Development of a Uniform Apheresis Case Report Form for Standardized Collection of Apheresis Data

IF 1.4 4区 医学 Q4 HEMATOLOGY
Andrew D. Johnson, Zbigniew M. Szczepiorkowski, Rasheed A. Balogun, Oliver Karam, Marianne Nellis, Jennifer Schneiderman, Joseph Schwartz, Jeffrey L. Winters, Yanyun Wu, Tomas Armendariz, Edwin Burgstaler, Laura Collins, Kira Geile, Katerina Pavenski, Amber P. Sanchez, Volker Witt, Amutha Muthusamy, Thomas Pederson, Vidhyalakshmi Ramesh, Mai Thao, Therese Chlebeck, Nicole D. Zantek
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引用次数: 0

Abstract

Apheresis is performed worldwide for an increasing number of indications. The development of common data elements (CDE) for apheresis related areas may facilitate conduct of new research, enhance quality initiatives including benchmarking, and improve patient care. This report describes the systematic development of the Uniform Apheresis Case Report Form (UACRF) as part of the Apheresis in the United States (ApheresUS) program. A consensus panel of 17 diverse experts in apheresis, related specialties, and electronic case report form (eCRF), and database development was assembled. The panel met via online conferencing from November 17, 2020 to December 1, 2021. A draft document was posted online for public comment from October 11, 2021 to November 10, 2021. Feedback was collected using an online survey tool. The consensus panel revised the UACRF. This version was converted to an eCRF with additional changes made to improve usability in this format. The final version of the UACRF was created on August 24, 2023. The UACRF contains 16 modules: procedure and subject eligibility, patient demographics, general procedure information, laboratory parameters, vascular access, common procedure elements, eight procedure specific modules (mononuclear cell collection and seven therapeutic modalities), outcomes, and site information. A total of 137 data elements were created, including 57 with one or more subelements. The UACRF is the first systematic attempt to develop CDE for therapeutic apheresis and white blood cell collections. Further validation of the UACRF is necessary to confirm the tool's ability to collect the relevant data elements and determine the usability of the form.

开发统一的血液透析病例报告表,实现血液透析数据的标准化收集
在全球范围内进行的血液净化适应症越来越多。为血液透析相关领域开发通用数据元素(CDE)可促进新研究的开展,提高包括基准在内的质量计划,并改善患者护理。本报告介绍了作为美国血液净化(ApheresUS)计划一部分的统一血液净化病例报告表(UACRF)的系统开发情况。由 17 位不同领域的专家组成了一个共识小组,这些专家分别来自无创抽吸、相关专科、电子病例报告表 (eCRF) 和数据库开发领域。专家小组于 2020 年 11 月 17 日至 2021 年 12 月 1 日通过在线会议召开了会议。2021 年 10 月 11 日至 2021 年 11 月 10 日,文件草案在网上公布,征求公众意见。使用在线调查工具收集反馈意见。共识小组修订了 UACRF。该版本被转换为 eCRF,并进行了更多修改,以提高该格式的可用性。UACRF 的最终版本于 2023 年 8 月 24 日创建。UACRF 包含 16 个模块:手术和受试者资格、患者人口统计学、一般手术信息、实验室参数、血管通路、常见手术元素、8 个特定手术模块(单核细胞采集和 7 种治疗方式)、结果和手术部位信息。共创建了 137 个数据元素,其中 57 个包含一个或多个子元素。UACRF 是为治疗性无细胞疗法和白细胞采集开发 CDE 的首次系统性尝试。有必要对 UACRF 进行进一步验证,以确认该工具收集相关数据元素的能力,并确定表格的可用性。
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来源期刊
CiteScore
2.80
自引率
13.30%
发文量
70
审稿时长
>12 weeks
期刊介绍: The Journal of Clinical Apheresis publishes articles dealing with all aspects of hemapheresis. Articles welcomed for review include those reporting basic research and clinical applications of therapeutic plasma exchange, therapeutic cytapheresis, therapeutic absorption, blood component collection and transfusion, donor recruitment and safety, administration of hemapheresis centers, and innovative applications of hemapheresis technology. Experimental studies, clinical trials, case reports, and concise reviews will be welcomed.
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