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Development of Korean Standardized Heart Failure Registry: Experience From Integration of KorAHF and KorHF III

Authors
 Kim, Eui-Soon  ;  Lee, Huijin  ;  Youn, Jong-Chan  ;  Yoo, Byung-Su  ;  Lee, Hae-Young  ;  Lee, Ju-Hee  ;  Cho, Dong-Hyuk  ;  Jung, Mi-Hyang  ;  Lee, Hye Sun  ;  Cho, Hyun-Jai 
Citation
 International Journal of Heart Failure, Vol.8(1) : 1-11, 2026-01 
Journal Title
International Journal of Heart Failure
ISSN
 2636-154X 
Issue Date
2026-01
Keywords
Data collection ; Heart failure ; Methods ; Registries ; Standards
Abstract
Heart failure (HF) prevalence and associated socio-economic costs have risen rapidly in Korea, creating urgent demand for a national, standardized prospective registry to support quality monitoring, outcome comparison, and real-world evidence. Standardized data definitions are essential for valid comparisons across studies and healthcare settings. We created a unified national HF cohort by integrating the two largest Korean registries, KorAHF (2011–2014; n=5,625) and KorHF III (2018–2023; n=7,351), yielding 12,976 hospitalized HF patients. Because heterogeneous variable definitions impeded direct comparisons, we implemented a harmonization pipeline across demographic, clinical, imaging, biomarker, therapeutic, and outcome domains, aligned with international standards and reinforced by systematic data quality checks. A multidisciplinary panel then conducted a structured decision process to produce the Korean HF Standard Dataset, a tiered and interoperable variable set spanning six domains: demographics, presentation at admission, in-hospital events and comorbidities, discharge status, outpatient follow-up, and readmission events. This integrated platform and standardized variables enable precise identification of HF patient phenotypes and prognostic factors, establishing an evidence-based foundation for disease management. This supports an analysis of temporal changes in treatment patterns and outcomes, generates data to inform future clinical practice guidelines, and provides a practical basis for planning large, continuous, prospective HF registries. Furthermore, it also facilitates pragmatic, registry-based randomized clinical trials and unmet-needs assessments that can guide national health policy. Establishing a foundation for future linkage with national health databases, this platform will allow for enhanced accuracy, comparability, and representativeness, powering quality improvement initiatives and population-level monitoring of Korea’s growing HF burden. © 2026. Korean Society of Heart Failure.
DOI
10.36628/ijhf.2025.0100
Appears in Collections:
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
Yonsei Authors
Lee, Hye Sun(이혜선) ORCID logo https://orcid.org/0000-0001-6328-6948
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/211720
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