赞比亚抗逆转录病毒药物、抗疟疾药物和抗结核药物的质量:上市后常规监测结果。

The journal of medicine access Pub Date : 2024-07-25 eCollection Date: 2024-01-01 DOI:10.1177/27550834241266755
Elimas Jere, Derrick Munkombwe, Moses Mukosha, Steward Mudenda, Aubrey Chichonyi Kalungia, Billy Chabalenge
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引用次数: 0

摘要

背景:在撒哈拉以南非洲地区,人们越来越担心劣质抗菌药物如果达不到既定的质量、安全和疗效标准,可能会影响对具有公共卫生重要性的传染病的管理:目的:旨在确定赞比亚公共卫生部门供应和提供的抗逆转录病毒药物、抗疟疾药物和抗结核药物的质量:设计:开展了一项描述性横断面研究,分析了赞比亚国内上市后连续例行监测计划的数据,评估了2018年1月至2023年6月期间向公共医疗机构供应的抗逆转录病毒、抗疟和抗结核药物的质量:数据提取自实验室质量分析结果,这些结果来自赞比亚药品管理局在 2018 年 1 月至 2023 年 6 月期间作为上市后例行监测的一部分而收集的样本。样品从赞比亚各地药品供应链的各个环节采集。样本在津巴布韦药品监管局质量控制实验室(世界卫生组织预认证实验室)按照各自的药典标准进行分析。使用结构化 Excel 数据库提取数据,使用 Microsoft Excel 进行分析,并使用 GraphPad Prism 软件进行可视化:在 198 份样本中,86 份(43.43%)为抗逆转录病毒药物,54 份(27.27%)为抗疟药物,58 份(29.29%)为抗结核药物。在这 198 个样本中,171 个(86.36%)来自亚洲,19 个(9.60%)来自非洲,8 个(4.04%)来自欧洲。所有抽样药品在外观、鉴别、化验、质量均匀性、重量变化、崩解度、溶解度、pH 值和比重等测试方面均符合各自的质量规格,符合率为 100%:结论:通过上市后常规监测从赞比亚公共医疗机构获得的抗逆转录病毒药物、抗疟药物和抗结核药物均符合其质量标准。这可能会对艾滋病毒/艾滋病、疟疾和结核病的治疗效果产生积极影响。有必要对药品质量进行大规模的持续监测,以确保质量得到维持,并将不合格产品从药品供应链中清除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quality of antiretroviral, antimalarial and antituberculosis medicines in Zambia: Findings of routine post-marketing surveillance.

Background: There is growing concern in sub-Saharan Africa that poor-quality antimicrobial medicines may negate management of infectious diseases of public health importance should they fail to meet the set criteria of quality, safety and efficacy.

Objectives: The objective was to ascertain the quality of antiretroviral, antimalarial and antituberculosis medicines supplied and available in the public health sector in Zambia.

Design: A descriptive cross-sectional study was conducted involving the analysis of data from the continuous routine in-country post-marketing surveillance programme in Zambia that assessed the quality of antiretroviral, antimalarial and antituberculosis medicines supplied to public healthcare facilities between January 2018 and June 2023.

Methods: Data were extracted from laboratory quality analysis results from samples collected as part of routine post-marketing surveillance by the Zambia Medicines Regulatory Authority between January 2018 and June 2023. The samples were collected from various levels of the pharmaceutical supply chain across Zambia. Samples were analysed according to their respective pharmacopoeia standards at the Medicines Control Authority of Zimbabwe Quality Control Laboratory, a World Health Organization prequalified laboratory. Data were extracted using a structured Excel database and analysed using Microsoft Excel, and GraphPad Prism Software was used for visualizations.

Results: Of the 198 samples, 86 (43.43%) were antiretrovirals, 54 (27.27%) antimalarials and 58 (29.29%) antituberculosis medicines. Of these 198 samples, 171 (86.36%) originated from Asia, 19 (9.60%) Africa and 8 (4.04%) Europe. All sampled medicines met their respective quality specifications with respect to tests, which included appearance, identification, assay, uniformity of mass, weight variation, disintegration, dissolution, pH and specific gravity, giving a compliance rate of 100%.

Conclusion: Antiretrovirals, antimalarials and antituberculosis medicines obtained from public healthcare facilities in Zambia through routine post-marketing surveillance met their quality standards. This might positively impact treatment outcomes for HIV/AIDS, malaria and tuberculosis. There is a need for large-scale continuous monitoring of the quality of medicines in order to ensure quality is maintained and substandard products removed from the pharmaceutical supply chain.

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