Department of Cardiothoracic Surgery, Erasmus University Medical Center, Rotterdam, Netherlands.
Department of Cardiac Surgery, Medical and Health Science Centre, University of Debrecen, Debrecen, Hungary.
Eur J Cardiothorac Surg. 2019 Jun 1;55(6):1025-1036. doi: 10.1093/ejcts/ezz034.
Intraoperative surgical prosthetic heart valve (SHV) choice is a key determinant of successful surgery and positive postoperative outcomes. Currently, many controversies exist around the sizing and labelling of SHVs rendering the comparison of different valves difficult. To explore solutions, an expert Valve Labelling Task Force was jointly initiated by the European Association for Cardio-Thoracic Surgery (EACTS), The Society of Thoracic Surgeons (STS) and the American Association for Thoracic Surgery (AATS). The EACTS-STS-AATS Valve Labelling Task Force, comprising cardiac surgeons, cardiologists, engineers, regulators and representatives from the International Organization for Standardization (ISO) and major valve manufacturers, held its first in-person meeting in February 2018 in Paris, France. This article was derived from the meeting's discussions. The Task Force identified the following areas for improvement and clarification: reporting of physical dimensions and characteristics of SHVs determining and labelling of SHV size, in vivo and in vitro testing and reporting of SHV haemodynamic performance and thrombogenicity. Furthermore, a thorough understanding of the regulatory background and the role of the applicable ISO standards, together with close cooperation between all stakeholders (including regulatory and standard-setting bodies), is necessary to improve the current situation. Cardiac surgeons should be provided with appropriate information to allow for optimal SHV choice. This first article from the EACTS-STS-AATS Valve Labelling Task Force summarizes the background of SHV sizing and labelling and identifies the most important elements where further standardization is necessary.
术中外科人工心脏瓣膜 (SHV) 的选择是手术成功和术后结果良好的关键决定因素。目前,SHV 的尺寸和标签存在许多争议,使得不同瓣膜的比较变得困难。为了解决这些问题,欧洲心胸外科学会 (EACTS)、胸外科医师学会 (STS) 和美国胸外科学会 (AATS) 共同发起了一个专家瓣膜标签工作组。EACTS-STS-AATS 瓣膜标签工作组由心脏外科医生、心脏病学家、工程师、监管机构以及国际标准化组织 (ISO) 和主要瓣膜制造商的代表组成,于 2018 年 2 月在法国巴黎举行了第一次面对面会议。本文源自会议讨论内容。工作组确定了以下需要改进和澄清的领域:报告 SHV 的物理尺寸和特性、确定和标记 SHV 尺寸、体内和体外测试以及报告 SHV 血液动力学性能和血栓形成。此外,深入了解监管背景和适用 ISO 标准的作用,以及所有利益相关者(包括监管和标准制定机构)之间的密切合作,对于改善现状至关重要。应该向心脏外科医生提供适当的信息,以便能够做出最佳的 SHV 选择。这是 EACTS-STS-AATS 瓣膜标签工作组的第一篇文章,总结了 SHV 尺寸和标签的背景,并确定了需要进一步标准化的最重要因素。