Valve-in-Valve Transcatheter Aortic Valve Replacement Versus Redo-Surgical Aortic Valve Replacement in Patients With Aortic Stenosis: A Systematic Review and Meta-analysis

被引:0
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作者
Nasir, Muhammad Moiz [1 ]
Ikram, Armeen [1 ]
Usman, Muhammad [1 ]
Sarwar, Jawad [1 ]
Ahmed, Jawad [1 ]
Hamza, Mohammad [2 ]
Farhan, Syed Ali [3 ]
Siddiqi, Rabbia [4 ]
Qadar, Laila Tul [5 ]
Shah, Syed Raza [6 ]
Khalid, Muhammad Rizwan [7 ]
Memon, Roha Saeed [8 ]
Hameed, Irbaz [9 ]
机构
[1] Dow Univ Hlth Sci, Dept Internal Med, Karachi, Pakistan
[2] Guthrie Med Grp, Dept Internal Med, Cortland, NY USA
[3] Ohio State Univ, Dept Surg, Columbus, OH USA
[4] Univ Toledo, Dept Internal Med, Toledo, OH USA
[5] St Vincents Med Ctr, Dept Internal Med, Bridgeport, CT USA
[6] Univ Louisville, Div Cardiovasc Med, Louisville, KY USA
[7] Texas Hlth Presbyterian Hosp, Dept Internal Med, Dallas, TX USA
[8] New York City Hlth Hosp Corp, Albert Einstein Coll Med, Jacobi Med Ctr, Dept Internal Med, Bronx, NY USA
[9] Yale Univ, Sch Med, Div Cardiac Surg, New Haven, CT USA
来源
关键词
aortic stenosis; redo-SAVR; redo-surgical aortic valve replacement; valve-in-valve transcatheter aortic valve replacement; ViV-TAVR; CLINICAL-OUTCOMES; IMPLANTATION; MISMATCH; SURGERY; IMPACT; DURABILITY; GUIDELINES; MANAGEMENT;
D O I
10.1016/j.amjcard.2024.04.057
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aortic stenosis is a common and significant valve condition requiring bioprosthetic heart valves with transcatheter aortic valve replacement (TAVR) being strongly recommended for high-risk patients or patients over 75 years. This meta-analysis aimed to pool existing data on postprocedural clinical as well as echocardiographic outcomes comparing valvein-valve (ViV)-TAVR to redo-surgical aortic valve replacement to assess the short-term and medium-term outcomes for both treatment methods. A systematic literature search on Cochrane Central, Scopus, and Medline (PubMed interface) electronic databases from inception to August 2023. We used odds ratios (OR) for dichotomous outcomes and mean differences (MD) for continuous outcomes. Twenty-four studies (25,216 patients) were pooled with a mean follow-up of 16.4 months. The analysis revealed that ViV-TAVR group showed a significant reduction in 30-day mortality (OR 0.50, 95% confidence interval [CI] 0.43 to 0.58, p < 0.00001), new-onset atrial fibrillation (OR 0.34, 95% CI 0.17 to 0.67, p = 0.002), major bleeding event (OR 0.28, 95% CI 0.17 to 0.45, p < 0.00001) and lower rate of device success (OR 0.25, 95% CI 0.12 to 0.53, p = 0.0003). There were no significant differences between either group when assessing 1-year mortality, stroke, myocardial infarction, postoperative left ventricular ejection fraction, and effective orifice area. ViV-TAVR cohort showed a significantly increased incidence of paravalvular leaks, aortic regurgitation, and increased mean aortic valve gradient. ViV-TAVR is a viable short-term option for older patients with high co-morbidities and operative risks, reducing perioperative complications and improving 30-day mortality with no significant cardiovascular adverse events. However, both treatment methods present similar results on short-term to medium-term complications assessment. (c) 2024 Elsevier Inc. All rights reserved.
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页码:151 / 159
页数:9
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