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经导管非急性取出基于钛丝的无导线心室起搏器。

Transcatheter non-acute retrieval of the tine-based leadless ventricular pacemaker.

机构信息

Cardiology Department, Na Homolce Hospital, Roentgenova 37/2, 15030 Prague, Czech Republic.

Medtronic, Minneapolis, MN, USA.

出版信息

Europace. 2024 Oct 3;26(10). doi: 10.1093/europace/euae256.

DOI:10.1093/europace/euae256
PMID:39374848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11503947/
Abstract

AIMS

We report our single-centre experience of mid-term to long-term retrieval and reimplantation of a tine-based leadless pacemaker [Micra transcatheter pacing system (TPS)]. The TPS is a clinically effective alternative to transvenous single-chamber ventricular pacemakers. Whereas it is currently recommended to abandon the TPS at the end of device life, catheter-based retrieval may be favourable in specific scenarios.

METHODS AND RESULTS

We report on nine consecutive patients with the implanted TPS who subsequently underwent transcatheter retrieval attempts. The retrieval system consists of the original TPS delivery catheter and an off-the-shelf single-loop 7 mm snare. The procedure was guided by fluoroscopy and intracardiac echocardiography. After an implantation duration of 3.1 ± 2.8 years (range 0.4-9.0), the overall retrieval success rate was 88.9% (8 of 9 patients). The mean procedure time was 89 ± 16 min, and the fluoroscopy time was 18.0 ± 6.6 min. No procedure-related adverse device events occurred. In the one unsuccessful retrieval, intracardiac echocardiography revealed that the TPS was partially embedded in the ventricular tissue surrounding the leadless pacemaker body in the right ventricle. After retrieval, three patients were reimplanted with a new TPS device. All implantations were successful without complications.

CONCLUSION

A series of transvenous late retrievals of implanted TPS devices demonstrated safety and feasibility, followed by elective replacement with a new leadless pacing device or conventional transvenous pacing system. This provides a viable end-of-life management alternative to simple abandonment of this leadless pacemaker.

摘要

目的

我们报告了我们中心对基于钛针的无导线起搏器[Micra 经导管起搏系统(TPS)]进行中期至长期取回和再植入的经验。TPS 是经静脉单腔心室起搏器的有效替代方案。尽管目前建议在设备寿命结束时放弃 TPS,但在特定情况下,基于导管的取回可能更为有利。

方法和结果

我们报告了 9 例连续植入 TPS 后接受经导管取回尝试的患者。取回系统由原始的 TPS 输送导管和现成的单环 7mm 圈套器组成。该程序由荧光透视和心腔内超声心动图引导。在植入 3.1±2.8 年后(范围 0.4-9.0),总体取回成功率为 88.9%(9 例中的 8 例)。平均手术时间为 89±16min,透视时间为 18.0±6.6min。没有发生与程序相关的不良设备事件。在一次不成功的取回中,心腔内超声心动图显示 TPS 部分嵌入了右心室中无导线起搏器体周围的心室组织中。取回后,3 例患者重新植入了新的 TPS 装置。所有植入均成功,无并发症。

结论

一系列经静脉晚期取回植入的 TPS 设备证明了其安全性和可行性,随后可选择更换新的无导线起搏装置或传统的经静脉起搏系统。这为这种无导线起搏器的简单废弃提供了一种可行的寿命终止管理替代方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/778ab197913e/euae256f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/cf44909799e4/euae256_ga.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/c2eaa0b03475/euae256f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/01dff0853a71/euae256f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/37d90442798a/euae256f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/778ab197913e/euae256f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/cf44909799e4/euae256_ga.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/c2eaa0b03475/euae256f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/01dff0853a71/euae256f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/37d90442798a/euae256f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9475/11503947/778ab197913e/euae256f4.jpg

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