Term
1. _____ is idiopathic high blood pressure that usually goes undetected due to a lack of symptoms. |
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Definition
PRIMARY/ESSENTIAL HYPERTENSION |
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Term
2. Primary/essential hypertension represents _____% of hypertension cases. |
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Definition
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Term
3. 4 causes of secondary hypertension. |
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Definition
1) CUSHINGS DISEASE, 3) PRIMARY ALDOSTERONISM, 3) PHEOCHROMOCYTOMA, 4) COARCTATION OF THE AORTA |
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Term
4. 9 risk factors of hypertension. |
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Definition
1) FAMILY HISTORY, 2) AGE, 3) MALE GENDER, 4) BLACK RACE, 5) OBESITY, 6) HIGH SODIUM DIET, 7) GLUCOSE INTOLERANCE, 8) SMOKING, 9) HEAVY ALCOHOL CONSUMPTION |
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Term
5. What is the best way to diagnose hypertension. . |
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Definition
TAKE BP AT THE SAME TIME OF DAY AND RECORD IT OVER A PERIOD OF DAYS |
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Term
6. If one has hypertension, there will be ophthalmic changes in the _____ of the eyes. |
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Definition
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Term
7. _____ is thong term effect of hypertension, so we should run kidney function tests when one presents with hypertension. |
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Definition
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Term
8. If one has hypertension, there will be a _____ in an ECG. |
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Definition
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Term
9. 7 steps in the pathyphysiology of hypertension. |
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Definition
1) HYPERTENSION DAMAGES THE WALLS OF THE SYSTEMIC VESSELS, 2) PROLONGED VASOCONSTRICTION AND HIGH PRESSURE CAUSES THE VESSELS TO THICKEN, 3) ARTERIAL SMOOTH MUSCLE UNDERGOES HYPERTROPHY, 4) TUNICA INTIMA AND MEDIA UNDERGO FIBROMUSCULAR THICKENING LEADING TO NARROWING OF THE LUMEN, 5) VESSELS BECOME PERMANENTLY NARROWED, 6) HYPERTENSIVE INJURY CAUSES INFLAMMATION TO INCREASE THE PERMEABILITY OF THE VASCULAR ENDOTHELIUM, 7) AS PERMEABILITY INCREASES MORE IONS ENTER THE VESSEL WALLS CAUSING FURTHER THICKENING |
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Term
10. When _____ occur, hypertension is usually far advanced. |
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Definition
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Term
11. 7 manifestations of hypertension. |
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Definition
1) UNSTEADINESS, 2) WALKING HEADACHE, 3) BLURRED VISION, 4) DEPRESSION, 5) RENAL DYSFUNCTION, 6) RETINAL CHANGES, 7) SIGNS OF VENTRICULAR FAILURE SUCH AS DYSPNEA OR EXERTION |
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Term
12. 4 hypertensive death related causes. |
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Definition
1) STROKE, 2) MI, 3) RENAL FAILURE, 4) ENCEPHALOPATHY |
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Term
13. _____ is a CVA when a blood clot lodges in a vessel leading to ischemic hypoxia. |
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Definition
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Term
14. _____ is a CVA when a clot comes from a far away source. |
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Definition
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Term
15. _____ is a CVA caused by bleeding. |
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Definition
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Term
16. Hypertension is the primary cause of _____ strokes. |
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Definition
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Term
17. _____ are small stroke like incidents that last 10 minutes or less. It leads to a loss in a patients senses. |
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Definition
TIA (TRANSIENT ISCHEMIC ATTACK) |
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Term
18. If one has a TIA, a patient will experience these 2 symptoms. |
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Definition
1) BRUITS, 2) THEY WILL SEE FLOATERS |
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Term
19. For something to be diagnosed as a stroke, symptoms must remain for _____ hours. |
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Definition
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Term
20. If a patient has a thrombotic stroke, _____ can be administered to bust out the clot that’s blocking the brain, and restore blood flow. This is able to completely resolve the stroke leading too complications. |
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Definition
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Term
21. Strokes tame time to _____ to completion. It might not look severe at first, but the next day the patient could look much worse. |
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Definition
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Term
22. Once a patient has completed a stoke they should work on _____ as quick as possible. |
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Definition
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Term
23. _____ and _____ are 2 agents used to treat thrombotic and embolic strokes. They must not be administered to a patient with a hemorrhagic stroke because they will bleed to death. |
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Definition
FIBRINOLYSIS AND FIBRINOLYTIC AGENTS |
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Term
24. 13 risk factors of cerebrovascular disease. |
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Definition
1) ATHEROSCLEROSIS, 2) HYPERTENSION, 3) HIGH CHOLESTEROL, 4) FAMILY HISTORY, 5) OBESITY, 6) SEDENTARY LIFESTYLE, 7) ORAL CONTRACEPTIVES, 8) SMOKING, 9) COAGULATION DISORDERS, 10) DEHYDRATION, 11) CHRONIC HYPOXIA, 12) CIGARETTE SMOKING |
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Term
25. 4 manifestations of a left hemispheric stroke. |
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Definition
1) RIGHT SIDED HEMIPLEGIA, 2) SLOW AND CAUTIOUS BEHAVIOR, 3) RIGHT VISUAL FIELD DEFECT, 4) EXPRESSIVE, RECEPTIVE OR GLOBAL DYSPHASIA |
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Term
26. 7 manifestations of a right hemispheric stroke. |
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Definition
1) LEFT SIDED HEMIPLEGIA, 2) SPATIAL-PERCEPTUAL DEFICITS, 3) IMPULSIVE BEHAVIOR, 4) DISTRACTABILITY, 5) DENIAL, 6) LEFT VISUAL FIELD DEFECTS, 7) PERSEVERATION (REPEATING A WORD OVER AND OVER) |
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Term
27. _____ is a medium by which we get transmission of a lot of different systems for the body. |
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Definition
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Term
28. The normal blood volume in the human body is _____. |
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Definition
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Term
29. _____is the fluid part of blood. |
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Definition
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Term
30. Plasma makes up _____% of blood. |
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Definition
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Term
31. _____ is a measure of albumin acting like a giant sponge that osmotically attracts fluids and holds the fluids together. It is due to the osmotic pressure created by solutes in the fluid. |
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Definition
COLLOID OSMOTIC PRESSURE (COP) |
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Term
32. Most plasma proteins are manufactured and synthesized by the _____. |
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Definition
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Term
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Definition
1) LIVER HYPERTENSION, 2) HYPOALBUMINEMEA, 3) EXCESS ALDOSTERONE |
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Term
34. Plasma is made up of _____% water, and _____% proteins. |
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Definition
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Term
35. _____ are the antibody making cells in the body. |
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Definition
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Term
36. _____ are antibodies that are the primary immune responders. |
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Definition
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Term
37. IgM antibodies are responsible for _____. |
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Definition
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Term
38. _____ are antibodies that are the secondary immune responders. |
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Definition
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Term
39. _____ are the most abundant immunoglobulin’s in the body. |
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Definition
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Term
40. IgG antibodies respond immediately after _____. |
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Definition
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Term
41. _____ are antibodies found in allergies and hypersensitivity responses. |
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Definition
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Term
42. _____ are antibodies found in most of bodily fluid secretions. |
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Definition
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Term
43. _____ is the main clotting protein in our blood. |
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Definition
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Term
44. _____ is the total amount of blood cells and blood cell fragments due to the RBC volume and the quantity of red cells. |
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Definition
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Term
45. _____ is another name for hematocrit. |
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Definition
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Term
46. A normal person has _____ platelets in their blood stream. |
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Definition
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Term
47. A normal person has _____ leukocytes in their blood stream. |
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Definition
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Term
48. Men have _____ erythrocytes in their blood stream. |
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Definition
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Term
49. Women have _____ erythrocytes in their blood stream. |
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Definition
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Term
50. _____ tissue is where RBC’s originate. |
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Definition
MYELOID TISSUE (RED BONE MARROW) |
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Term
51. During childhood, _____ are RBC producing. |
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Definition
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Term
52. As our bodies mature, the _____ and the _____ are the producers of RBC’s. |
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Definition
AXIAL SKELETON, AND THE ENDS OF LONG BONES |
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Term
53. _____ are the parent cells of all RBC’s. |
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Definition
HEMOCYTOBLAST (HEMATOPOETIC STEM CELL) |
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Term
54. _____ is an almost mature form of the RBC that has lost its nucleus. They consist of small cells which become biconcave. |
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Definition
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Term
55. There are _____ million hemoglobins per erythrocyte. |
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Definition
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Term
56. 1 molecule of hemoglobin can bind _____ oxygen cells. |
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Definition
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Term
57. _____ is the process of producing blood cells. |
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Definition
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Term
58. _____ is the iron element at the center of the hemoglobin molecule. |
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Definition
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Term
59. _____ is iron deficiency often due to blood loss or nutritional deficiencies. |
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Definition
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Term
60. The main stimulus for formation of erythrocytes is _____. |
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Definition
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Term
61. Decreased blood oxygen causes signals to be sent to the kidneys to release _____. This hormone causes an increase in the blood production of RBC in the bone marrow. |
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Definition
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Term
62. _____ is red blood cell making that occurs in the ends of long bones. |
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Definition
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Term
63. _____ is the inactive form of erythropoiesis formed in the liver. |
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Definition
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Term
64. _____ is secreted by the kidney that causes activation of erythropoitinogen. |
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Definition
RENAL ERYTHROPOITINOGEN FACTOR (EZ) |
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Term
65. _____ is the bone marrow that makes fatty cells used to beef up our bodies systems. |
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Definition
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Term
66. Erythrocytes have an average life span of _____ days. |
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Definition
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Term
67. Erythrocyte breakdown occurs in the _____, and the _____ is the chief cell used to break them down. |
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Definition
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Term
68. Hemoglobin is broken down into _____, which then becomes _____. |
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Definition
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Term
69. Bilirubin is responsible for giving _____ and _____ its color. |
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Definition
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Term
70. _____ coming off from the heme is recycled and reused in the future. |
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Definition
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Term
71. Excess bilirubin in the liver spills out in the skin causing _____. |
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Definition
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Term
72. Proerythroblasts are the precursor cells to _____. |
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Definition
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Term
73. Monoblasts are the precursor cells to _____. |
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Definition
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Term
74. Myeloblasts are the precursor cells to _____. |
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Definition
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Term
75. Lymphoblasts are the precursor cells to _____. |
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Definition
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Term
76. Megakaryocytes are the precursor cells to _____. |
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Definition
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Term
77. 3 types of granulocytes. |
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Definition
1) NEUTROPHILS, 2) BASOPHILS, 3) EOSINOPHILS |
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Term
78. _____ are the most numerous white blood cells in the body. They are important phagoc ytes in acute inflammation. |
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Definition
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Term
79. Neutrophils stain _____, and have a _____ nucleus. |
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Definition
LIGHT PURPLE; MULTI-LOBULED NUCLEUS |
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Term
80. _____are white blood cells that protect us against infections caused by parasitic worms, and they are involved in allergic reactions. |
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Definition
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Term
81. Eosinophils stain _____, and they have a _____ nucleus. |
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Definition
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Term
82. _____ are the least common white blood cells that are responsible for secreting heparin. |
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Definition
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Term
83. Basophils stain _____, and have a _____ nuclei. |
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Definition
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Term
84. 2 different types of agranulocytes. |
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Definition
1) LYMPHOCYTES, 2) MONOCYTES |
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Term
85. _____ are the second most common WBC’s that play an immunity role defense. |
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Definition
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Term
86. _____ lymphocytes are regulatory helper and suppressor cells. |
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Definition
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Term
87. _____ lymphocytes are responsible for antibody production. |
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Definition
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Term
88. Lymphocytes have a _____ stained cytoplasm. |
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Definition
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Term
89. _____ are key phagocytic agranulocytes that become macrophages in circulation as soon as they leave production. |
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Definition
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Term
90. _____ is a decrease in the number of white blood cells. |
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Definition
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Term
91. 3 causes of a shift to the left differential. |
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Definition
1) NEUTROPHILS RESPONDING TO ACUTE INFLAMMATION, 2) LEUKOCYTOSIS, 3) MORE BAND CELLS IN THE PLASMA |
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Term
92. 2 causes of a shift to the right differential. |
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Definition
1) INCREASED LYMPHOCYTES DURING CHRONIC INFLAMMATION, 2) LYMPHOCYTIC LEUKOCYTOSIS |
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Term
93. 88% neutrophils causes what? |
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Definition
SHIFT TO THE LEFT, ACUTE INFLAMMATION |
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Term
94. What is an example of a shift to the left? |
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Definition
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Term
95. 40% lymphocytes causes what? |
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Definition
SHIFT TO THE RIGHT, CHRONIC INFLAMMATION |
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Term
96. What is an example of a shift to the right? |
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Definition
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Term
97. _____ are cell fragments from megakaryocytes. |
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Definition
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Term
98. Platelets play a major role in _____ and _____, and they are released in response around tissue injury and clump together to stop bleeding. |
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Definition
HEMOSTASIS (STOP BLEEDING) AND COAGULATION |
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Term
99. The life span of platelets is typically _____ days. |
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Definition
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Term
100. The normal platelet count is between _____. |
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Definition
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Term
101. _____ is a deficiency in the number of WBC’s. |
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Definition
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Term
102. Leukopenia is a common side effect of _____. |
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Definition
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Term
103. _____ is having decreased numbers of neutrophils. |
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Definition
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Term
104. _____ is having decreased numbers of lymphocytes. |
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Definition
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Term
105. _____ is a decrease in the number of platelets (below 100,000 platelets/mm3). |
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Definition
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Term
106. Why do we worry about patients with thrombocytopenia. |
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Definition
WE WORRY ABOUT INTERNAL BLEEDING WHEN #’S FALL BELOW 40,000 |
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Term
107. What is another name for platelets? |
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Definition
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Term
108. How are platelets formed? |
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Definition
FROM CELL FRAGMENTS OF MEGAKARYOCYTES WHICH COME FROM STEM CELLS |
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Term
109. What is the average life span of platelets? |
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Definition
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Term
110. Red blood cells have surface _____ that have been given classification in the ABO system. |
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Definition
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Term
111. Type A blood has _____ on the RBC surface, and has _____ in plasma. |
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Definition
ANTIGEN A; TYPE B ANTIBODY |
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Term
112. Type B blood has _____ on the RBC surface, and has _____ in plasma. |
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Definition
ANTIGEN B; TYPE A ANTIBODIES |
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Term
113. Type AB blood has _____ on the RBC surface, and _____ in plasma. |
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Definition
ANTIGENS A AND B; NO A OR B ANTIBODIES |
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Term
114. Blood type AB is known as the _____. |
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Definition
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Term
115. Type O blood has _____ on the RBC surface, and _____ in plasma. |
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Definition
NO A OR B ANTIGENS; A AND B ANTIBODIES |
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Term
116. Type O blood is known as the _____. |
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Definition
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Term
117. _____ is when the D-antigen is present on the RBC surface. |
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Definition
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Term
118. _____ is when there is no D-antigen present on the RBC surface. |
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Definition
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Term
119. _____ is when there is a blood transfusion reaction for an RH(-) patient. The first time fused no reaction will occur, but the patient will develop antibodies against the RH factor causing a reaction each subsequent blood transfusion. |
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Definition
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Term
120. _____ is a condition when a RH(-) mother gets pregnant with an RH(+) baby. The mother body creates antibodies against the fetuses blood, causing a destruction of the baby’s erythrocytes. |
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Definition
ERYTHROBLASTOSIS FETALIS (HEMOLYTIC DISEASE OF THE NEWBORN) |
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Term
121. The dangers of erythroblastosis fetalis increases with _____. |
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Definition
EACH SUBSEQUENT PREGNANCY |
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Term
122. _____ is the medication given to the mother with erythroblastosis fetalis. It causes the mothers body to think it has already made antibodies to the D-antigen; fooling the mothers immune system to prevent the in utero attach on the fetus. |
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Definition
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Term
123. _____ means to stop bleeding. |
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Definition
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Term
124. 3 ways our bodies perform hemostasis. |
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Definition
1) VASCULAR SPASM, 2) PLATELET PLUG FORMATION, 3) FIBRIN FORMATION CAUSING COAGULATION |
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Term
125. _____ agents are direct dissolvers of blood clots. |
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Definition
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Term
126. _____ agents are clot prevents and prevent clots from forming, or already formed clots from getting any bigger. |
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Definition
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Term
127. _____ is having blood in the stool. |
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Definition
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Term
128. Blood clotting factors made in the liver are dependent on _____ for synthesis. |
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Definition
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Term
129. _____ is an immediate but temporary closure of a blood vessel resulting from contraction of smooth muscle within the blood vessels wall. |
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Definition
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Term
130. Vascular spasms are caused by these 2 bodily mechanisms. |
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Definition
1) NERVOUS SYSTEM REFLEXES, 2) CHEMICALS RELEASED FROM PLATELETS DURING FORMATION OF THE PLATELET PLUG |
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Term
131. In small vessels, vascular spasm can close the vessel _____. |
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Definition
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Term
132. When a blood vessel is damaged, the endothelium becomes torn and the underlying tissue is exposed. When this happen _____ adhere to the _____ in the connective tissue. |
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Definition
PLATELETS; COLLAGEN FIBERS |
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Term
133. When platelets adhere to the collagen fibers in the connective tissue during platelet plug formation, it causes the release of these 4 chemicals. |
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Definition
1) ADP, 2) THROMBOXANE, 3) SEROTONIN, 4) CHEMICALS INVOLVED IN COAGULATION |
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Term
134. _____ and _____ are 2 chemicals released by platelets that cause vascular spasm. |
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Definition
THROMBOXANE AND SEROTONIN |
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Term
135. _____ is a chemical released by platelets that makes their surface sticky, so additional platelets adhere to those already attached to the collagen fibers. |
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Definition
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Term
136. _____ is a chemical released by platelets that induces the aggregating platelets to release ADP, thromboxane, and other chemicals. |
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Definition
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Term
137. When platelets adhere to each other and release chemicals that cause other platelets to adhere, it forms an accumulating mass called a _____. |
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Definition
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Term
138. _____ is the formation of a blood clot that consists of a network of fibrin in which blood cells, platelets, and fluid become trapped. |
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Definition
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Term
139. Coagulation is dependent on coagulation factors present in the _____. |
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Definition
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Term
140. 3 main stages of coagulation. |
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Definition
STAGE 1) ACTIVATION OF FACTOR XII AND PRODUCTION OF PROTHROMBIN ACTIVATOR; STAGE 2) CONVERSION OF PROTHROMBIN TO THROMBIN BY PROTHROMBIN ACTIVATOR FACOR; STAGE 3) ENZYMATIC CONVERSION BY THROMBIN OF SOLUBLE FIBRINOGEN TO INSOLUBLE FIBRIN |
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Term
141. Coagulation operates via both the _____ and _____ pathways. |
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Definition
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Term
142. The _____ pathway of coagulation is turned on by factors that are outside the damaged blood vessel. If surrounding tissues are damages, a domino effect will occur that will form the prothrombin factor. |
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Definition
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Term
143. The _____ pathway of coagulation is when circulating clotting factors (factor XII) comes in contact with damaged blood vessels that starts a cascade which ends up as prothrombin factor. |
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Definition
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Term
144. _____ is needed in both the intrinsic and extrinsic coagulation pathways. |
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Definition
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Term
145. Once a blood clot forms, it condenses into a denser, compact structure through a process known as _____. |
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Definition
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Term
146. As a clot condenses _____ is squeezed out of the clot. |
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Definition
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Term
147. Consolidation of clots pull the edges of damaged vessels together, which may help _____, _____ and _____. |
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Definition
STOP BLOOD FLOW, REDUCE INFECTION, AND ENHANCE HEALING |
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Term
148. A clot usually dissolves within a few days after a clot formation by a process known as _____, which is a natural biochem reaction that occurs when the threat is over and the body returns its tissue to the original structure and function. |
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Definition
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Term
149. 3 steps of fibrinolysis. |
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Definition
1) PLASMINOGEN IS ACTIVATED BY THROMBIN FACTOR XII, TISSUE PLASMINOGEN ACTIVATOR, AND LYSOSOMAL ENZYMES RELEASED FROM DAMAGED TISSUES, 2) PLASMINOGEN FORMS PLASMIN, 3) PLASMIN HYDROLYZES FIBRIN DISSOLVING THE CLOT |
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Term
150. What is the difference between anticoagulants and thrombolytic agents? |
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Definition
ANTICOAGULANTS PREVENT FIBRIN FROM FORMING, WHILE THROMBOLITIC AGENTS DISSOLVE FIBRIN OR BUST THE CLOT |
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Term
151. _____ are medications that drive the production of plasmin to bust the clots. They are not anti-coagulants. |
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Definition
THROMBOLYTICS/FIBRINOLYTICS |
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Term
152. _____ do not dissolve clots, rather they prevents cots from forming or prevent existing clots from getting bigger. |
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Definition
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Term
153. _____ and _____ are common anticoagulant medications. |
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Definition
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Term
154. How does Coumadin work? |
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Definition
IT WORKS IN THE LIVER BY COMPETING WITH VITAMIN K. SINCE CLOTTING FACTORS ARE DEPENDENT ON VITAMIN K, COUMADIN WILL RESTRICT FIBRIN SYNTHESIS |
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Term
155. If patients eat foods with _____, it can counteract the effects of Coumadin. |
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Definition
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Term
156. How does heparin work? |
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Definition
IT WORKS IN THE PERIPHERY PREVENTING PROTHROMBIN FROM BEING CONVERTED TO THROMBIN |
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Term
157. Heparin takes up to _____hours to work. |
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Definition
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Term
158. _____ is an antidote for heparin overdose, which is made from fish sperm. |
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Definition
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Term
159. 3 signs of internal bleeding. |
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Definition
1) LARGE, DISTENDED HARD ABDOMEN, 2) FLANK PAIN, 3) BLOOD IN STOOL OR URINE |
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Term
160. 3 signs of over-coagulation. |
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Definition
1) EASY BRUISING, 2) PETECIAL HEMORRHAGES, 3) SHAVING CUTS THAT DO NOT STOP BLEEDING |
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Term
161. 2 coagulation factors found in our body. |
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Definition
1) FACTOR I- FIBRINOGEN, 2) FACTOR XII- FIBRIN STABILIZING FACTOR |
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Term
162. _____ is a test to determine clotting test times of people taking warfarin/Coumadin. |
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Definition
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Term
163. _____ is a test to determine clotting test times of people on heparin. |
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Definition
PARTIAL THROMBOPLASTIN TIME (PTT) |
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Term
164. The normal PTT time is between _____. |
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Definition
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Term
165. _____ is the standardized clotting times across the globe, it consists of a ration responsible for standardizing everything. |
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Definition
INTERNATIONAL NORMALIZED RATION (INR) |
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Term
166. The normal clotting time in the INR is between _____. |
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Definition
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Term
167. The normal ratio of INR is between _____ and _____. |
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Definition
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Term
168. The desirable anticoagulant effect of INR is between _____ and _____. |
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Definition
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Term
169. 3 components of a complete blood count. |
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Definition
1) WBC COUNT, 2) RBC COUNT, 3) PLATELET COUNT |
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Term
170. _____ is a test the counts the actual number of WBC’s per volume of blood. |
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Definition
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Term
171. _____ is a test that determines what types of WBC’s are present in the blood. |
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Definition
WHITE BLOOD CELL DIFFERENTIAL |
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Term
172. _____ is a test to determine the actual number of RBC’s per volume of blood. |
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Definition
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Term
173. _____ is a test to determine the amount of oxygen carrying protein in the blood. |
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Definition
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Term
174. _____ is a test to determine the rate of RBC production. |
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Definition
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Term
175. _____ is a test to determine the amount of space RBC’s take up in the blood. |
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Definition
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Term
176. _____ is a test to determine the number of platelets in a given volume of blood. |
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Definition
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Term
177. _____ is a test to measure the average size of RBC’s. |
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Definition
MEAN CORPUSCULAR VOLUME (MCV) |
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Term
178. MCV is an important in testing for _____. |
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Definition
ANEMIAS DUE TO B12 DEFICIENCY |
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Term
179. _____ is a test to calculate the amount of hemoglobin inside of the RBC’s. |
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Definition
MEAN CORPUSCULAR HEMOGLOBIN (MCH) |
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Term
180. _____ is a test to calculate the percentage of hemoglobin in red blood cells. |
|
Definition
MEAN CORPUSCULAR HEMOGLOBIN CONCENTRATION (MCHC) |
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Term
181. _____ is a test to determine how varied the size of RBC’s are in a sample. |
|
Definition
RED CELL DISTRIBUTION WIDTH (RDW) |
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Term
182. RDW helps determine the kind of _____ one may have. |
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Definition
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|
Term
183. _____ is the most life threatening skin carcinoma. |
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Definition
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Term
184. _____ for skin disorders serve as anti-inflammatory agents. |
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Definition
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|
Term
185. What is a cubitus ulcer? |
|
Definition
A BEDSORE (WHEELCHAIR BOUND PATIENT) |
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Term
186. Herpes zoster spreads along the _____. |
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Definition
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Term
187. _____ is a condition caused by a low number of circulating red cells, abnormally low number of hemoglobin, or both. |
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Definition
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Term
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Definition
1) BLOOD LOSS, 2) LACK OF OXYGEN DELIVERY TO CELLS/TISSUES, 3) DECREASED OXYGEN AFFINITY TO HEMOGLOBIN |
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Term
189. What increased oxygen’s affinity for hemoglobin? |
|
Definition
THE ACTUAL BINDING OF OXYGEN TO THE HEMOGLOBIN |
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Term
190. 3 things that decrease oxygen’s affinity for hemoglobin. |
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Definition
1) BINDING OF CO2 TO HEMOGLOBIN, 2) BINDING OF PROTONS TO SPECIFIC BASIC GROUPS, 3) BINDING OF CERTAIN ORGANIC PHOSPHATES |
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Term
191. _____ anemia is most common in menstruating women. |
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Definition
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|
Term
192. _____ anemia is due to an early destruction of RBC’s due to a pathology. |
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Definition
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|
Term
193. _____ is a major pathology that causes hemolytic anemia. |
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Definition
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|
Term
194. _____ anemia is caused by a vitamin B-12 deficiency. |
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Definition
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|
Term
195. 3 different types of nutritional deficiency anemia’s. |
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Definition
1) PERNICIOUS ANEMIA, 2) FOLIC ACID DEFICIENCY ANEMIA, 3) IRON DEFICIENCY ANEMIA |
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Term
196. _____ anemia is caused by a bone marrow depression causing a lack of adequate production of RBC’s. it is usually accompanied by depressions in other formed elements of the blood. |
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Definition
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|
Term
197. 9 signs and symptoms of general anemia. |
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Definition
1) FATIGUE/WEAKNESS, 2) PALLOR, 3) TACHYCARDIA, 4) ANXIETY, 5) SYSTOLIC MURMUR, 6) VENTRICULAR HYPERTROPHY, 7) CHF, 8) ERYTHROPOEISIS, 9) ANGINA AND NIGHT CRAMPS |
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Term
198. _____ anemia’s are due to an early destruction of red blood cells either due to extrinsic or intrinsic causes. |
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Definition
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Term
199. _____ is an intrinsic cause of hemolytic anemia that is caused by an autosomal trait causing spherical-shaped RBC’s rather than biconcave disc shape. |
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Definition
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Term
200. In hereditary spherocytosis, the tight spherical shape RBC’s will hemolyze and be _____ early in mass numbers. |
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Definition
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Term
201. _____ is sometimes used as the treatment of hemolytic anemia’s for adults, but it will not work in children. |
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Definition
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Term
202. _____ are conditions inherent to hemoglobin molecules. |
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Definition
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Term
203. Hemoglobin usually consists of _____ polypeptide chains. |
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Definition
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Term
204. Hemoglobinopathies occur when one hemoglobin polypeptide chain is substituted with an _____. |
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Definition
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Term
205. Sickle cell anemia is a condition when one of the hemoglobin amino acids is substituted with _____ rather than a polypeptide chain. |
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Definition
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Term
206. Sickle cell anemia typically occurs in _____. |
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Definition
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Term
207. _____ are sickle cells. |
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Definition
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Term
208. _____ are normal hemoglobin cells. |
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Definition
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Term
209. Is a person contains the _____ and _____ cells, they are carriers for the sickle cell trait. |
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Definition
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|
Term
210. If a person contains the _____ and _____ cells, they will have sickle cell anemia. |
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Definition
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|
Term
211. Why is sickle cell anemia more dangers in a low oxygen environment. |
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Definition
IN LOW OXYGEN ENVIORNMENTS, THE SICKLE HBS BECOMES AN AGGREGATE AND BOWS OUT THE CELL |
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Term
212. A sickling crisis can cause death by leading to _____. |
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Definition
HEMOLYSIS AT LOG-JAMMED CAPILLARIES |
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Term
213. Factors that precipitate sickling are related to _____. |
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Definition
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|
Term
214. 6 low oxygen situations that can lead to sickling. |
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Definition
1) EXERCISE, 2) HYPOXIA, 3) ACIDOSIS, 4) DEHYDRATION, 5) INFECTION, 6) REDUCED OXYGEN TENSION IN SLEEP |
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Term
215. 5 symptoms of sickle cell crisis. |
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Definition
1) SWOLLEN HANDS AND FEET, 2) STROKE, 3) MI, 4) KIDNEY FAILURE, 5) HEMOLYSIS |
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Term
216. What causes the painful crisis of sickle cell? |
|
Definition
VESSEL OCCLUSION THAT MAY APPEAR SUDDENLY IN ALMOST ANY PART OF THE BODY |
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Term
217. Hemoglobin is composed of _____, which is made up of 4 folded polypeptide chains, and 4 _____. |
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Definition
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|
Term
218. Each hemoglobin molecule can carry _____ molecules of oxygen. |
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Definition
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|
Term
219. When hemoglobin is called _____ when carrying oxygen, and _____ when not carrying oxygen. |
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Definition
OXYHEMOGLOBIN, REDUCED HEMOGLOBIN |
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Term
220. Hemoglobin can also combine with _____ to transport it from the tissues to the lungs for excretion. |
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Definition
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|
Term
221. _____ is a condition that results from absent or defective synthesis of either the alpha or beta chains of hemoglobin’s causing a decrease in the size of cells and a change in the MCV (size of RBC). |
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Definition
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|
Term
222. _____ is a repeated defect in the beta-chain synthesis of hemoglobin. |
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Definition
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Term
223. B-thalassemias is most common in the _____ population. |
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Definition
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|
Term
224. If a person receives the B-thalassemias trait from both parents it will cause transfusion-dependent anemia leading to death by _____. |
|
Definition
HEMOCHROMATOSIS (EXCESS IRON) |
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|
Term
225. 6 symptoms present in children with B-thalassemias. |
|
Definition
1) GROWTH RETARDATION, 2) SPLEENOMEGALY, 3) HEPATOMEGALY, 4) INCREASED RBC DISTRUCTION, 5) INCREASED STIM FOR HEMATOPORIESIS CAUSING BONE MARROW EXPANSION, 6) THINNING OF THE CORTICAL BONE |
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Term
226. A-thalassemias is most common in _____. |
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Definition
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|
Term
227. Most severe cases of A-thalassemias occurs in _____. |
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Definition
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|
Term
228. Anemia occurs in A-thalassemias due to _____ and _____. |
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Definition
DEFECTIVE HEMOGLOBIN PRODUCTION, ACCUMULATION OF UNPAIRED GLOBIN CHAINS |
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Term
229. What is more severe alpha or beta thalassemias? |
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Definition
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|
Term
230. Individuals with the mildest form of A-thalassemias are usually _____ having mild _____. |
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Definition
ASYMPTOMATIC, MICROCYTOSIS |
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Term
231. The minor form of A-thalassemias is associated with these 4 conditions. |
|
Definition
1) MILD MICROCYTITC HYPOCHROMIC RETICULOCYTOSIS (IMMATURE RBC’S), 2) BONE MARROW HYPERPLASIA, 3) INCREASED SERUM IRON CONCENTRATION, 4) MODERATE SPLENOMEGALY |
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Term
232. 2 factors that cause microcytic-hypochromic anemia in A-thalassemias. |
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Definition
1) REDUCED HEMOGLOBIN SYNTHESIS AND IMBALANCE IN GLOBIN CHAIN PRODUCTION, 2) UNPAIRED CHAINS ACCUMULATE IN RED CELLS CAUSING RBC DESTRUCTION AND ANEMIA |
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Term
233. The most common disorder associated with an inherited enzyme deficiency is _____. |
|
Definition
G-6-PD (GLUCOSE-6-PHOSPHO DEHYDROGENASE) |
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|
Term
234. G-6-PD causes the direct oxidation of hemoglobin which forms a _____. |
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Definition
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|
Term
235. 3 risk factors of the formation of methemoglobin. |
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Definition
1) THE CELL IS NOT FUNCTIONAL, 2) DENATURED HEMOGLOBIN MOLECULE RESULTS, 3) THEY CAN NOT MAKE IT THROUGH THE TIGHT CIRCULATORY AREAS OF THE BODY |
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Term
236. G-6-PD eventually results in _____. |
|
Definition
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|
Term
237. 6 extrinsic anemia factors. |
|
Definition
1) DRUGS, 2) CHEMICALS, 3) TOXINS, 4) ARTIFICIAL MECHANICAL BODY STRUCTURES, 5) BURNS, 6) ANY DIRECT INJURY TO THE RBC’S THEMSELVES |
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|
Term
238. _____ means the size of the RBC is normal. |
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Definition
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|
Term
239. _____ means the size of the RBC is small. |
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Definition
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|
Term
240. The most common cause of microcytic RBC’s is _____. |
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Definition
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|
Term
241. _____ means the size of the RBC is large. |
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Definition
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Term
242. _____ means the color of the RBC is normal. |
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Definition
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Term
243. _____ means there is a decrease in the color of the RBC. |
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Definition
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|
Term
244. These 2 criteria must be met for anemia to be classified as nutritional anemia. |
|
Definition
1) THERE MUST BE A DEFECIENCY OR LACK OF A NUTRIENT ALONE CAUSING THE ANEMIA, 2) HAVING THE NUTRIENT PROVIDED CORRECTS THE ANEMIA |
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|
Term
245. 4 symptoms associated with nutritional anemias. |
|
Definition
1) PALLOR, 2) WEAKNESS, 3) LETHARGY, 4) HEART RATE ELEVATION |
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Term
246. 2 additional symptoms associated with iron deficiency anemias. |
|
Definition
1) SOARS IN THE CORNER OF THE MOUTH, 2) PICA (EATING DIRT, CLAY OR ICE) |
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|
Term
247. If blood was drawn in a patient with iron deficiency anemia, the red blood cells would be _____ and _____. |
|
Definition
MICROCYTIC AND HYPOCHROMIC |
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Term
248. 3 classes of nutritional anemias. |
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Definition
1) IRON DEFICIENCY ANEMIA, 2) PERNICIOUS ANEMIA, 3) FOLIC ACID DEFICIENCY ANEMIA |
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Term
249. _____ is essential for heme, in that each heme unit has one of these molecules at its center to form hemoglobin. |
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Definition
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|
Term
250. 3 causes of iron deficiency during pregnancy and pre-natal development. |
|
Definition
1) IF MOM IS IRON DEFICIENT SO IS THE BABY, 2) MOMS WHO ARE IRON DEFICIENT AND BREAST FEED WILL TRANSFER IT TO THE BABY, 3) IF NOT BREAST FEEDING COWS MILK MUST BE IRON FORTIFIED |
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Term
251. What is the main symptom of iron deficiency during the infant/toddler years? |
|
Definition
PICA (EATING THINGS THAT ARE NOT NORMALLY EDIBLE) |
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|
Term
252. During the teenage years girls on their _____ and _____ are susceptible to iron deficiency. |
|
Definition
MENSTRUAL CYCLE, NOT EATING PROPERLY |
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Term
253. The most vulnerable time of iron deficiency in the adult years is during _____. |
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Definition
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Term
254. _____ is anemia caused by a lack of vitamin B12/intrinsic factor. |
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Definition
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Term
255. Pernicious anemia causes _____ RBC’s as well as _____ anemias. |
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Definition
MACROCYTIC, MEGALOBLASTIC |
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Term
256. The _____ is necessary for vitamin B-12 to be absorbed in the intestine. |
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Definition
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Term
257. Patients with pernicious anemia can have these 3 CNS related effects. |
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Definition
1) NEUROLOGIC DEGENERATION OF DORSAL AND LATERAL SPINAL COLUMNS, 2) PARASTHESIA, 3) SPASTIC ATAXIA |
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Term
258. Folic acid anemias cause _____ RBC’s and _____ anemias. |
|
Definition
MACROCYTIC, MEGALOBLASTIC |
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Term
259. _____ anemias usually have normal size and color RBC’s. |
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Definition
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Term
260. 3 causes of a shift to the right in the oxygen saturation curve. |
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Definition
1) EXERTION, 2) INFECTION (TEMP INCREASE), 3) SURGERY |
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Term
261. _____ is polycythemia caused by dehydration or fluid loss. |
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Definition
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Term
262. _____ is polycythemia caused by anything that increases the bone marrow production of RBC’s. |
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Definition
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Term
263. _____ polycythemia is caused by a congenital issue leading to a proliferative disease in the bone marrow causing an accelerated production of RBC’s. |
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Definition
PRIMARY POLYCYTHEMIA (POLYCYTHEMIA VERA) |
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Term
264. Polycythemia vera causes _____ blood due to extra RBC’s, and problems arise due to _____. |
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Definition
VISCOUS; INCREASED BLOOD VISCOSITY |
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Term
265. The skin of a patient with polycythemia vera will appear _____. |
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Definition
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Term
266. _____ is the treatment of polycythemia vera. |
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Definition
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Term
267. 7 conditions associated with polycythemia vera. |
|
Definition
1) BLOOD CLOTS, 2) HYPERTENSION, 3) PAINFUL ITCHING SENSATIONS, 4) SLUGGISH BLOOD FLOW, 5) PROBLEMS HEARING AND CONCENTRATING, 6) IRRITABILITY, 7) THROMBOSIS |
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Term
268. Suppressing the bone marrow of polycythemia vera requires _____, which is risky due to the side effects. |
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Definition
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Term
269. Polycythemia vera may lead to _____ or _____ due to stagnation and build-up of thick blood. |
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Definition
THROMBOSIS, FRANK HEMORRHAGING |
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Term
270. _____ disorders are caused by platelet issues and anything that causes a decrease in platelet production. |
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Definition
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Term
271. _____ is a condition when there is less than 100,000 platelets in the body. |
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Definition
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Term
272. 3 mechanisms behind thrombocytopenia. |
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Definition
1) DECREASE IN PLATELET PRODUCTION BY THE BONE MARROW, 2) INCREASED POOLING OF PLATELETS IN THE SPLEEN CAUSING SPLEENOMEGALY, 3) DECREASED PLATELET SURVIVAL |
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Term
273. 4 causes of thrombocytopenia. |
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Definition
1) VIRAL INFECTIONS, 2) DRUGS, 3) IDIOPATHIC, 4) BONE MARROW PROBLEMS |
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Term
274. 3 signs and symptoms of thrombocytopenia. |
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Definition
1) EASY BRUISING, 2) NOSE BLEEDS, 3) SHAVING CUTS THAT DON’T STOP BLEEDING |
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Term
275. _____ occurs 1-4 weeks after a viral infection, causing bruising and a generalized petechial rash that often occurs with acute onset. |
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Definition
IDIOPATHIC THROMBOCYTOPENIC PURPA (ITP) |
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Term
276. 4 conditions associated with idiopathic thrombocytopenic purpa. |
|
Definition
1) ASYMMETRICAL BLEEDING FOUND MOST FREQUENTLY COVERING THE LEGS, 2) HEMORRHAGE BULLAE OF THE MUCOUS MEMBRANES, 3) EPISTAXIS (NOSE BLEEDS), 4) SPONTANEOUS HEMORRHAGES THAT LAST 1-2 WEEKS |
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Term
277. _____ is used to slow down the platelet production in idiopathic thrombocytopenic purpa. |
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Definition
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Term
278. _____ is a condition that begins as a systemic clotting issue that ends up as a bleeding problem secondary to some other event. |
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Definition
DISIMINATED INTRAVASCULAR COAGULATION (DIC) |
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Term
279. _____ is the most common cause of disiminated intravascular coagulation. |
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Definition
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Term
280. 8 causes of disiminated intravascular coagulation. |
|
Definition
1) MASSIVE TRAUMA, 2) BURNS, 3) SEPSIS, 4) SHOCK, 5) MALIGNANT DISEASE, 6) MENONGOCOCCEMIA, 7) OBSTETRIC COMPLICATIONS, 8) SNAKE BITES |
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Term
281. _____ is a condition associated with disiminated intravascular coagulation that has a very high mortality rate. |
|
Definition
BLEEDING FROM EVERY ORIFICE |
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Term
282. What is the treatment of disiminated intravascular coagulation? |
|
Definition
STOP THE UNDERLYING PATHOLOGY AND ADMINISTER HEPARIN TO SUPPLY FRESH COAGULATION FACTORS AND PLATELETS |
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Term
283. _____ is a common bleeding pathology within the body. |
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Definition
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Term
284. _____ is classic hemophilia, which is an x-linked recessive disorder manifesting in males that is transmitted by females. |
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Definition
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Term
285. Hemophilia A is caused by a defect of _____, which is prevented from participating in the intrinsic clotting pathway. |
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Definition
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Term
286. _____ is the most common hemophilia and accounts for 80-85% of all cases. |
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Definition
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Term
287. Thrombin is nor normally found in circulating blood. In order for thrombin to be made in the intrinsic clotting pathway, prothrombin (factor II) requires _____ and _____ to be converted to thrombin. |
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Definition
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Term
288. _____ is the second most common hemophilia (15%) caused by an x-linked recessive trait that is clinically indistinguishable from a factor VIII deficiency. |
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Definition
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Term
289. Hemophilia B is caused by a _____ deficiency. |
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Definition
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Term
290. Hemophilia B is also referred to as _____. |
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Definition
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Term
291. How can a doctor distinguish between hemophila A and B? |
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Definition
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Term
292. _____ is a hemophilia that results from an autosomal recessive disease that occurs equally in males and females. |
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Definition
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Term
293. Hemophilia C is caused by a _____ deficiency. |
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Definition
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Term
294. In patients with hemophilia C, bleeding is usually _____ than in hemophilia A or B. |
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Definition
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Term
295. Hemophilia C does not present at birth, but rather around _____ when clotting factors begin to fail. |
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Definition
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Term
296. 4 symptoms of patients with hemophilia C. |
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Definition
1) EASY BRUISING, 2) BLEEDING GUMS OR JOINTS, 3) BLOOD IN URINE OR STOOL, 4) EPISTAXIS (NOSE BLEEDS) THAT DO NOT STOP |
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Term
297. _____ is a condition caused by a defect in a different subunit, co-factor, or carrier protein of factor VIII. It is an inherited autosomal dominant trait that is different from hemophilia A. |
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Definition
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Term
298. In von wilderband disease, rapidly circulating platelets are unable to stick to _____ and _____ cannot be formed. |
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Definition
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Term
299. What is mainly affected by von wildebrand disease? |
|
Definition
ENDOTHELIAL CELLS THAT LINE VESSELS |
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Term
300. _____ is the usual treatment of von wildebrand disease, which caused factor VIII activity to increase for several days. It temporarily induced endogenous synthesis of factor VIII. |
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Definition
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Term
301. _____ is a life threatening condition that causes a rapid proliferation of immature WBC’s by the bone marrow. |
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Definition
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Term
302. 11 endogenous findings associated with leukemia. |
|
Definition
1) ABNORMAL PATHOLOGICAL CELLS, 2) EXCESS BONE MARROW PROLIFERATION, 3) REPLACEMENT OF BONE MARROW WITH WBC’S (BONE MARROW DEPRESSION), 4) EXCESS NON-FUNCTIONAL WBC’S IN BLOOD, 5) SPLENOMEGALY, 6) HEPATOMEGALY, 7) LYMPHANDENOAPTHY, 8) WEIGHT LOSS, 9) NIGHT SWEATS, 10) LOW GRADE FEVER, 11) HYPERURICEMIA |
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Term
303. If a patient has leukemia, _____ and _____ will result due to decreased platelet and erythrocyte production. |
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Definition
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Term
304. _____ is present in 90% of all leukemia patients. |
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Definition
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Term
305. 6 CNS related conditions associated with leukemia. |
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Definition
1) ENCEPHALOPATHY, 2) MENINGITIS, 3) CRANIAL NERVE PALSIES, 4) BLURRED VISION, 5) HEADACHE, 6) SEIZURES |
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Term
306. The 2 acute forms of leukemia are _____ and _____. |
|
Definition
ACUTE LYMPHOCYTIC LEUKEMIA; ACUTE MYELOTIC LEUKEMIA OR ACUTE GRANULOCYTIC LEUKEMIA |
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Term
307. _____ is an acute form of leukemia with a sudden onset most commonly seen in children between the ages of 2 and 4. |
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Definition
ACUTE LYMPHOCYTIC LEUKEMIA |
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Term
308. In acute lymphocytic leukemia _____ are differentiated poorly. |
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Definition
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Term
309. The onset of acute lymphocytic leukemia is _____. |
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Definition
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Term
310. _____ accounts for 2/3 of all leukemia cases. |
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Definition
ACUT E LYMPHOCYTIC LEUKEMIA |
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|
Term
311. 6 symptoms associated with acute lymphocytic leukemia. |
|
Definition
1) FEVER, 2) MUSCLE FATIGUE, 3) BLEEDING, 4) BONE PAIN, 5) BONE MARROW DYSFUNCTION, 6) ANEMIA |
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Term
312. More than _____% of children with acute lymphocytic leukemia have complete remission, while _____% of children live 5 years or longer. 90%, |
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Definition
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Term
313. _____ is an acute form of leukemia with a low survival rate. It affects all the –phil cells, and symptoms arise abruptly which are similar to those of acute lymphocytic anemia. |
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Definition
ACUTE MYELOTIC LEUKEMIA (ACUTE GRANULOCYTIC LEUKEMIA) |
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Term
314. _____ is the most common type of leukemia found in adults. |
|
Definition
ACUTE MYELOTIC OR GRANULOCYTIC LEUKEMIA |
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Term
315. Acute myelotic leukemia is treated with intensive chemo to cause _____ of the bone marrow. |
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Definition
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Term
316. Only about _____% of acute myelotic leukemia patients who receive chemo will achieve long-term disease free survival. |
|
Definition
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|
Term
317. The more _____ a cell, the more malignant they can become and lead to a more progressive cancer. |
|
Definition
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Term
318. These are the 2 types of chronic leukemia’s. |
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Definition
1) CHRONIC LYMPHOCYTIC LEUKEMIA, 2) CHRONIC MYELOCYTIC OR GRANULOCYTIC LEUKEMIA |
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|
Term
319. _____ is a form of chronic leukemia that is often a disorder in older adults between the ages of 50-70. The disease consists of slightly differentiated cells which causes the disease to progress _____. |
|
Definition
CHRONIC LYMPHOCYTIC LEUKEMIA; SLOWLY |
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|
Term
320. Is chronic lymphocytic leukemia more common in men or women? |
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Definition
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Term
321. Unlike acute lymphocytic leukemia, in chronic lymphocytic leukemia the chronic cells are more _____ and easily identifiable. |
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Definition
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Term
322. Chronic lymphocytic leukemia cells develops _____, but _____ are affected. |
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Definition
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Term
323. Patients with chronic lymphocytic anemia are usually diagnosed when they are _____, and they life expectancy is _____ than those patients with acute lymphocytic anemia. |
|
Definition
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|
Term
324. _____ is a chronic form of leukemia that occurs in patients between the ages of 30-50. |
|
Definition
CHRONIC MYELOCYTIC OR GRANULOCYTIC LEUKEMIA |
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|
Term
325. In chronic myelocytic or granulocytic leukemia, bone marrow cells have the _____ chromosome that occurs in mitotic error with a shortened arm on chromosome _____. |
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Definition
PHILADELPHIA CHROMOSOME; CHROMOSOME 22 |
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|
Term
326. Chronic myelocytic or granulocytic leukemia patients are often _____ when diagnosed. |
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Definition
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Term
327. About _____% of chronic myelocytic or granulocytic leukemia patients enter an accelerated phase characteristic of acute leukemia which leads to _____ survival rates. |
|
Definition
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|
Term
328. 13 symptoms associated with chronic myelocytic or granulocytic leukemia. |
|
Definition
1) SPLENOMEAGALY, 2) IMMATURE LEUKOCYTES, 3) HIGH WBC COUNT, 4) ANEMIA, 5) THROMBOCYTOPENIA, 6) WEAKNESS, 7) FATIGUE, 8) DYSPNEA, 9) LOW GRADE FEVER, 10) NIGHT SWEATS, 11) WEIGHT LOSS, 12) HEPATOMEGALY, 13) LYMPHADENOPATHY |
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|
Term
329. 4 caused associated with chronic myelocytic or granulocytic leukemias. |
|
Definition
1) RADIATION, 2) CHEMICALS LIKE BENZENE, 3) TWINS, 4) ANIMALS |
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|
Term
330. _____ are cancers of WBC’s (lymphocytes). |
|
Definition
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|
Term
331. _____ is a malignant disorder or lymphoid tissue that constitutes 40% of all malignant lymphomas seen in younger adults between the ages of 20-40. |
|
Definition
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|
Term
332. In hodgkins lymphoma, lymphoid tissue is characterized by the presence of _____ upon biopsy. |
|
Definition
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|
Term
333. Manifestations of hogdkins lymphoma are due to rapid proliferation of abnormal _____. |
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Definition
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|
Term
334. Hodgkins lymphoma often begins in lymph tissue above the _____, which usually sends people to see the doctor. |
|
Definition
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|
Term
335. 10 symptoms associated with hodgkins lymphoma. |
|
Definition
1) PAINLESS ENLARGEMENT OF LYMPHOID TISSUE, 2) SPLENOMEGALY, 3) FEVER, 4) NIGHT SWEATS, 5) WEIGHT LOSS, 6) FATIGUE, 7) PURITIS, 8) WEAKENED IMMUNE SYSTEM, 9) INCREASED WBC COUNT, 10) AFFECTED LIVER, LUNGS, DIGESTIVE TRACT AND CNS |
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Term
336. 7 medical tests used to identify hodgkins lymphoma. |
|
Definition
1) LYMPH NODE BIOPSY, 2) CT SCANS OF ABDOMEN AND PELVIC LYMPH NODES, 3) LYMPHANGIOGRAPHY, 4) LAPAROTOMY, 5) LIVER BIOPSY, 6) BONE MARROW BIOPSY, 7) X RAYS AND LAB WORK |
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Term
337. In _____ of ann arbor staging of hodgkins lymphoma, a single lymph node or single extralymphatic region is affected. |
|
Definition
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|
Term
338. In _____ of ann arbor staging of hodgkins lymphoma, there is involvement of lymph nodes on the same side of the diaphragm. |
|
Definition
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|
Term
339. In _____ of ann arbor staging of hodgkins lymphoma, there is involvement of lymph nodes on both sides of the diaphragm. |
|
Definition
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|
Term
340. In _____ of ann arbor staging of hodgkins lymphoma, there is diffused or disseminated involvement of lymph nodes. |
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Definition
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|
Term
341. The incidence rate of hodgkins lymphoma is _____ cases a year with _____ deaths. |
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Definition
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|
Term
342. _____ is a type of lymphoma that typically affects immune suppressed people over the age of 50, which could be virus related. It consists of a group of neoplastic disorders of lymphoid tissue not characterized by reed-sternberg cells. |
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Definition
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|
Term
343. In patients with non-hodgkins lymphoma, there is early involvement of the lymph nodes in the _____ area. |
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Definition
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|
Term
344. There is less than _____% chance of curability of patients with non-hodgkins lymphoma. |
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Definition
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|
Term
345. Non-hodgkins lymphomas are divided into 3 main groups according to the cell types involved which are _____, _____ and _____. |
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Definition
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|
Term
346. The diagnosis of non-hodgkins lymphoma is through a _____. |
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Definition
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|
Term
347. 4 signs and symptoms of patients with non-hodgkins lymphoma. |
|
Definition
1) EARLY INVOLVELENT OF OROPHARYNGEAL LYMPHOID TISSUE, 2) CONSTITUTIONAL SIGNS, 3) LEUKEMIC TRANSFORMATIONS WITH HIGH NUMBERS OF WBC’S, 4) INCREASED SUSCEPTIBILITY TO INFECTIONS |
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Term
348. The incidence rate of non-hodgkins lymphoma is _____ new cases a year with _____ deaths. |
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Definition
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Term
350. _____ is a condition that consists of bone tumors of B-lymphocytes commonly affecting people between the ages of 50 and 60. |
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Definition
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Term
351. Multiple myelomas causing B-cell neoplasms leads to an excess production of _____ and _____. |
|
Definition
IMMATURE AND MATURE PLASMA CELLS |
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Term
352. Multiple myeloma affecting B-cells can be detectable by _____ of the long bones, sternum, or skull. |
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Definition
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Term
353. Multiple myeloma is characterized by multiple malignant tumor masses of _____ scattered throughout the skeletal system and sometimes soft tissues. |
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Definition
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Term
354. Incidence of multiple myelomas is _____ times greater than all other malignant tumors of the bone combined. |
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Definition
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Term
355. Chronic stimulation of the mononuclear phagocytic system by these 3 things have been proposed causes of multiple myelomas. |
|
Definition
1) BACTERIA, 2) CHEMICALS, 3) VIRUSES |
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Term
356. In the pathophysiology of multiple myeloma, _____ arise from 1 clone of B-cells that produce abnormally large amounts of _____. |
|
Definition
MALIGNANT PLASMA CELLS; CLASS 1 IMMUNOGLOBULINS (IgG) |
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Term
357. Laboratory examinations of the bone marrow of patients with multiple myeloma shows proliferation of _____ and _____ cells with 20% or more having multinucleated cytoplasms containing multiple immunoglobulins (whits blobs). These cells often completely replace _____. |
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Definition
IMMATURE AND MATURE PLASMA CELLS; BONE MARROW |
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Term
358. _____ proteins, which are fragments of IgG/A are present in the urine and blood of over 60% of patients with multiple myeloma. |
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Definition
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|
Term
359. Bence jones proteins are proliferations of the _____. |
|
Definition
LIGHT CHAINS OF IMMUNOGLOBULINS (M-CHAIN) |
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Term
360. In multiple myeloma patients, there is a higher frequency of _____ correlated with the amount of protein found in urine, since the excreted light chains are through to be toxin to the renal tubules. |
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Definition
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Term
361. The malignant neoplasm of multiple myeloma usually does not metastasize outside of the _____, rather the destructive lesions typically erode the _____ and cause _____ that are observable on radiographs. |
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Definition
BONE; BONE; LYTIC LESIONS |
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Term
362. Lytic lesions of multiple myeloma patients are most frequently visualized in these 7 places. |
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Definition
1) VERTEBRAL COLUMN, 2) RIBS, 3) SKULL, 4) PELVIS, 5) FEMUR, 6) CLAVICLE, 7) SCAPULA |
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Term
363. In multiple myeloma patients, pathological _____ usually occur in the areas with the lytic lesions, especially in the weigh bearing regions. |
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Definition
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|
Term
364. In multiple myeloma, calcium metabolism is usually abnormal resulting in elevated _____, because of _____. |
|
Definition
SERUM CALCIUM LEVELS; PLASMA CELL PROLIFERATION |
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Term
365. Multiple myeloma patients often experience _____ and _____ anemia with variable depression of _____ and _____ counts. |
|
Definition
NOMOCYTIC AND NONOCHROMIC ANEMIA; WBC AND PLATELET COUNTS |
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Term
366. The most common symptoms of multiple myeloma is _____ or _____ pain, as well as _____. |
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Definition
BONE OR BACK PAIN; COMPRESSION FRACTURES |
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Term
367. _____ and _____ may be caused by the secondary anemia of multiple myeloma. |
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Definition
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|
Term
368. Survival rates of multiple myeloma patients are generally poor, and rely largely on the persons response to _____. |
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Definition
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|
Term
1. _____ is idiopathic high blood pressure that usually goes undetected due to a lack of symptoms. |
|
Definition
PRIMARY/ESSENTIAL HYPERTENSION |
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Term
2. Primary/essential hypertension represents _____% of hypertension cases. |
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Definition
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|
Term
3. 4 causes of secondary hypertension. |
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Definition
1) CUSHINGS DISEASE, 3) PRIMARY ALDOSTERONISM, 3) PHEOCHROMOCYTOMA, 4) COARCTATION OF THE AORTA |
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Term
4. 9 risk factors of hypertension. |
|
Definition
1) FAMILY HISTORY, 2) AGE, 3) MALE GENDER, 4) BLACK RACE, 5) OBESITY, 6) HIGH SODIUM DIET, 7) GLUCOSE INTOLERANCE, 8) SMOKING, 9) HEAVY ALCOHOL CONSUMPTION |
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Term
5. What is the best way to diagnose hypertension. . |
|
Definition
TAKE BP AT THE SAME TIME OF DAY AND RECORD IT OVER A PERIOD OF DAYS |
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Term
6. If one has hypertension, there will be ophthalmic changes in the _____ of the eyes. |
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Definition
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|
Term
7. _____ is thong term effect of hypertension, so we should run kidney function tests when one presents with hypertension. |
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Definition
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|
Term
8. If one has hypertension, there will be a _____ in an ECG. |
|
Definition
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|
Term
9. 7 steps in the pathyphysiology of hypertension. |
|
Definition
1) HYPERTENSION DAMAGES THE WALLS OF THE SYSTEMIC VESSELS, 2) PROLONGED VASOCONSTRICTION AND HIGH PRESSURE CAUSES THE VESSELS TO THICKEN, 3) ARTERIAL SMOOTH MUSCLE UNDERGOES HYPERTROPHY, 4) TUNICA INTIMA AND MEDIA UNDERGO FIBROMUSCULAR THICKENING LEADING TO NARROWING OF THE LUMEN, 5) VESSELS BECOME PERMANENTLY NARROWED, 6) HYPERTENSIVE INJURY CAUSES INFLAMMATION TO INCREASE THE PERMEABILITY OF THE VASCULAR ENDOTHELIUM, 7) AS PERMEABILITY INCREASES MORE IONS ENTER THE VESSEL WALLS CAUSING FURTHER THICKENING |
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|
Term
10. When _____ occur, hypertension is usually far advanced. |
|
Definition
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|
Term
11. 7 manifestations of hypertension. |
|
Definition
1) UNSTEADINESS, 2) WALKING HEADACHE, 3) BLURRED VISION, 4) DEPRESSION, 5) RENAL DYSFUNCTION, 6) RETINAL CHANGES, 7) SIGNS OF VENTRICULAR FAILURE SUCH AS DYSPNEA OR EXERTION |
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Term
12. 4 hypertensive death related causes. |
|
Definition
1) STROKE, 2) MI, 3) RENAL FAILURE, 4) ENCEPHALOPATHY |
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Term
13. _____ is a CVA when a blood clot lodges in a vessel leading to ischemic hypoxia. |
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Definition
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|
Term
14. _____ is a CVA when a clot comes from a far away source. |
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Definition
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|
Term
15. _____ is a CVA caused by bleeding. |
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Definition
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|
Term
16. Hypertension is the primary cause of _____ strokes. |
|
Definition
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|
Term
17. _____ are small stroke like incidents that last 10 minutes or less. It leads to a loss in a patients senses. |
|
Definition
TIA (TRANSIENT ISCHEMIC ATTACK) |
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Term
18. If one has a TIA, a patient will experience these 2 symptoms. |
|
Definition
1) BRUITS, 2) THEY WILL SEE FLOATERS |
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Term
19. For something to be diagnosed as a stroke, symptoms must remain for _____ hours. |
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Definition
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Term
20. If a patient has a thrombotic stroke, _____ can be administered to bust out the clot that’s blocking the brain, and restore blood flow. This is able to completely resolve the stroke leading too complications. |
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Definition
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|
Term
21. Strokes tame time to _____ to completion. It might not look severe at first, but the next day the patient could look much worse. |
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Definition
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|
Term
22. Once a patient has completed a stoke they should work on _____ as quick as possible. |
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Definition
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Term
23. _____ and _____ are 2 agents used to treat thrombotic and embolic strokes. They must not be administered to a patient with a hemorrhagic stroke because they will bleed to death. |
|
Definition
FIBRINOLYSIS AND FIBRINOLYTIC AGENTS |
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|
Term
24. 13 risk factors of cerebrovascular disease. |
|
Definition
1) ATHEROSCLEROSIS, 2) HYPERTENSION, 3) HIGH CHOLESTEROL, 4) FAMILY HISTORY, 5) OBESITY, 6) SEDENTARY LIFESTYLE, 7) ORAL CONTRACEPTIVES, 8) SMOKING, 9) COAGULATION DISORDERS, 10) DEHYDRATION, 11) CHRONIC HYPOXIA, 12) CIGARETTE SMOKING |
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Term
25. 4 manifestations of a left hemispheric stroke. |
|
Definition
1) RIGHT SIDED HEMIPLEGIA, 2) SLOW AND CAUTIOUS BEHAVIOR, 3) RIGHT VISUAL FIELD DEFECT, 4) EXPRESSIVE, RECEPTIVE OR GLOBAL DYSPHASIA |
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Term
26. 7 manifestations of a right hemispheric stroke. |
|
Definition
1) LEFT SIDED HEMIPLEGIA, 2) SPATIAL-PERCEPTUAL DEFICITS, 3) IMPULSIVE BEHAVIOR, 4) DISTRACTABILITY, 5) DENIAL, 6) LEFT VISUAL FIELD DEFECTS, 7) PERSEVERATION (REPEATING A WORD OVER AND OVER) |
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Term
27. _____ is a medium by which we get transmission of a lot of different systems for the body. |
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Definition
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|
Term
28. The normal blood volume in the human body is _____. |
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Definition
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|
Term
29. _____is the fluid part of blood. |
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Definition
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|
Term
30. Plasma makes up _____% of blood. |
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Definition
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Term
31. _____ is a measure of albumin acting like a giant sponge that osmotically attracts fluids and holds the fluids together. It is due to the osmotic pressure created by solutes in the fluid. |
|
Definition
COLLOID OSMOTIC PRESSURE (COP) |
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Term
32. Most plasma proteins are manufactured and synthesized by the _____. |
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Definition
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Term
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Definition
1) LIVER HYPERTENSION, 2) HYPOALBUMINEMEA, 3) EXCESS ALDOSTERONE |
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Term
34. Plasma is made up of _____% water, and _____% proteins. |
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Definition
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Term
35. _____ are the antibody making cells in the body. |
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Definition
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Term
36. _____ are antibodies that are the primary immune responders. |
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Definition
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Term
37. IgM antibodies are responsible for _____. |
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Definition
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Term
38. _____ are antibodies that are the secondary immune responders. |
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Definition
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Term
39. _____ are the most abundant immunoglobulin’s in the body. |
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Definition
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Term
40. IgG antibodies respond immediately after _____. |
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Definition
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Term
41. _____ are antibodies found in allergies and hypersensitivity responses. |
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Definition
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Term
42. _____ are antibodies found in most of bodily fluid secretions. |
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Definition
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Term
43. _____ is the main clotting protein in our blood. |
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Definition
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Term
44. _____ is the total amount of blood cells and blood cell fragments due to the RBC volume and the quantity of red cells. |
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Definition
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Term
45. _____ is another name for hematocrit. |
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Definition
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Term
46. A normal person has _____ platelets in their blood stream. |
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Definition
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Term
47. A normal person has _____ leukocytes in their blood stream. |
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Definition
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Term
48. Men have _____ erythrocytes in their blood stream. |
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Definition
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Term
49. Women have _____ erythrocytes in their blood stream. |
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Definition
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Term
50. _____ tissue is where RBC’s originate. |
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Definition
MYELOID TISSUE (RED BONE MARROW) |
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Term
51. During childhood, _____ are RBC producing. |
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Definition
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Term
52. As our bodies mature, the _____ and the _____ are the producers of RBC’s. |
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Definition
AXIAL SKELETON, AND THE ENDS OF LONG BONES |
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Term
53. _____ are the parent cells of all RBC’s. |
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Definition
HEMOCYTOBLAST (HEMATOPOETIC STEM CELL) |
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Term
54. _____ is an almost mature form of the RBC that has lost its nucleus. They consist of small cells which become biconcave. |
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Definition
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Term
55. There are _____ million hemoglobins per erythrocyte. |
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Definition
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Term
56. 1 molecule of hemoglobin can bind _____ oxygen cells. |
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Definition
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Term
57. _____ is the process of producing blood cells. |
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Definition
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Term
58. _____ is the iron element at the center of the hemoglobin molecule. |
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Definition
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Term
59. _____ is iron deficiency often due to blood loss or nutritional deficiencies. |
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Definition
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Term
60. The main stimulus for formation of erythrocytes is _____. |
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Definition
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Term
61. Decreased blood oxygen causes signals to be sent to the kidneys to release _____. This hormone causes an increase in the blood production of RBC in the bone marrow. |
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Definition
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Term
62. _____ is red blood cell making that occurs in the ends of long bones. |
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Definition
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Term
63. _____ is the inactive form of erythropoiesis formed in the liver. |
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Definition
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Term
64. _____ is secreted by the kidney that causes activation of erythropoitinogen. |
|
Definition
RENAL ERYTHROPOITINOGEN FACTOR (EZ) |
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Term
65. _____ is the bone marrow that makes fatty cells used to beef up our bodies systems. |
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Definition
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Term
66. Erythrocytes have an average life span of _____ days. |
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Definition
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Term
67. Erythrocyte breakdown occurs in the _____, and the _____ is the chief cell used to break them down. |
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Definition
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Term
68. Hemoglobin is broken down into _____, which then becomes _____. |
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Definition
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Term
69. Bilirubin is responsible for giving _____ and _____ its color. |
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Definition
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Term
70. _____ coming off from the heme is recycled and reused in the future. |
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Definition
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Term
71. Excess bilirubin in the liver spills out in the skin causing _____. |
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Definition
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Term
72. Proerythroblasts are the precursor cells to _____. |
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Definition
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Term
73. Monoblasts are the precursor cells to _____. |
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Definition
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Term
74. Myeloblasts are the precursor cells to _____. |
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Definition
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Term
75. Lymphoblasts are the precursor cells to _____. |
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Definition
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Term
76. Megakaryocytes are the precursor cells to _____. |
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Definition
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Term
77. 3 types of granulocytes. |
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Definition
1) NEUTROPHILS, 2) BASOPHILS, 3) EOSINOPHILS |
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Term
78. _____ are the most numerous white blood cells in the body. They are important phagoc ytes in acute inflammation. |
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Definition
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Term
79. Neutrophils stain _____, and have a _____ nucleus. |
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Definition
LIGHT PURPLE; MULTI-LOBULED NUCLEUS |
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Term
80. _____are white blood cells that protect us against infections caused by parasitic worms, and they are involved in allergic reactions. |
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Definition
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Term
81. Eosinophils stain _____, and they have a _____ nucleus. |
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Definition
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Term
82. _____ are the least common white blood cells that are responsible for secreting heparin. |
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Definition
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Term
83. Basophils stain _____, and have a _____ nuclei. |
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Definition
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Term
84. 2 different types of agranulocytes. |
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Definition
1) LYMPHOCYTES, 2) MONOCYTES |
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Term
85. _____ are the second most common WBC’s that play an immunity role defense. |
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Definition
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Term
86. _____ lymphocytes are regulatory helper and suppressor cells. |
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Definition
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Term
87. _____ lymphocytes are responsible for antibody production. |
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Definition
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Term
88. Lymphocytes have a _____ stained cytoplasm. |
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Definition
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Term
89. _____ are key phagocytic agranulocytes that become macrophages in circulation as soon as they leave production. |
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Definition
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Term
90. _____ is a decrease in the number of white blood cells. |
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Definition
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|
Term
91. 3 causes of a shift to the left differential. |
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Definition
1) NEUTROPHILS RESPONDING TO ACUTE INFLAMMATION, 2) LEUKOCYTOSIS, 3) MORE BAND CELLS IN THE PLASMA |
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Term
92. 2 causes of a shift to the right differential. |
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Definition
1) INCREASED LYMPHOCYTES DURING CHRONIC INFLAMMATION, 2) LYMPHOCYTIC LEUKOCYTOSIS |
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Term
93. 88% neutrophils causes what? |
|
Definition
SHIFT TO THE LEFT, ACUTE INFLAMMATION |
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Term
94. What is an example of a shift to the left? |
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Definition
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Term
95. 40% lymphocytes causes what? |
|
Definition
SHIFT TO THE RIGHT, CHRONIC INFLAMMATION |
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Term
96. What is an example of a shift to the right? |
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Definition
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Term
97. _____ are cell fragments from megakaryocytes. |
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Definition
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Term
98. Platelets play a major role in _____ and _____, and they are released in response around tissue injury and clump together to stop bleeding. |
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Definition
HEMOSTASIS (STOP BLEEDING) AND COAGULATION |
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Term
99. The life span of platelets is typically _____ days. |
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Definition
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Term
100. The normal platelet count is between _____. |
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Definition
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Term
101. _____ is a deficiency in the number of WBC’s. |
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Definition
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Term
102. Leukopenia is a common side effect of _____. |
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Definition
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Term
103. _____ is having decreased numbers of neutrophils. |
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Definition
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Term
104. _____ is having decreased numbers of lymphocytes. |
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Definition
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Term
105. _____ is a decrease in the number of platelets (below 100,000 platelets/mm3). |
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Definition
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Term
106. Why do we worry about patients with thrombocytopenia. |
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Definition
WE WORRY ABOUT INTERNAL BLEEDING WHEN #’S FALL BELOW 40,000 |
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Term
107. What is another name for platelets? |
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Definition
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|
Term
108. How are platelets formed? |
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Definition
FROM CELL FRAGMENTS OF MEGAKARYOCYTES WHICH COME FROM STEM CELLS |
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Term
109. What is the average life span of platelets? |
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Definition
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|
Term
110. Red blood cells have surface _____ that have been given classification in the ABO system. |
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Definition
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Term
111. Type A blood has _____ on the RBC surface, and has _____ in plasma. |
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Definition
ANTIGEN A; TYPE B ANTIBODY |
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Term
112. Type B blood has _____ on the RBC surface, and has _____ in plasma. |
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Definition
ANTIGEN B; TYPE A ANTIBODIES |
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Term
113. Type AB blood has _____ on the RBC surface, and _____ in plasma. |
|
Definition
ANTIGENS A AND B; NO A OR B ANTIBODIES |
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Term
114. Blood type AB is known as the _____. |
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Definition
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Term
115. Type O blood has _____ on the RBC surface, and _____ in plasma. |
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Definition
NO A OR B ANTIGENS; A AND B ANTIBODIES |
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Term
116. Type O blood is known as the _____. |
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Definition
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Term
117. _____ is when the D-antigen is present on the RBC surface. |
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Definition
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Term
118. _____ is when there is no D-antigen present on the RBC surface. |
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Definition
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Term
119. _____ is when there is a blood transfusion reaction for an RH(-) patient. The first time fused no reaction will occur, but the patient will develop antibodies against the RH factor causing a reaction each subsequent blood transfusion. |
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Definition
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Term
120. _____ is a condition when a RH(-) mother gets pregnant with an RH(+) baby. The mother body creates antibodies against the fetuses blood, causing a destruction of the baby’s erythrocytes. |
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Definition
ERYTHROBLASTOSIS FETALIS (HEMOLYTIC DISEASE OF THE NEWBORN) |
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|
Term
121. The dangers of erythroblastosis fetalis increases with _____. |
|
Definition
EACH SUBSEQUENT PREGNANCY |
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Term
122. _____ is the medication given to the mother with erythroblastosis fetalis. It causes the mothers body to think it has already made antibodies to the D-antigen; fooling the mothers immune system to prevent the in utero attach on the fetus. |
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Definition
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|
Term
123. _____ means to stop bleeding. |
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Definition
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Term
124. 3 ways our bodies perform hemostasis. |
|
Definition
1) VASCULAR SPASM, 2) PLATELET PLUG FORMATION, 3) FIBRIN FORMATION CAUSING COAGULATION |
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Term
125. _____ agents are direct dissolvers of blood clots. |
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Definition
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Term
126. _____ agents are clot prevents and prevent clots from forming, or already formed clots from getting any bigger. |
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Definition
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Term
127. _____ is having blood in the stool. |
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Definition
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Term
128. Blood clotting factors made in the liver are dependent on _____ for synthesis. |
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Definition
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Term
129. _____ is an immediate but temporary closure of a blood vessel resulting from contraction of smooth muscle within the blood vessels wall. |
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Definition
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|
Term
130. Vascular spasms are caused by these 2 bodily mechanisms. |
|
Definition
1) NERVOUS SYSTEM REFLEXES, 2) CHEMICALS RELEASED FROM PLATELETS DURING FORMATION OF THE PLATELET PLUG |
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|
Term
131. In small vessels, vascular spasm can close the vessel _____. |
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Definition
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|
Term
132. When a blood vessel is damaged, the endothelium becomes torn and the underlying tissue is exposed. When this happen _____ adhere to the _____ in the connective tissue. |
|
Definition
PLATELETS; COLLAGEN FIBERS |
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|
Term
133. When platelets adhere to the collagen fibers in the connective tissue during platelet plug formation, it causes the release of these 4 chemicals. |
|
Definition
1) ADP, 2) THROMBOXANE, 3) SEROTONIN, 4) CHEMICALS INVOLVED IN COAGULATION |
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|
Term
134. _____ and _____ are 2 chemicals released by platelets that cause vascular spasm. |
|
Definition
THROMBOXANE AND SEROTONIN |
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Term
135. _____ is a chemical released by platelets that makes their surface sticky, so additional platelets adhere to those already attached to the collagen fibers. |
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Definition
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Term
136. _____ is a chemical released by platelets that induces the aggregating platelets to release ADP, thromboxane, and other chemicals. |
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Definition
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Term
137. When platelets adhere to each other and release chemicals that cause other platelets to adhere, it forms an accumulating mass called a _____. |
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Definition
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Term
138. _____ is the formation of a blood clot that consists of a network of fibrin in which blood cells, platelets, and fluid become trapped. |
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Definition
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|
Term
139. Coagulation is dependent on coagulation factors present in the _____. |
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Definition
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|
Term
140. 3 main stages of coagulation. |
|
Definition
STAGE 1) ACTIVATION OF FACTOR XII AND PRODUCTION OF PROTHROMBIN ACTIVATOR; STAGE 2) CONVERSION OF PROTHROMBIN TO THROMBIN BY PROTHROMBIN ACTIVATOR FACOR; STAGE 3) ENZYMATIC CONVERSION BY THROMBIN OF SOLUBLE FIBRINOGEN TO INSOLUBLE FIBRIN |
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Term
141. Coagulation operates via both the _____ and _____ pathways. |
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Definition
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Term
142. The _____ pathway of coagulation is turned on by factors that are outside the damaged blood vessel. If surrounding tissues are damages, a domino effect will occur that will form the prothrombin factor. |
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Definition
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Term
143. The _____ pathway of coagulation is when circulating clotting factors (factor XII) comes in contact with damaged blood vessels that starts a cascade which ends up as prothrombin factor. |
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Definition
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Term
144. _____ is needed in both the intrinsic and extrinsic coagulation pathways. |
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Definition
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Term
145. Once a blood clot forms, it condenses into a denser, compact structure through a process known as _____. |
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Definition
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Term
146. As a clot condenses _____ is squeezed out of the clot. |
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Definition
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Term
147. Consolidation of clots pull the edges of damaged vessels together, which may help _____, _____ and _____. |
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Definition
STOP BLOOD FLOW, REDUCE INFECTION, AND ENHANCE HEALING |
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Term
148. A clot usually dissolves within a few days after a clot formation by a process known as _____, which is a natural biochem reaction that occurs when the threat is over and the body returns its tissue to the original structure and function. |
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Definition
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Term
149. 3 steps of fibrinolysis. |
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Definition
1) PLASMINOGEN IS ACTIVATED BY THROMBIN FACTOR XII, TISSUE PLASMINOGEN ACTIVATOR, AND LYSOSOMAL ENZYMES RELEASED FROM DAMAGED TISSUES, 2) PLASMINOGEN FORMS PLASMIN, 3) PLASMIN HYDROLYZES FIBRIN DISSOLVING THE CLOT |
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Term
150. What is the difference between anticoagulants and thrombolytic agents? |
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Definition
ANTICOAGULANTS PREVENT FIBRIN FROM FORMING, WHILE THROMBOLITIC AGENTS DISSOLVE FIBRIN OR BUST THE CLOT |
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Term
151. _____ are medications that drive the production of plasmin to bust the clots. They are not anti-coagulants. |
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Definition
THROMBOLYTICS/FIBRINOLYTICS |
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Term
152. _____ do not dissolve clots, rather they prevents cots from forming or prevent existing clots from getting bigger. |
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Definition
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Term
153. _____ and _____ are common anticoagulant medications. |
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Definition
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Term
154. How does Coumadin work? |
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Definition
IT WORKS IN THE LIVER BY COMPETING WITH VITAMIN K. SINCE CLOTTING FACTORS ARE DEPENDENT ON VITAMIN K, COUMADIN WILL RESTRICT FIBRIN SYNTHESIS |
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Term
155. If patients eat foods with _____, it can counteract the effects of Coumadin. |
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Definition
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Term
156. How does heparin work? |
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Definition
IT WORKS IN THE PERIPHERY PREVENTING PROTHROMBIN FROM BEING CONVERTED TO THROMBIN |
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Term
157. Heparin takes up to _____hours to work. |
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Definition
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Term
158. _____ is an antidote for heparin overdose, which is made from fish sperm. |
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Definition
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Term
159. 3 signs of internal bleeding. |
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Definition
1) LARGE, DISTENDED HARD ABDOMEN, 2) FLANK PAIN, 3) BLOOD IN STOOL OR URINE |
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Term
160. 3 signs of over-coagulation. |
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Definition
1) EASY BRUISING, 2) PETECIAL HEMORRHAGES, 3) SHAVING CUTS THAT DO NOT STOP BLEEDING |
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Term
161. 2 coagulation factors found in our body. |
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Definition
1) FACTOR I- FIBRINOGEN, 2) FACTOR XII- FIBRIN STABILIZING FACTOR |
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Term
162. _____ is a test to determine clotting test times of people taking warfarin/Coumadin. |
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Definition
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Term
163. _____ is a test to determine clotting test times of people on heparin. |
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Definition
PARTIAL THROMBOPLASTIN TIME (PTT) |
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Term
164. The normal PTT time is between _____. |
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Definition
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Term
165. _____ is the standardized clotting times across the globe, it consists of a ration responsible for standardizing everything. |
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Definition
INTERNATIONAL NORMALIZED RATION (INR) |
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Term
166. The normal clotting time in the INR is between _____. |
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Definition
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Term
167. The normal ratio of INR is between _____ and _____. |
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Definition
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Term
168. The desirable anticoagulant effect of INR is between _____ and _____. |
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Definition
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Term
169. 3 components of a complete blood count. |
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Definition
1) WBC COUNT, 2) RBC COUNT, 3) PLATELET COUNT |
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Term
170. _____ is a test the counts the actual number of WBC’s per volume of blood. |
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Definition
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Term
171. _____ is a test that determines what types of WBC’s are present in the blood. |
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Definition
WHITE BLOOD CELL DIFFERENTIAL |
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Term
172. _____ is a test to determine the actual number of RBC’s per volume of blood. |
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Definition
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Term
173. _____ is a test to determine the amount of oxygen carrying protein in the blood. |
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Definition
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Term
174. _____ is a test to determine the rate of RBC production. |
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Definition
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Term
175. _____ is a test to determine the amount of space RBC’s take up in the blood. |
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Definition
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Term
176. _____ is a test to determine the number of platelets in a given volume of blood. |
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Definition
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Term
177. _____ is a test to measure the average size of RBC’s. |
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Definition
MEAN CORPUSCULAR VOLUME (MCV) |
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Term
178. MCV is an important in testing for _____. |
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Definition
ANEMIAS DUE TO B12 DEFICIENCY |
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Term
179. _____ is a test to calculate the amount of hemoglobin inside of the RBC’s. |
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Definition
MEAN CORPUSCULAR HEMOGLOBIN (MCH) |
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Term
180. _____ is a test to calculate the percentage of hemoglobin in red blood cells. |
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Definition
MEAN CORPUSCULAR HEMOGLOBIN CONCENTRATION (MCHC) |
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Term
181. _____ is a test to determine how varied the size of RBC’s are in a sample. |
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Definition
RED CELL DISTRIBUTION WIDTH (RDW) |
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Term
182. RDW helps determine the kind of _____ one may have. |
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Definition
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Term
183. _____ is the most life threatening skin carcinoma. |
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Definition
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Term
184. _____ for skin disorders serve as anti-inflammatory agents. |
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Definition
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Term
185. What is a cubitus ulcer? |
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Definition
A BEDSORE (WHEELCHAIR BOUND PATIENT) |
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Term
186. Herpes zoster spreads along the _____. |
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Definition
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Term
187. _____ is a condition caused by a low number of circulating red cells, abnormally low number of hemoglobin, or both. |
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Definition
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Term
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Definition
1) BLOOD LOSS, 2) LACK OF OXYGEN DELIVERY TO CELLS/TISSUES, 3) DECREASED OXYGEN AFFINITY TO HEMOGLOBIN |
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Term
189. What increased oxygen’s affinity for hemoglobin? |
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Definition
THE ACTUAL BINDING OF OXYGEN TO THE HEMOGLOBIN |
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Term
190. 3 things that decrease oxygen’s affinity for hemoglobin. |
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Definition
1) BINDING OF CO2 TO HEMOGLOBIN, 2) BINDING OF PROTONS TO SPECIFIC BASIC GROUPS, 3) BINDING OF CERTAIN ORGANIC PHOSPHATES |
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Term
191. _____ anemia is most common in menstruating women. |
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Definition
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Term
192. _____ anemia is due to an early destruction of RBC’s due to a pathology. |
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Definition
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Term
193. _____ is a major pathology that causes hemolytic anemia. |
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Definition
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Term
194. _____ anemia is caused by a vitamin B-12 deficiency. |
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Definition
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|
Term
195. 3 different types of nutritional deficiency anemia’s. |
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Definition
1) PERNICIOUS ANEMIA, 2) FOLIC ACID DEFICIENCY ANEMIA, 3) IRON DEFICIENCY ANEMIA |
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Term
196. _____ anemia is caused by a bone marrow depression causing a lack of adequate production of RBC’s. it is usually accompanied by depressions in other formed elements of the blood. |
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Definition
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Term
197. 9 signs and symptoms of general anemia. |
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Definition
1) FATIGUE/WEAKNESS, 2) PALLOR, 3) TACHYCARDIA, 4) ANXIETY, 5) SYSTOLIC MURMUR, 6) VENTRICULAR HYPERTROPHY, 7) CHF, 8) ERYTHROPOEISIS, 9) ANGINA AND NIGHT CRAMPS |
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Term
198. _____ anemia’s are due to an early destruction of red blood cells either due to extrinsic or intrinsic causes. |
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Definition
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Term
199. _____ is an intrinsic cause of hemolytic anemia that is caused by an autosomal trait causing spherical-shaped RBC’s rather than biconcave disc shape. |
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Definition
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Term
200. In hereditary spherocytosis, the tight spherical shape RBC’s will hemolyze and be _____ early in mass numbers. |
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Definition
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Term
201. _____ is sometimes used as the treatment of hemolytic anemia’s for adults, but it will not work in children. |
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Definition
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Term
202. _____ are conditions inherent to hemoglobin molecules. |
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Definition
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Term
203. Hemoglobin usually consists of _____ polypeptide chains. |
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Definition
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Term
204. Hemoglobinopathies occur when one hemoglobin polypeptide chain is substituted with an _____. |
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Definition
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Term
205. Sickle cell anemia is a condition when one of the hemoglobin amino acids is substituted with _____ rather than a polypeptide chain. |
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Definition
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Term
206. Sickle cell anemia typically occurs in _____. |
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Definition
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Term
207. _____ are sickle cells. |
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Definition
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Term
208. _____ are normal hemoglobin cells. |
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Definition
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Term
209. Is a person contains the _____ and _____ cells, they are carriers for the sickle cell trait. |
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Definition
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Term
210. If a person contains the _____ and _____ cells, they will have sickle cell anemia. |
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Definition
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Term
211. Why is sickle cell anemia more dangers in a low oxygen environment. |
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Definition
IN LOW OXYGEN ENVIORNMENTS, THE SICKLE HBS BECOMES AN AGGREGATE AND BOWS OUT THE CELL |
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Term
212. A sickling crisis can cause death by leading to _____. |
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Definition
HEMOLYSIS AT LOG-JAMMED CAPILLARIES |
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Term
213. Factors that precipitate sickling are related to _____. |
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Definition
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|
Term
214. 6 low oxygen situations that can lead to sickling. |
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Definition
1) EXERCISE, 2) HYPOXIA, 3) ACIDOSIS, 4) DEHYDRATION, 5) INFECTION, 6) REDUCED OXYGEN TENSION IN SLEEP |
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Term
215. 5 symptoms of sickle cell crisis. |
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Definition
1) SWOLLEN HANDS AND FEET, 2) STROKE, 3) MI, 4) KIDNEY FAILURE, 5) HEMOLYSIS |
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Term
216. What causes the painful crisis of sickle cell? |
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Definition
VESSEL OCCLUSION THAT MAY APPEAR SUDDENLY IN ALMOST ANY PART OF THE BODY |
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Term
217. Hemoglobin is composed of _____, which is made up of 4 folded polypeptide chains, and 4 _____. |
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Definition
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Term
218. Each hemoglobin molecule can carry _____ molecules of oxygen. |
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Definition
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Term
219. When hemoglobin is called _____ when carrying oxygen, and _____ when not carrying oxygen. |
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Definition
OXYHEMOGLOBIN, REDUCED HEMOGLOBIN |
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Term
220. Hemoglobin can also combine with _____ to transport it from the tissues to the lungs for excretion. |
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Definition
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Term
221. _____ is a condition that results from absent or defective synthesis of either the alpha or beta chains of hemoglobin’s causing a decrease in the size of cells and a change in the MCV (size of RBC). |
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Definition
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Term
222. _____ is a repeated defect in the beta-chain synthesis of hemoglobin. |
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Definition
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Term
223. B-thalassemias is most common in the _____ population. |
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Definition
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Term
224. If a person receives the B-thalassemias trait from both parents it will cause transfusion-dependent anemia leading to death by _____. |
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Definition
HEMOCHROMATOSIS (EXCESS IRON) |
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Term
225. 6 symptoms present in children with B-thalassemias. |
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Definition
1) GROWTH RETARDATION, 2) SPLEENOMEGALY, 3) HEPATOMEGALY, 4) INCREASED RBC DISTRUCTION, 5) INCREASED STIM FOR HEMATOPORIESIS CAUSING BONE MARROW EXPANSION, 6) THINNING OF THE CORTICAL BONE |
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Term
226. A-thalassemias is most common in _____. |
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Definition
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Term
227. Most severe cases of A-thalassemias occurs in _____. |
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Definition
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Term
228. Anemia occurs in A-thalassemias due to _____ and _____. |
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Definition
DEFECTIVE HEMOGLOBIN PRODUCTION, ACCUMULATION OF UNPAIRED GLOBIN CHAINS |
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Term
229. What is more severe alpha or beta thalassemias? |
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Definition
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Term
230. Individuals with the mildest form of A-thalassemias are usually _____ having mild _____. |
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Definition
ASYMPTOMATIC, MICROCYTOSIS |
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Term
231. The minor form of A-thalassemias is associated with these 4 conditions. |
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Definition
1) MILD MICROCYTITC HYPOCHROMIC RETICULOCYTOSIS (IMMATURE RBC’S), 2) BONE MARROW HYPERPLASIA, 3) INCREASED SERUM IRON CONCENTRATION, 4) MODERATE SPLENOMEGALY |
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Term
232. 2 factors that cause microcytic-hypochromic anemia in A-thalassemias. |
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Definition
1) REDUCED HEMOGLOBIN SYNTHESIS AND IMBALANCE IN GLOBIN CHAIN PRODUCTION, 2) UNPAIRED CHAINS ACCUMULATE IN RED CELLS CAUSING RBC DESTRUCTION AND ANEMIA |
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Term
233. The most common disorder associated with an inherited enzyme deficiency is _____. |
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Definition
G-6-PD (GLUCOSE-6-PHOSPHO DEHYDROGENASE) |
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Term
234. G-6-PD causes the direct oxidation of hemoglobin which forms a _____. |
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Definition
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Term
235. 3 risk factors of the formation of methemoglobin. |
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Definition
1) THE CELL IS NOT FUNCTIONAL, 2) DENATURED HEMOGLOBIN MOLECULE RESULTS, 3) THEY CAN NOT MAKE IT THROUGH THE TIGHT CIRCULATORY AREAS OF THE BODY |
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Term
236. G-6-PD eventually results in _____. |
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Definition
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Term
237. 6 extrinsic anemia factors. |
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Definition
1) DRUGS, 2) CHEMICALS, 3) TOXINS, 4) ARTIFICIAL MECHANICAL BODY STRUCTURES, 5) BURNS, 6) ANY DIRECT INJURY TO THE RBC’S THEMSELVES |
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Term
238. _____ means the size of the RBC is normal. |
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Definition
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Term
239. _____ means the size of the RBC is small. |
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Definition
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Term
240. The most common cause of microcytic RBC’s is _____. |
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Definition
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Term
241. _____ means the size of the RBC is large. |
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Definition
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Term
242. _____ means the color of the RBC is normal. |
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Definition
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Term
243. _____ means there is a decrease in the color of the RBC. |
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Definition
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Term
244. These 2 criteria must be met for anemia to be classified as nutritional anemia. |
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Definition
1) THERE MUST BE A DEFECIENCY OR LACK OF A NUTRIENT ALONE CAUSING THE ANEMIA, 2) HAVING THE NUTRIENT PROVIDED CORRECTS THE ANEMIA |
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Term
245. 4 symptoms associated with nutritional anemias. |
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Definition
1) PALLOR, 2) WEAKNESS, 3) LETHARGY, 4) HEART RATE ELEVATION |
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Term
246. 2 additional symptoms associated with iron deficiency anemias. |
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Definition
1) SOARS IN THE CORNER OF THE MOUTH, 2) PICA (EATING DIRT, CLAY OR ICE) |
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Term
247. If blood was drawn in a patient with iron deficiency anemia, the red blood cells would be _____ and _____. |
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Definition
MICROCYTIC AND HYPOCHROMIC |
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Term
248. 3 classes of nutritional anemias. |
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Definition
1) IRON DEFICIENCY ANEMIA, 2) PERNICIOUS ANEMIA, 3) FOLIC ACID DEFICIENCY ANEMIA |
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Term
249. _____ is essential for heme, in that each heme unit has one of these molecules at its center to form hemoglobin. |
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Definition
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Term
250. 3 causes of iron deficiency during pregnancy and pre-natal development. |
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Definition
1) IF MOM IS IRON DEFICIENT SO IS THE BABY, 2) MOMS WHO ARE IRON DEFICIENT AND BREAST FEED WILL TRANSFER IT TO THE BABY, 3) IF NOT BREAST FEEDING COWS MILK MUST BE IRON FORTIFIED |
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Term
251. What is the main symptom of iron deficiency during the infant/toddler years? |
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Definition
PICA (EATING THINGS THAT ARE NOT NORMALLY EDIBLE) |
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Term
252. During the teenage years girls on their _____ and _____ are susceptible to iron deficiency. |
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Definition
MENSTRUAL CYCLE, NOT EATING PROPERLY |
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Term
253. The most vulnerable time of iron deficiency in the adult years is during _____. |
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Definition
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Term
254. _____ is anemia caused by a lack of vitamin B12/intrinsic factor. |
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Definition
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Term
255. Pernicious anemia causes _____ RBC’s as well as _____ anemias. |
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Definition
MACROCYTIC, MEGALOBLASTIC |
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Term
256. The _____ is necessary for vitamin B-12 to be absorbed in the intestine. |
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Definition
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Term
257. Patients with pernicious anemia can have these 3 CNS related effects. |
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Definition
1) NEUROLOGIC DEGENERATION OF DORSAL AND LATERAL SPINAL COLUMNS, 2) PARASTHESIA, 3) SPASTIC ATAXIA |
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Term
258. Folic acid anemias cause _____ RBC’s and _____ anemias. |
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Definition
MACROCYTIC, MEGALOBLASTIC |
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Term
259. _____ anemias usually have normal size and color RBC’s. |
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Definition
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Term
260. 3 causes of a shift to the right in the oxygen saturation curve. |
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Definition
1) EXERTION, 2) INFECTION (TEMP INCREASE), 3) SURGERY |
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Term
261. _____ is polycythemia caused by dehydration or fluid loss. |
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Definition
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Term
262. _____ is polycythemia caused by anything that increases the bone marrow production of RBC’s. |
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Definition
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Term
263. _____ polycythemia is caused by a congenital issue leading to a proliferative disease in the bone marrow causing an accelerated production of RBC’s. |
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Definition
PRIMARY POLYCYTHEMIA (POLYCYTHEMIA VERA) |
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Term
264. Polycythemia vera causes _____ blood due to extra RBC’s, and problems arise due to _____. |
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Definition
VISCOUS; INCREASED BLOOD VISCOSITY |
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Term
265. The skin of a patient with polycythemia vera will appear _____. |
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Definition
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Term
266. _____ is the treatment of polycythemia vera. |
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Definition
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Term
267. 7 conditions associated with polycythemia vera. |
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Definition
1) BLOOD CLOTS, 2) HYPERTENSION, 3) PAINFUL ITCHING SENSATIONS, 4) SLUGGISH BLOOD FLOW, 5) PROBLEMS HEARING AND CONCENTRATING, 6) IRRITABILITY, 7) THROMBOSIS |
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Term
268. Suppressing the bone marrow of polycythemia vera requires _____, which is risky due to the side effects. |
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Definition
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Term
269. Polycythemia vera may lead to _____ or _____ due to stagnation and build-up of thick blood. |
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Definition
THROMBOSIS, FRANK HEMORRHAGING |
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Term
270. _____ disorders are caused by platelet issues and anything that causes a decrease in platelet production. |
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Definition
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Term
271. _____ is a condition when there is less than 100,000 platelets in the body. |
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Definition
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Term
272. 3 mechanisms behind thrombocytopenia. |
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Definition
1) DECREASE IN PLATELET PRODUCTION BY THE BONE MARROW, 2) INCREASED POOLING OF PLATELETS IN THE SPLEEN CAUSING SPLEENOMEGALY, 3) DECREASED PLATELET SURVIVAL |
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Term
273. 4 causes of thrombocytopenia. |
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Definition
1) VIRAL INFECTIONS, 2) DRUGS, 3) IDIOPATHIC, 4) BONE MARROW PROBLEMS |
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Term
274. 3 signs and symptoms of thrombocytopenia. |
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Definition
1) EASY BRUISING, 2) NOSE BLEEDS, 3) SHAVING CUTS THAT DON’T STOP BLEEDING |
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Term
275. _____ occurs 1-4 weeks after a viral infection, causing bruising and a generalized petechial rash that often occurs with acute onset. |
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Definition
IDIOPATHIC THROMBOCYTOPENIC PURPA (ITP) |
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|
Term
276. 4 conditions associated with idiopathic thrombocytopenic purpa. |
|
Definition
1) ASYMMETRICAL BLEEDING FOUND MOST FREQUENTLY COVERING THE LEGS, 2) HEMORRHAGE BULLAE OF THE MUCOUS MEMBRANES, 3) EPISTAXIS (NOSE BLEEDS), 4) SPONTANEOUS HEMORRHAGES THAT LAST 1-2 WEEKS |
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Term
277. _____ is used to slow down the platelet production in idiopathic thrombocytopenic purpa. |
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Definition
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Term
278. _____ is a condition that begins as a systemic clotting issue that ends up as a bleeding problem secondary to some other event. |
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Definition
DISIMINATED INTRAVASCULAR COAGULATION (DIC) |
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Term
279. _____ is the most common cause of disiminated intravascular coagulation. |
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Definition
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Term
280. 8 causes of disiminated intravascular coagulation. |
|
Definition
1) MASSIVE TRAUMA, 2) BURNS, 3) SEPSIS, 4) SHOCK, 5) MALIGNANT DISEASE, 6) MENONGOCOCCEMIA, 7) OBSTETRIC COMPLICATIONS, 8) SNAKE BITES |
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Term
281. _____ is a condition associated with disiminated intravascular coagulation that has a very high mortality rate. |
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Definition
BLEEDING FROM EVERY ORIFICE |
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|
Term
282. What is the treatment of disiminated intravascular coagulation? |
|
Definition
STOP THE UNDERLYING PATHOLOGY AND ADMINISTER HEPARIN TO SUPPLY FRESH COAGULATION FACTORS AND PLATELETS |
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Term
283. _____ is a common bleeding pathology within the body. |
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Definition
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Term
284. _____ is classic hemophilia, which is an x-linked recessive disorder manifesting in males that is transmitted by females. |
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Definition
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Term
285. Hemophilia A is caused by a defect of _____, which is prevented from participating in the intrinsic clotting pathway. |
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Definition
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Term
286. _____ is the most common hemophilia and accounts for 80-85% of all cases. |
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Definition
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Term
287. Thrombin is nor normally found in circulating blood. In order for thrombin to be made in the intrinsic clotting pathway, prothrombin (factor II) requires _____ and _____ to be converted to thrombin. |
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Definition
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Term
288. _____ is the second most common hemophilia (15%) caused by an x-linked recessive trait that is clinically indistinguishable from a factor VIII deficiency. |
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Definition
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Term
289. Hemophilia B is caused by a _____ deficiency. |
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Definition
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Term
290. Hemophilia B is also referred to as _____. |
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Definition
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Term
291. How can a doctor distinguish between hemophila A and B? |
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Definition
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Term
292. _____ is a hemophilia that results from an autosomal recessive disease that occurs equally in males and females. |
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Definition
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Term
293. Hemophilia C is caused by a _____ deficiency. |
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Definition
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Term
294. In patients with hemophilia C, bleeding is usually _____ than in hemophilia A or B. |
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Definition
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Term
295. Hemophilia C does not present at birth, but rather around _____ when clotting factors begin to fail. |
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Definition
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|
Term
296. 4 symptoms of patients with hemophilia C. |
|
Definition
1) EASY BRUISING, 2) BLEEDING GUMS OR JOINTS, 3) BLOOD IN URINE OR STOOL, 4) EPISTAXIS (NOSE BLEEDS) THAT DO NOT STOP |
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|
Term
297. _____ is a condition caused by a defect in a different subunit, co-factor, or carrier protein of factor VIII. It is an inherited autosomal dominant trait that is different from hemophilia A. |
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Definition
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Term
298. In von wilderband disease, rapidly circulating platelets are unable to stick to _____ and _____ cannot be formed. |
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Definition
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|
Term
299. What is mainly affected by von wildebrand disease? |
|
Definition
ENDOTHELIAL CELLS THAT LINE VESSELS |
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|
Term
300. _____ is the usual treatment of von wildebrand disease, which caused factor VIII activity to increase for several days. It temporarily induced endogenous synthesis of factor VIII. |
|
Definition
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|
Term
301. _____ is a life threatening condition that causes a rapid proliferation of immature WBC’s by the bone marrow. |
|
Definition
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|
Term
302. 11 endogenous findings associated with leukemia. |
|
Definition
1) ABNORMAL PATHOLOGICAL CELLS, 2) EXCESS BONE MARROW PROLIFERATION, 3) REPLACEMENT OF BONE MARROW WITH WBC’S (BONE MARROW DEPRESSION), 4) EXCESS NON-FUNCTIONAL WBC’S IN BLOOD, 5) SPLENOMEGALY, 6) HEPATOMEGALY, 7) LYMPHANDENOAPTHY, 8) WEIGHT LOSS, 9) NIGHT SWEATS, 10) LOW GRADE FEVER, 11) HYPERURICEMIA |
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Term
303. If a patient has leukemia, _____ and _____ will result due to decreased platelet and erythrocyte production. |
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Definition
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|
Term
304. _____ is present in 90% of all leukemia patients. |
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Definition
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|
Term
305. 6 CNS related conditions associated with leukemia. |
|
Definition
1) ENCEPHALOPATHY, 2) MENINGITIS, 3) CRANIAL NERVE PALSIES, 4) BLURRED VISION, 5) HEADACHE, 6) SEIZURES |
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Term
306. The 2 acute forms of leukemia are _____ and _____. |
|
Definition
ACUTE LYMPHOCYTIC LEUKEMIA; ACUTE MYELOTIC LEUKEMIA OR ACUTE GRANULOCYTIC LEUKEMIA |
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Term
307. _____ is an acute form of leukemia with a sudden onset most commonly seen in children between the ages of 2 and 4. |
|
Definition
ACUTE LYMPHOCYTIC LEUKEMIA |
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Term
308. In acute lymphocytic leukemia _____ are differentiated poorly. |
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Definition
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Term
309. The onset of acute lymphocytic leukemia is _____. |
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Definition
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Term
310. _____ accounts for 2/3 of all leukemia cases. |
|
Definition
ACUT E LYMPHOCYTIC LEUKEMIA |
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Term
311. 6 symptoms associated with acute lymphocytic leukemia. |
|
Definition
1) FEVER, 2) MUSCLE FATIGUE, 3) BLEEDING, 4) BONE PAIN, 5) BONE MARROW DYSFUNCTION, 6) ANEMIA |
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Term
312. More than _____% of children with acute lymphocytic leukemia have complete remission, while _____% of children live 5 years or longer. 90%, |
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Definition
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Term
313. _____ is an acute form of leukemia with a low survival rate. It affects all the –phil cells, and symptoms arise abruptly which are similar to those of acute lymphocytic anemia. |
|
Definition
ACUTE MYELOTIC LEUKEMIA (ACUTE GRANULOCYTIC LEUKEMIA) |
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Term
314. _____ is the most common type of leukemia found in adults. |
|
Definition
ACUTE MYELOTIC OR GRANULOCYTIC LEUKEMIA |
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Term
315. Acute myelotic leukemia is treated with intensive chemo to cause _____ of the bone marrow. |
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Definition
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Term
316. Only about _____% of acute myelotic leukemia patients who receive chemo will achieve long-term disease free survival. |
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Definition
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Term
317. The more _____ a cell, the more malignant they can become and lead to a more progressive cancer. |
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Definition
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Term
318. These are the 2 types of chronic leukemia’s. |
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Definition
1) CHRONIC LYMPHOCYTIC LEUKEMIA, 2) CHRONIC MYELOCYTIC OR GRANULOCYTIC LEUKEMIA |
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Term
319. _____ is a form of chronic leukemia that is often a disorder in older adults between the ages of 50-70. The disease consists of slightly differentiated cells which causes the disease to progress _____. |
|
Definition
CHRONIC LYMPHOCYTIC LEUKEMIA; SLOWLY |
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Term
320. Is chronic lymphocytic leukemia more common in men or women? |
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Definition
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Term
321. Unlike acute lymphocytic leukemia, in chronic lymphocytic leukemia the chronic cells are more _____ and easily identifiable. |
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Definition
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Term
322. Chronic lymphocytic leukemia cells develops _____, but _____ are affected. |
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Definition
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Term
323. Patients with chronic lymphocytic anemia are usually diagnosed when they are _____, and they life expectancy is _____ than those patients with acute lymphocytic anemia. |
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Definition
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Term
324. _____ is a chronic form of leukemia that occurs in patients between the ages of 30-50. |
|
Definition
CHRONIC MYELOCYTIC OR GRANULOCYTIC LEUKEMIA |
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Term
325. In chronic myelocytic or granulocytic leukemia, bone marrow cells have the _____ chromosome that occurs in mitotic error with a shortened arm on chromosome _____. |
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Definition
PHILADELPHIA CHROMOSOME; CHROMOSOME 22 |
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Term
326. Chronic myelocytic or granulocytic leukemia patients are often _____ when diagnosed. |
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Definition
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Term
327. About _____% of chronic myelocytic or granulocytic leukemia patients enter an accelerated phase characteristic of acute leukemia which leads to _____ survival rates. |
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Definition
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Term
328. 13 symptoms associated with chronic myelocytic or granulocytic leukemia. |
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Definition
1) SPLENOMEAGALY, 2) IMMATURE LEUKOCYTES, 3) HIGH WBC COUNT, 4) ANEMIA, 5) THROMBOCYTOPENIA, 6) WEAKNESS, 7) FATIGUE, 8) DYSPNEA, 9) LOW GRADE FEVER, 10) NIGHT SWEATS, 11) WEIGHT LOSS, 12) HEPATOMEGALY, 13) LYMPHADENOPATHY |
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Term
329. 4 caused associated with chronic myelocytic or granulocytic leukemias. |
|
Definition
1) RADIATION, 2) CHEMICALS LIKE BENZENE, 3) TWINS, 4) ANIMALS |
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Term
330. _____ are cancers of WBC’s (lymphocytes). |
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Definition
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|
Term
331. _____ is a malignant disorder or lymphoid tissue that constitutes 40% of all malignant lymphomas seen in younger adults between the ages of 20-40. |
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Definition
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|
Term
332. In hodgkins lymphoma, lymphoid tissue is characterized by the presence of _____ upon biopsy. |
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Definition
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|
Term
333. Manifestations of hogdkins lymphoma are due to rapid proliferation of abnormal _____. |
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Definition
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|
Term
334. Hodgkins lymphoma often begins in lymph tissue above the _____, which usually sends people to see the doctor. |
|
Definition
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|
Term
335. 10 symptoms associated with hodgkins lymphoma. |
|
Definition
1) PAINLESS ENLARGEMENT OF LYMPHOID TISSUE, 2) SPLENOMEGALY, 3) FEVER, 4) NIGHT SWEATS, 5) WEIGHT LOSS, 6) FATIGUE, 7) PURITIS, 8) WEAKENED IMMUNE SYSTEM, 9) INCREASED WBC COUNT, 10) AFFECTED LIVER, LUNGS, DIGESTIVE TRACT AND CNS |
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Term
336. 7 medical tests used to identify hodgkins lymphoma. |
|
Definition
1) LYMPH NODE BIOPSY, 2) CT SCANS OF ABDOMEN AND PELVIC LYMPH NODES, 3) LYMPHANGIOGRAPHY, 4) LAPAROTOMY, 5) LIVER BIOPSY, 6) BONE MARROW BIOPSY, 7) X RAYS AND LAB WORK |
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Term
337. In _____ of ann arbor staging of hodgkins lymphoma, a single lymph node or single extralymphatic region is affected. |
|
Definition
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|
Term
338. In _____ of ann arbor staging of hodgkins lymphoma, there is involvement of lymph nodes on the same side of the diaphragm. |
|
Definition
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|
Term
339. In _____ of ann arbor staging of hodgkins lymphoma, there is involvement of lymph nodes on both sides of the diaphragm. |
|
Definition
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|
Term
340. In _____ of ann arbor staging of hodgkins lymphoma, there is diffused or disseminated involvement of lymph nodes. |
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Definition
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|
Term
341. The incidence rate of hodgkins lymphoma is _____ cases a year with _____ deaths. |
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Definition
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|
Term
342. _____ is a type of lymphoma that typically affects immune suppressed people over the age of 50, which could be virus related. It consists of a group of neoplastic disorders of lymphoid tissue not characterized by reed-sternberg cells. |
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Definition
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|
Term
343. In patients with non-hodgkins lymphoma, there is early involvement of the lymph nodes in the _____ area. |
|
Definition
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|
Term
344. There is less than _____% chance of curability of patients with non-hodgkins lymphoma. |
|
Definition
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|
Term
345. Non-hodgkins lymphomas are divided into 3 main groups according to the cell types involved which are _____, _____ and _____. |
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Definition
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|
Term
346. The diagnosis of non-hodgkins lymphoma is through a _____. |
|
Definition
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|
Term
347. 4 signs and symptoms of patients with non-hodgkins lymphoma. |
|
Definition
1) EARLY INVOLVELENT OF OROPHARYNGEAL LYMPHOID TISSUE, 2) CONSTITUTIONAL SIGNS, 3) LEUKEMIC TRANSFORMATIONS WITH HIGH NUMBERS OF WBC’S, 4) INCREASED SUSCEPTIBILITY TO INFECTIONS |
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Term
348. The incidence rate of non-hodgkins lymphoma is _____ new cases a year with _____ deaths. |
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Definition
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|
Term
350. _____ is a condition that consists of bone tumors of B-lymphocytes commonly affecting people between the ages of 50 and 60. |
|
Definition
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|
Term
351. Multiple myelomas causing B-cell neoplasms leads to an excess production of _____ and _____. |
|
Definition
IMMATURE AND MATURE PLASMA CELLS |
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|
Term
352. Multiple myeloma affecting B-cells can be detectable by _____ of the long bones, sternum, or skull. |
|
Definition
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|
Term
353. Multiple myeloma is characterized by multiple malignant tumor masses of _____ scattered throughout the skeletal system and sometimes soft tissues. |
|
Definition
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|
Term
354. Incidence of multiple myelomas is _____ times greater than all other malignant tumors of the bone combined. |
|
Definition
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|
Term
355. Chronic stimulation of the mononuclear phagocytic system by these 3 things have been proposed causes of multiple myelomas. |
|
Definition
1) BACTERIA, 2) CHEMICALS, 3) VIRUSES |
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|
Term
356. In the pathophysiology of multiple myeloma, _____ arise from 1 clone of B-cells that produce abnormally large amounts of _____. |
|
Definition
MALIGNANT PLASMA CELLS; CLASS 1 IMMUNOGLOBULINS (IgG) |
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Term
357. Laboratory examinations of the bone marrow of patients with multiple myeloma shows proliferation of _____ and _____ cells with 20% or more having multinucleated cytoplasms containing multiple immunoglobulins (whits blobs). These cells often completely replace _____. |
|
Definition
IMMATURE AND MATURE PLASMA CELLS; BONE MARROW |
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|
Term
358. _____ proteins, which are fragments of IgG/A are present in the urine and blood of over 60% of patients with multiple myeloma. |
|
Definition
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|
Term
359. Bence jones proteins are proliferations of the _____. |
|
Definition
LIGHT CHAINS OF IMMUNOGLOBULINS (M-CHAIN) |
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|
Term
360. In multiple myeloma patients, there is a higher frequency of _____ correlated with the amount of protein found in urine, since the excreted light chains are through to be toxin to the renal tubules. |
|
Definition
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|
Term
361. The malignant neoplasm of multiple myeloma usually does not metastasize outside of the _____, rather the destructive lesions typically erode the _____ and cause _____ that are observable on radiographs. |
|
Definition
BONE; BONE; LYTIC LESIONS |
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Term
362. Lytic lesions of multiple myeloma patients are most frequently visualized in these 7 places. |
|
Definition
1) VERTEBRAL COLUMN, 2) RIBS, 3) SKULL, 4) PELVIS, 5) FEMUR, 6) CLAVICLE, 7) SCAPULA |
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|
Term
363. In multiple myeloma patients, pathological _____ usually occur in the areas with the lytic lesions, especially in the weigh bearing regions. |
|
Definition
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|
Term
364. In multiple myeloma, calcium metabolism is usually abnormal resulting in elevated _____, because of _____. |
|
Definition
SERUM CALCIUM LEVELS; PLASMA CELL PROLIFERATION |
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|
Term
365. Multiple myeloma patients often experience _____ and _____ anemia with variable depression of _____ and _____ counts. |
|
Definition
NOMOCYTIC AND NONOCHROMIC ANEMIA; WBC AND PLATELET COUNTS |
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|
Term
366. The most common symptoms of multiple myeloma is _____ or _____ pain, as well as _____. |
|
Definition
BONE OR BACK PAIN; COMPRESSION FRACTURES |
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Term
367. _____ and _____ may be caused by the secondary anemia of multiple myeloma. |
|
Definition
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|
Term
368. Survival rates of multiple myeloma patients are generally poor, and rely largely on the persons response to _____. |
|
Definition
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|
Term
1. _____ is idiopathic high blood pressure that usually goes undetected due to a lack of symptoms. |
|
Definition
PRIMARY/ESSENTIAL HYPERTENSION |
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|
Term
2. Primary/essential hypertension represents _____% of hypertension cases. |
|
Definition
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|
Term
3. 4 causes of secondary hypertension. |
|
Definition
1) CUSHINGS DISEASE, 3) PRIMARY ALDOSTERONISM, 3) PHEOCHROMOCYTOMA, 4) COARCTATION OF THE AORTA |
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|
Term
4. 9 risk factors of hypertension. |
|
Definition
1) FAMILY HISTORY, 2) AGE, 3) MALE GENDER, 4) BLACK RACE, 5) OBESITY, 6) HIGH SODIUM DIET, 7) GLUCOSE INTOLERANCE, 8) SMOKING, 9) HEAVY ALCOHOL CONSUMPTION |
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Term
5. What is the best way to diagnose hypertension. . |
|
Definition
TAKE BP AT THE SAME TIME OF DAY AND RECORD IT OVER A PERIOD OF DAYS |
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Term
6. If one has hypertension, there will be ophthalmic changes in the _____ of the eyes. |
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Definition
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|
Term
7. _____ is thong term effect of hypertension, so we should run kidney function tests when one presents with hypertension. |
|
Definition
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|
Term
8. If one has hypertension, there will be a _____ in an ECG. |
|
Definition
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|
Term
9. 7 steps in the pathyphysiology of hypertension. |
|
Definition
1) HYPERTENSION DAMAGES THE WALLS OF THE SYSTEMIC VESSELS, 2) PROLONGED VASOCONSTRICTION AND HIGH PRESSURE CAUSES THE VESSELS TO THICKEN, 3) ARTERIAL SMOOTH MUSCLE UNDERGOES HYPERTROPHY, 4) TUNICA INTIMA AND MEDIA UNDERGO FIBROMUSCULAR THICKENING LEADING TO NARROWING OF THE LUMEN, 5) VESSELS BECOME PERMANENTLY NARROWED, 6) HYPERTENSIVE INJURY CAUSES INFLAMMATION TO INCREASE THE PERMEABILITY OF THE VASCULAR ENDOTHELIUM, 7) AS PERMEABILITY INCREASES MORE IONS ENTER THE VESSEL WALLS CAUSING FURTHER THICKENING |
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Term
10. When _____ occur, hypertension is usually far advanced. |
|
Definition
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|
Term
11. 7 manifestations of hypertension. |
|
Definition
1) UNSTEADINESS, 2) WALKING HEADACHE, 3) BLURRED VISION, 4) DEPRESSION, 5) RENAL DYSFUNCTION, 6) RETINAL CHANGES, 7) SIGNS OF VENTRICULAR FAILURE SUCH AS DYSPNEA OR EXERTION |
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Term
12. 4 hypertensive death related causes. |
|
Definition
1) STROKE, 2) MI, 3) RENAL FAILURE, 4) ENCEPHALOPATHY |
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Term
13. _____ is a CVA when a blood clot lodges in a vessel leading to ischemic hypoxia. |
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Definition
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Term
14. _____ is a CVA when a clot comes from a far away source. |
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Definition
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Term
15. _____ is a CVA caused by bleeding. |
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Definition
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Term
16. Hypertension is the primary cause of _____ strokes. |
|
Definition
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Term
17. _____ are small stroke like incidents that last 10 minutes or less. It leads to a loss in a patients senses. |
|
Definition
TIA (TRANSIENT ISCHEMIC ATTACK) |
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Term
18. If one has a TIA, a patient will experience these 2 symptoms. |
|
Definition
1) BRUITS, 2) THEY WILL SEE FLOATERS |
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Term
19. For something to be diagnosed as a stroke, symptoms must remain for _____ hours. |
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Definition
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Term
20. If a patient has a thrombotic stroke, _____ can be administered to bust out the clot that’s blocking the brain, and restore blood flow. This is able to completely resolve the stroke leading too complications. |
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Definition
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Term
21. Strokes tame time to _____ to completion. It might not look severe at first, but the next day the patient could look much worse. |
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Definition
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Term
22. Once a patient has completed a stoke they should work on _____ as quick as possible. |
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Definition
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Term
23. _____ and _____ are 2 agents used to treat thrombotic and embolic strokes. They must not be administered to a patient with a hemorrhagic stroke because they will bleed to death. |
|
Definition
FIBRINOLYSIS AND FIBRINOLYTIC AGENTS |
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Term
24. 13 risk factors of cerebrovascular disease. |
|
Definition
1) ATHEROSCLEROSIS, 2) HYPERTENSION, 3) HIGH CHOLESTEROL, 4) FAMILY HISTORY, 5) OBESITY, 6) SEDENTARY LIFESTYLE, 7) ORAL CONTRACEPTIVES, 8) SMOKING, 9) COAGULATION DISORDERS, 10) DEHYDRATION, 11) CHRONIC HYPOXIA, 12) CIGARETTE SMOKING |
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Term
25. 4 manifestations of a left hemispheric stroke. |
|
Definition
1) RIGHT SIDED HEMIPLEGIA, 2) SLOW AND CAUTIOUS BEHAVIOR, 3) RIGHT VISUAL FIELD DEFECT, 4) EXPRESSIVE, RECEPTIVE OR GLOBAL DYSPHASIA |
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Term
26. 7 manifestations of a right hemispheric stroke. |
|
Definition
1) LEFT SIDED HEMIPLEGIA, 2) SPATIAL-PERCEPTUAL DEFICITS, 3) IMPULSIVE BEHAVIOR, 4) DISTRACTABILITY, 5) DENIAL, 6) LEFT VISUAL FIELD DEFECTS, 7) PERSEVERATION (REPEATING A WORD OVER AND OVER) |
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Term
27. _____ is a medium by which we get transmission of a lot of different systems for the body. |
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Definition
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Term
28. The normal blood volume in the human body is _____. |
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Definition
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Term
29. _____is the fluid part of blood. |
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Definition
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Term
30. Plasma makes up _____% of blood. |
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Definition
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Term
31. _____ is a measure of albumin acting like a giant sponge that osmotically attracts fluids and holds the fluids together. It is due to the osmotic pressure created by solutes in the fluid. |
|
Definition
COLLOID OSMOTIC PRESSURE (COP) |
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Term
32. Most plasma proteins are manufactured and synthesized by the _____. |
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Definition
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Term
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Definition
1) LIVER HYPERTENSION, 2) HYPOALBUMINEMEA, 3) EXCESS ALDOSTERONE |
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Term
34. Plasma is made up of _____% water, and _____% proteins. |
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Definition
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Term
35. _____ are the antibody making cells in the body. |
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Definition
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Term
36. _____ are antibodies that are the primary immune responders. |
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Definition
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Term
37. IgM antibodies are responsible for _____. |
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Definition
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Term
38. _____ are antibodies that are the secondary immune responders. |
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Definition
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Term
39. _____ are the most abundant immunoglobulin’s in the body. |
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Definition
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Term
40. IgG antibodies respond immediately after _____. |
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Definition
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Term
41. _____ are antibodies found in allergies and hypersensitivity responses. |
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Definition
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Term
42. _____ are antibodies found in most of bodily fluid secretions. |
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Definition
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Term
43. _____ is the main clotting protein in our blood. |
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Definition
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Term
44. _____ is the total amount of blood cells and blood cell fragments due to the RBC volume and the quantity of red cells. |
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Definition
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Term
45. _____ is another name for hematocrit. |
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Definition
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Term
46. A normal person has _____ platelets in their blood stream. |
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Definition
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Term
47. A normal person has _____ leukocytes in their blood stream. |
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Definition
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Term
48. Men have _____ erythrocytes in their blood stream. |
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Definition
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Term
49. Women have _____ erythrocytes in their blood stream. |
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Definition
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Term
50. _____ tissue is where RBC’s originate. |
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Definition
MYELOID TISSUE (RED BONE MARROW) |
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Term
51. During childhood, _____ are RBC producing. |
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Definition
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Term
52. As our bodies mature, the _____ and the _____ are the producers of RBC’s. |
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Definition
AXIAL SKELETON, AND THE ENDS OF LONG BONES |
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Term
53. _____ are the parent cells of all RBC’s. |
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Definition
HEMOCYTOBLAST (HEMATOPOETIC STEM CELL) |
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Term
54. _____ is an almost mature form of the RBC that has lost its nucleus. They consist of small cells which become biconcave. |
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Definition
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Term
55. There are _____ million hemoglobins per erythrocyte. |
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Definition
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Term
56. 1 molecule of hemoglobin can bind _____ oxygen cells. |
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Definition
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Term
57. _____ is the process of producing blood cells. |
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Definition
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Term
58. _____ is the iron element at the center of the hemoglobin molecule. |
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Definition
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Term
59. _____ is iron deficiency often due to blood loss or nutritional deficiencies. |
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Definition
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Term
60. The main stimulus for formation of erythrocytes is _____. |
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Definition
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Term
61. Decreased blood oxygen causes signals to be sent to the kidneys to release _____. This hormone causes an increase in the blood production of RBC in the bone marrow. |
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Definition
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Term
62. _____ is red blood cell making that occurs in the ends of long bones. |
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Definition
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Term
63. _____ is the inactive form of erythropoiesis formed in the liver. |
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Definition
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Term
64. _____ is secreted by the kidney that causes activation of erythropoitinogen. |
|
Definition
RENAL ERYTHROPOITINOGEN FACTOR (EZ) |
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Term
65. _____ is the bone marrow that makes fatty cells used to beef up our bodies systems. |
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Definition
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Term
66. Erythrocytes have an average life span of _____ days. |
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Definition
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Term
67. Erythrocyte breakdown occurs in the _____, and the _____ is the chief cell used to break them down. |
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Definition
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Term
68. Hemoglobin is broken down into _____, which then becomes _____. |
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Definition
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Term
69. Bilirubin is responsible for giving _____ and _____ its color. |
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Definition
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Term
70. _____ coming off from the heme is recycled and reused in the future. |
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Definition
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Term
71. Excess bilirubin in the liver spills out in the skin causing _____. |
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Definition
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Term
72. Proerythroblasts are the precursor cells to _____. |
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Definition
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Term
73. Monoblasts are the precursor cells to _____. |
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Definition
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Term
74. Myeloblasts are the precursor cells to _____. |
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Definition
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Term
75. Lymphoblasts are the precursor cells to _____. |
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Definition
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Term
76. Megakaryocytes are the precursor cells to _____. |
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Definition
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Term
77. 3 types of granulocytes. |
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Definition
1) NEUTROPHILS, 2) BASOPHILS, 3) EOSINOPHILS |
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Term
78. _____ are the most numerous white blood cells in the body. They are important phagoc ytes in acute inflammation. |
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Definition
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Term
79. Neutrophils stain _____, and have a _____ nucleus. |
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Definition
LIGHT PURPLE; MULTI-LOBULED NUCLEUS |
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Term
80. _____are white blood cells that protect us against infections caused by parasitic worms, and they are involved in allergic reactions. |
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Definition
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Term
81. Eosinophils stain _____, and they have a _____ nucleus. |
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Definition
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Term
82. _____ are the least common white blood cells that are responsible for secreting heparin. |
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Definition
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Term
83. Basophils stain _____, and have a _____ nuclei. |
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Definition
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Term
84. 2 different types of agranulocytes. |
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Definition
1) LYMPHOCYTES, 2) MONOCYTES |
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Term
85. _____ are the second most common WBC’s that play an immunity role defense. |
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Definition
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Term
86. _____ lymphocytes are regulatory helper and suppressor cells. |
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Definition
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Term
87. _____ lymphocytes are responsible for antibody production. |
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Definition
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Term
88. Lymphocytes have a _____ stained cytoplasm. |
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Definition
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Term
89. _____ are key phagocytic agranulocytes that become macrophages in circulation as soon as they leave production. |
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Definition
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Term
90. _____ is a decrease in the number of white blood cells. |
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Definition
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|
Term
91. 3 causes of a shift to the left differential. |
|
Definition
1) NEUTROPHILS RESPONDING TO ACUTE INFLAMMATION, 2) LEUKOCYTOSIS, 3) MORE BAND CELLS IN THE PLASMA |
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|
Term
92. 2 causes of a shift to the right differential. |
|
Definition
1) INCREASED LYMPHOCYTES DURING CHRONIC INFLAMMATION, 2) LYMPHOCYTIC LEUKOCYTOSIS |
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Term
93. 88% neutrophils causes what? |
|
Definition
SHIFT TO THE LEFT, ACUTE INFLAMMATION |
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|
Term
94. What is an example of a shift to the left? |
|
Definition
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Term
95. 40% lymphocytes causes what? |
|
Definition
SHIFT TO THE RIGHT, CHRONIC INFLAMMATION |
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|
Term
96. What is an example of a shift to the right? |
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Definition
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|
Term
97. _____ are cell fragments from megakaryocytes. |
|
Definition
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|
Term
98. Platelets play a major role in _____ and _____, and they are released in response around tissue injury and clump together to stop bleeding. |
|
Definition
HEMOSTASIS (STOP BLEEDING) AND COAGULATION |
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|
Term
99. The life span of platelets is typically _____ days. |
|
Definition
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|
Term
100. The normal platelet count is between _____. |
|
Definition
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|
Term
101. _____ is a deficiency in the number of WBC’s. |
|
Definition
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|
Term
102. Leukopenia is a common side effect of _____. |
|
Definition
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|
Term
103. _____ is having decreased numbers of neutrophils. |
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Definition
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|
Term
104. _____ is having decreased numbers of lymphocytes. |
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Definition
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|
Term
105. _____ is a decrease in the number of platelets (below 100,000 platelets/mm3). |
|
Definition
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|
Term
106. Why do we worry about patients with thrombocytopenia. |
|
Definition
WE WORRY ABOUT INTERNAL BLEEDING WHEN #’S FALL BELOW 40,000 |
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|
Term
107. What is another name for platelets? |
|
Definition
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|
Term
108. How are platelets formed? |
|
Definition
FROM CELL FRAGMENTS OF MEGAKARYOCYTES WHICH COME FROM STEM CELLS |
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|
Term
109. What is the average life span of platelets? |
|
Definition
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|
Term
110. Red blood cells have surface _____ that have been given classification in the ABO system. |
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Definition
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|
Term
111. Type A blood has _____ on the RBC surface, and has _____ in plasma. |
|
Definition
ANTIGEN A; TYPE B ANTIBODY |
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|
Term
112. Type B blood has _____ on the RBC surface, and has _____ in plasma. |
|
Definition
ANTIGEN B; TYPE A ANTIBODIES |
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Term
113. Type AB blood has _____ on the RBC surface, and _____ in plasma. |
|
Definition
ANTIGENS A AND B; NO A OR B ANTIBODIES |
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Term
114. Blood type AB is known as the _____. |
|
Definition
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|
Term
115. Type O blood has _____ on the RBC surface, and _____ in plasma. |
|
Definition
NO A OR B ANTIGENS; A AND B ANTIBODIES |
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Term
116. Type O blood is known as the _____. |
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Definition
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Term
117. _____ is when the D-antigen is present on the RBC surface. |
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Definition
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Term
118. _____ is when there is no D-antigen present on the RBC surface. |
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Definition
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Term
119. _____ is when there is a blood transfusion reaction for an RH(-) patient. The first time fused no reaction will occur, but the patient will develop antibodies against the RH factor causing a reaction each subsequent blood transfusion. |
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Definition
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Term
120. _____ is a condition when a RH(-) mother gets pregnant with an RH(+) baby. The mother body creates antibodies against the fetuses blood, causing a destruction of the baby’s erythrocytes. |
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Definition
ERYTHROBLASTOSIS FETALIS (HEMOLYTIC DISEASE OF THE NEWBORN) |
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Term
121. The dangers of erythroblastosis fetalis increases with _____. |
|
Definition
EACH SUBSEQUENT PREGNANCY |
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Term
122. _____ is the medication given to the mother with erythroblastosis fetalis. It causes the mothers body to think it has already made antibodies to the D-antigen; fooling the mothers immune system to prevent the in utero attach on the fetus. |
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Definition
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|
Term
123. _____ means to stop bleeding. |
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Definition
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Term
124. 3 ways our bodies perform hemostasis. |
|
Definition
1) VASCULAR SPASM, 2) PLATELET PLUG FORMATION, 3) FIBRIN FORMATION CAUSING COAGULATION |
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Term
125. _____ agents are direct dissolvers of blood clots. |
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Definition
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Term
126. _____ agents are clot prevents and prevent clots from forming, or already formed clots from getting any bigger. |
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Definition
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|
Term
127. _____ is having blood in the stool. |
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Definition
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|
Term
128. Blood clotting factors made in the liver are dependent on _____ for synthesis. |
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Definition
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Term
129. _____ is an immediate but temporary closure of a blood vessel resulting from contraction of smooth muscle within the blood vessels wall. |
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Definition
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|
Term
130. Vascular spasms are caused by these 2 bodily mechanisms. |
|
Definition
1) NERVOUS SYSTEM REFLEXES, 2) CHEMICALS RELEASED FROM PLATELETS DURING FORMATION OF THE PLATELET PLUG |
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|
Term
131. In small vessels, vascular spasm can close the vessel _____. |
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Definition
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|
Term
132. When a blood vessel is damaged, the endothelium becomes torn and the underlying tissue is exposed. When this happen _____ adhere to the _____ in the connective tissue. |
|
Definition
PLATELETS; COLLAGEN FIBERS |
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Term
133. When platelets adhere to the collagen fibers in the connective tissue during platelet plug formation, it causes the release of these 4 chemicals. |
|
Definition
1) ADP, 2) THROMBOXANE, 3) SEROTONIN, 4) CHEMICALS INVOLVED IN COAGULATION |
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|
Term
134. _____ and _____ are 2 chemicals released by platelets that cause vascular spasm. |
|
Definition
THROMBOXANE AND SEROTONIN |
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Term
135. _____ is a chemical released by platelets that makes their surface sticky, so additional platelets adhere to those already attached to the collagen fibers. |
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Definition
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|
Term
136. _____ is a chemical released by platelets that induces the aggregating platelets to release ADP, thromboxane, and other chemicals. |
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Definition
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|
Term
137. When platelets adhere to each other and release chemicals that cause other platelets to adhere, it forms an accumulating mass called a _____. |
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Definition
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|
Term
138. _____ is the formation of a blood clot that consists of a network of fibrin in which blood cells, platelets, and fluid become trapped. |
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Definition
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|
Term
139. Coagulation is dependent on coagulation factors present in the _____. |
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Definition
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|
Term
140. 3 main stages of coagulation. |
|
Definition
STAGE 1) ACTIVATION OF FACTOR XII AND PRODUCTION OF PROTHROMBIN ACTIVATOR; STAGE 2) CONVERSION OF PROTHROMBIN TO THROMBIN BY PROTHROMBIN ACTIVATOR FACOR; STAGE 3) ENZYMATIC CONVERSION BY THROMBIN OF SOLUBLE FIBRINOGEN TO INSOLUBLE FIBRIN |
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Term
141. Coagulation operates via both the _____ and _____ pathways. |
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Definition
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Term
142. The _____ pathway of coagulation is turned on by factors that are outside the damaged blood vessel. If surrounding tissues are damages, a domino effect will occur that will form the prothrombin factor. |
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Definition
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|
Term
143. The _____ pathway of coagulation is when circulating clotting factors (factor XII) comes in contact with damaged blood vessels that starts a cascade which ends up as prothrombin factor. |
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Definition
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|
Term
144. _____ is needed in both the intrinsic and extrinsic coagulation pathways. |
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Definition
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|
Term
145. Once a blood clot forms, it condenses into a denser, compact structure through a process known as _____. |
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Definition
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|
Term
146. As a clot condenses _____ is squeezed out of the clot. |
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Definition
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|
Term
147. Consolidation of clots pull the edges of damaged vessels together, which may help _____, _____ and _____. |
|
Definition
STOP BLOOD FLOW, REDUCE INFECTION, AND ENHANCE HEALING |
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|
Term
148. A clot usually dissolves within a few days after a clot formation by a process known as _____, which is a natural biochem reaction that occurs when the threat is over and the body returns its tissue to the original structure and function. |
|
Definition
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|
Term
149. 3 steps of fibrinolysis. |
|
Definition
1) PLASMINOGEN IS ACTIVATED BY THROMBIN FACTOR XII, TISSUE PLASMINOGEN ACTIVATOR, AND LYSOSOMAL ENZYMES RELEASED FROM DAMAGED TISSUES, 2) PLASMINOGEN FORMS PLASMIN, 3) PLASMIN HYDROLYZES FIBRIN DISSOLVING THE CLOT |
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|
Term
150. What is the difference between anticoagulants and thrombolytic agents? |
|
Definition
ANTICOAGULANTS PREVENT FIBRIN FROM FORMING, WHILE THROMBOLITIC AGENTS DISSOLVE FIBRIN OR BUST THE CLOT |
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|
Term
151. _____ are medications that drive the production of plasmin to bust the clots. They are not anti-coagulants. |
|
Definition
THROMBOLYTICS/FIBRINOLYTICS |
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Term
152. _____ do not dissolve clots, rather they prevents cots from forming or prevent existing clots from getting bigger. |
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Definition
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|
Term
153. _____ and _____ are common anticoagulant medications. |
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Definition
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|
Term
154. How does Coumadin work? |
|
Definition
IT WORKS IN THE LIVER BY COMPETING WITH VITAMIN K. SINCE CLOTTING FACTORS ARE DEPENDENT ON VITAMIN K, COUMADIN WILL RESTRICT FIBRIN SYNTHESIS |
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|
Term
155. If patients eat foods with _____, it can counteract the effects of Coumadin. |
|
Definition
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|
Term
156. How does heparin work? |
|
Definition
IT WORKS IN THE PERIPHERY PREVENTING PROTHROMBIN FROM BEING CONVERTED TO THROMBIN |
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|
Term
157. Heparin takes up to _____hours to work. |
|
Definition
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|
Term
158. _____ is an antidote for heparin overdose, which is made from fish sperm. |
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Definition
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|
Term
159. 3 signs of internal bleeding. |
|
Definition
1) LARGE, DISTENDED HARD ABDOMEN, 2) FLANK PAIN, 3) BLOOD IN STOOL OR URINE |
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|
Term
160. 3 signs of over-coagulation. |
|
Definition
1) EASY BRUISING, 2) PETECIAL HEMORRHAGES, 3) SHAVING CUTS THAT DO NOT STOP BLEEDING |
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|
Term
161. 2 coagulation factors found in our body. |
|
Definition
1) FACTOR I- FIBRINOGEN, 2) FACTOR XII- FIBRIN STABILIZING FACTOR |
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|
Term
162. _____ is a test to determine clotting test times of people taking warfarin/Coumadin. |
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Definition
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|
Term
163. _____ is a test to determine clotting test times of people on heparin. |
|
Definition
PARTIAL THROMBOPLASTIN TIME (PTT) |
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|
Term
164. The normal PTT time is between _____. |
|
Definition
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|
Term
165. _____ is the standardized clotting times across the globe, it consists of a ration responsible for standardizing everything. |
|
Definition
INTERNATIONAL NORMALIZED RATION (INR) |
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|
Term
166. The normal clotting time in the INR is between _____. |
|
Definition
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|
Term
167. The normal ratio of INR is between _____ and _____. |
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Definition
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|
Term
168. The desirable anticoagulant effect of INR is between _____ and _____. |
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Definition
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|
Term
169. 3 components of a complete blood count. |
|
Definition
1) WBC COUNT, 2) RBC COUNT, 3) PLATELET COUNT |
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|
Term
170. _____ is a test the counts the actual number of WBC’s per volume of blood. |
|
Definition
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|
Term
171. _____ is a test that determines what types of WBC’s are present in the blood. |
|
Definition
WHITE BLOOD CELL DIFFERENTIAL |
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|
Term
172. _____ is a test to determine the actual number of RBC’s per volume of blood. |
|
Definition
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|
Term
173. _____ is a test to determine the amount of oxygen carrying protein in the blood. |
|
Definition
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|
Term
174. _____ is a test to determine the rate of RBC production. |
|
Definition
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|
Term
175. _____ is a test to determine the amount of space RBC’s take up in the blood. |
|
Definition
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|
Term
176. _____ is a test to determine the number of platelets in a given volume of blood. |
|
Definition
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|
Term
177. _____ is a test to measure the average size of RBC’s. |
|
Definition
MEAN CORPUSCULAR VOLUME (MCV) |
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|
Term
178. MCV is an important in testing for _____. |
|
Definition
ANEMIAS DUE TO B12 DEFICIENCY |
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|
Term
179. _____ is a test to calculate the amount of hemoglobin inside of the RBC’s. |
|
Definition
MEAN CORPUSCULAR HEMOGLOBIN (MCH) |
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|
Term
180. _____ is a test to calculate the percentage of hemoglobin in red blood cells. |
|
Definition
MEAN CORPUSCULAR HEMOGLOBIN CONCENTRATION (MCHC) |
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|
Term
181. _____ is a test to determine how varied the size of RBC’s are in a sample. |
|
Definition
RED CELL DISTRIBUTION WIDTH (RDW) |
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|
Term
182. RDW helps determine the kind of _____ one may have. |
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Definition
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|
Term
183. _____ is the most life threatening skin carcinoma. |
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Definition
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|
Term
184. _____ for skin disorders serve as anti-inflammatory agents. |
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Definition
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|
Term
185. What is a cubitus ulcer? |
|
Definition
A BEDSORE (WHEELCHAIR BOUND PATIENT) |
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Term
186. Herpes zoster spreads along the _____. |
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Definition
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Term
187. _____ is a condition caused by a low number of circulating red cells, abnormally low number of hemoglobin, or both. |
|
Definition
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|
Term
|
Definition
1) BLOOD LOSS, 2) LACK OF OXYGEN DELIVERY TO CELLS/TISSUES, 3) DECREASED OXYGEN AFFINITY TO HEMOGLOBIN |
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|
Term
189. What increased oxygen’s affinity for hemoglobin? |
|
Definition
THE ACTUAL BINDING OF OXYGEN TO THE HEMOGLOBIN |
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|
Term
190. 3 things that decrease oxygen’s affinity for hemoglobin. |
|
Definition
1) BINDING OF CO2 TO HEMOGLOBIN, 2) BINDING OF PROTONS TO SPECIFIC BASIC GROUPS, 3) BINDING OF CERTAIN ORGANIC PHOSPHATES |
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Term
191. _____ anemia is most common in menstruating women. |
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Definition
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Term
192. _____ anemia is due to an early destruction of RBC’s due to a pathology. |
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Definition
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Term
193. _____ is a major pathology that causes hemolytic anemia. |
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Definition
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|
Term
194. _____ anemia is caused by a vitamin B-12 deficiency. |
|
Definition
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|
Term
195. 3 different types of nutritional deficiency anemia’s. |
|
Definition
1) PERNICIOUS ANEMIA, 2) FOLIC ACID DEFICIENCY ANEMIA, 3) IRON DEFICIENCY ANEMIA |
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|
Term
196. _____ anemia is caused by a bone marrow depression causing a lack of adequate production of RBC’s. it is usually accompanied by depressions in other formed elements of the blood. |
|
Definition
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|
Term
197. 9 signs and symptoms of general anemia. |
|
Definition
1) FATIGUE/WEAKNESS, 2) PALLOR, 3) TACHYCARDIA, 4) ANXIETY, 5) SYSTOLIC MURMUR, 6) VENTRICULAR HYPERTROPHY, 7) CHF, 8) ERYTHROPOEISIS, 9) ANGINA AND NIGHT CRAMPS |
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Term
198. _____ anemia’s are due to an early destruction of red blood cells either due to extrinsic or intrinsic causes. |
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Definition
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Term
199. _____ is an intrinsic cause of hemolytic anemia that is caused by an autosomal trait causing spherical-shaped RBC’s rather than biconcave disc shape. |
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Definition
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Term
200. In hereditary spherocytosis, the tight spherical shape RBC’s will hemolyze and be _____ early in mass numbers. |
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Definition
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Term
201. _____ is sometimes used as the treatment of hemolytic anemia’s for adults, but it will not work in children. |
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Definition
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Term
202. _____ are conditions inherent to hemoglobin molecules. |
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Definition
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Term
203. Hemoglobin usually consists of _____ polypeptide chains. |
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Definition
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Term
204. Hemoglobinopathies occur when one hemoglobin polypeptide chain is substituted with an _____. |
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Definition
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Term
205. Sickle cell anemia is a condition when one of the hemoglobin amino acids is substituted with _____ rather than a polypeptide chain. |
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Definition
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Term
206. Sickle cell anemia typically occurs in _____. |
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Definition
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|
Term
207. _____ are sickle cells. |
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Definition
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Term
208. _____ are normal hemoglobin cells. |
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Definition
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Term
209. Is a person contains the _____ and _____ cells, they are carriers for the sickle cell trait. |
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Definition
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|
Term
210. If a person contains the _____ and _____ cells, they will have sickle cell anemia. |
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Definition
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|
Term
211. Why is sickle cell anemia more dangers in a low oxygen environment. |
|
Definition
IN LOW OXYGEN ENVIORNMENTS, THE SICKLE HBS BECOMES AN AGGREGATE AND BOWS OUT THE CELL |
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|
Term
212. A sickling crisis can cause death by leading to _____. |
|
Definition
HEMOLYSIS AT LOG-JAMMED CAPILLARIES |
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|
Term
213. Factors that precipitate sickling are related to _____. |
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Definition
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|
Term
214. 6 low oxygen situations that can lead to sickling. |
|
Definition
1) EXERCISE, 2) HYPOXIA, 3) ACIDOSIS, 4) DEHYDRATION, 5) INFECTION, 6) REDUCED OXYGEN TENSION IN SLEEP |
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|
Term
215. 5 symptoms of sickle cell crisis. |
|
Definition
1) SWOLLEN HANDS AND FEET, 2) STROKE, 3) MI, 4) KIDNEY FAILURE, 5) HEMOLYSIS |
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|
Term
216. What causes the painful crisis of sickle cell? |
|
Definition
VESSEL OCCLUSION THAT MAY APPEAR SUDDENLY IN ALMOST ANY PART OF THE BODY |
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|
Term
217. Hemoglobin is composed of _____, which is made up of 4 folded polypeptide chains, and 4 _____. |
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Definition
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|
Term
218. Each hemoglobin molecule can carry _____ molecules of oxygen. |
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Definition
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|
Term
219. When hemoglobin is called _____ when carrying oxygen, and _____ when not carrying oxygen. |
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Definition
OXYHEMOGLOBIN, REDUCED HEMOGLOBIN |
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Term
220. Hemoglobin can also combine with _____ to transport it from the tissues to the lungs for excretion. |
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Definition
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|
Term
221. _____ is a condition that results from absent or defective synthesis of either the alpha or beta chains of hemoglobin’s causing a decrease in the size of cells and a change in the MCV (size of RBC). |
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Definition
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|
Term
222. _____ is a repeated defect in the beta-chain synthesis of hemoglobin. |
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Definition
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|
Term
223. B-thalassemias is most common in the _____ population. |
|
Definition
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|
Term
224. If a person receives the B-thalassemias trait from both parents it will cause transfusion-dependent anemia leading to death by _____. |
|
Definition
HEMOCHROMATOSIS (EXCESS IRON) |
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|
Term
225. 6 symptoms present in children with B-thalassemias. |
|
Definition
1) GROWTH RETARDATION, 2) SPLEENOMEGALY, 3) HEPATOMEGALY, 4) INCREASED RBC DISTRUCTION, 5) INCREASED STIM FOR HEMATOPORIESIS CAUSING BONE MARROW EXPANSION, 6) THINNING OF THE CORTICAL BONE |
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|
Term
226. A-thalassemias is most common in _____. |
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Definition
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|
Term
227. Most severe cases of A-thalassemias occurs in _____. |
|
Definition
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|
Term
228. Anemia occurs in A-thalassemias due to _____ and _____. |
|
Definition
DEFECTIVE HEMOGLOBIN PRODUCTION, ACCUMULATION OF UNPAIRED GLOBIN CHAINS |
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|
Term
229. What is more severe alpha or beta thalassemias? |
|
Definition
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|
Term
230. Individuals with the mildest form of A-thalassemias are usually _____ having mild _____. |
|
Definition
ASYMPTOMATIC, MICROCYTOSIS |
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|
Term
231. The minor form of A-thalassemias is associated with these 4 conditions. |
|
Definition
1) MILD MICROCYTITC HYPOCHROMIC RETICULOCYTOSIS (IMMATURE RBC’S), 2) BONE MARROW HYPERPLASIA, 3) INCREASED SERUM IRON CONCENTRATION, 4) MODERATE SPLENOMEGALY |
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|
Term
232. 2 factors that cause microcytic-hypochromic anemia in A-thalassemias. |
|
Definition
1) REDUCED HEMOGLOBIN SYNTHESIS AND IMBALANCE IN GLOBIN CHAIN PRODUCTION, 2) UNPAIRED CHAINS ACCUMULATE IN RED CELLS CAUSING RBC DESTRUCTION AND ANEMIA |
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|
Term
233. The most common disorder associated with an inherited enzyme deficiency is _____. |
|
Definition
G-6-PD (GLUCOSE-6-PHOSPHO DEHYDROGENASE) |
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|
Term
234. G-6-PD causes the direct oxidation of hemoglobin which forms a _____. |
|
Definition
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|
Term
235. 3 risk factors of the formation of methemoglobin. |
|
Definition
1) THE CELL IS NOT FUNCTIONAL, 2) DENATURED HEMOGLOBIN MOLECULE RESULTS, 3) THEY CAN NOT MAKE IT THROUGH THE TIGHT CIRCULATORY AREAS OF THE BODY |
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|
Term
236. G-6-PD eventually results in _____. |
|
Definition
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|
Term
237. 6 extrinsic anemia factors. |
|
Definition
1) DRUGS, 2) CHEMICALS, 3) TOXINS, 4) ARTIFICIAL MECHANICAL BODY STRUCTURES, 5) BURNS, 6) ANY DIRECT INJURY TO THE RBC’S THEMSELVES |
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|
Term
238. _____ means the size of the RBC is normal. |
|
Definition
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|
Term
239. _____ means the size of the RBC is small. |
|
Definition
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|
Term
240. The most common cause of microcytic RBC’s is _____. |
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Definition
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|
Term
241. _____ means the size of the RBC is large. |
|
Definition
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|
Term
242. _____ means the color of the RBC is normal. |
|
Definition
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|
Term
243. _____ means there is a decrease in the color of the RBC. |
|
Definition
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|
Term
244. These 2 criteria must be met for anemia to be classified as nutritional anemia. |
|
Definition
1) THERE MUST BE A DEFECIENCY OR LACK OF A NUTRIENT ALONE CAUSING THE ANEMIA, 2) HAVING THE NUTRIENT PROVIDED CORRECTS THE ANEMIA |
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|
Term
245. 4 symptoms associated with nutritional anemias. |
|
Definition
1) PALLOR, 2) WEAKNESS, 3) LETHARGY, 4) HEART RATE ELEVATION |
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|
Term
246. 2 additional symptoms associated with iron deficiency anemias. |
|
Definition
1) SOARS IN THE CORNER OF THE MOUTH, 2) PICA (EATING DIRT, CLAY OR ICE) |
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|
Term
247. If blood was drawn in a patient with iron deficiency anemia, the red blood cells would be _____ and _____. |
|
Definition
MICROCYTIC AND HYPOCHROMIC |
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|
Term
248. 3 classes of nutritional anemias. |
|
Definition
1) IRON DEFICIENCY ANEMIA, 2) PERNICIOUS ANEMIA, 3) FOLIC ACID DEFICIENCY ANEMIA |
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|
Term
249. _____ is essential for heme, in that each heme unit has one of these molecules at its center to form hemoglobin. |
|
Definition
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|
Term
250. 3 causes of iron deficiency during pregnancy and pre-natal development. |
|
Definition
1) IF MOM IS IRON DEFICIENT SO IS THE BABY, 2) MOMS WHO ARE IRON DEFICIENT AND BREAST FEED WILL TRANSFER IT TO THE BABY, 3) IF NOT BREAST FEEDING COWS MILK MUST BE IRON FORTIFIED |
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|
Term
251. What is the main symptom of iron deficiency during the infant/toddler years? |
|
Definition
PICA (EATING THINGS THAT ARE NOT NORMALLY EDIBLE) |
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|
Term
252. During the teenage years girls on their _____ and _____ are susceptible to iron deficiency. |
|
Definition
MENSTRUAL CYCLE, NOT EATING PROPERLY |
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|
Term
253. The most vulnerable time of iron deficiency in the adult years is during _____. |
|
Definition
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|
Term
254. _____ is anemia caused by a lack of vitamin B12/intrinsic factor. |
|
Definition
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|
Term
255. Pernicious anemia causes _____ RBC’s as well as _____ anemias. |
|
Definition
MACROCYTIC, MEGALOBLASTIC |
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|
Term
256. The _____ is necessary for vitamin B-12 to be absorbed in the intestine. |
|
Definition
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|
Term
257. Patients with pernicious anemia can have these 3 CNS related effects. |
|
Definition
1) NEUROLOGIC DEGENERATION OF DORSAL AND LATERAL SPINAL COLUMNS, 2) PARASTHESIA, 3) SPASTIC ATAXIA |
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|
Term
258. Folic acid anemias cause _____ RBC’s and _____ anemias. |
|
Definition
MACROCYTIC, MEGALOBLASTIC |
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|
Term
259. _____ anemias usually have normal size and color RBC’s. |
|
Definition
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|
Term
260. 3 causes of a shift to the right in the oxygen saturation curve. |
|
Definition
1) EXERTION, 2) INFECTION (TEMP INCREASE), 3) SURGERY |
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|
Term
261. _____ is polycythemia caused by dehydration or fluid loss. |
|
Definition
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|
Term
262. _____ is polycythemia caused by anything that increases the bone marrow production of RBC’s. |
|
Definition
|
|
Term
263. _____ polycythemia is caused by a congenital issue leading to a proliferative disease in the bone marrow causing an accelerated production of RBC’s. |
|
Definition
PRIMARY POLYCYTHEMIA (POLYCYTHEMIA VERA) |
|
|
Term
264. Polycythemia vera causes _____ blood due to extra RBC’s, and problems arise due to _____. |
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Definition
VISCOUS; INCREASED BLOOD VISCOSITY |
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Term
265. The skin of a patient with polycythemia vera will appear _____. |
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Definition
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Term
266. _____ is the treatment of polycythemia vera. |
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Definition
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Term
267. 7 conditions associated with polycythemia vera. |
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Definition
1) BLOOD CLOTS, 2) HYPERTENSION, 3) PAINFUL ITCHING SENSATIONS, 4) SLUGGISH BLOOD FLOW, 5) PROBLEMS HEARING AND CONCENTRATING, 6) IRRITABILITY, 7) THROMBOSIS |
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Term
268. Suppressing the bone marrow of polycythemia vera requires _____, which is risky due to the side effects. |
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Definition
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Term
269. Polycythemia vera may lead to _____ or _____ due to stagnation and build-up of thick blood. |
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Definition
THROMBOSIS, FRANK HEMORRHAGING |
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Term
270. _____ disorders are caused by platelet issues and anything that causes a decrease in platelet production. |
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Definition
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Term
271. _____ is a condition when there is less than 100,000 platelets in the body. |
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Definition
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Term
272. 3 mechanisms behind thrombocytopenia. |
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Definition
1) DECREASE IN PLATELET PRODUCTION BY THE BONE MARROW, 2) INCREASED POOLING OF PLATELETS IN THE SPLEEN CAUSING SPLEENOMEGALY, 3) DECREASED PLATELET SURVIVAL |
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Term
273. 4 causes of thrombocytopenia. |
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Definition
1) VIRAL INFECTIONS, 2) DRUGS, 3) IDIOPATHIC, 4) BONE MARROW PROBLEMS |
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Term
274. 3 signs and symptoms of thrombocytopenia. |
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Definition
1) EASY BRUISING, 2) NOSE BLEEDS, 3) SHAVING CUTS THAT DON’T STOP BLEEDING |
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Term
275. _____ occurs 1-4 weeks after a viral infection, causing bruising and a generalized petechial rash that often occurs with acute onset. |
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Definition
IDIOPATHIC THROMBOCYTOPENIC PURPA (ITP) |
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Term
276. 4 conditions associated with idiopathic thrombocytopenic purpa. |
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Definition
1) ASYMMETRICAL BLEEDING FOUND MOST FREQUENTLY COVERING THE LEGS, 2) HEMORRHAGE BULLAE OF THE MUCOUS MEMBRANES, 3) EPISTAXIS (NOSE BLEEDS), 4) SPONTANEOUS HEMORRHAGES THAT LAST 1-2 WEEKS |
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Term
277. _____ is used to slow down the platelet production in idiopathic thrombocytopenic purpa. |
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Definition
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Term
278. _____ is a condition that begins as a systemic clotting issue that ends up as a bleeding problem secondary to some other event. |
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Definition
DISIMINATED INTRAVASCULAR COAGULATION (DIC) |
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Term
279. _____ is the most common cause of disiminated intravascular coagulation. |
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Definition
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Term
280. 8 causes of disiminated intravascular coagulation. |
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Definition
1) MASSIVE TRAUMA, 2) BURNS, 3) SEPSIS, 4) SHOCK, 5) MALIGNANT DISEASE, 6) MENONGOCOCCEMIA, 7) OBSTETRIC COMPLICATIONS, 8) SNAKE BITES |
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Term
281. _____ is a condition associated with disiminated intravascular coagulation that has a very high mortality rate. |
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Definition
BLEEDING FROM EVERY ORIFICE |
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Term
282. What is the treatment of disiminated intravascular coagulation? |
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Definition
STOP THE UNDERLYING PATHOLOGY AND ADMINISTER HEPARIN TO SUPPLY FRESH COAGULATION FACTORS AND PLATELETS |
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Term
283. _____ is a common bleeding pathology within the body. |
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Definition
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Term
284. _____ is classic hemophilia, which is an x-linked recessive disorder manifesting in males that is transmitted by females. |
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Definition
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Term
285. Hemophilia A is caused by a defect of _____, which is prevented from participating in the intrinsic clotting pathway. |
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Definition
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Term
286. _____ is the most common hemophilia and accounts for 80-85% of all cases. |
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Definition
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Term
287. Thrombin is nor normally found in circulating blood. In order for thrombin to be made in the intrinsic clotting pathway, prothrombin (factor II) requires _____ and _____ to be converted to thrombin. |
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Definition
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Term
288. _____ is the second most common hemophilia (15%) caused by an x-linked recessive trait that is clinically indistinguishable from a factor VIII deficiency. |
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Definition
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Term
289. Hemophilia B is caused by a _____ deficiency. |
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Definition
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Term
290. Hemophilia B is also referred to as _____. |
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Definition
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Term
291. How can a doctor distinguish between hemophila A and B? |
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Definition
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Term
292. _____ is a hemophilia that results from an autosomal recessive disease that occurs equally in males and females. |
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Definition
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Term
293. Hemophilia C is caused by a _____ deficiency. |
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Definition
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Term
294. In patients with hemophilia C, bleeding is usually _____ than in hemophilia A or B. |
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Definition
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Term
295. Hemophilia C does not present at birth, but rather around _____ when clotting factors begin to fail. |
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Definition
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Term
296. 4 symptoms of patients with hemophilia C. |
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Definition
1) EASY BRUISING, 2) BLEEDING GUMS OR JOINTS, 3) BLOOD IN URINE OR STOOL, 4) EPISTAXIS (NOSE BLEEDS) THAT DO NOT STOP |
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Term
297. _____ is a condition caused by a defect in a different subunit, co-factor, or carrier protein of factor VIII. It is an inherited autosomal dominant trait that is different from hemophilia A. |
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Definition
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Term
298. In von wilderband disease, rapidly circulating platelets are unable to stick to _____ and _____ cannot be formed. |
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Definition
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Term
299. What is mainly affected by von wildebrand disease? |
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Definition
ENDOTHELIAL CELLS THAT LINE VESSELS |
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Term
300. _____ is the usual treatment of von wildebrand disease, which caused factor VIII activity to increase for several days. It temporarily induced endogenous synthesis of factor VIII. |
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Definition
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Term
301. _____ is a life threatening condition that causes a rapid proliferation of immature WBC’s by the bone marrow. |
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Definition
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Term
302. 11 endogenous findings associated with leukemia. |
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Definition
1) ABNORMAL PATHOLOGICAL CELLS, 2) EXCESS BONE MARROW PROLIFERATION, 3) REPLACEMENT OF BONE MARROW WITH WBC’S (BONE MARROW DEPRESSION), 4) EXCESS NON-FUNCTIONAL WBC’S IN BLOOD, 5) SPLENOMEGALY, 6) HEPATOMEGALY, 7) LYMPHANDENOAPTHY, 8) WEIGHT LOSS, 9) NIGHT SWEATS, 10) LOW GRADE FEVER, 11) HYPERURICEMIA |
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Term
303. If a patient has leukemia, _____ and _____ will result due to decreased platelet and erythrocyte production. |
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Definition
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Term
304. _____ is present in 90% of all leukemia patients. |
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Definition
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Term
305. 6 CNS related conditions associated with leukemia. |
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Definition
1) ENCEPHALOPATHY, 2) MENINGITIS, 3) CRANIAL NERVE PALSIES, 4) BLURRED VISION, 5) HEADACHE, 6) SEIZURES |
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Term
306. The 2 acute forms of leukemia are _____ and _____. |
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Definition
ACUTE LYMPHOCYTIC LEUKEMIA; ACUTE MYELOTIC LEUKEMIA OR ACUTE GRANULOCYTIC LEUKEMIA |
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Term
307. _____ is an acute form of leukemia with a sudden onset most commonly seen in children between the ages of 2 and 4. |
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Definition
ACUTE LYMPHOCYTIC LEUKEMIA |
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Term
308. In acute lymphocytic leukemia _____ are differentiated poorly. |
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Definition
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Term
309. The onset of acute lymphocytic leukemia is _____. |
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Definition
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Term
310. _____ accounts for 2/3 of all leukemia cases. |
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Definition
ACUT E LYMPHOCYTIC LEUKEMIA |
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Term
311. 6 symptoms associated with acute lymphocytic leukemia. |
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Definition
1) FEVER, 2) MUSCLE FATIGUE, 3) BLEEDING, 4) BONE PAIN, 5) BONE MARROW DYSFUNCTION, 6) ANEMIA |
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Term
312. More than _____% of children with acute lymphocytic leukemia have complete remission, while _____% of children live 5 years or longer. 90%, |
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Definition
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Term
313. _____ is an acute form of leukemia with a low survival rate. It affects all the –phil cells, and symptoms arise abruptly which are similar to those of acute lymphocytic anemia. |
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Definition
ACUTE MYELOTIC LEUKEMIA (ACUTE GRANULOCYTIC LEUKEMIA) |
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Term
314. _____ is the most common type of leukemia found in adults. |
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Definition
ACUTE MYELOTIC OR GRANULOCYTIC LEUKEMIA |
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Term
315. Acute myelotic leukemia is treated with intensive chemo to cause _____ of the bone marrow. |
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Definition
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Term
316. Only about _____% of acute myelotic leukemia patients who receive chemo will achieve long-term disease free survival. |
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Definition
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Term
317. The more _____ a cell, the more malignant they can become and lead to a more progressive cancer. |
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Definition
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Term
318. These are the 2 types of chronic leukemia’s. |
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Definition
1) CHRONIC LYMPHOCYTIC LEUKEMIA, 2) CHRONIC MYELOCYTIC OR GRANULOCYTIC LEUKEMIA |
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Term
319. _____ is a form of chronic leukemia that is often a disorder in older adults between the ages of 50-70. The disease consists of slightly differentiated cells which causes the disease to progress _____. |
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Definition
CHRONIC LYMPHOCYTIC LEUKEMIA; SLOWLY |
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Term
320. Is chronic lymphocytic leukemia more common in men or women? |
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Definition
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Term
321. Unlike acute lymphocytic leukemia, in chronic lymphocytic leukemia the chronic cells are more _____ and easily identifiable. |
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Definition
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Term
322. Chronic lymphocytic leukemia cells develops _____, but _____ are affected. |
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Definition
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Term
323. Patients with chronic lymphocytic anemia are usually diagnosed when they are _____, and they life expectancy is _____ than those patients with acute lymphocytic anemia. |
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Definition
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Term
324. _____ is a chronic form of leukemia that occurs in patients between the ages of 30-50. |
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Definition
CHRONIC MYELOCYTIC OR GRANULOCYTIC LEUKEMIA |
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Term
325. In chronic myelocytic or granulocytic leukemia, bone marrow cells have the _____ chromosome that occurs in mitotic error with a shortened arm on chromosome _____. |
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Definition
PHILADELPHIA CHROMOSOME; CHROMOSOME 22 |
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Term
326. Chronic myelocytic or granulocytic leukemia patients are often _____ when diagnosed. |
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Definition
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Term
327. About _____% of chronic myelocytic or granulocytic leukemia patients enter an accelerated phase characteristic of acute leukemia which leads to _____ survival rates. |
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Definition
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Term
328. 13 symptoms associated with chronic myelocytic or granulocytic leukemia. |
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Definition
1) SPLENOMEAGALY, 2) IMMATURE LEUKOCYTES, 3) HIGH WBC COUNT, 4) ANEMIA, 5) THROMBOCYTOPENIA, 6) WEAKNESS, 7) FATIGUE, 8) DYSPNEA, 9) LOW GRADE FEVER, 10) NIGHT SWEATS, 11) WEIGHT LOSS, 12) HEPATOMEGALY, 13) LYMPHADENOPATHY |
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Term
329. 4 caused associated with chronic myelocytic or granulocytic leukemias. |
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Definition
1) RADIATION, 2) CHEMICALS LIKE BENZENE, 3) TWINS, 4) ANIMALS |
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Term
330. _____ are cancers of WBC’s (lymphocytes). |
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Definition
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Term
331. _____ is a malignant disorder or lymphoid tissue that constitutes 40% of all malignant lymphomas seen in younger adults between the ages of 20-40. |
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Definition
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Term
332. In hodgkins lymphoma, lymphoid tissue is characterized by the presence of _____ upon biopsy. |
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Definition
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Term
333. Manifestations of hogdkins lymphoma are due to rapid proliferation of abnormal _____. |
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Definition
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Term
334. Hodgkins lymphoma often begins in lymph tissue above the _____, which usually sends people to see the doctor. |
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Definition
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Term
335. 10 symptoms associated with hodgkins lymphoma. |
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Definition
1) PAINLESS ENLARGEMENT OF LYMPHOID TISSUE, 2) SPLENOMEGALY, 3) FEVER, 4) NIGHT SWEATS, 5) WEIGHT LOSS, 6) FATIGUE, 7) PURITIS, 8) WEAKENED IMMUNE SYSTEM, 9) INCREASED WBC COUNT, 10) AFFECTED LIVER, LUNGS, DIGESTIVE TRACT AND CNS |
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Term
336. 7 medical tests used to identify hodgkins lymphoma. |
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Definition
1) LYMPH NODE BIOPSY, 2) CT SCANS OF ABDOMEN AND PELVIC LYMPH NODES, 3) LYMPHANGIOGRAPHY, 4) LAPAROTOMY, 5) LIVER BIOPSY, 6) BONE MARROW BIOPSY, 7) X RAYS AND LAB WORK |
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Term
337. In _____ of ann arbor staging of hodgkins lymphoma, a single lymph node or single extralymphatic region is affected. |
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Definition
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Term
338. In _____ of ann arbor staging of hodgkins lymphoma, there is involvement of lymph nodes on the same side of the diaphragm. |
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Definition
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Term
339. In _____ of ann arbor staging of hodgkins lymphoma, there is involvement of lymph nodes on both sides of the diaphragm. |
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Definition
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Term
340. In _____ of ann arbor staging of hodgkins lymphoma, there is diffused or disseminated involvement of lymph nodes. |
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Definition
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Term
341. The incidence rate of hodgkins lymphoma is _____ cases a year with _____ deaths. |
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Definition
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Term
342. _____ is a type of lymphoma that typically affects immune suppressed people over the age of 50, which could be virus related. It consists of a group of neoplastic disorders of lymphoid tissue not characterized by reed-sternberg cells. |
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Definition
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Term
343. In patients with non-hodgkins lymphoma, there is early involvement of the lymph nodes in the _____ area. |
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Definition
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Term
344. There is less than _____% chance of curability of patients with non-hodgkins lymphoma. |
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Definition
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Term
345. Non-hodgkins lymphomas are divided into 3 main groups according to the cell types involved which are _____, _____ and _____. |
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Definition
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Term
346. The diagnosis of non-hodgkins lymphoma is through a _____. |
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Definition
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Term
347. 4 signs and symptoms of patients with non-hodgkins lymphoma. |
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Definition
1) EARLY INVOLVELENT OF OROPHARYNGEAL LYMPHOID TISSUE, 2) CONSTITUTIONAL SIGNS, 3) LEUKEMIC TRANSFORMATIONS WITH HIGH NUMBERS OF WBC’S, 4) INCREASED SUSCEPTIBILITY TO INFECTIONS |
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Term
348. The incidence rate of non-hodgkins lymphoma is _____ new cases a year with _____ deaths. |
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Definition
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Term
350. _____ is a condition that consists of bone tumors of B-lymphocytes commonly affecting people between the ages of 50 and 60. |
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Definition
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Term
351. Multiple myelomas causing B-cell neoplasms leads to an excess production of _____ and _____. |
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Definition
IMMATURE AND MATURE PLASMA CELLS |
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Term
352. Multiple myeloma affecting B-cells can be detectable by _____ of the long bones, sternum, or skull. |
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Definition
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Term
353. Multiple myeloma is characterized by multiple malignant tumor masses of _____ scattered throughout the skeletal system and sometimes soft tissues. |
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Definition
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Term
354. Incidence of multiple myelomas is _____ times greater than all other malignant tumors of the bone combined. |
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Definition
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Term
355. Chronic stimulation of the mononuclear phagocytic system by these 3 things have been proposed causes of multiple myelomas. |
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Definition
1) BACTERIA, 2) CHEMICALS, 3) VIRUSES |
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Term
356. In the pathophysiology of multiple myeloma, _____ arise from 1 clone of B-cells that produce abnormally large amounts of _____. |
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Definition
MALIGNANT PLASMA CELLS; CLASS 1 IMMUNOGLOBULINS (IgG) |
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Term
357. Laboratory examinations of the bone marrow of patients with multiple myeloma shows proliferation of _____ and _____ cells with 20% or more having multinucleated cytoplasms containing multiple immunoglobulins (whits blobs). These cells often completely replace _____. |
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Definition
IMMATURE AND MATURE PLASMA CELLS; BONE MARROW |
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Term
358. _____ proteins, which are fragments of IgG/A are present in the urine and blood of over 60% of patients with multiple myeloma. |
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Definition
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Term
359. Bence jones proteins are proliferations of the _____. |
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Definition
LIGHT CHAINS OF IMMUNOGLOBULINS (M-CHAIN) |
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Term
360. In multiple myeloma patients, there is a higher frequency of _____ correlated with the amount of protein found in urine, since the excreted light chains are through to be toxin to the renal tubules. |
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Definition
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Term
361. The malignant neoplasm of multiple myeloma usually does not metastasize outside of the _____, rather the destructive lesions typically erode the _____ and cause _____ that are observable on radiographs. |
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Definition
BONE; BONE; LYTIC LESIONS |
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Term
362. Lytic lesions of multiple myeloma patients are most frequently visualized in these 7 places. |
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Definition
1) VERTEBRAL COLUMN, 2) RIBS, 3) SKULL, 4) PELVIS, 5) FEMUR, 6) CLAVICLE, 7) SCAPULA |
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Term
363. In multiple myeloma patients, pathological _____ usually occur in the areas with the lytic lesions, especially in the weigh bearing regions. |
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Definition
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Term
364. In multiple myeloma, calcium metabolism is usually abnormal resulting in elevated _____, because of _____. |
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Definition
SERUM CALCIUM LEVELS; PLASMA CELL PROLIFERATION |
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Term
365. Multiple myeloma patients often experience _____ and _____ anemia with variable depression of _____ and _____ counts. |
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Definition
NOMOCYTIC AND NONOCHROMIC ANEMIA; WBC AND PLATELET COUNTS |
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Term
366. The most common symptoms of multiple myeloma is _____ or _____ pain, as well as _____. |
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Definition
BONE OR BACK PAIN; COMPRESSION FRACTURES |
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Term
367. _____ and _____ may be caused by the secondary anemia of multiple myeloma. |
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Definition
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Term
368. Survival rates of multiple myeloma patients are generally poor, and rely largely on the persons response to _____. |
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Definition
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