Page 366 - Cardiac Nursing
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                                                      Monitor QT interval, QRS width, PR. Monitor NAPA level (active metabolite) Watch for hypotension with IV use  Amiodarone, cimeti- dine, ranitidine increase procainamide  procainamide levels Additive effects on conduction system dis- ease when given with other class IA, class IC, tricyclic antidepressants, or  Was not included in CAST but is same class as drugs shown to cause higher  digoxin levels.  c  blocker  -blocker and Ca 2
  Quinidine and cimetidine increase  Additive effects
                                                  Comments  Drug Interactions:  levels  Alcohol T  blockers  Ca 2
  mortality post-MI Watch for proarrhythmia  Drug interactions:  Potentiates coumadin  Has mild  effects  Cyclosporin levels  c  propafenone levels  Drug interactions:  digoxin
                                                      GI: nausea, vomiting, anorexia CV: bradycardia, heart block,  proarrhythmia (less than that with quinidine). Prolongs QT   Hypotension. With IV use CNS: headache, insomnia, dizziness, psy- chosis, hallucinations, depression Lupus-like syndrome with long-term use (15%–25% of patients who take drug Other: rash, fever, swollen joints, agranu-  locytosis, pancytopenia  GI: nausea, anorexia, constipation, CNS: dizziness, headache, blurred vision CV: HF, bradycardia, AV block, bundle- br
                                                  Side Effects  interval   1 year)  metallic taste          depression
                                             (continued)  PO dose (regular release form): loading dose of 1,000–1,200 mg; maintenance dose 50 mg/kg/day in divided doses three to four times a day (never more  SR forms: 750–1,500 mg q 6 hours IV loading dose: 17 mg/kg at 20 mg/min. If rapid loading is needed, give 100-mg doses over 5 minutes to total of 1g  4–10 mcg/mL (may be as high as 5–32 mg/L to prevent  about 3.5 hours Active metabolite is NAPA: therapeutic  0.2–3 mcg/mL 2–10 hours in normal metab- olizers, up to 32 hours in slow
                                                Dose/Administration  Therapeutic Level/Half-Life  than 6 hour between doses)  IV drip 2–4 mg/min  Therapeutic level    sustained VT)     Half-life  9–12 mg/L  level    150–300 mg t.i.d.  Therapeutic level       Half-life  lizers  IV: 1–3 mg at rate of 1 mg/min  50–100 ng/mL     Half-life
                                             DRUGS USED FOR HEART RATE AND RHYTHM CONTROL
                                                      Conversion of atrial fib to sinus and  maintenance of NSR  Treatment of AT, atrial flutter and fib Slows conduction through accessory path-  Treatment of monomorphic VT  Conversion of atrial fib to sinus and  maintenance of NSR Slow conduction through accessory path- Life-threatening ventricular arrhythmias  Ventricular rate control in atrial fib/  Treatment of SVT (slow AV node conduction): AVNRT, CMT Effective in some types of VT: exercise in-  duced, digitalis induced Effective in re








                                                  Indication  ways in WPW               ways  (sustained VT)  flutter









                                             ■        Procainamide (Pronestyl) (Class IA antiarrhythmic)  Propafenone (Rythmol) (Class IC antiarrhythmic, also has  -blocker effects)  Propranolol (Inderal)  (Noncardioselective  -
                                             Table 16-2  Drug (Class)                                     blocker)





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