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Does Bachmann's bundle pacing prevent atrial fibrillation in myotonic dystrophy type 1 patients? A 12 months follow-up study.

机译:Bachmann束起搏器是否可以防止1型强直性肌营养不良患者的房颤?为期12个月的随访研究。

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AIMS: Paroxysmal atrial arrhythmias occur in myotonic dystrophy type 1 (MD1) patients frequently. Pacemaker (PM) including detailed diagnostic functions may facilitate the diagnosis and management of frequent paroxysmal atrial tachyarrhythmias that may remain undetected during conventional clinical follow-up. Aim of our study was to evaluate the preventive effects of interatrial septum pacing in the Bachmann's Bundle region on atrial fibrillation (AF) in MD1 patients during 12 months follow up period. METHODS AND RESULTS: Thirty MD1 patients (age 50.3 +/- 7.3; 11 F) who underwent dual chamber PM implantation were randomized at implantation to receive right atrial appendage pacing (16 patients) or Bachmann's bundle pacing (14 patients). No statistically significant difference in the electrical parameters (P wave amplitude, pacing threshold and lead impedance) was found between the two groups at implantation. Patients were followed at 1 month, 3 months, and every 6 months thereafter. They underwent clinical assessment, a standard 12-lead ECG and assessment of device performance at every visit. We counted the number of episodes of atrial arrhythmia occurred during the collection period and the duration of each episode. At 12 months of follow-up, no statistically significant differences in the number of AF episodes or in AF duration were found. Lead parameters remained stable over time and there were no displacements of the electrodes after implantation. CONCLUSION: Implantation of an atrial-active fixation lead on the atrial septum is safe and feasible. However, this study showed no significant difference between septal pacing and high atrial pacing, using the endpoints of AF duration and number of AF episodes.
机译:目的:阵发性房性心律失常常发生于1型强直性肌营养不良(MD1)患者。具有详细诊断功能的起搏器(PM)可以促进对常见的阵发性房性心律失常的诊断和管理,而在常规的临床随访过程中仍可能未被发现。我们研究的目的是评估在12个月的随访期间,巴赫曼氏囊区域的房间隔起搏对MD1患者房颤的预防作用。方法和结果:30例接受双室PM植入的MD1患者(50.3 +/- 7.3岁; 11 F)在植入时被随机分配接受右心耳起搏(16例)或巴赫曼束起搏(14例)。在植入时两组之间在电学参数(P波幅度,起搏阈值和导线阻抗)上没有发现统计学上的显着差异。在1个月,3个月以及此后每6个月对患者进行随访。他们进行了临床评估,标准的12导联心电图并在每次就诊时评估了器械的性能。我们统计了收集期间发生的心律失常发作的次数以及每次发作的持续时间。随访12个月时,房颤发作次数或房颤持续时间无统计学意义差异。铅参数随时间保持稳定,并且植入后电极没有位移。结论:在房间隔上植入心房主动固定导线是安全可行的。然而,这项研究表明,使用房颤持续时间和房颤发作次数的终点,在间隔起搏和高心房起搏之间没有显着差异。

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