Beta-blocker use and acute exacerbations of COPD following myocardial infarction: a Danish nationwide cohort study

被引:6
|
作者
Rasmussen, Daniel B. [1 ,2 ,3 ]
Bodtger, Uffe [1 ,3 ,4 ]
Lamberts, Morten [2 ]
Torp-Pedersen, Christian [5 ,6 ]
Gislason, Gunnar [7 ,8 ,9 ]
Lange, Peter [10 ,11 ]
Jensen, Magnus T. [12 ]
机构
[1] Naestved Hosp, Dept Resp Med, Resp Res Unit Zealand, DK-4700 Naestved, Sjaelland, Denmark
[2] Herlev & Gentofte Univ Hosp, Dept Cardiol, Hellerup, Denmark
[3] Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark
[4] Zealand Univ Hosp, Dept Resp Med, Roskilde, Denmark
[5] Aalborg Univ Hosp, Unit Epidemiol & Biostat, Aalborg, Denmark
[6] Aalborg Univ, Dept Hlth Sci & Technol, Aalborg, Denmark
[7] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen, Denmark
[8] Univ Southern Denmark, Natl Inst Publ Hlth, Odense, Denmark
[9] Danish Heart Fdn, Copenhagen, Denmark
[10] Copenhagen Univ Hosp, Herlev & Gentofte Hosp, Sect Resp Med, Dept Internal Med, Herlev, Denmark
[11] Univ Copenhagen, Sect Epidemiol, Dept Publ Hlth, Copenhagen, Denmark
[12] Queen Mary Univ London, William Harvey Res Inst, NIHR Barts Biomed Ctr, Charterhouse Sq Campus, London, England
关键词
COPD exacerbations; COPD epidemiology; COPD pharmacology; OBSTRUCTIVE PULMONARY-DISEASE; HEART-DISEASE; RISK; THERAPY; OUTCOMES; MORTALITY; EXPOSURE; ROBUST;
D O I
10.1136/thoraxjnl-2019-214206
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction Patients with chronic obstructive pulmonary disease (COPD) are undertreated with beta-blockers following myocardial infarction (MI), possibly due to fear for acute exacerbations of COPD (AECOPD). Is beta-blocker use associated with increased risk of AECOPD in patients following first-time MI? Methods Danish nationwide study of patients with COPD following hospitalisation for MI from 2003 to 2015. Multivariable, time-dependent Cox regression accounting for varying beta-blocker use based on claimed prescriptions during up to 13 years of follow-up. Results A total of 10 884 patients with COPD were discharged after first-time MI. The 1-year rate of AECOPD was 35%, and 65% used beta-blockers at 1 year. Beta-blocker use was associated with a lower risk of AECOPD (multivariable-adjusted HR 0.78, 95% CI 0.74-0.83). This association was independent of the type of MI (HR 0.70, 95% CI 0.59-0.83 in ST-elevation MI (STEMI) and HR 0.80, 95% CI 0.75-0.84 in non-STEMI), presence or absence of heart failure (HR 0.82, 95% CI 0.74-0.90 and HR 0.77, 95% CI 0.72-0.82, respectively), beta-blocker dosage and type, as well as exacerbation severity. Results were similar in 1118 patients with full data on COPD severity and symptom burden (median forced expiratory volume in 1 s as percentage of predicted was 46 and majority had moderate dyspnoea), and in 1358 patients with severe COPD and frequent AECOPD with a high 1-year rate of AECOPD of 70%. Discussion Beta-blocker use was not associated with increased risk of AECOPD following MI. This finding was independent of COPD severity, symptom burden and exacerbation history, and supports the safety of beta-blockers in patients with COPD, including high-risk patients with severe disease.
引用
收藏
页码:928 / 933
页数:6
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