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Optimising immunisation in children with 22q11 microdeletion

BACKGROUND: The condition known as 22q11 microdeletion syndrome has a broad phenotypic spectrum, with many affected individuals experiencing mild-to-moderate immunodeficiency. Currently, there are significant variations in live vaccine practices and immunological testing prior to live vaccine admini...

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Autores principales: Berkhout, Angela, Preece, Kahn, Varghese, Vanil, Prasad, Vinita, Heussler, Helen, Clark, Julia, Wen, Sophie C. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580130/
https://www.ncbi.nlm.nih.gov/pubmed/33150298
http://dx.doi.org/10.1177/2515135520957139
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author Berkhout, Angela
Preece, Kahn
Varghese, Vanil
Prasad, Vinita
Heussler, Helen
Clark, Julia
Wen, Sophie C. H.
author_facet Berkhout, Angela
Preece, Kahn
Varghese, Vanil
Prasad, Vinita
Heussler, Helen
Clark, Julia
Wen, Sophie C. H.
author_sort Berkhout, Angela
collection PubMed
description BACKGROUND: The condition known as 22q11 microdeletion syndrome has a broad phenotypic spectrum, with many affected individuals experiencing mild-to-moderate immunodeficiency. Currently, there are significant variations in live vaccine practices and immunological testing prior to live vaccine administration due to safety concerns and limited established guidelines. METHODS: Queensland Children’s Hospital (QCH) Child Development Unit, offers a state-wide 22q11 microdeletion clinic. This is a retrospective single-centre review, capturing the majority of children with 22q11 microdeletion in Queensland, Australia. We describe the live vaccination status of 134 children, age 0 to 18 years under our care between 2000 and 2018, adverse events following immunisation (AEFI) and the proportion of children who received additional pneumococcal coverage. An immunological investigation pathway prior to live vaccine administration is proposed. RESULTS: Of the 134 children, 124 were eligible for live vaccinations as per the Australian National Immunisation Program: 82% had received dose one of measles, mumps and rubella (MMR) vaccine, 77% had completed MMR dose two and 66% had completed varicella immunisation. There were no AEFI notifications reported. Of the total sample of children, 18% received a fourth dose of conjugate pneumococcal vaccine (Prevenar 7 or 13) and 16% received a dose of Pneumovax 23 from 4 years of age. Immunology workup practices were demonstrated to vary widely prior to live vaccine administration. Most patients’ immune profiles were consistent with mild-to-moderate immunodeficiency. CONCLUSION: We propose an immunological investigation and vaccination pathway with the aim of providing guidance and consistency to clinicians caring for children with 22q11 microdeletion.
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spelling pubmed-75801302020-11-03 Optimising immunisation in children with 22q11 microdeletion Berkhout, Angela Preece, Kahn Varghese, Vanil Prasad, Vinita Heussler, Helen Clark, Julia Wen, Sophie C. H. Ther Adv Vaccines Immunother Original Research BACKGROUND: The condition known as 22q11 microdeletion syndrome has a broad phenotypic spectrum, with many affected individuals experiencing mild-to-moderate immunodeficiency. Currently, there are significant variations in live vaccine practices and immunological testing prior to live vaccine administration due to safety concerns and limited established guidelines. METHODS: Queensland Children’s Hospital (QCH) Child Development Unit, offers a state-wide 22q11 microdeletion clinic. This is a retrospective single-centre review, capturing the majority of children with 22q11 microdeletion in Queensland, Australia. We describe the live vaccination status of 134 children, age 0 to 18 years under our care between 2000 and 2018, adverse events following immunisation (AEFI) and the proportion of children who received additional pneumococcal coverage. An immunological investigation pathway prior to live vaccine administration is proposed. RESULTS: Of the 134 children, 124 were eligible for live vaccinations as per the Australian National Immunisation Program: 82% had received dose one of measles, mumps and rubella (MMR) vaccine, 77% had completed MMR dose two and 66% had completed varicella immunisation. There were no AEFI notifications reported. Of the total sample of children, 18% received a fourth dose of conjugate pneumococcal vaccine (Prevenar 7 or 13) and 16% received a dose of Pneumovax 23 from 4 years of age. Immunology workup practices were demonstrated to vary widely prior to live vaccine administration. Most patients’ immune profiles were consistent with mild-to-moderate immunodeficiency. CONCLUSION: We propose an immunological investigation and vaccination pathway with the aim of providing guidance and consistency to clinicians caring for children with 22q11 microdeletion. SAGE Publications 2020-10-16 /pmc/articles/PMC7580130/ /pubmed/33150298 http://dx.doi.org/10.1177/2515135520957139 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Berkhout, Angela
Preece, Kahn
Varghese, Vanil
Prasad, Vinita
Heussler, Helen
Clark, Julia
Wen, Sophie C. H.
Optimising immunisation in children with 22q11 microdeletion
title Optimising immunisation in children with 22q11 microdeletion
title_full Optimising immunisation in children with 22q11 microdeletion
title_fullStr Optimising immunisation in children with 22q11 microdeletion
title_full_unstemmed Optimising immunisation in children with 22q11 microdeletion
title_short Optimising immunisation in children with 22q11 microdeletion
title_sort optimising immunisation in children with 22q11 microdeletion
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580130/
https://www.ncbi.nlm.nih.gov/pubmed/33150298
http://dx.doi.org/10.1177/2515135520957139
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