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Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India

OBJECTIVE: To describe the comorbidities in children with cerebral palsy (CP) and determine the characteristics associated with different impairments. DESIGN: Cross-sectional study. SETTING: Tertiary care referral centre in India. PATIENTS: Between April 2018 and May 2022, all children aged 2–18 yea...

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Autores principales: Viswanath, Maya, Jha, Ruchika, Gambhirao, Ankita Dilip, Kurup, Arjun, Badal, Sachendra, Kohli, Sarvesh, Parappil, Parvathi, John, Biju M, Adhikari, Krishna Moorthi, Kovilapu, Uday Bhanu, Sondhi, Vishal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10335521/
https://www.ncbi.nlm.nih.gov/pubmed/37429681
http://dx.doi.org/10.1136/bmjopen-2023-072365
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author Viswanath, Maya
Jha, Ruchika
Gambhirao, Ankita Dilip
Kurup, Arjun
Badal, Sachendra
Kohli, Sarvesh
Parappil, Parvathi
John, Biju M
Adhikari, Krishna Moorthi
Kovilapu, Uday Bhanu
Sondhi, Vishal
author_facet Viswanath, Maya
Jha, Ruchika
Gambhirao, Ankita Dilip
Kurup, Arjun
Badal, Sachendra
Kohli, Sarvesh
Parappil, Parvathi
John, Biju M
Adhikari, Krishna Moorthi
Kovilapu, Uday Bhanu
Sondhi, Vishal
author_sort Viswanath, Maya
collection PubMed
description OBJECTIVE: To describe the comorbidities in children with cerebral palsy (CP) and determine the characteristics associated with different impairments. DESIGN: Cross-sectional study. SETTING: Tertiary care referral centre in India. PATIENTS: Between April 2018 and May 2022, all children aged 2–18 years with a confirmed diagnosis of CP were enrolled by systematic random sampling. Data on antenatal, birth and postnatal risk factors, clinical evaluation and investigations (neuroimaging and genetic/metabolic workup) were recorded. MAIN OUTCOME MEASURES: Prevalence of the co-occurring impairments was determined using clinical evaluation or investigations as indicated. RESULTS: Of the 436 children screened, 384 participated (spastic CP=214 (55.7%) (spastic hemiplegic=52 (13.5%); spastic diplegia=70 (18.2%); spastic quadriplegia=92 (24%)), dyskinetic CP=58 (15.1%) and mixed CP=110 (28.6%)). A primary antenatal/perinatal/neonatal and postneonatal risk factor was identified in 32 (8.3%), 320 (83.3%) and 26 (6.8%) patients, respectively. Prevalent comorbidities (the test used) included visual impairment (clinical assessment and visual evoked potential)=357/383(93.2%), hearing impairment (brainstem-evoked response audiometry)=113 (30%), no understanding of any communication (MacArthur Communicative Development Inventory)=137 (36%), cognitive impairment (Vineland scale of social maturity)=341 (88.8%), severe gastrointestinal dysfunction (clinical evaluation/interview)=90 (23%), significant pain (non-communicating children’s pain checklist)=230 (60%), epilepsy=245 (64%), drug-resistant epilepsy=163 (42.4%), sleep impairment (Children’s Sleep Habits Questionnaire)=176/290(60.7%) and behavioural abnormalities (Childhood behaviour checklist)=165 (43%). Overall, hemiparetic and diplegic CP and Gross Motor Function Classification System ≤3 were predictive of lesser co-occurring impairment. CONCLUSION: CP children have a high burden of comorbidities, which increase with increasing functional impairment. This calls for urgent actions to prioritise opportunities to prevent risk factors associated with CP and organise existing resources to identify and manage co-occurring impairments. TRIAL REGISTRATION NUMBER: CTRI/2018/07/014819.
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spelling pubmed-103355212023-07-12 Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India Viswanath, Maya Jha, Ruchika Gambhirao, Ankita Dilip Kurup, Arjun Badal, Sachendra Kohli, Sarvesh Parappil, Parvathi John, Biju M Adhikari, Krishna Moorthi Kovilapu, Uday Bhanu Sondhi, Vishal BMJ Open Paediatrics OBJECTIVE: To describe the comorbidities in children with cerebral palsy (CP) and determine the characteristics associated with different impairments. DESIGN: Cross-sectional study. SETTING: Tertiary care referral centre in India. PATIENTS: Between April 2018 and May 2022, all children aged 2–18 years with a confirmed diagnosis of CP were enrolled by systematic random sampling. Data on antenatal, birth and postnatal risk factors, clinical evaluation and investigations (neuroimaging and genetic/metabolic workup) were recorded. MAIN OUTCOME MEASURES: Prevalence of the co-occurring impairments was determined using clinical evaluation or investigations as indicated. RESULTS: Of the 436 children screened, 384 participated (spastic CP=214 (55.7%) (spastic hemiplegic=52 (13.5%); spastic diplegia=70 (18.2%); spastic quadriplegia=92 (24%)), dyskinetic CP=58 (15.1%) and mixed CP=110 (28.6%)). A primary antenatal/perinatal/neonatal and postneonatal risk factor was identified in 32 (8.3%), 320 (83.3%) and 26 (6.8%) patients, respectively. Prevalent comorbidities (the test used) included visual impairment (clinical assessment and visual evoked potential)=357/383(93.2%), hearing impairment (brainstem-evoked response audiometry)=113 (30%), no understanding of any communication (MacArthur Communicative Development Inventory)=137 (36%), cognitive impairment (Vineland scale of social maturity)=341 (88.8%), severe gastrointestinal dysfunction (clinical evaluation/interview)=90 (23%), significant pain (non-communicating children’s pain checklist)=230 (60%), epilepsy=245 (64%), drug-resistant epilepsy=163 (42.4%), sleep impairment (Children’s Sleep Habits Questionnaire)=176/290(60.7%) and behavioural abnormalities (Childhood behaviour checklist)=165 (43%). Overall, hemiparetic and diplegic CP and Gross Motor Function Classification System ≤3 were predictive of lesser co-occurring impairment. CONCLUSION: CP children have a high burden of comorbidities, which increase with increasing functional impairment. This calls for urgent actions to prioritise opportunities to prevent risk factors associated with CP and organise existing resources to identify and manage co-occurring impairments. TRIAL REGISTRATION NUMBER: CTRI/2018/07/014819. BMJ Publishing Group 2023-07-10 /pmc/articles/PMC10335521/ /pubmed/37429681 http://dx.doi.org/10.1136/bmjopen-2023-072365 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Paediatrics
Viswanath, Maya
Jha, Ruchika
Gambhirao, Ankita Dilip
Kurup, Arjun
Badal, Sachendra
Kohli, Sarvesh
Parappil, Parvathi
John, Biju M
Adhikari, Krishna Moorthi
Kovilapu, Uday Bhanu
Sondhi, Vishal
Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India
title Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India
title_full Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India
title_fullStr Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India
title_full_unstemmed Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India
title_short Comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from India
title_sort comorbidities in children with cerebral palsy: a single-centre cross-sectional hospital-based study from india
topic Paediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10335521/
https://www.ncbi.nlm.nih.gov/pubmed/37429681
http://dx.doi.org/10.1136/bmjopen-2023-072365
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