Abstract

BackgroundSeveral major ESRD-related regulatory and reimbursement changes were introduced in the United States in 2011. In several large, national datasets, these changes have been associated with decreases in erythropoiesis stimulating agent (ESA) utilization and hemoglobin concentrations in the ESRD population, as well as an increase in the use of red blood cell (RBC) transfusions in this population. Our objective was to examine the use of RBC transfusion before and after the regulatory and reimbursement changes implemented in 2011 in a prevalent population of chronic dialysis patients in a large national claims database.MethodsPatients in the Truven Health MarketScan Commercial and Medicare Databases with evidence of chronic dialysis were selected for the study. The proportion of chronic dialysis patients who received any RBC transfusion and RBC transfusion event rates per 100 patient-months were calculated in each month from January 1, 2007 to March 31, 2012. The results were analyzed overall and stratified by primary health insurance payer (commercial payer or Medicare).ResultsOverall, the percent of chronic dialysis patients with RBC transfusion and RBC transfusion event rates per 100 patient-months increased between January 2007 and March 2012. When stratified by primary health insurance payer, it appears that the increase was driven by the primary Medicare insurance population. While the percent of patients with RBC transfusion and RBC transfusion event rates did not increase in the commercially insured population between 2007 and 2012 they did increase in the primary Medicare insurance population; the majority of the increase occurred in 2011 during the same time frame as the ESRD-related regulatory and reimbursement changes.ConclusionsThe regulatory and reimbursement changes implemented in 2011 may have contributed to an increase in the use of RBC transfusions in chronic dialysis patients in the MarketScan dataset who were covered by Medicare plus Medicare supplemental insurance.

Highlights

  • Several major end-stage renal disease (ESRD)-related regulatory and reimbursement changes were introduced in the United States in 2011

  • The primary registration trials used for the approval of epoetin alfa demonstrated correction of anemia and virtual elimination of transfusions (>90% reduction) in patients treated with erythropoiesis stimulating agent (ESA) to a mean hemoglobin (Hb) of 11.7 g/dL [7]

  • After application of the remaining criteria for inclusion in the base-case analysis, there were 42,790 individuals who qualified as chronic dialysis patients

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Summary

Introduction

Several major ESRD-related regulatory and reimbursement changes were introduced in the United States in 2011. National datasets, these changes have been associated with decreases in erythropoiesis stimulating agent (ESA) utilization and hemoglobin concentrations in the ESRD population, as well as an increase in the use of red blood cell (RBC) transfusions in this population. Our objective was to examine the use of RBC transfusion before and after the regulatory and reimbursement changes implemented in 2011 in a prevalent population of chronic dialysis patients in a large national claims database. As of the end of 2010, the total treated end-stage renal disease (ESRD) population reached 594,374 patients in the United States [1]. Within this population, approximately 70% were treated with dialysis [1]. From 1992 to 2000, the mean population Hb in prevalent dialysis patients rose from about 9.8 to 11.2 g/dL while the overall transfusion rate was halved [8]

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