Effect of leukotriene receptor antagonist therapy in bronchial asthma – A prospective, preliminary, hospital-based, randomized study in rural Konaseema, Andhra Pradesh

B. Bathula, P. Bandela, P. Ravikumar, B. Duvvuri, Subba Polimati
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Abstract

BACKGROUND: The role of leukotriene receptor antagonist is well documented in the management of chronic asthma. However, the efficacy in acute asthma is not yet established. AIM AND OBJECTIVES: This study was designed to evaluate the clinical efficacy of oral montelukast as an add-on drug to the standard therapy of the acute attack of bronchial asthma. MATERIALS AND METHODS: A prospective, institutional-based, single-blinded, randomized control study was done. A total of 100 (aged between 18 and 60 years) participants diagnosed with acute exacerbations due to bronchial asthma were enrolled in the study. They were divided into study and control groups randomly. The study group patients were treated with 10 mg of montelukast once in a day for 4 weeks as an add-on drug, whereas the control group received only standard medication of acute bronchial asthma (as per Global Initiative for Asthma guidelines). All the participants were monitored at baseline to every week for a month. RESULTS: All the 100 participants were assessed finally without any dropouts. The baseline characteristics were noted similarly in both groups. The mean age was 35.46 + 13.17 years in the control and 37.86 + 14.43 years in the study group. Majority were males in both the groups. At the end of the 4 weeks of oral montelukast administration, there was improvement in forced expiratory volume in 1 s (FEV1) and peak expiratory flow rate at 2 weeks and 1 month. On many occasions, there was a strong improvement in FEV1 and other clinical parameters after continuous treatment with beta-2 agonists and parenteral corticosteroids for patients with acute asthma. Even though there was no improvement in FEV1/forced vital capacity ratio among both the groups at 2 weeks and 4 weeks, statistically significant improvement was seen between 2 weeks to 1 month on baseline parameters. CONCLUSION: Administration of oral montelukast 10 mg as an add-on drug to standard therapy may help in quick recovery from acute bronchial asthma and relapse.
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白三烯受体拮抗剂治疗支气管哮喘的效果——在安得拉邦科纳西马农村进行的一项前瞻性、初步、基于医院的随机研究
背景:白三烯受体拮抗剂在慢性哮喘治疗中的作用已被充分证实。然而,对急性哮喘的疗效尚未确定。目的和目的:本研究旨在评价口服孟鲁司特作为支气管哮喘急性发作标准治疗的附加药物的临床疗效。材料和方法:一项前瞻性、基于机构、单盲、随机对照研究。共有100名(年龄在18至60岁之间)被诊断为支气管哮喘急性加重的参与者参加了这项研究。他们被随机分为研究组和对照组。研究组患者接受10mg孟鲁司特治疗,每天1次,连续4周作为附加药物,而对照组仅接受急性支气管哮喘的标准药物治疗(根据全球哮喘倡议指南)。所有的参与者都在一个月的时间里每周进行一次基线监测。结果:100名受试者均完成最终评估,无一例中途退出。两组的基线特征相似。对照组平均年龄35.46 + 13.17岁,研究组平均年龄37.86 + 14.43岁。两组中的大多数都是男性。口服孟鲁司特4周后,1 s用力呼气量(FEV1)和2周及1个月呼气流量峰值均有改善。在许多情况下,急性哮喘患者在持续使用β -2激动剂和外注射皮质类固醇治疗后,FEV1和其他临床参数有较强的改善。尽管两组在2周和4周时FEV1/强迫肺活量比没有改善,但在2周至1个月的基线参数上有统计学显著改善。结论:口服孟鲁司特10mg作为标准治疗的附加药物,有助于急性支气管哮喘的快速康复和复发。
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