From the Division of Plastic and Reconstructive Surgery.
Lymphatic Education and Research Network.
Plast Reconstr Surg. 2023 Jul 1;152(1):222-234. doi: 10.1097/PRS.0000000000010239. Epub 2023 Jun 29.
This article describes the key stakeholders and process involved in developing an insurance policy in the United States to establish medical necessity criteria for lymphatic surgery procedures. Lymphedema is a chronic health issue that impacts over 1.2 million patients and is associated with lifelong health, economic, and psychosocial costs. Patients affected have been described as "medical nomads," as they often interface with multiple providers before receiving an accurate diagnosis and treatment. This underscores the lack of attention and understanding about this disease across all sectors of the medical system. Unlike nations including Sweden and the United Kingdom, which provide insurance coverage for treatment, the United States has lagged behind. As a country, we have neglected to fully recognize the consequences of inadequate treatment of lymphedema, including chronic morbidities such as loss of mobility, psychosocial sequelae, recurrent infections, and even death. Recently, the authors' lymphatic center had the unique opportunity to help develop a policy that merged their clinical experience, recently established lymphatic care center of excellence criteria, and third-party payer policy expertise. This experience spanned 1 year from June of 2018 to June of 2019. The authors identify how key partnerships helped fill evidentiary gaps that ultimately resulted in policy change.
本文介绍了在美国制定医疗保险政策以确立淋巴手术适应证的关键利益相关者和流程。淋巴水肿是一种影响超过 120 万患者的慢性健康问题,与终身健康、经济和心理社会成本相关。受影响的患者被描述为“医疗游牧民”,因为他们在获得准确诊断和治疗之前经常与多个提供者接触。这突显了医疗系统所有部门对这种疾病的关注和理解不足。与包括瑞典和英国在内的为治疗提供保险覆盖的国家不同,美国已经落后。作为一个国家,我们未能充分认识到淋巴水肿治疗不足的后果,包括行动不便、心理社会后遗症、反复感染,甚至死亡等慢性疾病。最近,作者的淋巴中心有机会帮助制定一项政策,该政策融合了他们的临床经验、最近确立的淋巴卓越护理中心标准以及第三方支付者政策专业知识。这一经验从 2018 年 6 月到 2019 年 6 月持续了 1 年。作者确定了关键合作伙伴关系如何帮助填补证据空白,最终导致政策的改变。