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Low Back Pain in Patients with Lumbar Spinal Stenosis―Hemodynamic and electrophysiological study of the lumbar multifidus muscles

INTRODUCTION: Several studies have demonstrated improvement in low back pain (LBP) after decompression surgery for lower extremity symptoms in lumbar spinal stenosis (LSS); however, the influence of neuropathic disorders on LBP is uncertain. Aim of this study is to identify the features of motion-in...

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Detalles Bibliográficos
Autores principales: Sakai, Yoshihito, Ito, Sadayuki, Hida, Tetsuro, Ito, Kenyu, Koshimizu, Hiroyuki, Harada, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Spine Surgery and Related Research 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698562/
https://www.ncbi.nlm.nih.gov/pubmed/31440617
http://dx.doi.org/10.22603/ssrr.1.2016-0016
Descripción
Sumario:INTRODUCTION: Several studies have demonstrated improvement in low back pain (LBP) after decompression surgery for lower extremity symptoms in lumbar spinal stenosis (LSS); however, the influence of neuropathic disorders on LBP is uncertain. Aim of this study is to identify the features of motion-induced and walking-induced LBP in patients with LSS and to assess whether neuropathic LBP develops. METHODS: In total, 234 patients with LSS including L4/5 lesion were asked to identify their LBP. Subjects were classified into three groups: walking-induced LBP that aggravated during walking (W group), motion-induced LBP that aggravated during sitting up (M group), and no LBP (N group). Cross-sectional areas of the dural sac, lumbar multifidus, and the erector spinae were measured. Intramuscular oxygenation was evaluated with near-infrared spectrophotometer. Surface electromyography (EMG) and mechanomyography (MMG) were performed on the lumbar multifidus. Morphological, hemodynamic, and electrophysiological differences in the onset of LBP were evaluated. RESULTS: The prevalence of W, M, and control groups was 31.2%, 32.1%, 36.8%, respectively. Concordance between the laterality of LBP and leg symptoms including pain and numbness was 86.3% in the W group and 47.0% in the M group. Dural sac area was lower in the W group than in the M and control groups. In the hemodynamic evaluation, the oxygenated hemoglobin level was significantly lower in the W group than in the M and N groups. In electrophysiological evaluation of lumbar multifidus, the mean power frequency in EMG was significantly higher in the W group than in the N group. Amplitude in MMG was significantly lower in the W group than in the N group. CONCLUSIONS: Neurologic disturbance in patients with LSS may be attributed to “neuropathic LBP.” Neuropathic multifidus disorder plays a role in walking-induced LBP.