Technical aspects and outcomes of using homografts in atrioventricular valve surgery: a systematic review

M. Nuzhdin, R. Komarov, D. A. Matsuganov, I. Melnikov, A.V. Tsaregorodtsev
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Abstract

Objective: To summarize and critically appraise the world experience with homografts in mitral and tricuspid valve surgery.Methods: We conducted a systematic review according to the PRISMA criteria. We searched the following terms in available databases, such as PubMed (National Center for Biotechnology Information), Cochrane Library, Web of Science (Clarivate), and Google Scholar: ((mitral homograft) OR (tricuspid homograft) OR (homograft) AND (valve replacement) OR (valve repair)).Results: We recruited 3 specialists to search the information matching our inclusion and exclusion criteria and selected 23 publications covering the period 1988-2021 for analysis. The mean follow-up period was 15 [6-60] months. Survival at the end of the follow-up period was 100% [90.7%-100.0%]; freedom from graft dysfunction was 100%, and freedom from reoperation was 100% [79%-100%].Conclusion: The world experience with homografts in atrioventricular valve surgery is limited to small case series with inconclusive surgical aspects and a heterogeneous follow-up period. The immediate results suggest that homografts could be used as an alternative valve substitute for a wide spectrum of diseases both in primary and revision surgery. Received 19 April 2023. Revised 14 May 2023. Accepted 15 May 2023. Funding: The study did not have sponsorship. Conflict of interest: The authors declare no conflict of interest. Contribution of the authorsConception and study design: M.D. Nuzhdin, R.N. KomarovData collection and analysis: M.D. Nuzhdin, D.A. Matsuganov, I.Yu. Melnikov, A.V. TsaregorodtsevStatistical analysis: D.A. MatsuganovDrafting the article: M.D. NuzhdinCritical revision of the article: R.N. Komarov, M.D. NuzhdinFinal approval of the version to be published: M.D. Nuzhdin, R.N. Komarov, D.A. Matsuganov, I.Yu. Melnikov, A.V. Tsaregorodtsev
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在房室瓣膜手术中使用同种移植物的技术方面和结果:系统回顾
目的:总结并批判评价国内外同种异体二尖瓣、三尖瓣移植手术的经验。方法:我们按照PRISMA标准进行系统评价。我们在PubMed(国家生物技术信息中心)、Cochrane图书馆、Web of Science (Clarivate)和Google Scholar等数据库中检索了以下术语:(二尖瓣同种移植物)或(三尖瓣同种移植物)或(同种移植物)和(瓣膜置换术)或(瓣膜修复))。结果:我们招募了3位专家来搜索符合我们的纳入和排除标准的信息,并选择了涵盖1988-2021年期间的23篇 出版物进行分析。平均随访15[6-60]个月。随访结束时生存率为100% [90.7% ~ 100.0%];移植物功能不全率为100%,再手术率为100%[79% ~ 100%]。结论:同种异体移植在房室瓣膜手术中的世界经验仅限于小病例系列,手术方面不确定,随访期不均匀。直接结果表明,同种异体移植物可以作为一种替代瓣膜替代物用于广泛的疾病,无论是在原发性手术还是翻修手术中。2023年4月19日收。2023年5月14日修订。2023年5月15日接受。经费来源:本研究未获得赞助。利益冲突:作者声明无利益冲突。作者贡献。研究构思与设计:M.D. Nuzhdin, R.N. komarov。资料收集与分析:M.D. Nuzhdin, D.A. Matsuganov, I.Yu。统计分析:d.a taregorodtsev论文起稿:M.D. nuzhdin文章批改:R.N. Komarov, M.D. nuzhdin终稿审定:M.D. Nuzhdin, R.N. Komarov, d.a tsuganov, i.u u。梅尼可夫,A.V.察列哥罗采夫
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来源期刊
Patologiya krovoobrashcheniya i kardiokhirurgiya
Patologiya krovoobrashcheniya i kardiokhirurgiya Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.00
自引率
0.00%
发文量
42
审稿时长
12 weeks
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