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Table 1 Patient demographics and characteristics (full analysis set)

From: Long-acting antimuscarinic therapy in patients with chronic obstructive pulmonary disease receiving beta-blockers

 

Beta-blocker users

(N = 1269)

Non-users

(N = 2320)

Patients

  

Age, years, mean (SD)

68.1 (7.9)

66.6 (8.6)

Male, %

64.4

55.5

White, %

90.6

90.7

BMI, kg/m2, mean (SD)

30.4 (6.7)

29.1 (6.8)

 Obese (≥ 30 kg/m2), n (%)

597 (47.0)

913 (39.4)

Current smoker, %

39.8

45.6

Prior CV events, %

67.9

36.7

Pre-BD FEV1 (mL), mean (SD)

1215 (486)

1213 (492)

Post-BD FEV1% predicted, mean (SD)

47.2 (14.2)

48.0 (15.4)

COPD severity, a %

  

 Moderate

42.0

46.2

 Severe

44.5

38.4

 Very severe

11.9

13.5

COPD exacerbations in previous year, %

60.5

59.8

 ≥ 2 prior COPD exacerbations, %

16.6

15.1

Exacerbation rate in previous year, mean (SD)

0.8 (0.9)

0.8 (1.0)

Prior and concomitant COPD medication, b n (%)

  

 LABA + ICS

706 (55.6)

1310 (56.5)

 SABA

638 (50.3)

1227 (52.9)

 ICS

125 (9.9)

200 (8.6)

 LABA

77 (6.1)

150 (6.5)

 Systemic corticoids

31 (2.4)

86 (3.7)

 SAMA

5 (0.4)

11 (0.5)

 SABA + SAMA

4 (0.3)

12 (0.5)

 LAMA

2 (0.2)

7 (0.3)

 Monoclonal antibody

1 (0.1)

0 (0.0)

 LABA + LAMA

1 (0.1)

1 (< 0.1)

  1. Full analysis set (N = 3589); included all patients randomized to treatment who received ≥ 1 dose of study drug
  2. BD bronchodilator, BMI body max index, COPD chronic obstructive pulmonary disease, CV cardiovascular, FEV1 forced expiratory volume in 1 s, GOLD Global Initiative for Chronic Obstructive Lung Disease, ICS inhaled corticosteroid, LABA long-acting β2-agonist, LAMA long-acting muscarinic antagonist, N number of subjects in treatment group, n number of subjects in category or analysis, SABA short-acting β2-agonist, SAMA short-acting muscarinic antagonist, SD standard deviation
  3. aBased on GOLD airflow obstruction grade: moderate (50% ≤ FEV1 < 80% predicted); severe (30% ≤ FEV1 < 50% predicted); very severe (FEV1 < 30% predicted)[1]
  4. bMedications started prior to randomization and continued after first dose of study drug