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Table 4 Spirometry outcomes in tiotropium and placebo groups according to different threshold criteria for bronchodilator responsiveness.

From: Acute bronchodilator responsiveness and health outcomes in COPD patients in the UPLIFT trial

A

Criterion A (∆ % Predicted FEV1≥12% and ≥200 mL)

Criterion B (∆ % Predicted FEV1≥15%)

Criterion C (∆ % Predicted FEV1≥10%)

 

Nonresponder

Responder

Nonresponder

Responder

Nonresponder

Responder

Prebronchodilator

            

   Difference in FEV1 at 4 years (mL)*

76 (54, 98)

98 (77, 119)

97 (69, 124)

83 (65, 101)

78 (58, 97)

105 (81, 130)

   Difference in FVC at 4 years (mL)*

134 (89, 178)

195 (153, 236)

143 (92, 194)

179 (140, 217)

139 (99, 179)

213 (165, 260)

B

Criterion A (∆ % Predicted FEV 1 ≥12% and ≥200 mL)

Criterion B (∆ % Predicted FEV 1 ≥15%)

Criterion C (∆ % Predicted FEV 1 ≥10%)

 

Nonresponder

Responder

Nonresponder

Responder

Nonresponder

Responder

 

Tio

Placebo

Tio

Placebo

Tio

Placebo

Tio

Placebo

Tio

Placebo

Tio

Placebo

Rate of change in FEV1 (mL/year)

            

   Prebronchodilator

-32 ± 2

-31 ± 2

-29 ± 2

-29 ± 2

-35 ± 2

-38 ± 2

-28 ± 2

-26 ± 2

-32 ± 2

-32 ± 2

-28 ± 2

-28 ± 2

   Postbronchodilator

-37 ± 2

-37 ± 2

-43 ± 2

-47 ± 2

-38 ± 2

-42 ± 2

-42 ± 2

-43 ± 2

-39 ± 2

-39 ± 2

-43 ± 2

-47 ± 2

  1. (A) mean differences (95%CI) at 4 years (tiotropium - placebo), (B) mean (SE) rate of change by treatment group.
  2. In patients with at least three measurements after Day 30. Change in FEV1 and FVC data are based on repeated-measures ANOVA model, adjusted for baseline. Rates of decline in FEV1 data are based on random-effects model.
  3. *p ≤ 0.001 versus placebo. Tio = tiotropium; FEV1 = forced expiratory volume in 1 second; FVC = forced vital capacity.