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Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis

While peanut oral immunotherapy (POIT) represents a promising treatment for peanut allergies in children, safety concerns remain a common barrier to widespread adoption. We aimed to systematically assess available evidence to determine the risk and frequency of adverse events occurring during POIT,...

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Autores principales: Grzeskowiak, Luke E., Tao, Billy, Knight, Emma, Cohen-Woods, Sarah, Chataway, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971009/
https://www.ncbi.nlm.nih.gov/pubmed/31959857
http://dx.doi.org/10.1038/s41598-019-56961-3
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author Grzeskowiak, Luke E.
Tao, Billy
Knight, Emma
Cohen-Woods, Sarah
Chataway, Timothy
author_facet Grzeskowiak, Luke E.
Tao, Billy
Knight, Emma
Cohen-Woods, Sarah
Chataway, Timothy
author_sort Grzeskowiak, Luke E.
collection PubMed
description While peanut oral immunotherapy (POIT) represents a promising treatment for peanut allergies in children, safety concerns remain a common barrier to widespread adoption. We aimed to systematically assess available evidence to determine the risk and frequency of adverse events occurring during POIT, and examine study-level characteristics associated with their occurrence and severity. A systematic search of MEDLINE, EMBASE, and Web of Science was conducted through April 2019. Controlled and non-controlled studies evaluating POIT were eligible. Twenty-seven studies, involving 1488 subjects, were included. Adverse events to POIT were common and led to treatment discontinuation in 6.6% of children (95% CI 4.4–9.0; 27 studies, I(2) = 48.7%). Adverse events requiring treatment with epinephrine occurred among 7.6% (4.5–11.4; 26 studies, I(2) = 75.5%) of participants, at a rate of 2.0 per 10,000 doses (0.8–3.7; 15 studies, I(2) = 64.4). Use of a rush treatment phase and targeting a higher maintenance dose were associated with a higher risk and frequency of epinephrine use, while using co-treatments in addition to POIT was associated with a lower risk of treatment discontinuation due to adverse events. While adverse events to POIT are common, this study provides promising explorative evidence that certain modifications to existing treatment protocols could significantly improve treatment outcomes.
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spelling pubmed-69710092020-01-27 Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis Grzeskowiak, Luke E. Tao, Billy Knight, Emma Cohen-Woods, Sarah Chataway, Timothy Sci Rep Article While peanut oral immunotherapy (POIT) represents a promising treatment for peanut allergies in children, safety concerns remain a common barrier to widespread adoption. We aimed to systematically assess available evidence to determine the risk and frequency of adverse events occurring during POIT, and examine study-level characteristics associated with their occurrence and severity. A systematic search of MEDLINE, EMBASE, and Web of Science was conducted through April 2019. Controlled and non-controlled studies evaluating POIT were eligible. Twenty-seven studies, involving 1488 subjects, were included. Adverse events to POIT were common and led to treatment discontinuation in 6.6% of children (95% CI 4.4–9.0; 27 studies, I(2) = 48.7%). Adverse events requiring treatment with epinephrine occurred among 7.6% (4.5–11.4; 26 studies, I(2) = 75.5%) of participants, at a rate of 2.0 per 10,000 doses (0.8–3.7; 15 studies, I(2) = 64.4). Use of a rush treatment phase and targeting a higher maintenance dose were associated with a higher risk and frequency of epinephrine use, while using co-treatments in addition to POIT was associated with a lower risk of treatment discontinuation due to adverse events. While adverse events to POIT are common, this study provides promising explorative evidence that certain modifications to existing treatment protocols could significantly improve treatment outcomes. Nature Publishing Group UK 2020-01-20 /pmc/articles/PMC6971009/ /pubmed/31959857 http://dx.doi.org/10.1038/s41598-019-56961-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Grzeskowiak, Luke E.
Tao, Billy
Knight, Emma
Cohen-Woods, Sarah
Chataway, Timothy
Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis
title Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis
title_full Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis
title_fullStr Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis
title_full_unstemmed Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis
title_short Adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis
title_sort adverse events associated with peanut oral immunotherapy in children – a systematic review and meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971009/
https://www.ncbi.nlm.nih.gov/pubmed/31959857
http://dx.doi.org/10.1038/s41598-019-56961-3
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