Preoperative imaging patterns and intracranial findings in single-suture craniosynostosis: a study from the Synostosis Research Group

Author:

Ravindra Vijay M.123,Awad Al-Wala1,Baker Cordell M.1,Lee Amy4,Anderson Richard C. E.5,Gociman Barbu6,Patel Kamlesh B.7,Smyth Matthew D.8,Birgfeld Craig9,Pollack Ian F.9,Goldstein Jesse A.10,Imahiyerobo Thomas11,Siddiqi Faizi A.6,Kestle John R. W.1,_ _

Affiliation:

1. Department of Neurosurgery, and

2. Division of Neurosurgery, University of California, San Diego;

3. Department of Neurosurgery, Naval Medical Center San Diego, California;

4. Department of Neurosurgery, Seattle Children’s Hospital, University of Washington, Seattle, Washington;

5. Department of Neurosurgery, Columbia University, Morgan Stanley Children’s Hospital, and

6. Division of Plastic and Reconstructive Surgery, University of Utah, Salt Lake City, Utah;

7. Division of Plastic and Reconstructive Surgery, Department of Surgery, and

8. Department of Neurosurgery, St. Louis Children’s Hospital, Washington University School of Medicine in St. Louis, Missouri;

9. and Departments of Pediatric Neurosurgery and

10. Plastic Surgery, Children’s Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania

11. Division of Plastic Surgery, Columbia University Medical Center, NewYork-Presbyterian Hospital, New York, New York;

Abstract

OBJECTIVE The diagnosis of single-suture craniosynostosis can be made by physical examination, but the use of confirmatory imaging is common practice. The authors sought to investigate preoperative imaging use and to describe intracranial findings in children with single-suture synostosis from a large, prospective multicenter cohort. METHODS In this study from the Synostosis Research Group, the study population included children with clinically diagnosed single-suture synostosis between March 1, 2017, and October 31, 2020, at 5 institutions. The primary analysis correlated the clinical diagnosis and imaging diagnosis; secondary outcomes included intracranial findings by pathological suture type. RESULTS A total of 403 children (67% male) were identified with single-suture synostosis. Sagittal (n = 267), metopic (n = 77), coronal (n = 52), and lambdoid (n = 7) synostoses were reported; the most common presentation was abnormal head shape (97%), followed by a palpable or visible ridge (37%). Preoperative cranial imaging was performed in 90% of children; findings on 97% of these imaging studies matched the initial clinical diagnosis. Thirty-one additional fused sutures were identified in 18 children (5%) that differed from the clinical diagnosis. The most commonly used imaging modality by far was CT (n = 360), followed by radiography (n = 9) and MRI (n = 7). Most preoperative imaging was ordered as part of a protocolized pathway (67%); some images were obtained as a result of a nondiagnostic clinical examination (5.2%). Of the 360 patients who had CT imaging, 150 underwent total cranial vault surgery and 210 underwent strip craniectomy. The imaging findings influenced the surgical treatment 0.95% of the time. Among the 24% of children with additional (nonsynostosis) abnormal findings on CT, only 3.5% required further monitoring. CONCLUSIONS The authors found that a clinical diagnosis of single-suture craniosynostosis and the findings on CT were the same with rare exceptions. CT imaging very rarely altered the surgical treatment of children with single-suture synostosis.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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