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从监测系统、文献和社交媒体获取的药物安全数据比较:来自一种中药的实证研究。

Comparison of drug safety data obtained from the monitoring system, literature, and social media: An empirical proof from a Chinese patent medicine.

机构信息

Centre for Evidence-Based Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.

Department of Health Sciences, University of York, York, England, United Kingdom.

出版信息

PLoS One. 2019 Nov 6;14(11):e0222077. doi: 10.1371/journal.pone.0222077. eCollection 2019.

Abstract

OBJECTIVES

To investigate the consistency of adverse events (AEs) and adverse drug reactions (ADRs) reported in the literature, monitoring and social media data.

METHODS

Using one Chinese patent medicine-Cordyceps sinensis extracts (CSE) as an example, we obtained safety data from the national monitoring system (July 2002 to February 2016), literature (up to November 2016) and social media (May 2019). For literature data, we searched the Chinese National Knowledge Infrastructure Database (CNKI), WanFang database, Chinese Science and Technology Periodical Database (VIP), Chinese Biomedical Literature Database (SinoMed), PubMed, Embase and the Cochrane Library. Social media data was from the Baidu post bar and Sina micro-blog. Two authors independently screened the literature and extracted data by PRISMA Harms checklist was followed. AEs and ADRs were coded using the World Health Organization Adverse Reaction Terminology (WHO-ART). AEs and ADRs were grouped into thirty-one organ-system classes for comparisons. Frequencies, relative frequencies and rank were used as metrics. Radar chart was used to manifest the features of the distributions and proportions.

RESULTS

610 AEs reported in CFDA monitoring data were associated with CSE, of which 537 (88.03%) were suspected ADRs (10.49% certain). 5568 AEs were identified from 172 papers (63% RCTs, 37% other types of studies including case series, case reports, ADR monitoring reports and reviews), in which 86 (1.54%) were ADRs (1.54% certain). 15 AEs (0 certain ADR) were identified from social media. AEs, ADRs and their affected system-organ classes, looked largely similar, but different in every aspect when looking at details. Data from RCTs demonstrated the most disparity.

CONCLUSIONS

In our study, the most prevalent AEs and ADRs, mainly gastro-intestinal system disorders including nausea, diarrhea and vomiting, in monitoring system were largely similar with those in literature and social media. But data from different sources varied if looked at details. Multiple data sources (the monitoring system, literature and social media) should be integrated to collect safety information of interventions. The distributions of AEs and ADRs from RCTs were least similar with the data from other sources. Our empirical proof is consistent with other similar studies.

摘要

目的

调查文献、监测和社交媒体数据中报告的不良事件(AE)和药物不良反应(ADR)的一致性。

方法

以一种中药-冬虫夏草提取物(CSE)为例,我们从国家监测系统(2002 年 7 月至 2016 年 2 月)、文献(截至 2016 年 11 月)和社交媒体(2019 年 5 月)获得安全性数据。对于文献数据,我们检索了中国国家知识基础设施数据库(CNKI)、万方数据库、中国科技期刊数据库(VIP)、中国生物医学文献数据库(SinoMed)、PubMed、Embase 和 Cochrane 图书馆。社交媒体数据来自百度贴吧和新浪微博。两位作者独立筛选文献,并按照 PRISMA 危害检查表提取数据。使用世界卫生组织不良反应术语(WHO-ART)对 AE 和 ADR 进行编码。将 AE 和 ADR 分为三十一个器官系统类别进行比较。频率、相对频率和等级用作指标。雷达图用于显示分布和比例的特征。

结果

CFDA 监测数据中报告了 610 例与 CSE 相关的 AE,其中 537 例(88.03%)为疑似 ADR(10.49%确定)。从 172 篇论文中确定了 5568 例 AE(63% RCT,37%其他类型的研究,包括病例系列、病例报告、ADR 监测报告和综述),其中 86 例(1.54%)为 ADR(1.54%确定)。从社交媒体中确定了 15 例 AE(0 例确定的 ADR)。AE、ADR 及其受影响的系统器官类别,在很大程度上相似,但细节上存在差异。RCT 数据显示出最大的差异。

结论

在我们的研究中,监测系统中最常见的 AE 和 ADR,主要是胃肠道系统紊乱,包括恶心、腹泻和呕吐,与文献和社交媒体中的相似。但从细节上看,不同来源的数据存在差异。应整合多种数据源(监测系统、文献和社交媒体)以收集干预措施的安全性信息。RCT 来源的 AE 和 ADR 分布与其他来源的数据最不相似。我们的实证证明与其他类似研究一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e870/6834258/7437fe992c3d/pone.0222077.g001.jpg

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