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Should we prescribe montelukast to allergic pediatric patients?

Should we prescribe montelukast to allergic pediatric patients?

Article information

Clin Exp Pediatr. 2020;63(10):389-390
Publication date (electronic) : 2020 August 24
doi : https://doi.org/10.3345/cep.2019.01662
Department of Pediatrics, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea
Corresponding author: Yong Mean Park, MD, PhD. Department of Pediatrics, Konkuk University Medical Center, Konkuk University School of Medicine, 120-1 Neungdongro, Gwanjingu, Seoul, Korea E-mail: pymcko@kuh.ac.kr
Received 2019 December 24; Revised 2020 July 29; Accepted 2020 August 8.

Montelukast, a representative leukotriene receptor antagonist (LTRA), was launched 20 years ago in Korea and, since then, has been used mainly to treat childhood asthma and allergic rhinitis.

Since 2010, LTRA has been prescribed more often than inhaled corticosteroids (ICS) to pediatric asthma patients in Korea [1]. Although the efficacy of LTRA is inferior to that of ICS, the effectiveness of LTRA is superior considering patient compliance and medication side effects as demonstrated in several real-world studies [2]. With the increasing use of LTRA, the symptoms of pediatric asthma patients are becoming well controlled and their quality of life is improving [2]. LTRA is safe, especially in young children, because it has fewer side effects than other asthma medications. Moreover, it rarely causes behavioral changes or Churg-Strauss syndrome [3].

Viral wheeze in childhood is well described as an episodic viral wheeze. Although highly controversial, LTRA has proven efficacy for episodic viral wheeze and can be useful when asthma exacerbates by viral infections [4]. It is difficult to identify practical biomarkers of LTRA that are safe, easy to take, and effective asthma controllers. To our knowledge, the best LTRA efficacy is seen for treating asthma in young children and asthma of short duration [5]. Many recent studies have determined the effectiveness of LTRA treatment by noninvasively measuring eosinophil-derived neurotoxin (EDN). EDN may act as a predictor of the development of recurrent wheezing in patients with postrespiratory syncytial virus bronchiolitis. A meta-analysis reported that montelukast reduced EDN levels in children with recurrent wheezing [5]. However, most studies of EDN examined patients with recurrent wheezing. Therefore, well-designed studies of EDN in asthma patients remain insufficient, making its application difficult in practical clinical practice.

Now, 20 years after the introduction of montelukast in Korea, this review article [6] addresses the effects of LTRA on asthma. However, LTRA also has a profound effect on symptom control in children with allergic rhinitis. Of course, as with asthma, LTRA is less effective at treating allergic rhinitis than intranasal steroids, with somewhat contradictory results compared to antihistamines [7]. Combination therapy of montelukast and a second-generation antihistamine may be more effective at controlling symptoms than administering monotherapy [8]. Intranasal steroid is the primary recommended drug for allergic rhinitis, but for patients who cannot use intranasal steroids, LTRA alone or in combination with an antihistamine may be recommended [9]. LTRA is also useful in the presence of asthma and allergic rhinitis and has some effectiveness at alleviating symptoms of allergic conjunctivitis [10].

In the absence of key tools for precision medicine, the most appropriate approach for the thoughtful clinician is to perform a therapeutic trial in an individual patient to assess the potential benefit of montelukast. Such a trial should be as objective as possible and finite in length considering the variable natural history of children who wheeze. A significant minority of children can undoubtedly benefit from montelukast, and this approach could be the most effective way to identify such children while minimizing over-prescription to children who do not benefit from this treatment.

Notes

No potential conflict of interest relevant to this article was reported.

References

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