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通过重复心电图检查和心动过缓检测起搏器评估双分支阻滞患者的房室传导阻滞进展情况。

Atrioventricular block progression in patients with bifascicular block assessed by repeated electrocardiography and a bradycardia-detecting pacemaker.

作者信息

Bergfeldt L, Edvardsson N, Rosenqvist M, Vallin H, Edhag O

机构信息

Department of Cardiology, Karolinska Institute, Karolinska Hospital, Stockholm, Sweden.

出版信息

Am J Cardiol. 1994 Dec 1;74(11):1129-32. doi: 10.1016/0002-9149(94)90465-0.

Abstract

Syncope may be due to intermittent high-degree atrioventricular (AV) block, but a cause-relation is sometimes difficult to prove. Diagnostic methods with high predictive value proven by instruments for safe and sensitive follow-up are needed. A bradycardia-detecting pacemaker was used in patients with bifascicular block, who had been the subjects of pharmacologic stress testing of the His-Purkinje system. Thirty-seven patients were included, of whom 26 had experienced at least 1 syncopal episode of suspected bradycardia origin, and 11 had previously documented transient high-degree AV block. The electrophysiologic study included injection of disopyramide 2 mg/kg (up to 150 mg) over 5 minutes. A positive test result was defined as spontaneous or pacing-induced His-Purkinje high-degree AV block after drug or a drug-induced HV prolongation of > or = 50%. Patients were followed an average 63 months with repeated electrocardiography and a diagnostic pacemaker (n = 23). Altogether, 24 patients had a significant bradycardia diagnosed by either or both methods. The sensitivity and positive predictive values were: HV interval > or = 70 ms at baseline, 47% and 88%; a positive disopyramide test result, 75% and 80%; and HV interval > or = 70 ms or a positive disopyramide test result, 93% and 74%, respectively. Thus, the diagnostic pacemaker is a safe and sensitive tool for evaluating the information obtained at electrophysiologic study, and pharmacologic stress testing with disopyramide has an informative value in patients with bifascicular block and syncope when results at baseline are inconclusive.

摘要

晕厥可能是由于间歇性高度房室(AV)传导阻滞引起的,但有时很难证明其因果关系。需要通过仪器证明具有高预测价值的诊断方法,以便进行安全、灵敏的随访。对双分支阻滞患者使用了一种心动过缓检测起搏器,这些患者曾是希氏-浦肯野系统药物应激试验的对象。共纳入37例患者,其中26例曾经历过至少1次疑似心动过缓起源的晕厥发作,11例曾记录有短暂性高度AV传导阻滞。电生理研究包括在5分钟内注射2mg/kg(最大150mg)丙吡胺。阳性试验结果定义为用药后自发或起搏诱发的希氏-浦肯野高度AV传导阻滞,或药物诱发的HV间期延长≥50%。对患者平均随访63个月,重复进行心电图检查并使用诊断性起搏器(n = 23)。总共有24例患者通过两种方法中的一种或两种被诊断为显著心动过缓。敏感性和阳性预测值分别为:基线时HV间期≥70ms,47%和88%;丙吡胺试验结果为阳性,75%和80%;HV间期≥70ms或丙吡胺试验结果为阳性,分别为93%和74%。因此,诊断性起搏器是评估电生理研究中获得信息的一种安全、灵敏的工具,当基线结果不明确时,丙吡胺药物应激试验对双分支阻滞和晕厥患者具有参考价值。

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