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A Retrospective Population-Based Survival Study of Idiopathic Pulmonary Arterial Hypertension in Korea

Shin Yi Jang, Eun Kyoung Kim, June Huh, Jinyoung Song, I‐Seok Kang, Seung Woo Park, Duk‐Kyung Kim, Sung‐A Chang

2022Journal of Korean Medical Science10 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Few studies used nationwide data to assess the survival rates (SRs) and death risk for idiopathic pulmonary arterial hypertension (IPAH; ICD-10 I27.0) in Korea. METHODS: IPAH data (N = 9,017; female:male = 6:4) were collected from the National Health Insurance Service in Korea, from 2006 through 2017. The data consisted of primary diagnoses related to IPAH. The Kaplan-Meier method and Cox proportional-hazards analyses were carried out. RESULTS: < 0.001). The one-, three-, five- and 10-year SRs for IPAH were 89.0%, 79.8%, 72.3% and 57.0%, respectively. The adjusted hazard ratio (HR) of IPAH was 1.81 (95% confidence interval [CI], 1.26-2.59) in 60-69 age group, 3.42 (95% CI, 2.40-4.87) in 70-79, and 7.73 (95% CI, 5.43-11.0) in 80s. Other risk factors were male, low-income status, diabetes, myocardial infarction, atrial fibrillation, ischemic stroke, hemorrhagic stroke, and malignant neoplasm. CONCLUSION: The 10-year SR of IPAH was 57% in Korea. The HR for IPAH was significantly high in patients with older age and other risk factors.

Topics & Concepts

MedicineRetrospective cohort studyPulmonary hypertensionPopulationInternal medicineCardiologyEnvironmental healthPulmonary Hypertension Research and TreatmentsChronic Obstructive Pulmonary Disease (COPD) ResearchInterstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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