Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article 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.

Download full-text PDF

Source
http://dx.doi.org/10.3171/2021.2.PEDS2113DOI Listing

Publication Analysis

Top Keywords

single-suture synostosis
16
clinical diagnosis
16
preoperative imaging
12
intracranial findings
12
single-suture craniosynostosis
12
imaging
10
study synostosis
8
synostosis group
8
diagnosis single-suture
8
children single-suture
8

Similar Publications

Leveraging novel diagnostic codes for craniosynostosis by suture type in surgical database research.

J Plast Reconstr Aesthet Surg

September 2025

Division of Plastic Surgery, Department of Surgery, Columbia University Irving Medical Center, New York, NY, United States. Electronic address:

Background: Craniosynostosis presents with a diverse range of presentations that influence surgical approach and postoperative outcomes. This study applies new diagnostic ICD-10 codes that stratify by craniosynostosis suture type to investigate trends in postoperative outcomes within a surgical database.

Methods: Patients undergoing craniosynostosis repair with specified suture types were identified in the 2023 National Surgical Quality Improvement Program (NSQIP) Pediatric database.

View Article and Find Full Text PDF

Endoscopic Strip Craniectomy for the Treatment of Single Suture Craniosynostosis.

Adv Tech Stand Neurosurg

July 2025

Neurosurgery, Pediatric Neurosurgery, C.S. Mott Children's Hospital, Department of Neurosurgery, University of Michigan, Ann Arbor, MI, USA.

The treatment of craniosynostosis has evolved significantly over the past few decades. While open calvarial vault reconstruction remains a good treatment option, minimally invasive techniques have been shown to yield excellent results in children treated at a young age. This chapter details the use of endoscopic strip craniectomy with postoperative helmet therapy.

View Article and Find Full Text PDF

Objective: Secondary bone closure following single-suture craniosynostosis (SSCS) correction has been previously reported. However, the incidence of such secondary closure, which leads to increased intracranial pressure (ICP), following strip craniectomy for sagittal synostosis (SS) has not been systematically described. The possibility of secondary closure must be taken into account when determining the optimal long-term follow-up regimen after the procedure.

View Article and Find Full Text PDF

Non-syndromic craniosynostosis.

Nat Rev Dis Primers

April 2025

Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

Craniosynostosis is characterized by the premature fusion of one or more major cranial sutures at birth or soon after. Single-suture non-syndromic craniosynostosis (NSC) is the most common form of craniosynostosis and includes the sagittal, metopic, unicoronal and unilambdoid subtypes. Characterized by an abnormal head shape specific to the fused suture type, NSC can cause increased intracranial pressure.

View Article and Find Full Text PDF

Multisutural syndromic craniosynostosis is strongly associated with secondary Chiari malformation. Although less commonly described, single suture synostosis can also be associated with secondary Chiari malformation due to craniocephalic disproportion. These children have traditionally been treated with posterior vault expansion; however, in patients with sagittal synostosis, increasing only the posterior vault volume can worsen the scaphocephalic deformity.

View Article and Find Full Text PDF