Literature DB >> 32114543

Factors associated with syrinx size in pediatric patients treated for Chiari malformation type I and syringomyelia: a study from the Park-Reeves Syringomyelia Research Consortium.

Andrew T Hale1,2, P David Adelson3, Gregory W Albert4, Philipp R Aldana5, Tord D Alden6, Richard C E Anderson7, David F Bauer8, Christopher M Bonfield2,9, Douglas L Brockmeyer10, Joshua J Chern11, Daniel E Couture12, David J Daniels13, Susan R Durham14, Richard G Ellenbogen15, Ramin Eskandari16, Timothy M George17, Gerald A Grant18, Patrick C Graupman19, Stephanie Greene20, Jeffrey P Greenfield21, Naina L Gross22, Daniel J Guillaume23, Gregory G Heuer24, Mark Iantosca25, Bermans J Iskandar26, Eric M Jackson27, James M Johnston28, Robert F Keating29, Jeffrey R Leonard30, Cormac O Maher31, Francesco T Mangano32, J Gordon McComb33, Thanda Meehan34, Arnold H Menezes35, Brent O'Neill36, Greg Olavarria37, Tae Sung Park34, John Ragheb38, Nathan R Selden39, Manish N Shah40, Matthew D Smyth34, Scellig S D Stone41, Jennifer M Strahle34, Scott D Wait42, John C Wellons2,9, William E Whitehead43, Chevis N Shannon2,9, David D Limbrick34.   

Abstract

OBJECTIVE: Factors associated with syrinx size in pediatric patients undergoing posterior fossa decompression (PFD) or PFD with duraplasty (PFDD) for Chiari malformation type I (CM-I) with syringomyelia (SM; CM-I+SM) are not well established.
METHODS: Using the Park-Reeves Syringomyelia Research Consortium registry, the authors analyzed variables associated with syrinx radiological outcomes in patients (< 20 years old at the time of surgery) with CM-I+SM undergoing PFD or PFDD. Syrinx resolution was defined as an anteroposterior (AP) diameter of ≤ 2 mm or ≤ 3 mm or a reduction in AP diameter of ≥ 50%. Syrinx regression or progression was defined using 1) change in syrinx AP diameter (≥ 1 mm), or 2) change in syrinx length (craniocaudal, ≥ 1 vertebral level). Syrinx stability was defined as a < 1-mm change in syrinx AP diameter and no change in syrinx length.
RESULTS: The authors identified 380 patients with CM-I+SM who underwent PFD or PFDD. Cox proportional hazards modeling revealed younger age at surgery and PFDD as being independently associated with syrinx resolution, defined as a ≤ 2-mm or ≤ 3-mm AP diameter or ≥ 50% reduction in AP diameter. Radiological syrinx resolution was associated with improvement in headache (p < 0.005) and neck pain (p < 0.011) after PFD or PFDD. Next, PFDD (p = 0.005), scoliosis (p = 0.007), and syrinx location across multiple spinal segments (p = 0.001) were associated with syrinx diameter regression, whereas increased preoperative frontal-occipital horn ratio (FOHR; p = 0.007) and syrinx location spanning multiple spinal segments (p = 0.04) were associated with syrinx length regression. Scoliosis (HR 0.38 [95% CI 0.16-0.91], p = 0.03) and smaller syrinx diameter (5.82 ± 3.38 vs 7.86 ± 3.05 mm; HR 0.60 [95% CI 0.34-1.03], p = 0.002) were associated with syrinx diameter stability, whereas shorter preoperative syrinx length (5.75 ± 4.01 vs 9.65 ± 4.31 levels; HR 0.21 [95% CI 0.12-0.38], p = 0.0001) and smaller pB-C2 distance (6.86 ± 1.27 vs 7.18 ± 1.38 mm; HR 1.44 [95% CI 1.02-2.05], p = 0.04) were associated with syrinx length stability. Finally, younger age at surgery (8.19 ± 5.02 vs 10.29 ± 4.25 years; HR 1.89 [95% CI 1.31-3.04], p = 0.01) was associated with syrinx diameter progression, whereas increased postoperative syrinx diameter (6.73 ± 3.64 vs 3.97 ± 3.07 mm; HR 3.10 [95% CI 1.67-5.76], p = 0.003), was associated with syrinx length progression. PFD versus PFDD was not associated with syrinx progression or reoperation rate.
CONCLUSIONS: These data suggest that PFDD and age are independently associated with radiological syrinx improvement, although forthcoming results from the PFDD versus PFD randomized controlled trial (NCT02669836, clinicaltrials.gov) will best answer this question.

Entities:  

Keywords:  AP = anteroposterior; CM-I = Chiari malformation type I; CM-I+SM = CM-I with SM; CPH = Cox proportional hazards; CXA = clivus canal angle; Chiari malformation type I; FOHR = frontal-occipital horn ratio; PFD = posterior fossa decompression; PFDD = PFD with duraplasty; PRSRC = Park-Reeves Syringomyelia Research Consortium; Park-Reeves Syringomyelia Research Consortium; SM = syringomyelia; pB-C2 distance = distance from the ventral dura perpendicular to the line between the basion and C2; syrinx

Year:  2020        PMID: 32114543     DOI: 10.3171/2020.1.PEDS19493

Source DB:  PubMed          Journal:  J Neurosurg Pediatr        ISSN: 1933-0707            Impact factor:   2.375


  3 in total

Review 1.  Chiari Malformation (Update on Diagnosis and Treatment).

Authors:  Jared S Rosenblum; I Jonathan Pomeraniec; John D Heiss
Journal:  Neurol Clin       Date:  2022-03-31       Impact factor: 3.787

2.  Specific microstructural changes of the cervical spinal cord in syringomyelia estimated by diffusion tensor imaging.

Authors:  Weifei Wu; Xiangxiang Li; Zong Yang; Neng Ru; Fan Zhang; Jie Liang; Ke Zhang
Journal:  Sci Rep       Date:  2021-03-04       Impact factor: 4.379

3.  Expansile duraplasty and obex exploration compared with bone-only decompression for Chiari malformation type I in children: retrospective review of outcomes and complications.

Authors:  Chibawanye I Ene; Anthony C Wang; Kelly L Collins; Robert H Bonow; Lynn B McGrath; Sharon J Durfy; Jason K Barber; Richard G Ellenbogen
Journal:  J Neurosurg Pediatr       Date:  2020-10-30       Impact factor: 2.375

  3 in total

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