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Updated: May 18, 2026

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Exploring the characteristics of children with obstructive adenoid responding to mometasone fuorate monohydrate:
Mohamed A Bitar1, Lorice Mahfoud, Jihad Nassar
1Department of Otolaryngology Head and Neck Surgery, American University of Beirut Medical Center, PO Box 11-0236/A52, Beirut, Lebanon. mb36@aub.edu.lb
Insights
Mometasone furoate monohydrate nasal spray effectively reduced obstructive adenoids in children. The treatment improved symptoms and obstruction, with effects independent of age or allergic rhinitis severity.
Area of Science:
- Otorhinolaryngology
- Pediatric Allergy
- Pharmacology
Background:
- Adenoid obstruction significantly impacts children's health.
- Current treatment options for obstructive adenoids are limited.
- Mometasone furoate monohydrate nasal spray is a potential therapeutic agent.
Purpose of the Study:
- To evaluate the efficacy of mometasone furoate monohydrate nasal spray in children with obstructive adenoids.
- To identify predictors of treatment response.
- To assess the impact on allergic rhinitis and obstructive symptoms.
Main Methods:
- Pilot study involving children aged 2-11 years with >50% adenoid obstruction.
- Daily administration of 100 μg mometasone furoate monohydrate nasal spray.
- Clinical and endoscopic evaluations at baseline, 6, and 12 weeks, compared to a control group.
Main Results:
- Significant reduction in adenoidal obstruction (58%) and obstructive symptoms (56%) within 6 weeks (P < 0.05).
- Marked improvement in allergic rhinitis scores (75%) (P < 0.05).
- Endoscopic obstruction decreased from 85% to 61% (P < 0.05); no significant changes after 6 weeks.
Conclusions:
- Mometasone furoate monohydrate nasal spray is effective for treating obstructive adenoids in children.
- Treatment benefits were observed regardless of patient age, allergic rhinitis presence, or symptom severity.
- No adverse effects were reported, suggesting a favorable safety profile.
Abstract:
This study aimed at observing the efficacy of mometasone fuorate monohydrate nasal spray on obstructive adenoids in children and identifying the characteristics of responders using a pilot study including children aged 2-11 years, with evidence of more than 50 % obstruction. Allergic rhinitis and nasal obstruction were evaluated on baseline (V0), 6- (V1), and 12-week (V2) visits. Degree of obstruction was evaluated by nasopharyngoscopy at V0 and V2. Subjects received 100 μg mometasone fuorate daily. Results were compared with those of a matching control group. Nineteen children (8 females, 11 males; 2.25-8.50 years old, mean 4.24 years, median 4.00 years) completed treatment and follow-up adequately. There was 58 % reduction in a clinical score assessing the severity of adenoidal obstruction (P < 0.05), 56 % reduction in severity of obstructive symptom (P < 0.05), and 75 % reduction in allergic rhinitis score (P < 0.05) between V0 and V1. No further significant improvement was noticed between V1 and V2. The degree of obstruction dropped from 85 to 61 % as noted on endoscopy (P < 0.05). None in the control group showed spontaneous decrease or resolution of the symptoms. Age of patients, allergic rhinitis score, and severity of the clinical score had no impact on the response parameters. No side effects were observed. Mometasone furoate monohydrate nasal spray appears to be effective in treating children with obstructive adenoids. The effect seems to be independent of the presence of mild intermittent allergic rhinitis, the age of patient, or the severity of symptoms.
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