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Development of a standardized definition for clinically significant bleeding in the ASPirin in Reducing Events in the Elderly (ASPREE) trial

机译:制定关于减少老年人中阿斯匹林中临床上重大出血的标准化定义(ASPREE)试验

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Background Bleeding is the major risk of aspirin treatment, especially in the elderly. A consensus definition for clinically significant bleeding (CSB) in aspirin primary prevention trials is lacking in the literature. Methods This paper details the development, modification, application, and quality control of a definition for clinically significant bleeding in the ASPirin in Reducing Events in the Elderly (ASPREE) trial, a primary prevention trial of aspirin in 19,114 community-dwelling elderly men and women. In ASPREE a confirmed bleeding event needed to meet criteria both for substantiated bleeding and clinical significance. Substantiated bleeding was defined as: 1) observed bleeding, 2) a reasonable report of symptoms of bleeding, 3) medical, nursing or paramedical report, or 4) imaging evidence. Bleeding was defined as clinically significant if it: 1) required transfusion of red blood cells, 2) required admission to the hospital for >24?h, or prolonged a hospitalization, with bleeding as the principal reason, 3) required surgery to stop the bleeding, or 4) resulted in death. Bleeding sites were subclassified as upper gastrointestinal, lower gastrointestinal, intracranial (hemorrhagic stroke, subarachnoid hemorrhage, subdural hematoma, extradural hematoma, or other), or other sites. Potential events were retrieved from medical records, self-report or notification from treating doctors. Two reviewers adjudicated each event using electronic adjudication software, and discordant cases were reviewed by a third reviewer. Adjudication rules evolved to become more strictly defined as the trial progressed and decision rules were added to assist with frequent scenarios such as post-operative bleeding. Conclusions This paper provides a detailed methodologic description of the development of a standardized definition for clinically significant bleeding and provides a benchmark for development of a consensus definition for future aspirin primary prevention trials. Trial registration ASPREE is registered on the International Standard Randomized Controlled Trial Number Register (ISRCTN83772183) and on clinicaltrials.gov ( NCT01038583 ).
机译:背景出血是阿司匹林治疗的主要风险,尤其是在老年人中。文献中缺乏对阿司匹林一级预防性临床上重大出血(CSB)的共识定义。方法本文详细介绍了阿司匹林在19,114例居住在社区的老年男性和女性的阿司匹林的初步预防性试验中阿司匹林的主要预防性临床试验中阿司匹林的临床上重大出血的定义的开发,修饰,应用和质量控制。 。在ASPREE中,确诊的出血事件需要符合证实的出血和临床意义的标准。实质性出血的定义为:1)观察到的出血; 2)出血症状的合理报告; 3)医疗,护理或辅助医疗报告;或4)影像学证据。如果出现以下情况,则出血被定义为具有临床意义:1)需要输注红细胞,2)需要入院> 24?h,或住院时间延长,出血是主要原因,3)需要手术以停止出血。出血,或4)导致死亡。出血部位分为上消化道,下消化道,颅内(出血性中风,蛛网膜下腔出血,硬膜下血肿,硬膜外血肿或其他部位)或其他部位。从医疗记录,自我报告或主治医生的通知中检索出潜在事件。两名审稿人使用电子裁判软件对每个事件进行裁决,第三名审稿人对不一致的案件进行了审理。随着试验的进行,裁决规则逐渐变得更加严格,并增加了决策规则以辅助诸如手术后出血等常见情况。结论本文为临床上重大出血的标准化定义的制定提供了详细的方法学描述,并为未来阿司匹林一级预防试验的共识定义的制定提供了基准。试验注册ASPREE在国际标准随机对照试验编号寄存器(ISRCTN83772183)和Clinicaltrials.gov(NCT01038583)上注册。

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