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. 2019 May 1;36(1):39–46. doi: 10.36141/svdld.v36i1.7117

Table 1.

Baseline characteristics at the time of IPF diagnosis

Characteristics
Subjects 107
  Male 82
Age (yrs) 66.9±7.1
Smoking history
  Never smoke 25
  Current smoker 3
  Ex-smoker 69
  Pack-year 40.2±25.5
Surgical lung biopsy (Yes) 107
Familial interstitial lung diseases (Yes) 16
Blood tests (n=107)
  KL-6 (U/mL) 1147±826
  SP-D (ng/mL) 219±139
  LDH (U/L) 225±43
  CRP (mg/dL) 0.40±1.81
  PaO2 (Torr) 84.9±8.3
Pulmonary function (n=107)
  FVC (L) 2.82±0.79
  FVC %pred (%) 85.3±17.0
  FEV1/FVC (%) 79.0±6.5
  DLco %pred (%) 82.1±19.3
  DLco (mL/min/mm Hg) 14.8±3.9
6-minute walk test (n=95)
  Distance (meter) 458±82
  Minimum SpO2 (%) 91±4
Bronchoalveolar lavage fluid findings (n=81)
  Total cell count (×10^5) 2.07±1.55
  Macrophages (%) 78.2±18.0
  Lymphocytes (%) 16.9±16.8
  Neutrophils (%) 3.4±5.0
Eosinophils (%) 1.6±1.9

Data are presented as n or mean±standard deviation. Definition of abbreviations: IPF: idiopathic pulmonary fibrosis, KL-6: Krebs von den Lungen-6, SP-D: surfactant protein-D, LDH: lactate dehydrogenase, CRP: C-reactive protein, PaO2: partial pressure of oxygen in arterial blood, FVC: forced vital capacity, %pred: % predicted, FEV1: forced expiratory volume in 1 second, DLco: diffusion capacity of the lung for carbon monoxide, SpO2: arterial oxygen saturation measured by pulse oximetry.