Treatment failure of syringomyelia associated with Chiari I malformation following foramen magnum decompression: how should we proceed?
Adolescent
Adult
Arnold-Chiari Malformation
/ complications
Child
Child, Preschool
Decompression, Surgical
/ adverse effects
Female
Foramen Magnum
/ surgery
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Neurosurgical Procedures
Radiography
Recurrence
Retrospective Studies
Syringomyelia
/ diagnostic imaging
Treatment Failure
Young Adult
Chiari I malformation
Foramen magnum decompression
Hydrocephalus
Spinal cord
Syringo-subarachnoid shunt
Syringomyelia
Journal
Neurosurgical review
ISSN: 1437-2320
Titre abrégé: Neurosurg Rev
Pays: Germany
ID NLM: 7908181
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
received:
01
08
2018
accepted:
04
12
2018
revised:
21
10
2018
pubmed:
17
12
2018
medline:
18
12
2019
entrez:
17
12
2018
Statut:
ppublish
Résumé
The preferred treatment of patients with persistent, recurrent, or progressive syringomyelia after foramen magnum decompression (FMD) for Chiari I (CMI)-associated syringomyelia is controversial, and may include redo FMD, stabilization, or shunting procedures (such as syringopleural or syringo-subarachnoid shunts). We describe our experience in treating these patients and discuss the treatment modalities for these patients. We retrospectively collected data of CMI patients with persistent, recurrent, or progressive syringomyelia after FMD. In addition to baseline characteristics, surgical treatments and neurological and radiological outcomes were assessed. Further, we assessed through uni- and multivariate analyses possible technical, surgical, and radiological factors which might lead to failed FMD. Between 1998 and 2017, 48 consecutive patients (35 females (73%), average age 16.8 ± 11.5 years) underwent FMD for a syringomyelia-Chiari complex. Twenty-four patients (50%) underwent surgical treatment for a persistent (n = 10), progressive (n = 12), or recurrent (n = 2) syringomyelia 21.4 ± 27.9 months (median 14.6 months, range 12 days-134.9 months) after FMD. Of all analyzed factors, only extradural FMD was significantly associated with lower failure rates. Two patients (8%) underwent redo FMD, 18 (75%) underwent 19 syringo-subarachnoid-shunts, and 4 (17%) had 6 cranial CSF diversion procedures. The overall follow-up time was 40.1 ± 47.4 months (median 25 months, range 3-230 months). Based on our results, 50% of the patients undergoing FMD for syringomyelia-Chiari complex may require further surgical treatment due to persistent, progressive, or recurrent syringomyelia. Treatment should be tailored to the suspected underlying pathology. A subgroup of patients may be managed conservatively; however, these patients need close clinical and radiological follow-ups. The technical aspects of FMD in CMI-syrinx complex should be the focus of larger studies, as an effort to improve failure rates.
Identifiants
pubmed: 30554294
doi: 10.1007/s10143-018-01066-0
pii: 10.1007/s10143-018-01066-0
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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