Salpeter Shelley R, Ormiston Thomas M, Salpeter Edwin E
Stanford University School of Medicine, Palo Alto, California, USA.
Ann Intern Med. 2002 Nov 5;137(9):715-25. doi: 10.7326/0003-4819-137-9-200211050-00035.
To assess the effect of cardioselective beta-blockers on respiratory function of patients with reactive airway disease.
Comprehensive searches of the EMBASE, MEDLINE, and CINAHL databases from 1966 to May 2001 and scanning of references of the identified articles and related reviews.
Randomized, blinded, placebo-controlled trials that studied the effects of cardioselective beta-blockers on FEV1, symptoms, and the use of inhaled beta2-agonists in patients with reactive airway disease were selected. Interventions studied were the administration of a cardioselective beta-blocker and administration of beta2-agonist after the study drug.
Outcomes measured were the change in FEV1 from baseline, the number of patients with respiratory symptoms, and the use of inhaled beta2-agonists with active treatment compared with placebo.
Nineteen studies on single-dose treatment and 10 studies on continued treatment were included. Administration of a single dose of a cardioselective beta-blocker was associated with a 7.46% (95% CI, 5.59% to 9.32%) decrease in FEV(1) and a 4.63% (CI, 2.47% to 6.78%) increase in FEV1 response to beta-agonist compared with placebo, with no increase in symptoms. Trials lasting from 3 days to 4 weeks produced no significant change in FEV1 (-0.42% [CI, -3.74% to 2.91%]), symptoms, or inhaler use compared with placebo but maintained an 8.74% (CI, 1.96% to 15.52%) increase in beta-agonist response. No significant treatment effect in terms of FEV1 was found in patients with concomitant chronic obstructive pulmonary disease, whether single doses (change in FEV1, -5.28% [CI, -10.03% to -0.54%]) or continued treatment (change in FEV1, 1.07% [CI, -3.3% to 5.44%]) was given.
Cardioselective beta-blockers do not produce clinically significant adverse respiratory effects in patients with mild to moderate reactive airway disease. The results were similar for patients with concomitant chronic airways obstruction. Given their demonstrated benefit in such conditions as heart failure, cardiac arrhythmias, and hypertension, cardioselective beta-blockers should not be withheld from patients with mild to moderate reactive airway disease.
评估心脏选择性β受体阻滞剂对反应性气道疾病患者呼吸功能的影响。
全面检索1966年至2001年5月的EMBASE、MEDLINE和CINAHL数据库,并查阅已识别文章的参考文献及相关综述。
选取随机、双盲、安慰剂对照试验,这些试验研究了心脏选择性β受体阻滞剂对反应性气道疾病患者第一秒用力呼气容积(FEV1)、症状以及吸入β2激动剂使用情况的影响。所研究的干预措施为给予心脏选择性β受体阻滞剂以及在研究药物后给予β2激动剂。
测量的结果包括与基线相比FEV1的变化、有呼吸道症状的患者数量以及与安慰剂相比在积极治疗时吸入β2激动剂的使用情况。
纳入了19项关于单剂量治疗的研究和10项关于持续治疗的研究。与安慰剂相比,给予单剂量心脏选择性β受体阻滞剂与FEV1降低7.46%(95%可信区间,5.59%至9.32%)以及FEV1对β激动剂的反应增加4.63%(可信区间,2.47%至6.78%)相关,且症状无增加。持续3天至4周的试验与安慰剂相比,FEV1(-0.42%[可信区间,-3.74%至2.91%])、症状或吸入器使用情况无显著变化,但β激动剂反应维持增加8.74%(可信区间,1.96%至15.52%)。对于合并慢性阻塞性肺疾病的患者,无论给予单剂量(FEV1变化,-5.28%[可信区间,-10.03%至-0.54%])还是持续治疗(FEV1变化,1.07%[可信区间,-3.3%至5.44%]),在FEV1方面均未发现显著治疗效果。
心脏选择性β受体阻滞剂在轻度至中度反应性气道疾病患者中不会产生具有临床意义的不良呼吸影响。对于合并慢性气道阻塞的患者,结果相似。鉴于其在心力衰竭、心律失常和高血压等疾病中已证实的益处,不应不给轻度至中度反应性气道疾病患者使用心脏选择性β受体阻滞剂。