Margraff Florence, Bertram Delphine
Délégation à la Recherche Clinique et à l'Innovation, Hospices Civils de Lyon, 3, quai des Célestins, 69229, Lyon Cedex 02, France.
Drug Saf. 2014 Jun;37(6):409-19. doi: 10.1007/s40264-014-0162-y.
The modalities and contributions to drug safety of patient adverse drug reaction reporting systems in 50 countries have been reviewed and analysed.
The means made available by National Health Competent Authorities (NCAs) for patients to report drug side effects were compared through literature review and questionnaire.
Among the 50 countries included in this study, we found that direct patient reporting systems exist in 44 countries and represent 9 % of total reports, the rest coming from healthcare professionals. Australia was the first, in 1964, and the United States has the system in which patients are the most involved. A total of 27 countries have a patient-specific reporting form, and 31 countries provide a form to complete online. In order to help patients, four countries constrain the description of the reaction and 12 constrain the choice of drug on the reporting form. Most of the surveyed countries request the patient's medical history (30 countries) and concomitant therapies (41 countries). The total number of fields per form ranges from 6 to 59, with a mean of 36 items.
Most of the surveyed countries have implemented a patient adverse drug reaction reporting system. From this study, it seems that an online reporting form increases the rate of reporting. Currently, many different forms exist worldwide; these should be harmonized by considering the strengths and weaknesses of all existing forms. But above all, to increase the number of reports, each country should promote NCA-initiated adverse drug reactions reporting systems.
对50个国家患者药品不良反应报告系统的模式及其对药物安全性的贡献进行了审查和分析。
通过文献综述和问卷调查,比较了国家卫生主管当局(NCA)为患者提供的报告药物副作用的方式。
在本研究纳入的50个国家中,我们发现44个国家存在直接患者报告系统,占报告总数的9%,其余报告来自医疗保健专业人员。澳大利亚于1964年率先建立该系统,美国的患者参与度最高。共有27个国家有针对患者的报告表格,31个国家提供在线填写的表格。为帮助患者,4个国家对反应描述进行限制,12个国家对报告表格上的药物选择进行限制。大多数接受调查的国家要求提供患者病史(30个国家)和伴随治疗情况(41个国家)。每个表格的字段总数从6个到59个不等,平均为36项。
大多数接受调查的国家已实施患者药品不良反应报告系统。从本研究来看,在线报告表格似乎提高了报告率。目前,全球存在许多不同的表格;应通过考虑所有现有表格的优缺点来进行统一。但最重要的是,为增加报告数量,每个国家都应推广由国家卫生主管当局发起的药品不良反应报告系统。