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手术风险评分较低患者的经导管主动脉瓣置换术与外科主动脉瓣置换术:早期结局的系统评价和荟萃分析

Transcatheter Versus Surgical Aortic Valve Replacement in Patients With Lower Surgical Risk Scores: A Systematic Review and Meta-Analysis of Early Outcomes.

作者信息

Arora Sameer, Strassle Paula D, Ramm Cassandra J, Rhodes Jeremy A, Vaidya Satyanarayana R, Caranasos Thomas G, Vavalle John P

机构信息

Division of Cardiology, University of North Carolina, Chapel Hill, NC, USA.

Division of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.

出版信息

Heart Lung Circ. 2017 Aug;26(8):840-845. doi: 10.1016/j.hlc.2016.12.003. Epub 2017 Jan 24.

DOI:10.1016/j.hlc.2016.12.003
PMID:28169084
Abstract

BACKGROUND

The results from the PARTNER 2 trial showed the feasibility of transcatheter aortic valve replacement (TAVR) in intermediate surgical risk patients. Although low risk clinical trials will take time to conclude, some data has emerged comparing TAVR with surgical aortic valve replacement (SAVR) in lower risk patients.

METHODS

A Medline search was conducted using standard methodology to search for studies reporting results comparing TAVR and SAVR. Studies were included if the overall mean Society of Thoracic Surgeons Score was less than 4% (or equivalent Euroscore). A meta-analysis comparing the 30-day risk of clinical outcomes between TAVR and SAVR in the lower surgical risk population was conducted.

RESULTS

A total of four studies, including one clinical trial and three propensity-matched cohort studies met the inclusion criteria. Compared to SAVR, TAVR had a lower risk of 30-day mortality (RR 0.67, 95% CI 0.41, 1.10), stroke (RR 0.60, 95% CI 0.30, 1.22), bleeding complications (RR 0.51, 95% CI 0.40, 0.67) and acute kidney injury (RR 0.66, 95% CI 0.47, 0.94). However, a higher risk of vascular complications (RR 11.72, 95% CI 3.75, 36.64), moderate or severe paravalvular leak (RR 5.04, 95% CI 3.01, 8.43), and permanent pacemaker implantations (RR 4.62, 95% CI 2.63, 8.12) was noted for TAVR.

CONCLUSION

Among lower risk patients, TAVR and SAVR appear to be comparable in short term outcomes. Additional high quality studies among patients classified as low risk are needed to further explore the feasibility of TAVR in all surgical risk patients.

摘要

背景

PARTNER 2试验结果显示经导管主动脉瓣置换术(TAVR)在外科手术风险中等的患者中具有可行性。尽管低风险临床试验尚需时日才能得出结论,但已有一些数据比较了TAVR与外科主动脉瓣置换术(SAVR)在低风险患者中的情况。

方法

采用标准方法在Medline上进行检索,以查找报告TAVR与SAVR比较结果的研究。如果胸外科医师协会总体平均评分低于4%(或等效的欧洲评分),则纳入该研究。对低手术风险人群中TAVR与SAVR的30天临床结局风险进行荟萃分析。

结果

共有四项研究符合纳入标准,包括一项临床试验和三项倾向匹配队列研究。与SAVR相比,TAVR的30天死亡率(风险比[RR]0.67,95%置信区间[CI]0.41,1.10)、中风(RR 0.60,95% CI 0.30,1.22)、出血并发症(RR 0.51,95% CI 0.40,0.67)和急性肾损伤(RR 0.66,95% CI 0.47,0.94)风险较低。然而,TAVR的血管并发症(RR 11.72,95% CI 3.75,36.64)、中度或重度瓣周漏(RR 5.04,95% CI 3.01,8.43)以及永久起搏器植入(RR 4.62,95% CI 2.63,8.12)风险较高。

结论

在低风险患者中,TAVR和SAVR的短期结局似乎相当。需要在分类为低风险的患者中开展更多高质量研究,以进一步探索TAVR在所有手术风险患者中的可行性。

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