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β-受体阻滞剂治疗慢性阻塞性肺疾病:一项来自TONADO®研究项目的队列研究

2018/05/30

   摘要
   背景:心血管疾病在慢性阻塞性肺疾病(COPD)患者中是一种常见的并发症。许多临床医师,特别是呼吸科医师,尽管已经有证据证实了预防心血管事件的有效性,但仍不愿意在COPD患者中使用β-肾上腺素受体阻断剂。
   方法:大型(5,162例)III期TONADO®研究评估了接受长效支气管扩张剂治疗1年以上的中、重度COPD患者的肺功能和患者报告的临床结局(PROs)情况。这项事后分析对研究中接受了β受体阻滞剂的亚组患者的肺功能变化,PROs和安全性进行了逐一分析。
   结果:总共有557 / 5,162名患者(11%)在基线时接受了β受体阻滞剂治疗。与未接收β受体阻滞剂组相比,β受体阻滞剂组的使用支气管扩张剂后的FEV1较高(1.362 L vs 1.470 L)。正如预期的那样,β受体阻滞剂组的患者有较多的心血管并发症和药物治疗史。在24或52周时,未观察到两组患者的基线肺功能改善情况有明显差异。β受体阻滞剂组患者的圣乔治呼吸问卷(SGRQ)评分和过渡期呼吸困难指数与未使用β受体阻滞剂组的患者相比,差异无统计学意义。两组之间的安全性结果相当。
   结论:基线β受体阻滞剂治疗对中重度COPD患者的肺功能,总体呼吸状态和安全性没有影响。来自这一大型患者队列的结果支持COPD同时存在心血管并发症的患者可以慎用β-阻滞剂。
 
(中日友好医院呼吸与危重症医学科 王圆方 摘译 林江涛 审校)
(Chest,Available online 31 January 2018)

 
 
 
β-blockers in Chronic Obstructive Pulmonary Disease: a Cohort Study from the TONADO® Research Programme
 
François Maltais, MD , Roland Buhl, MD, Andrea Koch, MD, Valeria C. Amatto, MD, MSc, Jim Reid, MBChB DipObs, FRNZCGP, FCCP, MPS, Lars Grönke, MD, Ulrich Bothner, MD, MSc
 
Abstract
BackgroundCardiovascular disease is a frequent co-morbidity in patients with chronic obstructive pulmonary disease (COPD). Many clinicians, particularly pulmonologists, are reluctant to use β-adrenoceptor blocking agents (β-blockers) in patients with COPD, despite their proven effectiveness in preventing cardiovascular events.
MethodsThe large (5,162 patients) phase III TONADO® 1 and 2 studies assessed lung function and patient-reported outcomes (PROs) in patients with moderate to very severe COPD receiving long-acting bronchodilator treatment over 1 year. This post hoc analysis characterised lung-function changes, PROs and safety in the subgroup of patients receiving β-blockers in the studies.
Resultstotal, 557/5,162 patients (11%) received β-blockers at baseline. Post-bronchodilator FEV1 at baseline was higher in the β-blocker group (1.470 L) compared to the no β-blocker group (1.362 L). As expected, patients on β-blockers had a more frequent history of cardiovascular co-morbidities and medications. Lung function improved from baseline in patients with or without β-blocker treatment, and no relevant between-group differences were observed in trough FEV1 or trough FVC at 24 or 52 weeks. No relevant differences were observed for SGRQ and Transition Dyspnoea Index in patients with β-blockers compared to those without. Safety findings were comparable between groups.
ConclusionsLung function, overall respiratory status and safety of tiotropium/olodaterol were not influenced by baseline β-blocker treatment in patients with moderate to very severe COPD. Results from this large patient cohort support the cautious and appropriate use of β-blockers in patients with COPD and cardiovascular co-morbidity.
 


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