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布地奈德/福莫特罗与沙丁胺醇治疗急性哮喘的疗效和安全性比较。

Efficacy and safety of budesonide/formoterol compared with salbutamol in the treatment of acute asthma.

作者信息

Balanag V M, Yunus F, Yang P-C, Jorup C

机构信息

Lung Center of The Philippines, Quezon City, The Philippines.

出版信息

Pulm Pharmacol Ther. 2006;19(2):139-47. doi: 10.1016/j.pupt.2005.04.009. Epub 2005 Jul 11.

DOI:10.1016/j.pupt.2005.04.009
PMID:16009588
Abstract

This study compared the efficacy and safety of budesonide/formoterol (Symbicort) Turbuhaler)) with salbutamol pressurized metered-dose inhaler (pMDI) with spacer for relief of acute bronchoconstriction in patients with asthma. In this randomized, double-blind, parallel-group study, patients (n = 104 allocated to treatment; n = 103 received treatment; mean age 45 years) seeking medical attention for acute asthma (mean FEV(1) 43% of predicted) received two doses repeated at t = -5 and 0 min of either budesonide/formoterol (320/9 microg, two inhalations) or salbutamol (100 microg x eight inhalations); total doses 1280/36 microg and 1600 microg, respectively. All patients received prednisolone 60 mg at 90 min and FEV(1) was assessed over 3h. FEV(1) 90 min after dosing (primary variable) increased compared with pre-dose FEV(1) by an average of 30% and 32% for budesonide/formoterol and salbutamol, respectively (P = 0.66), with similar increases at all timepoints from 3 to 180 min for both groups. Mean pulse rate over 3h was significantly higher in the salbutamol group versus the budesonide/formoterol group (92 vs. 88 bpm; P < 0.01). No treatment differences were seen for other vital signs, including ECG. High-dose budesonide/formoterol was effective and well tolerated for the treatment of acute asthma, with rapid onset of efficacy and a safety profile over 3h similar to high-dose salbutamol.

摘要

本研究比较了布地奈德/福莫特罗(信必可都保)都保与沙丁胺醇压力定量气雾剂加储雾罐缓解哮喘患者急性支气管收缩的疗效和安全性。在这项随机、双盲、平行组研究中,因急性哮喘(平均第一秒用力呼气容积[FEV₁]为预测值的43%)就医的患者(n = 104分配至治疗组;n = 103接受治疗;平均年龄45岁)在t = -5分钟和0分钟时重复接受两剂布地奈德/福莫特罗(320/9微克,两次吸入)或沙丁胺醇(100微克×八次吸入);总剂量分别为1280/36微克和1600微克。所有患者在90分钟时接受60毫克泼尼松龙,并在3小时内评估FEV₁。给药后90分钟时的FEV₁(主要变量)与给药前FEV₁相比,布地奈德/福莫特罗组和沙丁胺醇组分别平均增加30%和32%(P = 0.66),两组在3至180分钟的所有时间点均有相似增加。沙丁胺醇组3小时内的平均脉搏率显著高于布地奈德/福莫特罗组(92次/分钟对88次/分钟;P < 0.01)。其他生命体征(包括心电图)未见治疗差异。高剂量布地奈德/福莫特罗治疗急性哮喘有效且耐受性良好,起效迅速,3小时内的安全性与高剂量沙丁胺醇相似。

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