Temporary Right Ventricular Mechanical Circulatory Support Devices in Acute Right Ventricular Failure and Cardiogenic Shock: A Cross-Device Systematic Review and Single-Arm Meta-Analysis.

IF 2.2 3区 医学 Q3 ENGINEERING, BIOMEDICAL
Hussein Elghazaly, Omar Naeim, Anna Collins, Mohamed Abouegla, Omar Elsiraffy, Syed Yusuf Maududi
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引用次数: 0

Abstract

Background: Evidence for temporary right ventricular assist devices (tRVADs) is fragmented. We characterized outcomes among adults receiving temporary support for acute right ventricular (RV) failure or RV-predominant cardiogenic shock.

Methods: MEDLINE, Embase, CENTRAL, and ClinicalTrials.gov were searched from inception to June 2026. Arm-level outcome proportions were pooled on the logit scale using three-level random-effects models, with arms nested within studies. Device-stratified estimates, meta-regression, and sensitivity analyses were examined.

Results: We included 106 studies (119 device arms; 4653 patients), including 57 conference-abstract studies (53.8%). Concurrent left-sided support was reported in 85.8% of patients with available data; post-LVAD RV failure predominated in 47.5% of arms. Separately pooled survival to discharge was 60.4% (95% CI 56.0-64.7; 63 arms), successful weaning 60.6% (54.8-66.2; 68 arms), and 30-day mortality 30.1% (24.1-36.9; 31 arms). The survival prediction interval was wide (34.4%-81.6%). Pooled bleeding, renal complications (acute kidney injury and/or renal replacement therapy, as reported), and stroke were 36.5%, 46.6%, and 14.5%, respectively. Device-stratified estimates were vulnerable to confounding. No meta-regression association remained significant after multiplicity correction.

Conclusions: These descriptive estimates characterize selected, heterogeneous treated cohorts, predominantly receiving left-sided or biventricular support; they do not establish treatment benefit or comparative device effectiveness. Complication rates were high. Applicability to isolated primary RV shock is limited. Standardized prospective data are needed to inform patient selection, timing, and device strategy.

Trial registration: PROSPERO registration number: CRD420261406088.

临时右心室机械循环支持装置在急性右心室衰竭和心源性休克中的应用:一项跨装置系统评价和单组meta分析。
背景:临时右心室辅助装置(tRVADs)的证据是碎片化的。我们对急性右心室(RV)衰竭或RV为主的心源性休克接受临时支持的成年人的结局进行了分析。方法:检索MEDLINE、Embase、CENTRAL和ClinicalTrials.gov网站从创建到2026年6月。采用三水平随机效应模型在logit量表上汇总臂水平结果比例,在研究中嵌套臂。检查了器械分层估计、元回归和敏感性分析。结果:我们纳入106项研究(119个器械臂;4653名患者),包括57项会议摘要研究(53.8%)。在现有数据中,85.8%的患者报告了并发左侧支持;在47.5%的组中,lvad后RV衰竭占主导地位。单独的总生存率为60.4% (95% CI 56.0-64.7; 63组),成功断奶60.6%(54.8-66.2;68组),30天死亡率30.1%(24.1-36.9;31组)。生存预测区间较宽(34.4% ~ 81.6%)。合并出血、肾脏并发症(据报道急性肾损伤和/或肾替代治疗)和中风分别为36.5%、46.6%和14.5%。器械分层估计容易出现混淆。多重性校正后,meta回归相关性不显著。结论:这些描述性估计描述了选择的异质治疗队列,主要接受左侧或双心室支持;他们没有建立治疗效益或比较器械的有效性。并发症发生率高。适用于孤立的初级RV冲击是有限的。需要标准化的前瞻性数据来为患者选择、时机和设备策略提供信息。试验注册:普洛斯彼罗注册号:CRD420261406088。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Artificial organs
Artificial organs 工程技术-工程:生物医学
CiteScore
4.30
自引率
12.50%
发文量
303
审稿时长
4-8 weeks
期刊介绍: Artificial Organs is the official peer reviewed journal of The International Federation for Artificial Organs (Members of the Federation are: The American Society for Artificial Internal Organs, The European Society for Artificial Organs, and The Japanese Society for Artificial Organs), The International Faculty for Artificial Organs, the International Society for Rotary Blood Pumps, The International Society for Pediatric Mechanical Cardiopulmonary Support, and the Vienna International Workshop on Functional Electrical Stimulation. Artificial Organs publishes original research articles dealing with developments in artificial organs applications and treatment modalities and their clinical applications worldwide. Membership in the Societies listed above is not a prerequisite for publication. Articles are published without charge to the author except for color figures and excess page charges as noted.
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