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Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study
OBJECTIVES: To assess neurological sequelae and growth in the first 12 months of life in a cohort of congenital cytomegalovirus (cCMV) infected infants compared to cCMV uninfected infants. STUDY DESIGN: This was a prospective matched cohort study conducted in Soweto, South Africa where forty-six con...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498063/ https://www.ncbi.nlm.nih.gov/pubmed/32941484 http://dx.doi.org/10.1371/journal.pone.0238102 |
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author | Pathirana, Jayani Texeira, Leanne Munian, Hannah Nakwa, Firdose Mayet, Ismail Maposa, Innocent Groome, Michelle J. Boppana, Suresh Madhi, Shabir A. |
author_facet | Pathirana, Jayani Texeira, Leanne Munian, Hannah Nakwa, Firdose Mayet, Ismail Maposa, Innocent Groome, Michelle J. Boppana, Suresh Madhi, Shabir A. |
author_sort | Pathirana, Jayani |
collection | PubMed |
description | OBJECTIVES: To assess neurological sequelae and growth in the first 12 months of life in a cohort of congenital cytomegalovirus (cCMV) infected infants compared to cCMV uninfected infants. STUDY DESIGN: This was a prospective matched cohort study conducted in Soweto, South Africa where forty-six confirmed cCMV cases were matched on HIV-exposure, gender and gestational age (±two weeks) to 84 cCMV-uninfected controls in a 1:2 ratio. Cases and controls were followed up until 12 months of age to assess anthropometry, hearing and neurodevelopmental outcomes. RESULTS: Thirty-four (73.9%) cCMV cases and 74 (88.1%) controls, completed all assessments at 12 months age. At 12 months, one cCMV case had died, none of the children in either group had SNHL and neurodevelopmental delay was present in a similar percentage of cCMV cases (n = 2; 6%) and controls (n = 1, 4%; OR 1.09, 95% CI 0.04–27.84, p = 0.958). Anthropometry did not differ between cases and controls overall throughout the follow up period. HIV-exposed cases had smaller head circumference for age at 6 and 12 months when compared with HIV-exposed controls. CONCLUSION: By 12 months of age, there was no evidence of a difference in neurological sequelae between cCMV infected South African children and cCMV uninfected children in this study. Further follow-up is warranted to detect late-onset hearing loss and neurodevelopmental delay beyond 12 months of age. |
format | Online Article Text |
id | pubmed-7498063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74980632020-09-24 Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study Pathirana, Jayani Texeira, Leanne Munian, Hannah Nakwa, Firdose Mayet, Ismail Maposa, Innocent Groome, Michelle J. Boppana, Suresh Madhi, Shabir A. PLoS One Research Article OBJECTIVES: To assess neurological sequelae and growth in the first 12 months of life in a cohort of congenital cytomegalovirus (cCMV) infected infants compared to cCMV uninfected infants. STUDY DESIGN: This was a prospective matched cohort study conducted in Soweto, South Africa where forty-six confirmed cCMV cases were matched on HIV-exposure, gender and gestational age (±two weeks) to 84 cCMV-uninfected controls in a 1:2 ratio. Cases and controls were followed up until 12 months of age to assess anthropometry, hearing and neurodevelopmental outcomes. RESULTS: Thirty-four (73.9%) cCMV cases and 74 (88.1%) controls, completed all assessments at 12 months age. At 12 months, one cCMV case had died, none of the children in either group had SNHL and neurodevelopmental delay was present in a similar percentage of cCMV cases (n = 2; 6%) and controls (n = 1, 4%; OR 1.09, 95% CI 0.04–27.84, p = 0.958). Anthropometry did not differ between cases and controls overall throughout the follow up period. HIV-exposed cases had smaller head circumference for age at 6 and 12 months when compared with HIV-exposed controls. CONCLUSION: By 12 months of age, there was no evidence of a difference in neurological sequelae between cCMV infected South African children and cCMV uninfected children in this study. Further follow-up is warranted to detect late-onset hearing loss and neurodevelopmental delay beyond 12 months of age. Public Library of Science 2020-09-17 /pmc/articles/PMC7498063/ /pubmed/32941484 http://dx.doi.org/10.1371/journal.pone.0238102 Text en © 2020 Pathirana et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Pathirana, Jayani Texeira, Leanne Munian, Hannah Nakwa, Firdose Mayet, Ismail Maposa, Innocent Groome, Michelle J. Boppana, Suresh Madhi, Shabir A. Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study |
title | Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study |
title_full | Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study |
title_fullStr | Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study |
title_full_unstemmed | Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study |
title_short | Neurological and growth outcomes in South African children with congenital cytomegalovirus: A cohort study |
title_sort | neurological and growth outcomes in south african children with congenital cytomegalovirus: a cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498063/ https://www.ncbi.nlm.nih.gov/pubmed/32941484 http://dx.doi.org/10.1371/journal.pone.0238102 |
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