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色甘酸钠(定量吸入器)与二丙酸倍氯米松(定量吸入器)治疗成人轻至中度支气管哮喘的比较。一项双盲、双模拟随机平行组研究。

Comparison between sodium cromoglycate (MDI: metered-dose inhaler) and beclomethasone dipropionate (MDI) in treatment of adult patients with mild to moderate bronchial asthma. A double-blind, double-dummy randomized, parallel-group study.

作者信息

Faurschou P, Bing J, Edman G, Engel A M

机构信息

Department of Pulmonary Medicine, Gentofte University Hospital, Hellerup, Denmark.

出版信息

Allergy. 1994 Sep;49(8):659-63. doi: 10.1111/j.1398-9995.1994.tb00136.x.

Abstract

This study compared the efficacy and tolerability of sodium cromoglycate (SC) and beclomethasone dipropionate (BDP) in adult patients with bronchial asthma inadequately treated with bronchodilators alone. The study was a double-blind, randomized, double-dummy, parallel-group study. Patients with mild to moderate symptomatic asthma, inadequately treated with bronchodilators only, were, after a 2-week run-in (base-line) period, randomized to 8 weeks of treatment with either SC 10 mg four times daily or BDP 100 micrograms four times daily. Salbutamol metered-dose inhaler was given as relief medication. A total of 37 patients were randomized for treatment, 19 patients in the SC group and 18 patients in the BD group. Efficacy and safety were determined by daily record card data: morning and evening peak-expiratory-flow rates (PEFR), daytime and nighttime asthma symptom scores, and rescue salbutamol use. At clinic visits, FEV1 and FVC were measured, as were the physician's and the patient's assessment of the medication at the end of the study. The safety and tolerability of the trial medication were assessed by monitoring adverse events throughout the study. A clinically and statistically significant improvement of the asthma in FEV1, symptom scores, rescue medication, and global opinion of efficacy was observed, and both groups provided equivalent efficacy. The morning PEFR as well as the evening PEFR for both groups improved, but was statistically significant only for the BDP group (M-PEFR). Both drugs were well tolerated with only a few minor adverse events. This trial shows that SC and BDP are equally effective anti-inflammatory treatments for mild to moderate bronchial asthma in adults.

摘要

本研究比较了色甘酸钠(SC)和二丙酸倍氯米松(BDP)对仅使用支气管扩张剂治疗效果不佳的成年支气管哮喘患者的疗效和耐受性。该研究为双盲、随机、双模拟、平行组研究。仅使用支气管扩张剂治疗症状控制不佳的轻至中度哮喘患者,在经过2周的导入(基线)期后,随机分为两组,分别接受为期8周的治疗,一组每日4次,每次10 mg的SC治疗,另一组每日4次,每次100μg的BDP治疗。沙丁胺醇定量气雾剂用作缓解药物。共有37例患者被随机分组进行治疗,SC组19例,BD组18例。通过每日记录卡数据确定疗效和安全性:早晚呼气峰值流速(PEFR)、白天和夜间哮喘症状评分以及沙丁胺醇急救药物的使用情况。在门诊就诊时,测量第1秒用力呼气容积(FEV1)和用力肺活量(FVC),以及研究结束时医生和患者对药物的评估。通过在整个研究过程中监测不良事件来评估试验药物的安全性和耐受性。观察到哮喘患者的FEV1、症状评分、急救药物使用情况以及总体疗效评价在临床和统计学上有显著改善,且两组疗效相当。两组的早晨PEFR和晚上PEFR均有所改善,但仅BDP组的早晨PEFR(M-PEFR)有统计学意义。两种药物耐受性良好,仅出现少数轻微不良事件。该试验表明,SC和BDP对成人轻至中度支气管哮喘是同样有效的抗炎治疗药物。

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