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1.
Journal of Clinical Neurology ; : 31-33, 2011.
Article in English | WPRIM | ID: wpr-103349

ABSTRACT

BACKGROUND AND PURPOSE: Amyotrophic lateral sclerosis (ALS) patients display easy fatigability and abnormal decrements on repetitive nerve stimulation (RNS) test of clinically involved limb muscles, which can result in ALS being misdiagnosed as myasthenia gravis. We retrospectively analyzed the RNS tests of ten ALS patients with only or predominant oropharyngeal symptoms without ocular or facial weakness. METHODS: RNS tests were performed on the abductor digiti quinti, flexor carpi ulnaris, orbicularis oculi (OO), nasalis and trapezius muscles at low-rate stimulation frequencies of 3 and 5-Hz. Decrements greater than 10% of the compound muscle action potential amplitude on the fifth stimulation compared to the first was regarded as abnormal. RESULTS: Six patients complained of muscular fatigue or diurnal fluctuation. Among the ten patients, three exhibited abnormal decrements during low-rate stimulation in the facial muscles but not in the limb muscles, two exhibited abnormal decrements in the OO and nasalis muscles, and one exhibited abnormal decrements in the OO muscle. CONCLUSIONS: These findings show that the facial muscles may be involved in some early oropharyngeal forms of ALS, although facial weakness may not be clinically evident. We confirm herein that abnormal decrement of facial muscles to RNS test cannot make a definite diagnose for myasthenia gravis.


Subject(s)
Humans , Action Potentials , Amyotrophic Lateral Sclerosis , Extremities , Facial Muscles , Muscle Fatigue , Muscles , Myasthenia Gravis , Retrospective Studies
2.
Journal of the Korean Neurological Association ; : 47-49, 2010.
Article in Korean | WPRIM | ID: wpr-95208

ABSTRACT

Botulinum toxin type A (BTA) is widely used for both medical treatment and cosmetic purposes. A 46-year-old woman presented with progressive generalized weakness and dysphagia. The patient had injected BTA into her both of her calves by herself for cosmetic purposes. Repetitive nerve stimulation of the right facial nerve demonstrated reduced compound muscle action potential amplitudes of the orbicularis oculi and nasalis muscles, and a reduced response to low-frequency, repetitive stimulation. The possibility of iatrogenic botulism should be considered when using BTA.


Subject(s)
Female , Humans , Middle Aged , Action Potentials , Botulinum Toxins , Botulinum Toxins, Type A , Botulism , Cosmetics , Deglutition Disorders , Facial Nerve , Injections, Intramuscular , Muscles
4.
Journal of the Korean Academy of Rehabilitation Medicine ; : 152-160, 2002.
Article in Korean | WPRIM | ID: wpr-722647

ABSTRACT

OBJECTIVE: The purpose of this study was to measure the local and distant effects of BTX-A of different dosage through the electrophysiologic study. METHOD: Sixteen Sprague-Dawley rats were used and divided into four groups by the dosage of BTX-A (Botox , Allergan Co.): 2, 4, 6, 8 U for each of the four rats. BTX-A was injected into tibialis anterior (TA) muscles. Slow rate (3 Hz) and fast rate (20 Hz) repetitive nerve stimulation test (RNST) was performed before and after BTX-A injection. The schedule of postinjection was as follows: 2 days after the injection, every seven days till 10 weeks postinjection, once a month for 4 months. RESULTS: In the fast rate RNST of the treated TA muscle, dose-dependent increments were seen on the 2nd day postin jection and thereafter dose-dependent decrements appeared and weakened over the course of time. In the slow rate RNST of the treated TA, dose-dependent decrements were observed through ten weeks postinjection in all groups. In the fast rate RNST of the untreated TA, incremental responses were produced in all groups in a dose-dependent manner. In the slow rate RNST of the untreated TA, there were no changes. CONCLUSION: The BTX-A injection causes local paralysis in the treated muscles and presynaptic dysfunction of the neuro muscular junction in the distant untreated muscles in a dosedependent manner. This study could not be differentiated between neuromuscular dysfunction, myopathy or neuropathy through these RNST studies.


Subject(s)
Animals , Rats , Appointments and Schedules , Botulinum Toxins , Muscles , Muscular Diseases , Neuromuscular Junction , Paralysis , Rats, Sprague-Dawley
5.
Yeungnam University Journal of Medicine ; : 277-286, 2001.
Article in Korean | WPRIM | ID: wpr-73168

ABSTRACT

BACKGROUND: This study was undertaken to evaluate the diagnostic sensitivity of several muscles in repetitive nerve stimulation test (RNST) for myasthenia gravis (MG) patients. MATERIALS AND METHODS: The study population consisted of 39 MG patients classified by modified Ossermann's classification. Using Stalberg's method, RNST was systematically performed in facial (orbicularis oculi and nasalis) and upper extremity (flexor carpi ulnaris, abductor digiti quinti and anconeus) muscles. RESULTS: The significant electrodecremental response of RNST were noted in orbicularis oculi (58.9%), nasalis (51.3%), flexor carpi ulnaris (42%), anconeus (41%) and abductor digiti quinti muscles (27%). Among the 3 muscles of upper extremity (abductor digiti quinti, flexor carpi ulnaris and anconeus), the positive electrodecremental response of anconeus muscles was significantly higher than other two muscles (p<0.05) in type IIa, IIb and there were no statistical differences of the positive electrodecremental response between orbicularis oculi and nasalis muscles. The facial muscles showed more prominent decremental responses than upper extremity muscles in type I MG(p<0.05). In type IIa MG patients, there were no significant statistical differences between facial and upper extremity muscles but significant statistical differences among upper extremity muscles. In type IIb MG patients, there were no significant statistical differences in all tested muscles in spite of the increased positive electrodecremental response of RNST. CONCLUSION: On the basis of this study, RNST would be initially performed for the orbicularis or nasalis in type I MG and for the anconeus in type IIa or IIb MG.


Subject(s)
Humans , Classification , Facial Muscles , Muscles , Myasthenia Gravis , Upper Extremity
6.
Journal of the Korean Neurological Association ; : 425-430, 2000.
Article in Korean | WPRIM | ID: wpr-146858

ABSTRACT

BACKGROUND: The axonal stimulation single fiber electromyography (S-SFEMG) is a relatively new electrophysio-logical technique and has several advantages over conventional voluntarily activated single fiber electromyography (V-SFEMG). This study was performed in patients with myasthenia gravis (MG) in order to analyze their neuromuscular transmission defects and thus to verify the usefulness of the S-SFEMG technique. METHODS: In 44 patients with MG, S-SFEMG was performed on the extensor digitorum communis muscle. The repetitive nerve stimulation test (RNST) on orbicularis oculi, trapezius, flexor carpi ulnaris, and abductor digiti quinti muscles was also performed at the same time. The results of the RNS and S-SFEMG were then analysed in detail. RESULTS: The S-SFEMG was found abnormal in 84.1%, while RNST was found abnormal in 75.0% of the patients tested. The normal S-SFEMG result was observed exclusively among 7 ocular type MG patients. The mean of the mean consecutive difference (MCD) value, % of fibers with blocking and % of fibers with abnormal jitter, was more increased in patients with generalized type MG than those with ocular type MG. This difference was statistically significant (P<0.01) in all 3 variables. CONCLUSIONS The S-SFEMG is a highly sensitive and useful diagnostic tool in MG. Although it demands more strict technical consideration than V-SFEMG, it is less time-consuming and applicable to uncooperative patients including children. Our study shows S-SFEMG to be especially useful in patients with ocular type MG whose RNST results do not show definite decremen-tal responses.


Subject(s)
Child , Humans , Axons , Electromyography , Muscles , Myasthenia Gravis , Superficial Back Muscles
7.
Journal of the Korean Neurological Association ; : 319-325, 2000.
Article in Korean | WPRIM | ID: wpr-91903

ABSTRACT

BACKGROUND: The repetitive nerve stimulation (RNS) test is a useful tool in the evaluation of neuromuscular transmission disorders. In our laboratory, we frequently use Oh's method, which tests 5 kinds of muscles (flexor carpi ulnaris (FCU), abductor digiti quinti (ADQ), orbicularis oculi, nasalis and trapezius) with 3 kinds of low rate stimulation (LRS) and high rate stimulation (HRS). This method has the advantage of high sensitivity, but is time consuming and painful to patients. So, we tried to reestablish the stage of RNS to overcome this problem and to create a useful test. METHODS: We analyzed RNS data from 369 patients, retrospectively. The number of patients with myasthenia gravis (MG) was 357 and the number with myasthenic syndrome was 12. We compared the sensitivity of individual muscle as well as individual stimulation rate. And we analyzed the results of MG and myasthenic syndrome to verify the usefulness of HRS. RESULTS: The sensitivity of RNS (LRS) was 69.7% in MG (generalized symptom 86.4%, only ocular symptom 40.3%). The sensitivity was higher with 3 pps and 5 pps than with 2 pps, while the exclusion of 2 pps did not affect the sensitivity. We found only 3 cases (1.0%) with post-tetanic exhaustion (PTE) in MG patients with negative results on LRS. The distributions of resting CMAP and post-exercise CMAP were different between MG and myasthenic syndrome. In most cases of myasthenic syndrome, the resting CMAP of ADQ and FCU was below 4.0 mV and post-exercise CMAP of ADQ and FCU was above 50%. CONCLUSIONS: LRS may be done with only 3 and 5 pps, and HRS of the ulnar nerve was helpful only if there was a suspicion of myasthenic syndrome (resting CMAP50%, in ADQ & FCU) or a borderline decremental response in LRS.


Subject(s)
Humans , Muscles , Myasthenia Gravis , Neuromuscular Junction Diseases , Retrospective Studies , Ulnar Nerve
8.
Journal of the Korean Academy of Rehabilitation Medicine ; : 408-414, 1998.
Article in Korean | WPRIM | ID: wpr-723753

ABSTRACT

The low rate repetitive nerve stimulation test(RST) using the electric stimulation has been known the best procedure among the electroliagnostic evaluations for the neuromuscular transmission. However, the electric stimulation often causes a considerable discomfort and pain during the procedure. On the contrary, the magnetic stimulation is much easier and less painful in activating to activate the deep seated nerves. The purpose of this study was to compare the effect of repetitive magnetic and electric stimulation for the induction of compound muscle action potentials(CMAP) of abductor digiti quinti and deltoid muscles in 25 healthy subjects. The results were showed there were no significant differences in the amplitudes of CMAP of axillary and ulnar nerves between the magnetic and electric stimulations. And there were no significant differences in the decremental ratio of CMAP between the magnetic and electric stimulations. The magnetic stimulations were less painful for the subjects than electric stimulations in both proximal and distal muscles. In conclusion, the magnetic stimulation proved to be a useful method for repetitive nerve stimulations in the diagnosis of neuromuscular disease.


Subject(s)
Deltoid Muscle , Diagnosis , Electric Stimulation , Muscles , Neuromuscular Diseases , Ulnar Nerve
9.
Journal of the Korean Neurological Association ; : 366-371, 1998.
Article in Korean | WPRIM | ID: wpr-228312

ABSTRACT

BACKGROUND AND PURPOSE: For diagnosis of acquired autoimmune myasthenia gravis (MG), single fiber electromyography (SFEMG) is known to be much more sensitive than repetitive nerve stimulation test (RNST) in demonstrating the electrophysiological defects of neuromuscular transmission. Neuromuscular blocking in SFEMG is presumed to have the same physiologic basis with decremental response in RNST. The authors performed the study to know the correlations between the electrophysiological parameters of the RNST (decremental response) and the SFEMG (jitter and blocking) and to understand the basic physiological mechanisms in MG. METHODS: In 28 patients with definite MG (12 : ocular MG, 16 : generalized MG), RNST and SFEMG tests were done in orbicularis oculi and abductor digiti quinti and in extensor digitorum communis, respectively. The correlations between several factors, such as maximum decremental response (%) in RNST, mean value of mean consecutive differences (MCD's) (?sec) and blocking pairs (%) were analyzed. RESULTS: In 12 ocular MG patients, RNST and SFEMG abnormalities were found in 4 (33.3%) and in 10 (83.3%), respectively. In 16 generalized MG patients, abnormal decremental responses were found in 13 (81.3%) and increased jitters in 15 (93.8%). SFEMG showed significant correlations between blockings and mean MCD's (R=0.54, p<0.01). When the correlation between RNST and SFEMG was analyzed, increased percentage of blockings in extensor digitorum communis were correlated with maximum degree of decremental responses in abductor digiti quinti or orbicularis oculi (R=0.60, p<0.001). The degree of mean MCD's was poorly correlated with maximum decremental responses (R=0.23, p=0.229). But the correlation became significant (R=0.43, p<0.05) by analyzing mean MCD's and maximum decremental responses only from abductor digiti quinti, reflecting that blockings have similar electrophysiological meanings with increased mean MCD's. CONCLUSION: The good correlation between decremental response in RNST and blocking or mean MCD's in SFEMG was found. Therefore the authors concluded that the parameters of the RNST and the SFEMG show similar electrophysiologic phenomena of the abnormal neuromuscular transmission in MG.


Subject(s)
Humans , Diagnosis , Electromyography , Electrophysiological Phenomena , Myasthenia Gravis , Neuromuscular Blockade
10.
Journal of the Korean Academy of Rehabilitation Medicine ; : 772-783, 1997.
Article in Korean | WPRIM | ID: wpr-722880

ABSTRACT

Botulinum toxin develops muscular paralysis through the inhibition of acetylcholine release from presynaptic membrane in neuromuscular junction. It has been used clinically to treat strabismus, blepharospasm and spasmodic dysphonia. Recently it was introduced for the treatment of limb spasticity as well. Serial compound muscle action potential(CMAP) amplitudes were measured and repetitive nerve stimulation test(RNST) was performed with 2Hz and 30Hz on the rat gastrocnemius muscle to observe the effect of muscle paralysis. Also, Periodic acid Schiff (PAS) staining sections of the muscle for glycogen was studied to quantify the degree of muscular paralysis. Thirty Sprague-Dawley rats, 10 for control and 20 for experimental group were studied for 12 weeks. Normal saline 0.025 ml and 0.125 ml was injected into gastrocnemius muscle in cotrol group 1 and 2, respectively. Botulinum toxin type A(Botox) was injected 5.0U/0.025 ml in experimental group 1, 2.5U/0.025 ml in group 2, 2.5U/0.125 ml in group 3, and 0.5U/0.025 ml in group 4. The amplitudes of CMAP declined markedly by 81.1% to 96.5% of basal amplitudes on the first week after Botox injection, but slightly recovered on 12th week by 20.8% to 42.2% with greater recovery in lower dose group. RNST with 2Hz produced no remarkable 1 : 5 amplitude change in experimental group. RNST with 30Hz produced marked increment in 1 : 5 amplitude up to 24.4%. PAS staining for muscle sections showed residual glycogen after tetanic stimulation due to neuromuscular block by Botox.


Subject(s)
Animals , Rats , Acetylcholine , Action Potentials , Blepharospasm , Botulinum Toxins , Dysphonia , Extremities , Glycogen , Membranes , Muscle Spasticity , Muscle, Skeletal , Neuromuscular Blockade , Neuromuscular Junction , Paralysis , Periodic Acid , Rats, Sprague-Dawley , Strabismus
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