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美国肺动脉高压(PAH)给医保支付方和患者带来的经济负担。

The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients.

作者信息

Sikirica Mirko, Iorga Serban R, Bancroft Tim, Potash Jesse

机构信息

Value Evidence and Outcomes, GlaxoSmithKline, 2301 Renaissance Blvd, King of Prussia, PA, 19406, USA.

Health Economics and Outcomes Research, Optum, 12125 Technology Drive, Eden Prairie, MN, 55344, USA.

出版信息

BMC Health Serv Res. 2014 Dec 24;14:676. doi: 10.1186/s12913-014-0676-0.

Abstract

BACKGROUND

Pulmonary arterial hypertension (PAH) is a rare condition that can ultimately lead to right heart failure and death. In this study we estimated the health care costs and resource utilization associated with PAH in a large US managed care health plan.

METHODS

Subjects with claims-based evidence of PAH from 1/1/2004 to 6/30/2010 (identification period) were selected. To be included in the final PAH study sample, subjects were required to have ≥2 claims with a primary PH diagnosis; ≥2 claims with a PAH related-diagnosis (connective tissue diseases, congenital heart diseases, portal hypertension); and ≥1 claim with evidence of a PAH-indicated medication. The earliest date of a claim with evidence of PAH-indicated medication during the identification period was set as the index date. Health care costs and resource utilization were compared between an annualized baseline period and a 12 month follow-up period.

RESULTS

504 PAH subjects were selected for the final study cohort. Estimated average total health care costs were approximately 16% lower in the follow-up period compared to the baseline period (follow-up costs = $98,243 [SD = 110,615] vs. baseline costs = $116,681 [SD = 368,094], p < 0.001), but substantively high in each period relative to costs reported for other chronic diseases. Pharmacy costs were significantly higher in the follow-up period vs. the baseline period, ($38,514 [SD = 34,817] vs. $6,440 [SD = 12,186], p < 0.001) but medical costs were significantly lower in the follow-up vs. baseline ($59,729 [SD = 106,683] vs. $110,241 [SD = 368,725], p < 0.001). These costs were mirrored in health-care resource utilization estimates. The average counts of ambulatory visits and inpatient stays were lower in the follow-up vs. the baseline (both p < 0.001). Results varied in exploratory analyses when less restrictive subject identification algorithms were used.

CONCLUSIONS

Subjects with evidence of PAH had substantively high health care costs. Medical costs appeared to decrease following PAH medication use, but with a concomitant increase in pharmacy costs.

摘要

背景

肺动脉高压(PAH)是一种罕见疾病,最终可导致右心衰竭和死亡。在本研究中,我们估算了美国一个大型管理式医疗保健计划中与PAH相关的医疗保健成本和资源利用情况。

方法

选取2004年1月1日至2010年6月30日(识别期)有基于索赔证据的PAH患者。要纳入最终的PAH研究样本,患者需有≥2次主要PH诊断的索赔;≥2次与PAH相关诊断(结缔组织病、先天性心脏病、门静脉高压)的索赔;以及≥1次有PAH指示药物证据的索赔。识别期内有PAH指示药物证据的最早索赔日期被设定为索引日期。比较了年化基线期和12个月随访期之间的医疗保健成本和资源利用情况。

结果

504名PAH患者被选入最终研究队列。与基线期相比,随访期估计的平均总医疗保健成本降低了约16%(随访成本 = 98,243美元[标准差 = 110,615],基线成本 = 116,681美元[标准差 = 368,094],p < 0.001),但相对于其他慢性病报告的成本,每个时期的成本都很高。随访期的药房成本显著高于基线期(38,514美元[标准差 = 34,817]对6,440美元[标准差 = 12,186],p < 0.001),但随访期的医疗成本显著低于基线期(59,729美元[标准差 = 106,683]对110,241美元[标准差 = 368,725],p < 0.001)。这些成本反映在医疗保健资源利用估计中。随访期的门诊就诊和住院次数平均计数低于基线期(均p < 0.001)。当使用限制较少的患者识别算法时,探索性分析结果有所不同。

结论

有PAH证据的患者医疗保健成本很高。使用PAH药物后医疗成本似乎下降,但药房成本随之增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1d5/4301626/e2be0b8f0bab/12913_2014_676_Fig1_HTML.jpg

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