Cerebrospinal fluid velocity amplitudes within the cerebral aqueduct in healthy children and patients with Chiari I malformation

• Published in: Journal of magnetic resonance imaging Vol. 44; no. 2; pp. 463 - 470
• Main Authors: Bapuraj, J. Rajiv, Londy, Frank J., Delavari, Nader, Maher, Cormac O., Garton, Hugh J.L., Martin, Bryn A., Muraszko, Karin M., Ibrahim, El-Sayed H., Quint, Douglas J.
• Format: Journal Article
• Language: English
• Published: United States Blackwell Publishing Ltd 01.08.2016; Wiley Subscription Services, Inc
• Subjects: Amplitudes; Arnold-Chiari Malformation - cerebrospinal fluid; Arnold-Chiari Malformation - diagnostic imaging; Arnold-Chiari Malformation - surgery; Brain; cerebral aqueduct; Cerebral Aqueduct - diagnostic imaging; Cerebral Aqueduct - pathology; Cerebrospinal fluid; Cerebrospinal Fluid - cytology; Cerebrospinal Fluid - diagnostic imaging; Chiari malformation; Children; Compartments; Congenital defects; Decompression, Surgical; Female; Humans; Image Interpretation, Computer-Assisted - methods; Magnetic resonance imaging; Magnetic Resonance Imaging - methods; Male; MRI phase contrast imaging; Neural tube defects; Patients; Pediatrics; Phase contrast; Reproducibility of Results; Rheology - methods; Sensitivity and Specificity; Skull; Subarachnoid space; Surgery; Treatment Outcome; Velocity; cerebral aqueduct; MRI phase contrast imaging; Chiari malformation; cerebrospinal fluid
• DOI: 10.1002/jmri.25160
• ISSN: 1053-1807

Purpose To assess the effects of cerebrospinal fluid (CSF) bidirectional motion in Chiari malformation type I (CMI), we monitored CSF velocity amplitudes on phase contrast MRI (PC‐MRI) in patients before and after surgery; and in healthy volunteers. Materials and Methods 10 pediatric volunteers and 10 CMI patients participated in this study. CMI patients underwent PC‐MRI scans before and approximately 14 months following surgery. Two parameters—amplitude of mean velocity (AMV) and amplitude of peak velocity (APV) of CSF—were derived from the data. Measurements were made at the mid‐portion of the cerebral aqueduct, and anterior and posterior compartments of the spinal canal at the craniovertebral junction (CVJ). Results AMV and APV within the cerebral aqueduct were greater in preoperative assessments of the CMI patients compared to normal volunteers. Statistical significance was noted when comparing aqueductal AMV between the preoperative values and normal controls (P = 0.03), and before and after surgery in the CMI patients (P = 0.02). Lower values of AMV (P = 0.02) were noted in the anterior CVJ compartment in the patients before and after surgery when compared to the normal volunteers. There were no significant correlations (P = 0.06) noted for the APV at the CVJ between the normal control and patients, before or after surgery. Conclusion In pediatric CMI patients, AMV for CSF within the cerebral aqueduct and anterior CVJ subarachnoid space are significantly elevated preoperatively and normalize following surgery. Given the biphasic CSF motion, measuring amplitude accounts for cranial and caudal flow. It may offer an alternative parameter to assess postsurgical outcome. J. Magn. Reson. Imaging 2016;44:463–470.