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]
日期:2024-10-28
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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