Goy J J, Fromer M
Department of Internal Medicine, University Hospital, Lausanne, Switzerland.
J Cardiovasc Pharmacol. 1991;17 Suppl 6:S36-40.
Atrioventricular (AV) tachycardia includes both AV nodal reentrant tachycardia (AVNRT) and AV reentrant tachycardia (AVRT) using an accessory pathway. The treatment of the acute attack is different from the long-term treatment of both AVNRT and AVRT. Verapamil and adenosine, by prolonging the refractory period of the AV node, are highly effective in terminating acute attacks of AVNRT and orthodromic AVRT. Conversion to sinus rhythm is achieved in approximately 90% of the episodes of tachycardias with both agents given intravenously. The initial dose of verapamil is 0.075-0.1 mg/kg and a subsequent bolus of 5 mg can be given to a maximal dose of 15-20 mg. The initial dose of adenosine is 3 or 6 mg, but doses of 9 or 12 mg can be administered if smaller dosages have been unsuccessful. Other agents producing lengthening of the refractory period of the accessory pathway in AVRT or of the fast pathway in AVNRT often terminate reentry tachycardia. Such agents are class IC antiarrhythmic drugs such as flecainide or propafenone and class IA drugs such as procainamide. In patients with accessory pathways and antidromic tachycardia or atrial fibrillation conducting via an accessory pathway, treatment with verapamil or digoxin should be avoided because these agents may enhance the conduction properties of the accessory pathway, thereby leading to an increase of the ventricular rate or even to ventricular fibrillation. Prevention of AVNRT episodes can be obtained with various antiarrhythmic drugs. Digoxin alone or in combination with beta-blockers is effective in approximately 50% of the cases and especially when the combination proved to be successful during electrophysiological testing.(ABSTRACT TRUNCATED AT 250 WORDS)
房室(AV)性心动过速包括房室结折返性心动过速(AVNRT)和利用旁路的房室折返性心动过速(AVRT)。急性发作的治疗与AVNRT和AVRT的长期治疗不同。维拉帕米和腺苷通过延长房室结的不应期,在终止AVNRT和正向AVRT的急性发作方面非常有效。静脉给予这两种药物时,约90%的心动过速发作可转为窦性心律。维拉帕米的初始剂量为0.075 - 0.1mg/kg,随后可给予5mg的推注剂量,最大剂量为15 - 20mg。腺苷的初始剂量为3或6mg,但如果较小剂量未成功,可给予9或12mg的剂量。其他能延长AVRT中旁路不应期或AVNRT中快径不应期的药物通常可终止折返性心动过速。这类药物包括IC类抗心律失常药物,如氟卡尼或普罗帕酮,以及IA类药物,如普鲁卡因胺。对于有旁路且存在逆向性心动过速或通过旁路传导的房颤患者,应避免使用维拉帕米或地高辛治疗,因为这些药物可能增强旁路的传导特性,从而导致心室率增加甚至心室颤动。多种抗心律失常药物可用于预防AVNRT发作。单独使用地高辛或与β受体阻滞剂联合使用在约50%的病例中有效,尤其是在电生理测试中联合使用被证明成功的情况下。(摘要截选于250字)