TABLE 2

Primary end-point outcomes

Patients with pre-existing cardiovascular diseasePatients without pre-existing cardiovascular disease
Patients with COPD and asthmaPatients with COPD without asthmaPatients with COPD and asthmaPatients with COPD without asthma
Patients n36907236677513 205
Primary outcome
Severe MACE591 (15.9)978 (6.8)301 (4.4)550 (2.0)
  HR (95% CI)1.25 (1.13–1.39)#Reference1.22 (1.06–1.41)Reference
Secondary outcome
 Any MACE654 (17.6)1093 (7.6)388 (5.7)696 (2.5)
  HR (95% CI)1.22 (1.11–1.34)#Reference1.22 (1.07–1.38)Reference
Severe MACE analysis
 Lethal cardiovascular events72 (1.9)148 (1.0)42 (0.6)88 (0.3)
  HR (95% CI)1.14 (0.86–1.51)Reference1.09 (0.75–1.57)Reference
 Nonlethal cardiovascular events requiring revascularisation102 (2.8)152 (1.1)45 (0.7)113 (0.4)
  HR (95% CI)1.53 (1.19–1.97)#Reference0.92 (0.65–1.29)Reference
 Non-lethal cardiovascular events requiring admission417 (11.2)678 (4.7)214 (3.1)349 (1.3)
  HR (95% CI)1.28 (1.15–1.43)#Reference1.25 (1.08–1.45)#Reference
All-cause mortality (not MACE)843 (22.7)1807 (12.5)991 (14.5)2169 (7.9)
 HR (95% CI)1.11 (1.03–1.21)#Reference1.06 (0.98–1.14)Reference

Data are presented as n (%), unless otherwise stated. Hazard ratios (HR) analysed by unadjusted Cox method with other cause mortality as a competing risk on the propensity-matched cohorts stratified by pre-existing cardiovascular disease. Patients with COPD and asthma and with COPD without asthma were propensity matched 1:2 by age, gender, tobacco exposure, Medical Research Council dyspnoea score, body mass index and forced expiratory volume in 1 s stratified into populations based on pre-existing cardiovascular disease. “Severe major adverse cardiac events (MACE)” defined as lethal cardiovascular events, and cardiovascular events requiring revascularisation or hospitalisation; “any MACE” defined as a severe MACE or an event requiring a prescription of ADP receptor inhibitors or nitrates. #: statistical significance >0.95 by regression analysis.