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Biomedical subjects

E L Logigian

Publications and source records attributed to E L Logigian.

At least 55 records · Page 3Linked to original sources
PubMed1996

Detection of Borrelia burgdorferi DNA by polymerase chain reaction in cerebrospinal fluid in Lyme neuroborreliosis.

A polymerase chain reaction (PCR) assay that detects Borrelia burgdorferi DNA in cerebrospinal fluid (CSF) was evaluated as a diagnostic test for acute or chronic Lyme neuroborreliosis. In one laboratory, 102 samples were tested blindly, and 40 samples were retested in a second laboratory. In the first laboratory, B. burgdorferi DNA was detected in CSF samples in 6 (38%) of 16 patients with acute neuroborreliosis, 11 (25%) of 44 with chronic neuroborreliosis, and none of 42 samples from patients with other illnesses. There was a significant correlation between PCR results and the duration of previous intravenous antibiotic therapy. The overall frequency of positive results was similar in the second laboratory, but concordance between the laboratories and among primer-probe sets was limited because many samples were positive with only one primer-probe set. Thus, PCR testing can sometimes detect B. burgdorferi DNA in CSF in patients with acute or chronic neuroborreliosis, but with current methods, the sensitivity of the test is limited.

Adolescent↗
PubMed1996

Activity-dependent conduction in single motor units.

Vertebrate sensory and motor axons vary in their responses to submaximal stimuli as a function of time since prior activation. When two equal but submaximal stimuli are presented in pairs, the response to the second stimulus may be greater or less than the response to the first stimulus, depending on the interstimulus interval (ISI). We studied both the supernormal period (ISI between 6 and 25 msec) and the subnormal period (ISI between 25 and 100 msec) under conditions where only single motor axons were stimulated. Twenty single motor units from eight normal subjects were studied. The behavior of single units was very similar to that observed in compound motor action potentials, with the supernormal period lasting approximately 20 msec, followed by a subnormal period lasting at least 80 msec. Surprisingly, a supernormal period could be evoked by a stimulus that did not produce a response in the motor unit being studied; however, the presence of subnormality was dependent on an action potential being generated in response to the first stimulus. Based on these results, we conclude that the supernormal period does not require the opening of voltage-dependent ion channels, in contrast to the later occurring subnormal period.

Action Potentials↗
PubMed1996

[Chronic neuroborreliosis in Lyme disease].

Acute and chronic syndromes of Lyme neuroborreliosis are recognized. Acute syndromes are clinically pronounced and comprise meningitis, neuritis of the cranial nerve, radiculoneuritis. Chronic syndromes are less evident. These are moderate encephalopathy and radiculoneuropathy. The diagnosis of the chronic syndrome is based on the presence of early classic signs of BL. CSF must be tested for routine procedure and in pair with serum in the test for selective accumulation of antibodies to Bb in the CSF. Neurophysiological studies help detect memory defects. Electrophysiological tests verify radiculoneuropathy. NMR investigation of the brain and SPECT-scanning may demonstrate damage to the white brain matter. We have much experience with i.v. administration of ceftriaxone (2 g/day for 4 weeks) which relieved neurological syndromes several months later.

Acute Disease↗
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.

Action Potentials↗
PubMed1995

Does ulnar neuropathy predispose to focal dystonia?

We have observed a high incidence of ulnar neuropathy in musicians with dystonic flexion of the ipsilateral little and ring fingers. To investigate the relationship between ulnar neuropathy and focal dystonia, we compared the patterns of surface EMG activity in extensor digitorum communis (EDC4) and flexor digitorum superficialis (FDS4) during tapping of the ring finger in normal controls and patients with ulnar neuropathy or focal dystonia. Ten of 10 normal subjects exhibited well-formed alternating EMG bursts in EDC4 and FDS4 separated by clear silent periods. Seven of 7 patients with dystonic flexion of the little and ring fingers showed loss of silent periods between poorly formed bursts in FDS or EDC. Surprisingly, 9 of 10 patients with ulnar neuropathy showed burst pattern abnormalities qualitatively similar to those observed in the dystonic patients. These data suggest that ulnar neuropathy alters the execution of a motor task involving multiple peripheral nerves.

Adult↗
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.

Action Potentials↗
PubMed1995

Electrophysiological and urodynamic studies to monitor surgical outcome in children with tethered spinal cords.

Children with myelodysplasia often develop tethering of their spinal cord within 2-3 years after correction of their initial birth defect, leading to either neurological or urological dysfunction. Surveillance of these children includes electrophysiologic/urodynamic (EMG/UDS) studies to monitor improvement or deterioration of their neurological function. We reviewed 39 patients who underwent surgical untethering from 1979 to 1994 to determine whether postoperative EMG/UDS studies were useful in assessing outcome after surgery. All patients had a complete neurologic examination and an EMG/UDS prior to and 3 months after surgery. Twenty patients (51%) showed improvement in their EMG/UDS study after untethering, 15 (39%) demonstrated no significant change, and 4 (10%) showed deterioration. Improvement consisted of either return of previously absent motor units, return of sacral reflexes, or improved bladder dynamics. In a further 3 patients, subsequent deterioration on serial postoperative EMG/UDS testing was the first indication of recurrent tethering. We conclude that serial EMG/UDS evaluation in patients at risk for tethering of the spinal cord may serve as a useful adjunct to close clinical observation.

Child↗
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↗
PubMed1995

Nitrous oxide depresses the H-reflex in children with cerebral palsy.

Hoffmann's reflex or H-reflex (HR) is an electrically elicited reflex that measures excitability of motoneurons and shares some physiologic properties with the deep tendon reflex. Children with tendon hyperreflexia due to cerebral palsy usually have higher amplitude HRs. Nitrous oxide (N2O) depresses the HR in patients with normal spinal reflexes, although the effect of N2O in conditions with hyperreflexia such as cerebral palsy is not known. We propose to determine the effect of N2O on the amplitude of the HR under general anesthesia in children with hyperreflexia due to cerebral palsy. We studied eight children undergoing selective dorsal rhizotomy (SDR) for the relief of spasticity. The maximum amplitudes of the HR (HRmax) and direct motor response (MRmax) were routinely evoked under the following anesthetic conditions: 1) sufentanil and 66% N2O/33% oxygen; and 2) sufentanil and 100% oxygen. The HRmax amplitude was significantly lower when N2O was part of the inspired gas mixture. The differences between the no N2O and the 66% N2O groups were significant. The MRmax did not change significantly. Abnormal spinal reflexes seen in spastic diplegia can be abolished by inhaled N2O. This finding also suggests that N2O-induced depression of spinal reflexes should be a consideration during physiologic monitoring of the spinal cord under general anesthesia.

Cerebral Palsy↗
PubMed1994

The long-term clinical outcomes of Lyme disease. A population-based retrospective cohort study.

OBJECTIVE: To ascertain the prevalence of and risk factors for long-term sequelae from acute Lyme disease. DESIGN: Population-based, retrospective cohort study. SETTING: A coastal region endemic for Lyme disease. PARTICIPANTS: Patients with a history of Lyme disease who were previously treated with antibiotics were compared with randomly selected controls. MEASUREMENTS: A standardized physical examination, health status measure (Short Form 36), psychometric test battery, and serologic analysis. RESULTS: Compared with the control group (n = 43), the Lyme group (n = 38; mean duration from disease onset to study evaluation, 6.2 years) had more arthralgias (61% compared with 16%; P < 0.0001); distal paresthesias (16% compared with 2%; P = 0.03); concentration difficulties (16% compared with 2%; P = 0.03); and fatigue (26% compared with 9%; P = 0.04), and they had poorer global health status scores (P = 0.04). The Lyme group also had more abnormal joints (P = 0.02) and more verbal memory deficits (P = 0.01) than did the control group. Overall, 13 patients (34%; 95% CI, 19% to 49%) had long-term sequelae from Lyme disease (arthritis or recurrent arthralgias [n = 6], neurocognitive impairment [n = 4], and neuropathy or myelopathy [n = 3]). Compared with controls, patients who had long-term sequelae had higher IgG antibody titers to the spirochete (P = 0.03) and received treatment later (34.5 months compared with 2.7 months; P < 0.0001). CONCLUSIONS: Persons with a history of Lyme disease have more musculoskeletal impairment and a higher prevalence of verbal memory impairment when compared with those without a history of Lyme disease. Our findings suggest that disseminated Lyme disease may be associated with long-term morbidity.

Cohort Studies↗
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

H reflex studies in cerebral palsy patients undergoing partial dorsal rhizotomy.

H reflex studies were performed in ten spastic children with cerebral palsy who underwent partial dorsal rhizotomy (PDR). Under anesthesia prior to PDR, H reflex amplitude evoked by percutaneous peripheral nerve stimulation gradually declined in all patients and became unobtainable in five. Motor responses could still be evoked by apparent dorsal root stimulation in these five, but since it was shown that they were M responses and not reflexes, PDR was performed randomly. In the other five patients, in whom H reflexes were still evokable, dorsal root stimulation evoked motor responses which were true reflex responses, and PDR was performed "selectively." Compared to preoperative values, postoperative Hmax/Mmax ratios declined, but no more so in selective than in random PDR. We conclude that current intraoperative methods for selection of "abnormal" dorsal rootlets for section may be invalid and may have no bearing on successful outcome, since spasticity improves even with random PDR.

Analysis of Variance↗
PubMed1994

Conduction velocity in motor, cutaneous afferent, and muscle afferent fibers within the same mixed nerve.

Mammalian axons subserving different functions have different conduction velocities (CV); motor fibers conduct more slowly than cutaneous fibers, which conduct slower than muscle afferents. However, human studies have yielded conflicting results. We studied isolated fiber populations in human sciatic nerve to examine further this question. Motor studies were performed in standard fashion, stimulating at gluteal fold (GF) and popliteal fossa (PF) and recording soleus. In addition, conduction velocity of a pure motor nerve volley was calculated for 3 subjects. Stimulating and recording electrodes were needles placed close to the nerve. Cutaneous afferents were studied by stimulating the sural nerve at the ankle and recording at PF and GF. Muscle afferent velocity was assessed by comparing soleus H reflex latency with stimulation at PF and GF. Results in 10 subjects showed muscle afferent CV of 57.6, cutaneous afferent CV of 55.1, motor CV of 52.4, and mixed nerve CV of 56.3 m/s. Although statistically significant, these differences are much smaller than in animal studies. These results have implications for understanding what fibers contribute to spinal reflexes.

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↗