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经静脉腔内心内 3830 起搏导线在心脏传导系统起搏中的提取:单中心经验。

Transvenous lead extraction of lumenless 3830 pacing lead in conduction system pacing: a single-center experience.

机构信息

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova, Via N. Giustiniani 2, Padova, Italy.

Arrhythmia and Electrophysiology Unit, Division of Cardiology, Santa Maria Della Misericordia General Hospital, Rovigo, Italy.

出版信息

J Interv Card Electrophysiol. 2024 Jan;67(1):175-182. doi: 10.1007/s10840-023-01590-0. Epub 2023 Jun 27.

Abstract

BACKGROUND

The Medtronic SelectSecure Model 3830 lumenless lead (Medtronic, Inc., Minneapolis, MN) is commonly used for conduction system pacing (CSP). However, with this increased use, the potential need for transvenous lead extraction (TLE) also will increase. While extraction of endocardial 3830 leads is rather well described especially in pediatric and adult congenital heart disease population, there is very limited data on extraction of CSP leads. In the present study, we reported our preliminary experience on TLE of CSP leads and provided technical considerations.

METHODS

The study population comprised 6 consecutive patients (67% male; mean age 70 ± 22 years) with CSP leads (3830 leads), including left bundle branch pacing (LBBP) lead (n = 3) and His pacing lead (n = 3) undergoing TLE. Overall target leads were 17. The mean implant duration time of CSP leads was 97 ± 90 months [range 8-193).

RESULTS

Manual traction was successful in 2 cases and mechanical extraction tools were required in the remaining cases. Sixteen leads (94%) were completely extracted, whereas incomplete removal was observed in one lead (6%) among 1 patient. Of note, in the only lead incompletely removed, we observed retention of < 1-cm remnant of lead material consisting of the screw of 3830 LBBP lead into the interventricular septum. No failure of lead extraction was reported and no major complications occurred.

CONCLUSIONS

Our findings demonstrated that at an experienced center the success of TLE of chronically implanted CSP leads is high in the absence of major complications also when mechanical extraction tools are needed.

摘要

背景

美敦力 SelectSecure Model 3830 无管腔导联(美敦力公司,明尼苏达州明尼阿波利斯)常用于心脏传导系统起搏(CSP)。然而,随着这种应用的增加,经静脉导联拔除(TLE)的需求也会增加。虽然心内膜 3830 导联的拔除已有相当详细的描述,特别是在儿科和成人先天性心脏病患者中,但关于 CSP 导联拔除的资料非常有限。在本研究中,我们报告了我们在 CSP 导联 TLE 方面的初步经验,并提供了技术考虑因素。

方法

研究人群包括 6 例连续患者(67%为男性;平均年龄 70 ± 22 岁),植入 CSP 导联(3830 导联),包括左束支起搏(LBBP)导联(n=3)和希氏束起搏导联(n=3),行 TLE。总的目标导联为 17 个。CSP 导联的平均植入时间为 97 ± 90 个月[范围 8-193 个月]。

结果

手动牵引在 2 例中成功,其余病例需要使用机械拔除工具。16 个导联(94%)完全拔除,而 1 例患者中有 1 个导联(6%)不完全拔除。值得注意的是,在唯一不完全拔除的导联中,我们观察到 3830 LBBP 导联的螺丝残留在间隔内,长度<1 厘米。无导联拔除失败,无重大并发症发生。

结论

我们的研究结果表明,在有经验的中心,即使需要使用机械拔除工具,慢性植入的 CSP 导联 TLE 的成功率也很高,且无重大并发症发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e5/10769925/4e42769b925a/10840_2023_1590_Fig1_HTML.jpg

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