Iraqi Board Clinical Pharmacy flashcards
Iraqi Board Clinical Pharmacy · Build recall with a focused review session.
32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Volume of distribution
- Apparent volume relating the amount of drug in the body to its plasma concentration (Vd = dose/C0); a large Vd indicates extensive tissue distribution and limits removal by dialysis.
- Clearance
- Volume of plasma cleared of drug per unit time; determines the maintenance dose needed to achieve a target steady-state concentration, independent of dose size in first-order kinetics.
- Michaelis-Menten kinetics
- Saturable elimination described by rate = Vmax × C/(Km + C); at high concentrations clearance falls and small dose increases produce disproportionate rises in plasma level, as with phenytoin.
- Therapeutic drug monitoring
- Measurement of plasma drug concentrations for narrow-therapeutic-index drugs to individualize dosing; interpretation requires correct sampling time, steady state, and knowledge of interacting factors.
- ARNI in heart failure
- Sacubitril/valsartan replaces an ACE inhibitor in HFrEF to reduce mortality; a 36-hour washout is required when switching from an ACE inhibitor to avoid angioedema.
- CHA2DS2-VASc score
- Stroke risk score in atrial fibrillation: congestive failure, hypertension, age ≥75 (2 points), diabetes, stroke (2 points), vascular disease, age 65–74, female sex; guides anticoagulation.
- Cockcroft-Gault equation
- Estimates creatinine clearance from age, weight, and serum creatinine, with a 0.85 factor for women; used for renal drug dosing even though eGFR is used for CKD staging.
- RAAS inhibitor monitoring
- After starting an ACE inhibitor or ARB, check creatinine and potassium within 1–2 weeks; a creatinine rise up to 30% is acceptable, but greater rises warrant investigation.
- Extended-interval aminoglycosides
- Once-daily dosing uses high peaks for concentration-dependent killing and a low trough to reduce nephrotoxicity; monitor levels in renal impairment, obesity, and pregnancy.
- Antimicrobial de-escalation
- Narrowing empiric therapy once culture and susceptibility results are available, stopping redundant agents, and switching to oral therapy when clinically stable.
- Surgical prophylaxis timing
- Give a single preoperative antibiotic dose within 60 minutes of incision (vancomycin and fluoroquinolones within 120 minutes); redose for long procedures and stop within 24 hours.
- Penicillin allergy delabeling
- A detailed history identifies low-risk reactions; direct oral challenge or graded challenge can remove an inaccurate penicillin allergy label and reduce use of broader-spectrum antibiotics.
- Metformin first-line therapy
- First-line pharmacotherapy for type 2 diabetes unless contraindicated; SGLT2 inhibitors or GLP-1 receptor agonists are added when atherosclerotic cardiovascular disease, heart failure, or CKD is present.
- Diabetic ketoacidosis management
- Isotonic fluids, insulin infusion after potassium is at least 3.3 mmol/L, potassium replacement, and glucose monitoring; bicarbonate is reserved for pH below 6.9.
- Levothyroxine administration
- Take on an empty stomach 30–60 minutes before food and separate by 4 hours from calcium, iron, and proton pump inhibitors; titrate using TSH every 6–8 weeks.
- Steroid equivalence
- Hydrocortisone 20 mg equals prednisone 5 mg, methylprednisolone 4 mg, and dexamethasone 0.75 mg; prolonged use requires tapering to prevent adrenal insufficiency.
- Asthma MART regimen
- Maintenance and reliever therapy using low-dose inhaled corticosteroid-formoterol; SABA-only treatment is no longer recommended because undertreated inflammation increases exacerbation and death risk.
- H. pylori quadruple therapy
- A 14-day regimen of proton pump inhibitor, bismuth, tetracycline, and metronidazole, preferred where clarithromycin resistance is high; confirm eradication after treatment.
- N-acetylcysteine for acetaminophen
- Antidote for acetaminophen overdose, most effective within 8 hours of ingestion; the Rumack-Matthew nomogram guides treatment for acute single ingestions.
- R ratio in liver injury
- R = (ALT/upper limit of normal) ÷ (ALP/upper limit of normal); R ≥5 indicates hepatocellular, R ≤2 cholestatic, and 2–5 mixed drug-induced liver injury.
- Serotonin syndrome
- Life-threatening toxidrome with clonus, hyperreflexia, agitation, and hyperthermia after serotonergic drugs; stop offending agents, give benzodiazepines, and use cyproheptadine in severe cases.
- Lithium therapeutic range
- Trough level of 0.6–1.0 mmol/L drawn 12 hours after the dose; dehydration, NSAIDs, and thiazides raise levels and risk toxicity, so monitor renal and thyroid function.
- Alcohol withdrawal treatment
- Benzodiazepines are first-line, dosed by symptom-triggered CIWA-Ar scoring; thiamine is given before glucose to prevent Wernicke encephalopathy.
- Febrile neutropenia
- Fever with absolute neutrophil count below 500 cells/µL; start empiric antipseudomonal beta-lactam within 1 hour; add vancomycin for line infection or instability.
- Tumor lysis syndrome
- Metabolic emergency with hyperkalemia, hyperphosphatemia, hyperuricemia, and hypocalcemia after rapid tumor breakdown; prevent with hydration and allopurinol or rasburicase.
- Leucovorin rescue
- Folinic acid given after high-dose methotrexate to bypass dihydrofolate reductase blockade and reduce toxicity; glucarpidase is used for toxic levels with renal impairment.
- Heparin-induced thrombocytopenia
- Immune-mediated platelet activation causing thrombocytopenia and thrombosis; stop heparin and start a non-heparin anticoagulant such as argatroban or fondaparinux.
- Anion gap
- Calculated as sodium minus chloride minus bicarbonate, normally 8–12 mmol/L; an elevated gap suggests ketoacidosis, lactic acidosis, renal failure, or toxin ingestion.
- Corrected calcium
- Measured calcium plus 0.8 × (4.0 − albumin in g/dL); ionized calcium is preferred in critical illness or when albumin is abnormal.
- Number needed to treat
- The reciprocal of the absolute risk reduction; it estimates how many patients must be treated to prevent one additional adverse outcome and depends on baseline risk.
- Sensitivity and specificity
- Sensitivity is the proportion of diseased patients testing positive; specificity is the proportion of nondiseased patients testing negative; predictive values also depend on disease prevalence.
- Pharmacovigilance reporting
- Systematic detection, assessment, and prevention of adverse drug reactions; serious, unexpected, and new-drug reactions are reported to the national center, with causality assessed by validated scales.