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Thyrotoxic periodic paralysis

Periodic paralysis - thyrotoxic

 

Thyrotoxic periodic paralysis is a condition in which there are episodes of muscle weakness . It occurs in people who have high levels of thyroid hormone in their blood ( hyperthyroidism , thyrotoxicosis).

Causes

 

This is a rare condition that occurs only in people with high thyroid hormone levels (thyrotoxicosis). It is common in Asian and Hispanic men.

There is a similar disorder, called hypokalemic , or familial, periodic paralysis. It is an inherited condition and not related to high thyroid levels.

Risk factors include a family history of periodic paralysis and hyperthyroidism.

 

Symptoms

 

Symptoms involve attacks of muscle weakness or paralysis .The attacks alternate with periods of normal muscle function. Attacks often begin after symptoms of hyperthyroidism have developed.

The frequency of attacks varies from daily to yearly. Episodes of muscle weakness may last for a few hours or several days.

The weakness or paralysis:

  • Comes and goes
  • Can last for up to several days
  • Is more common in the legs than the arms
  • Is most common in the shoulders and hips
  • Is triggered by heavy, high-carbohydrate, high-salt meals
  • Is triggered during rest after exercise

Other rare symptoms may include any of the following:

  • Difficulty breathing
  • Speech difficulty
  • Swallowing difficulty
  • Vision changes

People are alert during attacks and can answer questions. Normal strength returns between attacks. Muscle weakness may develop over time with repeated attacks.

Symptoms of hyperthyroidism include:

  • Excessive sweating
  • Fast heart rate
  • Fatigue
  • Headache
  • Heat intolerance
  • Increased appetite
  • Insomnia
  • More frequent bowel movements
  • Sensation of feeling a strong heartbeat ( palpitations )
  • Tremors of the hand
  • Warm, moist skin
  • Weight loss

 

Exams and Tests

 

The health care provider may suspect thyrotoxic periodic paralysis based on:

  • Abnormal thyroid hormone levels
  • A family history of the disorder
  • Low potassium level during attacks
  • Symptoms that come and go in episodes

Diagnosis involves ruling out disorders associated with low potassium.

The provider may try to trigger an attack by giving you insulin and sugar (glucose, which reduces potassium level) or thyroid hormone.

The following signs may be seen during the attack:

  • Decreased or no reflexes
  • Heart arrhythmias
  • Low potassium in the bloodstream ( serum potassium levels are normal between attacks)

Between attacks, the examination is normal. Or, there may be signs of hyperthyroidism, such as an enlarged thyroid changes in the eyes, tremor, hair and nail changes.

The following tests are used to diagnose hyperthyroidism:

  • High thyroid hormone levels ( T3 or T4 )
  • Low serum TSH (thyroid stimulating hormone) levels
  • Thyroid uptake and scan

Other test results:

  • Abnormal electrocardiogram ( ECG ) during attacks
  • Abnormal electromyogram ( EMG ) during attacks
  • Low serum potassium during attacks, but normal between attacks

A muscle biopsy may sometimes be taken.

 

Treatment

 

Potassium should also be given during the attack, usually by mouth. If weakness is severe, you may need to get potassium through a vein ( intravenously ). Note: You should only get intravenous potassium if your kidney function is normal and you are monitored in the hospital.

Weakness that involves the muscles used for breathing or swallowing is an emergency. People must be taken to a hospital. Serious irregularity of heartbeat may also occur during attacks.

Your provider may recommend a diet that is low in carbohydrates and salt to prevent attacks. Medicines called beta-blockers may reduce the number and severity of attacks while your hyperthyroidism is brought under control.

Acetazolamide is effective at preventing attacks in people with familial periodic paralysis . It is usually not effective for thyrotoxic periodic paralysis.

 

Outlook (Prognosis)

 

If an attack isn't treated and the breathing muscles are affected, death can occur.

Chronic attacks over time can lead to muscle weakness. This weakness can continue even between attacks if the thyrotoxicosis is not treated.

Thyrotoxic periodic paralysis responds well to treatment. Treating hyperthyroidism will prevent attacks and may even reverse muscle weakness.

 

Possible Complications

 

Untreated thyrotoxic periodic paralysis can lead to:

  • Difficulty breathing, speaking, or swallowing during attacks (rare)
  • Heart arrhythmias during attacks
  • Muscle weakness that gets worse over time

 

When to Contact a Medical Professional

 

Call the local emergency number (such as 911) or go to the emergency room if you have periods of muscle weakness. This is especially important if you have a family history of periodic paralysis or thyroid disorders.

Emergency symptoms include:

  • Difficulty breathing, speaking, or swallowing
  • Falls due to muscle weakness

 

Prevention

 

Genetic counseling may be advised. Treating the thyroid disorder prevents attacks of weakness.

 

 

Open References

References

Davies TF, Laurberg P, Bahn RS. Hyperthyroid disorders. In: Melmed S, Polonsky K, Larsen R, Kronenberg HM, eds. Williams textbook of Endocrinology . 13th ed. Philadelphia, PA: Elsevier; 2016:chap 12.

Ferri FF. Hyperthyroidism. In: Ferri FF, ed. Ferri's Clinical Advisor 2016 . Philadelphia, PA: Elsevier; 2016:672-673.

 
  • Thyroid gland

    Thyroid gland - illustration

    The thyroid gland, a part of the endocrine (hormone) system, plays a major role in regulating the body's metabolism.

    Thyroid gland

    illustration

    • Thyroid gland

      Thyroid gland - illustration

      The thyroid gland, a part of the endocrine (hormone) system, plays a major role in regulating the body's metabolism.

      Thyroid gland

      illustration

    A Closer Look

     

    Tests for Thyrotoxic periodic paralysis

     
     

    Review Date: 2/3/2016

    Reviewed By: Brent Wisse, MD, Associate Professor of Medicine, Division of Metabolism, Endocrinology & Nutrition, University of Washington School of Medicine, Seattle, WA. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.

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