首页> 外文期刊>Circulation: An Official Journal of the American Heart Association >Pacemaker therapy in patients with neurally mediated syncope and documented asystole: Third international study on syncope of uncertain etiology (ISSUE-3): A randomized trial
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Pacemaker therapy in patients with neurally mediated syncope and documented asystole: Third international study on syncope of uncertain etiology (ISSUE-3): A randomized trial

机译:神经介导性晕厥和心搏停止的起搏器治疗:不确定病因性晕厥的第三次国际研究(ISSUE-3):一项随机试验

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Background-The efficacy of cardiac pacing for prevention of syncopal recurrences in patients with neurally mediated syncope is controversial. We wanted to determine whether pacing therapy reduces syncopal recurrences in patients with severe asystolic neurally mediated syncope. Methods and Results-Double-blind, randomized placebo-controlled study conducted in 29 centers in the Third International Study on Syncope of Uncertain Etiology (ISSUE-3) trial. Patients were 40 years, had experienced 3 syncopal episodes in the previous 2 years. Initially, 511 patients, received an implantable loop recorder; 89 of these had documentation of syncope with 3 s asystole or 6 s asystole without syncope within 12±10 months and met criteria for pacemaker implantation; 77 of 89 patients were randomly assigned to dual-chamber pacing with rate drop response or to sensing only. The data were analyzed on intention-to-treat principle. There was syncope recurrence during follow-up in 27 patients, 19 of whom had been assigned to pacemaker OFF and 8 to pacemaker ON. The 2-year estimated syncope recurrence rate was 57% (95% CI, 40-74) with pacemaker OFF and 25% (95% CI, 13-45) with pacemaker ON (log rank: P=0.039 at the threshold of statistical significance of 0.04). The risk of recurrence was reduced by 57% (95% CI, 4-81). Five patients had procedural complications: lead dislodgment in 4 requiring correction and subclavian vein thrombosis in 1 patient. Conclusions-Dual-chamber permanent pacing is effective in reducing recurrence of syncope in patients 40 years with severe asystolic neurally mediated syncope. The observed 32% absolute and 57% relative reduction in syncope recurrence support this invasive treatment for the relatively benign neurally mediated syncope. Clinical Trial Registration-URL: http://www. clinicaltrials.gov. Unique identifier: NCT00359203.
机译:背景-心脏起搏在神经介导性晕厥患者中预防晕厥复发的功效尚存争议。我们想确定起搏治疗是否可以降低严重的收缩期神经介导性晕厥患者的晕厥复发。方法和结果-在第三次不确定病因晕厥国际研究(ISSUE-3)试验中,在29个中心进行了双盲,随机安慰剂对照研究。患者为40岁,在过去2年中经历过3次晕厥发作。最初,有511名患者接受了植入式循环记录仪;其中89例在12±10个月内有3 s搏动或6 s搏动无晕厥的晕厥记录,并符合起搏器植入的标准。在89例患者中,有77例被随机分配至双室起搏并伴有降速反应或仅进行感知。数据按意向治疗原则进行分析。随访期间有27例患者发生晕厥复发,其中19例被分配给起搏器OFF,8例被分配给起搏器ON。在起搏器关闭的情况下,两年的估计晕厥复发率为57%(95%CI,40-74),在起搏器打开的情况下为25%(95%CI,13-45)(对数统计学上为P = 0.039)显着性为0.04)。复发风险降低了57%(95%CI,4-81)。 5例患者存在手术并发症:4例需要纠正的铅移位,1例患者的锁骨下静脉血栓形成。结论:双腔永久起搏可有效减少40岁重度收缩性神经介导性晕厥患者的晕厥复发。所观察到的晕厥复发绝对值减少了32%,相对减少了57%,支持这种侵入性治疗相对良性的神经介导的晕厥。临床试验注册-URL:http:// www。临床试验网唯一标识符:NCT00359203。

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