University of York, York, United Kingdom.
University of Pennsylvannia, Philadelphia, PA, United States.
JMIR Public Health Surveill. 2024 Sep 6;10:e59167. doi: 10.2196/59167.
Adverse drug events pose an enormous public health burden, leading to hospitalization, disability, and death. Even the adverse events (AEs) categorized as nonserious can severely impact on patient's quality of life, adherence, and persistence. Monitoring medication safety is challenging. Web-based patient reports on social media may be a useful supplementary source of real-world data. Despite the growth of sophisticated techniques for identifying AEs using social media data, a consensus has not been reached as to the value of social media in relation to more traditional data sources.
This study aims to evaluate and characterize the utility of social media analysis in adverse drug event detection and pharmacovigilance as compared with other data sources (such as spontaneous reporting systems and the clinical literature).
In this scoping review, we searched 11 bibliographical databases and Google Scholar, followed by handsearching and forward and backward citation searching. Each record was screened by 2 independent reviewers at both the title and abstract stage and the full-text screening stage. Studies were included if they used any type of social media (such as Twitter or patient forums) to detect AEs associated with any drug medication and compared the results ascertained from social media to any other data source. Study information was collated using a piloted data extraction sheet. Data were extracted on the AEs and drugs searched for and included; the methods used (such as machine learning); social media data source; volume of data analyzed; limitations of the methodology; availability of data and code; comparison data source and comparison methods; results, including the volume of AEs, and how the AEs found compared with other data sources in their seriousness, frequencies, and expectedness or novelty (new vs known knowledge); and conclusions.
Of the 6538 unique records screened, 73 publications representing 60 studies with a wide variety of extraction methods met our inclusion criteria. The most common social media platforms used were Twitter and online health forums. The most common comparator data source was spontaneous reporting systems, although other comparisons were also made, such as with scientific literature and product labels. Although similar patterns of AE reporting tended to be identified, the frequencies were lower in social media. Social media data were found to be useful in identifying new or unexpected AEs and in identifying AEs in a timelier manner.
There is a large body of research comparing AEs from social media to other sources. Most studies advocate the use of social media as an adjunct to traditional data sources. Some studies also indicate the value of social media in understanding patient perspectives such as the impact of AEs, which could be better explored.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR2-10.2196/47068.
药物不良反应给公共健康带来了巨大的负担,导致住院、残疾和死亡。即使是非严重的不良反应(AE)也会严重影响患者的生活质量、治疗依从性和持久性。监测药物安全性具有挑战性。基于社交媒体的患者报告可能是真实世界数据的有用补充来源。尽管使用社交媒体数据识别不良反应的复杂技术不断发展,但在社交媒体与更传统数据源的价值方面尚未达成共识。
本研究旨在评估和描述与其他数据源(如自发报告系统和临床文献)相比,社交媒体分析在药物不良反应检测和药物警戒中的作用。
在本次范围综述中,我们搜索了 11 个文献数据库和 Google Scholar,并进行了手工搜索和向前及向后引文搜索。每个记录均由 2 名独立的审查员在标题和摘要阶段以及全文筛选阶段进行筛选。如果研究使用任何类型的社交媒体(如 Twitter 或患者论坛)来检测与任何药物相关的不良反应,并将从社交媒体中确定的结果与任何其他数据源进行比较,则将其纳入研究。使用预先制定的数据提取表对研究信息进行了整理。提取的信息包括:搜索的不良反应和药物;所使用的方法(如机器学习);社交媒体数据源;分析的数据量;方法学的局限性;数据和代码的可用性;比较数据源和比较方法;结果,包括不良反应的数量,以及从严重程度、频率和预期或新颖性(新与已知知识)方面来看,从社交媒体中发现的不良反应与其他数据源相比的情况;以及结论。
在筛选出的 6538 条独特记录中,有 73 篇出版物代表了 60 项研究,这些研究采用了广泛的提取方法,符合我们的纳入标准。最常使用的社交媒体平台是 Twitter 和在线健康论坛。最常见的比较数据源是自发报告系统,尽管也进行了其他比较,如与科学文献和产品标签的比较。尽管相似的不良反应报告模式往往是一致的,但社交媒体中的频率较低。研究发现,社交媒体数据可用于识别新的或意外的不良反应,并以更及时的方式识别不良反应。
有大量研究比较了来自社交媒体和其他来源的不良反应。大多数研究主张将社交媒体用作传统数据源的辅助手段。一些研究还表明,社交媒体在了解患者观点(如不良反应的影响)方面具有价值,这方面可以进一步探讨。
国际注册报告摘要识别码(IRRID):RR2-10.2196/47068。