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《平价医疗法案》之后早期肿瘤学临床试验的保险审批

Insurance Clearance for Early-Phase Oncology Clinical Trials Following the Affordable Care Act.

作者信息

Kehl Kenneth L, Fullmer Cheryl P, Fu Siqing, George Goldy C, Hess Kenneth R, Janku Filip, Karp Daniel D, Kato Shumei, Kizer Cynthia K, Kurzrock Razelle, Naing Aung, Pant Shubham, Piha-Paul Sarina A, Subbiah Vivek, Tsimberidou Apostolia M, Hong David S

机构信息

Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

出版信息

Clin Cancer Res. 2017 Aug 1;23(15):4155-4162. doi: 10.1158/1078-0432.CCR-16-3027. Epub 2017 Jul 20.

Abstract

The Affordable Care Act (ACA) required that private insurance plans allow clinical trial participation and cover standard-of-care costs, but the impact of this provision has not been well-characterized. We assessed rates of insurance clearance for trial participation within our large early-phase clinical trials program, before and after implementation of the requirement. We analyzed the departmental database for the Clinical Center for Targeted Therapy (CCTT) at MD Anderson Cancer Center (Houston, TX). Among patients referred for sponsored trials, we described rates of insurance clearance and prolonged time to clearance (at least 14 days) from July 2012 to June 2013 (baseline), July 2013-December 2013 (following CCTT staffing changes in July 2103), and January 2014-June 2015 (following implementation of the ACA). We used multivariable logistic regression models to compare rates across these time periods. We identified 2,404 referrals for insurance clearance. Among privately insured patients, insurance clearance rates were higher for those referred from January 2014 to June 2015 than for those referred from July 2012 to June 2013 (OR, 4.72; 95% CI, 2.96-7.51). There was no association between referral period and clearance rates for Medicare/Medicaid patients ( = 0.25). Referral from January 2014 to June 2015 was associated with lower rates of prolonged clearance among both privately insured (OR 0.57; 95% CI, 0.38-0.86) and Medicare/Medicaid patients (OR 0.39; 95% CI, 0.19-0.83). Within our large early-phase clinical trials program, insurance clearance rates among privately insured patients improved following implementation of the ACA's requirement for coverage of standard-of-care costs. .

摘要

《平价医疗法案》(ACA)要求私人保险计划允许患者参与临床试验并支付标准治疗费用,但这一规定的影响尚未得到充分描述。我们评估了在该要求实施前后,我们大型早期临床试验项目中试验参与的保险审批率。我们分析了德克萨斯州休斯顿市MD安德森癌症中心靶向治疗临床中心(CCTT)的部门数据库。在被转诊参加申办试验的患者中,我们描述了2012年7月至2013年6月(基线期)、2013年7月至2013年12月(2013年7月CCTT人员配置变化之后)以及2014年1月至2015年6月(ACA实施之后)的保险审批率和审批延长时间(至少14天)。我们使用多变量逻辑回归模型来比较这些时间段的比率。我们确定了2404例保险审批转诊病例。在私人投保患者中,2014年1月至2015年6月被转诊者的保险审批率高于2012年7月至2013年6月被转诊者(比值比,4.72;95%置信区间,2.96 - 7.51)。医疗保险/医疗补助患者的转诊期与审批率之间无关联(P = 0.25)。2014年1月至2015年6月的转诊与私人投保患者(比值比0.57;95%置信区间,0.38 - 0.86)和医疗保险/医疗补助患者(比值比0.39;95%置信区间,0.19 - 0.83)中延长审批率较低相关。在我们大型早期临床试验项目中,ACA关于标准治疗费用覆盖要求实施后,私人投保患者的保险审批率有所提高。

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Responsibility for costs associated with clinical trials.临床试验相关费用的责任。
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