首页> 外文期刊>The Journal of heart valve disease >Artificial Valve Endocarditis Reduction Trial (AVERT): protocol of a multicenter randomized trial.
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Artificial Valve Endocarditis Reduction Trial (AVERT): protocol of a multicenter randomized trial.

机译:人工瓣膜减少心内膜炎试验(AVERT):一项多中心随机试验的协议。

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BACKGROUND AND AIM OF THE STUDY: This article presents the protocol of the Artificial Valve Endocarditis Reduction Trial (AVERT), a multicenter, international randomized trial to assess the efficacy of the SilzoneTM coating of St. Jude Medical Masters Series mechanical heart valves in the prevention of prosthetic heart valve endocarditis (PVE). A total of 4,400 eligible patients will be randomized within three years of study commencement at 17 participating clinical centers in North America and Europe, with study completion within four years. ELIGIBILITY CRITERIA: Eligible patients are candidates for St. Jude mechanical valves with either the Silzone or conventional cuff, in the mitral and/or aortic position, who give informed written consent to participate. Major exclusion criteria are the presence of prosthetic valves that do not require replacement, and the need for tricuspid valve replacement. Bypass surgery and valve repair are allowed during the implant operation. Patients will be randomized using an envelope-based intraoperative randomization scheme, stratified by clinical center and by the presence of endocarditis at the time of surgery. FOLLOW UP: Patients will be contacted at discharge, three months, and each anniversary of the implant procedure. A brief follow up survey, administered via clinic interview, telephone or mail, will elicit events associated with possible endocarditis (unexplained fever, worsening angina, hospitalization) that will initiate contact with the patient's following physician. OUTCOME ANALYSIS: The primary PVE endpoint will be based upon a published algorithm, with two infectious disease specialists making the final determination of cases classified as possible endocarditis. Study data will be periodically reviewed by a Data Safety Monitoring Board. The primary analysis will be an intention-to-treat comparison of freedom from PVE curves between the Silzone and conventional cuff treatment groups. CONCLUSIONS: AVERT will provide much-needed information on the effectiveness of Silzone in preventing PVE, as well as practice patterns and outcomes of valve replacement.
机译:研究背景和目的:本文介绍了一项减少人工瓣膜性心内膜炎试验(AVERT)的方案,这项多中心国际随机试验旨在评估St. Jude Medical Masters系列机械心脏瓣膜SilzoneTM涂层在预防中的功效。人工心脏瓣膜心内膜炎(PVE)。在研究开始的三年内,将在北美和欧洲的17个参与临床中心将4400名合格患者随机分组,并在四年内完成研究。合格标准:符合条件的患者是二尖瓣和/或主动脉位置带有Silzone或常规袖带的St. Jude机械瓣膜的候选人,并应征得他们的书面同意。主要的排除标准是不需要更换人工瓣膜,以及需要更换三尖瓣。植入手术期间允许进行旁路手术和瓣膜修复。将使用基于包膜的术中随机方案对患者进行随机化,并按临床中心和手术时是否存在心内膜炎进行分层。随访:出院时,三个月以及植入手术的每个周年日都将与患者联系。通过临床访谈,电话或邮件进行的简短随访调查将引发与可能的心内膜炎相关的事件(不明原因的发热,心绞痛加重,住院),这些事件将开始与患者的后续医师接触。结果分析:主要的PVE终点将基于已发布的算法,由两名传染病专家对被归类为可能的心内膜炎的病例进行最终确定。研究数据将由数据安全监控委员会定期审查。主要分析将是对Silzone和常规袖带治疗组之间从PVE曲线获得的自由度进行意向性治疗比较。结论:AVERT将提供有关Silzone预防PVE的有效性以及实践模式和瓣膜置换结果的急需信息。

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