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为阿尔茨海默病的诊断和治疗提供报销理由:寻求证据的一致性。

Justifying reimbursement for Alzheimer's diagnostics and treatments: Seeking alignment on evidence.

机构信息

Center for Alzheimer's Care, Imaging and Research, Department of Neurology, University of Utah, Salt Lake City, UT, USA.

AstraZeneca, Boston, MA, USA.

出版信息

Alzheimers Dement. 2014 Jul;10(4):503-508. doi: 10.1016/j.jalz.2014.05.003.

Abstract

The increasing cost of health care combined with expensive new drugs and diagnostics is leading to more frequent gaps between regulatory and subsequent reimbursement approval decisions. As a result, persons with Alzheimer's disease may have difficulty accessing the benefit of medical advances. In contrast to the long history and established structure for drug approval, payer decision making is dispersed, not standardized, and perspectives on necessary evidence and the evaluation of this evidence differ and are often poorly defined. Particularly challenging is how to demonstrate the value of drugs and diagnostics for patients who do not yet have significant functional decline. Although discussions to develop consensus continue, clinical trials should begin to incorporate health system and patient-oriented outcomes. In some situations, additional studies designed to demonstrate value and comparative effectiveness will be needed. Such studies should examine outcomes of representative populations in community settings. To assure scientific advances in diagnosis and treatment benefit in patients, developing evidence to support reimbursement will become as important as obtaining regulatory approval.

摘要

医疗保健成本的不断增加,加上昂贵的新药和诊断技术,导致监管和后续报销审批决策之间的差距越来越大。因此,阿尔茨海默病患者可能难以受益于医学的进步。与药物批准的悠久历史和既定结构相比,支付者的决策分散,不标准化,对必要证据的看法以及对这些证据的评估也存在差异,而且往往定义不明确。特别具有挑战性的是如何为尚未出现明显功能下降的患者证明药物和诊断的价值。尽管继续进行达成共识的讨论,但临床试验应开始纳入以卫生系统和患者为导向的结果。在某些情况下,可能需要进行额外的研究以证明药物和诊断的价值和比较效果。此类研究应在社区环境中检查具有代表性人群的结果。为确保诊断和治疗方面的科学进步使患者受益,制定支持报销的证据将与获得监管批准同样重要。

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