Cranial vault remodeling for sagittal craniosynostosis in older children

被引:30
作者
Rottgers, S. Alex [1 ,2 ]
Kim, Peter D. [1 ,3 ]
Kumar, Anand Raj [1 ,2 ]
Cray, James J. [1 ,2 ]
Losee, Joseph E. [1 ,2 ]
Pollack, Ian F. [1 ,3 ]
机构
[1] UPMC, Childrens Hosp Pittsburgh, Pittsburgh, PA 15224 USA
[2] Univ Pittsburgh, Div Pediat Plast Surg, Div Plast & Reconstruct Surg, Pittsburgh, PA USA
[3] Univ Pittsburgh, Div Pediat Neurosurg, Dept Neurosurg, Pittsburgh, PA USA
关键词
craniosynostosis; sagittal craniosynostosis; scaphocephaly; dolicocephaly; cranioplasty; craniofacial deformity; PI-PLASTY; SYNOSTOSIS; RECONSTRUCTION; CRANIOPLASTY; CRANIECTOMY; DEFORMITY; DEFECTS; GROWTH;
D O I
10.3171/2011.5.FOCUS1196
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Sagittal craniosynostosis is the most common form of craniosynostosis and is commonly treated within the first year of life. Optimal treatment of patients older than 1 year of age is not well characterized. The authors reviewed cases of sagittal craniosynostosis involving patients who were treated surgically at their institution when they were older than 1 year in order to determine the rate of intracranial hypertension (ICH), potential to develop nonhealing cranial defects, and the need for various surgical procedures to treat the more mature phenotype. Methods. A retrospective chart review was conducted of all cases in the Children's Hospital of Pittsburgh Neurosurgery Database involving patients who underwent cranial vault remodeling for scaphocephaly after 1 year of age between October 2000 and December 2010. Results. Ten patients were identified who met the inclusion criteria. Five patients underwent anterior two-thirds cranial vault remodeling procedures, 3 patients underwent posterior vault remodeling, and 2 patients underwent 2-staged total vault remodeling. All patients had improved head shapes, and mean cephalic indices improved from 65.4 to 69.1 (p = 0.05). Six patients exhibited signs of ICH. No patients with more than 3 months of follow-up exhibited palpable calvarial defects. Conclusions. Patients with sagittal synostosis treated after 1 year of age demonstrate increased rates of ICH, warranting diligent evaluations and surveillance to detect it; rarely develop clinically significant cranial defects if appropriate bone grafting is performed at the time of surgery; and achieve acceptable improvements in head shape. (DOI: 10.3171/2011.5.FOCUS1196)
引用
收藏
页数:6
相关论文
共 19 条
[1]   A single-center experience with symptomatic postoperative calvarial growth restriction after extended strip craniectomy for sagittal craniosynostosis Clinical article [J].
Adamo, Matthew A. ;
Pollack, Ian F. .
JOURNAL OF NEUROSURGERY-PEDIATRICS, 2010, 5 (01) :131-135
[2]   PROGNOSIS FOR MENTAL FUNCTION IN SCAPHOCEPHALY [J].
ARNAUD, E ;
RENIER, D ;
MARCHAC, D .
JOURNAL OF NEUROSURGERY, 1995, 83 (03) :476-479
[3]   Demineralized Bone Matrix and Resorbable Mesh Bilaminate Cranioplasty: A Novel Method for Reconstruction of Large-Scale Defects in the Pediatric Calvaria [J].
Chao, Mimi T. ;
Jiang, Shao ;
Smith, Darren ;
DeCesare, Gary E. ;
Cooper, Gregory M. ;
Pollack, Ian F. ;
Girotto, John ;
Losee, Joseph E. .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2009, 123 (03) :976-982
[4]   The reversal exchange technique of total calvarial reconstruction for sagittal synostosis [J].
Fata, JJ ;
Turner, MS .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2001, 107 (07) :1637-1646
[5]   Sagittal craniosynostosis: Surgical outcomes and long-term growth [J].
Fearon, JA ;
McLaughlin, EB ;
Kolar, JC .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2006, 117 (02) :532-541
[6]   Clinical outcome of the modified pi-plasty procedure for sagittal synostosis [J].
Guimaraes-Ferreira, J ;
Gewalli, F ;
David, L ;
Olsson, R ;
Friede, H ;
Lauritzen, CGK .
JOURNAL OF CRANIOFACIAL SURGERY, 2001, 12 (03) :218-224
[7]   IMMEDIATE CORRECTION OF SAGITTAL SYNOSTOSIS [J].
JANE, JA ;
EDGERTON, MT ;
FUTRELL, JW ;
PARK, TS .
JOURNAL OF NEUROSURGERY, 1978, 49 (05) :705-710
[8]   Endoscopic craniectomy for early surgical correction of sagittal craniosynostosis [J].
Jimenez, DF ;
Barone, CM .
JOURNAL OF NEUROSURGERY, 1998, 88 (01) :77-81
[9]  
Lajeunie E, 1996, AM J MED GENET, V62, P282, DOI 10.1002/(SICI)1096-8628(19960329)62:3<282::AID-AJMG15>3.0.CO
[10]  
2-G