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一种基于人群的方法,用于实现从退出式到加入式研究许可的转变。

A population-based approach for implementing change from opt-out to opt-in research permissions.

作者信息

Marshall Elizabeth A, Oates Jim C, Shoaibi Azza, Obeid Jihad S, Habrat Melissa L, Warren Robert W, Brady Kathleen T, Lenert Leslie A

机构信息

Biomedical Informatics Center, Medical University of South Carolina, Charleston, South Carolina, United States of America.

Department of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, United States of America.

出版信息

PLoS One. 2017 Apr 25;12(4):e0168223. doi: 10.1371/journal.pone.0168223. eCollection 2017.

Abstract

Due to recently proposed changes in the Common Rule regarding the collection of research preferences, there is an increased need for efficient methods to document opt-in research preferences at a population level. Previously, our institution developed an opt-out paper-based workflow that could not be utilized for research in a scalable fashion. This project was designed to demonstrate the feasibility of implementing an electronic health record (EHR)-based active opt-in research preferences program. The first phase of implementation required creating and disseminating a patient questionnaire through the EHR portal to populate discreet fields within the EHR indicating patients' preferences for future research study contact (contact) and their willingness to allow anonymised use of excess tissue and fluid specimens (biobank). In the second phase, the questionnaire was presented within a clinic nurse intake workflow in an obstetrical clinic. These permissions were tabulated in registries for use by investigators for feasibility studies and recruitment. The registry was also used for research patient contact management using a new EHR encounter type to differentiate research from clinical encounters. The research permissions questionnaire was sent to 59,670 patients via the EHR portal. Within four months, 21,814 responses (75% willing to participate in biobanking, and 72% willing to be contacted for future research) were received. Each response was recorded within a patient portal encounter to enable longitudinal analysis of responses. We obtained a significantly lower positive response from the 264 females who completed the questionnaire in the obstetrical clinic (55% volunteers for biobank and 52% for contact). We demonstrate that it is possible to establish a research permissions registry using the EHR portal and clinic-based workflows. This patient-centric, population-based, opt-in approach documents preferences in the EHR, allowing linkage of these preferences to health record information.

摘要

由于最近《通用规则》中关于研究偏好收集的提议变更,在人群层面记录主动选择参与研究偏好的高效方法的需求日益增加。此前,我们机构开发了一种基于纸质的退出式工作流程,无法以可扩展的方式用于研究。本项目旨在证明实施基于电子健康记录(EHR)的主动选择参与研究偏好计划的可行性。实施的第一阶段要求通过EHR门户创建并分发一份患者问卷,以填充EHR内的离散字段,表明患者对未来研究联系(联系)的偏好以及他们允许匿名使用多余组织和液体标本(生物样本库)的意愿。在第二阶段,该问卷在产科诊所的临床护士接诊工作流程中呈现。这些许可被列入登记册,供研究人员用于可行性研究和招募。该登记册还用于使用新的EHR会诊类型进行研究患者联系管理,以区分研究会诊和临床会诊。研究许可问卷通过EHR门户发送给了59670名患者。在四个月内,收到了21814份回复(75%愿意参与生物样本库,72%愿意在未来研究中被联系)。每份回复都记录在患者门户会诊中,以便对回复进行纵向分析。我们从在产科诊所完成问卷的264名女性中获得的积极回复明显较低(55%自愿参与生物样本库,52%自愿被联系)。我们证明了使用EHR门户和基于诊所的工作流程建立研究许可登记册是可行的。这种以患者为中心、基于人群的主动选择参与方法在EHR中记录偏好,允许将这些偏好与健康记录信息相联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14ff/5404843/a419b3e1367d/pone.0168223.g001.jpg

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