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Impact of a National Follow-Up Program on the Age at Diagnosis for Cerebral Palsy.
Fabricius, Rebecca Alison; Larsen, Mads Langager; Debes, Nanette Mol; Rackauskaite, Gija; Hoei-Hansen, Christina Engel.
Afiliação
  • Fabricius RA; Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark; Department of Orthopedic Surgery, Hospital South West Jutland, University Hospital of Southern Denmark, Esbjerg, Denmark. Electronic address: rebecca.alison.fabricius@regionh.dk.
  • Larsen ML; Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Debes NM; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark; Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital - Herlev, Herlev, Denmark.
  • Rackauskaite G; Department of Paediatrics and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.
  • Hoei-Hansen CE; Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Pediatr Neurol ; 152: 56-61, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38211417
ABSTRACT

BACKGROUND:

The Danish National Cerebral Palsy Follow-up Program (CPOP) is a nationwide program offering standardized treatment to all children with cerebral palsy (CP) since 2004. We aimed to establish if its implementation had a positive impact on the diagnostic age of CP.

METHODS:

Children with validated CP diagnoses were identified from the Danish Cerebral Palsy Registry and the CPOP. We then compared the age at diagnosis and the clinical features of children with CP born in 2000 to 2003 with those born in 2010 to 2013. Differences in time to diagnosis were compared using log-rank test.

RESULTS:

The age at diagnosis was not different in the two periods (P = 0.23), with identical overall median diagnostic ages at 13.0 months. The number of children with severe motor disability decreased markedly from 47.5% in 2000 to 2003 to 32.0% in 2010 to 2013 (P < 0.001). There was increased usage of cerebral magnetic resonance imaging; however, this was not associated with lower diagnostic age.

CONCLUSIONS:

The diagnostic age of CP did not change after the implementation of a nationwide follow-up program, offering standardized and early assessments. However, central clinical aspects also changed significantly between the periods compared, which possibly affected the diagnostic age.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Cerebral / Pessoas com Deficiência / Transtornos Motores Tipo de estudo: Diagnostic_studies Limite: Adult / Child / Humans Idioma: En Revista: Pediatr Neurol / Pediatr. neurol / Pediatric Neurology Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Cerebral / Pessoas com Deficiência / Transtornos Motores Tipo de estudo: Diagnostic_studies Limite: Adult / Child / Humans Idioma: En Revista: Pediatr Neurol / Pediatr. neurol / Pediatric Neurology Ano de publicação: 2024 Tipo de documento: Article