Literature DB >> 21721888

Treatment for delayed presentation of sagittal synostosis: challenges pertaining to occult intracranial hypertension.

Mitchel Seruya1, Albert K Oh, Michael J Boyajian, Jeffrey C Posnick, Robert F Keating.   

Abstract

OBJECT: Patients with delayed presentation of isolated sagittal synostosis (ISS) pose unique surgical challenges. Intracranial hypertension can be missed in the absence of overt findings. Here, an algorithm is presented for the elucidation of intracranial hypertension and approaches to surgical treatment during calvarial reconstruction.
METHODS: Patients with delayed presentation (age > 15 months) of ISS between 1997 and 2009 were identified. Symptoms, signs, and radiological evidence of intracranial hypertension were noted. Intraoperative management included calvarial reconstruction in conjunction with ventriculostomy for intracranial pressure (ICP) monitoring and CSF drainage in the setting of suspected intracranial hypertension.
RESULTS: Seventeen patients underwent calvarial reconstruction for delayed presentation of ISS. The mean surgical age was 40.5 months (16.2-82.9 months), and the average follow-up was 34.2 months (0.6-92.2 months). Eleven patients with subtle findings of intracranial hypertension underwent ICP monitoring during calvarial reconstruction. The mean opening ICP was 23.5 cm H(2)O (16.5-29.5 cm H(2)O), and the mean closing ICP was 7.0 cm H(2)O (3.5-17.0 cm H(2)O). Nine (81.8%) of 11 monitored patients demonstrated intracranial hypertension (ICP ≥ 20 cm H(2)O); the other 2 had borderline increased ICP. Perioperative morbidity was 5.9%, with 1 patient medically treated for transient, new-onset intracranial hypertension. The postoperative Whitaker category was I in 94.1% of patients, II in 5.9%, and III/IV in 0%. There were no reoperations or deaths.
CONCLUSIONS: In this consecutive series, 11 of 17 patients with delayed presentation of ISS underwent ICP monitoring during calvarial reconstruction as a result of subtle clinical findings of intracranial hypertension. Nine (81.8%) of 11 monitored patients demonstrated intracranial hypertension. Calvarial reshaping along with ICP monitoring and CSF drainage facilitated reconstruction and resulted in good outcomes and the resolution of intracranial hypertension.

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Mesh:

Year:  2011        PMID: 21721888     DOI: 10.3171/2011.4.PEDS1160

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  6 in total

1.  Occult Scaphocephaly: A Forme Fruste Phenotype of Sagittal Craniosynostosis.

Authors:  Esperanza Mantilla-Rivas; Liyun Tu; Agnes Goldrich; Monica Manrique; Antonio R Porras; Robert F Keating; Albert K Oh; Marius George Linguraru; Gary F Rogers
Journal:  J Craniofac Surg       Date:  2020 Jul-Aug       Impact factor: 1.046

2.  Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.

Authors:  Jin Liu; Hwa Kyung Nam; Estee Wang; Nan E Hatch
Journal:  Calcif Tissue Int       Date:  2013-01-29       Impact factor: 4.333

3.  Tissue-nonspecific alkaline phosphatase deficiency causes abnormal craniofacial bone development in the Alpl(-/-) mouse model of infantile hypophosphatasia.

Authors:  Jin Liu; Hwa Kyung Nam; Cassie Campbell; Kellen Cristina da Silva Gasque; José Luis Millán; Nan E Hatch
Journal:  Bone       Date:  2014-07-09       Impact factor: 4.398

4.  Materials and Orthopedic Applications for Bioresorbable Inductively Coupled Resonance Sensors.

Authors:  Aleksi Palmroth; Timo Salpavaara; Petri Vuoristo; Sanna Karjalainen; Tommi Kääriäinen; Susanna Miettinen; Jonathan Massera; Jukka Lekkala; Minna Kellomäki
Journal:  ACS Appl Mater Interfaces       Date:  2020-07-02       Impact factor: 9.229

5.  Craniosynostosis-associated Fgfr2(C342Y) mutant bone marrow stromal cells exhibit cell autonomous abnormalities in osteoblast differentiation and bone formation.

Authors:  J Liu; T-G Kwon; H K Nam; N E Hatch
Journal:  Biomed Res Int       Date:  2013-05-09       Impact factor: 3.411

Review 6.  Cranial Neural Crest Cells and Their Role in the Pathogenesis of Craniofacial Anomalies and Coronal Craniosynostosis.

Authors:  Erica M Siismets; Nan E Hatch
Journal:  J Dev Biol       Date:  2020-09-09
  6 in total

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