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dc.contributor.authorAsamoah, Felix
dc.contributor.authorKakourou, Artemisia
dc.contributor.authorDhami, Sangeeta
dc.contributor.authorLau, Susanne
dc.contributor.authorAgache, Ioana
dc.contributor.authorMuraro, Antonella
dc.contributor.authorRoberts, Graham
dc.contributor.authorAkdis, Cezmi
dc.contributor.authorBonini, Matteo
dc.contributor.authorCavkaytar, Ozlem
dc.contributor.authorFlood, Breda
dc.contributor.authorIzuhara, Kenji
dc.contributor.authorJutel, Marek
dc.contributor.authorKalayci, Omer
dc.contributor.authorPfaar, Oliver
dc.contributor.authorSheikh, Aziz
dc.date.accessioned2019-12-10T11:10:13Z
dc.date.available2019-12-10T11:10:13Z
dc.date.issued2017
dc.identifier.issn2045-7022
dc.identifier.urihttps://doi.org/10.1186/s13601-017-0160-0
dc.identifier.urihttp://hdl.handle.net/11655/14826
dc.description.abstractBackground: There is clinical uncertainty about the effectiveness and safety of allergen immunotherapy (AIT) for the treatment of allergic asthma. Objectives: To undertake a systematic overview of the effectiveness, cost-effectiveness and safety of AIT for the treatment of allergic asthma. Methods: We searched nine electronic databases from inception to October 31, 2015. Systematic reviews were independently screened by two reviewers against pre-defined eligibility criteria and critically appraised using the Critical Appraisal Skills Programme quality assessment tool for systematic reviews. Data were descriptively and thematically synthesized. Results: We identified nine eligible systematic reviews; these focused on delivery of AIT through the following routes: subcutaneous (SCIT; n = 3); sublingual (SLIT; n = 4); and both SCIT and SLIT (n = 2). This evidence found that AIT delivered by SCIT and SLIT can improve medication and symptom scores and measures of bronchial hyper-reactivity. The impact on measures of lung function or asthma control was however less clear. We found no systematic review level evidence on the cost-effectiveness of SCIT or SLIT. SLIT had a favorable safety profile when compared to SCIT, particularly in relation to the risk of systemic reactions. Conclusions: AIT has the potential to achieve reductions in symptom and medication scores, but there is no clear or consistent evidence that measures of lung function can be improved. Bearing in mind the limitations of synthesizing evidence from systematic reviews and the fact that these reviews include mainly dated studies, a systematic review of current primary studies is now needed to update this evidence base, estimate the effectiveness of AIT on asthma outcomes and to investigate the relative effectiveness, cost-effectiveness and safety of SCIT and SLIT.
dc.language.isoen
dc.publisherBioMed Central
dc.relation.isversionof10.1186/s13601-017-0160-0
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAllergy
dc.titleAllergen Immunotherapy for Allergic Asthma: A Systematic Overview of Systematic Reviews
dc.typeinfo:eu-repo/semantics/review
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalClinical And Translational Allergy
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume7
dc.description.indexWoS
dc.description.indexScopus


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