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Posterior Cranial Vault Distraction

A Guide for Parents

The moment a parent hears their child needs skull surgery, a flood of emotions takes over—fear, confusion, and an overwhelming need to understand every possible detail. For children with certain forms of craniosynostosis, the skull doesn’t grow as it should, creating pressure on the brain and affecting its natural development. In the past, large, single-stage surgeries were the primary solution, but surgical advancements have paved the way for posterior cranial vault distraction (PCVD)—a technique that offers a safer, gradual, and more adaptable way to expand the skull and create space for the growing brain.

What Is Posterior Cranial Vault Distraction?

PCVD is a two-stage surgical technique used to gradually expand the back of a child’s skull (the occipital region) over time. Unlike traditional skull surgeries that require large sections of bone to be removed and reshaped in a single procedure, PCVD harnesses the body’s natural ability to generate new bone, allowing for a controlled and predictable expansion of the skull.

The technique involves carefully cutting and separating the bone in the back of the head and placing small distraction devices that slowly pull the bones apart over several weeks. This slow movement stimulates the body’s natural bone-healing process, causing new bone to form in the created gap. The result is an expanded posterior skull, increased intracranial volume, and improved overall head shape—all achieved with less trauma and a lower risk of complications compared with traditional methods.

Why and When Is Posterior Cranial Vault Distraction Used?

  • Chosen Over Traditional CVR
Sagittal

Metopic

Overview

Metopic synostosis, also known as trigonocephaly, is characterized by the premature fusion of the metopic suture, which runs from the top of the head down the middle of the forehead to the nose. This fusion results in a triangular-shaped forehead and a prominent ridge along the suture line.

metopic

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Metopic synostosis is relatively rare, accounting for between 5% and 15% of all craniosynostosis cases.

Diagnosis

Diagnostically, the condition can be identified through a physical examination, where the triangular shape of the forehead and ridging are noticeable. Imaging techniques, such as computed tomography (CT) scans, can confirm the diagnosis and assess the extent of the fusion.

Treatment

Treatment typically involves surgery to correct the skull shape and allow for normal brain growth. The surgical procedure, usually performed in the first year of life, involves removing and reshaping the fused bones to create a more typical skull contour. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Overview

PCVD is primarily used in children who have restricted skull growth at the back of the head, often due to premature suture fusion in conditions such as:

  • Syndromic craniosynostosis (such as Apert, Crouzon, or Pfeiffer syndrome), where multiple sutures are affected, leading to increased intracranial pressure (ICP)
  • Selective nonsyndromic cases where traditional expansion may not be ideal
metopic
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Metopic synostosis is relatively rare, accounting for between 5% and 15% of all craniosynostosis cases.

Diagnosis

Diagnostically, the condition can be identified through a physical examination, where the triangular shape of the forehead and ridging are noticeable. Imaging techniques, such as computed tomography (CT) scans, can confirm the diagnosis and assess the extent of the fusion.

Treatment

Treatment typically involves surgery to correct the skull shape and allow for normal brain growth. The surgical procedure, usually performed in the first year of life, involves removing and reshaping the fused bones to create a more typical skull contour. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Metopic

Coronal

Overview

The primary goals of PCVD include:

  • Relieving ICP, which can cause headaches, developmental delays, or vision issues
  • Creating more room for brain growth to ensure proper neurological development
  • Improving head shape and symmetry, particularly in cases where flattening of the back of the skull is severe
posterior cranioynostosis
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Coronal synostosis accounts for approximately 20% to 30% of all craniosynostosis cases.

Diagnosis

Diagnosis of coronal synostosis involves a thorough physical examination where asymmetry or brachycephaly is apparent. Imaging techniques, including CT scans, help confirm the diagnosis and plan the surgical intervention.

Treatment

Overview

Coronal synostosis involves the premature fusion of one (unilateral) or both (bilateral) coronal sutures, which run from ear to ear over the top of the skull. Unilateral coronal synostosis, also known as synostotic anterior plagiocephaly, results in an asymmetrical skull with a flattened forehead on the affected side and a raised eyebrow. Bilateral coronal synostosis, also known as brachycephaly, leads to a brachycephalic head shape, characterized by a broad, short skull.

Synostotic Anterior Plagiocephaly

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Coronal synostosis accounts for approximately 20% to 30% of all craniosynostosis cases.

Diagnosis

Diagnosis of coronal synostosis involves a thorough physical examination where asymmetry or brachycephaly is apparent. Imaging techniques, including CT scans, help confirm the diagnosis and plan the surgical intervention.

Treatment

Surgical correction is typically recommended to improve skull shape and symmetry. The timing of the surgery is crucial; it is often performed within the first year of life to maximize the benefits. Procedures may involve fronto-orbital advancement and reshaping of the forehead and eye sockets. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Unilateral Coronal

Sagittal

Overview

PCVD is often chosen over traditional cranial vault remodeling (CVR) when a more controlled and gradual expansion is needed. By expanding the skull over weeks rather than all at once, PCVD offers several benefits:

  • Less blood loss
  • More stable long-term results due to the natural bone formation process
  • The ability to adjust the expansion process based on the child’s response to treatment
Scaphocephaly
Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Sagittal synostosis accounts for approximately 40% to 55% of all craniosynostosis cases.

Diagnosis

Physical examination often reveals a long, narrow head shape with a prominent ridge along the sagittal suture. Confirmatory diagnosis is achieved through imaging studies such as CT scans, which provide detailed views of the fused suture and skull shape.

Treatment

Surgical treatment for sagittal synostosis aims to expand the width of the skull and improve its overall shape. Depending on the severity of the condition, procedures may include minimally invasive endoscopic suturectomy or a more complex procedure referred to as cranial vault remodeling. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

Overview

Sagittal synostosis, also known as scaphocephaly, is the most common form of craniosynostosis. It involves the premature fusion of the sagittal suture, which runs from the front to the back of the skull along the midline. This fusion causes the head to grow long and narrow, a condition known as scaphocephaly.

Synostotic Anterior Plagiocephaly

Incidence

The overall incidence of Craniosynostosis is approximately 1 in 2000/3000 births. Sagittal synostosis accounts for approximately 40% to 55% of all craniosynostosis cases.

Diagnosis

Physical examination often reveals a long, narrow head shape with a prominent ridge along the sagittal suture. Confirmatory diagnosis is achieved through imaging studies such as CT scans, which provide detailed views of the fused suture and skull shape.

Treatment

Surgical treatment for sagittal synostosis aims to expand the width of the skull and improve its overall shape. Depending on the severity of the condition, procedures may include minimally invasive endoscopic suturectomy or a more complex procedure referred to as cranial vault remodeling. Please refer to our Treatment Options page for a more detailed explanation of these surgical procedures.

How Posterior Cranial Vault Distraction Differs From Traditional Skull Expansion Surgery

Before PCVD, most children with restricted skull growth underwent CVR, a complex surgery that involves removing and reshaping large pieces of skull bone in a single operation. While effective, CVR has some drawbacks compared with PCVD:

  • It requires a longer surgery that has a higher risk of blood loss.
  • The skull is immediately reshaped, meaning there’s less control over how the bone heals and adapts.
  • In some cases, children still need additional surgeries later in life for further expansion.

With PCVD, the distraction devices allow for a slower and more controlled expansion, giving the brain more room over time and leading to a more natural skull shape with less surgical trauma. This gradual process mimics the body’s natural bone growth, resulting in a stronger, more stable skull structure.

The Benefits of Posterior Cranial Vault Distraction

For parents exploring treatment options, PCVD offers several advantages over CVR:

A Life-Changing Innovation in Craniofacial Surgery

PCVD represents a major advancement in treating craniosynostosis, offering a less invasive and more adaptable solution for children needing skull expansion. While the idea of multiple stages (surgery plus the distraction phase) may feel overwhelming for parents, the long-term benefits—improved brain space, reduced complications, and a more natural skull shape—make PCVD a preferred option for many craniofacial surgeons.

In the next section, we’ll explore the history and evolution of PCVD—how it was developed, how it improved upon traditional methods, and how today’s technology has made it even safer and more effective.

The Evolution of Posterior Vault Expansion

For decades, the surgical treatment of craniosynostosis remained essentially unchanged: large, single-stage skull reconstructions that required removing and reshaping significant portions of bone in one procedure. While effective, these surgeries carried risks, including high blood loss, unpredictable healing patterns, and the potential need for reoperation as the child’s skull continued to grow.

As medical technology advanced, so did the search for less invasive, more controlled methods for expanding the skull. The introduction of distraction osteogenesis—a technique originally used for limb lengthening—transformed craniofacial surgery. It allowed surgeons to move bones gradually rather than all at once, reducing surgical trauma and improving long-term outcomes.

Among the most impactful applications of this technique was the development of PCVD—a method specifically designed to expand the back of the skull in children with restricted growth, particularly those with ICP.

The Introduction of Distraction Osteogenesis in Craniofacial Surgery

The breakthrough came from an unexpected field: limb lengthening surgery. In the 1950s, Russian orthopedic surgeon Dr. Gavriil Ilizarov discovered that slowly pulling apart bone segments stimulated the body to form new bone in the gap—a process known as distraction osteogenesis. This technique revolutionized orthopedic surgery, allowing for controlled limb lengthening with stronger, more stable bone formation.

By the late 1990s and early 2000s, craniofacial surgeons began adapting distraction osteogenesis for skull expansion. Instead of instantly reshaping the skull in a single surgery, they experimented with gradual bone movement using distraction devices. The first applications focused on the midface and jaw, but surgeons soon realized the posterior skull (occipital region) could also be expanded using this method.

The Birth of Posterior Cranial Vault Distraction

Posterior vault distraction scaled

The Distraction Osteogenesis Process

Distraction osteogenesis is a biological process that occurs when bone is slowly pulled apart in a controlled manner, prompting the body to fill the gap with newly generated bone tissue. This technique has been widely used in orthopedic and craniofacial surgery as it enables the creation of strong, stable bone structures over time.

Step-By-Step Breakdown of the Bone Growth Process:

Once your baby is fully asleep under anesthesia, the surgical team will proceed with the following steps:

 1.

Osteotomy (bone cutting)

During the initial surgery, the craniofacial surgeon makes precise cuts in the occipital (posterior) skull bone, separating it from the rest of the skull while keeping the underlying dura mater (brain covering) intact.

 

 2.

Placement of distraction devices

Specialized internal or external distraction devices are carefully positioned and secured to the bone segments.

 

 3.

Latency period (resting phase)

 After surgery, there is a short waiting period (usually five to seven days) to allow early bone healing to begin before the distraction phase starts

 4.

Activation phase (gradual expansion)

Parents or surgeons slowly adjust the distractor daily or every other day, moving the skull segments apart by approximately one millimeter per day. This controlled movement creates a growing gap that is gradually filled with new bone tissue.

 

 5.

Consolidation phase (bone hardening)

Once the desired skull expansion is reached (typically after three to six weeks), no further adjustments are made, and the newly formed bone is allowed to harden and fully integrate with the surrounding skull.

 

 6.

Device removal

 After several months, once the new bone is stable, a second surgery is performed to remove the distraction device.

 

Why Posterior Cranial Vault Distraction Provides Stronger, More Stable Skull Growth

Compared with traditional CVR, PCVD offers several biomechanical advantages:

  • The gradual process allows for more robust bone formation, reducing the risk of re-fusion or irregular skull shape.
  • The skull expands naturally, following the body’s own healing patterns rather than being forced into an immediate new shape.
  • Less tension is placed on the dura mater and surrounding tissues, which reduces complications and improves postsurgical comfort.

How the Skull Changes Over Time

As the distraction phase progresses, parents will notice a gradual change in the shape of the back of the skull. Over weeks to months, the newly formed bone integrates seamlessly with the existing skull, ensuring a smooth and natural-looking result.

In the next section, we will explore how families prepare for PCVD surgery, including preoperative imaging, surgical planning, and what to expect before, during, and after the procedure.

Preparing for Posterior Cranial Vault Distraction Surgery

The decision to move forward with PCVD can feel overwhelming for you as a parent. Understanding what to expect before, during, and after surgery can help ease concerns and ensure that your family is fully prepared for each step of the process.

Preoperative Evaluation: Assessing the Need for Posterior Cranial Vault Distraction

Before surgery, a comprehensive evaluation is performed to determine whether PCVD is the best approach for your child. This process involves:

The Posterior Cranial Vault Distraction Surgery

The thought of your child undergoing skull surgery can be daunting. Understanding the step-by-step process of PCVD can help ease your concerns and provide clarity on what happens in the operating room. This section will cover how the surgery is performed, what to expect during and immediately after the procedure, and how the distraction devices are placed.

Step-By-Step Breakdown of the Surgery

 1.

Anesthesia and presurgical preparation

  • The child is placed under general anesthesia to ensure they are completely asleep and pain-free during the procedure.
  • The surgical team carefully positions the child to allow full access to the posterior skull.
  • Antibiotics are administered to minimize the risk of infection.

 2.

Making the incision

  • An incision is made across the back of the head. The incision is made in the most appropriate manner to minimize noticeable scarring.
  • The scalp and soft tissues are carefully lifted to expose the skull while protecting underlying structures, such as the dura mater (the protective layer covering the brain).

 3.

Osteotomy (cutting and mobilizing the skull bone)

  • The surgeon makes precise bone cuts (osteotomies) in the occipital (posterior) skull.
  • The goal is to free a large segment of bone while keeping it connected to the dura mater, which supplies blood and promotes new bone growth.
  • Unlike with traditional CVR, no bone is removed; instead, the existing bone is repositioned and gradually expanded over time.

 4.

Placement of the distraction devices

  • Small distraction devices (internal or external) are securely attached to the mobilized bone segment.
  • The devices function as controlled expanders, gradually increasing the distance between the separated bones.
  • Depending on the surgical plan, one or two distractors may be used to achieve symmetrical skull expansion.

 5.

Closing the incision and final adjustments

  • The scalp is carefully repositioned and sutured in place, ensuring a secure and natural-looking closure.
  • The distractor arms (if external) are positioned to allow for postoperative adjustments.

 6.

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Types of Distractors Used in Posterior Cranial Vault Distraction

Surgeons may use different types of distraction devices, depending on the child’s needs:

  • Internal distractors are hidden beneath the scalp and activated manually by turning a small key or screw.
  • External distractors are less common and involve adjustment rods visible outside the scalp.

The Consolidation Phase and Device Removal

Once the activation phase of PCVD is complete, the next critical step is the consolidation phase. This is the period where the newly formed bone hardens and strengthens, ensuring that the skull maintains its expanded shape. After sufficient bone maturation, the distraction devices are surgically removed, completing the process.

What Happens During the Consolidation Phase?

1. Stopping adjustments and allowing bone to harden:

  • Once the desired skull expansion has been reached (typically after three to six weeks of activation), adjustments to the distraction devices are stopped.

  • The bone is left undisturbed for several weeks to allow the new tissue to solidify and integrate with the existing skull.

  • The consolidation phase typically lasts 8 to 12 weeks, but the exact duration depends on your child’s age, healing ability, and bone growth rate.

2. Monitoring bone formation:

  • Regular follow-up appointments will include X-rays or CT scans to confirm that sufficient bone has filled the expansion gap.

  • If the bone is not forming as expected, additional time may be needed before device removal.

  • You should continue to monitor the surgical site for any redness, swelling, or discomfort.

The Second Surgery: Removing the Distraction Devices

Once the surgeon confirms that the new bone is stable, a second procedure is scheduled to remove the distraction devices.

1. The device removal surgery:

  • The procedure is shorter and less invasive than the initial surgery.
  • Your child is placed under general anesthesia, and a small incision is made to access the distractors.
  • The devices are carefully detached and removed, leaving the newly expanded skull intact.
  • The incisions are closed with sutures, and the scalp heals naturally over the following weeks.

2. Recovery after the device removal:

  • Most children recover quickly and are discharged the same day or after one night in the hospital.
  • Some mild swelling or tenderness is expected but clears up within a few days.
  • The bone continues to strengthen over the next several months, ensuring long-term stability.

What Happens After Posterior Cranial Vault Distraction Is Complete?

After the distraction devices are removed, follow-up care is essential to monitor the long-term success of the skull expansion. This aftercare includes:

  • Periodic skull imaging (CT scans or X-rays) to assess continued skull growth
  • Neurological evaluations to ensure there are no concerns related to brain development or ICP
  • Discussion of future surgical needs if additional interventions are required as your child grows

For many children, PCVD provides a permanent solution for increasing skull volume, reducing the need for additional surgeries in the future.

In the next section, we’ll discuss the overall recovery process, long-term outcomes, and what parents should expect as their child grows after PCVD.

Recovery and Long-Term Outcomes

After the distraction devices are removed, the recovery process focuses on allowing the skull to heal fully and monitoring the long-term effects of PCVD. Most children experience a smooth recovery with gradual improvements in skull shape, brain space, and overall head symmetry.

laughing mother lifting her adorable newborn baby son air scaled

Final Thoughts and Key Takeaways

PCVD has transformed the treatment of certain forms of craniosynostosis, offering a gradual, controlled, and effective way to expand the skull. As you navigate this journey, understanding each phase of the process—from surgical planning to recovery—can make the experience less overwhelming and more manageable.

Key Takeaways for Parents:

  • PCVD is a gradual skull expansion method that allows the body to form new bone naturally, reducing the risks associated with traditional CVR.
  • It is primarily used for children with restricted skull growth in the back of the head, particularly those with increased ICP or syndromic craniosynostosis.
  • The procedure involves two surgeries: the initial placement of the distractors and a later procedure to remove them after the bone has fully formed.
  • The activation phase requires daily adjustments to gradually expand the skull over several weeks. As a parent, you will likely be involved in this process and receive training from the medical team.
  • The consolidation phase allows the new bone to harden, ensuring long-term skull stability. This phase typically lasts several months and is followed by device removal.
  • Recovery after PCVD is usually smooth, with minimal pain after the initial healing period. Most children can resume regular activities within weeks of the distraction device being removed.
  • Regular follow-up visits and imaging are essential to ensure proper skull development and monitor long-term outcomes.

Empowering Parents With Knowledge and Support

PCVD is a highly effective treatment, but as with any medical procedure, it requires patience, understanding, and close collaboration with a craniofacial team. You should feel empowered to:

  • Ask questions and seek clarification about your child’s treatment plan
  • Stay actively involved in postsurgical care, including distractor activation and incision monitoring
  • Lean on support networks—including medical professionals, other families, and patient advocacy groups—to navigate the emotional and practical aspects of your journey

A Future of Continued Innovation

With advancements in distraction device technology, 3D surgical planning, and regenerative medicine, the future of PCVD is promising. Ongoing research and innovation will continue to improve the procedure’s safety, precision, and overall outcomes.

For you, the journey through PCVD may seem complex at first, but with the right medical team and the knowledge gained from this guide, you can confidently support your child through the treatment and into the future with a healthy, well-developed skull.

 

Frequently Asked Questions

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