从底层提取药物:在停止使用抗疟疾药物金尼丁时的伦理考虑
Joshua F Craft1, John J Openshaw2, Priya M Travassos3
1Division of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
伊利利利公司停止了关键的疟疾药物金尼丁的生产,这影响了患者的护理,并引发了伦理方面的担忧. 这凸显了需要更好的监督,以确保获得基本药物和道德医疗保健的提供.
科学领域:
- 医药伦理学 医药伦理学
- 医疗保健政策 医疗保健政策
- 制造业 制造业 制造业 制造业 制造业
背景情况:
- 伊利利利在2017年停止了胺的生产,取消了美国FDA批准的唯一一种针对严重疟疾的治疗方法.
- 这种停药为患者和提供者创造了关键的访问问题,延迟了拯救生命的治疗.
研究的目的:
- 检查制药公司决定停止使用一种必需药物的伦理影响.
- 为了调查医疗保健系统监督的缺乏如何允许企业行为损害患者护理伦理.
- 提出干预措施,以保护伦理的病人护理免受未来的利益冲突.
主要方法:
- 对Eli Lilly公司停止生产胺的伦理影响的分析.
- 检查医疗保健系统的问责制和监督机制.
- 审查潜在的干预措施,以确保获得基本药物的机会.
主要成果:
- 伊利莉莉公司停止生产胺,通过限制获得医疗标准来破坏道德医疗服务.
- 该案揭示了问责制和监督方面的系统性弱点,允许企业利益凌驾于患者福利之上.
- 现有的医疗保健结构未能防止对患者护理的负面影响.
结论:
- 需要紧急,协作和可执行的机制来优先考虑道德患者护理.
- 拟议的干预措施包括修订的生产协议,对必要疗法的加速批准,以及咨询机构.
- 需要采取积极的战略,以防止这种在药品供应链中的伦理违规事件再次发生.
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