π‘οΈ Pharmacokinetics (What the body does to the drug)
4 processes:
- Absorption β from GI tract β bloodstream
- Disintegration: break drug into particles
- Dissolution: dissolve in fluid
- Methods:
- Passive (diffusion, facilitated)
- Active (needs carrier + energy)
- Pinocytosis (engulfing drug particles)
- Factors: blood flow, pain/stress, pH, food, exercise, route
- First-pass effect: liver metabolism before reaching circulation
- Bioavailability: % of drug that actually reaches circulation
- Distribution β drug movement from blood β tissues
- Influenced by protein binding, free drug levels, blood-brain barrier, placenta transfer
- Metabolism (Biotransformation) β drug chemically changed (mainly in liver)
- Prodrug = inactive until metabolized
- Half-life (tΒ½) = time for drug level to fall by 50%
- Steady state = consistent drug level
- Loading dose = large first dose to reach effect quickly
- Excretion (Elimination) β main routes: kidneys, liver (bile), lungs, saliva, sweat, breast milk
π Pharmacodynamics (What the drug does to the body)
- Primary effect = desired therapeutic response
- Secondary effect = can be helpful or harmful
Drug Response Concepts:
- Potency β how much drug is needed
- Maximal efficacy β maximum effect drug can give
- Therapeutic index β margin between effective and toxic dose
- Onset, Peak, Duration β how fast, how strong, how long drug acts
- Therapeutic monitoring:
- Peak = highest plasma concentration
- Trough = lowest level before next dose
Receptor Theory:
- Agonist β activates receptor β response
- Partial agonist β weaker effect, blocks stronger drugs
- Antagonist β blocks receptor β no response
Other Mechanisms:
- Stimulation, Depression, Irritation, Replacement, Cytotoxic, Antimicrobial, Immune modification
Side Effects & Risks:
- Side effects β secondary effects (mild, expected)
- Adverse reactions β severe, unexpected, harmful
- Toxicity β drug levels above therapeutic range
- Tolerance β less response over time β higher dose needed
- Tachyphylaxis β rapid decrease in response
- Placebo effect β response due to expectation, not drug
π Drug Interactions
- Pharmacokinetic (absorption, distribution, metabolism, excretion changes)
- Pharmacodynamic:
- Additive = sum of two drugs
- Synergistic = effect much greater together
- Antagonistic = one drug blocks/reduces the other
- Other interactions:
- Drug-food (e.g., delayed absorption)
- Drug-lab (false test results)
- Drug-induced photosensitivity
π§ Clinical Judgment (PK & PD)
- Recognize cues: Look for possible interactions, check patientβs meds
- Analyze: Anxiety, knowledge gaps
- Generate solutions: Patient explains why regimen is important
- Take action:
- No high-fat food before enteric-coated meds
- Monitor drugs with narrow therapeutic ranges
- Notify provider of antagonistic combinations
- Evaluate: Check if outcomes met safely
β In short:
- Pharmacokinetics = ADME (Absorption, Distribution, Metabolism, Excretion).
- Pharmacodynamics = drug effects (agonists, antagonists, therapeutic effects, side/adverse effects).
- Nurses monitor interactions, therapeutic ranges, and patient teaching to keep drug therapy safe.