Introduction to Psychopharmacology Flashcards
What determines a patient’s response /tolerance in one drug over another?
Individual patients may better respond to or tolerate one agent over another because of differences in each drug’s pharmacokinetics
1. Absorption
2. Distribution
3. Metabolism
4. Excretion
Factors that may influence drug choice?
- Patient’s personal/family hx of response/tolerance to a drug
- Potential for interaction with/concurrent medications
- Patient preference
- Comorbid medical conditions
- Comorbid psychiatric conditions
Dangers of polypharmacy?
- Polypharmacy increases risk of drug-drug interactions and should be minimized/avoided
- Number of medications may be reduced by making use of drug’s secondary pharmacological effects
e.g. prescribing a sedating agent to someone who has insomnia
Note: Where possible patients need to be involved in drug selection
Strategies to maximize medication adherence?
- Patient education (adverse effects, speed of onset of therapeutic effect, tolerance)
- Arrange a convenient dosing schedule
- Minimize adverse effects
- Check for patient adherence
- Schedule office/phone visits to discuss adherence and adverse effects for newly prescribed drugs
- Reduce pill burden where necessary
Drug Metabolism in pharmacokinetics?
The most common pharmacokinetic drug–drug interaction involves changes in the CYP-mediated metabolism of the substrate drug by an interacting drug
1. Enzyme inducers - will decrease amount of circulating parent drug
2. Enzyme inhibitors - leading to high circulating drug levels
Note: Attempt to avoid medications that significantly inhibit or induce CYP enzymes
Drug Absorption in pharmacokinetics?
Many orally administered drugs, including a number of psychotropics, have poor bioavailability due to extensive first-pass metabolism
Drug Distribution in pharmacokinetics?
Changes in drug protein binding, either disease-induced or the result of a protein-binding drug interaction
Drug Excretion in pharmacokinetics?
Drug interactions altering renal drug elimination may be clinically significant if the parent drug or its active metabolite undergoes renal excretion
E.g. some antihypertensive agents (thiazide diuretics, angiotensin- converting enzyme inhibitors), decrease GFR and impair renal elimination, which may lead to lithium toxicity
Pharmacodynamic drug interactions?
- Occur when drugs with similar or opposing effects are combined
- Leads to addition or antagonism of the pharmacological and toxic effects of each
- More common with compromised physiological function
e.g. in cardiovascular disease, or the elderly - For example multiple drugs with anticholinergic activity may exacerbate cognitive impairment in the elderly
Anticholinergic adverse effects?
- dry mouth
- constipation
- blurred vision, mydriasis
- urinary retention
- tachycardia
Diffuse neurotransmitters?
- Glutamate
- GABA
Circumscribed neurotransmitters?
- Serotonergic
- Noradrenergic
- Dopaminergic
- Histaminergic
- Cholinergic