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. 2019 Jul 4;19:120. doi: 10.1186/s12890-019-0868-9

Table 4.

Variables analyses for prediction of mortality in the study patients

Univariate Multivariate
Characteristics P HR 95% CI P HR 95% CI
Age < 0.001 1.035 1.018–1.052 0.034 1.022 1.002–1.044
Male/Female 0.011 1.563 1.106–2.210 0.945 0.976 0.493–1.934
Smoking history 0.032 1.463 1.034–2.071 0.110 1.758 0.879–3.513
Positive autoimmune Ab < 0.001 0.498 0.347–0.714 0.433 0.804 0.467–1.386
First line treatment 0.549
 Systemic corticosteroid 1
 Antifibrotics 1.417 0.453–4.432
Emphysema from HRCT 0.514 1.132 0.780–1.642
FVC (%) < 0.001 0.964 0.954–0.975 < 0.001 0.970 0.955–0.984
DLCO (%) < 0.001 0.978 0.969–0.988 0.051 0.988 0.976–1.000
ILD exacerbation (yes/no) 0.003 1.654 1.180–2.317 0.001 2.074 1.366–3.148
ILD type < 0.001 0.039
 IPF 1 1
 IPAF 0.008 0.470 0.269–0.821 0.047 0.436 0.192–0.990
 CTD-ILD < 0.001 0.235 0.135–0.410 0.026 0.401 0.179–0.898

Abbreviations: Ab antibody, CTD-ILD connective tissue disease-related interstitial lung disease, DLCO Diffusing capacity of the lungs for carbon monoxide, FVC forced vital capacity, HRCT high-resolution computed tomography scan, ILD interstitial lung disease, IPAF interstitial pneumonia with autoimmune features, IPF idiopathic pulmonary fibrosis