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Methods of Testing Neuromuscular Transmission in the Intensive Care Unit

Published online by Cambridge University Press:  18 September 2015

François Grand'Maison*
Affiliation:
Service de Neurologie, Hôpital Charles-LeMoyne, Geenfield Park, Québec
*
Hôpital Charles-LeMoyne, Service de Neurologie, 3120 boul., Geenfield Park, Québec, Canada J4V 2H1
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Abstract

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All disorders of neuromuscular transmission (NMT) may cause ventilatory failure, albeit rarely. Respiratory muscle weakness is occasionally the presenting feature of myasthenia gravis (MG), the Lambert-Eaton myasthenic syndrome (LEMS), hypermagnesemia and botulism. Chronic MG, congenital myasthenic syndromes and LEMS may be acutely exacerbated by various intercurrent conditions and by drugs which interfere with NMT. Finally, in the ICU, difficulty in weaning from the ventilator may be caused by prolonged use of neuromuscular blocking agents. Electrophysiological studies of NMT disorders in the intensive care unit have rarely been reported. Nevertheless, the available data indicates that the electrodiagnosis of severe NMT disorders can be misleading. With severe NMT defects, the electrophysiological distinction between post-synaptic and pre-synaptic disorders is blurred and the differential diagnosis with myopathies may be difficult. A clinically suspected NMT disorder should therefore not be ruled out when electrodiagnosis fails to demonstrate the expected abnormalities.

Type
Research Article
Copyright
Copyright © Canadian Neurological Sciences Federation 1998

References

REFERENCES

1.Oh, SJ, Eslami, N, Nishihira, T, et al. Electrophysiological and clinical correlation in myasthenia gravis. Ann Neurol 1982; 12: 348354.CrossRefGoogle ScholarPubMed
2.Howard, JF, Sanders, DB, Massey, JM. The electrodiagnosis of myasthenia gravis and the Lambert-Eaton myastheic syndrome. Neurologic Clinics 1994; 12 (2): 305330.CrossRefGoogle Scholar
3.Grand’Maison, F, Lamoureux, L. Acute fulminating myasthenia gravis: Misleading electrophysiological findings in one patient during a myasthenic crisis. Can J Neurol Sci 1993; 20 (Suppl 2): S52.Google Scholar
4.Maher, J, Bolton, CF, Grand’Maison, F, Strong, M. Diagnostic difficulties in myasthenia gravis. Can J Neurol Sci 1995; 22 (Suppl 1):S51.Google Scholar
5.Engel, AG. Congenital disorders of neuromuscular transmission. Semin Neurol 1990; 10: 1226.CrossRefGoogle ScholarPubMed
6.O’Neill, JH, Murray, MF, Newsom-Davis, J. The Lambert-Eaton myasthenic syndrome. Brain 1988; 111: 577596.CrossRefGoogle ScholarPubMed
7.Bady, B, Vial, C, Chauplannaz, G. Syndrome de Lambert-Eaton: Étude clinique et électrophysiologique de 18 cas associés à un cancer du poumon. Revue Neurologique 1992; 148: 513519.Google Scholar
8.Nicolle, MW, Stewart, DJ, Remtulla, H, Chen, R, Bolton, CF. Lambert-Eaton myasthenic syndrome presenting with severe respiratory failure. Muscle Nerve 1996; 19: 13281333.3.0.CO;2-Q>CrossRefGoogle ScholarPubMed
9.Segredo, V, Caldwell, JW, Matthay, MA, et al. Persistent paralysis in critically ill patients after long-term administration of vecuronium. N Engl J Med 1992; 327: 524528.CrossRefGoogle ScholarPubMed
10.Zochodne, DW, Ramsay, DA. Acute quadriplegic myopathy. Neurology 1994; 44: 988.CrossRefGoogle ScholarPubMed
11.Oh, SJ. Diverse electrophysiological spectrum ot the Lambert-Eaton myasthenic syndrome. Muscle & Nerve 1989; 21: 464469.CrossRefGoogle Scholar
12.Pickett, JB III. AAEE Case Report 16: Botulism. Muscle & Nerve 1988; 11: 12011205.CrossRefGoogle ScholarPubMed
13.Trontelj, JV, Stalberg, EV. Jitter measurement by axonal microstimulation: Guidelines and technical notes. Electroencephalogr Clin Neurophysiol 1992; 85: 3037.CrossRefGoogle ScholarPubMed
14.Oh, SJ, Kim, DE, Kuruoglu, R, et al. Edrophonium responsiveness not necessarily diagnostic of myasthenia gravis. Muscle & Nerve 1990; 13: 187191.CrossRefGoogle Scholar
15.Motomura, M, Lang, B, Johnston, I, et al. Incidence of serum anti-P/O-type and anti-N-type calcium channel autoantibodies in the Lambert-Eaton myasthenic syndrome. J Neurol Sci 1997; 20: 3542.CrossRefGoogle Scholar