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The good the bad and the ugly of medication coverage: Is altering a diagnosis to ensure medication coverage ethical?

机译:药物覆盖的好坏和丑陋:是否正在更改诊断以确保药物覆盖符合伦理?

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摘要

Recently, a patient presented to the dermatology clinic suffering from disabling, recurrent palmoplantar vesicles and pustules. Biopsy demonstrated nondiagnostic histologic findings without unequivocal evidence for psoriasis. The localized rash was recalcitrant to a host of standard therapies. An anti-tumor necrosis factor biologic was considered, and experience suggested that this expensive medication would only be approved for coverage if a diagnosis was submitted for a Food and Drug Administration–approved indication as psoriasis. All health-care providers face similar dilemmas in caring for their own patients. To whom is the physician’s primary responsibility when what is best for the patient may not align with the realities of our health-care system? Should a physician alter or exaggerate a medical diagnosis to obtain insurance coverage for a needed medication? What are the ethical implications of this action? If the physician’s fiduciary duty to the patient had no limits, there would be multiple potential consequences including compromise of the health-care provider’s integrity and relationships with patients, other providers, and third-party payers as well as the risk to an individual patient’s health and creation of injustices within the health-care system.
机译:近来,一位到皮肤科诊所就诊的患者患有残疾,复发性掌足囊泡和脓疱。活检显示无诊断性组织学发现,没有明确的银屑病证据。局部皮疹对许多标准疗法都是顽固的。考虑了一种抗肿瘤坏死因子的生物制剂,经验表明,这种昂贵的药物只有在获得美国食品药品监督管理局批准的银屑病适应症诊断后才能批准。所有医疗服务提供者在照顾自己的患者时都面临着类似的难题。当对患者最有利的事情可能与我们的医疗体系不符时,医师的主要责任是谁?医生是否应该改变或夸大医学诊断以获得所需药物的保险?此动作的伦理含义是什么?如果医师对患者的信托义务不受限制,则将产生多种潜在后果,包括损害医疗服务提供者的诚信以及与患者,其他提供者和第三方付款人的关系以及对单个患者健康的风险以及在卫生保健系统内造成不公正现象。

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