Cardiovascular Event Rates According to Cardiovascular Disorders at Baseline
Risk factors recorded at baseline included the presence of hypertension, diabetes mellitus, hyperlipidemia, and a history of heart disease (Table 1). Adjudicated event rates were higher in patients with baseline cardiovascular risk factors than in those without baseline cardiovascular risk (Table 4). HRs for MACEs found in patients treated with roflumilast relative to placebo in patients without cardiovascular diseases or risk factors at baseline were lower than in those with cardiovascular comorbid conditions. Adjusting for cardiovascular risk factors at baseline did not materially affect the HR for MACEs.
Rates and HRs for MACEs |
There were significantly fewer MACEs for roflumilast than for placebo in the subgroup of patients with COPD who did not have cardiovascular comorbid conditions at baseline (Table 1).
Cardiovascular Event Rates According to Other Factors at Baseline
Adjudicated event rates according to age, sex, smoking status, COPD severity, and concomitant long-term pulmonary medication use are shown in Figure 3. HRs were similar across age, sex, and smoking status. There were no significant interactions for COPD severity, concomitant inhaled corticosteroid use, or long-acting b-agonist use.
However, reductions in MACEs were significant in patients with severe COPD (GOLD [Global Initiative for Chronic Obstructive Lung Disease] stage III), in those using concomitant inhaled corticosteroids, and in those not using long-acting Ь-agonists and not in the corresponding subgroups.
Cardiovascular Event Rates According to COPD Exacerbations
Subanalyses of the four trials carried out for 1 year demonstrated that exacerbations of COPD were reduced significantly by roflumilast relative to placebo.
Between patients with and without exacerbations, the proportions with MACEs were similar (1.7% and 1.6%, respectively). Between patients with and without MACEs, the proportions experiencing exacerbations were similar (43.2% and 42.1%, respectively).
Table 4—Incidence Rates and HRs for MACEs According to Baseline CV Comorbid Diseases
Patient Group | Roflumilast | Placebo | HR (Roflumilast vs Placebo) | 95% CI | P Value |
No. patients with CV comorbid conditions | 3,584 | 3,056 | |||
Composite MACE | 43 (1.2) | 51 (1.7) | 0.75 | 0.50-1.14 | .185 |
CV death | 27 (0.8) | 31 (1.0) | 0.72 | 0.43-1.23 | .232 |
Nonfatal MI | 10 (0.3) | 12 (0.4) | 0.94 | 0.40-2.20 | .893 |
Nonfatal stroke | 6 (0.2) | 9 (0.3) | 0.55 | 0.18-1.66 | .288 |
No. patients without CV comorbid conditions | 2,979 | 2,435 | |||
Composite MACE | 9 (0.3) | 25 (1.0) | 0.36 | 0.17-0.77 | .009 |
CV death | 8 (0.3) | 12 (0.5) | 0.65 | 0.26-1.59 | .340 |
Nonfatal MI | 1 (0.0) | 10 (0.4) | 0.09 | 0.01-0.70 | .021 |
Nonfatal stroke | 0 (0.0) | 3(0.1) | 0 | .996 |
Data are presented as No. (%), unless otherwise indicated. See Table 3 legend for expansion of abbreviations. “Calculated using Cox proportional hazard model with terms for treatment, age, sex, smoking status, and country pool. Includes ischemic heart disease, type 2 diabetes, dyslipidemia, and hypertension.