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药物警戒与药品不良反应报告:坦桑尼亚南部高地医疗服务提供者的经验

Pharmacovigilance and Adverse Drug Reactions Reporting: Healthcare Providers' Experiences from Southern Highland Tanzania.

作者信息

Mwakawanga Dorkasi L, Kilonzi Manase, Philipo Erick G, Martine Aron, Mbilinyi Tusaligwe, Kileo Nancy F, Mkinga Bryceson, Shonyella Cleopatra Justine, Mohamedi Juma A, Clement Aurelia, Mwasomola Davance, Mushy Stella E, Sirili Nathanael

机构信息

School of Nursing, The Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania.

School of Pharmacy, The Muhimbili University of Health and Allied Sciences, P.O. Box 65013, Dar es Salaam, Tanzania.

出版信息

Adv Pharmacol Pharm Sci. 2023 Oct 16;2023:5537592. doi: 10.1155/2023/5537592. eCollection 2023.

Abstract

PURPOSE

This exploratory qualitative study aimed to analyze the experiences of healthcare providers (HCPs) in pharmacovigilance (PV) and ADR reporting in the southern highland zone of Tanzania.

METHODS

In 2022, an exploratory qualitative case study using in-depth interviews (IDIs) was conducted to explore the experiences of PV and ADR reporting among HCPs (doctors, nurses, and pharmacists). The study was carried out in a zonal referral hospital and a regional referral hospital of the Tanzanian southern highlands zone. Inductive-deductive thematic analysis was adopted for data analysis.

RESULTS

Participants demonstrated adequate knowledge of PV and its related activities including ADR reporting. Knowing the interactions and wrong medication dosage as sources of ADR, signs, and symptoms, stopping the drug, and treating the symptoms following ADR emerged as subthemes linked with adequate knowledge in identifying and managing ADR. Participants perceived reporting ADR as laborious, posing a subjective burden and that not all ADRs needed to be reported. The latter contributed to limited participation in ADR reporting despite that participants were conversant with both physical and online ADR reporting platforms.

CONCLUSION

Although HCPs are well informed about PV and ADR reporting including the benefits to public health, their involvement in ADR reporting is low. In addition to the ongoing on-the-job training and regular supportive supervision for HCPs to improve the ADR practice, there is still a need to explore other strategies to be used as motives for HCPs to report ADR regularly.

摘要

目的

本探索性定性研究旨在分析坦桑尼亚南部高地地区医疗服务提供者(HCPs)在药物警戒(PV)和药品不良反应(ADR)报告方面的经历。

方法

2022年,采用深入访谈(IDI)进行了一项探索性定性案例研究,以探究HCPs(医生、护士和药剂师)在PV和ADR报告方面的经历。该研究在坦桑尼亚南部高地地区的一家地区转诊医院和一家区域转诊医院开展。数据分析采用归纳 - 演绎主题分析法。

结果

参与者对PV及其相关活动(包括ADR报告)表现出足够的了解。将药物相互作用和错误的药物剂量视为ADR的来源、体征和症状,在出现ADR后停药并治疗症状,这些成为与识别和管理ADR的足够知识相关的子主题。参与者认为报告ADR很费力,会带来主观负担,且并非所有ADR都需要报告。尽管参与者熟悉纸质和在线ADR报告平台,但后者导致ADR报告的参与度有限。

结论

尽管HCPs充分了解PV和ADR报告,包括其对公众健康的益处,但他们在ADR报告方面的参与度较低。除了持续为HCPs提供在职培训和定期支持性监督以改善ADR实践外,仍有必要探索其他策略,作为促使HCPs定期报告ADR的动机。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6769/10593552/807e856727a9/APS2023-5537592.001.jpg

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