Temporary and highly variable recovery of neuromuscular dysfunction by electrical stimulation in the follow-up of acute critical illness neuromyopathy: a pilot study
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Published:2023-12-28
Issue:1
Volume:5
Page:
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ISSN:2524-3489
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Container-title:Neurological Research and Practice
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language:en
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Short-container-title:Neurol. Res. Pract.
Author:
Sekhniashvili MadonaORCID, Baum Petra, Toyka Klaus V.
Abstract
Abstract
Background
In sepsis-associated critical illness neuromyopathy (CIPNM) serial electrical stimulation of motor nerves induces a short-lived temporary recovery of compound muscle action potentials (CMAPs) termed facilitation phenomenon (FP). This technique is different from other stimulation techniques published. The identification of FP suggests a major functional component in acute CIPNM.
Methods
From our previous study cohort of 18 intensive care unit patients with sepsis associated CIPNM showing profound muscle weakness and low or missing CMAPs on nerve conduction studies, six patients with different severity could be followed. In a pilot sub-study we analyzed the variability of FP during follow up. Over up to 6 weeks we performed 2–6 nerve conduction studies with our novel stimulation paradigm. Motor nerves were stimulated at 0.2–0.5 Hz with 60–100 mA at 0.2–0.5 ms duration, and CMAP responses were recorded. Standard motor nerve conduction velocities (NCV) could be done when utilizing facilitated CMAPs. Needle electromyography was checked once for spontaneous activity to discover potential denervation and muscle fiber degeneration. Serum electrolytes were checked before any examination and corrected if abnormal.
Results
In all six patients a striking variability in the magnitude and pattern of FP could be observed at each examination in the same and in different motor nerves over time. With the first stimulus most CMAPs were below 0.1 mV or absent. With slow serial pulses CMAPs could gradually recover with normal shape and near normal amplitudes. With facilitated CMAPs NCV measurements revealed low normal values. With improvement of muscle weakness subsequent tests revealed larger first CMAP amplitudes and smaller magnitudes of FP. Needle EMG showed occasional spontaneous activity in the tibialis anterior muscle.
Conclusion
In this pilot study striking variability and magnitude of FP during follow-up was a reproducible feature indicating major fluctuations of neuromuscular excitability that may improve during follow-up. FP can be assessed by generally available electrophysiological techniques, even before patients could be tested for muscle strength. Large scale prospective studies of the facilitation phenomenon in CIPNM with or without sepsis are needed to define diagnostic specificity and to better understand the still enigmatic pathophysiology.
Trial registration: This trial was registered at the Leipzig University Medical Center in 2021 after approval by the Ethics Committee.
Funder
Deutscher Akademischer Austauschdienst Würzburg University Research Fund the Leipzig University Research Fund Kurt-Goldstein Research Institute, Kreischa, Germany
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference20 articles.
1. de Letter, M. A., Schmitz, P. I., Visser, L. H., Verheul, F. A., Schellens, R. L., Op de Coul, D. A., et al. (2001). Risk factors for the development of polyneuropathy and myopathy in critically ill patients. Critical Care Medicine, 29(12), 2281–2286. https://doi.org/10.1097/00003246-200112000-00008 2. Bolton, C. F. (2005). Neuromuscular manifestations of critical illness. Muscle and Nerve, 32, 140–163. https://doi.org/10.1002/mus.20304 3. Z’Graggen, W. J., Lin, C. S., Howard, R. S., Beale, R. J., & Bostock, H. (2006). Nerve excitability changes in critical illness polyneuropathy. Brain, 129(Pt 9), 2461–2470. https://doi.org/10.1093/brain/awl191. Epub 2006 Aug 10 PMID: 16901913. 4. Stevens, R. D., Marshall, S. A., Cornblath, D. R., Hoke, A., Needham, D. M., de Jonghe, B., et al. (2009). A framework for diagnosing and classifying intensive care unit-acquired weakness. Critical Care Medicine, 37(10 Suppl), S299-308. https://doi.org/10.1097/CCM.0b013e3181b6ef67 5. Z’Graggen, W. J., Brander, L., Tuchscherer, D., Scheidegger, O., Takala, J., & Bostock, H. (2011). Muscle membrane dysfunction in critical illness myopathy assessed by velocity recovery cycles. Clinical Neurophysiology, 122(4), 834–841. https://doi.org/10.1016/j.clinph.2010.09.024. Epub 2010 Nov 1 PMID: 21044861.
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