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Hypertonic saline monotherapy in children with perennial allergic rhinitis: a pilot study
S Barberi1, E D'Auria2, L Bernardo1
1Department of Pediatrics, A.O. Fatebenefratelli, Milan, Italy.
Insights
This pilot study found that 3% hypertonic saline nasal spray effectively improved nasal symptoms and parental-reported outcomes in children with perennial allergic rhinitis (PAR) caused by house dust mites (HDM). The treatment was safe and well-tolerated.
Area of Science:
- Pediatric Allergy and Immunology
- Otolaryngology
- Nasal Therapeutics
Background:
- Perennial allergic rhinitis (PAR) significantly impacts children's quality of life and family well-being.
- House dust mites (HDM) are a primary trigger for PAR in pediatric populations.
- Effective and safe monotherapy options for pediatric PAR require further investigation.
Purpose of the Study:
- To assess the efficacy of 3% hypertonic saline nasal spray as monotherapy for pediatric PAR.
- To evaluate improvements in nasal symptom severity and parental perception of rhinitis control.
- To determine the impact on children's sleep and school performance.
Main Methods:
- Pilot study involving 25 children (mean age 9.5 years) with HDM-sensitized PAR.
- Treatment with 3% hypertonic saline nasal spray for 3 weeks.
- Assessments at baseline, end of treatment, and 2-week follow-up.
Main Results:
- Significant reduction in total nasal symptom scores.
- Improved parental perception of rhinitis control.
- Enhanced sleep quality and school performance reported by parents.
Conclusions:
- 3% hypertonic saline monotherapy demonstrates efficacy in relieving nasal symptoms in children with PAR.
- The treatment positively influences parental perception of rhinitis control, sleep, and school performance.
- Hypertonic saline nasal spray is a safe and well-tolerated option for pediatric PAR.
Abstract:
Perennial allergic rhinitis (PAR) is very common in children and has a relevant impact on their families. House dust mites (HDM) are the most relevant cause of PAR. The present pilot study aimed to evaluate whether hypertonic saline (3%) nasal spray as monotherapy is able to improve: nasal symptom severity and parental perception of rhinitis control, sleep, and school performance in HDM-mono-sensitized children with PAR. Globally, 25 children (13 males and 12 females; mean age 9.5±3.1 years) were treated for 3 weeks. They were visited at baseline, at the end of treatment, and after a 2-week follow-up. Hypertonic saline significantly reduced total symptom score, and improved the perception, according to their parents, of rhinitis control, sleep, and school performance. In conclusion, the present pilot study provided the first evidence that 3% hypertonic saline monotherapy was able to relieve nasal symptoms and parental perception of PAR impact as well as being safe and well tolerated.
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