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Craniofacial Collaboration UK: Developmental Outcomes in 5-Year-Old Children With Sagittal Synostosis
Helen Care1, Patrick Kennedy-Williams1, Laura Culshaw2
1Oxford Craniofacial Unit, Oxford University Hospitals NHS Foundation Trust.
Insights
Children with single-suture sagittal synostosis (SS) generally develop typically by age 5. However, they show increased fine motor and hyperactivity issues, alongside unexpectedly strong problem-solving skills.
Area of Science:
- Pediatric developmental outcomes
- Craniosynostosis research
- Clinical child psychology
Background:
- Single-suture sagittal synostosis (SS) is a common craniosynostosis affecting skull development.
- Previous research on developmental outcomes in SS patients has limitations due to data heterogeneity.
- The Craniofacial Collaboration UK (CC-UK) initiative aims to collect robust, standardized data.
Purpose of the Study:
- To outline developmental outcomes at age 5 for children with SS post-primary surgery.
- To compare developmental trajectories of SS children with normative data.
- To identify potential early indicators of subtle neurodevelopmental differences.
Main Methods:
- Systematically collected, robust data from clinically and chronologically homogenous samples.
- Assessment of developmental, behavioral, and emotional domains at age 5.
- Comparison of SS cohort group means against established normative data.
Main Results:
- Majority of children with SS perform within the average range across developmental domains.
- Significantly greater difficulties observed in fine motor skills and hyperactivity compared to peers.
- Unexpectedly superior problem-solving skills noted in the SS cohort.
Conclusions:
- Most children with SS demonstrate broadly typical development by age 5.
- Subtle but significant differences in fine motor skills, hyperactivity, and problem-solving warrant further investigation.
- Longitudinal follow-up is crucial for understanding developmental trajectories and identifying at-risk subgroups.
Abstract:
The Craniofacial Collaboration UK (CC-UK) is a joint initiative that seeks to address some of the limitations of previous developmental research with this patient group by providing systematically collected, robust data from clinically and chronologically homogenous representative samples of children. The current paper outlines the developmental outcomes at the age of 5 for children who had previously undergone primary surgery for single-suture sagittal synostosis (SS). It shows broad consistencies with the previous CC-UK work, indicating that the majority of children with SS will perform within the average range compared to peers across a number of developmental, behavioral and emotional domains. However, the group mean for children with SS indicates significantly greater difficulties with fine motor skills and hyperactivity, relative to normative data. Unexpectedly, children with SS had significantly better problem solving skills. While it is reassuring that the majority of children are broadly developing in line with their unaffected peers, these small but significant differences may be early indicators of some of the subtle difficulties documented in older children with craniosynostosis. Longitudinal follow up is therefore important to understand the developmental trajectory for children with SS and identification of potentially 'at risk' sub groups within this diagnostic cohort.
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