Pelvic floor electrophysiology in spinal cord injury
- PMID: 26975618
- DOI: 10.1016/j.clinph.2015.12.022
Pelvic floor electrophysiology in spinal cord injury
Abstract
Objective: The study aimed to investigate sacral peripheral nerve function and continuity of pudendal nerve in patients with chronic spinal cord injury (SCI) using pelvic floor electrophysiological tests.
Methods: Twelve patients with low cervical or thoracic SCI were prospectively included. Quantitative external anal sphincter (EAS) muscle electromyography (EMG), pudendal nerve terminal motor latency (PNTML) testing, bulbocavernosus reflex (BCR) testing and pudendal short-latency somatosensory-evoked potential (SEP) measurement were performed.
Results: In EAS muscle EMG, two patients had abnormal increased spontaneous activity and seven prolonged motor unit potential duration. PNTML was normal in 10 patients. BCR was present with normal latency in 11 patients and with prolonged latency in one. The second component of BCR could be recorded in four patients. SEPs showed absent cortical responses in 11 patients and normal latency in one.
Conclusions: Pudendal nerve and sacral lower motor neuron involvement are significantly associated with chronic SCI, most prominently in EAS muscle EMG. The frequent finding of normal PNTML latencies supports earlier concerns on the utility of this test; however, BCR and pudendal SEPs may have clinical relevance.
Significance: As intact peripheral nerves including pudendal nerve are essential for efficient supportive therapies, pelvic floor electrophysiological testing prior to these interventions is highly recommended.
Keywords: Bulbocavernosus reflex; Electromyography; Pelvic floor electrophysiology; Pudendal nerve terminal motor latency; Spinal cord injury.
Copyright © 2016 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
Comment in
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Double spinal cord lesions and pelvic floor electrophysiology.Clin Neurophysiol. 2016 May;127(5):2317-8. doi: 10.1016/j.clinph.2016.01.007. Epub 2016 Jan 23. Clin Neurophysiol. 2016. PMID: 26857848 No abstract available.
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