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Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary

Tuberculosis (TB) remains a significant, yet under-recognized cause of death in the pediatric population, with a WHO estimate of 1 million new cases of childhood TB in 2016 resulting in 250,000 deaths. Diagnosis is notoriously difficult; manifestations are protean due to the high proportion of cases...

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Autores principales: Atherton, Rachel R., Cresswell, Fiona V., Ellis, Jayne, Kitaka, Sabrina B., Boulware, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403143/
https://www.ncbi.nlm.nih.gov/pubmed/30873392
http://dx.doi.org/10.3389/fped.2019.00034
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author Atherton, Rachel R.
Cresswell, Fiona V.
Ellis, Jayne
Kitaka, Sabrina B.
Boulware, David R.
author_facet Atherton, Rachel R.
Cresswell, Fiona V.
Ellis, Jayne
Kitaka, Sabrina B.
Boulware, David R.
author_sort Atherton, Rachel R.
collection PubMed
description Tuberculosis (TB) remains a significant, yet under-recognized cause of death in the pediatric population, with a WHO estimate of 1 million new cases of childhood TB in 2016 resulting in 250,000 deaths. Diagnosis is notoriously difficult; manifestations are protean due to the high proportion of cases of extra-pulmonary TB in children, and logistical problems exist in obtaining suitable specimens. These issues are compounded by the paucibacillary nature of disease with the result that an estimated 96% of pediatric TB-associated mortality occurs prior to commencing anti-tuberculous treatment. Further development of sensitive, rapid diagnostic tests and their incorporation into diagnostic algorithms is vital in this population, and central to the WHO End-TB strategy. Initial gains were made with the expansion of nucleic acid amplification technology, particularly the introduction of the GeneXpert fully-automated PCR Xpert MTB/Rif assay in 2010, and more recently, the Xpert MTB/Rif Ultra (Ultra) assay in 2017. Ultra provides increased analytical sensitivity when compared with the initial Xpert assay in vitro; a finding now also supported by six clinical studies to date, two of which included pediatric samples. Here, we review the published evidence for the performance of Ultra in TB diagnosis in children, as well as studies in adults with paucibacillary disease providing results relevant to the pediatric population. Following on from this, we speculate upon future directions for Ultra, with focus on its potential use with alternative diagnostic specimens, which may be of particular utility in children.
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spelling pubmed-64031432019-03-14 Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary Atherton, Rachel R. Cresswell, Fiona V. Ellis, Jayne Kitaka, Sabrina B. Boulware, David R. Front Pediatr Pediatrics Tuberculosis (TB) remains a significant, yet under-recognized cause of death in the pediatric population, with a WHO estimate of 1 million new cases of childhood TB in 2016 resulting in 250,000 deaths. Diagnosis is notoriously difficult; manifestations are protean due to the high proportion of cases of extra-pulmonary TB in children, and logistical problems exist in obtaining suitable specimens. These issues are compounded by the paucibacillary nature of disease with the result that an estimated 96% of pediatric TB-associated mortality occurs prior to commencing anti-tuberculous treatment. Further development of sensitive, rapid diagnostic tests and their incorporation into diagnostic algorithms is vital in this population, and central to the WHO End-TB strategy. Initial gains were made with the expansion of nucleic acid amplification technology, particularly the introduction of the GeneXpert fully-automated PCR Xpert MTB/Rif assay in 2010, and more recently, the Xpert MTB/Rif Ultra (Ultra) assay in 2017. Ultra provides increased analytical sensitivity when compared with the initial Xpert assay in vitro; a finding now also supported by six clinical studies to date, two of which included pediatric samples. Here, we review the published evidence for the performance of Ultra in TB diagnosis in children, as well as studies in adults with paucibacillary disease providing results relevant to the pediatric population. Following on from this, we speculate upon future directions for Ultra, with focus on its potential use with alternative diagnostic specimens, which may be of particular utility in children. Frontiers Media S.A. 2019-02-28 /pmc/articles/PMC6403143/ /pubmed/30873392 http://dx.doi.org/10.3389/fped.2019.00034 Text en Copyright © 2019 Atherton, Cresswell, Ellis, Kitaka and Boulware. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Atherton, Rachel R.
Cresswell, Fiona V.
Ellis, Jayne
Kitaka, Sabrina B.
Boulware, David R.
Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary
title Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary
title_full Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary
title_fullStr Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary
title_full_unstemmed Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary
title_short Xpert MTB/RIF Ultra for Tuberculosis Testing in Children: A Mini-Review and Commentary
title_sort xpert mtb/rif ultra for tuberculosis testing in children: a mini-review and commentary
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403143/
https://www.ncbi.nlm.nih.gov/pubmed/30873392
http://dx.doi.org/10.3389/fped.2019.00034
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