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人工耳蜗植入适应症:第三方支付方关于标准适应症和扩展适应症政策的综述

Cochlear implant indications: a review of third-party payers' policies for standard and expanded indications.

作者信息

Moses Lindsey E, Friedmann David R

机构信息

Department of Otolaryngology - Head & Neck Surgery, New York University Langone Health, 550 First Avenue, Skirball Suite 7Q, New York, NY 10016, USA.

出版信息

Cochlear Implants Int. 2021 Jul;22(4):237-244. doi: 10.1080/14670100.2021.1877865. Epub 2021 Jan 28.

Abstract

As cochlear implant (CI) candidacy has expanded, commercial payers in the United States have varied in their adoption of new indications, potentially confusing providers' knowledge about appropriate patients for referral. We reviewed how third-party payers classify the medical necessity of cochlear implants for a variety of indications across the lifespan.We compared policies of the six largest commercial payers in our region, focusing on clinical scenarios for which many centers experience difficulty obtaining pre-authorization. These include: (1) CI in children under 12 months, (2) audiometric and speech perception criteria in children, (3) sequential bilateral CI, (4) electro-acoustic stimulation, (5) impending cochlear ossification, and (6) single-sided deafness (SSD).Of the more notable findings for the clinical scenarios half of commercial payers have a pediatric age requirement of greater than 12 months. Generally, audiologic and speech perception criteria are more stringent for children than adults across all policies. SSD is considered investigational by most policies.Third-party payers employ variable criteria regarding the medical necessity of CI, many of which are not contemporaneous with clinical knowledge and best practices. This may impact referral patterns among audiologists. More methodologically rigorous clinical trials may help shift such restrictive policies to benefit a greater number of patients.

摘要

随着人工耳蜗(CI)适用症范围的扩大,美国的商业医保支付方在采用新适应症方面存在差异,这可能会让医疗服务提供者对合适的转诊患者的了解产生困惑。我们回顾了第三方支付方如何对不同年龄段人工耳蜗植入的医疗必要性进行分类。我们比较了本地区六大商业医保支付方的政策,重点关注许多中心在获得预授权方面存在困难的临床情况。这些情况包括:(1)12个月以下儿童的人工耳蜗植入;(2)儿童的听力测定和言语感知标准;(3)序贯双侧人工耳蜗植入;(4)电声刺激;(5)即将发生的耳蜗骨化;(6)单侧耳聋(SSD)。在这些临床情况中,比较显著的发现是,一半的商业医保支付方对儿童的年龄要求大于12个月。一般来说,在所有政策中,儿童的听力学和言语感知标准都比成人更为严格。大多数政策将单侧耳聋视为试验性治疗。第三方支付方在人工耳蜗植入医疗必要性方面采用的标准各不相同,其中许多标准与临床知识和最佳实践并不同步。这可能会影响听力学家的转诊模式。方法学上更严谨的临床试验可能有助于改变这种限制性政策,使更多患者受益。

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