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Screening for developmental delay in urban Rwandan children: a cross sectional study

BACKGROUND: Systematic or targeted screening for developmental delay (DD) is critical to the early identification of developmental disabilities. With limited available information for urban Rwandan children, this study aimed to determine the prevalence of DD and associated risk factors in infants ag...

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Autores principales: Tuyisenge, Victoire, Mushimiyimana, Febronie, Kanyamuhunga, Aimable, Rukabyarwema, Jean Paul, Patel, Archana A., O’Callahan, Cliff
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588090/
https://www.ncbi.nlm.nih.gov/pubmed/37864138
http://dx.doi.org/10.1186/s12887-023-04332-3
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author Tuyisenge, Victoire
Mushimiyimana, Febronie
Kanyamuhunga, Aimable
Rukabyarwema, Jean Paul
Patel, Archana A.
O’Callahan, Cliff
author_facet Tuyisenge, Victoire
Mushimiyimana, Febronie
Kanyamuhunga, Aimable
Rukabyarwema, Jean Paul
Patel, Archana A.
O’Callahan, Cliff
author_sort Tuyisenge, Victoire
collection PubMed
description BACKGROUND: Systematic or targeted screening for developmental delay (DD) is critical to the early identification of developmental disabilities. With limited available information for urban Rwandan children, this study aimed to determine the prevalence of DD and associated risk factors in infants aged 9 to 16 months living in the urban Rwandan city of Kigali. METHODS: A cross-sectional study was conducted in Rwanda from August to November 2019. A convenience sample of 376 Rwandan parents/caregivers and their children attending urban health centers for their routine immunization visits at 9 and 15 months of age was studied. Parents/caregivers completed the official Kinyarwandan version of the Ages and Stages Questionnaire (ASQ-3) and established cutoffs were used to identify DD. Frequency and percentages were used to summarise the data. Logistic regression analysis was used to identify factors associated with DD. RESULTS: Of the 358 children screened using the ASQ-3, the overall prevalence of DD was 24.6%, with a 27.2% prevalence among 9–10-month old children and 22.4% prevalence among 15–16-month old children. Delays in the combined group among the domains of gross motor, communication, fine motor, personal social, and problem solving were 12.8%, 2.5%, 8.4%, 1.7% and 7.5%, respectively. Gestational age at delivery and district of origin were most highly associated with DD, with preterm children at significantly higher risk of having DD compared to term children (Adjusted Odd Ratio AOR = 8.3; 95% CI = 2.5–27.4) and children from Nyarugenge District at high risk of DD compared to children from Gasabo district (AOR = 2.15; 95% CI = 1.2–3.9). CONCLUSIONS: The prevalence of ASQ-detectable DD among urban Rwandan children between 9 and 16 months of age was 24.6%, with a high correlation to a history of prematurity and district of origin. This study demonstrates the need for thoughtful health planning regarding integrated developmental surveillance for children, particularly those at high risk, to allow for earlier identification and intervention in the urban area of Kigali, Rwanda.
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spelling pubmed-105880902023-10-21 Screening for developmental delay in urban Rwandan children: a cross sectional study Tuyisenge, Victoire Mushimiyimana, Febronie Kanyamuhunga, Aimable Rukabyarwema, Jean Paul Patel, Archana A. O’Callahan, Cliff BMC Pediatr Research BACKGROUND: Systematic or targeted screening for developmental delay (DD) is critical to the early identification of developmental disabilities. With limited available information for urban Rwandan children, this study aimed to determine the prevalence of DD and associated risk factors in infants aged 9 to 16 months living in the urban Rwandan city of Kigali. METHODS: A cross-sectional study was conducted in Rwanda from August to November 2019. A convenience sample of 376 Rwandan parents/caregivers and their children attending urban health centers for their routine immunization visits at 9 and 15 months of age was studied. Parents/caregivers completed the official Kinyarwandan version of the Ages and Stages Questionnaire (ASQ-3) and established cutoffs were used to identify DD. Frequency and percentages were used to summarise the data. Logistic regression analysis was used to identify factors associated with DD. RESULTS: Of the 358 children screened using the ASQ-3, the overall prevalence of DD was 24.6%, with a 27.2% prevalence among 9–10-month old children and 22.4% prevalence among 15–16-month old children. Delays in the combined group among the domains of gross motor, communication, fine motor, personal social, and problem solving were 12.8%, 2.5%, 8.4%, 1.7% and 7.5%, respectively. Gestational age at delivery and district of origin were most highly associated with DD, with preterm children at significantly higher risk of having DD compared to term children (Adjusted Odd Ratio AOR = 8.3; 95% CI = 2.5–27.4) and children from Nyarugenge District at high risk of DD compared to children from Gasabo district (AOR = 2.15; 95% CI = 1.2–3.9). CONCLUSIONS: The prevalence of ASQ-detectable DD among urban Rwandan children between 9 and 16 months of age was 24.6%, with a high correlation to a history of prematurity and district of origin. This study demonstrates the need for thoughtful health planning regarding integrated developmental surveillance for children, particularly those at high risk, to allow for earlier identification and intervention in the urban area of Kigali, Rwanda. BioMed Central 2023-10-20 /pmc/articles/PMC10588090/ /pubmed/37864138 http://dx.doi.org/10.1186/s12887-023-04332-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Tuyisenge, Victoire
Mushimiyimana, Febronie
Kanyamuhunga, Aimable
Rukabyarwema, Jean Paul
Patel, Archana A.
O’Callahan, Cliff
Screening for developmental delay in urban Rwandan children: a cross sectional study
title Screening for developmental delay in urban Rwandan children: a cross sectional study
title_full Screening for developmental delay in urban Rwandan children: a cross sectional study
title_fullStr Screening for developmental delay in urban Rwandan children: a cross sectional study
title_full_unstemmed Screening for developmental delay in urban Rwandan children: a cross sectional study
title_short Screening for developmental delay in urban Rwandan children: a cross sectional study
title_sort screening for developmental delay in urban rwandan children: a cross sectional study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588090/
https://www.ncbi.nlm.nih.gov/pubmed/37864138
http://dx.doi.org/10.1186/s12887-023-04332-3
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