Literature DB >> 26850429

Thoracolumbar kyphosis in patients with mucopolysaccharidoses: clinical outcomes and predictive radiographic factors for progression of deformity.

S B Roberts1, R Dryden1, A I Tsirikos2.   

Abstract

AIMS: Clinical and radiological data were reviewed for all patients with mucopolysaccharidoses (MPS) with thoracolumbar kyphosis managed non-operatively or operatively in our institution.
METHODS: In all 16 patients were included (eight female: eight male; 50% male), of whom nine had Hurler, five Morquio and two Hunter syndrome. Six patients were treated non-operatively (mean age at presentation of 6.3 years; 0.4 to 12.9); mean kyphotic progression +1.5(o)/year; mean follow-up of 3.1 years (1 to 5.1) and ten patients operatively (mean age at presentation of 4.7 years; 0.9 to 14.4); mean kyphotic progression 10.8(o)/year; mean follow-up of 8.2 years; 4.8 to 11.8) by circumferential arthrodesis with posterior instrumentation in patients with flexible deformities (n = 6).
RESULTS: In the surgical group (mean age at surgery of 6.6 years; 2.4 to 16.8); mean post-operative follow-up of 6.3 years (3.5 to 10.3), mean pre-operative thoracolumbar kyphosis of 74.3(o) (42(o) to 110(o)) was corrected to mean of 28.6(o) (0(o) to 65(o)) post-operatively, relating to a mean deformity correction of 66.9% (31% to 100%). Surgical complications included a deep wound infection treated by early debridement, apical non-union treated by posterior re-grafting, and stable adjacent segment spondylolisthesis managed non-operatively. Thoracolumbar kyphosis > +38(o) at initial presentation was identified as predicting progressively severe deformity with 90% sensitivity and 83% specificity. DISCUSSION: This study demonstrates that severe thoracolumbar kyphosis in patients with MPS can be effectively treated by circumferential arthrodesis. Severity of kyphosis at initial presentation may predict progression of thoracolumbar deformity. Patients with MPS may be particularly susceptible to post-operative complications due to the underlying connective tissue disorder and inherent immunological compromise. TAKE HOME MESSAGE: Clinical and radiological data were reviewed for all patients with mucopolysaccharidoses with thoracolumbar kyphosis managed non-operatively or operatively in our institution. ©2016 The British Editorial Society of Bone & Joint Surgery.

Entities:  

Keywords:  instrumentation; kyphosis; mucopolysaccharidosis; spinal fusion; thoracolumbar; treatment

Mesh:

Year:  2016        PMID: 26850429     DOI: 10.1302/0301-620X.98B2.36144

Source DB:  PubMed          Journal:  Bone Joint J        ISSN: 2049-4394            Impact factor:   5.082


  7 in total

1.  Incidence of spinal deformity surgery in a national health service from 2005 to 2018: an analysis of 2,205 children and adolescents.

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Review 3.  Pathogenesis and treatment of spine disease in the mucopolysaccharidoses.

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Journal:  Mol Genet Metab       Date:  2016-06-04       Impact factor: 4.797

4.  Dwarf with dual spinal kyphotic deformity at the cervical and dorsal spine unassociated with odontoid hypoplasia: Surgical management.

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Review 5.  Treatment of thoracolumbar kyphosis in patients with mucopolysaccharidosis type I: results of an international consensus procedure.

Authors:  Gé-Ann Kuiper; Eveline J Langereis; Sandra Breyer; Marco Carbone; René M Castelein; Deborah M Eastwood; Christophe Garin; Nathalie Guffon; Peter M van Hasselt; Pauline Hensman; Simon A Jones; Vladimir Kenis; Moyo Kruyt; Johanna H van der Lee; William G Mackenzie; Paul J Orchard; Neil Oxborrow; Rossella Parini; Amy Robinson; Elke Schubert Hjalmarsson; Klane K White; Frits A Wijburg
Journal:  Orphanet J Rare Dis       Date:  2019-01-18       Impact factor: 4.123

Review 6.  Surgical Management of Spinal Disorders in People with Mucopolysaccharidoses.

Authors:  Hidetomi Terai; Hiroaki Nakamura
Journal:  Int J Mol Sci       Date:  2020-02-10       Impact factor: 5.923

7.  Does orthopaedic surgery improve quality of life and function in patients with mucopolysaccharidoses?

Authors:  N Williams; D Challoumas; D M Eastwood
Journal:  J Child Orthop       Date:  2017-08-01       Impact factor: 1.548

  7 in total

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