TY - JOUR
T1 - What to do with an incidental finding of a fused sagittal suture
T2 - a modified Delphi study
AU - for the Synostosis Research Group (SynRG)
AU - Chiang, Sarah N.
AU - Reckford, Jocelyn
AU - Alexander, Allyson L.
AU - Birgfeld, Craig B.
AU - Bonfield, Christopher M.
AU - Couture, Daniel E.
AU - David, Lisa R.
AU - French, Brooke
AU - Gociman, Barbu
AU - Goldstein, Jesse A.
AU - Golinko, Michael S.
AU - Kestle, John R.W.
AU - Lee, Amy
AU - Magge, Suresh N.
AU - Pollack, Ian F.
AU - Rottgers, S. Alex
AU - Runyan, Christopher M.
AU - Smyth, Matthew D.
AU - Wilkinson, C. Corbett
AU - Skolnick, Gary B.
AU - Strahle, Jennifer M.
AU - Patel, Kamlesh B.
N1 - Publisher Copyright:
©AANS 2024, except where prohibited by US copyright law.
PY - 2024/8
Y1 - 2024/8
N2 - OBJECTIVE As many as 5% of normocephalic children may have a prematurely fused sagittal suture, yet the clinical significance and best course of management of this finding remain unclear. Providers in the Synostosis Research Group were surveyed to create a multicenter consensus on an optimal treatment and monitoring algorithm for this condition. METHODS A four-round modified Delphi method was utilized. The first two rounds consisted of anonymous surveys distributed to 10 neurosurgeons and 9 plastic surgeons with expertise in craniosynostosis across 9 institutions, and presented 3 patients (aged 3 years, 2 years, and 2 months) with incidentally discovered fused sagittal sutures, normal cephalic indices, and no parietal dysmorphology. Surgeons were queried about their preferred term for this entity and how best to manage these patients. Results were synthesized to create a treatment algorithm. The third and fourth feedback rounds consisted of open discussion of the algorithm until no further concerns arose. RESULTS Most surgeons preferred the term “premature fusion of the sagittal suture” (93%). At the conclusion of the final round, all surgeons agreed to not operate on the 3- and 2-year-old patients unless symptoms of intracranial hypertension or papilledema were present. In contrast, 50% preferred to operate on the 2-month-old. However, all agreed to utilize shared decision-making, taking into account any concerns about future head shape and neurodevelopment. Panelists agreed that patients over 18 months of age without signs or symptoms suggesting elevated intracranial pressure (ICP) should not undergo surgical treatment. CONCLUSIONS Through the Delphi method, a consensus regarding management of premature fusion of the sagittal suture was obtained from a panel of North American craniofacial surgeons. Without signs or symptoms of ICP elevation, surgery is not recommended in patients over 18 months of age. However, for children younger than 18 months, surgery should be discussed with caregivers using a shared decision-making process.
AB - OBJECTIVE As many as 5% of normocephalic children may have a prematurely fused sagittal suture, yet the clinical significance and best course of management of this finding remain unclear. Providers in the Synostosis Research Group were surveyed to create a multicenter consensus on an optimal treatment and monitoring algorithm for this condition. METHODS A four-round modified Delphi method was utilized. The first two rounds consisted of anonymous surveys distributed to 10 neurosurgeons and 9 plastic surgeons with expertise in craniosynostosis across 9 institutions, and presented 3 patients (aged 3 years, 2 years, and 2 months) with incidentally discovered fused sagittal sutures, normal cephalic indices, and no parietal dysmorphology. Surgeons were queried about their preferred term for this entity and how best to manage these patients. Results were synthesized to create a treatment algorithm. The third and fourth feedback rounds consisted of open discussion of the algorithm until no further concerns arose. RESULTS Most surgeons preferred the term “premature fusion of the sagittal suture” (93%). At the conclusion of the final round, all surgeons agreed to not operate on the 3- and 2-year-old patients unless symptoms of intracranial hypertension or papilledema were present. In contrast, 50% preferred to operate on the 2-month-old. However, all agreed to utilize shared decision-making, taking into account any concerns about future head shape and neurodevelopment. Panelists agreed that patients over 18 months of age without signs or symptoms suggesting elevated intracranial pressure (ICP) should not undergo surgical treatment. CONCLUSIONS Through the Delphi method, a consensus regarding management of premature fusion of the sagittal suture was obtained from a panel of North American craniofacial surgeons. Without signs or symptoms of ICP elevation, surgery is not recommended in patients over 18 months of age. However, for children younger than 18 months, surgery should be discussed with caregivers using a shared decision-making process.
KW - consensus
KW - craniofacial
KW - craniosynostosis
KW - sagittal synostosis
KW - survey
UR - http://www.scopus.com/inward/record.url?scp=85200523651&partnerID=8YFLogxK
U2 - 10.3171/2024.2.PEDS23521
DO - 10.3171/2024.2.PEDS23521
M3 - Article
C2 - 38728754
AN - SCOPUS:85200523651
SN - 1933-0707
VL - 34
SP - 182
EP - 189
JO - Journal of Neurosurgery: Pediatrics
JF - Journal of Neurosurgery: Pediatrics
IS - 2
ER -