Class Ia Antiarrhythmic Agents Flashcards
Quinidine Adverse Effects
“cinchonism” (CNS and GI symptoms, tinnitus),
strong vagolytic and anticholinergic properties
Quinidine PK/DI
PK: Half-life 5–9 hr
Potent inhibitor of CYP2D6 (Digoxin); substrate and
inhibitor of CYP3A4 (Warfarin)
Quinidine (Quinidex,
Quinaglute) Dosing
AF and VT maintenance:
Sulfate: 200–400 mg PO every 6 hr
Gluconate (CR): 324 mg PO every 8–12 hr
Quinidine Dose Adjustment
Decrease dose by 25% if CrCl < 10 mL/min
Procainamide Contraindication
LVEF < 40%
Procainamide Elimination
Active metabolite NAPA (class III effects) may accumulate in renal dysfunction (reduce in renal and liver dysfunction)
Procainamide (Pronestyl) Dosing
AF conversion: 1 g IV for 30 min; then 2 mg/min
VT conversion: 20 mg/min IV until 17 mg/kg, arrhythmia ceases, hypotension, or QRS widens > 50%
VT maintenance: 1–4 mg/min
Disopyramide Contraindications
potent negative inotropic effect- Cardiogenic shock, congenital long QT syndrome, second- or third-degree AVB,
glaucoma
Disopyramide PK/DI
PK: Half-life 4–8 hr
Substrate of CYP2D6
DI: May enhance the effect of β-blockers
Disopyramide (Norpace) Dosing
AF conversion: IR 200 mg (if < 50 kg) or 300 mg
(if > 50 kg) PO every 6 hr
AF maintenance: 400–800 mg/day in divided doses IR every 6 hr or CR every 12 hr
Disopyramide Dose Adjustments
If < 50 kg, moderate renal dysfunction (CrCl > 40 mL/ min) or hepatic dysfunction, max 400 mg/day
If severe renal dysfunction (IR only; avoid CR)
CrCl 30–40 mL/min, 100 mg every 8 hr
CrCl 15–30 mL/min, 100 mg every 12 hr
CrCl < 15 mL/min, 100 mg every 24 hr
Class Ia Adverse Effect
Tdp
Class Ia Caution
Avoid in heart failure and acute MI