Sagittal Synostosis

163 Sagittal Synostosis
Amer F. Samdani and Phillip B. Storm


♦ Preoperative


Operative Planning



  • Physical exam

    • Clinical features include palpable ridge along sagittal suture, biparietal narrowing, occipital bossing
    • Closed fontanelle does not indicate sagittal synostosis (or any craniosynostosis). Craniosynostosis is a problem of the sutures, not the fontanelles.
    • Much more common in boys than girls (8:1)

  • Review imaging

    • Three-dimensional computed tomography scan (only in cases that the diagnosis is not clear on physical exam)

      • Look for fused sagittal suture; plain films are not helpful in ruling in or out sagittal synostosis

  • Reconstructive procedure, discuss risks/benefits with family
  • Ophthalmologic consult to rule out papilledema if the family elects not to perform surgery. Elevated intracranial pressure is rare in single suture craniosynostosis but has been reported.
  • Discuss timing of surgery; ideally the infant should be between 6 to 8 weeks because the earlier the surgery the better the reconstructive result. After 8 months a cranial vault reconstruction procedure may be required with the plastic surgery craniofacial team.
  • Discuss donor-directed blood

Special Equipment



  • Gel rolls for chest and hips
  • Horseshoe head holder
  • Hudson brace hand drill or perforator with pediatric burr
  • Local anesthetic (bupivacaine 0.25% with 1:200,000 epinephrine, 1 mL/kg maximum dose)
  • FloSeal or equivalent (thrombin with Gelfoam)

Anesthetic Issues



♦ Intraoperative


Positioning



Sterile Scrub and Prep



  • Clean incision line and surrounding area with 70% ethanol followed by a prescrub with scrub brush followed by a two-step Betadine prep, first with Betadine soap followed by Betadine scrub
  • Patient is draped with a U-shaped drape; no occlusive Ioban dressing is used

Incision and Exposure


Jul 11, 2016 | Posted by in NEUROSURGERY | Comments Off on Sagittal Synostosis

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