Radiological and clinical associations with scoliosis outcomes after posterior fossa decompression in patients with Chiari malformation and syrinx from the Park-Reeves Syringomyelia Research Consortium.

Chiari malformation posterior fossa decompression scoliosis spine syrinx

Journal

Journal of neurosurgery. Pediatrics
ISSN: 1933-0715
Titre abrégé: J Neurosurg Pediatr
Pays: United States
ID NLM: 101463759

Informations de publication

Date de publication:
10 Apr 2020
Historique:
received: 30 06 2019
accepted: 07 01 2020
pubmed: 11 4 2020
medline: 11 4 2020
entrez: 11 4 2020
Statut: epublish

Résumé

In patients with Chiari malformation type I (CM-I) and a syrinx who also have scoliosis, clinical and radiological predictors of curve regression after posterior fossa decompression are not well known. Prior reports indicate that age younger than 10 years and a curve magnitude < 35° are favorable predictors of curve regression following surgery. The aim of this study was to determine baseline radiological factors, including craniocervical junction alignment, that might predict curve stability or improvement after posterior fossa decompression. A large multicenter retrospective and prospective registry of pediatric patients with CM-I (tonsils ≥ 5 mm below the foramen magnum) and a syrinx (≥ 3 mm in width) was reviewed for clinical and radiological characteristics of CM-I, syrinx, and scoliosis (coronal curve ≥ 10°) in patients who underwent posterior fossa decompression and who also had follow-up imaging. Of 825 patients with CM-I and a syrinx, 251 (30.4%) were noted to have scoliosis present at the time of diagnosis. Forty-one (16.3%) of these patients underwent posterior fossa decompression and had follow-up imaging to assess for scoliosis. Twenty-three patients (56%) were female, the mean age at time of CM-I decompression was 10.0 years, and the mean follow-up duration was 1.3 years. Nine patients (22%) had stable curves, 16 (39%) showed improvement (> 5°), and 16 (39%) displayed curve progression (> 5°) during the follow-up period. Younger age at the time of decompression was associated with improvement in curve magnitude; for those with curves of ≤ 35°, 17% of patients younger than 10 years of age had curve progression compared with 64% of those 10 years of age or older (p = 0.008). There was no difference by age for those with curves > 35°. Tonsil position, baseline syrinx dimensions, and change in syrinx size were not associated with the change in curve magnitude. There was no difference in progression after surgery in patients who were also treated with a brace compared to those who were not treated with a brace for scoliosis. In this cohort of patients with CM-I, a syrinx, and scoliosis, younger age at the time of decompression was associated with improvement in curve magnitude following surgery, especially in patients younger than 10 years of age with curves of ≤ 35°. Baseline tonsil position, syrinx dimensions, frontooccipital horn ratio, and craniocervical junction morphology were not associated with changes in curve magnitude after surgery.

Identifiants

pubmed: 32276246
doi: 10.3171/2020.1.PEDS18755
pii: 2020.1.PEDS18755
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

53-59

Auteurs

Jennifer M Strahle (JM)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Rukayat Taiwo (R)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Christine Averill (C)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

James Torner (J)

2Department of Epidemiology, University of Iowa, Iowa City, Iowa.

Jordan I Gewirtz (JI)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Chevis N Shannon (CN)

3Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.

Christopher M Bonfield (CM)

3Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.

Gerald F Tuite (GF)

4Department of Neurosurgery, Neuroscience Institute, Johns Hopkins All Children's Hospital, St. Petersburg, Florida.

Tammy Bethel-Anderson (T)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Richard C E Anderson (RCE)

6Department of Neurological Surgery, Columbia University College of Physicians and Surgeons, New York, New York; and.

Michael P Kelly (MP)

7Department of Orthopedic Surgery, Washington University School of Medicine, St. Louis, Missouri.

Joshua S Shimony (JS)

5Department of Radiology, Washington University School of Medicine, St. Louis, Missouri.

Ralph G Dacey (RG)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Matthew D Smyth (MD)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Tae Sung Park (TS)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

David D Limbrick (DD)

1Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri.

Classifications MeSH