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经导管二尖瓣瓣中瓣置换术与再次二尖瓣置换术治疗退行性生物瓣二尖瓣置换术:系统评价和荟萃分析。

Valve-in-valve transcatheter mitral valve replacement versus redo-surgical mitral valve replacement for degenerated bioprosthetic mitral valves: A systematic review and meta-analysis.

机构信息

Department of Internal Medicine, Dow University of Health Sciences, Karachi, Pakistan.

Department of Internal Medicine, United Health Services Hospital, Johnson City, NY, USA.

出版信息

Int J Cardiol. 2024 Nov 15;415:132448. doi: 10.1016/j.ijcard.2024.132448. Epub 2024 Aug 15.

Abstract

Bioprosthetic mitral valve degeneration is traditionally treated with Redo-SMVR, but the latest ViV-TMVR procedure offers a less invasive and lower risk alternative. A systematic literature search was conducted on Cochrane Central, Scopus, and Medline (PubMed interface) electronic databases from inception till 15th April 2024. We used risk ratios (RR) for dichotomous outcomes and mean differences (MD) for continuous outcomes. We included a total of eleven studies with 11,931 patients in the final quantitative and qualitative analysis. When comparing ViV-TMVR with Redo-SMVR, no significant difference was found for 30-day mortality (P = 0.13) and 1-year mortality (P = 0.91), whereas patients in the ViV-TMVR showed significantly reduced incidence of stroke (P < 0.00001), In-hospital mortality (P), bleeding complications (P = 0.003), AKI (P = 0.0006), arrhythmias (P = 0.01), LVOT obstruction (P = 0.04), and PPI (P < 0.00001). Furthermore, no significant difference was observed between either group when comparing vascular complications (P = 0.97), 2-year mortality (P = 0.60) and 3-year mortality. ViV-TMVR was associated with a significant risk of paravalvular leakage (P = 0.008). Although, ViV-TMVR reduces the risk of complications associated with Redo-SMVR, larger studies are imperative to reach conclusive results.

摘要

生物瓣二尖瓣退行性变传统上采用 redo-SMVR 治疗,但最新的 ViV-TMVR 手术提供了一种侵袭性更小、风险更低的替代方法。我们对 Cochrane Central、Scopus 和 Medline(PubMed 界面)电子数据库进行了系统的文献检索,检索时间从建库至 2024 年 4 月 15 日。我们使用二分类结局的风险比(RR)和连续结局的均数差(MD)。我们共纳入了 11 项研究,共 11931 例患者进行了最终的定量和定性分析。与 redo-SMVR 相比,ViV-TMVR 组 30 天死亡率(P=0.13)和 1 年死亡率(P=0.91)无显著差异,而 ViV-TMVR 组患者的中风发生率显著降低(P<0.00001)、住院死亡率(P)、出血并发症(P=0.003)、急性肾损伤(AKI)(P=0.0006)、心律失常(P=0.01)、LVOT 梗阻(P=0.04)和 PPI(P<0.00001)。此外,两组间血管并发症(P=0.97)、2 年死亡率(P=0.60)和 3 年死亡率均无显著差异。ViV-TMVR 与瓣周漏的发生风险显著相关(P=0.008)。尽管 ViV-TMVR 降低了 redo-SMVR 相关并发症的风险,但仍需要更大规模的研究来得出明确的结论。

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