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室性心动过速的减慢作为电生理研究中系列药物测试的一个可能终点。

Slowing of ventricular tachycardia as a possible endpoint for serial drug testing at electrophysiological study.

作者信息

Handlin L R, Brodine W N, Gibbs H, Vacek J L

机构信息

Research Medical Center, University of Missouri-Kansas City.

出版信息

Pacing Clin Electrophysiol. 1992 Jun;15(6):864-9. doi: 10.1111/j.1540-8159.1992.tb03076.x.

DOI:10.1111/j.1540-8159.1992.tb03076.x
PMID:1376898
Abstract

Certain patients who cannot be rendered noninducible by serial drug testing during electrophysiology study demonstrate significant slowing of their ventricular tachycardia rate with selected agents. We evaluated the characteristics and outcome of 19 such patients to assess whether this slowing could be considered an acceptable endpoint for treatment. This group consisted of 14 males and 5 females (mean age 63 +/- 9) with a mean ejection fraction of 28 +/- 13% and inducible sustained ventricular tachycardia. Sixteen patients had known coronary artery disease and 13 had prior myocardial infarction. The other three patients had idiopathic cardiomyopathy. Serial drug testing during an electrophysiology protocol that used up to three extrastimuli at two or three cycle lengths at two right ventricular sites was used to select a medication regimen that provided optimal ventricular tachycardia slowing without limiting side effects. Five patients were treated with amiodarone, three with Ic agents (all with ejection fraction greater than 30%), and the remainder with Ia and Ib agents alone or in combination. Mean initial ventricular tachycardia rate was 219 +/- 26 beats/min with posttreatment ventricular tachycardia rate 137 +/- 17 (mean initial cycle length 278 +/- 35 msec, posttreatment 443 +/- 53 msec). Two groups were identified, those who had recurrent (although well-tolerated) ventricular tachycardia (group I, n = 8, mean time to recurrence = 15 months), and those who did not (group II, n = 11, mean follow-up 22 months). Overall sudden death rate was 5%, while total mortality was 11% (all mortality in group I).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在电生理研究期间,某些患者通过系列药物测试无法被诱导为不诱发状态,但使用特定药物后其室性心动过速速率显著减慢。我们评估了19例此类患者的特征及预后,以判断这种减慢是否可被视为可接受的治疗终点。该组包括14名男性和5名女性(平均年龄63±9岁),平均射血分数为28±13%,且可诱导出持续性室性心动过速。16例患者患有已知冠状动脉疾病,13例有既往心肌梗死史。另外3例患者患有特发性心肌病。在电生理方案中,通过在两个右心室部位以两个或三个周期长度使用多达三个额外刺激进行系列药物测试,以选择一种能提供最佳室性心动过速减慢效果且无明显副作用的药物方案。5例患者接受胺碘酮治疗,3例接受Ic类药物治疗(均射血分数大于30%),其余患者单独或联合使用Ia类和Ib类药物。平均初始室性心动过速速率为219±26次/分钟,治疗后室性心动过速速率为137±17次/分钟(平均初始周期长度278±35毫秒,治疗后443±53毫秒)。分为两组,一组为有复发性(尽管耐受性良好)室性心动过速的患者(第一组,n = 8,平均复发时间 = 15个月),另一组为无复发性室性心动过速的患者(第二组,n = 11,平均随访22个月)。总体猝死率为5%,总死亡率为11%(所有死亡均在第一组)。(摘要截断于250字)

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