Biblo L A, Carlson M D, Waldo A L
Department of Medicine, Case Western Reserve University/University Hospitals of Cleveland, Ohio, USA.
J Am Coll Cardiol. 1995 Jun;25(7):1601-4. doi: 10.1016/0735-1097(95)00087-k.
We hypothesized that if the Electrophysiology Study Versus Electrocardiographic Monitoring (ESVEM) trial programmed stimulation protocol misclassified some drug trials as effective, then the misclassification rate would be proportionally greater for drugs other than sotalol.
In the ESVEM trial, patients treated with sotalol had fewer arrhythmic recurrences than those treated with other antiarrhythmic drugs despite similar efficacy predictions during electrophysiologic testing.
We retrospectively compared the standard programmed stimulation protocol used at Case Western Reserve University, which used three extrastimuli during all follow-up studies, with the ESVEM protocol in 176 antiarrhythmic drug trials: sotalol (n = 54), procainamide (n = 73) and quinidine/mexiletine (n = 49).
Predictions of efficacy were higher in the sotalol trials (14 of 54 standard, 20 of 54 ESVEM) than in procainamide trials (7 of 73 standard, 14 of 73 ESVEM) or quinidine/mexiletine trials (1 of 49 standard, 7 of 49 ESVEM). Thus, the two protocols classified 19 of 176 trials differently: not effective by the standard protocol but effective by the ESVEM trial. Discordant predictions of drug efficacy constituted a smaller proportion of ESVEM protocol efficacy predictions for sotalol (6 [30%] of 20) than for the other drugs (13 [62%] of 21, p < or = 0.05).
In the present study, the ESVEM programmed stimulation protocol predicted efficacy more often than the standard protocol. Discordant predictions represented a smaller portion of efficacy predictions for sotalol than for the other drugs. Thus, in the ESVEM trial, the superior long-term follow-up observed in patients assigned to sotalol may have been an artifact of the stimulation protocol utilized by the ESVEM investigators.
我们假设,如果电生理研究与心电图监测(ESVEM)试验的程控刺激方案将一些药物试验错误分类为有效,那么对于除索他洛尔之外的药物,错误分类率将成比例地更高。
在ESVEM试验中,尽管在电生理测试期间疗效预测相似,但接受索他洛尔治疗的患者心律失常复发次数少于接受其他抗心律失常药物治疗的患者。
我们回顾性地比较了凯斯西储大学使用的标准程控刺激方案(在所有随访研究中使用三个额外刺激)与176项抗心律失常药物试验中的ESVEM方案:索他洛尔(n = 54)、普鲁卡因胺(n = 73)和奎尼丁/美西律(n = 49)。
索他洛尔试验中疗效预测高于普鲁卡因胺试验(标准方案73项中的7项,ESVEM方案73项中的14项)或奎尼丁/美西律试验(标准方案49项中的1项,ESVEM方案49项中的7项)。因此,两种方案对176项试验中的19项分类不同:标准方案判定无效但ESVEM试验判定有效。药物疗效的不一致预测在索他洛尔的ESVEM方案疗效预测中所占比例(20项中的6项[30%])小于其他药物(21项中的13项[62%],p≤0.05)。
在本研究中,ESVEM程控刺激方案比标准方案更常预测疗效。不一致预测在索他洛尔疗效预测中所占比例小于其他药物。因此,在ESVEM试验中,分配接受索他洛尔治疗的患者观察到的更好的长期随访结果可能是ESVEM研究人员使用的刺激方案造成的假象。