Pharm Final

Properties of an Ideal Drug

  • Effectiveness: This is the most important property a drug can have. It implies that the drug elicits the response for which it is given.
  • Safety: A safe drug is defined as one that cannot produce harmful effects—even if administered in very high doses and for a very long time. It is important to note that all drugs have the ability to cause injury, especially with high doses and prolonged use.
  • Selectivity: A selective drug is defined as one that elicits only the response for which it is given. There is no such thing as a wholly selective drug because all drugs cause side effects.
  • Reversible Action: For most drugs, it is important that effects be reversible (e.g., general anesthetics must wear off).
  • Predictability: It is helpful to know with certainty how a given patient will respond to a particular drug, though every patient is unique.
  • Ease of Administration: An ideal drug should be simple to administer. This can enhance patient adherence and decrease risk of administration errors.
  • Freedom from Drug Interactions: When a patient is taking multiple drugs, these agents can interact. An ideal drug would not interact with other agents.
  • Low Cost: An ideal drug would be easy to afford.
  • Chemical Stability: Some drugs lose effectiveness during storage or when put into solution; an ideal drug retains activity.
  • Possession of a Simple Generic Name: Generic names are often complex and difficult to remember; a simple name is preferable.

Therapeutic Objective and Response Factors

  • Therapeutic Objective/Goal: The ultimate objective of drug therapy is to provide maximum benefit with minimum harm.
  • Factors Determining Intensity of Drug Responses:
    • Administration: Dosage size, route, and timing are important determinants of drug responses. Toxicity can occur if dosage is too high; treatment failure occurs if it is too low.
    • Pharmacokinetics: Processes that determine how much of an administered dose gets to its sites of action. The four major processes are absorption, distribution, metabolism, and excretion.
    • Pharmacodynamics: The impact of drugs on the body. Once a drug has reached its site of action, pharmacodynamic processes determine the nature and intensity of the response.
    • Sources of Individual Variation: Physiological variables (age, gender, weight), Pathological variables (kidney/liver function), and Genetic variables.

Application of Pharmacology in Nursing Practice

  • Drug Cards to Know:
    • Acetaminophen
    • Ibuprofen
  • Pre-administration Assessment:
    • Collecting Baseline Data: Needed to evaluate therapeutic and adverse responses.
    • Identifying High-Risk Patients: Factors include liver/kidney impairment, genetic factors, drug allergies, pregnancy, and pediatric/elderly age groups.
  • Dosage and Administration:
    • Different indications may require different dosages.
    • Dosages may differ depending on the route of administration.
    • Guideline Steps for Correct Administration:
      1. Check the medication order.
      2. Verify the identity of the patient (e.g., using wristbands or asking for name/DOB).
      3. Read the medication label.
      4. Verify dosage calculations.
      5. Implement any special handling the drug may require.
      6. Critical Safety Rule: Do not administer any drug if you do not understand the reason for its use!
  • Nursing Responsibilities:
    • Promoting therapeutic effects.
    • Minimizing adverse effects and adverse interactions.
    • Making PRN (pro re nata) decisions.
    • Evaluating responses to medications.
    • Managing toxicity.
  • Patient Education:
    • Nurses must educate patients on the drug name, dosage, schedule, adherence, technique of administration (e.g., injection, inhaler), duration of use, and drug storage.

New Drug Development and Naming

  • The Randomized Controlled Trial (RCT):
    • Use of Controls: Comparing new drugs with standard drugs or placebos.
    • Randomization: Subjects are assigned randomly to groups to prevent bias.
    • Blinding: People involved do not know which group is receiving the drug or placebo (single or double-blind).
  • Stages of New Drug Development:
    • Pre-clinical Testing: Conducted in animals to assess toxicity, pharmacokinetics, and useful effects.
    • Clinical Testing:
      • Phase I: Conducted in healthy volunteers to evaluate metabolism, pharmacokinetics, and biologic effects.
      • Phases II and III: Conducted in patients to determine therapeutic effects, dosage range, safety, and effectiveness.
      • Phase IV: Post-marketing Surveillance: The drug is released for general use, allowing for the observation of effects in a large population.
  • Limitations of Testing:
    • There is historically limited information on women and children.
    • Testing fails to detect all adverse effects before a drug is marketed.
  • Drug Names:
    • Chemical Name: Description of the drug using the nomenclature of chemistry.
    • Generic Name: Assigned by the U.S. Adopted Names Council; each drug has only one generic name (nonproprietary name).
    • Brand Name: Proprietary or trade names under which the drug is marketed. One drug may have many brand names.
  • Generic vs. Brand Name: Generic products are generally preferred and contain the same dose of the same drug, but rates of absorption may differ between formulations.

Pharmacokinetics

  • Drug Cards to Know:
    • Warfarin
    • Nitroglycerin
  • Passing Membranes: Drugs must cross cell membranes through channels/pores, transport systems (e.g., P-glycoprotein), or direct penetration (most common, requires lipid solubility).
  • Absorption Routes:
    • Intravenous (IV): No barriers to absorption; instantaneous absorption. Advantages include rapid onset and control; disadvantages include cost, irreversibility, and risk of fluid overload or infection.
    • Intramuscular (IM) / Subcutaneous (SubQ): Barrier is the capillary wall. Absorption is rapid with water-soluble drugs and slow with poorly soluble ones.
    • Oral (PO): Barriers include the GI epithelium and capillary wall. Absorption is highly variable. Advantages include safety and convenience; disadvantages include inactivation by digestive enzymes/liver and patient requirements (conscious/cooperative).
  • Pharmaceutical Preparations (Oral):
    • Tablets: Compressed drug mix.
    • Enteric-Coated: Dissolve in the intestine, not the stomach.
    • Sustained-Release: Capsules filled with spheres that dissolve at different rates to release drug steadily.
  • Distribution:
    • Blood-Brain Barrier (BBB): Only lipid-soluble drugs or those with a transport system can cross.
    • Placental Drug Transfer: Not an absolute barrier; lipid-soluble non-ionized drugs pass easily.
    • Protein Binding: Many drugs bind to albumin. Bound molecules cannot leave the bloodstream.
  • Metabolism (Biotransformation):
    • Primarily occurs in the liver via hepatic drug-metabolizing enzymes (P450 system).
    • First-Pass Effect: Rapid hepatic inactivation of certain oral drugs before they reach systemic circulation.
    • Prodrugs: Inactive compounds that become active through metabolism.
  • Excretion:
    • Renal: Glomerular filtration, Passive tubular reabsorption, and Active tubular secretion.
    • Factors affecting renal excretion: pH-dependent ionization and competition for active transport.
    • Non-renal: Breast milk, bile, sweat, saliva, and expired air.
  • Time Course of Responses:
    • Minimum Effective Concentration (MEC): The plasma drug level below which therapeutic effects will not occur.
    • Toxic Concentration: Plasma level at which toxic effects begin.
    • Therapeutic Range: The range between the MEC and toxic concentration.
    • Half-Life (t1/2t_{1/2}): The time required for the amount of drug in the body to decrease by 50%50\%.
    • Plateau (Steady State): Reached when the amount of drug eliminated between doses equals the amount administered. It takes approximately four half-lives to reach a plateau.
    • Loading Dose: Large initial dose used to reach plateau quickly for drugs with long half-lives.

Complementary and Alternative Therapy (Chapter 86)

  • Dietary Supplement Health and Education Act of 1994 (DSHEA):
    • Categorizes botanical products, vitamins, and minerals as "dietary supplements" rather than drugs.
    • Exempts products from FDA scrutiny and approval before marketing.
    • Manufacturers do not need to prove safety or efficacy; the FDA must prove a product is unsafe to intervene.
  • Key Herbs and Supplements (* denotes increased bleeding risk):
    • Black cohosh: Used for menopause symptoms (hot flashes, vaginal dryness, depression).
    • Butterbur: Used for migraines, allergies, and asthma; has anti-inflammatory and vasodilatory effects.
    • Feverfew (increases bleeding risk): Suppresses arachidonic acid release and platelet aggregation. Used for migraine prophylaxis and immune disorders. Must discontinue 22 weeks before surgery.
    • Ginkgo biloba (increases bleeding risk): Used for memory, dementia, and intermittent claudication. Use caution with anticoagulants.
    • Echinacea: Used to stimulate immune function and treat viral infections.
    • St. John’s wort: Used for mild to moderate depression.
    • Garlic (increases bleeding risk): Used for cardiovascular effects (lower BP, lower LDL/triglycerides, higher HDL) and suppressing platelet aggregation.
    • Cranberry Juice (increases bleeding risk if taking warfarin): Used to prevent UTIs by preventing bacteria from adhering to the urinary tract wall.
    • Ginger Root (increases bleeding risk): Inhibits thromboxane production to suppress platelet aggregation. Used for vertigo and nausea/vomiting.
    • Green Tea: Used for weight loss, mental clarity, and cancer prevention.
    • Saw Palmetto: Used to relieve urinary symptoms of Benign Prostatic Hyperplasia (BPH).

Neuropharmacology and Adrenergic/Muscarinic Drugs

  • Basic Principles: Understanding the physiology of the Peripheral Nervous System (PNS).
  • Muscarinic Agonists: Activate muscarinic receptors.
  • Muscarinic Antagonists: Block muscarinic receptors.
  • Adrenergic Agonists: Activate adrenergic receptors.
  • Adrenergic Antagonists: Block adrenergic receptors.

Medication Management and Specific Topics

  • Disulfiram Reaction: Patient must consume NO alcohol.
  • Substance Use Disorders: Basic terms and concepts from Chapter 40.
  • Nutritional Considerations:
    • Tyramine containing foods: Often interact with MAOIs.
    • Vitamin K containing foods: Interact with Warfarin (Vitamin K is the antagonist).
    • Potassium containing foods: Important for patients on diuretics or heart medications.
  • Selected Medications:
    • Furosemide: A diuretic.
    • Heparin: An anticoagulant.
    • Morphine: An opioid analgesic.
    • Naloxone: An opioid antagonist.
    • Benzodiazepines: Often used for anxiety or sedation.
    • Flumazenil: A benzodiazepine antagonist.
  • Rights of Medication Administration: Includes right patient, right drug, right dose, right route, and right time.

Newer Content and Specialized Chapters

  • Drugs for Headache:
    • NSAIDs: Aspirin, Ibuprofen.
    • Acetaminophen.
    • Selective Serotonin Receptor Agonists: Sumatriptan.
    • Ergot Alkaloids: Ergotamine.
  • Opioid Analgesics (Chapter 31):
    • Pure Agonist: Morphine.
    • Pure Antagonist: Naloxone.
  • Anesthetics:
    • Local (Amide-type): Lidocaine.
    • General (Inhalation): Nitrous Oxide.
    • General (Intravenous): Propofol, Ketamine.