4.5 Article

Prognostic factors and causes of death in Korean patients with idiopathic pulmonary fibrosis

Journal

RESPIRATORY MEDICINE
Volume 100, Issue 3, Pages 451-457

Publisher

W B SAUNDERS CO LTD
DOI: 10.1016/j.rmed.2005.06.013

Keywords

interstitial lung disease; pulmonary fibrosis; survival; cause of death

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The purpose of this study was to investigate the prognostic factors at initial presentation and the causes of death in Korean patients with idiopathic pulmonary fibrosis (IPF), which might be different report wise, in comparison to the western countries. A retrospective review of 88 patients (mean 60.3 years, 69 mate) was carried out and they were diagnosed as IPF positive. After diagnosis, the survival rate was 57% and 41% for third and fifth year, respectively (mean follow-up 39.1 months). Mortality was closely correlated with severe dyspnea at presentation (Hazard Ratio [HR], 2.6 per grade; p = 0.015), lower initial forced vital capacity (HR, 1.7 per 10% predicted; p = 0.004) and lower initial diffusing capacity of the lung (HR, 1.5 per 10% predicted; p = 0.033). Treatment with specific drugs was ineffective against the survival when compared with symptomatic supportive care. Thirty-four patients (68%) died of worsened respiratory failure, seven (14%) died of infection and only one patient showed cardiovascular death. In conclusion, our study suggests that the severity of dyspnea and lung function tests at the time of diagnosis are the predictive factors for the survival of patients with IPF. In comparison to the reports from western countries, we observed that respiratory failure and pulmonary infection were more frequent causes of death, while cardiovascular death was rare in Korean patients with IPF. (c) 2005 Elsevier Ltd. All rights reserved.

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