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EMG protocol for periodic paralyses and myotonic syndromes diagnosis Long and repeated short exercise tests. Dr. Emmanuel Fournier La Salpêtrière Hospital, Paris, France. Overview of the protocol.
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EMG protocol for periodic paralyses and myotonic syndromes diagnosisLong and repeated short exercise tests Dr. Emmanuel Fournier La Salpêtrière Hospital, Paris, France
Overview of the protocol • The EMG protocol includes several tests performed successively or simultaneously in order to reduce the total examination duration : • Long (5 mn) exercise test on right hand, with post-exercise rest • Repeated short (10s, three times) exercise test performed two times, on left hand and on right foot • Needle electromyography of five muscles • References for the precise description of technical conditions, protocol and main results : • Fournier, E.M.Inter, Cachan, 1998, pp 253-262 • Fournier et al. Annals of Neurology, 2004, 56: 650-661 • Fournier, Rev Neurol (Paris), 2005, in press
Preparation • Three sets of surface recording electrodes are installed • Best stimulation and recording sites are located • Baseline compound muscle action potentials (CMAP) are recorded • Recording electrodes are left in the optimal position throughout the examination • The purposes are threefold : • Electrodes will serve to different exercise tests • A rapid nerve conduction study checks the absence of nerve alterations. If necessary, neuromuscular transmission is tested by 3 Hz repetitive nerve stimulation. • Baseline recordings would serve as reference values if an attack of paralysis occurs during the examination
Preparation (I, II, III) • Recording of the extensor digitorum brevis (EDB) muscle • Stimulation of the anterior tibial nerve • Electrodes will be used for one of the repeated short exercise tests • Recording of the left abductor digiti minimi (ADM) • Stimulation of the ulnar nerve • Electrodes will be used for one of the repeated short exercise tests • Recording of the right abductor digiti minimi (ADM) • Stimulation of the ulnar nerve • Electrodes will be used for the long exercise test
Preparation (IV) • A bandage prevents articulation displacements and changes in muscle volume during the exercise tests • Skin temperature is measured and must be maintained between 32 and 34°C throughout the EMG session • The purpose is to prevent any decrease in CMAP amplitude and area which could be caused by muscle warming during the examination
Long exercise test on right hand (I) • CMAP is monitored before exercise (top trace) • The subject is asked to spread the little finger as strong as possible against resistance during 5 minutes • Brief resting periods (2-3 seconds) are respected every 30-45 seconds to prevent ischemia • After completion of the exercise, the subject is instructed to completely relax while CMAP are recorded • 2 seconds immediately after cessation of exercise (second trace) • and then 30 seconds after (third trace)
Long exercise test (I)Normal changes immediately after exercise • Immediately after exercise cessation, normal results are : • Slightly decreased amplitude (-6 %) of the CMAP • Increased duration (+38 %) disappearing in 30 seconds • If the amplitude decline is more marked, it must be carefully checked that nerve stimulation is still supramaximal
Long exercise test (I)Immediate changes after exercise cessationin muscle channelopathies • Patients with Paramyotonia Congenita • Decreased CMAP amplitude • Presence of Post-exercise myotonic potentials (PEMP) • Patients with Periodic Paralysis • No change of the CMAP in most cases • Early decreased amplitude if an attack of paralysis has been triggered by the exercise achievement • Increased amplitude in patients with Hyperkalemic Periodic Paralysis, especially when pre-exercise CMAP amplitude was small
Long exercise test (II)Changes 1-5 minutes after exercise • CMAP is recorded every minute during the first 5 minutes after exercise cessation (traces 4-8 on the screen) • Normal results during this rest period are no change of the CMAP as compared with pre-exercise values : • Otherwise, it must be carefully checked that nerve stimulation is still supramaximal
Long exercise test (II)Changes 1-5 minutes after exercisein muscle channelopathies • Patients with Paramyotonia Congenita • Disappearance of PEMP, persistence of decreased CMAP amplitude • Patients with Periodic Paralysis • No change or progressive decline of CMAP amplitude • Persistence of the increased amplitude if previously present, in Hyperkalemic Periodic Paralysis
Continuation of the long exercise test • CMAP of the right ADM is recorded every 5 minutes during the 40 minutes rest after exercise cessation. • Recording electrodes and bandage are left on the right hand • During the 5 minutes interval between two recordings, different others tests are performed : • Repeated short exercise test on the left hand • Repeated short exercise test on the right foot • Search for myotonic discharges by needle-EMG
Repeated short exercise teston left hand (I) • A second bandage is installed on the left hand, and CMAP of the ADM is monitored before exercise (top trace) • The subject is asked to spread the little finger as strong as possible against resistance during 10 seconds • After completion of the exercise, the subject is instructed to completely relax while CMAP are recorded at rest : • 2 seconds immediately after cessation of exercise (second trace) • and then every 7-8 seconds for 50 seconds (traces 3-8 on the screen) • This sequence (10 s contraction - 50 s rest) is repeated three times
Repeated short exercise test (II)Normal CMAP changes after exercise • Immediately after exercise cessation, normal results are : • Slightly increased amplitude (+5 %) of the CMAP (second trace) • Return to pre-exercise values in 10 seconds (third and next traces) • If an amplitude decline appeared, it must be carefully checked that nerve stimulation is still supramaximal
Repeated short exercise test (II)CMAP changes between the exercisesin muscle channelopathies • Patients with myotonic syndromes • Presence of Post-exercise myotonic potentials (PEMP) immediately after the first short exercise, especially in Paramyotonia Congenita • Decrease in CMAP amplitude, worsening or disappearing with repeating exercise in Paramyotonia Congenita and Myotonia Congenita respectively • Patients with Periodic Paralysis • No change of the CMAP in most cases • Increased amplitude in patients with Hyperkalemic Periodic Paralysis, worsening with repeating exercise, especially when pre-exercise CMAP amplitude was small
Long exercise test (III) • Back to the right hand for recording CMAP of the ADM at 10 minutes rest after exercise cessation. • If an amplitude decline appeared, it must be carefully checked that nerve stimulation is still supramaximal
Repeated short exercise teston right foot • CMAP of the EDB is monitored before exercise (top trace) • The subject is asked to raise the toes as strong as possible against resistance during 10 seconds • After completion of the exercise, the subject is instructed to completely relax while CMAP are recorded at rest : • 2 seconds immediately after cessation of exercise (second trace) • and then every 7-8 seconds for 50 seconds (traces 3-8 on the screen) • This sequence (10 s contraction - 50 s rest) is repeated three times
Long exercise test (IV) • Back to the right hand for recording CMAP of the ADM at 15 minutes rest after exercise cessation. • If an amplitude decline appeared, it must be carefully checked that nerve stimulation is still supramaximal
Needle Electromyography • EMG recording of 5 muscles at rest and during voluntary contraction : • Deltoid • Extensor digitorum brevis • First interosseus dorsalis • Tibialis anterior • Vastus medialis • Searching for myotonic discharges : • Abundant in myotonic syndromes • Rare and inconstant in Hyperkalemic Periodic Paralysis • Absent in Hypokalemic Periodic Paralysis
End of the long exercise test (V) • Back to the right hand for recording CMAP of the ADM at 20, 25, 30, 35, 40 minutes rest after exercise cessation. • Changes in CMAP amplitude between -20 and +10 % of the pre-exercise value can be considered normal. • If an amplitude decline appeared, it must be carefully checked that nerve stimulation is still supramaximal
End of the long exercise test (V)Changes 20-40 minutes after exercisein muscle channelopathies • Patients with Paramyotonia Congenita • Progressive disappearance of the immediate post-exercise decline in CMAP amplitude • Patients with Periodic Paralysis • Progressive installation of a marked decline of CMAP amplitude of the right ADM • In some cases, a paralysis of the four limbs occurs during the post-exercise rest, with marked CMAP amplitude declines not only of the right ADM, but also of the left ADM and of the EDB.
Conclusion • Total duration of the protocol realization : 50 minutes • Preparation : 5 mn; Long exercise : 5 mn; Rest after long exercise with repeated short exercises and needle EMG : 40 mn • By comparing EMG findings and responses to long and repeated short exercise tests, five main patterns of muscle abnormalities could be defined (Type I-V), each of them corresponding to a defined group of ion channel mutations. • References for the results : • Fournier et al. Annals of Neurology, 2004, 56: 650-661 • Fournier, Rev Neurol (Paris), 2005, in press
Ackowledgments • Thanks to Ghislaine Therme for technical assistance and Nicolas Danziger for filming and comments. • This video tape was ordered and supported by Periodic Paralysis Association. • The work on muscle channelopathies was supported by Résocanaux and Association Française contre les Myopathies (AFM).