Literature DB >> 18831658

Clinical predictors of developmental outcome in patients with cephaloceles.

Benjamin W Y Lo1, Abhaya V Kulkarni, James T Rutka, Andrew Jea, James M Drake, Maria Lamberti-Pasculli, Peter B Dirks, Lehana Thabane.   

Abstract

OBJECT: Cephaloceles represent primary axial mesodermal defects, occurring in 0.8-4 per 10,000 live births. Prior studies have reported posterior location, hydrocephalus, microcephaly, seizure, and presence of brain tissue as poor prognostic markers for neurological outcome. However, these studies were small and the results were analyzed using univariate tests. The purpose of this study was to investigate the potential risk factors for the occurrence of developmental delay in patients with cephaloceles, using both univariate and multivariable regression techniques.
METHODS: This is a retrospective cohort study of cephalocele cases treated at the Hospital for Sick Children between 1990 and 2006. Two independent investigators collected the data from the Hospital for Sick Children Encephalocele Database and hospital charts. Developmental assessments were made by general pediatricians and neuropsychologists. Both univariate analysis (alpha=0.10) and multivariable logistic regression analysis (alpha=0.05) were performed.
RESULTS: Eighty-five cases of cephaloceles were identified. The patient group consisted of 48 boys and 37 girls. Sixty-eight lesions were encephaloceles and 17 were meningoceles. The distribution was as follows: frontal (40 lesions), occipital (33), and parietal (12). Associated conditions included hydrocephalus (23), seizure disorder (17), microcephaly (6), corpus callosal abnormalities (15), heterotopias (9), cerebral dysgenesis (11), and myelomeningocele (1). Evaluation of long-term development revealed that 41 patients (48%) had normal development, 9 (11%) had mild delay, 14 (16%) had moderate delay, and 21 (25%) had severe delay. Hydrocephalus, seizure disorder, microcephaly, presence of associated intracranial abnormalities, and presence of brain tissue were significantly associated with poor outcome on univariate analysis. Multivariable analysis revealed hydrocephalus and presence of intracranial abnormalities to be statistically significant predictors of developmental delay.
CONCLUSIONS: To the authors' knowledge, this is one of the largest North American cephalocele series documented. Unlike prior studies, location of the cephaloceles is not a significant predictor of outcome. The multivariable regression analysis demonstrates hydrocephalus and the presence of associated intracranial abnormalities as variables with cumulative predictive effects for developmental delay.

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Year:  2008        PMID: 18831658     DOI: 10.3171/PED.2008.2.10.254

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


  17 in total

1.  Dural sinus filling defect: intrasigmoid encephalocele.

Authors:  Ozan Karatag; Murat Cosar; Betul Kizildag; Halil Murat Sen
Journal:  BMJ Case Rep       Date:  2013-12-05

Review 2.  Hydrocephalus associated with neural tube defects: characteristics, management, and outcome in sub-Saharan Africa.

Authors:  Benjamin C Warf
Journal:  Childs Nerv Syst       Date:  2011-09-17       Impact factor: 1.475

3.  Late-onset obstructive hydrocephalus associated with occipital encephalocele with large skull defect successfully treated by endoscopic third ventriculostomy.

Authors:  Yuki Munekata; Taku Sugiyama; Yuki Ueda; Makoto Mizushima; Hiroaki Motegi; Miki Fujimura
Journal:  Childs Nerv Syst       Date:  2022-07-29       Impact factor: 1.532

Review 4.  Occipital encephalocele associated with Dandy-Walker malformation: a case-based review.

Authors:  Felipe Gutierrez; Matheus Ballestero; David Herrera; Catalina Gonzalez; Alejandra Cardona; Laura Mora
Journal:  Childs Nerv Syst       Date:  2022-05-19       Impact factor: 1.532

5.  A new phenotype of amniotic band syndrome with occipital encephalocele-like morphology: a case report.

Authors:  Osamu Yazawa; Daisuke Hirokawa; Kaede Okamoto; Mio Tanaka; Jun Shibasaki; Hironobu Sato
Journal:  Childs Nerv Syst       Date:  2021-11-05       Impact factor: 1.532

6.  Spontaneous Third Ventriculostomy in Krabbe Disease.

Authors:  Giulio Zuccoli; Aram Kim; Michele Poe; Maria L Escolar
Journal:  Pediatr Neurol       Date:  2019-12-02       Impact factor: 3.372

Review 7.  Vertex cephaloceles: a review.

Authors:  Zeng Gao; Luca Massimi; Simone Rogerio; Charles Raybaud; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2013-08-29       Impact factor: 1.475

8.  Correction of a vertex encephalocele related to amniotic band syndrome.

Authors:  Aaron M Yengo-Kahn; Andreas C Plackis; Christopher M Bonfield; Srijaya K Reddy
Journal:  BMJ Case Rep       Date:  2020-03-31

9.  Giant occipital meningocele in an 8-year-old child with Dandy-Walker malformation.

Authors:  Giuseppe Talamonti; Marco Picano; Alberto Debernardi; Moreno Bolzon; Mario Teruzzi; Giuseppe D'Aliberti
Journal:  Childs Nerv Syst       Date:  2010-05-19       Impact factor: 1.475

10.  Antenatal Diagnosis of a Rare Neural Tube Defect: Sincipital Encephalocele.

Authors:  Mehdi Kehila; Sana Ghades; Hassine Saber Abouda; Aida Masmoudi; Mohamed Badis Chanoufi
Journal:  Case Rep Obstet Gynecol       Date:  2015-07-29
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