Literature DB >> 16284567

Incidence and characteristics of spinal decompression surgery after the onset of symptoms of amyotrophic lateral sclerosis.

Daniel Yoshor1, Arnett Klugh, Stanley H Appel, Lanny J Haverkamp.   

Abstract

OBJECTIVE: The high incidence of spondylosis in patients at the mean age of onset (55.7 yr) of amyotrophic lateral sclerosis (ALS) can make recognition of ALS as a cause of weakness difficult.
METHODS: To assess the impact of this diagnostic dilemma on neurosurgical practice, we performed a retrospective analysis of a database of more than 1500 patients with motor neuron disease.
RESULTS: Of 1131 patients with typical, sporadic ALS, 47 (4.2%) underwent decompressive spinal surgery after the onset of retrospectively recognized symptoms of ALS. Among 55 operations in 47 ALS patients, 86% yielded no improvement, 9% produced minor improvement, and only 5% provided significant benefit. Cervical decompression was performed in 56%, lumbar in 42%, and thoracic in 2%. Foot drop was a symptom prompting surgery in 11 patients, and in 10, this finding was subsequently attributed solely to ALS. No differences between ALS patients who underwent spinal decompression and other ALS patients were noted regarding age at symptom onset, severity of impairment at time of diagnosis, or rate of disease progression. Not surprisingly, patients who had spinal surgery tended to have a longer interval between retrospectively recognized symptom onset and diagnosis of ALS.
CONCLUSION: A small but significant number of patients with unrecognized ALS undergo spinal surgery that in retrospect may be inappropriate. The possibility of ALS must be considered in the evaluation of patients with weakness even in the presence of radiographic evidence of spondylosis and nerve root or spinal cord impingement.

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Year:  2005        PMID: 16284567     DOI: 10.1227/01.neu.0000180028.64385.d3

Source DB:  PubMed          Journal:  Neurosurgery        ISSN: 0148-396X            Impact factor:   4.654


  7 in total

1.  Radiculopathy at the C5/6 intervertebral foramen resulting in isolated atrophy of the deltoid: an aberrant innervation complicating diagnosis. Report of two cases.

Authors:  Satoru Shimizu; Shigekuni Tachibana; Takao Sagiuchi; Mari Kurita; Kiyotaka Fujii
Journal:  Eur Spine J       Date:  2008-04-19       Impact factor: 3.134

2.  Clinical Course of Amyotrophic Lateral Sclerosis according to Initial Symptoms: An Analysis of 500 Cases.

Authors:  Jang Woo Lee; Seong Woong Kang; Won Ah Choi
Journal:  Yonsei Med J       Date:  2021-04       Impact factor: 2.759

3.  Neuron-specific enolase level is a useful biomarker for distinguishing amyotrophic lateral sclerosis from cervical spondylotic myelopathy.

Authors:  Akihiro Tsukahara; Takafumi Hosokawa; Daisuke Nishioka; Takuya Kotani; Shimon Ishida; Tohru Takeuchi; Fumiharu Kimura; Shigeki Arawaka
Journal:  Sci Rep       Date:  2021-11-24       Impact factor: 4.379

4.  Treatment of progressive paralysis associated with cervical myelopathy and suspected amyotrophic lateral sclerosis: A case report.

Authors:  Yoshinori Ishikawa; Naohisa Miyakoshi; Takashi Kobayashi; Toshihiko Kikuchi
Journal:  Surg Neurol Int       Date:  2021-11-02

5.  Limb-onset amyotrophic lateral sclerosis patients visiting orthopedist show a longer time-to-diagnosis since symptom onset.

Authors:  Osamu Kano; Konosuke Iwamoto; Hirono Ito; Yuji Kawase; Derek Cridebring; Ken Ikeda; Yasuo Iwasaki
Journal:  BMC Neurol       Date:  2013-02-09       Impact factor: 2.474

6.  Diagnosis pathway for patients with amyotrophic lateral sclerosis: retrospective analysis of the US Medicare longitudinal claims database.

Authors:  James R Williams; David Fitzhenry; Lauren Grant; Derek Martyn; Douglas A Kerr
Journal:  BMC Neurol       Date:  2013-11-04       Impact factor: 2.474

Review 7.  Current Diagnosis and Management of Cervical Spondylotic Myelopathy.

Authors:  Joshua Bakhsheshian; Vivek A Mehta; John C Liu
Journal:  Global Spine J       Date:  2017-05-31
  7 in total

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