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Definition
The study of drugs Medicinal purposes Toxic characteristics Social or recreational use |
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Definition
Describes the drug using exact chemical nomenclature to show atomic and molecular structure |
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Definition
derived from the chemical name |
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Trade or Brand naming of drugs |
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Definition
Provided by the drug manufacturer for ease i pronouncing and remembering. Protected by trademark. |
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It is the Responsibility of the Nurse to know what in pharmacology? |
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Definition
Generic/trade name Drug class Clinical use Mechanism of action Side effects Other specifics (non-pharmacological use, cultural implications, life span implications) |
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Term
Identify interactions between core drug knowledge and core patient variables to |
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Definition
Maximize therapeutic effects Minimize adverse effects Provide patient and family education Evaluate effectiveness of the drug therapy |
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Definition
Health Status Drug History Medical History Current Diagnosis Personal (Diet, lifestyle, habits, typical source of information, support system, financial support) |
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Term
When giving a nursing diagnosis for pharmacology, remember: |
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Definition
Actual or current diagnosis Potential or at risk diagnosis Wellness diagnosis |
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Potential Pharmacology Nursing Diagnosis's |
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Definition
Knowledge Deficit Management of therapeutic regimen, ineffective Alteration in health maintenance Noncompliance (be careful with this ‘label’) Alteration in………. Potential for injury |
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Planning or Outcomes (NOC) for Pharmacology |
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Definition
Client focused Resources in the environment Future but in measurable terms |
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Implementation (NIC) for Pharmacology: |
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Definition
One of the most important functions Carries the most legal vulnerability Continuous assessment Teaching, teaching, teaching Monitor diagnostic and lab tests Proper and timely documentation |
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Implementation (NIC) for Pharmacology: |
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Definition
One of the most important functions Carries the most legal vulnerability Continuous assessment Teaching, teaching, teaching Monitor diagnostic and lab tests Proper and timely documentation |
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Term
5 Rights of Safe Handling and Administration |
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Definition
1. Right Drug 2. Right Dose 3. Right Client 4. Right Route 5. Right Time |
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Evaluation of Pharmacology |
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Definition
Therapeutic response to the drug Non-therapeutic response to the drug Side effects nearly unavoidable effects Adverse reactions unintended & undesirable Level of clients knowledge Ability of client to manage the therapeutic regimen |
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Definition
Study of the biological effects of chemicals |
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Definition
Use of drugs to treat, prevent or diagnose disease |
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Definition
the effects of the drug on the body |
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Definition
the effects of genes on drug behavior |
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Definition
the effects of the body on the drug |
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Term
Four phases of Pharmacokinetics |
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Definition
Absorption Distribution Metabolism/Biotransformation Excretion |
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Term
Drug absorption is dependent upon |
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Definition
Route of administration Solubility and concentration of the drug Circulation Surface conditions Contact time pH at the absorption site Cell membrane transport mechanisms |
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Term
How drugs move across the cellular membranes |
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Definition
Passage through channels or ports Passage with aid of transport system Direct Penetration |
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Term
Passage through channels or ports |
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Definition
Few move in this manner Examples: K* or Na* |
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Passage with aid of transport system |
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Definition
Active or Passive Transport |
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Term
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Definition
Increased with lipophilic drug (lipid soluble) |
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Active Transport requires what from the cell |
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Definition
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Definition
Movement of drug molecules against the concentration gradient |
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Term
In active transport, carriers form... |
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Definition
complexes with drug molecules on membrane surface |
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Definition
Movement of substance from higher concentration to lower until equilibrium obtained |
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Term
Most drugs use what type of transport system |
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Definition
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Dose passive transport require energy? |
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Definition
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Drug movement is dependent on: |
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Definition
Drug flow to the tissues (cardiovascular functions) Drug’s ability to leave the vascular system and enter cells (permeability of capillary membranes) Drug’s lipid affinity (lipophilic) or water affinity (hydrophilic) Drug’s ability to bind with protein in the blood (protein binding) |
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An increase in the number of free drug particles (from low protein levels) will |
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Definition
increase the drug’s effect, even though the dose of the drug is unchanged |
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Term
An increase in the number of free drug particles (from low protein levels) will |
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Definition
increase the drug’s effect, even though the dose of the drug is unchanged |
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Term
Drug particles that are not bound to protein (“free” drug) are |
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Definition
active and exert an effect |
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Term
Competition between drugs to bind may |
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Definition
displace drugs and increase their toxicity |
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Term
Blood/Brain Barrier allows |
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Definition
distribution of lipid soluble drugs into brain and CSF |
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Term
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Definition
Lipid and non-lipid soluble drugs can pass to fetus |
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Term
Metabolism changes the drug from its |
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Definition
pharmcologically active form to a more water soluble form to enhance excretion |
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Term
Most metabolism occurs in |
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Definition
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Term
The percentage of drug metabolized each time the drug is circulated to the liver |
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Definition
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Term
When drugs are highly metabolized during the first circulation to the liver (first pass), |
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Definition
little or no active drug is sent to the general circulation |
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Term
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Definition
the time it takes for the amount of drug in the body to decrease to one-half of the peak level it previously achieved |
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Term
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Definition
oral drugs are usually absorbed from the small intestine directly into the portal venous system and delivered to the liver which transforms most of the chemicals into metabolites, some of which are deactivated and excreted without reaching the tissue/organ they were intended for |
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Term
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Definition
Drug swallowed Drug dissolved in gastrointestional fluid (lost in acid) Dissolved drug reaches intestine (lost in food, acid, digestion) Drug absorbed in portal system to liver (biotransformed to noneffective state Bound to plasma proteins- decrease free drug) Drug in circulation (Broken down in tissues if not bound) Drug distributed throughout body (Reaches reactive tissue and ‘does it’s thing’ Excreted by kidneys, lungs, skin, etc.Bound to fat tissue) |
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Term
Elimination or excretion of drugs occurs in |
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Definition
the kidneys (primarily), liver, gastrointestinal (GI) tract, lungs, sweat and salivary glands, skin, and breast milk |
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Term
Pathology of these systems will |
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Definition
decrease excretion of the drug |
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Term
Decreased excretion does what to blood levels of the drug |
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Definition
increases them even though the dose is unchanged |
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Definition
General study all the various genes that determine drug behavior |
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Term
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Definition
study of the genetic material in the cell |
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Definition
science of heredity & variations |
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Definition
study of inherited variations in drug metabolism and responses |
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Term
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Definition
appearance of an individual resulting from the effects of both environment and genes |
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Term
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Definition
genetic constitution of an individual |
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Term
CYP450 enzymes are essential for |
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Definition
the metabolism of numerous medications, nutrients, & herbal therapies |
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Term
System can be inhibited or induced by drugs and may lead to |
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Definition
altered drug responses (ADR) |
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Term
In a 1994 report, ADRs accounted for |
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Definition
more than 2.2 million serious cases & over 100,000 deaths in the U.S. |
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Term
Pharmacodynamics process includes: |
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Definition
Uptake Movement Binding Interactions of pharmacologically active molecules with their site(s) of action |
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Definition
largest effect the drug can produce. The innate ability of the drug to produce a desired effect |
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Term
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Definition
amount of drug needed to elicit an effect. How many particles of a drug are needed to produce a desired effect |
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Definition
usually a larger then standard dose given at the beginning of therapy to raise blood level |
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Definition
dose that continues to keep the drug in the desired therapeutic range |
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Term
Drug-Receptor Interactions |
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Definition
Chemical bond between drugs and specific receptor sites 'Lock and Key effect' |
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Term
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Definition
Intensity of response proportional to number of receptors occupied |
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Modified Occupancy Theory |
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Definition
Involves affinity and intrinsic activity |
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Term
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Definition
strength of the attraction |
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Term
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Definition
ability of drug to activate the receptor following binding |
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Definition
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Term
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Definition
Adrenergic Cholinergic Histamine |
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Examples of Adrenergic Receptors |
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Definition
Alpha 1 Alpha 2 Beta 1 Beta 2 Dopaminergic |
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Examples of Cholinergic Receptors |
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Definition
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Examples of Histamine Receptors |
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Definition
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Term
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Definition
Side effects Adverse reactions Allergic reactions |
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Term
Side effects are nearly ____ and are produced at ____ |
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Definition
unavoidable secondary drug effects therapeutic doses |
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Term
Adverse reactions are ____ and are produced at___ |
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Definition
Noxious, unintended, and undesirable normal doses |
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Term
Allergic reactions are an____ and result from ___ |
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Definition
Immune response prior sensitization |
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Term
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Definition
Altered physiologic reactions to a drug that occurs because of a prior exposure to the drug stimulated the immune system to develop antibodies |
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What is the most serious type of allergic reaction |
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Definition
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4 types of allergic reactions |
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Definition
Type I Type II Type III Type IV |
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Definition
Occurs soon after exposure Involves IgE |
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Type II Allergic Reaction |
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Definition
Delayed reaction Involves IgE & IgG |
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Type III Allergic Reaction |
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Definition
Delayed reaction Involves IgE, IgM, and IgG |
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Type IV Allergic Reaction |
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Definition
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Term
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Definition
Molecules that activate receptors |
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Term
When drugs act as agonists, they... |
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Definition
bind to receptors and mimic the actions of the body's own regulatory molecules |
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Term
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Definition
prevent receptor activation by endogenous regulatory molecules and drugs |
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Term
Antagonists produce their effects by... |
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Definition
preventing the activation of receptors by agonists |
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Term
FDA Testing Sequence for Investigational Drugs |
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Definition
Part I: Animal Studies Part II: Human Studies |
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Term
Part One of the FDA Animal study involves... |
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Definition
Toxicity Therapeutic Index |
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Part II of the FDA Human Studies involves... |
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Definition
Phase 1-Initial evaluation Phase 2-Limited Control Phase 3-Extended clinical trials |
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The 8 elements of informed consent |
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Definition
Information about the study Risks involved Benefits Alternatives Confidentiality Compensation and Care Contact information Volunteer's Rights |
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Term
What is required for consent for investigational drugs? |
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Definition
Informed consent Nuremberg code Review boards for research institute (IRBS) |
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Term
Different Classifications of Drugs |
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Definition
Prescription (legend) Drugs vs. OTCs CSA Classification (Controlled Substance Act) Pregnancy Safety Classification |
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CSA classification is based on... |
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Definition
The abuse potential and accepted use |
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Schedule I CSA Classification |
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Definition
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Schedule II CSA Classification |
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Definition
Prescription for 6 months with no refills |
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Schedule III CSA Classification |
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Definition
Prescription for 5 refills in 6 months |
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Schedule IV CSA Classification |
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Definition
Prescription required; accepted medical use |
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Schedule V CSA Classification |
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Definition
May not require a prescription |
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Category A Pregnancy Safety Classification |
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Definition
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Term
Category B Pregnancy Safety Classification |
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Definition
Animal studies show no risks but no human studies done |
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Term
Category C Pregnancy Safety Classification |
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Definition
Animal studies show adverse effects and no human studies done |
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Category D Pregnancy Safety Classification |
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Definition
Human fetal risk reported |
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Category X Pregnancy Safety Classification |
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Definition
Fetal abnormalities and fetal risks shown in studies |
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Definition
Basis for professional status Nurses' role with Medication Prescription situations |
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Definition
Self determination; the right of individuals to govern themselves according to their own reason |
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Definition
Person who is capable of making a decision has freely and voluntarily agreed after receiving the information needed to make a decision |
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Definition
Doing good or promoting good |
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Definition
Avoiding harm, wrong doing or misconduct |
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Truthfulness; accuracy of statement corresponding with fact or reality |
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Definition
Keeping promises; acting in good faith (confidentiality & privacy) |
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Definition
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Treating people fairly, impartiality, honestly and with equity |
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Definition
Quality or state of being of sound moral principle; uprightness, honesty and sincerity |
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Definition
Holds that an authority figure knows best and that the individual is obligated to comply with the authority figure; overrides patient autonomy |
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JCAHO Pain Management Standards- The Fifth Vital Sign |
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Definition
F - First Assess I - Initiate Intervention V - Verify effectiveness and document E - Educate self and patient |
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Term
Unrelieved pain will do what do the body |
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Definition
Causes unnecessary suffering Stimulates sympathetic response Decreases immune function Weakens already debilitated patients Increases poor compliance with therapy Impinges on work, leisure, role in family and society Diminishes hope |
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Term
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Definition
Inadequate assessment Patient reluctance to report pain Patient reluctance to take opioids Physician reluctance to prescribe opioids Lack of knowledge |
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Term
When the patient reports pain relief following a placebo, this means that |
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Definition
the patient is a malingerer or that the pain is psychogenic |
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Term
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Definition
Primary, chronic, neurobiologic disease, with genetic, psychosocial, and environmental factors influencing its development and manifestations. |
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Term
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Definition
clients that are inadequately treated for pain and as a result, develop a pattern of drug-seeking behaviors to achieve pain control |
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Definition
a pharmacologic property causing the occurrence of withdrawal symptoms with abrupt discontinuation or administration of an antagonist. |
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Term
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Definition
the pharmacologic effect in which, with repeated administration, increasing doses are necessary to provide the same effect |
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Term
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Definition
Physical - sensation of pain involves nerve pathways and brain
Psychological - emotional response to pain |
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Term
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Definition
sudden onset and subsides with treatment |
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Term
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Definition
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Term
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Definition
transient flare in pain, occurs in conjunction with persistent pain |
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Term
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Definition
originates in smooth muscle or sympathetically innerviated organ systems; may be referred pain |
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Term
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Definition
activation of nociceptors in skeletal muscles, fascia, ligaments vessels or joints; may be more localized |
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Term
Neuropathic (deafferentation) Pain |
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Definition
caused by peripheral nerve injury |
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Term
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Definition
Injury causes the release of substances, such as prostaglandines Nociceptors send pain impulses through myelinated afferent fibers to spinal cord in area of dorsal horn Activation of nociceptive system up spinal cord to brain Pain is perceived Descending pathways suppress pain input |
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Term
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Definition
Mu - mediate supraspinal analgesia, euphoria, respiratory depression, constipation, pruritus, urinary retention, nausea, vomiting, and physical dependence Kappa - activation at the spinal cord level mediates sedation, miosis, and analgesia |
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Term
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Definition
Tricyclic antidepressants Anticonvulsants Muscle relaxants Benzodiazepines Corticosteroids |
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Term
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Definition
morphine-like compound that produces bodily effects including pain relief, sedation, constipation, and respiratory depression |
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Term
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Definition
compounds that block the opioid analgesics from their receptor sites |
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Term
Opioid Agonists/Antagonists |
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Definition
exact mechanism of action is unknown but both act and block the opioid receptors |
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Term
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Definition
effective for mild to moderate pain and are often combined with opiod analgesics to enhance pain control in cases of severe pain . Also used for antiinflammatory effect |
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Term
Titration of Opioid Doses |
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Definition
When titrating opioid doses, increases of 25-50% should be administered until there is either a 50% reduction in the patient’s pain rating on a numerical or visual analog scale or the patient reports satisfactory pain relief |
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Term
A repeat dose can be safely administered at |
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Definition
the time of the peak if previous dose is ineffective and side effects are minimal. |
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Term
For mild to moderate pain increase the dose by |
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Definition
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Term
For moderate to severe pain, increase the dose by |
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Definition
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Term
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Definition
Around the clock doses are more effective than prn administration for pain that is expected to continue. Analgesic is more effective if given before pain becomes severe. Provide analgesia to allow for uninterrupted sleep. |
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Term
Breakthrough Pain "Rules" |
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Definition
Doses should be equivalent to about 10-15% of the 24-hour total dose Doses may be given every 2 hours as needed Doses of immediate-release opioid may be taken at same time as sustained-release opioid Do not use sustained-release opioid for breakthrough pain |
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Term
Opioid-Induced Side Effects |
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Definition
constipation nausea & vomiting sedation respiratory depression |
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Term
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Definition
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Nursing Interventions for Constipation |
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Definition
Assess bowel function routinely. Prevention of constipation should be instituted with increased intake of fluids and bulk and with laxatives to minimize constipating effects. Stimulant laxatives (ie. Senokot) should be administered routinely if opioid use exceeds 2-3 days, unless contraindicated. |
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Term
Causes of Nausea and Vomiting |
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Definition
Stimulation of the chemoreceptor trigger zone Inhibition of GI motility Vestibular stimulation |
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Term
Management of Nausea and Vomiting |
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Definition
Tolerance Change opioids Multiple antiemetics Decrease ambulation |
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Term
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Definition
If respiratory rate is <10/minute, assess level of sedation. Physical stimulation may be sufficient to prevent significant hypoventilation. Subsequent doses may need to be decreased by 25-50%. Initial drowsiness will diminish with continued use. |
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Term
Fixing Respiratory Depression |
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Definition
If an opioid antagonist is required -- naloxone (Narcan) is the antidote. Dilute the 0.4-mg ampule of naloxone in 10 ml of 0.9% NaCl and administer 0.5 ml (0.02 mg) by direct IV push every 2 min. Titrate dose to avoid withdrawal, seizures, and severe pain. |
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Term
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Definition
CNS depressants issued to induce a loss of sensation, especially the sensation of pain |
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Term
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Definition
Induces a state of unconsciousness and varying amount of analgesia, amnesia, muscle relaxation, and loss o f reflexes (sensory and autonomic) and is achieved by intravenous or inhalation routes |
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Term
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Definition
blocks pain sensations in specific areas of the body without loss of consciousness |
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Term
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Definition
combination of drugs to induce anesthesia with each used for its specific effect |
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Term
General Anesthetics Stages |
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Definition
Stage 1 – Analgesia
Stage 2 - Excitement
Stage 3 - Surgical anesthesia
Stage 4 – Medullary Paralysis (toxic stage) |
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Term
Special Considerations for Anesthetic use |
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Definition
Alcoholism – increase liver-metabolizing enzymes and cross-tolerance Obesity – cardiac and respiratory considerations; avoid fat-soluble anesthetics Smoking – increased rigidity in arterial vascular system Pregnancy Neonate/Child Elderly |
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Term
Nursing Considerations for Anesthetics |
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Definition
Preoperative – assessment, informed consent, decrease anxiety, patient teaching Intraoperative – ensure patient safety and monitor patient’s level of sedation Postoperative – Assessment: Airway and breathing Circulation Metabolic (skin integrity, temp, I & O) General – drains, catheters, bowel sounds, status of incision, positioning, LOC, ability to communicate |
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Term
Postoperative Nursing Responsibilities for Inhalation Anesthetics |
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Definition
Monitor BP, pulse, and temperature Support respiratory function Prevent aspiration Keep the patient warm Assess for return of normal bowel sounds and urinary output |
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Term
General Anesthetics: Parental |
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Definition
Barbiturates
Non-Barbiturates
Benzodiazepines
Opioid Analgesia |
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Term
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Definition
Nondepolarizing: antagonists to acetylcholine at neuromuscular junction and prevent depolarization of muscle cells |
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Term
Depolarizing Nerve Block/Regional |
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Definition
Act as acetylcholine agonist at the neuromuscular junction stimulating the muscle cell and then preventing it from repolarizing |
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