Epidemiology, Health Care Resource Utilization, and Costs of Hemophilia A and B by Treatment Regimen: A Retrospective Analysis of German Claims Data from 2016 to 2021

被引:0
作者
Obermueller, Dominik [1 ]
Berger, Karin [2 ,3 ,4 ]
Klamroth, Robert [5 ]
Kleppisch, Maria [6 ]
Rauchensteiner, Stephan [6 ]
Ecke, Ines [6 ]
Hermann, Sandra [6 ]
Pawlowska-Phelan, Dorota [1 ]
Haeckl, Dennis [7 ]
Kisser, Agnes [6 ]
机构
[1] InGef Inst Angew Gesundheitsforsch Berlin GmbH, Berlin, Germany
[2] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Med 3, Munich, Germany
[3] Bavarian Canc Res Ctr BZKF, Munich, Germany
[4] German Canc Consortium DKTK, Partner Site Munich, Munich, Germany
[5] Vivantes Klinikum Friedrichshain, Klin Innere Med Angiol & Hamostaseol, Zentrum Gefassmed, Berlin, Germany
[6] Pfizer Pharm GmbH, Friedrichstr 110, D-10117 Berlin, Germany
[7] Wig2 GmbH, Leipzig, Saxony, Germany
来源
HAMOSTASEOLOGIE | 2025年
关键词
hemophilia A; hemophilia B; health care resource utilization; healthcare costs; Germany; PREVALENCE; BURDEN;
D O I
10.1055/a-2558-9886
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction In Germany, hemophilia patients with a severe bleeding phenotype receive lifelong prophylactic treatment with intravenous concentrated factor VIII (FVIII) or IX (FIX) to prevent bleeding events. To assess the economic value of emerging treatment options, studies describing the economic burden of hemophilia under the current standard of care in Germany are needed.<br /> Aim This study classified hemophilia A (HA) and B (HB) patients by treatment regimen in administrative claims data to examine the real-world economic burden of Hemophilia in Germany from 2016 to 2021.<br /> Methods Hemophilia patients were identified in InGef statutory health insurance claims data via ICD-10 codes D66 (HA) and D67 (HB) in combination with one or more claims for hemophilia-related medication. Each patient's factor regimen was classified as either indicative of a severe phenotype needing prophylaxis or a non-severe phenotype treated on demand using a classification threshold of 100,000 International Units (IU) FVIII/year (HA) and 80,000 IU FIX/year (HB). Health care resource utilization and cost outcomes were captured for each study year.Methods Hemophilia patients were identified in InGef statutory health insurance claims data via ICD-10 codes D66 (HA) and D67 (HB) in combination with one or more claims for hemophilia-related medication. Each patient's factor regimen was classified as either indicative of a severe phenotype needing prophylaxis or a non-severe phenotype treated on demand using a classification threshold of 100,000 International Units (IU) FVIII/year (HA) and 80,000 IU FIX/year (HB). Health care resource utilization and cost outcomes were captured for each study year.<br /> Results Male prevalence per 100,000 ranged from 6.39 to 7.81 (HA) and 1.26 to 1.89 (HB), with 43 to 53% (HA) and 40 to 56% (HB) categorized as severe. In 2021, mean (standard deviation [SD]) per-patient medication costs were <euro>321,987 (<euro>157,915) in the severe treatment group versus <euro>43,487 (<euro>92,821) in the non-severe group for HA and <euro>289,411 (<euro>132,400) versus <euro>19,253 (<euro>23,655) for HB.<br /> Conclusion The results demonstrate the high economic burden of severe HA and HB in Germany, driven by the need for continuous factor replacement therapy, and give an estimate of treatment costs based on a real-world therapy mix.
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页数:14
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