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Examining the Quality of Medicines at Kenyan Healthcare Facilities: A Validation of an Alternative Post-Market Surveillance Model That Uses Standardized Patients

机译:在肯尼亚医疗机构中检查药品质量:使用标准化患者的替代上市后监测模型的验证

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BackgroundPromoting access to medicines requires concurrent efforts to strengthen quality assurance for sustained impact. Although problems of substandard and falsified medicines have been documented in low- and middle-income countries, reliable information on quality is rarely available. ObjectiveThe aim of this study was to validate an alternative post-market surveillance model to complement existing models. MethodsThe study used standardized patients or mystery clients (people recruited from the local community and trained to pose as real patients) to collect medicine samples after presenting a pre-specified condition. The patients presented four standardized conditions to 42 blinded facilities in Nairobi, Kenya, resulting in 166 patient–clinician interactions and dispensing of 300 medicines at facilities or nearby retail pharmacies. The medicine samples obtained thus resemble those that would be given to real patients. ResultsSixty samples were selected from the 300, and sent for analysis at the Kenya National Quality Control Laboratory. Of these, ten (17%) did not comply with monograph specifications (three ibuprofen, two cetirizine, two amoxicillin/clavulanic acid combinations, and one each for prednisone, salbutamol and zinc). Five of the ten samples that failed had been inappropriately prescribed to patients who had presented symptoms of unstable angina. There was no association between medicine quality and ownership, size or location of the facilities. ConclusionThe study shows that the standardized patient model can provide insights into multiple dimensions of care, thus helping to link primary care encounters with medicine quality. Furthermore, it makes it possible to obtain medicines from blinded sellers, thus minimizing the risk of obtaining biased samples.
机译:背景促进获得药物需要同时努力加强质量保证以产生持续影响。尽管在低收入和中等收入国家中已经记录了药品不合格和伪造的问题,但是很少有关于质量的可靠信息。目的本研究的目的是验证替代市场后的监视模型以补充现有模型。方法该研究使用标准化患者或神秘来访者(从当地社区招募并受过训练以冒充真实患者的人)在出现预定条件后收集药物样本。这些患者向肯尼亚内罗毕的42个盲区提供了四种标准化条件,从而导致166位患者与临床医生的互动,并在该机构或附近的零售药店分发了300种药品。因此,所获得的药物样品类似于将要提供给真实患者的药物样品。结果从300个样本中选择了60个样本,并送往肯尼亚国家质量控制实验室进行分析。其中有十种(17%)不符合专论规范(三种布洛芬,两种西替利嗪,两种阿莫西林/克拉维酸组合,以及一种用于泼尼松,沙丁胺醇和锌的组合)。十个失败的样本中有五个被不适当地给患有不稳定型心绞痛症状的患者开了处方。药品质量与设施的所有权,规模或位置之间没有关联。结论该研究表明,标准化的患者模型可以提供对医疗服务多个维度的见解,从而有助于将初级医疗服务与药物质量联系起来。此外,它有可能从盲目的卖家那里获得药品,从而将获得有偏见的样本的风险降到最低。

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