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Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view
Atopic dermatitis (AD) is a common chronic skin condition in children that has a proven association with other atopic conditions and allergies. These associations, like the general pathophysiology of AD, are complex and not fully understood. While there is evidence for the efficacy of specific immun...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836074/ https://www.ncbi.nlm.nih.gov/pubmed/27134697 http://dx.doi.org/10.1186/s40413-016-0107-2 |
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author | Ginsberg, David N. Eichenfield, Lawrence F. |
author_facet | Ginsberg, David N. Eichenfield, Lawrence F. |
author_sort | Ginsberg, David N. |
collection | PubMed |
description | Atopic dermatitis (AD) is a common chronic skin condition in children that has a proven association with other atopic conditions and allergies. These associations, like the general pathophysiology of AD, are complex and not fully understood. While there is evidence for the efficacy of specific immunotherapy (SIT) in pediatric asthma and allergic rhinitis (AR), there is a lack of strong data to support its use in AD. IgE has been shown to be elevated in many patients with AD, but it is an unreliable biomarker due to variability and great fluctuation over time, poor positive predictive value for clinically relevant allergy, and poor correlation with disease state. In spite of this, almost all studies of SIT use either positive skin prick testing (SPT) or serum specific IgE levels to guide therapy. Allergen avoidance, with some exceptions, is generally not effective at controlling AD in children. The few studies that have investigated the efficacy of SIT in children with AD have produced conflicting results, and a lack of reproducibility with a standard treatment protocol. Limited studies have shown clinical improvement in mild to moderate AD cases, but no effect on more severe patients. Uncontrolled studies are difficult to interpret, due to the natural history of remission or “outgrowing” of AD over time in many patients without specific interventions. Drawbacks to SIT include the length of treatment, poor compliance, cost, and potential side effect profile. The potential for misdirection of time and energy away from skin directed therapy could negatively impact on AD outcomes. |
format | Online Article Text |
id | pubmed-4836074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48360742016-04-29 Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view Ginsberg, David N. Eichenfield, Lawrence F. World Allergy Organ J Debate Atopic dermatitis (AD) is a common chronic skin condition in children that has a proven association with other atopic conditions and allergies. These associations, like the general pathophysiology of AD, are complex and not fully understood. While there is evidence for the efficacy of specific immunotherapy (SIT) in pediatric asthma and allergic rhinitis (AR), there is a lack of strong data to support its use in AD. IgE has been shown to be elevated in many patients with AD, but it is an unreliable biomarker due to variability and great fluctuation over time, poor positive predictive value for clinically relevant allergy, and poor correlation with disease state. In spite of this, almost all studies of SIT use either positive skin prick testing (SPT) or serum specific IgE levels to guide therapy. Allergen avoidance, with some exceptions, is generally not effective at controlling AD in children. The few studies that have investigated the efficacy of SIT in children with AD have produced conflicting results, and a lack of reproducibility with a standard treatment protocol. Limited studies have shown clinical improvement in mild to moderate AD cases, but no effect on more severe patients. Uncontrolled studies are difficult to interpret, due to the natural history of remission or “outgrowing” of AD over time in many patients without specific interventions. Drawbacks to SIT include the length of treatment, poor compliance, cost, and potential side effect profile. The potential for misdirection of time and energy away from skin directed therapy could negatively impact on AD outcomes. BioMed Central 2016-04-18 /pmc/articles/PMC4836074/ /pubmed/27134697 http://dx.doi.org/10.1186/s40413-016-0107-2 Text en © Ginsberg and Eichenfield. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Debate Ginsberg, David N. Eichenfield, Lawrence F. Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view |
title | Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view |
title_full | Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view |
title_fullStr | Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view |
title_full_unstemmed | Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view |
title_short | Debates in allergy medicine: Specific immunotherapy in children with atopic dermatitis, the “con” view |
title_sort | debates in allergy medicine: specific immunotherapy in children with atopic dermatitis, the “con” view |
topic | Debate |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836074/ https://www.ncbi.nlm.nih.gov/pubmed/27134697 http://dx.doi.org/10.1186/s40413-016-0107-2 |
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