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Table 2 Day 85 trough FEV1 (mL) by patient subgroup

From: Efficacy of revefenacin, a long-acting muscarinic antagonist for nebulized therapy, in patients with markers of more severe COPD: a post hoc subgroup analysis

Subgroups

Revefenacin 175 μg

(n = 395)

Placebo

(n = 417)

ITT

 Evaluable n

310

296

 LS mean difference (95% CI)

148.1 (115.2, 181.1); p < 0.0001

 

FEV130%–< 50% pred

 Evaluable n

101

78

 LS mean difference (95% CI)

131.2 (70.7, 191.6), p < 0.0001

 

FEV1 < 30% pred

 Evaluable n

17

9

 LS mean difference (95% CI)

176.2 (14.7, 337.5), p = 0.0324

 

2011 GOLD category D

 Evaluable n

108

83

 LS mean difference (95% CI)

124.6 (66.5, 182.7), p < 0.0001

 

ICS use

 Evaluable n

135

108

 LS mean difference (95% CI)

130.6 (78.7, 182.5), p < 0.001

 

LABA or ICS/LABA use

 Evaluable n

118

89

 LS mean difference (95% CI)

139.2 (82.9, 195.5), p < 0.0001

 

> 65 years

 Evaluable n

143

128

 LS mean difference (95% CI)

140.3 (91.0, 189.7), p < 0.0001

 

> 75 years

 Evaluable n

28

25

 LS mean difference (95% CI)

129.2 (18.9, 239.5), p = 0.0217

 

Reversible to ipratropium and albuterol

 Evaluable n

70

57

 LS mean difference (95% CI)

286.5 (214.8, 358.2), p < 0.0001

 

History of CV disease

 Evaluable n

21

27

 LS mean difference (95% CI)

140.7 (18.4, 263.0), p = 0.0242

 

History of diabetes

 Evaluable n

85

57

 LS mean difference (95% CI)

101.6 (27.0, 176.3), p = 0.0077

 

History of cognitive/mental impairments

 Evaluable n

45

44

 LS mean difference (95% CI)

149.5 (64.5, 234.5), p = 0.0006

 
  1. CI confidence intervals; CV cardiovascular; FEV1 forced expiratory volume in 1 s; GOLD Global Initiative for Chronic Obstructive Lung Disease, LABA long-acting ß agonist; ICS inhaled corticosteroids; ITT intention-to-treat; pred predicted