Cargando…
Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population
BACKGROUND: Pediatric mpox cases comprise less than 0.3% of the total cases reported in the United States during the global 2022 outbreak. As a result, relatively little is known about the epidemiology or performance characteristics of clinical testing in this group. METHODS: We retrospectively extr...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier B.V.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089974/ https://www.ncbi.nlm.nih.gov/pubmed/37068452 http://dx.doi.org/10.1016/j.jcv.2023.105447 |
_version_ | 1785022863809445888 |
---|---|
author | Ma, Angela Bradley, Benjamin T. |
author_facet | Ma, Angela Bradley, Benjamin T. |
author_sort | Ma, Angela |
collection | PubMed |
description | BACKGROUND: Pediatric mpox cases comprise less than 0.3% of the total cases reported in the United States during the global 2022 outbreak. As a result, relatively little is known about the epidemiology or performance characteristics of clinical testing in this group. METHODS: We retrospectively extracted and analyzed results for pediatric mpox specimens tested at a national reference laboratory from July to December 2022. RESULTS: During our study period 13.4% (2,063/15,385) of specimens were from individuals <18 years of age. The positivity rate of pediatric specimens was significantly lower than in adults (1.3% vs 22.3%). The pediatric cohort also consisted of a higher percentage of females (42.7% vs 31.0%) and lower percentage of specimens from genital sources (9.0% vs 19.7%) as compared to adults. In children, specimens were most frequently collected from 1-year-olds (10.1%) and least frequently from 11-year-olds (3.5%). Positivity rates were disproportionately elevated in the less than 1-year-old and 17-year-old age groups (7.8% and 6.4%, respectively). Ct values of positive cases were not statistically different between pediatric and adult cohorts (25.2 vs 22.2, p>0.05). When all pediatric cases with an initial positive mpox result were examined, 5/26 were classified as inconclusive and 2/26 were determined to be false positives. The positive predictive value of monkeypox virus detection was 90.5% (95% CI: 70.4–97.4%) in children. CONCLUSION: These results highlight important differences between pediatric and adult mpox populations and reinforce the need for clinical correlation when reporting positive results from a low prevalence population. |
format | Online Article Text |
id | pubmed-10089974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Author(s). Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100899742023-04-12 Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population Ma, Angela Bradley, Benjamin T. J Clin Virol Article BACKGROUND: Pediatric mpox cases comprise less than 0.3% of the total cases reported in the United States during the global 2022 outbreak. As a result, relatively little is known about the epidemiology or performance characteristics of clinical testing in this group. METHODS: We retrospectively extracted and analyzed results for pediatric mpox specimens tested at a national reference laboratory from July to December 2022. RESULTS: During our study period 13.4% (2,063/15,385) of specimens were from individuals <18 years of age. The positivity rate of pediatric specimens was significantly lower than in adults (1.3% vs 22.3%). The pediatric cohort also consisted of a higher percentage of females (42.7% vs 31.0%) and lower percentage of specimens from genital sources (9.0% vs 19.7%) as compared to adults. In children, specimens were most frequently collected from 1-year-olds (10.1%) and least frequently from 11-year-olds (3.5%). Positivity rates were disproportionately elevated in the less than 1-year-old and 17-year-old age groups (7.8% and 6.4%, respectively). Ct values of positive cases were not statistically different between pediatric and adult cohorts (25.2 vs 22.2, p>0.05). When all pediatric cases with an initial positive mpox result were examined, 5/26 were classified as inconclusive and 2/26 were determined to be false positives. The positive predictive value of monkeypox virus detection was 90.5% (95% CI: 70.4–97.4%) in children. CONCLUSION: These results highlight important differences between pediatric and adult mpox populations and reinforce the need for clinical correlation when reporting positive results from a low prevalence population. The Author(s). Published by Elsevier B.V. 2023-06 2023-04-12 /pmc/articles/PMC10089974/ /pubmed/37068452 http://dx.doi.org/10.1016/j.jcv.2023.105447 Text en © 2023 The Author(s) Elsevier has created a Monkeypox Information Center (https://www.elsevier.com/connect/monkeypox-information-center) in response to the declared public health emergency of international concern, with free information in English on the monkeypox virus. The Monkeypox Information Center is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its monkeypox related research that is available on the Monkeypox Information Center - including this research content - immediately available in publicly funded repositories, with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the Monkeypox Information Center remains active. |
spellingShingle | Article Ma, Angela Bradley, Benjamin T. Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population |
title | Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population |
title_full | Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population |
title_fullStr | Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population |
title_full_unstemmed | Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population |
title_short | Clinical testing of pediatric mpox specimens: Unique features and challenges in a low prevalence population |
title_sort | clinical testing of pediatric mpox specimens: unique features and challenges in a low prevalence population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089974/ https://www.ncbi.nlm.nih.gov/pubmed/37068452 http://dx.doi.org/10.1016/j.jcv.2023.105447 |
work_keys_str_mv | AT maangela clinicaltestingofpediatricmpoxspecimensuniquefeaturesandchallengesinalowprevalencepopulation AT bradleybenjamint clinicaltestingofpediatricmpoxspecimensuniquefeaturesandchallengesinalowprevalencepopulation |