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终末期肾病需血液透析患者肌肉内植入皮下心脏复律除颤器:5年随访

Subcutaneous cardioverter defibrillator implanted intermuscularly in patients with end-stage renal disease requiring hemodialysis: 5-year follow-up.

作者信息

Kloppe Axel, Winter Joachim, Prull Magnus, Aweimer Assem, El-Battrawy Ibrahim, Hanefeld Christoph, O'Connor Stephen, Mügge Andreas, Schiedat Fabian

机构信息

Department of Cardiology, Intensive Medicine and Angiology, Marienhospital Gelsenkirchen, Academic Hospital of the Ruhr University Bochum, Virchowstraße 122, 45886, Gelsenkirchen, Germany.

Department of Cardiology and Angiology, University Hospital Bergmannsheil Bochum, Ruhr University Bochum, Bochum, Germany.

出版信息

J Interv Card Electrophysiol. 2024 Feb 22. doi: 10.1007/s10840-024-01767-1.

Abstract

BACKGROUND

The aim of the present study was to evaluate the long-term safety and effectiveness of the subcutaneous implantable cardioverter defibrillator (S-ICD) when implanted intermuscularly in patients with end-stage renal disease and hemodialysis.

METHODS

This study is a retrospective analysis of 21 consecutive patients implanted with S-ICDs at three experienced centers in Germany with comorbid renal insufficiency requiring hemodialysis, as well as being at risk of sudden cardiac death. The S-ICD was placed intermuscularly in all patients. Follow-ups (FUs) were performed every 6 months.

RESULTS

The mean ± standard deviation FU duration was 60.0 ± 11.4 months, with a range of 39 to 78 months. There were no deaths due to arrhythmia, or device-associated infections and complications. Four patients (19.1%) died during FU due to respiratory insufficiency during dialysis, systolic heart failure, septic infection of the urogenital tract, and colorectal cancer, respectively. There were six non-device-related hospitalizations with a duration of 12.7 ± 5.1 days and a hospitalization rate of 4.1 per 100 patient years.

CONCLUSIONS

In the long-term FU of this small population of seriously compromised hemodialysis patients at risk of sudden cardiac death, the intermuscularly implanted S-ICD system was safe and effective. No arrhythmic complications, device-associated infections, or complications compromised survival. These data are encouraging and support testing in a larger group of similarly compromised patients.

摘要

背景

本研究的目的是评估皮下植入式心律转复除颤器(S-ICD)在终末期肾病和血液透析患者肌肉内植入时的长期安全性和有效性。

方法

本研究是一项回顾性分析,对德国三个经验丰富的中心连续21例植入S-ICD的患者进行研究,这些患者合并肾功能不全需要血液透析,且有心脏性猝死风险。所有患者的S-ICD均植入肌肉内。每6个月进行一次随访(FU)。

结果

随访时间的均值±标准差为60.0±11.4个月,范围为39至78个月。没有因心律失常、与设备相关的感染及并发症导致的死亡。4例患者(19.1%)在随访期间分别因透析期间呼吸功能不全、收缩性心力衰竭、泌尿生殖道败血症感染和结直肠癌死亡。有6次与设备无关的住院,住院时间为12.7±5.1天,住院率为每100患者年4.1次。

结论

在这一小部分有心脏性猝死风险的严重血液透析患者的长期随访中,肌肉内植入的S-ICD系统是安全有效的。没有心律失常并发症、与设备相关的感染或并发症影响生存。这些数据令人鼓舞,并支持在更多类似的患者群体中进行测试。

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