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Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa

BACKGROUND: Improved survival in extremely low birth weight infants (ELBWI) in Sub-Saharan Africa has raised the question whether these survivors have an increased chance of adverse neurodevelopmental outcomes. OBJECTIVES: To describe neurodevelopmental outcomes of ELBWI in a neonatal unit in South...

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Autores principales: Ramdin, Tanusha D., Saggers, Robin T., Bandini, Rossella M., Magadla, Yoliswa, Mphaphuli, Aripfani V., Ballot, Daynia E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160720/
https://www.ncbi.nlm.nih.gov/pubmed/35664886
http://dx.doi.org/10.3389/fped.2022.902263
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author Ramdin, Tanusha D.
Saggers, Robin T.
Bandini, Rossella M.
Magadla, Yoliswa
Mphaphuli, Aripfani V.
Ballot, Daynia E.
author_facet Ramdin, Tanusha D.
Saggers, Robin T.
Bandini, Rossella M.
Magadla, Yoliswa
Mphaphuli, Aripfani V.
Ballot, Daynia E.
author_sort Ramdin, Tanusha D.
collection PubMed
description BACKGROUND: Improved survival in extremely low birth weight infants (ELBWI) in Sub-Saharan Africa has raised the question whether these survivors have an increased chance of adverse neurodevelopmental outcomes. OBJECTIVES: To describe neurodevelopmental outcomes of ELBWI in a neonatal unit in South Africa. METHODS: This was a prospective follow-up study. All ELBWI who survived to discharge between 1 July 2013 and 31 December 2017 were invited to attend the clinic. Bayley Scales of Infant and Toddler Development (version III) were conducted at 9 to 12 months and 18 to 24 months. RESULTS: There were 723 ELBWI admissions during the study period, 292 (40.4%) survived to hospital discharge and 85/292 (29.1%) attended the neonatal follow up clinic. The mean birth weight was 857.7 g (95% CI: 838.2–877.2) and the mean gestational age was 27.5 weeks (95% CI 27.1–27.9). None of the infants had any major complication of prematurity. A total of 76/85 (89.4%) of the infants had a Bayley-III assessment at a mean corrected age of 17.21 months (95% CI: 16.2–18.3). The mean composite scores for cognition were 98.4 (95% CI 95.1–101.7), language 89.9 (95% CI 87.3–92.5) and motor 97.6 (95% CI 94.5–100.6). All mean scores fell within the normal range, The study found 28 (36.8%) infants to be “at risk” for neurodevelopmental delay. CONCLUSION: Our study demonstrates good neurodevelopmental outcome in a small group of surviving ELBWI, but these results must be interpreted in the context of the high mortality in this group of infants.
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spelling pubmed-91607202022-06-03 Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa Ramdin, Tanusha D. Saggers, Robin T. Bandini, Rossella M. Magadla, Yoliswa Mphaphuli, Aripfani V. Ballot, Daynia E. Front Pediatr Pediatrics BACKGROUND: Improved survival in extremely low birth weight infants (ELBWI) in Sub-Saharan Africa has raised the question whether these survivors have an increased chance of adverse neurodevelopmental outcomes. OBJECTIVES: To describe neurodevelopmental outcomes of ELBWI in a neonatal unit in South Africa. METHODS: This was a prospective follow-up study. All ELBWI who survived to discharge between 1 July 2013 and 31 December 2017 were invited to attend the clinic. Bayley Scales of Infant and Toddler Development (version III) were conducted at 9 to 12 months and 18 to 24 months. RESULTS: There were 723 ELBWI admissions during the study period, 292 (40.4%) survived to hospital discharge and 85/292 (29.1%) attended the neonatal follow up clinic. The mean birth weight was 857.7 g (95% CI: 838.2–877.2) and the mean gestational age was 27.5 weeks (95% CI 27.1–27.9). None of the infants had any major complication of prematurity. A total of 76/85 (89.4%) of the infants had a Bayley-III assessment at a mean corrected age of 17.21 months (95% CI: 16.2–18.3). The mean composite scores for cognition were 98.4 (95% CI 95.1–101.7), language 89.9 (95% CI 87.3–92.5) and motor 97.6 (95% CI 94.5–100.6). All mean scores fell within the normal range, The study found 28 (36.8%) infants to be “at risk” for neurodevelopmental delay. CONCLUSION: Our study demonstrates good neurodevelopmental outcome in a small group of surviving ELBWI, but these results must be interpreted in the context of the high mortality in this group of infants. Frontiers Media S.A. 2022-05-19 /pmc/articles/PMC9160720/ /pubmed/35664886 http://dx.doi.org/10.3389/fped.2022.902263 Text en Copyright © 2022 Ramdin, Saggers, Bandini, Magadla, Mphaphuli and Ballot. https://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
Ramdin, Tanusha D.
Saggers, Robin T.
Bandini, Rossella M.
Magadla, Yoliswa
Mphaphuli, Aripfani V.
Ballot, Daynia E.
Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa
title Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa
title_full Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa
title_fullStr Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa
title_full_unstemmed Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa
title_short Neurodevelopmental Outcomes of Extremely Low Birth Weight Survivors in Johannesburg, South Africa
title_sort neurodevelopmental outcomes of extremely low birth weight survivors in johannesburg, south africa
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160720/
https://www.ncbi.nlm.nih.gov/pubmed/35664886
http://dx.doi.org/10.3389/fped.2022.902263
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