Craniosynostosis Repair – Indications, Procedure, Risk

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Article Summary

Craniectomy - child; Synostectomy; Strip craniectomy; Endoscopy-assisted craniectomy; Sagittal craniectomy; Frontal-orbital advancement; FOA Craniosynostosis repair is surgery to correct a problem that causes the bones of a child's skull to grow together (fuse) too early. Description This surgery is done in the operating room under general anesthesia. This means your child will be asleep and will not feel pain. Traditional surgery is called open repair. It...

Key Takeaways

  • This article explains Description in simple medical language.
  • This article explains Why the Procedure Is Performed in simple medical language.
  • This article explains Risks in simple medical language.
  • This article explains Before the Procedure in simple medical language.
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Definition

Craniectomy – child; Synostectomy; Strip craniectomy; -assisted craniectomy; Sagittal craniectomy; Frontal-orbital advancement; FOA

Craniosynostosis repair is surgery to correct a problem that causes the bones of a child’s to grow together (fuse) too early.

Description

This surgery is done in the operating room under general anesthesia. This means your child will be asleep and will not feel .

Traditional surgery is called open repair. It includes these steps:

  • The most common place for a surgical cut to be made is over the top of the head, from just above one ear to just above the other ear. The cut is usually wavy. Where the cut is made depends on the specific problem.
  • A flap of skin, tissue, and muscle below the skin, and the tissue covering the bone are loosened and raised up so the surgeon can see the bone.
  • A strip of bone is usually removed where two sutures connect. This is called a strip craniectomy. Sometimes, larger pieces of bone must also be removed. This is called synostectomy. Parts of these bones may be changed or reshaped when they are removed. Then, they are put back. Other times, they are not.
  • Sometimes, bones that are left in place need to be shifted or moved.
  • Sometimes, the bones around the eyes are cut and reshaped.
  • Bones are fastened using a plate with screws that go into the skull. More and more surgeons are using resorbable plates and screws. The plates may expand as the skull grows.

Surgery usually takes 3 to 7 hours. Your child will probably need to have a blood transfusion during or after surgery to replace blood that is lost during the surgery.

A newer kind of surgery is used for some children. This type is usually done for children younger than 3 to 6 months old.

  • The surgeon makes one or two small cuts in the scalp. Most times these cuts are each just 1 inch (2.5 centimeters) long. These cuts are made above the area where the bone needs to be removed.
  • A tube that allows the doctor to see in (endoscope) is passed through the small cuts. Special medical devices and a camera are passed through the endoscope. Using these devices, the surgeon removes some bone through the cuts.
  • This surgery usually takes about 1 hour. There is much less blood loss with this kind of surgery.
  • Most children need to wear a special helmet to protect their head for a period of time after surgery.

Children do best when they have this surgery when they are 3 months old. The surgery should be done before the child is 6 months old

Why the Procedure Is Performed

A baby’s head, or skull, is made up of many different bones. The connections between these bones are called sutures. When a baby is born, it is normal for these sutures to be open a little. This gives the baby’s brain room to grow.

Craniosynostosis is a condition that causes one or more of the baby’s sutures to close too early. This can cause the shape of your baby’s head to be different than normal.

An or () scan can be used to diagnose craniosynostosis. Surgery is usually needed to correct it.

Surgery frees the sutures that are fused. It also reshapes the brow, eye sockets, and skull as needed. The goals of surgery are:

  • To relieve pressure on the child’s brain
  • To make sure there is enough room in the skull to allow the brain to properly grow
  • To improve the appearance of the child’s head

Risks

Risks for any surgery are:

  • Breathing problems
  • , including in the lungs and urinary tract
  • Blood loss (children having an open repair may need a transfusion)
  • Reaction to medicines

Possible risks of having this surgery are:

  • Infection in the brain
  • Bones connect together again, and more surgery is needed
  • Brain
  • Damage to brain tissue

Before the Procedure

If the surgery is planned, you will need to take the following steps:

During the days before the surgery:

  • Tell your health care provider what medicines, vitamins, or herbs you are giving your child. This includes anything you bought without a . You may be asked to stop giving your child some of these medicines in the days before the surgery.
  • Ask the doctor which medicines your child should still take on the day of the surgery.

On the day of the surgery:

  • Give your child a small sip of water with any medicines your doctor told you to give your child.
  • Your child’s provider will tell you when to arrive for the surgery.

Ask your provider if your child can eat or drink before surgery. In general:

  • Older children should not eat any food or drink any milk after midnight before the operation. They can have clear juice, water, and breast milk up to 4 hours before surgery.
  • Infants younger than 12 months can usually eat formula, cereal, or baby food until about 6 hours before surgery. They may have clear fluids and breast milk until 4 hours before surgery.

Your doctor may ask you to wash your child with a special soap on the morning of the surgery. Rinse your child well.

After the Procedure

After surgery, your child will be taken to an intensive care unit (ICU). Your child will be moved to a regular hospital room after a day or two. Your child will stay in the hospital for 3 to 7 days.

  • Your child will have a large bandage wrapped around the head. There will also be a tube going into a . This is called an IV.
  • The nurses will watch your child closely.
  • Tests will be done to see if your child lost too much blood during surgery. A blood transfusion will be given, if needed.
  • Your child will have swelling and around the eyes and face. Sometimes, the eyes may be swollen shut. This often gets worse in the first 3 days after surgery. It should be better by day 7.
  • Your child should stay in bed for the first few days. The head of your child’s bed will be raised. This helps keep the swelling down.

Talking, singing, playing music, and telling stories may help soothe your child. Acetaminophen (Tylenol) is used for pain. Your doctor can prescribe other pain medicines if your child needs them.

Most children who have endoscopic surgery can go home after staying in the hospital 1 night.

Outlook ()

Most of the time, the outcome from craniosynostosis repair is good.

 

Baskin JZ. Craniofacial surgery for and acquired deforminities. In: Cummings CW, Flint PW, Haughey BH, et al, eds. Otolaryngology: Head & Neck Surgery . 5th ed. Philadelphia, PA: Elsevier Mosby; 2010:chap 185.

Persing JA, Jane JA, Piatt JH. Craniosynostosis. In: Winn HR. Youman’s Neurological Surgery . 6th ed. Philadelphia, PA: Elsevier Saunders; 2011:chap 182.

Warren SM, Proctor MR, Bartlett SP, et al. Parameters of care for craniosynostosis: craniofacial and neurologic surgery perspectives. Plast Reconstry Surg . 2012;129:731-7. PMID 22373978  www.ncbi.nlm.nih.gov/pubmed/22373978 .

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Start with a registered doctor or the nearest qualified health center.

What to tell the doctor

  • Write when the problem started and how it changed.
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Questions to ask

  • What is the most likely cause of my symptoms?
  • Which danger signs mean I should go to hospital quickly?
  • Which tests are necessary now, and which can wait?
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  • Drink warm safe fluids and avoid smoke/dust exposure.
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  • Breathing difficulty should be treated as a warning sign.

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  • Cough syrups are not always needed; ask a clinician or pharmacist, especially for children.
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Get urgent help if

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  • Relevant blood, urine, imaging, or specialist tests only after clinical assessment
Questions to ask
  • What is the most likely cause of my symptoms?
  • Which warning signs mean I should go to emergency care?
  • Which tests are really needed now?
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Emergency warning signs such as chest pain, severe breathing difficulty, sudden weakness, confusion, severe dehydration, major injury, or loss of bladder/bowel control need urgent medical care. Do not wait for online information.

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Care roadmap for: Craniosynostosis Repair – Indications, Procedure, Risk

Use this simple roadmap to understand the next safe steps. It is educational and does not replace examination by a doctor.

Go to emergency care if you notice:
  • Severe or rapidly worsening symptoms
  • Breathing difficulty, chest pain, fainting, confusion, severe weakness, major injury, or severe dehydration
Doctor / service to discuss: Qualified healthcare provider; specialist depends on symptoms and examination.
  1. Step 1

    Check danger signs first

    If danger signs are present, seek emergency care and do not wait for online information.

  2. Step 2

    Record the symptom story

    Write when symptoms started, severity, medicines already taken, allergies, pregnancy status, and test results.

  3. Step 3

    Visit a qualified clinician

    A doctor, nurse, or qualified healthcare provider can examine you and decide which tests or treatment are needed.

  4. Step 4

    Do only useful tests

    Do tests after clinical assessment. Avoid unnecessary tests, random antibiotics, or repeated medicines without diagnosis.

  5. Step 5

    Follow up and return early if worse

    If symptoms worsen, new warning signs appear, or treatment is not helping, return for review quickly.

Rural patient practical tips
  • Take a written symptom diary and all previous prescriptions/test reports.
  • Do not hide medicines already taken, even herbal or over-the-counter medicines.
  • Ask which warning signs mean urgent referral to hospital.

This roadmap is for education. A real diagnosis and treatment plan requires history, examination, and clinical judgment.

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