NSAID Flashcards
What is the definition of pain?
An unpleasant sensation due to actual or potential tissue damage. Pain is both sensory and emotional, influenced by physiological and psychological factors.
What are the four main effects of NSAIDs?
Anti-inflammatory, antipyretic, analgesic, and anti-platelet effects.
How are NSAIDs classified based on their chemical structure?
Salicylates (e.g., aspirin), acetic acid derivatives (e.g., diclofenac), propionic acid derivatives (e.g., ibuprofen), enolic acids (e.g., piroxicam), and others (e.g., celecoxib).
What is the mechanism of action of NSAIDs?
NSAIDs inhibit cyclo-oxygenase (COX) enzymes, blocking prostaglandin synthesis.
What are the two isoforms of COX enzymes?
COX-1 (housekeeping enzyme) and COX-2 (inducible in inflammation).
What are the housekeeping roles of prostaglandins?
Protect gastric mucosa, maintain renal blood flow, and inhibit gastric acid synthesis.
What are the pharmacokinetics of NSAIDs?
Absorbed in the GI tract, metabolized in the liver, and excreted by the kidneys.
What factors should be considered when choosing an NSAID?
Age, safety, efficacy, tolerance, formulation, convenience, and cost.
What are common side effects of NSAIDs?
GI issues (e.g., dyspepsia, ulcers), renal toxicity, cardiovascular risks, and hepatotoxicity.
What are risk factors for NSAID-induced GI toxicity?
Age >60 years, alcohol use, smoking, H. pylori infection, multiple NSAIDs, prednisolone use, and history of GI issues.
What are risk factors for NSAID-induced renal toxicity?
Advanced age, hypertension, diabetes, dehydration, and pre-existing renal disease.
What are analgesics derived from para-aminophenol?
Phenacetin and acetaminophen (paracetamol).
What are the effects of acetaminophen?
Analgesic and antipyretic effects. It lacks anti-inflammatory and anti-platelet functions.
What are the pharmacokinetics of acetaminophen?
Rapid GI absorption, liver metabolism, and renal excretion.
What is the recommended dose of acetaminophen?
500–1000 mg orally daily (maximum 2 g daily); parenteral dose: 300 mg intramuscularly or intravenously.