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Real-World Eligibility and Cost-Effectiveness Analysis of Empagliflozin for Heart Failure in Korea

Authors
 Eui-Soon Kim  ;  Sun-Kyeong Park  ;  Jong-Chan Youn  ;  Hye Sun Lee  ;  Hae-Young Lee  ;  Hyun-Jai Cho  ;  Jin-Oh Choi  ;  Eun-Seok Jeon  ;  Sang Eun Lee  ;  Min-Seok Kim  ;  Jae-Joong Kim  ;  Kyung-Kuk Hwang  ;  Myeong-Chan Cho  ;  Shung Chull Chae  ;  Seok-Min Kang  ;  Jin Joo Park  ;  Dong-Ju Choi  ;  Byung-Su Yoo  ;  Jae Yeong Cho  ;  Kye Hun Kim  ;  Byung-Hee Oh  ;  Barry Greenberg  ;  Sang Hong Baek 
Citation
 JOURNAL OF KOREAN MEDICAL SCIENCE, Vol.39(1) : e8, 2024-01 
Journal Title
JOURNAL OF KOREAN MEDICAL SCIENCE
ISSN
 1011-8934 
Issue Date
2024-01
MeSH
Cost-Effectiveness Analysis ; Heart Failure* / drug therapy ; Humans ; Prospective Studies ; Republic of Korea ; Stroke Volume ; United States
Keywords
Cost-Effectiveness Analysis ; Drug Therapy ; Empagliflozin ; Heart Failure ; SGLT2 Inhibitors
Abstract
Background: The US Food and Drug Administration (FDA) and European Medicines Agency (EMA) approved empagliflozin for reducing cardiovascular mortality and heart failure (HF) hospitalization in patients with both HF with reduced ejection fraction (HFrEF) and HF with preserved ejection fraction (HFpEF). However, limited data are available on the generalizability of empagliflozin to clinical practice. Therefore, we evaluated real-world eligibility and potential cost-effectiveness based on a nationwide prospective HF registry.

Methods: A total of 3,108 HFrEF and 2,070 HFpEF patients from the Korean Acute Heart Failure (KorAHF) registry were analyzed. Eligibility was estimated by inclusion and exclusion criteria of EMPagliflozin outcomE tRial in Patients With chrOnic heaRt Failure With Reduced Ejection Fraction (EMPEROR-Reduced) and EMPagliflozin outcomE tRial in Patients With chrOnic heaRt Failure With Preserved Ejection Fraction (EMPEROR-Preserved) trials and by FDA & EMA label criteria. The cost-utility analysis was done using a Markov model to project the lifetime medical cost and quality-adjusted life year (QALY).

Results: Among the KorAHF patients, 91.4% met FDA & EMA label criteria, while 44.7% met the clinical trial criteria. The incremental cost-effectiveness ratio of empagliflozin was calculated at US$6,764 per QALY in the overall population, which is far below a threshold of US$18,182 per QALY. The cost-effectiveness benefit was more evident in patients with HFrEF (US$5,012 per QALY) than HFpEF (US$8,971 per QALY).

Conclusion: There is a large discrepancy in real-world eligibility for empagliflozin between FDA & EMA labels and clinical trial criteria. Empagliflozin is cost-effective in HF patients regardless of ejection fraction in South Korea health care setting. The efficacy and safety of empagliflozin in real-world HF patients should be further investigated for a broader range of clinical applications.
Files in This Item:
T202403153.pdf Download
DOI
10.3346/jkms.2024.39.e8
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
Yonsei Authors
Kang, Seok Min(강석민) ORCID logo https://orcid.org/0000-0001-9856-9227
Lee, Hye Sun(이혜선) ORCID logo https://orcid.org/0000-0001-6328-6948
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/199777
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