Cough-specific Quality of Life Predicts Disease Progression Among Patients with Interstitial Lung Disease: Data from the Pulmonary Fibrosis Foundation Patient Registry

医学 特发性肺纤维化 间质性肺病 内科学 危险系数 比例危险模型 生活质量(医疗保健) 肺功能测试 优势比 人口 肺移植 肺纤维化
作者
Janet Lee,Emily White,Elizabeth Freiheit,Mary Beth Scholand,Mary E. Strek,Anna J. Podolanczuk,Nina M. Patel
出处
期刊:Chest [Elsevier]
标识
DOI:10.1016/j.chest.2022.03.025
摘要

Cough is a common symptom of interstitial lung disease (ILD) and negatively impacts health-related quality of life (QOL). Previous studies have shown that among patients with idiopathic pulmonary fibrosis, cough may predict progression of lung disease and perhaps even respiratory hospitalizations and mortality.Does cough-specific QOL predict disease progression, respiratory hospitalization, lung transplantation, and death among patients with ILD?We analyzed data from the Pulmonary Fibrosis Foundation Registry, which comprises a multicenter population of well-characterized patients with ILD. We first examined associations between patient factors and baseline scores on the Leicester Cough Questionnaire (LCQ), a cough-specific QOL tool, using a proportional odds model. Next, we examined associations between baseline LCQ scores and patient-centered clinical outcomes, as well as pulmonary function parameters, using a univariate and multivariate proportional hazards model that was adjusted for clinically relevant variables, including measures of disease severity.One thousand four hundred forty-seven patients with ILD were included in our study. In the multivariate proportional odds model, we found that the following patient factors were associated with worse cough-specific QOL: younger age, diagnosis of "other ILD," gastroesophageal reflux disease, and lower FVC % predicted. Multivariate Cox regression models, adjusting for several variables including baseline disease severity, showed that a 1-point decrease in LCQ score (indicating lower cough-specific QOL) was associated with a 6.5% higher risk of respiratory-related hospitalization (hazard ratio [HR], 1.065; 95% CI, 1.025-1.107), a 7.4% higher risk of death (HR, 1.074; 95% CI, 1.020-1.130), and an 8.7% higher risk of lung transplantation (HR, 1.087; 95% CI, 1.022-1.156).Among a large population of well-characterized patients with ILD, cough-specific QOL was associated independently with respiratory hospitalization, death, and lung transplantation.
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