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州自闭症保险强制令实施后的支出和服务使用变化。

Changes in spending and service use after a state autism insurance mandate.

机构信息

Johns Hopkins Bloomberg School of Public Health, USA.

出版信息

Autism. 2019 Jan;23(1):167-174. doi: 10.1177/1362361317728205. Epub 2017 Nov 10.

Abstract

Almost all states have insurance coverage mandates for childhood autism spectrum disorder treatment, yet little is known about how mandates affect spending and service use. We evaluated a 2011 Kansas law mandating comprehensive coverage of autism spectrum disorder treatments in the State Employee Health Plan. Data were extracted from the Kansas All-Payer Claims Database from 2009 to 2013 for enrollees of State Employee Health Plan and private health plans. The sample included children aged 0-18 years with >2 claims with an autism spectrum disorder diagnosis insured through State Employee Health Plan or a comparison group enrolled through private health plans. We estimated differences-in-differences regression models to compare trends among State Employee Health Plan to privately insured children. Average annual total spending on autism spectrum disorder services increased by US$912 (95% confidence interval: US$331-US$1492) and average annual out-of-pocket spending on autism spectrum disorder services increased by US$138 (95% confidence interval: US$53-US$223) among diagnosed children in the State Employee Health Plan relative to the comparison group following the mandate, representing 92% and 75% increases over baseline total and out-of-pocket autism spectrum disorder spending, respectively. Average annual quantity of outpatient autism spectrum disorder services increased by 15.0 services (95% confidence interval: 8.4-21.6) among children in the State Employee Health Plan, more than doubling the baseline average. Implementation of a comprehensive autism spectrum disorder mandate in the Kansas State Employee Health Plan was associated with substantial increases in service use and spending for autism spectrum disorder treatment among autism spectrum disorder-diagnosed children.

摘要

几乎所有州都对儿童自闭症谱系障碍的治疗制定了保险覆盖要求,但对于这些要求如何影响支出和服务使用,我们知之甚少。我们评估了堪萨斯州 2011 年的一项法律,该法律要求堪萨斯州员工健康计划全面涵盖自闭症谱系障碍的治疗。数据来自堪萨斯州全付费索赔数据库,时间范围为 2009 年至 2013 年,涵盖了州员工健康计划和私人健康计划的参保人。样本包括年龄在 0-18 岁之间、有>2 次自闭症谱系障碍诊断索赔且通过州员工健康计划或私人健康计划参保的儿童。我们采用差分模型评估了州员工健康计划与私人保险儿童之间的趋势差异。在该命令颁布后,州员工健康计划中被诊断为自闭症谱系障碍的儿童的自闭症谱系障碍服务的平均年总支出增加了 912 美元(95%置信区间:331 美元-1492 美元),自付费用增加了 138 美元(95%置信区间:53 美元-223 美元),与对照组相比,这分别代表自闭症谱系障碍总支出和自付支出分别比基线增加了 92%和 75%。州员工健康计划中自闭症谱系障碍儿童的门诊自闭症谱系障碍服务平均年用量增加了 15.0 次(95%置信区间:8.4-21.6),比基线平均水平增加了一倍多。在堪萨斯州员工健康计划中实施全面的自闭症谱系障碍要求,与自闭症谱系障碍诊断儿童的自闭症谱系障碍治疗服务使用和支出的大幅增加有关。

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