Abstract

BackgroundPulmonary 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.MethodsSubjects 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.Results504 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.ConclusionsSubjects 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.Electronic supplementary materialThe online version of this article (doi:10.1186/s12913-014-0676-0) contains supplementary material, which is available to authorized users.

Highlights

  • Pulmonary arterial hypertension (PAH) is a rare condition that can lead to right heart failure and death

  • The objective of this study was to explore the health care costs and resource utilization associated with PAH in a large, national US managed care health plan using contemporary real-world data with a substantial time frame

  • In this study we investigated the health care costs and resource use associated with PAH using a large, national US managed care health plan database

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Summary

Introduction

Pulmonary arterial hypertension (PAH) is a rare condition that can lead to right heart failure and death. PAH is characterized by constriction of pulmonary arteries and an increase in pulmonary vascular resistance, leading to right heart failure [2]. As symptoms of PAH are similar to those of other diseases, diagnosis may be delayed until more advanced disease stage, when treatment is not as successful [14]. Surgical intervention, such as lung transplant or balloon atrial septostomy, may be needed for patients who are not adequately controlled with medication [4]

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