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知情同意过程中的数字工具:一项系统综述

Digital tools in the informed consent process: a systematic review.

作者信息

Gesualdo Francesco, Daverio Margherita, Palazzani Laura, Dimitriou Dimitris, Diez-Domingo Javier, Fons-Martinez Jaime, Jackson Sally, Vignally Pascal, Rizzo Caterina, Tozzi Alberto Eugenio

机构信息

Ospedale Pediatrico Bambino Gesù (OPBG), Piazza di Sant'Onofrio, 4, 00165, Rome, Italy.

Libera Università Maria Ss. Assunta (LUMSA), Via della Traspontina, 21, 00193, Rome, Italy.

出版信息

BMC Med Ethics. 2021 Feb 27;22(1):18. doi: 10.1186/s12910-021-00585-8.

Abstract

BACKGROUND

Providing understandable information to patients is necessary to achieve the aims of the Informed Consent process: respecting and promoting patients' autonomy and protecting patients from harm. In recent decades, new, primarily digital technologies have been used to apply and test innovative formats of Informed Consent. We conducted a systematic review to explore the impact of using digital tools for Informed Consent in both clinical research and in clinical practice. Understanding, satisfaction and participation were compared for digital tools versus the non-digital Informed Consent process.

METHODS

We searched for studies on available electronic databases, including Pubmed, EMBASE, and Cochrane. Studies were identified using specific Mesh-terms/keywords. We included studies, published from January 2012 to October 2020, that focused on the use of digital Informed Consent tools for clinical research, or clinical procedures. Digital interventions were defined as interventions that used multimedia or audio-video to provide information to patients. We classified the interventions into 3 different categories: video only, non-interactive multimedia, and interactive multimedia.

RESULTS

Our search yielded 19,579 publications. After title and abstract screening 100 studies were retained for full-text analysis, of which 73 publications were included. Studies examined interactive multimedia (29/73), non-interactive multimedia (13/73), and videos (31/73), and most (34/38) studies were conducted on adults. Innovations in consent were tested for clinical/surgical procedures (26/38) and clinical research (12/38). For research IC, 21 outcomes were explored, with a positive effect on at least one of the studied outcomes being observed in 8/12 studies. For clinical/surgical procedures 49 outcomes were explored, and 21/26 studies reported a positive effect on at least one of the studied outcomes.

CONCLUSIONS

Digital technologies for informed consent were not found to negatively affect any of the outcomes, and overall, multimedia tools seem desirable. Multimedia tools indicated a higher impact than videos only. Presence of a researcher may potentially enhance efficacy of different outcomes in research IC processes. Studies were heterogeneous in design, making evaluation of impact challenging. Robust study design including standardization is needed to conclusively assess impact.

摘要

背景

向患者提供易于理解的信息对于实现知情同意过程的目标至关重要:尊重和促进患者的自主权,并保护患者免受伤害。近几十年来,新的、主要是数字技术已被用于应用和测试创新的知情同意形式。我们进行了一项系统综述,以探讨在临床研究和临床实践中使用数字工具进行知情同意的影响。比较了数字工具与非数字知情同意过程在理解、满意度和参与度方面的差异。

方法

我们在包括PubMed、EMBASE和Cochrane在内的可用电子数据库中搜索研究。使用特定的医学主题词/关键词识别研究。我们纳入了2012年1月至2020年10月发表的、专注于在临床研究或临床程序中使用数字知情同意工具的研究。数字干预被定义为使用多媒体或视听手段向患者提供信息的干预措施。我们将干预措施分为3种不同类别:仅视频、非交互式多媒体和交互式多媒体。

结果

我们的搜索产生了19579篇出版物。经过标题和摘要筛选,保留了100项研究进行全文分析,其中纳入了73篇出版物。研究考察了交互式多媒体(29/73)、非交互式多媒体(13/73)和视频(31/73),并且大多数(34/38)研究是在成年人中进行的。对临床/外科手术(26/38)和临床研究(12/38)的知情同意创新进行了测试。对于研究知情同意,探索了21项结果,在12项研究中的8项研究中观察到对至少一项研究结果有积极影响。对于临床/外科手术,探索了49项结果,26项研究中的21项报告对至少一项研究结果有积极影响。

结论

未发现用于知情同意的数字技术对任何结果有负面影响,总体而言,多媒体工具似乎是可取的。多媒体工具显示出比仅视频更高的影响。研究人员的在场可能会提高研究知情同意过程中不同结果的有效性。研究在设计上存在异质性,使得评估影响具有挑战性。需要包括标准化在内的稳健研究设计来最终评估影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a21/7913441/40a6e3923afb/12910_2021_585_Fig1_HTML.jpg

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