Page 363 - Cardiac Nursing
P. 363

M
                                        M
                                     6 A
                                          Pa
                                           g
                                           g
                                          Pa
                                     6 A
                                                      c.
                                                   a
                                   1
                                                      c.
                                                      c.
                                   2:1
                                   2:1
                                                 p
                                                 p
                                                 p
                                                  t
                                                  ara
                                                  ara
                                                  t
                                                A
                                            e 3
                                            e 3
                                           g
                                              39
                                                A
                                                A
                                              39
                      3-3
                                                     In
                    33
                      3-3
                        87.
                        87.
                                                     In
         LWB
         LWBK340-c16_
         LWB K34 0-c 16_ p p pp333-387.qxd  6/30/09  12:16 AM  Page 339 Aptara Inc.
            K34
                    33
                 16_
               0-c
                             6
                              6
                                /09
                             6
                                /09
                              /30
                              /30
                          q
                          q
                                                   a
                          q
                                   1
                           xd
                           xd
                    Phys-             Additive effects on  potential  blockers, digoxin  Incompatible with  T  digoxin levels: Ery-  Additive effects on  poten-  May potentiate effect   -  blockers. Phenobarbi-  disopyramide  disopyramide level
                    Special precautions with IV form: ically incompatible with aminophylline, heparin, cefamandole, cefazolin, mezlocillin, sodium bicarbonate Must be delivered using a volumetric (not drop counter) because drop  pump  size is altered by drug Cardioselective  -blocker used primarily for hypertension and angina  Drug interactions: HR, AV conduction, BP , and c for HF when given with negative  inotropic drugs, Ca 2
 Doses (0.5 mg may cause paradoxical  bradycardia Causes pupils to dilate (significant when checking pupils
                                   Hypotension, bradycardia, AV block. Di-  arrhea, wheezing, HF  CV: tachycardia, chest pain, VT/fibrilla-  tion (rare) CNS: drowsiness, confusion, dizziness,  insomnia, nervousness  GI motility, constipa- GI: dry mouth, T  tion, nausea Other: urinary retention, hot flushed skin,  rash  CV: bradycardia, AV block Digoxin toxicity: sinus exit block, AV block, AT with block, bidirectional VT, fascicular tachycardia, accelerated junc- tional rhythm, regularization of ventric- ular response to atrial fib Visua
                        800–1600 mg q.d.  600–800 mg q.d.
                      PO dose  400 mg q.d. Very long half-life (26–107 days; average Initial dose: 12.5–25 mg PO q.d. Mainte- nance dose: 50–100 mg PO q.d. IV: 5 mg over 5 minutes, may repeat in   Symptomatic bradycardia: 0.5 mg IV. May repeat q 3–5 minutes to a total of Asystole: 1 mg IV, repeat q 3–5 minutes to a total vagolytic dose of 0.04 mg/kg  cardiac arrest if no IV available:  PO loading dose: 0.5–1 mg divided into three or four doses at 6–8-hour PO maintenance dose: 0.125–0.5 mg q.d. IV loading dose: 0.5–1 mg divided into th
                    IV to PO transition:  Duration of IV   1 week  1–3 weeks   3 weeks Therapeutic level   0.5–2 mcg/mL  53 days)  5 minutes    6–7 hours  Half-life  3 mg  May be given down ET tube during  use 2–2.5 mg    2–5 hours  Half-life  intervals  intervals Therapeutic level   0.8–2 ng/mL    36–48 hours  Half-life  120–360 mg/day in divided doses  2 minutes  IV infusion: 5–15 mg/h Therapeutic level   50–200 ng/mL    4–6 hours  Half-life  Total daily dose  SR form   Therapeutic level   3–6 mcg/mL    4–10 hours  Half-life




                                   Ventricular rate control in atrial  fib/flutter Slow conduction through AV node in  AVNRT and CMT  Treatment of symptomatic bradycardia (sinus, junctional, AV block) and  asystole  Ventricular rate control in atrial fib/  flutter Rarely used as an antiarrhythmic  anymore Used as an inotropic agent in HF  Ventricular rate control in atrial fib/flutter Slow conduction through AV node in  AVNRT and CMT  Used to prevent recurrence of VT or VF Effective in preventing atrial fib and  flutter Slows conduction throu













                                     -blocker)
                                   Atenolol (Tenormin)  (Cardioselective  Atropine (Anticholinergic, parasympa-  tholytic)  Digoxin  Diltiazem (Cardizem) (Calcium channel blocker:  nondihydropyridine,  “heart rate lowering”  blocker)  Ca 2
  Disopyramide (Norpace) (Class IA antiarrhythmic)








                                                                                                                   339
   358   359   360   361   362   363   364   365   366   367   368