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Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities

BACKGROUND: Cerebral palsy (CP) is a common chronic childhood disorder worldwide. There is limited information about the CP panorama in sub-Saharan Africa. Our aim was to describe the clinical subtypes, gross and fine motor functions and presence of co-morbidities in a group of children with CP atte...

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Autores principales: Kakooza-Mwesige, Angelina, Forssberg, Hans, Eliasson, Ann-Christin, Tumwine, James K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421914/
https://www.ncbi.nlm.nih.gov/pubmed/25902796
http://dx.doi.org/10.1186/s13104-015-1125-9
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author Kakooza-Mwesige, Angelina
Forssberg, Hans
Eliasson, Ann-Christin
Tumwine, James K
author_facet Kakooza-Mwesige, Angelina
Forssberg, Hans
Eliasson, Ann-Christin
Tumwine, James K
author_sort Kakooza-Mwesige, Angelina
collection PubMed
description BACKGROUND: Cerebral palsy (CP) is a common chronic childhood disorder worldwide. There is limited information about the CP panorama in sub-Saharan Africa. Our aim was to describe the clinical subtypes, gross and fine motor functions and presence of co-morbidities in a group of children with CP attending a tertiary hospital in Uganda. METHODS: Children with CP in the age range of 2-12 years visiting the paediatric CP clinic at Mulago Hospital, Kampala, were enrolled. Screening and inclusion were based on a three-stage procedure: i) Two screening questions from the Ten Question Screen; ii) Clinical assessments adapted from the Surveillance for Cerebral Palsy in Europe (SCPE); iii) Clinical examinations and diagnoses of subtype, severity level and co-morbidities. Caregivers were interviewed using questionnaires to provide information on child’s medical history and co-morbidities. Co-morbidity scores were calculated for each child. RESULTS: One hundred and thirty five children with CP were enrolled (72 males, 63 females, median age 3 years 5 months, IQR-2 years 4 months-5 years 6 months). Bilateral spastic type was commonest (45%); moderate impairment in gross motor function was present in 43%, with comparable numbers (37%) in the mild and severely impaired fine motor function groups. The severe gross and fine motor function levels were seen in the bilateral spastic and dyskinetic CP subtypes. Signs of learning disability (75%) and epilepsy (45%) were the commonest co-morbidities. Higher co-morbidity scores were obtained in children with dyskinetic CP and severe levels of gross and fine motor function. There was a significant difference in distribution of the co-morbidity scores between the CP subtypes, gross motor and fine motor function levels (p <0.001). Signs of speech and language impairments were associated with bilateral spastic CP and severe gross and fine motor dysfunction (p < 0.05). CONCLUSIONS: Bilateral spastic CP was the main clinical subtype, with signs of learning disability and epilepsy as major causes of co-morbidity. The severity of gross and fine motor function levels was related to severity of clinical CP subtypes. Our findings imply a higher occurrence of birth asphyxia or post natally acquired infections. Improvement in emergency obstetric and postnatal care may reduce this burden. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-015-1125-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-44219142015-05-07 Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities Kakooza-Mwesige, Angelina Forssberg, Hans Eliasson, Ann-Christin Tumwine, James K BMC Res Notes Research Article BACKGROUND: Cerebral palsy (CP) is a common chronic childhood disorder worldwide. There is limited information about the CP panorama in sub-Saharan Africa. Our aim was to describe the clinical subtypes, gross and fine motor functions and presence of co-morbidities in a group of children with CP attending a tertiary hospital in Uganda. METHODS: Children with CP in the age range of 2-12 years visiting the paediatric CP clinic at Mulago Hospital, Kampala, were enrolled. Screening and inclusion were based on a three-stage procedure: i) Two screening questions from the Ten Question Screen; ii) Clinical assessments adapted from the Surveillance for Cerebral Palsy in Europe (SCPE); iii) Clinical examinations and diagnoses of subtype, severity level and co-morbidities. Caregivers were interviewed using questionnaires to provide information on child’s medical history and co-morbidities. Co-morbidity scores were calculated for each child. RESULTS: One hundred and thirty five children with CP were enrolled (72 males, 63 females, median age 3 years 5 months, IQR-2 years 4 months-5 years 6 months). Bilateral spastic type was commonest (45%); moderate impairment in gross motor function was present in 43%, with comparable numbers (37%) in the mild and severely impaired fine motor function groups. The severe gross and fine motor function levels were seen in the bilateral spastic and dyskinetic CP subtypes. Signs of learning disability (75%) and epilepsy (45%) were the commonest co-morbidities. Higher co-morbidity scores were obtained in children with dyskinetic CP and severe levels of gross and fine motor function. There was a significant difference in distribution of the co-morbidity scores between the CP subtypes, gross motor and fine motor function levels (p <0.001). Signs of speech and language impairments were associated with bilateral spastic CP and severe gross and fine motor dysfunction (p < 0.05). CONCLUSIONS: Bilateral spastic CP was the main clinical subtype, with signs of learning disability and epilepsy as major causes of co-morbidity. The severity of gross and fine motor function levels was related to severity of clinical CP subtypes. Our findings imply a higher occurrence of birth asphyxia or post natally acquired infections. Improvement in emergency obstetric and postnatal care may reduce this burden. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-015-1125-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-23 /pmc/articles/PMC4421914/ /pubmed/25902796 http://dx.doi.org/10.1186/s13104-015-1125-9 Text en © Kakooza-Mwesige et al.; licensee BioMed Central. 2015 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kakooza-Mwesige, Angelina
Forssberg, Hans
Eliasson, Ann-Christin
Tumwine, James K
Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities
title Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities
title_full Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities
title_fullStr Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities
title_full_unstemmed Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities
title_short Cerebral palsy in children in Kampala, Uganda: clinical subtypes, motor function and co-morbidities
title_sort cerebral palsy in children in kampala, uganda: clinical subtypes, motor function and co-morbidities
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421914/
https://www.ncbi.nlm.nih.gov/pubmed/25902796
http://dx.doi.org/10.1186/s13104-015-1125-9
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