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Author: Jonathan B Strober, MD, Director, Pediatric Muscular Dystrophy Association Clinic; Assistant Clinical Professor, Departments of Pediatrics and Neurology, Division of Child Neurology, University of California at San Francisco

Jonathan B Strober is a member of the following medical societies: American Academy of Neurology, American Academy of Pediatrics, Child Neurology Society, and Society for Pediatric Research

Editors: Stephen T Gancher, MD, Adjunct Associate Professor, Department of Neurology, Oregon Health Sciences University; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Nestor Galvez-Jimenez, MD, Program Director of Movement Disorders, Department of Neurology, Division of Medicine, Director of Neurology Residency Training Program, Cleveland Clinic Florida; Matthew J Baker, MD, Consulting Staff, Collier Neurologic Specialists, Naples Community Hospital; Nicholas Y Lorenzo, MD, Chief Editor, eMedicine Neurology; Consulting Staff, Neurology Specialists and Consultants

Author and Editor Disclosure

Synonyms and related keywords: focal hand dystonia, graphospasm, musician's cramp, writer's cramp, focal dystonia, dystonic conditions, repetitive movements, spinal reciprocal inhibition

Background

Writer's cramp is a form of task-specific focal dystonia. Dystonia is an involuntary, sustained muscle contraction causing twisting movements and abnormal postures; focal dystonia means only one body part is affected. Writer's cramp is the most common dystonia occurring in the setting of repetitive movement disorders. A focal dystonia can sometimes be the first manifestation of a generalized dystonia.

Pathophysiology

Normally, an antagonist muscle relaxes when an agonist muscle is contracted. Patients with dystonia have simultaneous contraction of both groups of muscles. Spinal reciprocal inhibition, a process that inhibits the antagonist muscles when the agonist muscles are active, is reduced in patients with writer's cramp. This is most probably due to aberrant descending commands.

Abnormalities in the basal ganglia lead to abnormalities of sensory processing and motor output. The normal increase in cerebral blood flow in the supplementary motor area is reduced in response to vibration and abnormal somatosensory evoked potentials. These provide evidence for the abnormal sensory processing in patients with dystonia. Increased motor cortex excitability along with decreased cortical inhibition causes abnormal motor output.

Frequency

United States

One study estimated the prevalence to be 69 cases per 100,000 population; this is thought to be an underestimation because a high percentage of patients never seek medical assistance.

International

Again, because of the small percentage of affected patients seeking medical attention, accurate prevalence estimates are not available.

Sex

Prevalence is slightly higher in men; the male-to-female ratio is 1.3:1.

Age

Typically, patients present in the third to fifth decades, and women usually present earlier than men.



History

  • Incoordination, cramping, and aching of the hand with task-specific movements are usually the initial complaints.
  • The hand assumes a semiflexed position of the fingers with possible hyperextension of the fingers and hyperflexion or extension of the wrist with supination or pronation.
  • The symptoms become exaggerated with attempts to perform a specific task, such as writing. In some cases, the hand may dart across the page with a sudden jerk.
  • A related condition is primary writing tremor. Affected individuals exhibit a prominent large-amplitude tremor only with writing.

Physical

  • Neurologic examination findings are usually normal.
  • Subtle findings include mild dystonic postures developing either spontaneously or with movement and reduced arm swing.
  • One third of patients have a tremor in the affected arm or hand while writing or when the extremity is outstretched. Observation of the limb during writing is an important part of the examination; the assumption of dystonic postures should be demonstrable. Patients affected with primary writing tremor, a variant of writer's cramp, may exhibit a large-amplitude tremor only during writing. In contrast to essential tremor, action or sustentation tremors are not seen with other tasks such as holding a full cup of liquid or coordination testing. Dystonic posturing is usually not seen with this condition.

Causes

  • Writer's cramp frequently affects persons who write a great deal or perform other repetitive hand movements such as typing.
  • Approximately 5% of patients have a positive family history of a similar condition.
  • Five to ten percent report an accident or injury to the hand or arm immediately preceding the onset of symptoms.
  • Several possible, but rare, associations have been reported, including C6 ruptured disk, lithium use, basal ganglia or cortical tumors, arteriovenous malformations (AVMs), and stroke. However, most cases are idiopathic.



Dopamine-Responsive Dystonia
Multiple Sclerosis
Parkinson Disease
Wilson Disease

Other Problems to be Considered

Primary writing tremor
Postural tremor
Idiopathic torsion dystonia



Imaging Studies

  • MRI - If a structural lesion is suspected

Procedures

  • Electromyography/nerve conduction studies
    • To evaluate for nerve injury, if trauma is the suspected cause
    • Confirm diagnosis by showing simultaneous contraction of agonist and antagonist muscles



Medical Care

  • Approximately 5% of patients have spontaneous remission, most probably in the first 5 years. However, the majority of these patients have relapses.
  • Treatment is generally disappointing.
  • Transcutaneous electrical nerve stimulation (TENS) delivered to the forearm flexor muscles for a 2-week period has been found to improve symptoms for up to 3 weeks after treatment.
  • Behavioral changes may help.
  • Biofeedback, hypnotherapy, and relaxation therapy have been tried.

Activity

  • Altering the grip of the pen and/or increasing the diameter of the pen used is the first step in treatment.
  • Patients can use a writing device or other means of transcription, such as typing or dictation.



Several classes of drugs have been used in patients with writer's cramp. Anticholinergics have had conflicting results. Beta-blockers have helped the tremor in a few patients. Botulinum toxin injections seem to have the best results.

Drug Category: Anticholinergic

Blocking cholinergic innervation of the basal ganglia is hypothesized to increase the dopaminergic effect, thereby reducing dystonia.

Drug NameTrihexyphenidyl (Artane)
DescriptionSubstituted piperidine that inhibits parasympathetic system. Available as 2 mg tab or 2 mg/5 cc elixir.
Adult DoseStart with 1 mg PO qd, then increase by 2 mg at intervals of 3-5 d up to 6-15 mg/d divided tid
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity; glaucoma; peptic ulcer; pyloric or duodenal obstruction; stenosing prostatic hypertrophy or bladder neck obstructions; achalasia; toxic megacolon
InteractionsAmantadine may increase anticholinergic adverse effects, which disappear when dose reduced; when taken with haloperidol, may decrease haloperidol serum concentration, resulting in worsening of schizophrenic symptoms; may reduce pharmacologic/therapeutic actions of phenothiazines
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsDose adjustment may be required in geriatric patients; caution in patients with tachycardia, cardiac hypotension, prostatic hypertrophy, arrhythmias, hypertension, or any tendency toward urinary retention, liver or kidney disorders, or obstructive disease of GI or GU tract; if dry mouth severe and impairs swallowing or speaking, or if loss of appetite and weight occurs, reduce dosage or discontinue medication temporarily

Drug Category: Beta-adrenergic blockers

These agents help reduce the tremor.

Drug NamePropranolol (Inderal, Betachron E-R)
DescriptionClass II antiarrhythmic, nonselective, beta-adrenergic, receptor blocker with membrane-stabilizing activity that decreases automaticity of contractions. Available as 10 mg, 20 mg, 40 mg, and 80 mg tablets and 60 mg, 80 mg, 120 mg, and 160 mg long-acting tablets (Inderal LA)
Adult Dose40 mg PO bid initially; increase as tolerated; not to exceed 240-320 mg/d divided bid/tid
Pediatric Dose2-4 mg/kg PO divided bid; increase as tolerated; not to exceed 16 mg/kg/d
ContraindicationsDocumented hypersensitivity; uncompensated congestive heart failure; bradycardia; cardiogenic shock; AV conduction abnormalities
InteractionsAluminum salts, barbiturates, NSAIDs, penicillins, calcium salts, cholestyramine, and rifampin may decrease effects; calcium channel blockers, cimetidine, loop diuretics, and MAOIs may increase toxicity; may increase toxicity of hydralazine, haloperidol, benzodiazepines, and phenothiazines
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsMay decrease signs of acute hypoglycemia and hyperthyroidism; abrupt withdrawal may exacerbate symptoms of hyperthyroidism, including thyroid storm; withdraw drug slowly and monitor closely

Drug Category: Neurotoxins

Neurotoxin complex blocks neuromuscular conduction by binding to receptor sites on motor nerve terminals, entering the nerve terminals, and inhibiting the release of acetylcholine. When injected intramuscularly, it produces a localized chemical denervation muscle paralysis.

Drug NameBotulinum toxin type A (BOTOX®)
DescriptionLocal intramuscular injections weaken overactive muscles, reducing dystonic symptoms.
Adult DoseInjections usually given under EMG guidance and should be administered by physicians experienced in giving the injections
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity
InteractionsAminoglycosides or drugs that interfere with neuromuscular transmission may potentiate effects
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsDo not exceed recommended dosages and frequencies of administration; presence of antibodies to botulinum toxin type A may reduce effects of therapy; not known if toxin excreted in breast milk



Prognosis

  • The prognosis is good.

Patient Education

  • Patients should reduce the task-specific activities that precipitate the condition.



Medical/Legal Pitfalls

  • Do not consider patients with writer's cramp and other action dystonias as having a psychiatric disorder. This could deprive the patient of evaluation by a movement disorder specialist and hence the benefit of adequate treatment. Patients with writer's cramp do not have a higher incidence of psychiatric disorder than the general population.



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Writer's Cramp excerpt

Article Last Updated: Nov 2, 2006