ECG-based risk factors for adverse cardiopulmonary events and treatment outcomes in COPD

医学 慢性阻塞性肺病 内科学 优势比 不利影响 心脏病学
作者
Raymond Wade,Fernando J. Martinez,Gerard J. Criner,Lee Tombs,David A. Lipson,David Halpin,MeiLan K. Han,Dave Singh,Robert A. Wise,Ravi Kalhan,Mark T. Dransfield
出处
期刊:The European respiratory journal [European Respiratory Society]
卷期号:: 2400171-2400171
标识
DOI:10.1183/13993003.00171-2024
摘要

Background COPD has high mortality, compounded by comorbid cardiovascular disease. We investigated two electrocardiogram (ECG) markers, Cardiac Infarction Injury Score (CIIS) and P pulmonale, as prognostic tools for adverse cardiopulmonary events in COPD. Methods Post hoc analysis of the IMPACT trial. Outcomes included odds (odds ratio [95% confidence intervals]) of adverse cardiopulmonary events stratified by CIIS threshold (<20/≥20) and P pulmonale (baseline). Events included all-cause death, hospitalisation/death, cardiovascular adverse event of special interest (CVAESI), severe COPD exacerbations, and moderate/severe COPD exacerbations. Effects of fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) versus FF/VI or UMEC/VI based on CIIS and P pulmonale were also assessed. Results We included 9448 patients. Patients with CIIS ≥20 had greater odds of all-cause death (1.73[1.27–2.37]; p <0.001), hospitalisation/death (1.33[1.17–1.50]; p <0.001), CVAESI (1.27[1.08–1.48]; p <0.005), severe COPD exacerbations (1.41[1.21–1.64]; p <0.001) and moderate/severe COPD exacerbations (1.25[1.13–1.40]; p <0.001) versus CIIS <20. Patients with P pulmonale ( versus without) had greater odds of all-cause death (2.25[1.54–3.29]; p <0.001), hospitalisation/death (1.51[1.28–1.79]; p <0.001), severe COPD exacerbations (2.00[1.65–2.41]; p <0.001) and moderate/severe COPD exacerbations (1.25[1.08–1.46]; p <0.001). A combined model demonstrated patients with CIIS ≥20 and P pulmonale had increased risk of all-cause death (3.38[1.23–9.30]; p=0.019), hospitalisation/death (1.61[1.14–2.22]; p=0.004), and rate of severe COPD exacerbations (1.89[1.22–2.91]; p=0.004) and moderate/severe COPD exacerbations (1.25[1.00–1.56]; p=0.046). The risk of all-cause death and CVAESI was reduced with FF/UMEC/VI versus UMEC/VI in patients with CIIS ≥20, but not CIIS <20. Conclusions These findings suggest potential clinical relevance of CIIS and P pulmonale as risk indicators for adverse cardiopulmonary events in COPD.

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