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为电同步编程心脏再同步治疗:超越左束支阻滞和左心室激活延迟。

Programming Cardiac Resynchronization Therapy for Electrical Synchrony: Reaching Beyond Left Bundle Branch Block and Left Ventricular Activation Delay.

机构信息

Cleveland Clinic, Cleveland, OH

Cardiology, Austin Health, Melbourne, Australia.

出版信息

J Am Heart Assoc. 2018 Feb 6;7(3):e007489. doi: 10.1161/JAHA.117.007489.

DOI:10.1161/JAHA.117.007489
PMID:29432133
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5850248/
Abstract

BACKGROUND

QRS narrowing following cardiac resynchronization therapy with biventricular (BiV) or left ventricular (LV) pacing is likely affected by patient-specific conduction characteristics (PR, qLV, LV-paced propagation interval), making a universal programming strategy likely ineffective. We tested these factors using a novel, device-based algorithm (SyncAV) that automatically adjusts paced atrioventricular delay (default or programmable offset) according to intrinsic atrioventricular conduction.

METHODS AND RESULTS

Seventy-five patients undergoing cardiac resynchronization therapy (age 66±11 years; 65% male; 32% with ischemic cardiomyopathy; LV ejection fraction 28±8%; QRS duration 162±16 ms) with intact atrioventricular conduction (PR interval 194±34, range 128-300 ms), left bundle branch block, and optimized LV lead position were studied at implant. QRS duration (QRSd) reduction was compared for the following pacing configurations: nominal simultaneous BiV (Mode I: paced/sensed atrioventricular delay=140/110 ms), BiV+SyncAV with 50 ms offset (Mode II), BiV+SyncAV with offset that minimized QRSd (Mode III), or LV-only pacing+SyncAV with 50 ms offset (Mode IV). The intrinsic QRSd (162±16 ms) was reduced to 142±17 ms (-11.8%) by Mode I, 136±14 ms (-15.6%) by Mode IV, and 132±13 ms (-17.8%) by Mode II. Mode III yielded the shortest overall QRSd (123±12 ms, -23.9% [<0.001 versus all modes]) and was the only configuration without QRSd prolongation in any patient. QRS narrowing occurred regardless of QRSd, PR, or LV-paced intervals, or underlying ischemic disease.

CONCLUSIONS

Post-implant electrical optimization in already well-selected patients with left bundle branch block and optimized LV lead position is facilitated by patient-tailored BiV pacing adjusted to intrinsic atrioventricular timing using an automatic device-based algorithm.

摘要

背景

心脏再同步治疗后 QRS 波变窄(双心室[BiV]或左心室[LV]起搏)可能受患者特定的传导特征(PR、qLV、LV 起搏传播间隔)影响,因此通用程控策略可能无效。我们使用一种新的基于设备的算法(SyncAV)来测试这些因素,该算法根据固有房室传导自动调整起搏房室延迟(默认或可编程偏移)。

方法和结果

在植入时,对 75 例接受心脏再同步治疗(年龄 66±11 岁;65%为男性;32%为缺血性心肌病;LV 射血分数 28±8%;QRS 时限 162±16 ms)的患者进行了研究,这些患者具有完整的房室传导(PR 间期 194±34,范围 128-300 ms)、左束支传导阻滞和优化的 LV 导联位置。比较了以下起搏配置的 QRS 时限(QRSd)降低情况:名义上同时的 BiV(模式 I:起搏/感知房室延迟=140/110 ms)、带 50 ms 偏移的 BiV+SyncAV(模式 II)、使 QRSd 最小化的 BiV+SyncAV 偏移(模式 III)或仅 LV 起搏+带 50 ms 偏移的 SyncAV(模式 IV)。固有 QRSd(162±16 ms)在模式 I 下降低至 142±17 ms(-11.8%),在模式 IV 下降低至 136±14 ms(-15.6%),在模式 II 下降低至 132±13 ms(-17.8%)。模式 III 产生的总体 QRSd 最短(123±12 ms,-23.9% [<0.001 与所有模式]),并且是唯一一种在任何患者中都没有 QRSd 延长的配置。QRS 变窄发生与 QRSd、PR 或 LV 起搏间隔或潜在的缺血性疾病无关。

结论

在已经选择良好的左束支传导阻滞患者中,通过自动设备算法调整至固有房室时间的患者定制的 BiV 起搏,可以实现已优化 LV 导联位置的患者的术后电优化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/afcd86567fff/JAH3-7-e007489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/920aa418cc5b/JAH3-7-e007489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/2af811269bcb/JAH3-7-e007489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/c35d7ed1b8b3/JAH3-7-e007489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/af5df8b902fd/JAH3-7-e007489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/c040788d4719/JAH3-7-e007489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/afcd86567fff/JAH3-7-e007489-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/920aa418cc5b/JAH3-7-e007489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/2af811269bcb/JAH3-7-e007489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/c35d7ed1b8b3/JAH3-7-e007489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/af5df8b902fd/JAH3-7-e007489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/c040788d4719/JAH3-7-e007489-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42d9/5850248/afcd86567fff/JAH3-7-e007489-g006.jpg

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