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D C Preston

Publications and source records attributed to D C Preston.

34 records · Page 2Linked to original sources
PubMed1995

Comparison of the flexed and extended elbow positions in localizing ulnar neuropathy at the elbow.

Electrophysiologic localization of ulnar neuropathy at the elbow often depends on demonstration of segmental slowing. Based on normative data obtained from 50 control subjects, we compared the utility of flexed and extended elbow positions in demonstrating focal slowing at the elbow as compared to the forearm segment in patients with ulnar neuropathy. We studied 35 patients with ulnar neuropathy with definite electrophysiologic localization to the elbow segment defined by conduction block across the elbow segment or by focal slowing demonstrated either in the flexed or extended position. Applying cutoff values from the control group, all 35 patients demonstrated focal slowing at the elbow in the flexed position, whereas only 5 of 35 (14%) patients did so in the extended position. We conclude that the flexed elbow position is more sensitive than the extended position in localizing ulnar neuropathy at the elbow and should be the preferred method when performing ulnar motor conduction studies.

Adult↗
PubMed1995

Differentiation between axonal and demyelinating neuropathies: identical segments recorded from proximal and distal muscles.

The presence of significant slowing of motor nerve conduction velocity is considered one of the electrodiagnostic hallmarks of demyelinating neuropathies; however, slowing of conduction velocity may also accompany severe axonal loss. When compound muscle action potential (CMAP) amplitudes are markedly reduced, it is frequently difficult to determine if conduction velocity slowing is due to axonal loss with dropout of the fastest conducting fibers or demyelination. To evaluate the relationship between conduction velocity and axonal dropout, we compared conduction velocities through the same segment of nerve recording from distal and proximal peroneal muscles in patients with chronic neuropathies, in patients with motor neuron disease, and in control subjects. In controls and patients with motor neuron disease, conduction velocities were normal with no significant difference between proximal and distal sites. In patients with axonal neuropathies, conduction velocities were preferentially slowed when recording from distal muscles and relatively normal when recording from proximal sites. Patients with demyelinating neuropathies showed marked slowing of conduction at both sites. We conclude that comparing conduction velocity obtained from proximal versus distal muscle recordings provides a simple, reliable aid for differentiating between chronic axonal and demyelinating polyneuropathies, especially in cases with conduction velocity slowing and low CMAP amplitudes.

Action Potentials↗
PubMed1995

Stimulation distal to the lesion in patients with carpal tunnel syndrome.

In patients with carpal tunnel syndrome, low action potential amplitude after stimulation at the wrist (proximal to the lesion) is due to either demyelination or axonal degeneration. Demyelination can be distinguished from axonal degeneration by the presence of amplitude drop across the lesion. Amplitude drop is determined by comparison of action potential amplitude evoked by stimulation at the palm (distal to the lesion) with that of the wrist. Of 59 consecutive CTS patient hands, 36 (61%) showed significant reduction in CMAP and/or antidromic SNAP amplitudes at the wrist compared to the palm, indicating the presence of focal demyelination resulting in conduction block vs. pathologic dispersion with phase cancellation. Moreover, the smaller the wrist-evoked action potential amplitude, the greater the amplitude drop across the lesion. We conclude that in patients with CTS, as in other entrapment neuropathies, stimulation both proximal and distal to the lesion provides important pathophysiological information about the median nerve lesion.

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PubMed1995

Comparison of digital sensory studies in patients with carpal tunnel syndrome.

Electrodiagnosis of carpal tunnel syndrome (CTS) often depends on the demonstration of focal slowing of median sensory fibers across the wrist. We compared the relative sensitivity of the four median innervated digits in demonstrating focal slowing in patients with CTS. Antidromic sensory studies of digits 1, 2, 3, and 4 were performed on 30 control subjects to develop normative data. Fifty-nine consecutive patients with CTS were then studied to determine the sensitivity of focal slowing of each median innervated digit. In the 26 CTS patients with a normal distal motor latency (DML) to abductor pollicis brevis, digit 1 was abnormal in 81%, digit 2 in 42%, digit 3 in 54%, and digit 4 in 38%. In the 33 CTS patients with a prolonged DML, digit 1 was abnormal in 94%, digit 2 in 88%, digit 3 in 91%, and digit 4 in 88%. We conclude that in milder cases of CTS with a normal DML, digit 1 is the most sensitive in identifying focal slowing of sensory conduction across the wrist. However, in patients with a prolonged DML, the sensitivity of sensory conduction is not significantly different among the four digits.

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PubMed1995

Electromyography: do the diagnostic ends justify the means?

BACKGROUND: Physicians are sometimes reluctant to refer patients for electrodiagnostic studies (electromyography with nerve conduction studies [EMG/NCS]) believing the test is too painful and of little benefit. METHODS: We performed two separate surveys on 126 and 100 consecutive patients referred to our laboratory to determine if EMG/NCS was beneficial to the referring physician and to compare the level of anxiety experienced by patients before the study with the pain actually experienced during the study. RESULTS: The electrodiagnosis was discordant from the referring diagnosis in 39% of the patients with an abnormal EMG/NCS. Pretest anxiety levels were low in 59% of the patients, medium in 27%, and high in 14%. After the tests, 82% of the patients said that the test was not as bad as expected, and was generally only mildly painful. Ninety-three responded that they would have the test performed again. CONCLUSIONS: EMG/NCS often suggest alternative diagnoses, and the actual pain experienced during an EMG/NCS study is significantly less than expected.

Adult↗
PubMed1994

Submaximal stimuli activate different nerve fiber populations at different sites.

Theoretically, the largest and fastest nerve fibers are preferentially stimulated with submaximal stimuli. However, it is also well known that intraneural fascicular topography changes substantially along a proximal to distal axis. Because of this change in fascicular topography, we hypothesized the percutaneous submaximal stimuli applied to a nerve at different locations would stimulate different subpopulations of large fibers. We performed a series of collision studies by stimulating the ulnar nerve submaximally at proximal and distal sites at varying levels of stimulation intensity from motor threshold to supramaximal stimulation. The results suggest that variation in intraneural topography at different sites allows different large diameter nerve fiber subpopulations to be activated at submaximal stimuli, and emphasizes the importance of supramaximal stimulation to determine a valid conduction velocity.

Action Potentials↗
PubMed1994

Sensory and mixed nerve conduction studies in the evaluation of ulnar neuropathy at the elbow.

The relative sensitivities of sensory, mixed nerve, and motor conduction studies in assessing ulnar neuropathy at the elbow have not yet been established. Using surface electrodes, we performed conduction studies across the elbow segment in 43 patients with symptoms referable to the ulnar nerve and 40 control subjects. Segmental slowing of motor conduction localized the lesion to the elbow in 14 of 21 patients (67%) with clear evidence of ulnar neuropathy on physical examination but only in 2 of 22 (9%) with subtle or no physical examination abnormalities. The diagnostic yield was increased by the finding of segmental slowing of sensory or mixed nerve conduction across the elbow to 86% and 68%, respectively, for each of the groups. We conclude that surface-recorded sensory and mixed nerve conduction studies appear to be more sensitive than motor studies in the electrodiagnosis of ulnar neuropathy at the elbow and are especially valuable in patients with subtle clinical involvement.

Action Potentials↗
PubMed1993

Demyelinating neuropathy and acute lymphocytic leukemia.

We report a 67-year-old man with acute lymphocytic leukemia (ALL) who developed a rapidly progressive areflexic quadriparesis following chemotherapy. Electrophysiologic studies demonstrated an acute demyelinating polyneuropathy. Although peripheral nervous system dysfunction in ALL is often attributed to leukemic infiltration or chemotherapy, a diligent search with electrophysiologic evaluation should be considered and may suggest alternative diagnoses.

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PubMed1992

Lumbrical and interossei recording in carpal tunnel syndrome.

Median motor studies are commonly "normal" in mild carpal tunnel syndrome (CTS). This reflects either the sparing of motor compared to sensory fibers, or the inability of conventional studies to detect an abnormality. A novel approach to demonstrate early motor fiber involvement in CTS is the placement of the same active electrode lateral to the third metacarpal, allowing recording from the second lumbrical or the deeper interossei, when stimulating the median or ulnar nerves at the wrist, respectively. We compared the difference between these latencies in 51 normal control hands to 107 consecutive patient hands referred with symptoms and signs suggestive of CTS, who were subsequently proven to have electrophysiologic CTS by standard nerve conduction criteria. A prolonged lumbrical-interossei latency difference (> 0.4 ms) was found to be a sensitive indicator of CTS in all patient groups. It was also helpful in patients with coexistent polyneuropathy, where localization at the wrist was otherwise difficult.

Adult↗
PubMed1991

"Pseudospasticity" in Guillain-Barré syndrome.

We report a woman with Guillain-Barré syndrome who developed a flexion posture of the right arm and hand resembling upper motor neuron dysfunction. EMG demonstrated that involuntary peripherally generated continuous motor unit discharges caused the posture.

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