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经导管二尖瓣修复术的监管批准审查-美国和日本之间的适应证差异。

Regulatory approval review of transcatheter mitral valve repair - Difference in the indication between the USA and Japan.

机构信息

Pharmaceuticals and Medical Devices Agency, Tokyo, Japan.

Pharmaceuticals and Medical Devices Agency, Tokyo, Japan.

出版信息

J Cardiol. 2019 Jul;74(1):13-18. doi: 10.1016/j.jjcc.2019.03.013. Epub 2019 Apr 17.

DOI:10.1016/j.jjcc.2019.03.013
PMID:31005388
Abstract

The indication for MitraClip (Abbott Vascular, Santa Clara, CA, USA) in the USA is degenerative mitral regurgitation (DMR), but the Japanese indication includes both DMR and functional mitral regurgitation (FMR), in patients without severe left ventricular dysfunction. One of the reasons for this difference is that the Japanese Circulation Society submitted a formal request to the Japanese government for early approval of MitraClip for both DMR and FMR on the basis of unmet medical need for MR patients resistant to medical therapy, but at prohibitive risk for mitral valve surgery. Here, we describe the regulatory approval review process of MitraClip in Japan. Clinical data from outside Japan indicated that MitraClip provides significant improvements from baseline in New York Heart Association Class and hospitalizations for heart failure due to the reduction of MR grade without adversely affecting long-term prognosis in FMR patients as well as DMR patients. Also, a Japanese domestic trial showed a favorable acute procedural success rate without serious adverse events with MitraClip in both DMR and FMR patients. Further, it is considered in Japan that improvement of MR mechanically is clinically important in both DMR and FMR, in patients without severe left ventricular dysfunction. On the basis of these considerations, the MitraClip was approved in Japan for indications of both DMR and FMR with preserved cardiac function in patients at prohibitive risk for mitral valve surgery.

摘要

MitraClip(美国雅培血管公司,加利福尼亚州圣克拉拉)在美国的适应证为退行性二尖瓣反流(DMR),但日本的适应证包括 DMR 和射血分数保留的心力衰竭(HFpEF)伴功能性二尖瓣反流(FMR),且适用于无严重左心室功能障碍的患者。造成这一差异的原因之一是,日本循环学会基于对不耐受药物治疗的 MR 患者的未满足的医疗需求,向日本政府提出了正式请求,要求早期批准 MitraClip 用于 DMR 和 FMR,尽管二尖瓣手术的风险很高。在此,我们描述了 MitraClip 在日本的监管审批审查过程。来自日本以外的临床数据表明,MitraClip 可显著改善纽约心脏协会(NYHA)心功能分级和因 MR 分级降低导致的心力衰竭住院率,而不会对 FMR 患者和 DMR 患者的长期预后产生不利影响。此外,一项日本国内试验表明,在 DMR 和 FMR 患者中,MitraClip 的急性程序成功率高,且无严重不良事件。此外,在日本,考虑到在无严重左心室功能障碍的情况下,DMR 和 FMR 患者机械性改善 MR 被认为具有重要的临床意义。基于这些考虑,MitraClip 在日本被批准用于二尖瓣手术风险高的 DMR 和 FMR 患者,且这些患者的心功能保存。

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