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首页> 外文期刊>BMC Health Services Research >The development and appraisal of a tool designed to find patients harmed by falsely labelled, falsified (counterfeit) medicines
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The development and appraisal of a tool designed to find patients harmed by falsely labelled, falsified (counterfeit) medicines

机译:一种工具的开发和评估,该工具旨在发现被错误标签,伪造(假冒)药物伤害的患者

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Background Falsely labelled, falsified (counterfeit) medicines (FFCm’s) are produced or distributed illegally and can harm patients. Although the occurrence of FFCm’s is increasing in Europe, harm is rarely reported. The European Directorate for the Quality of Medicines & Health-Care (EDQM) has therefore coordinated the development and validation of a screening tool. Methods The tool consists of a questionnaire referring to a watch-list of FFCm’s identified in Europe, including symptoms of their use and individual risk factors, and a scoring form. To refine the questionnaire and reference method, a pilot-study was performed in 105 self-reported users of watch-list medicines. Subsequently, the tool was validated under “real-life conditions” in 371 patients in 5 ambulatory and in-patient care sites (“sub-studies”). The physicians participating in the study scored the patients and classified their risk of harm as “unlikely” or “probable” (cut-off level: presence of ≥2 of 5 risk factors). They assessed all medical records retrospectively (independent reference method) to validate the risk classification and documented their perception of the tool’s value. Results In 3 ambulatory care sites (180 patients), the tool correctly classified 5 patients as harmed by FFCm’s. The positive and negative likelihood ratios (LR+/LR-) and the discrimination power were calculated for two cut-off levels: a) 1 site (50 patients): presence of two risk factors (at 10% estimated health care system contamination with FFCm’s): LR?+?4.9/LR-0, post-test probability: 35%; b) 2 sites (130 patients): presence of three risk factors (at 5% estimated prevalence of use of non-prescribed medicines (FFCm’s) by certain risk groups): LR?+?9.7/LR-0, post-test probability: 33%. In 2 in-patient care sites (191 patients), no patient was confirmed as harmed by FFCm’s. The physicians perceived the tool as valuable for finding harm, and as an information source regarding risk factors. Conclusions This “decision aid” is a systematic tool which helps find in medical practice patients harmed by FFCm’s. This study supports its value in ambulatory care in regions with health care system contamination and in certain risk groups. The establishment of systematic communication between authorities and the medical community concerning FFCm’s, current patterns of use and case reports may sustain positive public health impacts.
机译:背景带有非法标签,伪造(假冒)药品(FFCm)的产品是非法生产或散布的,可能伤害患者。尽管在欧洲,FFCm的发生率正在上升,但危害却鲜有报道。因此,欧洲药品和保健质量局(EDQM)协调了筛查工具的开发和验证。方法该工具由一份问卷调查表和一个评分表组成,该问卷调查表涉及在欧洲确定的FFCm监视清单,包括其使用症状和个人危险因素。为了完善调查表和参考方法,对105名自我报告的观察名单药物使用者进行了一项试点研究。随后,该工具在5个门诊和住院治疗地点的371名患者的“真实条件”下进行了验证(“子研究”)。参与研究的医生对患者进行了评分,并将其受到伤害的风险分类为“不太可能”或“可能”(临界值:存在5种危险因素中的≥2)。他们对所有病历进行了回顾性评估(独立参考方法),以验证风险分类并记录他们对工具价值的看法。结果在3个门诊护理场所(180位患者)中,该工具正确地将5位患者归类为FFCm伤害。计算两个截断水平的阳性和阴性似然比(LR + / LR-)和判别力:a)1个部位(50例患者):存在两个危险因素(估计的FFCm污染了10%的卫生保健系统污染) ):LR≥4.9/ LR-0,测试后概率:35%; b)2个部位(130例患者):存在三个危险因素(某些危险人群估计使用非处方药(FFCm's的估计患病率为5%)):LR≥9.7/ LR-0,测后概率:33%。在2个住院护理场所(191名患者)中,没有患者被证实受到FFCm的伤害。医师认为该工具对于发现危害非常有价值,并且是有关危险因素的信息来源。结论该“决策辅助工具”是系统的工具,可帮助在医疗实践中发现受到FFCm伤害的患者。这项研究支持其在医疗系统受到污染的地区以及某些风险人群中在非卧床护理中的价值。当局与医学界之间就FFCm的使用,当前使用方式和病例报告建立系统的沟通,可能会维持对公共健康的积极影响。

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