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Division of Clinical Electrophysiology, Department of Neurology. University of lowa Hospitals and Clinics. Iowa City. IA.
Address correspondence and reprint requests to Dr. Yamada. Division of Clinical Electrophysiology. Department Neurology, University of Iowa Hospitals and Clinics, Iowa City. IA 52242.
We studied the effect of tourniquet-induced ischemia on the somatosensory evoked potential (SEPI. During 24 minutes of ischemia, short-latency components (P9, P14, and N18) and Erb's potential were abolished earlier than the iong-latency components iP22, N30, P40, and N60). The latency increase was the same for Erbs potential and for P9, P14, and N18, but it was greater for P22, N30, and P40 and greatest for N60. These dissociated effects suggest that SEP components are not transmitted through a single pathway but are mediated through independent routes, possibly involving different first-order afferent fibers. Selective abnormalities of the early SEP peaks in association with relative preservation of late peaks may occur in peripheral nerve disorders.
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