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关于巴基斯坦利益相关者对药物警戒系统、政策及协调的观点的定性研究

A Qualitative Study of Stakeholders' Views on Pharmacovigilance System, Policy, and Coordination in Pakistan.

作者信息

Khan Muhammad Akhtar Abbas, Hamid Saima, Khan Shahzad Ali, Sarfraz Mariyam, Babar Zaheer-Ud-Din

机构信息

Health Services Academy Islamabad, Islamabad, Pakistan.

Fatima Jinnah Women University, Rawalpindi, Pakistan.

出版信息

Front Pharmacol. 2022 Jun 9;13:891954. doi: 10.3389/fphar.2022.891954. eCollection 2022.

Abstract

Due to the absence of necessary rules, poor coordination, and various challenges, the pharmacovigilance system of Pakistan is not optimally functional at all levels of the health system. The objective of the study was to assess the stakeholders' perceptions of the current ADR reporting system and to identify the pharmacovigilance policy issues and problems of effective coordination. Stakeholders from a broad range of disciplines, academia, regulatory authorities, the pharmaceutical industry, international health organizations, as well as pharmacovigilance experts, and healthcare professionals were included in the study. A total of 25 stakeholders throughout Pakistan were interviewed during exploratory semi-structured interviews. The interviews were recorded digitally, transcribed, coded, compared, and grouped according to their similarity of themes. Participants provided insights into gaps, limitations, and challenges of Pakistan's current ADR reporting system, issues with proposed pharmacovigilance rules, and coordination difficulties. The majority of the participants considered the ADR reporting system in Pakistan to be improving but in a nascent phase. The identified gaps, challenges, limitations of the system, and barriers to reporting were labeled as reasons for limited functioning. Almost all stakeholders were aware of the existence of draft pharmacovigilance rules; however, participants in the industry were familiar with the contents and context of draft pharmacovigilance rules. Bureaucratic red tape and lack of political will appeared to be the top reasons for delaying the approval of the pharmacovigilance rules. Wider consultation, advocacy, and awareness sessions of policymakers and HCPs were suggested for early approval of rules. Participants unanimously agreed that the approval of rules shall improve the quality of life and reduce the economic burden along with morbidity and mortality rates. The need for greater and collaborative coordination among the stakeholders in promoting medicines' safety was highlighted. All participants suggested the use of media and celebrities to disseminate the safety information. Participants showed partial satisfaction with the way pharmacovigilance in Pakistan is moving forward. However, stakeholders believed that engagement of multi-stakeholders, approval of pharmacovigilance rules, and the establishment of pharmacovigilance centers in provinces, hospitals, and public health programs (PHPs) shall support in achieving the desired results.

摘要

由于缺乏必要的规则、协调不力以及各种挑战,巴基斯坦的药物警戒系统在卫生系统的各个层面都未能达到最佳运行状态。本研究的目的是评估利益相关者对当前药品不良反应报告系统的看法,并确定药物警戒政策问题和有效协调方面的问题。来自广泛学科领域的利益相关者、学术界、监管机构、制药行业、国际卫生组织以及药物警戒专家和医疗保健专业人员都参与了这项研究。在探索性半结构化访谈中,对巴基斯坦各地的25名利益相关者进行了访谈。访谈进行了数字记录、转录、编码、比较,并根据主题的相似性进行了分组。参与者深入探讨了巴基斯坦当前药品不良反应报告系统的差距、局限性和挑战、拟议的药物警戒规则存在的问题以及协调困难。大多数参与者认为巴基斯坦的药品不良反应报告系统正在改进,但仍处于初期阶段。所发现的系统差距、挑战、局限性以及报告障碍被视为系统运行受限的原因。几乎所有利益相关者都知道药物警戒规则草案的存在;然而,行业参与者熟悉药物警戒规则草案的内容和背景。官僚主义的繁文缛节和缺乏政治意愿似乎是延迟药物警戒规则批准的首要原因。建议对政策制定者和医疗保健专业人员进行更广泛的咨询、宣传和提高认识活动,以便早日批准规则。参与者一致认为,规则的批准将改善生活质量,减轻经济负担,同时降低发病率和死亡率。强调了利益相关者之间在促进药品安全方面加强协作协调的必要性。所有参与者都建议利用媒体和名人传播安全信息。参与者对巴基斯坦药物警戒的发展方式表示部分满意。然而,利益相关者认为,多利益相关者的参与、药物警戒规则的批准以及在各省、医院和公共卫生项目中设立药物警戒中心将有助于实现预期结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdd2/9218668/ffd4c54d1e8a/fphar-13-891954-g001.jpg

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