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患者对疑似药物不良反应的报告:已发表文献及国际经验综述

Patient reporting of suspected adverse drug reactions: a review of published literature and international experience.

作者信息

Blenkinsopp A, Wilkie P, Wang M, Routledge P A

机构信息

Department of Medicines Management, Keele University, Keele, UK.

出版信息

Br J Clin Pharmacol. 2007 Feb;63(2):148-56. doi: 10.1111/j.1365-2125.2006.02746.x.

Abstract

AIMS

To synthesize data from published studies and international experience to identify evidence of potential benefits and drawbacks of direct patient reporting of suspected adverse drug reactions (ADRs) by patients.

METHODS

Structured search of MEDLINE, CINAHL and PsycINFO supplemented by internet searches and requests for information to key contacts.

RESULTS

Seven studies (eight papers) were included in the review. None of the studies concerned spontaneous reporting by patients. Information on patient reporting systems was obtained for six countries, with summary data reported by four. Patient reports identified possible new ADRs that had not previously been reported by health professionals. The quality of patient reports appears to be similar to that of health professional reports. There is some evidence that patients report an ADR when they consider their health professional has not paid attention to their concerns. Patient reports may, at least initially, be more time consuming to process.

CONCLUSIONS

Overall, the evidence indicates that patient reporting of suspected ADRs has more potential benefits than drawbacks. Evaluation of patient reporting systems is needed to provide further evidence.

摘要

目的

综合已发表研究的数据和国际经验,以确定患者直接报告疑似药物不良反应(ADR)的潜在益处和弊端的证据。

方法

对MEDLINE、CINAHL和PsycINFO进行结构化检索,并辅以互联网检索以及向关键联系人索取信息。

结果

该综述纳入了7项研究(8篇论文)。没有一项研究涉及患者的自发报告。获取了6个国家患者报告系统的信息,其中4个国家报告了汇总数据。患者报告识别出了卫生专业人员之前未报告过的可能的新ADR。患者报告的质量似乎与卫生专业人员报告的质量相似。有一些证据表明,当患者认为其卫生专业人员没有关注他们的担忧时,他们会报告ADR。至少在最初阶段,处理患者报告可能会更耗时。

结论

总体而言,证据表明患者报告疑似ADR的潜在益处多于弊端。需要对患者报告系统进行评估以提供进一步的证据。

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