Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions

Detalhes bibliográficos
Ano de defesa: 2025
Autor(a) principal: Ferreira, Jéssica Luchi
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: eng
Instituição de defesa: Biblioteca Digitais de Teses e Dissertações da USP
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://www.teses.usp.br/teses/disponiveis/61/61132/tde-22042025-112324/
Resumo: Purpose: Craniosynostosis\'s physical manifestations are well known, while its impact on neurodevelopment and cognitive functions is still under-researched. Evaluating neurodevelopment and cognition helps define cognitive functions\' baseline in surgical procedures, aiding in therapeutic and rehabilitation approaches post-discharge. This study aims to characterise the cognitive profile and neuropsychomotor development to identify the most affected functions in this group. Methods: This retrospective cross-sectional study analysed 65 individuals with craniosynostosis (syndromic=39; isolated=26) who underwent neuropsychological assessments and used social-demographic data obtained from medical records in a specialised hospital of craniofacial anomalies. The study employed five instruments to assess neuropsychomotor development - Dimensional Inventory of Child Development Assessment; Behaviour Developmental Scale of Gesell and Amatruda and cognitive function - Wechsler Abbreviated Scale of Intelligence; Wechsler Intelligence Scale for Children; Raven Progressive Matrices; and SON-R 2 ½ -7 based on age groups. Results: There are significant differences between the two groups in Neuropsychological assessment outcomes (p=0.026), with 68.4% of syndromic patients showing altered neuropsychological results, compared to 40.7% in the isolated group. Language skills were the most frequently altered cognitive domain across all tests, followed by motor skills. Among the other cognitive domains, fluid intelligence showed deficits in 7.7% of patients, and motor skills were affected in 9.2%, predominantly in the isolated group (p=0.0047). Although a weak negative correlation was found between the age at surgery and cognitive improvement (r=-0.32), it shows an impact on cognitive outcomes: early surgery (0-1 year) showed mixed results, while later surgery (3+ years) generally resulted in poorer cognitive outcomes. Conclusion: The study highlights that early interventions are crucial for reducing developmental delays, though individual variability and syndromic conditions affect their effectiveness. Focusing on early intervention, targeted rehabilitation, and a smooth transition back to school can optimize cognitive development and manage delays. The differences in the tests used for comparison may affect the relevance of some findings.
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spelling Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functionsDesenvolvimento cognitivo e neuropsicomotor em craniossinostoses: uma avaliação das funções mais afetadasCogniçãoCognitionCraniossinostoseCraniosynostosesNeuropsicologiaNeuropsychologyPurpose: Craniosynostosis\'s physical manifestations are well known, while its impact on neurodevelopment and cognitive functions is still under-researched. Evaluating neurodevelopment and cognition helps define cognitive functions\' baseline in surgical procedures, aiding in therapeutic and rehabilitation approaches post-discharge. This study aims to characterise the cognitive profile and neuropsychomotor development to identify the most affected functions in this group. Methods: This retrospective cross-sectional study analysed 65 individuals with craniosynostosis (syndromic=39; isolated=26) who underwent neuropsychological assessments and used social-demographic data obtained from medical records in a specialised hospital of craniofacial anomalies. The study employed five instruments to assess neuropsychomotor development - Dimensional Inventory of Child Development Assessment; Behaviour Developmental Scale of Gesell and Amatruda and cognitive function - Wechsler Abbreviated Scale of Intelligence; Wechsler Intelligence Scale for Children; Raven Progressive Matrices; and SON-R 2 ½ -7 based on age groups. Results: There are significant differences between the two groups in Neuropsychological assessment outcomes (p=0.026), with 68.4% of syndromic patients showing altered neuropsychological results, compared to 40.7% in the isolated group. Language skills were the most frequently altered cognitive domain across all tests, followed by motor skills. Among the other cognitive domains, fluid intelligence showed deficits in 7.7% of patients, and motor skills were affected in 9.2%, predominantly in the isolated group (p=0.0047). Although a weak negative correlation was found between the age at surgery and cognitive improvement (r=-0.32), it shows an impact on cognitive outcomes: early surgery (0-1 year) showed mixed results, while later surgery (3+ years) generally resulted in poorer cognitive outcomes. Conclusion: The study highlights that early interventions are crucial for reducing developmental delays, though individual variability and syndromic conditions affect their effectiveness. Focusing on early intervention, targeted rehabilitation, and a smooth transition back to school can optimize cognitive development and manage delays. The differences in the tests used for comparison may affect the relevance of some findings.Introdução: As manifestações físicas da craniossinostose são bem conhecidas, enquanto seu impacto no neurodesenvolvimento e nas funções cognitivas ainda é pouco pesquisado. Avaliar o neurodesenvolvimento e a cognição ajuda a definir a linha de base das funções cognitivas nos procedimentos cirúrgicos, auxiliando nas abordagens terapêuticas e de reabilitação após a alta. Este estudo tem como objetivo caracterizar o perfil cognitivo e o neurodesenvolvimento psicomotor para identificar as funções mais afetadas neste grupo. Métodos: Este estudo transversal retrospectivo analisou 65 indivíduos com craniossinostose (sindrômicos= 39; não sindrômicos= 26) que realizaram avaliações neuropsicológicas e usou dados sociodemográficos obtidos dos prontuários médicos em um hospital especializado em anomalias craniofaciais. O estudo utilizou cinco instrumentos para avaliar o desenvolvimento psicomotor o Inventário Dimensional de Avaliação do Desenvolvimento Infantil; a Escala de Desenvolvimento Comportamental de Gesell e Amatruda e a função cognitiva a Escala Abreviada de Inteligência de Wechsler; Escala Wechsler para Crianças; Matrizes Progressivas de Raven; e SON-R 2 ½ -7 com base nos grupos etários. Resultados: Foram observadas diferenças significativas entre os dois grupos nos resultados das avaliações neuropsicológicas (p=0,026), com 68,4% dos pacientes sindrômicos apresentando resultados neuropsicológicos alterados, comparados a 40,7% no grupo não sindrômico. As habilidades de linguagem foram o domínio cognitivo mais frequentemente alterado em todos os testes, seguidas pelas habilidades motoras. Entre os outros domínios cognitivos, a inteligência fluida apresentou déficits em 7,7% dos pacientes, e as habilidades motoras foram afetadas em 9,2%, predominantemente no grupo não sindrômico (p=0,0047). Embora tenha sido encontrada uma correlação negativa fraca entre a idade da cirurgia e a melhora cognitiva (r=-0,32), ela mostra um impacto nos resultados cognitivos: cirurgias precoces (0-1 ano) apresentaram resultados mistos, enquanto cirurgias mais tardias (3+ anos) geralmente resultaram em piores resultados cognitivos. Conclusão: Intervenções precoces são cruciais para reduzir atrasos no desenvolvimento, embora a variabilidade individual e as condições sindrômicas impactem sua eficácia. A reabilitação direcionada e o acompanhamento profissional na transição de volta à escola pode otimizar o desenvolvimento cognitivo e gerenciar os atrasos. As diferenças nos testes utilizados para comparação podem afetar a relevância de alguns achados.Biblioteca Digitais de Teses e Dissertações da USPTonello, CristianoFerreira, Jéssica Luchi2025-02-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttps://www.teses.usp.br/teses/disponiveis/61/61132/tde-22042025-112324/reponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USPReter o conteúdo por motivos de patente, publicação e/ou direitos autoriais.info:eu-repo/semantics/openAccesseng2025-06-18T19:18:02Zoai:teses.usp.br:tde-22042025-112324Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212025-06-18T19:18:02Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
Desenvolvimento cognitivo e neuropsicomotor em craniossinostoses: uma avaliação das funções mais afetadas
title Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
spellingShingle Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
Ferreira, Jéssica Luchi
Cognição
Cognition
Craniossinostose
Craniosynostoses
Neuropsicologia
Neuropsychology
title_short Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
title_full Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
title_fullStr Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
title_full_unstemmed Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
title_sort Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions
author Ferreira, Jéssica Luchi
author_facet Ferreira, Jéssica Luchi
author_role author
dc.contributor.none.fl_str_mv Tonello, Cristiano
dc.contributor.author.fl_str_mv Ferreira, Jéssica Luchi
dc.subject.por.fl_str_mv Cognição
Cognition
Craniossinostose
Craniosynostoses
Neuropsicologia
Neuropsychology
topic Cognição
Cognition
Craniossinostose
Craniosynostoses
Neuropsicologia
Neuropsychology
description Purpose: Craniosynostosis\'s physical manifestations are well known, while its impact on neurodevelopment and cognitive functions is still under-researched. Evaluating neurodevelopment and cognition helps define cognitive functions\' baseline in surgical procedures, aiding in therapeutic and rehabilitation approaches post-discharge. This study aims to characterise the cognitive profile and neuropsychomotor development to identify the most affected functions in this group. Methods: This retrospective cross-sectional study analysed 65 individuals with craniosynostosis (syndromic=39; isolated=26) who underwent neuropsychological assessments and used social-demographic data obtained from medical records in a specialised hospital of craniofacial anomalies. The study employed five instruments to assess neuropsychomotor development - Dimensional Inventory of Child Development Assessment; Behaviour Developmental Scale of Gesell and Amatruda and cognitive function - Wechsler Abbreviated Scale of Intelligence; Wechsler Intelligence Scale for Children; Raven Progressive Matrices; and SON-R 2 ½ -7 based on age groups. Results: There are significant differences between the two groups in Neuropsychological assessment outcomes (p=0.026), with 68.4% of syndromic patients showing altered neuropsychological results, compared to 40.7% in the isolated group. Language skills were the most frequently altered cognitive domain across all tests, followed by motor skills. Among the other cognitive domains, fluid intelligence showed deficits in 7.7% of patients, and motor skills were affected in 9.2%, predominantly in the isolated group (p=0.0047). Although a weak negative correlation was found between the age at surgery and cognitive improvement (r=-0.32), it shows an impact on cognitive outcomes: early surgery (0-1 year) showed mixed results, while later surgery (3+ years) generally resulted in poorer cognitive outcomes. Conclusion: The study highlights that early interventions are crucial for reducing developmental delays, though individual variability and syndromic conditions affect their effectiveness. Focusing on early intervention, targeted rehabilitation, and a smooth transition back to school can optimize cognitive development and manage delays. The differences in the tests used for comparison may affect the relevance of some findings.
publishDate 2025
dc.date.none.fl_str_mv 2025-02-13
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dc.language.iso.fl_str_mv eng
language eng
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