Efficacy of sublingual immunotherapy in children with asthma and rhinitis:A double-blind, placebo-controlled study

Citation
Nn. Bahceciler et al., Efficacy of sublingual immunotherapy in children with asthma and rhinitis:A double-blind, placebo-controlled study, PEDIAT PULM, 32(1), 2001, pp. 49-55
Citations number
21
Categorie Soggetti
Pediatrics
Journal title
PEDIATRIC PULMONOLOGY
ISSN journal
87556863 → ACNP
Volume
32
Issue
1
Year of publication
2001
Pages
49 - 55
Database
ISI
SICI code
8755-6863(200107)32:1<49:EOSIIC>2.0.ZU;2-V
Abstract
To evaluate the efficacy of specific sublingual immunotherapy (SLIT), we en rolled 15 children with asthma and rhinitis (7 girls, 8 boys, mean +/- SD a ge of 11.7 +/- 3.3) allergic to house dust mite (HDM) into a double-blind, placebo-controlled study. After a run-in period, patients were randomized t o receive either placebo (n = 7) or SLIT (n = 8) with a standardized Dermat ophagoides pteronyssinus (D. pteronyssinus) + Dermatophagoides farinea (D. farinea) 50/50 extract. They received increasing doses up to 100 index unit s of reactivity (IR) every day for 4 weeks, then 100 IR/day for another 4 w eeks, followed by maintenance therapy consisting of 20 drops 2 times a week for 4 months. Efficacy was assessed at the end of 6 months of therapy acco rding to symptom and medication scores, serum total IgE levels, results of lung function tests, methacholine provocation tests, and skin prick tests. Daily means for the asthma score and use of inhaled beta-2-mimetics decreas ed significantly in the SLIT group (P = 0.05, P = 0.028, respectively), whe reas no such difference was observed in the placebo group. At the end of fo llow-up, mean daily doses of intranasal steroids needed for control of rhin itis symptoms decreased significantly in the SLIT group (P = 0.04). Baselin e skin sensitivity to D. pteronyssinus and D. farinea was not significantly different between in the two groups, whereas end-point wheal diameter obta ined with D.pteronyssinus extract was significantly less in the SLIT vs. th e placebo group (p = 0.026). At the end of 6 months, peak expiratory flow ( PEF) values in the placebo group was significantly lower than in the SLIT g roup (P = 0.049). Throughout the treatment period, the SLIT group was found to have less asthma exacerbations than the placebo group (p = 0.007). The provocation concentration causing a 20% drop in forced expired volume in 1 sec did not change throughout the treatment period in either groups. None o f the patients reported local or systemic side effects from SLIT. Results of this study suggests that SLIT may be a useful alternative or add itional therapy in the treatment of children with asthma/rhinitis due to HD M. (C) 2001 Wiley-Liss, Inc.