Al-Abcha Abdullah, Saleh Yehia, Khan Safi U, Salazar Adolfo Martinez, Zaid Syed, Abdelkarim Ola, Halboni Adnan, Abdelfattah Omar M, Goel Sachin S, Kleiman Neal S, Guerrero Mayra
Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota.
Department of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston, Texas.
J Soc Cardiovasc Angiogr Interv. 2022 Nov 25;2(1):100516. doi: 10.1016/j.jscai.2022.100516. eCollection 2023 Jan-Feb.
Transcatheter mitral valve-in-valve (MViV) replacement has emerged as an alternative to redo surgical mitral valve replacement (redo-SMVR) in patients with failed mitral bioprostheses deemed to be at a high surgical risk. The aim of this analysis was to compare the outcomes of MViV replacement with those of redo-SMVR in patients with a failed bioprosthetic mitral valve.
We performed a study-level meta-analysis that compared MViV replacement with redo-SMVR in patients with failed mitral bioprostheses. Seven observational studies, with a total of 5083 patients, were included (1138 patients [22.4%] in the MViV replacement arm). The primary focus was all-cause mortality. Additional outcomes included major bleeding, stroke, vascular complications, and mean mitral valve gradient at follow-up.
The in-hospital mortality was lower in patients who underwent MViV replacement than in those who underwent redo-SMVR (odds ratio [OR], 0.64; 95% CI, 0.53-0.78; = .0023). The short-term mortality (<1 year) was numerically lower in the MViV replacement group (OR, 0.45; 95% CI, 0.18-1.13; = .069). At 1 year, the risk of mortality was similar in the 2 groups (OR, 0.99; 95% CI, 0.69-1.40; = .906), and at midterm follow-up (≥1 year), there was a numerically higher risk of mortality in the MViV replacement group (OR, 1.51; 95% CI, 1.00-2.29; = .051). The risk of major bleeding was significantly lower in the MViV replacement group (OR, 0.23; 95% CI, 0.10-0.56; = .01). Additionally, stroke and vascular complications were similar between the 2 groups.
The in-hospital mortality was lower in the MViV replacement group than in the redo-SMVR group. There were no differences in mortality at short-term (<1 year), 1-year, or midterm (≥1 year) follow-ups.
经导管二尖瓣瓣中瓣置换术(MViV)已成为二尖瓣生物瓣功能衰竭且手术风险高的患者再次行二尖瓣置换术(redo-SMVR)的替代方案。本分析的目的是比较二尖瓣生物瓣功能衰竭患者行MViV置换术与redo-SMVR的疗效。
我们进行了一项研究水平的荟萃分析,比较二尖瓣生物瓣功能衰竭患者行MViV置换术与redo-SMVR的情况。纳入了7项观察性研究,共5083例患者(MViV置换术组1138例患者[22.4%])。主要关注全因死亡率。其他结局包括大出血、中风、血管并发症以及随访时的平均二尖瓣跨瓣压差。
行MViV置换术患者的住院死亡率低于行redo-SMVR的患者(优势比[OR],0.64;95%置信区间[CI],0.53-0.78;P = 0.0023)。MViV置换术组的短期死亡率(<1年)在数值上较低(OR,0.45;95%CI,0.18-1.13;P = 0.069)。1年时,两组的死亡风险相似(OR,0.99;95%CI,0.69-1.40;P = 0.906),在中期随访(≥1年)时,MViV置换术组的死亡风险在数值上更高(OR,1.51;95%CI,1.00-2.29;P = 0.051)。MViV置换术组的大出血风险显著较低(OR,0.23;95%CI,0.10-0.56;P = 0.01)。此外,两组之间的中风和血管并发症相似。
MViV置换术组的住院死亡率低于redo-SMVR组。在短期(<1年)、1年或中期(≥1年)随访时,死亡率无差异。