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Epidemiology of PAH in Korea: An Analysis of the National Health Insurance Data, 2002-2018

  • Albert Youngwoo Jang (Gachon Cardiovascular Research Institute, Gachon University) ;
  • Hyeok-Hee Lee (Department of Preventive Medicine, Yonsei University College of Medicine) ;
  • Hokyou Lee (Department of Preventive Medicine, Yonsei University College of Medicine) ;
  • Hyeon Chang Kim (Department of Preventive Medicine, Yonsei University College of Medicine) ;
  • Wook-Jin Chung (Gachon Cardiovascular Research Institute, Gachon University)
  • Received : 2022.08.25
  • Accepted : 2023.01.18
  • Published : 2023.05.01

Abstract

Background and Objectives: Pulmonary arterial hypertension (PAH) is a rare but fatal disease. Recent advances in PAH-specific drugs have improved its outcomes, although the healthcare burden of novel therapeutics may lead to a discrepancy in outcomes between developing and developed countries. We analyzed how the epidemiology and clinical features of PAH has changed through the rapidly advancing healthcare infrastructure in South Korea. Methods: PAH was defined according to a newly devised 3-component algorithm. Using a nationwide health insurance claims database, we delineated annual trends in the prevalence, incidence, medication prescription pattern, and 5-year survival of PAH in Korea. Cumulative survival and potential predictors of mortality were also assessed among 2,151 incident PAH cases. Results: Between 2002 or 2004 and 2018, the prevalence and incidence of PAH increased 75-fold (0.4 to 29.9 per million people) and 12-fold (0.5 to 6.3 per million person-years), respectively. The proportion of patients on combination PAH-specific drug therapy has also steadily increased up to 29.0% in 2018. Among 2,151 incident PAH cases (median [interquartile range] age, 50 [37-62] years; 67.2% female), the 5-year survival rate and median survival duration were 71.8% and 13.1 years, respectively. Independent predictors of mortality were age, sex, etiology of PAH, diabetes, dyslipidemia, and chronic kidney disease. Conclusions: This nationwide study delineated that the prevalence and incidence of PAH have grown rapidly in Korea since the early 2000s. The use of combination therapy has also increased, and the 5-year survival rate of PAH in Korea was similar to those in western countries.

Keywords

Acknowledgement

This work was supported by the Korean Society of Cardiology (2020); the Korea Disease Control and Prevention Agency (grant numbers 2021-ER0902-00, 2021-ER0902-01, 2021-ER0902-02, 2018-ER6304-00, 2018-ER6304-01, 2018-ER6304-02); Gachon University (grant number 202209630001); Gachon University Gil Medical Center (grant number FRD2020-11, grant number FRD2022-05); the Korea Medical Device Development Fund (grant numbers 9991006834, KMDF_PR_20200901_0164, 9991007387, KMDF_PR_20200901_0170) funded by the Korean government (the Ministry of Science and ICT, the Ministry of Trade, Industry and Energy, the Ministry of Health and Welfare, the Ministry of Food and Drug Safety); the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (No. NRF-2021R1A5A2030333); The Korean Cardiac Research Foundation (grant number 202103-03); and Asia-pacific Cardiometabolic Society (grant number: 2021-06).

References

  1. Jang AY, Chung WJ. Current status of pulmonary arterial hypertension in Korea. Korean J Intern Med 2019;34:696-707.
  2. Oh S, Jung JH, Ahn KJ, et al. Stem cell and exosome therapy in pulmonary hypertension. Korean Circ J 2022;52:110-22.
  3. Gillmeyer KR, Lee MM, Link AP, Klings ES, Rinne ST, Wiener RS. Accuracy of algorithms to identify pulmonary arterial hypertension in administrative data: a systematic review. Chest 2019;155:680-8.
  4. Ahn KJ, Jang AY, Park SJ, Chung WJ. 15 years journey of idiopathic pulmonary arterial hypertension with BMPR2 mutation. Clin Hypertens 2019;25:22.
  5. Choi EK. Cardiovascular research using the Korean National Health Information Database. Korean Circ J 2020;50:754-72.
  6. Lee HY, Lee SW, Kim HC, Ihm SH, Park SH, Kim TH. Cost-effectiveness analysis of hypertension screening in the Korea National Health Screening Program. Korean Circ J 2021;51:610-22.
  7. Kim HC, Cho SM, Lee H, et al. Korea hypertension fact sheet 2020: analysis of nationwide populationbased data. Clin Hypertens 2021;27:8.
  8. Ko SH, Han K, Lee YH, et al. Past and current status of adult type 2 diabetes mellitus management in Korea: a national health insurance service database analysis. Diabetes Metab J 2018;42:93-100.
  9. Cho SM, Lee H, Lee HH, et al. Dyslipidemia fact sheets in Korea 2020: an analysis of nationwide population-based data. J Lipid Atheroscler 2021;10:202-9.
  10. Gall H, Felix JF, Schneck FK, et al. The giessen pulmonary hypertension registry: survival in pulmonary hypertension subgroups. J Heart Lung Transplant 2017;36:957-67.
  11. Wijeratne DT, Lajkosz K, Brogly SB, et al. increasing incidence and prevalence of World Health Organization groups 1 to 4 pulmonary hypertension: a population-based cohort study in Ontario, Canada. Circ Cardiovasc Qual Outcomes 2018;11:e003973.
  12. Anand V, Roy SS, Archer SL, et al. Trends and outcomes of pulmonary arterial hypertension-related hospitalizations in the United States: analysis of the nationwide inpatient sample database from 2001 through 2012. JAMA Cardiol 2016;1:1021-9.
  13. Lim SS, Lee W, Kim YK, et al. The cumulative incidence and trends of rare diseases in South Korea: a nationwide study of the administrative data from the National Health Insurance Service database from 2011-2015. Orphanet J Rare Dis 2019;14:49.
  14. Mayeux JD, Pan IZ, Dechand J, et al. Management of pulmonary arterial hypertension. Curr Cardiovasc Risk Rep 2021;15:2.
  15. Chung WJ, Park YB, Jeon CH, et al. Baseline characteristics of the Korean registry of pulmonary arterial hypertension. J Korean Med Sci 2015;30:1429-38.
  16. Greiner S, Jud A, Aurich M, et al. Reliability of noninvasive assessment of systolic pulmonary artery pressure by Doppler echocardiography compared to right heart catheterization: analysis in a large patient population. J Am Heart Assoc 2014;3:3.
  17. Song S, Lee SE, Oh SK, et al. Demographics, treatment trends, and survival rate in incident pulmonary artery hypertension in Korea: a nationwide study based on the health insurance review and assessment service database. PLoS One 2018;13:e0209148.
  18. D'Alonzo GE, Barst RJ, Ayres SM, et al. Survival in patients with primary pulmonary hypertension. Results from a national prospective registry. Ann Intern Med 1991;115:343-9.
  19. Farber HW, Miller DP, Poms AD, et al. Five-year outcomes of patients enrolled in the REVEAL registry. Chest 2015;148:1043-54.
  20. Hoeper MM, Kramer T, Pan Z, et al. Mortality in pulmonary arterial hypertension: prediction by the 2015 European pulmonary hypertension guidelines risk stratification model. Eur Respir J 2017;50:1700740.
  21. Jing ZC, Xu XQ, Han ZY, et al. Registry and survival study in chinese patients with idiopathic and familial pulmonary arterial hypertension. Chest 2007;132:373-9.
  22. Zeng WJ, Sun YJ, Gu Q, Xiong CM, Li JJ, He JG. The impact of pulmonary arterial hypertension-targeted therapy on survival in Chinese patients with idiopathic pulmonary arterial hypertension. Pulm Circ 2012;2:373-8.
  23. Kozu K, Sugimura K, Ito M, et al. Current status of long-term prognosis among all subtypes of pulmonary hypertension in Japan. Int J Cardiol 2020;300:228-35.
  24. Chang WT, Weng SF, Hsu CH, et al. Prognostic factors in patients with pulmonary hypertension-a nationwide cohort study. J Am Heart Assoc 2016;5:e003579.
  25. Fukuda K, Date H, Doi S, et al. Guidelines for the treatment of pulmonary hypertension (JCS 2017/JPCPHS 2017). Circ J 2019;83:842-945.
  26. Klinger JR, Elliott CG, Levine DJ, et al. Therapy for pulmonary arterial hypertension in adults: update of the CHEST guideline and expert panel report. Chest 2019;155:565-86.
  27. Jang AY, Kim BG, Kwon S, et al. Prevalence and clinical features of bone morphogenetic protein receptor type 2 mutation in Korean idiopathic pulmonary arterial hypertension patients: the PILGRIM explorative cohort. PLoS One 2020;15:e0238698.
  28. Jang AY, Kim S, Park SJ, et al. A Nationwide multicenter registry and biobank program for deep phenotyping of idiopathic and hereditary pulmonary arterial hypertension in Korea: the PAH platform for deep phenotyping in Korean subjects (PHOENIKS) cohort. Clin Hypertens 2019;25:21.
  29. Copher R, Cerulli A, Watkins A, Laura Monsalvo M. Treatment patterns and healthcare system burden of managed care patients with suspected pulmonary arterial hypertension in the United States. J Med Econ 2012;15:947-55.
  30. Papani R, Sharma G, Agarwal A, et al. Validation of claims-based algorithms for pulmonary arterial hypertension. Pulm Circ 2018;8:2045894018759246.