Table 1

Baseline characteristics of the 81 randomised patients according to treatment assignment

CharacteristicEtanercept (N=41)Prednisone (N=40)
Age, mean (SD)69.0 (8.6)65.1 (9.7)
Women, n (%)13 (31.7%)17 (42.5%)
White race (%)97.6100
BMI (kg/m2), mean (SD)26.6 (7.0)26.6 (7.3)
Current smoker (%)19.527.5
Pack-year history, mean (SD)50.0 (29.0)45.7 (27.6)
Years of chronic dyspnea, mean (SD)11.2 (7.9)13.0 (11.5)
Presenting symptoms (%)
 Increased dyspnoea95.090.0
 Increased cough82.987.5
 Increased sputum volume82.975.0
 Increased sputum purulence70.775.0
 Admitted to hospital for initial treatment of AECOPD, n (%)1 (2.4%)6 (15%)
Lung function at randomisation
 FEV1 (l), mean (SD)0.97 (0.50)0.90 (0.44)
 FEV1 (% predicted), mean (SD)35.7 (15.8)33.1 (11.6)
 FVC (l), mean (SD)2.42 (1.02)2.23 (0.97)
 FVC (% predicted), mean (SD)68.7 (21.6)64.6 (20.1)
 Baseline Dyspnoea Index score4.85 (2.47)4.75 (1.88)
Comorbid illnesses (%)
 Diabetes12.215.0
 Coronary artery disease12.227.5
 Congestive heart failure2.42.5
 Cancer7.75.0
Concomitant medications (%)
 Home oxygen14.615.4
 Long-acting anticholinergics90.287.2
 Inhaled steroid/long-acting β-agonist combination medication92.797.4
 Long-acting β-agonist7.30
 Inhaled steroid7.30
 Theophylline17.010.3
  • BMI, body mass index; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity.