Department of Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Agency for Medicinal Products and Medical Devices of Croatia (HALMED), Zagreb, Croatia.
Drug Saf. 2021 Oct;44(10):1073-1083. doi: 10.1007/s40264-021-01098-4. Epub 2021 Aug 8.
Healthcare professionals (HCPs) and patients have various motives to report adverse drug reactions (ADRs) to their national agency. These motives may differ between countries.
The aim of this study was to assess to what extent motives of HCPs and patients to report ADRs differ between countries.
HCPs and patients from Croatia (HR), The Netherlands (NL), and the UK were asked to complete a web-based survey containing questions regarding demographics and ADR reporting. HCPs and patients could select all motives for reporting that applied to them, with a total of 23 and 24 motives, respectively. Descriptive statistics are presented and Chi-square tests were used to test for differences across the countries, with effect sizes calculated using Cramer's V.
In total, 296 HCPs and 423 patients were included (60% and 32% from Croatia, 19% and 44% from NL, and 21% and 24% from the UK, respectively). For most of the motives to report or not to report an ADR, there were no differences between countries. Most HCPs from all countries would be motivated to report an ADR if there was a strong suspicion of causality (89%), if it concerned a severe/serious ADR (86%), and if it concerned an ADR for a new, recently marketed drug (77%). Most patients from all countries agreed that they would report an ADR if it concerned a severe ADR (96%), if the ADR influenced their daily activities (91%), and if they were worried about their own situation (90%). Differences across the countries (p < 0.05 and V ≥ 0.21) were observed for three and four of the HCP and patient motives, respectively. For HCPs, these differences were seen in motives related to legal obligation (65% HR, 24% NL, 38% UK), black triangle medicines (27% HR, 4% NL, 77% UK), and the reporting of well-known ADRs (53% HR, 85% NL, 69% UK). For patients, these differences were seen in motives related to a linkage between the ADR report and the medical notes (59% HR, 60% NL, 30% UK), complexity and time taken to report (25% HR, 13% NL, 40% UK), medicines purchased on the internet (59% HR, 39% NL, 65% UK), and the reporting of embarrassing ADRs (32% HR, 11% NL, 35% UK).
HCPs' and patients' motives to report or not to report ADRs to the national agency were mostly similar across the three countries. Such motives can be used in general strategies to promote and increase ADR reporting. The observed differences provide guidance to further fine-tune ADR reporting at a national level.
医疗保健专业人员(HCPs)和患者有各种动机向其国家机构报告药物不良反应(ADRs)。这些动机在不同国家可能有所不同。
本研究旨在评估 HCPs 和患者报告 ADR 的动机在国家间有何差异。
来自克罗地亚(HR)、荷兰(NL)和英国的 HCPs 和患者被要求完成一项基于网络的调查,其中包含有关人口统计学和 ADR 报告的问题。HCPs 和患者可以选择适用于他们的所有报告动机,分别有 23 项和 24 项动机。呈现描述性统计数据,并使用卡方检验测试国家间的差异,使用 Cramer's V 计算效应大小。
共有 296 名 HCPs 和 423 名患者入组(分别有 60%和 32%来自克罗地亚、19%和 44%来自 NL、21%和 24%来自英国)。对于报告或不报告 ADR 的大多数动机,国家间没有差异。来自所有国家的大多数 HCPs 如果有强烈的因果关系怀疑(89%)、涉及严重/严重 ADR(86%)以及涉及新的、最近上市的药物的 ADR(77%),他们会有动力报告 ADR。来自所有国家的大多数患者都同意,如果涉及严重 ADR(96%)、ADR 影响他们的日常生活活动(91%)或他们担心自己的情况(90%),他们会报告 ADR。在 HCP 和患者动机中,分别有三个和四个观察到国家间的差异(p<0.05 且 V≥0.21)。对于 HCPs,这些差异存在于与法律义务相关的动机(65% HR、24% NL、38% UK)、黑三角药物(27% HR、4% NL、77% UK)和知名 ADR 报告(53% HR、85% NL、69% UK)方面。对于患者,这些差异存在于与 ADR 报告与医疗记录之间的联系相关的动机(59% HR、60% NL、30% UK)、报告的复杂性和时间(25% HR、13% NL、40% UK)、互联网购买的药物(59% HR、39% NL、65% UK)和尴尬 ADR 报告(32% HR、11% NL、35% UK)方面。
HCPs 和患者向国家机构报告或不报告 ADR 的动机在三个国家基本相似。这些动机可用于促进和增加 ADR 报告的总体策略。观察到的差异为进一步调整国家一级的 ADR 报告提供了指导。