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首页> 外文期刊>International Journal of Chronic Obstructive Pulmonary Disease >Clinical efficacy of farcosolvin syrup (ambroxol–theophylline–guaiphenesin mixture) in the treatment of acute exacerbation of chronic bronchitis
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Clinical efficacy of farcosolvin syrup (ambroxol–theophylline–guaiphenesin mixture) in the treatment of acute exacerbation of chronic bronchitis

机译:Farcosolvin糖浆(氨溴索-茶碱-愈创甘油醚混合物)在治疗慢性支气管炎急性加重中的临床疗效

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Background: Acute exacerbations of chronic bronchitis (AECB) are defined as recurrent attacks of worsening bronchial inflammation that are marked by an increase in the volume of daily sputum produced, a change in color of the expectorated sputum, and worsening dyspnea. Farcosolvin? (Pharco Pharmaceuticals, Alexandria, Egypt) is a mixture of ambroxol (15 mg); theophylline (50 mg); and guaiphenesin (30 mg), per 5 mL syrup.Objective: To test the clinical efficacy of Farcosolvin in the treatment of AECB in a randomized, single-blinded, controlled study design.Patients and methods: One hundred patients with AECB were randomized to either Farcosolvin or guaiphenesin treatment groups, in addition to the standard medical treatment for their cases. Baseline clinical symptomatolgy of breathlessness, cough, and sputum severity scoring were compared before and after 3 and 7 days of treatment in both groups and the differences compared between groups. Changes in perceived improvement were also compared between groups using the Clinical Global Impression of Improvement or Change Scale (CGIC).Results: There were statistically significant improvements in breathlessness and cough scores in both groups (pretreatment versus posttreatment at day 3 and at day 7; P < 0.05). There were highly statistically significant differences between groups in improvement in -breathlessness and cough scores, after 3 and 7 days treatment, in favor of the Farcosolvin -treatment group (P < 0.001). Out of 50 patients, 48 (96%) in the Farcosolvin-treated group rated their -improvement on the CGIC scale as “much” and “very much” improved, while only 41 patients (82%) reported such a degree of improvement in the control group. The difference was statistically significant (P < 0.05).Conclusion: We concluded from our study that Farcosolvin syrup might be safe and effective in improving symptoms in cases of acute exacerbation of chronic bronchitis.
机译:背景:慢性支气管炎(AECB)的急性加重被定义为支气管炎症恶化的反复发作,其特征在于每日产生的痰量增加,痰液颜色改变和呼吸困难加重。 Farcosolvin? (Pharco Pharmaceuticals,Alexandria,埃及)是氨溴索(15毫克)的混合物;茶碱(50毫克);目的:每5毫升糖浆中加入30毫克和愈创木酚素(30毫克)。目的:通过随机,单盲,对照研究设计,测试Farcosolvin治疗AECB的临床疗效。患者和方法:将100例AECB患者随机分配至Farcosolvin或guaiphenesin治疗组,以及针对其病例的标准药物治疗。比较两组在治疗前后3天和7天的呼吸困难,咳嗽和痰严重程度评分的基线临床症状,并比较两组之间的差异。结果:两组患者的呼吸困难和咳嗽得分均有统计学意义的显着改善(治疗前和治疗后第3天和第7天;两组之间的差异均有统计学意义)。 P <0.05)。在治疗3天和7天后,两组之间呼吸困难和咳嗽得分的改善在统计学上具有显着统计学差异,而使用Farcosolvin治疗组更为有利(P <0.001)。在50例患者中,接受Farcosolvin治疗的组中有48例(96%)认为他们在CGIC量表上的改善为“很多”和“很多”改善,而只有41例患者(82%)表示其CGIC改善程度对照组。差异具有统计学意义(P <0.05)。结论:我们的研究得出结论,在慢性支气管炎急性加重的情况下,Farcosolvin糖浆可以安全有效地改善症状。

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