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Pharmacology principles
Name, classification, pharmacokinetics, medication response
Drug naming process
Generic name, trade/brand name, chemical name
Generic name (nonproprietary name)
Name given by the United States Adopted Names Council
Trade/brand name (proprietary name)
Drug has a registered trademark, use of name restricted by drug’s patent owner
Drug classification
Drug class → grouped together based on similar properties → commonly classified by therapeutic use → subclasses
Pharmacokinetics
What the body does to the drug; absorption, distribution, metabolism, excretion
Absorption
Transmission of medications from location of administration (oral, muscle, skin, mucous membranes, subcutaneous tissue) to the bloodstream
Distribution
Delivery to intended tissue
Metabolism
How drug is broken down, changes drugs into less active or inactive forms by action of enzymes, usually happens in liver
Excretion
Removing drug from body, primarily kidney’s responsibility, bowel also plays role, kidney dysfunction can lead to an increase in duration and intensity of a medication response
Bioavailability
How much of the drug is absorbed, oral meds have <100%
First pass effect
Drug from GI tract (enteral) much less available because liver destroys it before entering circulation
Pharmaceutics
How drug form influences the speed in which the drug is absorbed by the body
Factors altering absorption of oral drugs
Gastric ph and emptying time, presence of food in the stomach, forms of meds (enteric coating or sustained release), other medications
Factors influencing distribution
Circulation, plasma protein binding
Circulation
Conditions that inhibit perfusion (vascular or cv disease) can delay distribution
Plasma protein binding
Drugs compete for protein binding sites within the bloodstream (albumin), ability to bind to a protein can affect how much of the drug will travel to the target site, drugs can compete for the same binding sites (toxicity)
Distribution affecting factors
Low albumin levels, taking multiple medications at same time that are highly protein bound (Drug-Drug Interaction)
Factors influencing rate of metabolism
Age, higher level of drug-metabolizing enzymes (genetics), similar metabolic pathways (drug-drug interaction), leads to slowing metabolism, nutritional status
Outcomes of metabolism
Increased excretion, unactivation of medications, increased therapeutic effect, activation of pro-drugs into active form
Medication responses
Medication dosage attempts to maintain plasma levels between minimum effective concentration and toxic concentration, therapeutic index + therapeutic levels (peak and trough), half-life, pharmacodynamics
Peak level
Max concentration of drug in body after administration. (30 minutes after IV, 1 hour after PO)
Trough level
Lowest concentration in body after fall from peak level. (measured immediately before next
dose)
Half-life
Time for the medication in the body to drop by 50%, takes 4 half-lives to achieve a steady blood concentration, considered eliminated (no longer exerting effect) after 5 half lives, liver and kidney function affect half-life
Short half-life
Medications leave the body quickly (4-8 hrs), short dosing intervals (q4 hrs)
Long half-life
Medications leave the body slowly, greater risk for accumulation and toxicity, meds can be given at longer intervals, but take longer to reach a steady state
Pharmacodynamics
Interactions between medications and target cells to produce effects
Mechanisms of action
Acting on receptors (Agonist, Antagonist, Partial), blocking or stimulating enzymes, altering ion channels, affecting transporters or pumps, replacing missing substances, direct physical or chemical action
Uncontrolled substances
Do not generally pose risks of misuse and addiction
Controlled substances
Have a potential for misuse and dependence, have a “schedule” classification; schedule I has no medical use in the US
Medication prescriptions
Most often written (usually electronically through EMR), use verbal prescriptions only for emergencies, and follow facility’s protocol for telephone prescriptions, nursing students cannot accept verbal or telephone prescriptions
Types of medication prescriptions
Routine, single or one-time, stat, PRN
Components of medication prescription
Patient Name and medical record number, date and time order was written, generic drug name, dosage, route of administration, frequency of dosing, prescriber signatur
Medication reconciliation
TJC requires policies and procedures; list of current medications, including med name, dosage, frequency, is compiled; nurses compare list with new medication prescriptions and reconcile it with provider to resolve discrepancies; takes place upon admission, transferring to another unit or facility, at discharge
Medication rights
Right patient, drug, dose, time, indiction, route, response, documentation, education
Common medication errors
Wrong medication or IV fluid, incorrect dose or IV rate, wrong client, route, or time, administration of allergy-inducing medication, omission of a dose or administration of an extra dose, incorrect discontinuation of a medication or IV fluid, inaccurate prescribing, inadvertently giving a medication with a similar name
Bar code scanning
Leads to safer practice/less medication errors, integrated in almost every setting (esp. acute care), expected standard of practice, supports documentation of administration
Drugs commonly involved in severe medication errors
Insulins, anticoagulants, opioids, chemotherapeutic drugs
Committing a medication error
Ensure patient safety first, notify appropriate people, monitor and intervene, document objectively, learn from error