Efficacy and safety of montelukast adjuvant therapy in adults with cough variant asthma: A systematic review and meta‐analysis

Author:

Xu Qian123,Lu Tingting23,Song Zhongyang4,Zhu Peng1,Wu Yana1,Zhang Lumei1,Yang Kehu23,Zhang Zhiming5ORCID

Affiliation:

1. Clinical College of Traditional Chinese Medicine Gansu University of Chinese Medicine Lanzhou Gansu China

2. Institute of Clinical Research and Evidence‐Based Medicine Gansu Provincial Hospital Lanzhou Gansu China

3. Evidence‐Based Medicine Center, School of Basic Medical Sciences Lanzhou University Lanzhou Gansu China

4. Gansu Provincial Cancer Clinical Research Center of Integrated Traditional Chinese and Western Medicine Affiliated Hospital of Gansu University of Chinese Medicine Lanzhou Gansu China

5. Gansu Provincial Hospital of Traditional Chinese Medicine Lanzhou Gansu China

Abstract

AbstractBackgroundMontelukast is a highly selective and specific cysteinyl leukotriene receptor antagonist used in the treatment of asthma. Whether montelukast as adjuvant therapy can significantly and safely treat adults with cough variant asthma (CVA) remains inconclusive.AimsThis meta‐analysis systematically evaluated the efficacy and safety of montelukast as an adjuvant treatment for adults with CVA.Materials and methodsRandomized controlled trials (RCTs) on montelukast combined with inhaled corticosteroids (ICS) and long‐acting β2 agonists (LABAs) to treat CVA in adults, from inception to March 6, 2023, were retrieved from the CNKI, Wanfang, VIP, CBM, PubMed, Embase, Cochrane Library, and Web of Science databases and Clinical Trials website. Review Manager (version 5.4) and Stata (version 15.0) were used to conduct the meta‐analysis.ResultsA total of 15 RCTs were ultimately included in the meta‐analysis. It was established that montelukast as adjuvant therapy raised the total effective rate (RR = 1.20, 95% confidence interval [CI] [1.13, 1.27], P < 0.01) and improved the FEV1% (SMD = 0.91, 95% CI [0.40, 1.41], P < 0.01), PEF% (SMD = 0.63, 95% CI [0.38, 0.88], P < 0.01), FEV1 (SMD = 1.15, 95% CI [0.53, 1.77], P < 0.01), PEF (SMD = 0.64, 95% CI [0.42, 0.86], P < 0.01), and FEV1/FVC% (SMD = 0.76, 95% CI [0.51, 1.01], P < 0.01) and reduced the recurrence rate (RR = 0.28, 95% CI [0.15, 0.53], P < 0.01). The incidence of adverse reactions was higher in the montelukast auxiliary group compared to the control group but with no statistical difference (RR = 1.32, 95% CI [0.89, 1.96], P = 0.17).ConclusionExisting evidence indicated that the use of montelukast as an adjuvant therapy had therapeutic efficacy superior to ICS + LABA alone for the treatment of adult patients with CVA. However, further research is needed, especially a combination of high‐quality long‐term prospective studies and carefully designed RCTs.

Publisher

Wiley

Subject

Genetics (clinical),Pulmonary and Respiratory Medicine,Immunology and Allergy

Reference41 articles.

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