πŸ•‹
Trisquel.ink/Nursing
/
πŸ•‹
Pharmacology
/
No organized

Chapter 3

🌑️ Pharmacokinetics (What the body does to the drug)

4 processes:

  1. Absorption – 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
  2. Distribution – drug movement from blood β†’ tissues
    • Influenced by protein binding, free drug levels, blood-brain barrier, placenta transfer
  3. Metabolism (Biotransformation) – 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
  4. Excretion (Elimination) – main routes: kidneys, liver (bile), lungs, saliva, sweat, breast milk

πŸ’Š Pharmacodynamics (What the drug does to the body)

  • Primary effect = desired therapeutic response
  • Secondary effect = can be helpful or harmful

Drug Response Concepts:

  • Potency – how much drug is needed
  • Maximal efficacy – maximum effect drug can give
  • Therapeutic index – margin between effective and toxic dose
  • Onset, Peak, Duration – how fast, how strong, how long drug acts
  • Therapeutic monitoring:
    • Peak = highest plasma concentration
    • Trough = lowest level before next dose

Receptor Theory:

  • Agonist – activates receptor β†’ response
  • Partial agonist – weaker effect, blocks stronger drugs
  • Antagonist – blocks receptor β†’ no response

Other Mechanisms:

  • Stimulation, Depression, Irritation, Replacement, Cytotoxic, Antimicrobial, Immune modification

Side Effects & Risks:

  • Side effects – secondary effects (mild, expected)
  • Adverse reactions – severe, unexpected, harmful
  • Toxicity – drug levels above therapeutic range
  • Tolerance – less response over time β†’ higher dose needed
  • Tachyphylaxis – rapid decrease in response
  • Placebo effect – response due to expectation, not drug

πŸ”„ 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

🧠 Clinical Judgment (PK & PD)

  • Recognize cues: Look for possible interactions, check patient’s 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

βœ… 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.