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Long-Term Imaging Follow-up from the Management of Myelomeningocele Study.
George, E; MacPherson, C; Pruthi, S; Bilaniuk, L; Fletcher, J; Houtrow, A; Gupta, N; Glenn, O A.
Affiliation
  • George E; From the Departments of Radiology and Biomedical Imaging (E.G., O.A.G.).
  • MacPherson C; Biostatistics Center (C.M.), Milken Institute School of Public Health, The George Washington University, Washington, DC.
  • Pruthi S; Department of Radiology (S.P.), Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee.
  • Bilaniuk L; Department of Radiology (L.B.), Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Fletcher J; Department of Psychology (J.F.), University of Houston, Houston, Texas.
  • Houtrow A; Department of Physical Medicine and Rehabilitation (A.H.), University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Gupta N; Neurological Surgery (N.G.).
  • Glenn OA; Pediatrics (N.G.), University of California, San Francisco, San Francisco, California.
AJNR Am J Neuroradiol ; 44(7): 861-866, 2023 07.
Article de En | MEDLINE | ID: mdl-37385677
ABSTRACT
BACKGROUND AND

PURPOSE:

Short-term results demonstrate that prenatal repair of a myelomeningocele is associated with a reduction in hydrocephalus and an increased likelihood of the reversal of Chiari II malformations compared with postnatal repair. The purpose of this study was to identify the long-term imaging findings at school age among subjects who underwent pre- versus postnatal repair of a myelomeningocele. MATERIALS AND

METHODS:

A subset of subjects enrolled in the Management of Myelomeningocele Study who underwent either prenatal (n = 66) or postnatal (n = 63) repair of a lumbosacral myelomeningocele and had follow-up brain MR imaging at school age were included. The prevalence of posterior fossa features of Chiari II malformation and supratentorial abnormalities and the change in these findings from fetal to school-age MR imaging were compared between the 2 groups.

RESULTS:

Prenatal repair of a myelomeningocele was associated with higher rates of normal location of fourth ventricle and lower rates of hindbrain herniation, cerebellar herniation, tectal beaking, brainstem distortion, and kinking at school age compared with postnatal repair (all P < .01). Supratentorial abnormalities, including corpus callosal abnormalities, gyral abnormalities, heterotopia, and hemorrhage, were not significantly different between the 2 groups (all P > .05). The rates of resolution of brainstem kinking, tectal beaking, cerebellar and hindbrain herniation, and normalization of fourth ventricle size from fetal to school age MR imaging were higher among the prenatal compared with postnatal surgery group (all, P < .02).

CONCLUSIONS:

Prenatal repair of a myelomeningocele is associated with persistent improvement in posterior fossa imaging findings of Chiari II malformation at school age compared with postnatal repair.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Malformation d&apos;Arnold-Chiari / Myéloméningocèle / Hydrocéphalie Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Female / Humans / Pregnancy Langue: En Journal: AJNR Am J Neuroradiol Année: 2023 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Malformation d&apos;Arnold-Chiari / Myéloméningocèle / Hydrocéphalie Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Female / Humans / Pregnancy Langue: En Journal: AJNR Am J Neuroradiol Année: 2023 Type de document: Article
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