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Published on: February 2, 2015
Increased utilization of healthcare services in children with craniosynostosis
Gabriela D Ruiz Colón1, Michael C Jin1, Gerald A Grant1,2
11Department of Neurosurgery, Stanford University School of Medicine; and.
Insights
Children with craniosynostosis, both syndromic and nonsyndromic, utilize mental health care and rehabilitation therapies more than healthy children. Longitudinal monitoring for developmental and mental health support is crucial for all affected children.
Area of Science:
- Pediatric Health
- Medical Services Utilization
- Craniosynostosis Research
Background:
- Craniosynostosis, the premature fusion of cranial sutures, can be syndromic or nonsyndromic.
- While developmental, behavioral, and mental health support may benefit affected children, data on healthcare service utilization are limited.
- Understanding service use patterns is vital for comprehensive patient care.
Purpose of the Study:
- To compare healthcare service utilization among children with craniosynostosis (syndromic and nonsyndromic), plagiocephaly, and healthy controls.
- To analyze the utilization of mental health care, rehabilitation therapies, and other subspecialty medical services.
- To identify potential disparities or trends in service use based on diagnosis and demographics.
Main Methods:
- Utilized the Optum Clinformatics Data Mart database to identify cohorts.
- Included 1340 patients with craniosynostosis (200 syndromic), 1249 with plagiocephaly, and 1577 healthy controls.
- Calculated and compared long-term utilization of services up to age 6.
Main Results:
- Craniosynostosis patients used mental health services more frequently than plagiocephaly or healthy controls.
- Rehabilitation therapies were more utilized in syndromic craniosynostosis and plagiocephaly groups compared to controls.
- Other subspecialty services were significantly higher in craniosynostosis and plagiocephaly groups versus controls.
- Mental health care utilization increased with age in craniosynostosis patients.
Conclusions:
- Patients with syndromic and nonsyndromic craniosynostosis show similar, elevated rates of mental health care, rehabilitation, and subspecialty service utilization compared to healthy controls.
- Providers and parents should ensure ongoing monitoring for developmental and mental health needs in all children with craniosynostosis.
- Further research should investigate factors influencing service utilization, such as specific suture involvement and comorbidities.
Objective:
Craniosynostosis is characterized by the premature fusion of at least one cranial suture. Although evidence suggests that patients with both syndromic and nonsyndromic craniosynostosis may benefit from developmental, behavioral, and mental health support, data on utilization of healthcare services are lacking. In this study the authors compared utilization of mental health care, rehabilitation therapies, and other specialty medical services among children with craniosynostosis, children with plagiocephaly, and healthy controls.
Methods:
The Optum Clinformatics Data Mart database was queried to identify 1340 patients with craniosynostosis, of whom 200 had syndromic craniosynostosis. Long-term utilization of mental health care, rehabilitation therapies, and other medical services up to the age of 6 years was calculated. Rates of utilization were compared to healthy controls (n = 1577) and children with plagiocephaly (n = 1249).
Results:
Patients with syndromic and nonsyndromic craniosynostosis used mental health care, occupational therapy, speech-language pathology, and other medical services at similar rates (p = 0.1198, p > 0.9999, p = 0.1097, and p = 0.8119, respectively). Mental health services were used more frequently by patients with craniosynostosis (11.0% in patients with syndromic craniosynostosis and 7.5% in those with nonsyndromic craniosynostosis) compared to patients in the plagiocephaly (5.0%, p = 0.0020) and healthy control (2.9%, p < 0.0001) cohorts. Rehabilitation therapies were more frequently used by patients with syndromic craniosynostosis and plagiocephaly (16.0% and 14.1%, respectively), which was significantly higher than use by healthy controls (p < 0.0001). Other medical subspecialty services (developmental pediatrics, ophthalmology, optometry, and audiology) were used by 37.0% of patients with craniosynostosis, compared with 20.9% (p < 0.0001) and 15.1% (p < 0.0001) of patients with plagiocephaly and healthy controls, respectively. Among patients with craniosynostosis, utilization did not differ by race or household income, but it was not uniform by age. Whereas ophthalmology utilization did not differ by age (p = 0.1003), mental health care was most commonly used among older children (p = 0.0107).
Conclusions:
In this study, the authors demonstrate that rates of utilization of mental health care, rehabilitation therapies, and other medical subspecialty services are similar between patients with syndromic and those with nonsyndromic craniosynostosis, but higher than in healthy controls. Although surgical correction may be considered an isolated event, providers and parents need to monitor all children with craniosynostosis-syndromic and nonsyndromic-for developmental and mental health support longitudinally. Future work should explore risk factors driving utilization, including suture involvement, repair type, and comorbidities.
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