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马拉维南部住院患者中不合格抗生素及其临床结局:一项试点研究。

Substandard antibiotics and their clinical outcomes among hospitalized patients in southern Malawi: a pilot study.

作者信息

Chiumia Francis Kachidza, Sinjani Muula Adamson, Chimimba Frider, Nyirongo Happy Magwaza, Kampira Elizabeth, Khuluza Felix

机构信息

Department of Pharmacy, Kamuzu University of Health Sciences, Blantyre, Malawi.

Department of Community and Environmental Health, Kamuzu University of Health Sciences, Blantyre, Malawi.

出版信息

Front Pharmacol. 2025 Mar 18;16:1535501. doi: 10.3389/fphar.2025.1535501. eCollection 2025.

Abstract

BACKGROUND

The burden of substandard antibiotics is high in low-middle income countries including Malawi. These poor-quality antibiotics may cause deleterious effects on patients and promote drug resistance. We assessed the quality of antibiotics and the associated clinical outcomes among hospitalized patients in southern Malawi.

METHODS

A cross-sectional study involving review of retrospective records was conducted among hospitalized adult patients at Zomba central, Machinga and Nsanje district hospitals in October 2022 and January 2024. Trained pharmacy personnel recorded the parenteral antibiotics that were issued to the medical wards. We used these records for matching and sampling of the administered medicine batches to the patient files. In total, we reviewed 224 patient management files for eligible patients, aiming to assess the patient recovery and the occurrence of adverse drug reactions (ADRs) using a global trigger tool. We collected nine medicine samples of ceftriaxone and benzylpenicillin which were administered to these patients and subjected them to tests for the content of active pharmaceutical ingredients using methods adapted from the United States Pharmacopeia. For each sample, we collected at least ten dosage units and used Agilent 1120 High Performance Liquid Chromatography for quality analysis.

RESULTS

Of the 224 reviewed files, ADRs occurred in 18.3% % (n = 41) of patients while 12.05% (n = 27) did not recover from their illness. One benzylpenicillin sample was found out of specifications with only 61.8% of declared amount of active ingredients. Among patients who received benzylpenicillin with optimal API content, 15.8% experienced ADRs while 10.5% failed to recover from illness. For patients who received benzylpenicillin containing lower than required amount of API, only 7.1% experienced an ADR while 14.3% failed to recover from illness. These differences were, however, not statistically significant. Patient outcomes were significantly associated with the patient's age and Charlson comorbidity index (CCI), p < 0.05.

CONCLUSION

The present findings did not reveal statistically significant differences in patient outcomes based on the assessed medicine quality. Therefore, we recommend a larger prospective study to further validate these results and encourage stakeholders to be more vigilant on the quality of antibiotic medicines, as this is a crucial measure for improving clinical outcomes and preventing antibiotic resistance in Malawi.

摘要

背景

包括马拉维在内的中低收入国家,不合格抗生素的负担很重。这些质量不佳的抗生素可能会对患者造成有害影响,并促进耐药性。我们评估了马拉维南部住院患者使用的抗生素质量及其相关临床结局。

方法

2022年10月和2024年1月,在松巴中心医院、马钦加医院和恩桑杰区医院对住院成年患者开展了一项涉及回顾性记录审查的横断面研究。经过培训的药学人员记录发放至内科病房的注射用抗生素。我们利用这些记录将所用药剂批次与患者档案进行匹配和抽样。总共,我们审查了224份符合条件患者的病历,旨在使用全球触发工具评估患者的康复情况和药物不良反应(ADR)的发生情况。我们收集了9份给这些患者使用的头孢曲松和苄星青霉素药物样本,并采用源自美国药典的方法对其活性药物成分含量进行检测。对于每个样本,我们收集了至少10个剂量单位,并使用安捷伦1120高效液相色谱仪进行质量分析。

结果

在审查的224份病历中,18.3%(n = 41)的患者发生了药物不良反应,而12.05%(n = 27)的患者未康复。发现1份苄星青霉素样本不符合规格,其活性成分含量仅为申报量的61.8%。在接受活性药物成分含量最佳的苄星青霉素治疗的患者中,15.8%发生了药物不良反应,10.5%未康复。对于接受活性药物成分含量低于要求量的苄星青霉素治疗的患者,只有7.1%发生了药物不良反应,14.3%未康复。然而,这些差异无统计学意义。患者结局与患者年龄和查尔森合并症指数(CCI)显著相关,p < 0.05。

结论

目前的研究结果未显示基于所评估药物质量的患者结局存在统计学显著差异。因此,我们建议开展一项更大规模的前瞻性研究以进一步验证这些结果,并鼓励利益相关者对抗生素药物质量更加警惕,因为这是改善马拉维临床结局和预防抗生素耐药性的关键措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac1b/11959087/d6f0b63be0a9/fphar-16-1535501-g001.jpg

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