既往无心房颤动病史患者的设备检测到的心房高频率发作的结果:系统回顾与元分析》。

IF 2.6 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Arrhythmia & Electrophysiology Review Pub Date : 2024-06-18 eCollection Date: 2024-01-01 DOI:10.15420/aer.2024.11
Hasaan Ahmed, Mahmoud Ismayl, Anirudh Palicherla, Anthony Kashou, Jalal Dufani, Andrew Goldsweig, Nandan Anavekar, Ahmed Aboeata
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引用次数: 0

摘要

背景:对于既往无房颤病史的患者,设备检测出房颤的结果仍不明确:方法:我们进行了一项荟萃分析,以评估既往无房颤病史但经历过设备检测房颤的患者的治疗效果。评估的结果包括临床房颤、血栓栓塞和全因死亡率。采用固定效应模型计算RRs和95% CI:结果:与没有经历过设备检测到房颤的人相比,经历过设备检测到房颤的人发生临床房颤的风险更高(RR 3.33,95% CI [1.99.5.57];pCI):虽然装置检测到房颤的患者发生临床房颤和血栓栓塞的风险会增加,但死亡率并不显著。
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Outcomes of Device-detected Atrial High-rate Episodes in Patients with No Prior History of Atrial Fibrillation: A Systematic Review and Meta-analysis.

Background: Outcomes of device-detected AF remain unclear in individuals without a prior history of AF.

Methods: A meta-analysis was conducted to evaluate outcomes in individuals with no prior history of AF who experienced device-detected AF. Outcomes assessed were clinical AF, thromboembolism and all-cause mortality. A fixed-effects model was used to calculate RRs with 95% CI.

Results: Compared to individuals who did not experience device-detected AF, those who did had increased risks of clinical AF (RR 3.33, 95% CI [1.99.5.57]; p<0.0001) and thromboembolic events (RR 2.21; 95% CI [1.72.2.85]; p<0.0001). The risk of all-cause mortality was similar between both groups (RR 1.19; 95% CI [0.95.1.49]; p=0.13). Subgroup analysis revealed an increased risk of thromboembolic events among device-detected AF .24 hours (RR 12.34; 95% CI [2.70.56.36]).

Conclusion: While there is an increased risk of clinical AF and thromboembolism in individuals with device-detected AF, mortality was insignificant.

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来源期刊
Arrhythmia & Electrophysiology Review
Arrhythmia & Electrophysiology Review CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
5.10
自引率
6.70%
发文量
22
审稿时长
7 weeks
期刊最新文献
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