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Posterior only instrumented fusion provides incomplete curve control for early-onset scoliosis in type 1 neurofibromatosis.

Authors :
Cai, Siyi
Li, Zhengyao
Qiu, Guixing
Shen, Jianxiong
Zhao, Hong
Zhao, Yu
Wang, Yipeng
Zhang, Jianguo
Source :
BMC Pediatrics; 2/10/2020, Vol. 20 Issue 1, p1-9, 9p, 1 Color Photograph, 1 Black and White Photograph, 3 Charts
Publication Year :
2020

Abstract

<bold>Background: </bold>The mid-long term outcomes of posterior spinal fusion in pediatric neurofibromatosis type 1 (NF-1) patients are rarely reported, so does the effectiveness of itsorthopeidc maintenance function. This study aims to evaluate the mid-long term surgical outcomes of posterior only instrumented spinal fusion for early-onset scoliosis (EOS) in NF-1 patients.<bold>Methods: </bold>A retrospective review was performed on a cohort of 10 NF-1 patients having EOS from 2008 to 2014 in our hospital, the age averaged at 7.8 years old when they underwent posterior only instrumented spinal fusion for their EOS. Both general clinical data and surgical specific data of the patients were collected and reviewed, and the dystrophic progression of EOS was evaluated during the follow-up.<bold>Results: </bold>The average duration of follow-up was 54 months (24 to 88 months). All patients underwent posterior only instrumented spinal fusion at 1 stage. The primary curves of EOS were thoracic in 9 cases and 1 patient had lumbar scoliosis. Preoperative major curve was significantly corrected (from 66.1 to 31.1 degrees). However, the major curve deteriorated significantly to 40.1 degrees on average at the end of the follow-up. The T1-S1 distance increased 2.8 cm on average and kept increasing at a rate of 0.6 cm/year during the follow-up.<bold>Conclusions: </bold>Posterior only fusion surgery was not a good option to treat the EOS in NF-1 patients despite the relatively short segments involvement in the disease. The maintenance of orthopedic effect after treatment was not satisfactory. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712431
Volume :
20
Issue :
1
Database :
Complementary Index
Journal :
BMC Pediatrics
Publication Type :
Academic Journal
Accession number :
141662276
Full Text :
https://doi.org/10.1186/s12887-020-1956-y