重度抑郁症是一种常见的心理健康状况,影响着美国约1620万成年人和310万青少年。然而,在临床实践和研究环境中对抑郁症的测量和监测仍然缺乏一致性。该项目旨在开发一套与患者和临床医生相关的最低标准结果测量方法,可在抑郁症登记处和临床实践中收集。确定了29个抑郁症登记处和相关数据收集工作,并邀请他们提交结果措施。通过文献检索和质量措施的回顾确定了其他措施。代表临床医生的多利益攸关方小组;纳税人;政府机构;产业;医疗专业、卫生保健质量和患者倡导组织使用医疗保健研究和质量局支持的结果衡量框架对27种确定的措施进行了分类。 The panel identified 10 broadly relevant measures and harmonized definitions for these measures through in-person and virtual meetings. The harmonized measures represent a minimum set of outcomes that are relevant to clinicians and patients and appropriate for use in depression research and clinical practice. Routine and consistent collection of these measures in registries and other systems would support creation of a national research infrastructure to efficiently address new questions, improve patient management and outcomes, and facilitate care coordination.
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