Systematic review and meta-analysis on effectiveness of strategies for enhancing adverse drug reaction reporting.

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Journal of the American Pharmacists Association Pub Date : 2024-11-09 DOI:10.1016/j.japh.2024.102293
Niphonh Mongkhonmath, Phayom Sookaneknun Olson, Panupong Puttarak, Nathorn Chaiyakunapruk, Ratree Sawangjit
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Abstract

Background: Pharmacovigilance is essential for patient safety, but underreporting adverse drug reactions (ADRs) is a global challenge.

Objectives: This review evaluated the effectiveness of strategies for enhancing ADR reporting by healthcare professionals (HCPs).

Methods: This systematic review was conducted following the Cochrane and the PRISMA guidelines. Five international databases were searched from inception to December 2023 and updated search to September 2024. Randomized clinical controlled trials (RCTs) and non-RCTs on enhancing ADR reporting were included. The primary outcomes were the number of overall ADR and high-quality ADR reports. Study quality was assessed using the Effective Practice and Organization of Care risk of bias (ROB), and ROBIN-I for RCT, and non-RCT. All data were evaluated using a random-effects model, and heterogeneity was assessed using I2 statistic and chi-squared tests.

Results: From 1672 studies, 13 studies (10 RCTs, and 3 non-RCTs) with 28,116 participants were included. Two of 10 RCTs had low ROB while the remaining were judged as unclear and moderate ROB. Most studies were in high-income countries, and the main strategy was educating HCPs through workshops. Meta-analysis showed significant increases in overall ADR reporting through educating HCPs with a rate ratio (RR) of 5.09 (95% CI: 3.36-7.71, I2 = 84.5%, low certainty), and in high-quality reporting with 1.31 (95% CI: 1.09-1.58, I2 = 0.0%, moderate certainty). Subgroup analysis indicated that educating HCPs through face-to-face workshops combined with the Tawai app (RR:10.5, 95% CI: 8.74-12.61), a face-to-face workshop alone (RR:6.69, 95% CI: 5.43-8.25, I2 = 0.0%), and repeated telephone (RR:2.59, 95% CI: 1.75-3.84, I2 = 8.8%) significantly increased the overall number of ADR reports with moderate certainty. Email or letter communications showed no significant effect.

Conclusion: Educating HCPs via interactive strategies like face-to-face workshops with or without a mobile app and repeated phone calls improved ADR reporting. However, long-term, high-quality studies are needed to confirm these findings before recommending widespread implementation in clinical practice, especially in low-and middle-income countries.

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关于加强药物不良反应报告策略有效性的系统回顾和元分析。
背景:药物警戒对患者安全至关重要,但药物不良反应(ADRs)报告不足是一项全球性挑战:本综述评估了加强医疗保健专业人员(HCPs)报告药物不良反应的策略的有效性:本系统性综述遵循 Cochrane 和 PRISMA 指南。检索了五个国际数据库,检索期从开始至 2023 年 12 月,更新检索期至 2024 年 9 月。纳入了有关加强 ADR 报告的随机临床对照试验 (RCT) 和非 RCT。主要结果是总体 ADR 报告和高质量 ADR 报告的数量。研究质量采用 EPOC 偏倚风险 (ROB) 和 ROBIN-I 对 RCT 和非 RCT 进行评估。所有数据均采用随机效应模型进行评估,异质性采用 I2 统计量和卡方检验进行评估:在 1,672 项研究中,共纳入了 13 项研究(10 项 RCT 和 3 项非 RCT),28,116 名参与者。在 10 项研究性试验中,有两项研究的投资回报率较低,其余研究的投资回报率被判定为不明确和中等。大多数研究都在高收入国家进行,主要策略是通过研讨会对保健医生进行教育。Meta 分析表明,通过对 HCPs 进行教育,ADR 报告率 (RR) 明显增加,达到 5.09(95%CI:3.36-7.71,I2=84.5%,低度确定性),高质量报告率为 1.31(95%CI:1.09-1.58,I2=0.0%,中度确定性)。亚组分析表明,通过结合 Tawai 应用程序的面对面研讨会(RR:10.5,95%CI:8.74-12.61)、单独的面对面研讨会(RR:6.69,95%CI:5.43-8.25,I2=0.0%)和重复电话(RR:2.59,95%CI:1.75-3.84,I2=8.8%)对 HCP 进行教育可显著增加 ADR 报告的总数,确定性为中等。电子邮件或信件沟通没有明显效果:结论:通过互动策略(如使用或不使用移动应用程序的面对面研讨会以及反复拨打电话)对初级保健人员进行教育可提高ADR报告率。然而,在建议在临床实践中(尤其是在低收入国家)广泛实施之前,需要进行长期、高质量的研究来证实这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.30
自引率
14.30%
发文量
336
审稿时长
46 days
期刊介绍: The Journal of the American Pharmacists Association is the official peer-reviewed journal of the American Pharmacists Association (APhA), providing information on pharmaceutical care, drug therapy, diseases and other health issues, trends in pharmacy practice and therapeutics, informed opinion, and original research. JAPhA publishes original research, reviews, experiences, and opinion articles that link science to contemporary pharmacy practice to improve patient care.
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