Pitfalls in electrodiagnosis

Abstract This review describes some of the factors that may lead to erroneous interpretations of electromyographic and nerve conduction studies. Such errors may be due either to technical or to biological factors, and it is imperative that the consequent limitations of the methods be considered in a diagnostic setting. Electrodiagnostic findings should always be interpreted in the clinical context, and since they are rarely specific for a particular disorder or pathology, it is necessary to satisfy several criteria to make a specific diagnosis. The aim of electromyographic examination is to ascertain whether weakness is due to a neurogenic lesion or to myopathy. It is, however, not sufficient to show the presence of denervation activity since this may occur in either condition. Therefore the motor unit potentials from both weak and nonaffected muscles should be examined quantitatively. Nerve conduction studies are carried out to ascertain whether motor or sensory myelinated fibers are lost, and whether the primary pathology is due to demyelination or axonal loss or to both. The nerve conduction velocity is of primary importance in this distinction. However, loss of large myelinated fibers leads to slowing of conduction; in some instances the conduction velocity may be normal if only a few large fibers are spared. In addition collateral sprouting in chronic conditions may lead to apparent sparing of motor fibers. Hence an erroneous diagnosis may be made of a sensory neuropathy if additional electromyography or other tests are not carried out. Conduction studies investigate only large myelinated fibers, and therefore in some instances there is discordance between the morphology and physiology. Acquired demyelinating neuropathies are sometimes associated with focal slowing of conduction or with conduction block. The demonstration of conduction block is important, but several requirements must be fulfilled in terms of technique, clinical context, and temporal development in order to avoid errors.

[1]  S. Lipton,et al.  A syndrome of asymmetric limb weakness with motor conduction block , 1990, Neurology.

[2]  A. Sumner,et al.  The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies , 1982, Neurology.

[3]  W C Wiederholt,et al.  Threshold and conduction velocity in isolated mixed mammalian nerves , 1970, Neurology.

[4]  B Conrad,et al.  Is there an age-dependent continuous increase in the duration of the motor unit action potential? , 1991, Electroencephalography and clinical neurophysiology.

[5]  P. Fullerton Electrophysiological and histological observations on peripheral nerves in acrylamide poisoning in man. , 1969, Journal of neurology, neurosurgery, and psychiatry.

[6]  J. England,et al.  A computer simulation of conduction block: Effects produced by actual block versus interphase cancellation , 1990, Annals of neurology.

[7]  F Buchthal,et al.  The diagnostic yield of quantified electromyography and quantified muscle biopsy in neuromuscular disorders , 1982, Muscle & nerve.

[8]  M. Rasminsky,et al.  Conduction block in rat myelinated fibres following acute exposure to antigalactocerebroside serum , 1982, The Journal of physiology.

[9]  S. Boniface,et al.  Pure motor demyelinating neuropathy: deterioration after steroid treatment and improvement with intravenous immunoglobulin. , 1994, Journal of neurology, neurosurgery, and psychiatry.

[10]  J. Meulstee,et al.  Patterns of conduction failure in the Guillain-Barré syndrome. , 1988, Brain : a journal of neurology.

[11]  J. Kimura Consequences of peripheral nerve demyelination: basic and clinical aspects. , 1993, The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques.

[12]  T. Yamada,et al.  Effect of desynchronized inputs on compound sensory and muscle action potentials , 1988, Muscle & nerve.

[13]  G. Mckhann,et al.  Patterns of recovery in the Guillain-Barre syndromes , 1997, Neurology.

[14]  G. Mckhann,et al.  Plasmapheresis and guillain‐barré syndrome: Analysis of prognostic factors and the effect of plasmapheresis , 1988, Annals of neurology.

[15]  C. Krarup,et al.  Conduction studies in peripheral nerve. , 1985, Neurobehavioral toxicology and teratology.

[16]  P. Schmitz,et al.  A randomized trial comparing intravenous immune globulin and plasma exchange in Guillain-Barré syndrome. Dutch Guillain-Barré Study Group. , 1992, The New England journal of medicine.

[17]  Fritz Buchthal,et al.  An introduction to electromyography , 1957 .

[18]  Mark J. Brown,et al.  Multifocal demyelinating neuropathy with persistent conduction block , 1982, Neurology.

[19]  F. Buchthal Spontaneous electrical activity: an overview. , 1982, Muscle & nerve.

[20]  F Buchthal,et al.  Diagnostic yield of the analysis of the pattern of electrical activity of muscle and of individual motor unit potentials in neurogenic involvement. , 1977, Journal of neurology, neurosurgery, and psychiatry.

[21]  W. Brown,et al.  Conduction block in clinical practice , 1991, Muscle & nerve.

[22]  J. Griffin,et al.  Multifocal motor neuropathy: Electrodiagnostic features , 1994, Muscle & nerve.

[23]  P. D. Lewis,et al.  Pseudoaxonal Guillain-Barré syndrome: severe demyelination mimicking axonopathy. A case with pupillary involvement. , 1992, Journal of neurology, neurosurgery, and psychiatry.

[24]  R. Kaji,et al.  Ouabain reverses conduction disturbances in single demyelinated nerve fibers , 1989, Neurology.

[25]  J Kimura,et al.  Relation between size of compound sensory or muscle action potentials, and length of nerve segment , 1986, Neurology.

[26]  P. Grafe,et al.  Activity‐dependent excitability changes in normal and demyelinated rat spinal root axons. , 1985, The Journal of physiology.

[27]  Fritz Buchthal,et al.  Evoked action potentials and conduction velocity in human sensory nerves , 1966 .

[28]  F Buchthal,et al.  Diagnostic yield of analysis of the pattern of electrical activity and of individual motor unit potentials in myopathy. , 1976, Journal of neurology, neurosurgery, and psychiatry.

[29]  J. Desmedt,et al.  Collateral Innervation of Muscle Fibres by Motor Axons of Dystrophic Motor Units , 1973, Nature.

[30]  F. Buchthal Electromyography in the evaluation of muscle diseases. , 1985, Neurologic clinics.

[31]  B. Shahani,et al.  Motor nerve inexcitability in Guillain-Barré syndrome. The spectrum of distal conduction block and axonal degeneration. , 1992, Brain : a journal of neurology.

[32]  C. Krarup,et al.  Sensory pathophysiology in chronic acquired demyelinating neuropathy. , 1996, Brain : a journal of neurology.