Foramen magnum cerebrospinal fluid flow characteristics in children with Chiari I malformation before and after craniocervical decompression
- PMID: 15835104
- DOI: 10.3171/ped.2004.101.2.0169
Foramen magnum cerebrospinal fluid flow characteristics in children with Chiari I malformation before and after craniocervical decompression
Abstract
Object: The Chiari I malformation presents significant challenges to clinicians because its pathophysiology is not well understood. In conducting cerebrospinal fluid (CSF) flow studies, investigators have attempted to correlate the clinical severity of these lesions with general flow velocity or bulk flow at the foramen magnum; however, these techniques have not allowed consistent prediction of symptomatology, explanation of the presence of syringomyelia, or the assessment of the hydrodynamic characteristics of the decompression. The authors used temporally and spatially resolved flow analyses to assess the characteristics of CSF flow in children with Chiari I malformation and the changes in these flow characteristics that occur after suboccipital decompression.
Methods: The authors studied eight children with symptomatic Chiari I malformation with or without syringomyelia and two children without Chiari I malformation. All patients underwent phase-contrast magnetic resonance imaging before and after posterior fossa decompression. Velocity plots were displayed for each voxel. Several indices of CSF flow were developed to characterize the flow patterns associated with Chiari I malformation. In children with symptomatic Chiari I malformation, even though bulk flow or velocity is often normal, there was marked heterogeneity of flow at the foramen magnum. This was evident for several reasons: 1) an increase in cephalad and caudad peak velocities; 2) spatial inhomogeneity in velocities; 3) simultaneous bidirectional flow; and 4) substantial net craniad or caudad flows within particular voxels and subregions during the cardiac cycle. After posterior fossa decompression, the severity of these flow abnormalities decreased.
Conclusions: Foramen magnum CSF flow in children with symptomatic Chiari I malformations is spatially and temporally heterogeneous, and this heterogeneity improves postoperatively. The authors propose that relying on mean flow parameters in patients with Chiari I malformation is no longer sufficient; instead, more elaborate techniques to analyze foramen magnum CSF flow have become necessary.
Similar articles
-
Relationship of cine phase-contrast magnetic resonance imaging with outcome after decompression for Chiari I malformations.Neurosurgery. 2006 Jul;59(1):140-6; discussion 140-6. doi: 10.1227/01.NEU.0000219841.73999.B3. Neurosurgery. 2006. PMID: 16823310
-
A detailed morphologic and functional magnetic resonance imaging study of the craniocervical junction in adolescent idiopathic scoliosis.Spine (Phila Pa 1976). 2007 Jul 1;32(15):1667-74. doi: 10.1097/BRS.0b013e318074d539. Spine (Phila Pa 1976). 2007. PMID: 17621216
-
Chiari malformation: CSF flow dynamics in the craniocervical junction and syrinx.Acta Neurochir (Wien). 2005 Dec;147(12):1223-33. doi: 10.1007/s00701-005-0645-9. Epub 2005 Oct 17. Acta Neurochir (Wien). 2005. PMID: 16228125
-
The pathogenesis of syringomyelia associated with lesions at the foramen magnum: a critical review of existing theories and proposal of a new hypothesis.J Neurol Sci. 2004 May 15;220(1-2):3-21. doi: 10.1016/j.jns.2004.01.014. J Neurol Sci. 2004. PMID: 15140600 Review.
-
Cranio-cervical decompression for Chiari type I-malformation, adding extreme lateral foramen magnum opening and expansile duroplasty with arachnoid preservation. Technique and long-term functional results in 44 consecutive adult cases -- comparison with literature data.Acta Neurochir (Wien). 2002 Oct;144(10):1005-19. doi: 10.1007/s00701-002-1004-8. Acta Neurochir (Wien). 2002. PMID: 12382129 Review.
Cited by
-
Chiari I malformation: management evolution and technical innovation.Childs Nerv Syst. 2023 Oct;39(10):2757-2769. doi: 10.1007/s00381-023-06051-7. Epub 2023 Jun 27. Childs Nerv Syst. 2023. PMID: 37368069
-
Potential association among posterior fossa bony volume and crowdedness, tonsillar hernia, syringomyelia, and CSF dynamics at the craniocervical junction in Chiari malformation type I.Front Neurol. 2023 Feb 20;14:1069861. doi: 10.3389/fneur.2023.1069861. eCollection 2023. Front Neurol. 2023. PMID: 36891476 Free PMC article.
-
Posterior fossa decompression for children with Chiari I malformation and hydrocephalus.Childs Nerv Syst. 2022 Jan;38(1):153-161. doi: 10.1007/s00381-021-05377-4. Epub 2021 Oct 20. Childs Nerv Syst. 2022. PMID: 34671850
-
Assessment of Cerebrospinal Fluid Hydrodynamics Using Magnetic Resonance Imaging in Postcraniospinal Surgery Patients.Indian J Radiol Imaging. 2021 Apr;31(2):304-310. doi: 10.1055/s-0041-1734362. Epub 2021 Jul 27. Indian J Radiol Imaging. 2021. PMID: 34556912 Free PMC article.
-
Functional and morphological changes in hypoplasic posterior fossa.Childs Nerv Syst. 2021 Oct;37(10):3093-3104. doi: 10.1007/s00381-021-05193-w. Epub 2021 Jun 25. Childs Nerv Syst. 2021. PMID: 34169386 Free PMC article. Review.
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
