TY - JOUR
T1 - Outcomes in children undergoing posterior fossa decompression and duraplasty with and without tonsillar reduction for Chiari malformation type i and syringomyelia
T2 - A pilot prospective multicenter cohort study
AU - Koueik, Joyce
AU - Sandoval-Garcia, Carolina
AU - Kestle, John R.W.
AU - Rocque, Brandon G.
AU - Frim, David M.
AU - Grant, Gerald A.
AU - Keating, Robert F.
AU - Muh, Carrie R.
AU - Jerry Oakes, W.
AU - Pollack, Ian F.
AU - Selden, Nathan R.
AU - Tubbs, R. Shane
AU - Tuite, Gerald F.
AU - Warf, Benjamin
AU - Rajamanickam, Victoria
AU - Broman, Aimee Teo
AU - Haughton, Victor
AU - Rebsamen, Susan
AU - George, Timothy M.
AU - Iskandar, Bermans J.
N1 - Publisher Copyright:
©AANS 2020.
PY - 2020
Y1 - 2020
N2 - OBJECTIVE Despite significant advances in diagnostic and surgical techniques, the surgical management of Chiari malformation type I (CM-I) with associated syringomyelia remains controversial, and the type of surgery performed is surgeon dependent. This study's goal was to determine the feasibility of a prospective, multicenter, cohort study for CM-I/syringomyelia patients and to provide pilot data that compare posterior fossa decompression and duraplasty (PFDD) with and without tonsillar reduction. METHODS Participating centers prospectively enrolled children suffering from both CM-I and syringomyelia who were scheduled to undergo surgical decompression. Clinical data were entered into a database preoperatively and at 1-2 weeks, 3-6 months, and 1 year postoperatively. MR images were evaluated by 3 independent, blinded teams of neurosurgeons and neuroradiologists. The primary endpoint was improvement or resolution of the syrinx. RESULTS Eight clinical sites were chosen based on the results of a published questionnaire intended to remove geographic and surgeon bias. Data from 68 patients were analyzed after exclusions, and complete clinical and imaging records were obtained for 55 and 58 individuals, respectively. There was strong agreement among the 3 radiology teams, and there was no difference in patient demographics among sites, surgeons, or surgery types. Tonsillar reduction was not associated with > 50% syrinx improvement (RR = 1.22, p = 0.39) or any syrinx improvement (RR = 1.00, p = 0.99). There were no surgical complications. CONCLUSIONS This study demonstrated the feasibility of a prospective, multicenter surgical trial in CM-I/syringomyelia and provides pilot data indicating no discernible difference in 1-year outcomes between PFDD with and without tonsillar reduction, with power calculations for larger future studies. In addition, the study revealed important technical factors to consider when setting up future trials. The long-Term sequelae of tonsillar reduction have not been addressed and would be an important consideration in future investigations.
AB - OBJECTIVE Despite significant advances in diagnostic and surgical techniques, the surgical management of Chiari malformation type I (CM-I) with associated syringomyelia remains controversial, and the type of surgery performed is surgeon dependent. This study's goal was to determine the feasibility of a prospective, multicenter, cohort study for CM-I/syringomyelia patients and to provide pilot data that compare posterior fossa decompression and duraplasty (PFDD) with and without tonsillar reduction. METHODS Participating centers prospectively enrolled children suffering from both CM-I and syringomyelia who were scheduled to undergo surgical decompression. Clinical data were entered into a database preoperatively and at 1-2 weeks, 3-6 months, and 1 year postoperatively. MR images were evaluated by 3 independent, blinded teams of neurosurgeons and neuroradiologists. The primary endpoint was improvement or resolution of the syrinx. RESULTS Eight clinical sites were chosen based on the results of a published questionnaire intended to remove geographic and surgeon bias. Data from 68 patients were analyzed after exclusions, and complete clinical and imaging records were obtained for 55 and 58 individuals, respectively. There was strong agreement among the 3 radiology teams, and there was no difference in patient demographics among sites, surgeons, or surgery types. Tonsillar reduction was not associated with > 50% syrinx improvement (RR = 1.22, p = 0.39) or any syrinx improvement (RR = 1.00, p = 0.99). There were no surgical complications. CONCLUSIONS This study demonstrated the feasibility of a prospective, multicenter surgical trial in CM-I/syringomyelia and provides pilot data indicating no discernible difference in 1-year outcomes between PFDD with and without tonsillar reduction, with power calculations for larger future studies. In addition, the study revealed important technical factors to consider when setting up future trials. The long-Term sequelae of tonsillar reduction have not been addressed and would be an important consideration in future investigations.
KW - Chiari malformation decompression
KW - Surgical outcomes
KW - Syrinx improvement
KW - Tonsillar resection
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UR - http://www.scopus.com/inward/citedby.url?scp=85077620914&partnerID=8YFLogxK
U2 - 10.3171/2019.8.PEDS19154
DO - 10.3171/2019.8.PEDS19154
M3 - Article
C2 - 31628281
AN - SCOPUS:85077620914
SN - 1933-0707
VL - 25
SP - 21
EP - 29
JO - Journal of neurosurgery. Pediatrics
JF - Journal of neurosurgery. Pediatrics
IS - 1
ER -