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Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore
BACKGROUND: The predictive decision points for both peanut skin prick test (SPT) wheal size and serum IgE concentrations, in peanut-sensitized children, have not been evaluated in Singapore. OBJECTIVE: We aim to derive clinically useful predictive decision points to be used for risk stratification o...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Asia Pacific Association of Allergy, Asthma and Clinical Immunology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676064/ https://www.ncbi.nlm.nih.gov/pubmed/31384576 http://dx.doi.org/10.5415/apallergy.2019.9.e21 |
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author | Chong, Kok Wee Saffari, Seyed Ehsan Chan, Nicole Seah, Raynian Tan, Chek Han Goh, Si Hui Goh, Anne Loh, Wenyin |
author_facet | Chong, Kok Wee Saffari, Seyed Ehsan Chan, Nicole Seah, Raynian Tan, Chek Han Goh, Si Hui Goh, Anne Loh, Wenyin |
author_sort | Chong, Kok Wee |
collection | PubMed |
description | BACKGROUND: The predictive decision points for both peanut skin prick test (SPT) wheal size and serum IgE concentrations, in peanut-sensitized children, have not been evaluated in Singapore. OBJECTIVE: We aim to derive clinically useful predictive decision points to be used for risk stratification of oral food challenge (OFC) in peanut-sensitized patients. METHODS: Patients with a positive SPT to peanut, performed during a 4-year period between 2012 and 2016, were included in a retrospective chart review. The patients were assessed for their peanut allergy status based on a convincing clinical history. Their first SPT and serum IgE results done at presentation to our centre were used. RESULTS: There were 269 patients with a clinical diagnosis of peanut allergy based on recent immediate reaction to peanut and 59 patients whom were tolerating peanuts regularly. There were 251 patients sensitized to peanut, without prior known peanut exposure. A wheal size of ≥8 mm and a peanut-specific IgE of ≥6 kU/L each provided for a 95% positive predictive value of clinical reaction to peanuts; the larger the wheal size on SPT, the higher the probability. CONCLUSION: The cutoff values derived in this study can help clinicians in the risk assessment of OFC in peanut-sensitized patients. Prospective studies using OFCs for the diagnosis of peanut allergy are needed to confirm the diagnostic performance of these tests in predicting OFC outcomes. |
format | Online Article Text |
id | pubmed-6676064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Asia Pacific Association of Allergy, Asthma and Clinical Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-66760642019-08-05 Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore Chong, Kok Wee Saffari, Seyed Ehsan Chan, Nicole Seah, Raynian Tan, Chek Han Goh, Si Hui Goh, Anne Loh, Wenyin Asia Pac Allergy Original Article BACKGROUND: The predictive decision points for both peanut skin prick test (SPT) wheal size and serum IgE concentrations, in peanut-sensitized children, have not been evaluated in Singapore. OBJECTIVE: We aim to derive clinically useful predictive decision points to be used for risk stratification of oral food challenge (OFC) in peanut-sensitized patients. METHODS: Patients with a positive SPT to peanut, performed during a 4-year period between 2012 and 2016, were included in a retrospective chart review. The patients were assessed for their peanut allergy status based on a convincing clinical history. Their first SPT and serum IgE results done at presentation to our centre were used. RESULTS: There were 269 patients with a clinical diagnosis of peanut allergy based on recent immediate reaction to peanut and 59 patients whom were tolerating peanuts regularly. There were 251 patients sensitized to peanut, without prior known peanut exposure. A wheal size of ≥8 mm and a peanut-specific IgE of ≥6 kU/L each provided for a 95% positive predictive value of clinical reaction to peanuts; the larger the wheal size on SPT, the higher the probability. CONCLUSION: The cutoff values derived in this study can help clinicians in the risk assessment of OFC in peanut-sensitized patients. Prospective studies using OFCs for the diagnosis of peanut allergy are needed to confirm the diagnostic performance of these tests in predicting OFC outcomes. Asia Pacific Association of Allergy, Asthma and Clinical Immunology 2019-07-08 /pmc/articles/PMC6676064/ /pubmed/31384576 http://dx.doi.org/10.5415/apallergy.2019.9.e21 Text en Copyright © 2019. Asia Pacific Association of Allergy, Asthma and Clinical Immunology. https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Chong, Kok Wee Saffari, Seyed Ehsan Chan, Nicole Seah, Raynian Tan, Chek Han Goh, Si Hui Goh, Anne Loh, Wenyin Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore |
title | Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore |
title_full | Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore |
title_fullStr | Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore |
title_full_unstemmed | Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore |
title_short | Predictive value of peanut skin prick test, specific IgE in peanut-sensitized children in Singapore |
title_sort | predictive value of peanut skin prick test, specific ige in peanut-sensitized children in singapore |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676064/ https://www.ncbi.nlm.nih.gov/pubmed/31384576 http://dx.doi.org/10.5415/apallergy.2019.9.e21 |
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