1. Prevalence of Pulmonary Arterial Hypertension in Korean Adult Patients with Systemic Sclerosis: Result of a Pilot Echocardiographic Screening Study
- Author
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In Seol Yoo, Jae-Hwan Lee, Seung Cheol Shim, Jae-Hyeong Park, Su-Jin Yoo, Yunseon Park, Jinhyun Kim, Seong Wook Kang, and Byung Joo Sun
- Subjects
Right heart catheterization ,medicine.medical_specialty ,Early detection ,030204 cardiovascular system & hematology ,Pulmonary arterial pressure ,Pulmonary arterial hypertension ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,polycyclic compounds ,Radiology, Nuclear Medicine and imaging ,skin and connective tissue diseases ,Screening study ,030203 arthritis & rheumatology ,Adult patients ,integumentary system ,business.industry ,University hospital ,Echocardiography ,Cardiology ,Screening ,Systemic sclerosis ,Original Article ,Cardiology and Cardiovascular Medicine ,business ,Pulmonary vasodilators - Abstract
BACKGROUND Pulmonary arterial hypertension (PAH) is a major cause of morbidity and mortality among patients with systemic sclerosis (SSc). Early detection and prompt treatment of PAH associated with SSc (SSc-PAH) result in better prognosis. We conducted echocardiographic study to presume the prevalence of PAH in Korean adult SSc patients and to diagnose SSc-PAH in their early stages with right heart catheterization (RHC). METHODS We performed free of charge echocardiographic study including 37 adult SSc patients at the Chungnam National University Hospital. The possibility of PAH is determined by the estimation of pulmonary arterial pressure by peak tricuspid regurgitation velocity of > 3.0 m/s. Patients with possible PAH were recommended to undergo RHC to confirm the diagnosis. RESULTS In 37 patients, 8 patients were suspected with PAH. Among them, 6 patients agreed to be examined with RHC, and 4 were confirmed with PAH. The prevalence of possible PAH was 21.6% (8 of 37 patients), and that of confirmed PAH was 10.8% (4 of 37 patients). Four patients who were confirmed with SSc-PAH through RHC have been treated with specific pulmonary vasodilators and maintained stable. CONCLUSION Eight patients (21.6%) were possible PAH and 4 (10.8%) were diagnosed as SSc-PAH by RHC after the echocardiographic screening study of 37 adult SSc patients.
- Published
- 2016