Efficacy and Safety of Montelukast Sodium Tablets Combined with Budesonide Suspension in the Treatment of Patients with Bronchial Asthma

IF 0.8 4区 医学 Q4 CHEMISTRY, MEDICINAL Pharmaceutical Chemistry Journal Pub Date : 2024-07-13 DOI:10.1007/s11094-024-03156-4
Deyun Liu, Dawei Fei
{"title":"Efficacy and Safety of Montelukast Sodium Tablets Combined with Budesonide Suspension in the Treatment of Patients with Bronchial Asthma","authors":"Deyun Liu, Dawei Fei","doi":"10.1007/s11094-024-03156-4","DOIUrl":null,"url":null,"abstract":"<p>To evaluate the efficacy and safety of montelukast sodium tablets combined with budesonide suspension in the treatment of patients with bronchial asthma, ninety patients with bronchial asthma treated in The People’s Hospital of Quanjiao from January 2018 to April 2021 were randomly included in the study and then randomly divided into an observation group and a control group with 45 cases in each group. Patients in both groups were given clinical routine and symptomatic treatment. Patients in the control group were given budesonide suspension treatment on the basis of routine treatment, and patients in the observation group were treated with montelukast sodium tablets on the basis of the control group. The daytime and nighttime cough scores and asthma control scores (ACT scores) of the two groups were recorded before and after treatment. The pulmonary function indexes such as forced expiratory volume in one second (FEV1), forced vital capacity (FVC), peak expiratory flow (PEFR), etc., were measured. The daytime cough score and nighttime cough score of the patients in the observation group after treatment were significantly lower than those before treatment and the control group at the same period, and the act score was significantly higher than that before treatment and the control group during the same period (<i>P</i> &lt; 0.05). FEV1, FVC, PEFR and other pulmonary function indexes were significantly better than those before treatment and the control group at the same period (<i>P</i> &lt; 0.05). The total clinical effective rate of the observation group was 93.33%, which was significantly higher than 71.11% of the control group (<i>P</i> &lt; 0.05). There was no significant difference in the incidence of adverse reactions between the other two groups (<i>P</i> &gt; 0.05). Montelukast sodium tablets combined with budesonide suspension can effectively improve cough, asthma symptoms and lung function of patients with bronchial asthma.</p>","PeriodicalId":19990,"journal":{"name":"Pharmaceutical Chemistry Journal","volume":"30 1","pages":""},"PeriodicalIF":0.8000,"publicationDate":"2024-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Chemistry Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11094-024-03156-4","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

To evaluate the efficacy and safety of montelukast sodium tablets combined with budesonide suspension in the treatment of patients with bronchial asthma, ninety patients with bronchial asthma treated in The People’s Hospital of Quanjiao from January 2018 to April 2021 were randomly included in the study and then randomly divided into an observation group and a control group with 45 cases in each group. Patients in both groups were given clinical routine and symptomatic treatment. Patients in the control group were given budesonide suspension treatment on the basis of routine treatment, and patients in the observation group were treated with montelukast sodium tablets on the basis of the control group. The daytime and nighttime cough scores and asthma control scores (ACT scores) of the two groups were recorded before and after treatment. The pulmonary function indexes such as forced expiratory volume in one second (FEV1), forced vital capacity (FVC), peak expiratory flow (PEFR), etc., were measured. The daytime cough score and nighttime cough score of the patients in the observation group after treatment were significantly lower than those before treatment and the control group at the same period, and the act score was significantly higher than that before treatment and the control group during the same period (P < 0.05). FEV1, FVC, PEFR and other pulmonary function indexes were significantly better than those before treatment and the control group at the same period (P < 0.05). The total clinical effective rate of the observation group was 93.33%, which was significantly higher than 71.11% of the control group (P < 0.05). There was no significant difference in the incidence of adverse reactions between the other two groups (P > 0.05). Montelukast sodium tablets combined with budesonide suspension can effectively improve cough, asthma symptoms and lung function of patients with bronchial asthma.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
孟鲁司特钠片联合布地奈德混悬液治疗支气管哮喘患者的疗效和安全性
为评价孟鲁司特钠片联合布地奈德混悬液治疗支气管哮喘患者的疗效和安全性,将2018年1月至2021年4月在全椒县人民医院接受治疗的90例支气管哮喘患者随机纳入研究,然后随机分为观察组和对照组,每组45例。两组患者均给予临床常规治疗和对症治疗。对照组患者在常规治疗的基础上给予布地奈德混悬液治疗,观察组患者在对照组的基础上给予孟鲁司特钠片治疗。记录两组患者治疗前后的昼夜咳嗽评分和哮喘控制评分(ACT 评分)。测量一秒用力呼气容积(FEV1)、用力肺活量(FVC)、呼气峰流速(PEFR)等肺功能指标。治疗后观察组患者的白天咳嗽评分和夜间咳嗽评分明显低于治疗前和同期对照组,而行为评分明显高于治疗前和同期对照组(P <0.05)。FEV1、FVC、PEFR等肺功能指标明显优于治疗前及同期对照组(P< 0.05)。观察组临床总有效率为 93.33%,明显高于对照组的 71.11%(P <0.05)。其他两组不良反应发生率无明显差异(P >0.05)。孟鲁司特钠片联合布地奈德混悬液能有效改善支气管哮喘患者的咳嗽、哮喘症状和肺功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Pharmaceutical Chemistry Journal
Pharmaceutical Chemistry Journal CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
1.30
自引率
22.20%
发文量
226
审稿时长
3-8 weeks
期刊介绍: Pharmaceutical Chemistry Journal is a monthly publication devoted to scientific and technical research on the creation of new drugs and the improvement of manufacturing technology of drugs and intermediates. International contributors cover the entire spectrum of new drug research, including: methods of synthesis; results of pharmacological, toxicological, and biochemical studies; investigation of structure - activity relationships in prediction of new compounds; methods and technical facilities used; and problems associated with the development of ecologically safe and economically feasible methods of industrial production. In addition, analytical reviews of the international literature in the field provide coverage of the most recent developments around the world. Pharmaceutical Chemistry Journal is a translation of the Russian journal Khimiko-Farmatsevticheskii Zhurnal. The Russian Volume Year is published in English from April. All articles are peer-reviewed.
期刊最新文献
Synthesis, In Vitro Antimycobacterial Activity of Some 2-((5-Amino-1,3,4-Thiadiazol-2-YL)Methyl)-6-Aryl-Tetrahydropyridazin-3-One Derivatives Long-Acting Hydrogel Eye Drops Composite Sequentially Releases Basic Fibroblast Growth Factor and Carbomer for Synergistic Promotion of the Repair of Corneal Epithelium Study of Changes in Enterosgel Structure in Case of Violation of Drug Storage Conditions HPLC Determination of Myricitrin in Leaves of Common Myrtle (Myrtus communis L.) Preparation, Physicochemical Properties, and Antibacterial Activity of Hydrogel Films Based on Starch and Poly(Vinyl Alcohol) with Added Ethonium
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1