Original Article

Epidemiologic Assessment of Craniosynostosis in Mississippi’s Pediatric Population from 2015 to 2020

Authors: Martin G. McCandless, MD, Madyson I. Brown, BS, James M. Shiflett, MD, Kristin J. Weaver, MD, PhD, Ian C. Hoppe, MD, Laura S. Humphries, MD

Abstract

Objectives: This study aimed to report geographic and demographic patterns of patients with craniosynostosis (CS) treated at Children’s of Mississippi, the state’s only American Cleft Palate-Craniofacial Association–approved craniofacial team.

Methods: Patients with CS were treated at a tertiary pediatric hospital cared for by craniofacial surgeons and neurosurgeons from 2015 to 2020. Demographic, geographic, and CS diagnosis details, including sex, gestational age, race, ethnicity, insurance status, and affected cranial suture type(s), number, and associated syndromic diagnosis were collected, including birth county and total live births from state data. Significant differences between prevalence of CS in four regions of Mississippi were examined using two-tailed t tests (P < 0.05).

Results: Among 222,819 live births in Mississippi between 2015 and 2020, 79 pediatric patients presented to Children’s of Mississippi with CS, with an overall incidence of 0.355/1000 live births. Most cases were nonsyndromic CS (82%, n = 65) affecting a single major cranial suture (81%, n = 64). The overall incidence of CS was higher in the coastal and central regions compared with northeast Mississippi, at 0.333 and 0.527 vs 0.132/1000 live births (P = 0.012 and P = 0.004), respectively.

Conclusions: Results from this study suggest regional patterns of CS in Mississippi, which may reflect actual incidence patterns or proximity to Children’s of Mississippi. Further study could reveal regional differences in risk factors underlying CS incidence or access to specialized CS care for different regions in the state. This will lead to opportunities for institutional outreach to decrease the burden of CS care in Mississippi.

This content is limited to qualifying members.

Existing members, please login first

If you have an existing account please login now to access this article or view purchase options.

Purchase only this article ($25)

Create a free account, then purchase this article to download or access it online for 24 hours.

Purchase an SMJ online subscription ($75)

Create a free account, then purchase a subscription to get complete access to all articles for a full year.

Purchase a membership plan (fees vary)

Premium members can access all articles plus recieve many more benefits. View all membership plans and benefit packages.

References

1. Cornelissen M, Ottelander B, Rizopoulos D, et al. Increase of prevalence of craniosynostosis. J Craniomaxillofac Surg 2016;44:1273-1279.
 
2. Singer S, Bower C, Southall P, et al. Craniosynostosis in Western Australia, 1980-1994: a population-based study. Am J Med Genet 1999;83:382-387.
 
3. Boulet SL, Rasmussen SA, Honein MA. A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003. Am J Med Genet A 2008;146a:984-991.
 
4. Selber J, Reid RR, Chike-Obi CJ, et al. The changing epidemiologic spectrum of single-suture synostoses. Plast Reconstr Surg 2008;122:527-533.
 
5. Di Rocco F, Arnaud E, Renier D. Evolution in the frequency of nonsyndromic craniosynostosis. J Neurosurg Pediatr 2009;4:21-25.
 
6. Lee HQ, Hutson JM, Wray AC, et al. Changing epidemiology of nonsyndromic craniosynostosis and revisiting the risk factors. J Craniofac Surg 2012;23: 1245-1251.
 
7. van der Meulen J, van der Hulst R, van Adrichem L, et al. The increase of metopic synostosis: a pan-European observation. J Craniofac Surg 2009; 20:283-286.
 
8. Bennett KG, Bickham RS, Robinson AB, et al. Metopic craniosynostosis: a demographic analysis outside an urban environment. J Craniofac Surg 2016; 27:544-547.
 
9. Munn IA, Hussain A, Grebner DL, et al. Mississippi private landowner willingness for diverting land to growing short rotation woody crops for bioenergy enterprises. Forest Sci 2018;64:471-479.
 
10. Mississippi State Department of Health, Office of Public Health Statistics. Vital statistics. https://msdh.ms.gov/phs/statisti.htm. Accessed March 11, 2022.
 
11. Mississippi State Department of Health. Mississippi Birth Defects Surveillance Registry Fact Sheet. https://msdh.ms.gov/page/resources/2402.pdf. Accessed March 11, 2022.
 
12. Kweldam CF, van der Vlugt JJ, van der Meulen JJ. The incidence of craniosynostosis in the Netherlands, 1997-2007. J Plast Reconstr Aesthet Surg 2011;64:583-588.
 
13. Junaid M, Slack-Smith L, Wong K, et al. Epidemiology of rare craniofacial anomalies: retrospective Western Australian population data linkage study. J Pediatr 2022;241:162-172.e9.
 
14. US Census Bureau. Population and housing unit estimates datasets. https://www.census.gov/programs-surveys/popest/data/data-sets.html. Accessed March 11, 2022.
 
15. Wilkie AO, Byren JC, Hurst JA, et al. Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis. Pediatrics 2010;126:e391-e400.
 
16. Lajeunie E, Le Merrer M, Bonaïti-Pellie C, et al. Genetic study of scaphocephaly. Am J Med Genet 1996;62:282-285.
 
17. Byun IH, Hong JW, Hussein MA, et al. Demographic characteristics of craniosynostosis patients in Asia. J Craniomaxillofac Surg 2018;46:674-678.
 
18. Gandolfi BM, Sobol DL, Farjat AE, et al. Risk factors for delayed referral to a craniofacial specialist for treatment of craniosynostosis. J Pediatr 2017; 186:165-171.e2.
 
19. Badiee RK, Maru J, Yang SC, et al. Racial and socioeconomic disparities in prompt craniosynostosis workup and treatment. J Craniofac Surg 2022;33: 2422-2426.
 
20. KFF. State health facts. Total monthly Medicaid/CHIP enrollment and pre-ACA enrollment, May 2022. https://www.kff.org/affordable-care-act/state-indicator/total-monthly-medicaid-and-chip-enrollment/?currentTimeframe=0&sortModel=%7B%22colId%22:%22Location%22,%22sort%22:%22asc%22%7D. Accessed March 11, 2022.
 
21. Hoffman C, Valenti AB, Odigie E, et al. Impact of health disparities on treatment for single-suture craniosynostosis in an era of multimodal care. Neurosurg Focus 2021;50:E13.