Publication:
Sublingual immunotherapy in children with allergic rhinoconjunctivitis mono-sensitized to house-dust-mites: A double-blind-placebo-controlled randomised trial

dc.contributor.authorAKKOÇ, TUNÇ
dc.contributor.authorsAydogan, Metin; Eifan, Aarif O.; Keles, Sevgi; Akkoc, Tunc; Nursoy, Mustafa A.; Bahceciler, Nerrin N.; Barlan, Isil B.
dc.date.accessioned2022-03-14T10:56:04Z
dc.date.accessioned2026-01-10T19:01:53Z
dc.date.available2022-03-14T10:56:04Z
dc.date.issued2013-09
dc.description.abstractBackground: Although sublingual immunotherapy (SLIT) has been demonstrated to be a safe and efficient treatment in children with seasonal allergic rhinitis (AR), there is little evidence on the efficacy of SLIT with house-dust-mite (HDM) extract in children with isolated perennial AR. Objectives: We sought to assess the clinical efficacy and safety of HDM-SLIT in children with isolated allergic rhinitis-conjunctivitis mono-sensitized to HDM without asthma symptoms. Methods: Twenty-two children (aged 5-10 years) with perennial AR and conjunctivitis symptoms mono-sensitized to Dermatophagoides pteronyssinus and Dermatophagoides farinae were enrolled. During a 2 months run-in period, symptom and medication scores, lung functions, bronchial hyperreactivity, nasal provocation and skin prick tests were evaluated. Subjects were randomized to active or placebo using a double-blind method. A total of eighteen subjects were randomised to receive either active SLIT or placebo for 12 months. Daily symptom and medication scores, baseline lung functions, bronchial hyperreactivity, nasal provocation and skin prick tests were recorded and re-evaluated at the end of treatment. Results: After one year of treatment, no significant differences were detected in the between groups and within group comparisons based on total rhinitis symptom/medication scores (p > 0.05). Skin reactivity to Dermatophagoides pteronyssinus was significantly reduced in HDM-SLIT compared to placebo group (p = 0.018). A significant reduction in nasal sensitivity was observed in SLIT group after one year treatment when compared to baseline (p = 0.04). Total conjunctivitis symptoms were reduced significantly in both active and lacebo group at the end of treatment compared to baseline. The proportion of patients with nonspecific bronchial hyperreactivity increased to almost 3-fold in placebo group compared to baseline. Conclusion: HDM-SLIT was not superior to placebo in reducing isolated rhinoconjunctivitis symptoms within 12 months of treatment. However, HDM-SLIT has a modulating effect on allergen-specific nasal and skin reactivity in isolated perennial AR children. Clinical Trial Registration: The trial was registered at Anzctr.org.au number, ACTRN1261 3000315718. (C) 2013 Elsevier Ltd. All rights reserved.
dc.identifier.doi10.1016/j.rmed.2013.06.021
dc.identifier.eissn1532-3064
dc.identifier.issn0954-6111
dc.identifier.pubmed23886432
dc.identifier.urihttps://hdl.handle.net/11424/245512
dc.identifier.wosWOS:000330271600005
dc.language.isoeng
dc.publisherW B SAUNDERS CO LTD
dc.relation.ispartofRESPIRATORY MEDICINE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAllergy
dc.subjectAsthma
dc.subjectConjunctivitis
dc.subjectDust mite
dc.subjectRhinitis
dc.subjectSublingual immunotherapy
dc.subjectRHINITIS
dc.subjectASTHMA
dc.subjectEFFICACY
dc.subjectCHILDHOOD
dc.subjectCONJUNCTIVITIS
dc.subjectPARAMETERS
dc.subjectEXTRACT
dc.subjectIMPACT
dc.titleSublingual immunotherapy in children with allergic rhinoconjunctivitis mono-sensitized to house-dust-mites: A double-blind-placebo-controlled randomised trial
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage1329
oaire.citation.issue9
oaire.citation.startPage1322
oaire.citation.titleRESPIRATORY MEDICINE
oaire.citation.volume107

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