Myokymia Medication

  • Author: Suying Song; Chief Editor: Nicholas Lorenzo, MD   more...
 
Updated: Feb 3, 2012
 

Medication Summary

Phenytoin and carbamazepine have been proven to be effective in treating patients with generalized myokymia, specifically patients with continuous muscle fiber activity described by Isaacs syndrome. High therapeutic drug levels usually are required to reach satisfactory control of symptoms. EMG can objectively document the disappearance of myokymic discharges. Other medications, such as benzodiazepines, have been tried with no consistent benefit. Monitoring of potential adverse effects of phenytoin and carbamazepine and precautions for these drugs are no different from when they are used to treat epilepsy.

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Antiepileptic agents

Class Summary

These agents prevent seizure recurrence and terminate clinical and electrical seizure activity.

Phenytoin (Dilantin)

 

Has promising results in patients with Isaacs syndrome. Relieves cramps and pain of involved muscles. EMG can document objective resolution of myokymic discharges. Mechanism of action possibly related to its effect on sodium channel.

Dosage adjusted according to blood level. Target level should be at high therapeutic range.

Carbamazepine (Tegretol)

 

Has promising results in patients with Isaacs syndrome. Relieves cramps and pain of involved muscles. EMG can document objective resolution of myokymic discharges. Mechanism of action possibly related to its effect on sodium channel.

Dosage adjusted according to blood level. Target level should be at high therapeutic range.

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Contributor Information and Disclosures
Author

Suying Song  MD, Assistant Clinical Professor, Department of Neurology, NYU Medical Center

Suying Song is a member of the following medical societies: American Academy of Neurology and American Association of Neuromuscular and Electrodiagnostic Medicine

Disclosure: Nothing to disclose.

Specialty Editor Board

Carmel Armon, MD, MSc, MHS  Professor of Neurology, Tufts University School of Medicine; Chief, Division of Neurology, Baystate Medical Center

Carmel Armon, MD, MSc, MHS is a member of the following medical societies: American Academy of Neurology, American Academy of Sleep Medicine, American Association of Neuromuscular and Electrodiagnostic Medicine, American Clinical Neurophysiology Society, American College of Physicians, American Epilepsy Society, American Medical Association, American Neurological Association, American Stroke Association, Massachusetts Medical Society, Movement Disorders Society, and Sigma Xi

Disclosure: Avanir Pharmaceuticals Consulting fee Consulting

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

Neil A Busis, MD  Chief, Division of Neurology, Department of Medicine, Head, Clinical Neurophysiology Laboratory, University of Pittsburgh Medical Center-Shadyside

Neil A Busis, MD is a member of the following medical societies: American Academy of Neurology and American Association of Neuromuscular and Electrodiagnostic Medicine

Disclosure: Nothing to disclose.

Selim R Benbadis, MD  Professor, Director of Comprehensive Epilepsy Program, Departments of Neurology and Neurosurgery, Tampa General Hospital, University of South Florida College of Medicine

Selim R Benbadis, MD is a member of the following medical societies: American Academy of Neurology, American Academy of Sleep Medicine, American Clinical Neurophysiology Society, American Epilepsy Society, and American Medical Association

Disclosure: UCB Pharma Honoraria Speaking, consulting; Lundbeck Honoraria Speaking, consulting; Cyberonics Honoraria Speaking, consulting; Glaxo Smith Kline Honoraria Speaking, consulting; Pfizer Honoraria Speaking, consulting; Sleepmed/DigiTrace Honoraria Speaking, consulting

Chief Editor

Nicholas Lorenzo, MD  Consulting Staff, Neurology Specialists and Consultants

Nicholas Lorenzo, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Neurology, and American College of Physician Executives

Disclosure: Nothing to disclose.

References
  1. Schultze F. Beitrage zur Muskelpathologie. Deutsch Z Nervenheilk. 1895;6:65-167.

  2. Kny E. Ueber ein dem Paramyoclonus multiplex (Friedreich) nahestehendes Krankheitsbild. Arch Psychiat Nervenkr. 1888;19:577.

  3. Jackson DL, Satya-Murti S, Davis L, Drachman DB. Isaacs syndrome with laryngeal involvement: an unusual presentation of myokymia. Neurology. Dec 1979;29(12):1612-5. [Medline].

  4. Isaacs H. A syndrome of continuous muscle-fibre activity. J Neurol Neurosurg Psychiat. 1961;24:319-325.

  5. Doi H, Arimura K, Ohyagi Y, Kira J. Frostbite-like skin lesion as an autonomic symptom of Isaacs' syndrome. Intern Med. 2011;50(10):1113-5. [Medline].

  6. Hayashi Y, Kimura A, Watanabe N, Yamada M, Sakurai T, Tanaka Y, et al. Serial monitoring of basal metabolic rate for therapeutic evaluation in an Isaacs' syndrome patient with chronic fluctuating symptoms. Intern Med. 2010;49(5):475-7. [Medline].

  7. Daube JR, Kelly JJ, Martin RA. Facial myokymia with polyradiculoneuropathy. Neurology. May 1979;29(5):662-9. [Medline].

  8. Alapati A, Glaussen G, Oh SJ. Myokymia as an initial and predominant manifestation of dermatomyositis. AAEM Abstracts. 1999;95.

  9. Albers JW, Allen AA, Bastron JA, Daube JR. Limb myokymia. Muscle Nerve. Nov-Dec 1981;4(6):494-504. [Medline].

  10. Andermann F, Cosgrove J, Lloyd-Smith DL. Facial myokymia in multiple sclerosis. Brain. 1961;84:31-44.

  11. Brick JF, Gutmann L, McComas CF. Calcium effect on generation and amplification of myokymic discharges. Neurology. Jun 1982;32(6):618-22. [Medline].

  12. Denny-Brown D, Foley JM. Myokymia and the benign fasciculation of muscular cramps. Trans Assoc Am Physicians. 1948;61:88-96.

  13. Gardner-Medwin D, Walton JN. Myokymia with impaired muscular relaxation. Lancet. Jan 18 1969;1(7586):127-30. [Medline].

  14. Greenhouse AH, Bicknell JM, Pesch RN, Seelinger DF. Myotonia, myokymia, hyperhidrois and wasting of muscle. Neurology. Mar 1967;17(3):263-8. [Medline].

  15. Gutmann L, Gutmann L. Myokymia and neuromyotonia 2004. J Neurol. Feb 2004;251(2):138-42. [Medline].

  16. Hudson AJ, Brown WF, Gilbert JJ. The muscular pain-fasciculation syndrome. Neurology. Nov 1978;28(11):1105-9. [Medline].

  17. Isaacs H. Continuous muscle fibre activity in an Indian male with additional evidence of terminal motor fibre abnormality. J Neurol Neurosurg Psychiatry. Apr 1967;30(2):126-33. [Medline].

  18. Isaacs H, Frere G. Syndrome of continuous muscle fibre activity. Histochemical, nerve terminal and end-plate study of two cases. S Afr Med J. Aug 10 1974;48(38):1601-7. [Medline].

  19. Lance JW, Burke D, Pollard J. Hyperexcitability of motor and sensory neurons in neuromyotonia. Ann Neurol. Jun 1979;5(6):523-32. [Medline].

  20. Lublin FD, Tsairis P, Streletz LJ, et al. Myokymia and impaired muscular relaxation with continuous motor unit activity. J Neurol Neurosurg Psychiatry. Jun 1979;42(6):557-62. [Medline].

  21. Lutschg J, Jerusalem F, Ludin HP, et al. The syndrome of 'continuous muscle fiber activity.'. Arch Neurol. Apr 1978;35(4):198-205. [Medline].

  22. Matthews WB. Facial myokymia. J Neurol Neurosurg Psychiatry. Feb 1966;29(1):35-9. [Medline].

  23. Medina JL, Chokroverty S, Reyes M. Localized myokymia caused by peripheral nerve injury. Arch Neurol. Aug 1976;33(8):587-8. [Medline].

  24. Parry-Jones NO, Stephens JA, Taylor A, Yates DA. Myokymia, not myotonia. Br Med J. Jul 30 1977;2(6082):300. [Medline].

  25. Roth G. The origin of fasciculations. Ann Neurol. Dec 1982;12(6):542-7. [Medline].

  26. Solimena M, Folli F, Denis-Donini S, et al. Autoantibodies to glutamic acid decarboxylase in a patient with stiff-man syndrome, epilepsy, and type I diabetes mellitus. N Engl J Med. Apr 21 1988;318(16):1012-20. [Medline].

  27. Valenstein E, Watson RT, Parker JL. Myokymia, muscle hypertrophy and percussion "myotonia" in chronic recurrent polyneuropathy. Neurology. Nov 1978;28(11):1130-4. [Medline].

  28. Wallis WE, Van Poznak A, Plum F. Generalized muscular stiffness, fasciculations, and myokymia of peripheral nerve origin. Arch Neurol. May 1970;22(5):430-9. [Medline].

  29. Welch LK, Appenzeller O, Bicknell JM. Peripheral neuropathy with myokymia, sustained muscular contraction, and continuous motor unit activity. Neurology. Feb 1972;22(2):161-9. [Medline].

  30. Williamson E, Brooke MH. Myokymia and the motor unit. A histochemical study. Arch Neurol. Jan 1972;26(1):11-6. [Medline].

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