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DOI 10.1016/j.clinph.2008.07.003

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2008

Somatosensory evoked potentials (SEPs) for the evaluation of cervical spondylotic myelopathy: utility of the onset-latency parameters.

Nakai Shun-ichi, Sonoo Masahiro, Shimizu Teruo

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

Peak latencies have been traditionally employed for the evaluation of somatosensory evoked potentials (SEPs). Some authors have argued for the theoretical superiority of the onset latencies, which has never been verified in actual clinical cases. We aimed to investigate the utility of onset-latency parameters of median nerve SEPs in the cervical spondylotic myelopathy (CSM) patients, as well as several other issues concerned with the SEP diagnosis of CSM.

METHODS

We retrospectively enrolled 42 CSM patients and investigated their SEP findings.

RESULTS

The N9o (N9 onset)-P13/14o interval showed the highest sensitivity (83%) followed by N9o-N20o (74%). The sensitivities of corresponding peak latency parameters were lower (62% and 33%). The amplitude of the lower cervical N13 also showed the highest sensitivity (83%). The sensitivity of tibial nerve SEPs examined in 21 patients was lower (71%) than that of median nerve SEPs (90%). When clinical signs alone were used as the gold standard, the sensitivity of median SEPs was 90% whereas that of MRI was 88%.

CONCLUSIONS

Higher diagnostic yield of onset-latency parameters of median nerve SEPs has been documented in CSM.

SIGNIFICANCE: SEPs are useful in the diagnosis of CSM having equal sensitivity and probably higher specificity than MRI.

Для цитирования: Nakai Shun-ichi, Sonoo Masahiro, Shimizu Teruo. Somatosensory evoked potentials (SEPs) for the evaluation of cervical spondylotic myelopathy: utility of the onset-latency parameters.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2008. DOI: 10.1016/j.clinph.2008.07.003.

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