| Literature DB >> 21906303 |
Olugbenga A Akingbola1, Dinesh Singh, Sudesh K Srivastav, John W Walsh, David A Jansen, Edwin M Frieberg.
Abstract
BACKGROUND: Craniosynostosis (CSS) results from the premature closure of one or more cranial sutures, leading to deformed calvaria at birth. It is a common finding in children with an incidence of one in 2000 births. Surgery is required in order to release the synostotic constraint and promote normal calvaria growth. Cranial vault remodeling is the surgical approach to CSS repair at our institution and it involves excision of the frontal, parietal, and occipital bones. The purpose of this article is to describe the post-operative course of infants and children admitted to our PICU after undergoing cranial vault remodeling for primary CSS.Entities:
Year: 2011 PMID: 21906303 PMCID: PMC3228509 DOI: 10.1186/1756-0500-4-347
Source DB: PubMed Journal: BMC Res Notes ISSN: 1756-0500
Figure 1Cranial sutures in infancy. Premature closure of any of the calvarial sutures produces a restriction of growth vectors leading to craniosynostosis.
Age distribution in patients with craniosynostosis at the time of surgery
| Age group (months) | Number of patients | % |
|---|---|---|
| 4 | 5 | |
| 28 | 34 | |
| 26 | 32 | |
| 10 | 12 | |
| 14 | 17 | |
Majority of patients were greater than 4 months at diagnosis; intra-operative blood loss and post-operative morbidities were higher in older patients
Figure 2Total number of each category of suture involved in the different types of craniosynostosis is shown at the top of each bar; coronal and sagittal suture synostoses were predominant in our series.
Syndromes associated with craniosynostosis
| Syndromes | N = 8 |
|---|---|
| Apert | 1 |
| Pierre Robin | 2 |
| Goldenhar | 1 |
| Turner | 1 |
| Dandy-Walker malformation | 1 |
| VATER | 1 |
| Arnold-Chiari malformation | 1 |
9.7% of our patients had associated syndromes. Incidence of recurrent synostosis is higher in patients with associated syndromes.
Figure 3There was a tend towards longer duration of surgery in older patients but this was not statistically significant (p > 0.005).
Figure 4Blood loss during surgery was higher in older patients (P < 0.05) but a spike in blood loss occurred in the 6 mo-12 mo group because of presence of associated syndromes and a more complicated/protracted surgery in 2 pts in this group.
Figure 5Post-op blood loss in the PICU was higher in older patients in the time period indicated.
Figure 6There was a trend towards increased use of crystalloid intra-operatively and in the first 36 hours in PICU. This trend reached statistical significance (P < 0.05) and correlated with age.
Figure 7Urine output was a surrogate marker for intravascular volume status; increased urine output correlates with crystalloid administration (P < 0.001).
Number of patients requiring repeat operation for cosmetic and other problems after initial surgery for craniosynostosis
| Age at first surgery (suture category) | Age at re-operation | Reasons for re-operation |
|---|---|---|
| 8 yrs | ↑ICP, headache, unsteady gait | |
| 11 mo** | temporalis muscle re-suspension | |
| 4 yrs | bony defect over posterior sagittal sinus | |
| 18 mo* | hemifacial reconstruction | |
| 6 yrs | Facial asymmetry & orbital dystopia | |
| 6 yrs | Repair of multiple cranial defects | |
| 7 yrs | cranioplasty for frontal skull defects | |
| 4 yrs | Non-healing coronal incision, craniofacial deformity, repair of Lt encephalocoele | |
*3 days after first surgery; **4 days after first surgery;
Patients with recurrent synostosis and major surgical complications were 6 months or older at time of initial surgery. Poor cosmetic outcomes appear to be common in patients older than 6 months at the time of initial surgery.