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基于网络的患者叙述的风险与益处:系统评价

Risks and Benefits of Web-Based Patient Narratives: Systematic Review.

作者信息

Drewniak Daniel, Glässel Andrea, Hodel Martina, Biller-Andorno Nikola

机构信息

Institute of Biomedical Ethics and History of Medicine, University of Zurich, Zurich, Switzerland.

Institute of Health Sciences, Zurich University of Applied Sciences, Winterthur, Switzerland.

出版信息

J Med Internet Res. 2020 Mar 26;22(3):e15772. doi: 10.2196/15772.

Abstract

BACKGROUND

Patient narratives are illustrative, individual accounts of patients' experiences with certain health conditions. Web-based patient narratives have become widely available on the internet and in social media, as part of electronically available patient decision aids or Web-based databases. In recent years, the role of patient narratives as a source of information, insight, and support for both health care users and providers has increasingly been emphasized. Although the potential impact of patient stories has high immediate plausibility, it is of interest to know if this impact can be captured in quantitative studies.

OBJECTIVE

This review aimed to evaluate whether research-generated Web-based patient narratives have quantifiable risks or benefits for (potential) patients, relatives, or health care professionals.

METHODS

We searched the following databases from August 2017 to March 2019: Medical Literature Analysis and Retrieval System Online, PsycInfo, Sociological Abstracts, Web of Science, and EMBASE. Titles and abstracts of the retrieved studies were reviewed and assessed for the inclusion and exclusion criteria. Papers were included if they studied the following: (1) (potential) patients, relatives, or health care professionals; (2) the effects of Web-based patient narratives that were generated scientifically (eg, through qualitative research methods); and (3) were quantitative studies. Furthermore, 2 authors independently performed an assessment of the quality of the included studies using a validated checklist.

RESULTS

Of 4226 documents, 17 studies met the inclusion criteria. The studies investigated 10 different sources of Web-based patient narratives. Sample sizes ranged from 23 to 2458. The mean score of the quality assessment was 82.6 (range 61-100). Effects regarding five different purposes were identified as follows: provide information, engage, model behavior, persuade, and comfort. We found positive effects in every category and negative effects in one category (persuade). Several of the reported effects are rather small or were identified under specific experimental conditions.

CONCLUSIONS

Patient narratives seem to be a promising means to support users in improving their understanding of certain health conditions and possibly to provide emotional support and have an impact on behavioral changes. There is limited evidence for beneficial effects on some outcomes. However, narratives are characterized by considerable heterogeneity and the investigated outcomes are hardly comparable with each other, which makes the overall judgment difficult. As there are numerous possible measures and purposes of narratives, quantifying the impact of Web-based patient narratives remains a challenge. Future research is needed to define the optimal standards for quantitative approaches to narrative-based interventions.

摘要

背景

患者叙述是患者对某些健康状况经历的具有说明性的个人描述。基于网络的患者叙述在互联网和社交媒体上已广泛可得,作为电子可用的患者决策辅助工具或基于网络的数据库的一部分。近年来,患者叙述作为医疗保健使用者和提供者的信息、见解及支持来源的作用日益受到重视。尽管患者故事的潜在影响看似具有很高的直接可信度,但了解这种影响能否在定量研究中得到体现仍很有意义。

目的

本综述旨在评估基于研究生成的网络患者叙述对(潜在)患者、亲属或医疗保健专业人员是否具有可量化的风险或益处。

方法

我们在2017年8月至2019年3月期间检索了以下数据库:医学文献分析与检索系统在线数据库(Medical Literature Analysis and Retrieval System Online)、心理学文摘数据库(PsycInfo)、社会学文摘数据库(Sociological Abstracts)、科学引文索引数据库(Web of Science)和荷兰医学文摘数据库(EMBASE)。对检索到的研究的标题和摘要进行审查,并根据纳入和排除标准进行评估。若论文研究以下内容则纳入:(1)(潜在)患者、亲属或医疗保健专业人员;(2)科学生成的基于网络的患者叙述的影响(例如,通过定性研究方法);(3)为定量研究。此外,两名作者使用经过验证的清单独立对纳入研究的质量进行评估。

结果

在4226篇文献中,17项研究符合纳入标准。这些研究调查了10种不同的基于网络的患者叙述来源。样本量从23至2458不等。质量评估的平均分数为82.(范围为61 - 100)。确定了关于五个不同目的的影响如下:提供信息、吸引、示范行为、说服和安慰。我们在每个类别中都发现了积极影响,在一个类别(说服)中发现了消极影响。所报告的一些影响相当小,或者是在特定实验条件下确定的。

结论

患者叙述似乎是一种有前景的手段,可支持使用者更好地理解某些健康状况,并可能提供情感支持以及对行为改变产生影响。对某些结果有有益影响的证据有限。然而,叙述具有相当大的异质性,且所研究的结果彼此之间几乎无法比较,这使得整体判断困难。由于叙述有众多可能的衡量标准和目的,量化基于网络的患者叙述的影响仍然是一项挑战。未来需要开展研究来确定基于叙述的干预措施定量方法的最佳标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e7/7146251/202d2c22ca0b/jmir_v22i3e15772_fig1.jpg

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