Reduction of inappropriate shock rate through signal filtering (smart-pass) in patients with implantable subcutaneous cardioverter-defibrillator: a systematic review and meta-analysis.

IF 0.8 Q4 RESPIRATORY SYSTEM Monaldi Archives for Chest Disease Pub Date : 2025-10-14 Epub Date: 2024-08-29 DOI:10.4081/monaldi.2024.3013
Maurizio Santomauro, Mario Petretta, Carla Riganti, Mario Alberto Santomauro, Mariarosaria De Luca, Andrea Santomauro, Antonio Cittadini
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Abstract

Subcutaneous implantable cardioverter-defibrillators (S-ICD) are effective in protecting patients against sudden death but expose them to a higher risk of inappropriate shock (IAS). We performed a systematic search of studies published between January 2010 and December 2019 assessing IAS due to cardiac oversensing by the selection process (PRISMA) and identified 17 eligible articles. A total of 15 studies were observational, and 2 were retrospective. For the meta-analysis, the final population included 6111 patients: 3356 without the SMART-pass (SP) filter (group 1) and 2755 with the SP filter (group 2). A total of 1614 shocks (appropriate shocks plus IAS) were registered (1245 in group 1 and 369 in group 2). The random effects meta-analysis estimated an overall IAS rate of 7.78% (95% confidence interval: 4.93-10.64) with substantial variability between studies (I2=96.05%, p<0.001). The IAS rate was 10.75% (95% confidence interval: 8.49-13.02) for group 1 and 3.61% (95% confidence interval: 1.36-5.86) for group 2 (p<0.001). Third-generation S-ICD technology with SP filters reduced the risk of cardiac signal-related IAS.

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通过信号滤波(智能滤波)降低植入式皮下心律转复除颤器患者的不当电击率:系统综述和荟萃分析。
皮下植入式心律转复除颤器(S-ICD)可有效保护患者免于猝死,但却使患者面临更高的不适当休克(IAS)风险。我们对 2010 年 1 月至 2019 年 12 月间发表的研究进行了系统性检索,通过筛选过程(PRISMA)评估了心脏超感引起的 IAS,并确定了 17 篇符合条件的文章。其中 15 篇为观察性研究,2 篇为回顾性研究。荟萃分析的最终研究对象包括 6111 名患者:3356名患者未使用SMART通过(SP)过滤器(第1组),2755名患者使用SP过滤器(第2组)。共登记了 1614 次冲击(适当冲击加 IAS)(第一组 1245 次,第二组 369 次)。随机效应荟萃分析估计总体 IAS 率为 7.78%(95% 置信区间:4.93-10.64),不同研究之间存在很大差异(I 平方=96.05%,p
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
1
审稿时长
12 weeks
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