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《平价医疗法案》强制实施后癌症临床试验参与的保险拒赔情况。

Insurance denials for cancer clinical trial participation after the Affordable Care Act mandate.

作者信息

Mackay Christine B, Antonelli Kaitlyn R, Bruinooge Suanna S, Saint Onge Jarron M, Ellis Shellie D

机构信息

Department of Health Policy and Management, University of Kansas Medical Center, Fairway, Kansas.

University of Kansas Cancer Center, Fairway, Kansas.

出版信息

Cancer. 2017 Aug 1;123(15):2893-2900. doi: 10.1002/cncr.30689. Epub 2017 Mar 23.

Abstract

BACKGROUND

The Affordable Care Act (ACA) includes a mandate requiring most private health insurers to cover routine patient care costs for cancer clinical trial participation; however, the impact of this provision on cancer centers' efforts to accrue patients to clinical trials has not been well described.

METHODS

First, members of cancer research centers and community-based institutions (n = 252) were surveyed to assess the status of insurance denials, and then, a focused survey (n = 77) collected denial details. Univariate and multivariate analyses were used to examine associations between the receipt of denials and site characteristics.

RESULTS

Overall, 62.7% of the initial survey respondents reported at least 1 insurance denial during 2014. Sites using a precertification process were 3.04 times more likely to experience denials (95% confidence interval, 1.55-5.99; P ≤ .001), and similar rates of denials were reported from sites located in states with preexisting clinical trial coverage laws versus states without them (82.3% vs 85.1%; χ = 50.7; P ≤ .001). Among the focused survey sites, academic centers reported denials more often than community sites (71.4% vs 46.4%). The failure of plans to cover trial participation was cited as the most common reason provided for denials (n = 33 [80.5%]), with nearly 80% of sites (n = 61) not receiving a coverage response from the insurer within 72 hours.

CONCLUSIONS

Despite the ACA's mandate for most insurers to cover routine care costs for cancer clinical trial participation, denials and delays continue. Denials may continue because some insurers remain exempt from the law, or they may signal an implementation failure. Delays in coverage may affect patient participation in trials. Additional efforts to eliminate this barrier will be needed to achieve federal initiatives to double the pace of cancer research over the next 5 years. Future work should assess the law's effectiveness at the patient level to inform these efforts. Cancer 2017;123:2893-900. © 2017 American Cancer Society.

摘要

背景

《平价医疗法案》(ACA)包含一项强制要求,即大多数私人健康保险公司须承担癌症临床试验参与的常规患者护理费用;然而,这一规定对癌症中心招募患者参与临床试验的努力所产生的影响尚未得到充分描述。

方法

首先,对癌症研究中心和社区机构的成员(n = 252)进行调查,以评估保险拒付的情况,然后,进行一项针对性调查(n = 77)收集拒付细节。采用单因素和多因素分析来检验拒付的发生与机构特征之间的关联。

结果

总体而言,62.7%的初始调查受访者报告在2014年期间至少有1次保险拒付。采用预认证流程的机构经历拒付的可能性高出3.04倍(95%置信区间,1.55 - 5.99;P≤0.001),并且在已有临床试验覆盖法律的州与没有此类法律的州的机构,报告的拒付率相似(82.3%对85.1%;χ = 50.7;P≤0.001)。在针对性调查的机构中,学术中心报告拒付的情况比社区机构更频繁(71.4%对46.4%)。计划未能涵盖试验参与被列为拒付最常见的原因(n = 33 [80.5%]),近80%的机构(n = 61)在72小时内未收到保险公司的承保回复。

结论

尽管ACA强制要求大多数保险公司承担癌症临床试验参与的常规护理费用,但拒付和延误仍在继续。拒付可能持续存在,因为一些保险公司仍不受该法律约束,或者这可能表明实施失败。承保延误可能会影响患者参与试验。为实现未来5年将癌症研究速度提高一倍的联邦倡议,需要做出更多努力来消除这一障碍。未来的工作应在患者层面评估该法律的有效性,为这些努力提供信息。《癌症》2017年;123:2893 - 900。©2017美国癌症协会。

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