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Evaluation of neurocognitive and social developments after craniosynostosis surgery.
Aksogan, Yigit; Kuzucu, Pelin; Soysal Acar, Azime S; Sahin, Merve Büke; Gücüyener, Kivilcim; Börcek, Alp Ö.
Afiliación
  • Aksogan Y; Department of Neurosurgery, Bayburt State Hospital, Bayburt, Turkey. yigitaksogan@hotmail.com.
  • Kuzucu P; Division of Pediatric Neurosurgery, Gazi University Faculty of Medicine, Ankara, Turkey.
  • Soysal Acar AS; Department of Pediatric Health and Diseases, Gazi University Faculty of Medicine, Ankara, Turkey.
  • Sahin MB; Department of Public Health, Etimesgut District Health Directorate, Ankara, Turkey.
  • Gücüyener K; Division of Pediatric Neurology, Gazi University, Faculty of Medicine, Ankara, Turkey.
  • Börcek AÖ; Division of Pediatric Neurosurgery, Gazi University Faculty of Medicine, Ankara, Turkey.
Childs Nerv Syst ; 40(5): 1489-1499, 2024 May.
Article en En | MEDLINE | ID: mdl-38294493
ABSTRACT

OBJECTIVE:

The study focused on assessing the potential neurocognitive and social developmental issues in children with non-syndromic craniosynostosis (NSC) who received optimal surgical treatment. The primary objective was to determine whether NSC, even after optimal surgical treatment, could have negative effects on brain development.

METHODS:

The study included a total of 73 pediatric patients aged between 2 and 6 years who had previously undergone surgery for NSC at the Gazi University Faculty of Medicine, Department of Neurosurgery. These patients were carefully matched with 107 healthy children who visited the outpatient clinic of the same department in terms of sociodemographic characteristics such as age, gender, and social status. To assess the neurocognitive and social development of the participants, the child psychologist administered a developmental scale to the child and his/her family via video conference. This scale was adapted from the Bayley-III Infant and Child Development Scale by the Gazi University Faculty of Medicine, Division of Pediatric Neurology.

RESULTS:

The study found no social or gross motor developmental issues in patients who had undergone optimal surgical treatment for NSC. However, the risk of fine motor developmental deficiencies was 4.79 times higher than that of the normal population, and the risk of language developmental deficiencies was 5.75 times higher than that of the normal population.

CONCLUSIONS:

Despite timely treatment of NSC, long-term neurocognitive and social development issues may arise in affected children. Therefore, it is crucial to monitor these patients after completing surgical treatment and thoroughly examine their development using a multidisciplinary approach.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Cambio Social / Craneosinostosis Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Childs Nerv Syst Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Asunto principal: Cambio Social / Craneosinostosis Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Childs Nerv Syst Asunto de la revista: NEUROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Turquía