Hypokalemic periodic paralysis: Difference between revisions

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<big>'''Background'''</big><br />
===Background===
* Autosomal dominant channelopathy
*Autosomal dominant channelopathy<ref>June-Bum Kim, MD, PhD. Channelopathies. Korean J Pediatr. 2014 Jan;57(1):1-18 [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935107/ Full Text]</ref>
      * Symptoms include muscle weakness or paralysis with associated hypokalemia (though potassium levels can be normal), sometimes painful        
*Symptoms include muscle weakness or paralysis with associated hypokalemia (though potassium levels can be normal), sometimes painful though often painless. Weakness can be from hand to leg to complete paralysis.
        though often painless. Weakness can be from hand to leg to complete paralysis.
*Triggered by strenuous exercise, high carbohydrate meal, high sodium meals, sudden changes in temperature or emotional stress
              * Triggered by strenuous exercise, high carbohydrate meal, high sodium meals, sudden changes in temperature or emotional stress
*Attacks can last several hours to several days
              * Attacks can last several hours to several days
*Most first attacks happen by age 16
              * Most first attacks happen by age 16


<big>'''Differential Diagnosis'''</big>
===Differential Diagnosis===
      * Guillan Barre - Deep tendon reflexes spared, CN 7 spared
*[[Guillan Barre]] - Deep tendon reflexes spared, CN 7 spared
      * Thyrotoxic Periodic Paralysis - Distinguished by thyroid studies
*[[Thyrotoxic Periodic Paralysis]] - Distinguished by thyroid studies
      * Multiple Sclerosis
*[[Multiple Sclerosis]]
      * Myasthenia Gravis
*[[Myasthenia Gravis]]
      * Conversion Disorder
*[[Conversion Disorder]]
      * Spinal Impingement/Epidural Abscess
*Spinal Impingement/[[Epidural Abscess]]
      * ALS
*[[ALS]]


'''<big>Treatment</big>'''
===Treatment===
      * Replace potassium appropriately - do not try to correct to normal level as once the muscles release potassium you will likely overcorrect
*Replace potassium appropriately - do not try to correct to normal level as once the muscles release potassium you will likely overcorrect
      ''* Long Term Treatment:'' Should be initiated by PMD
*Long Term Treatment: Should be initiated by PMD
              * Avoid exacerbating factors
**Avoid exacerbating factors
              * Medications to increase potassium: Acetazolomide, Spironolactone, Potassium tablets,  
** Medications to increase potassium: Acetazolomide, Spironolactone, Potassium tablets,  


'''<big>Disposition</big>'''
===Disposition===


Can be discharged from ED after potassium repletion and resolution of symptoms.
Can be discharged from ED after potassium repletion and resolution of symptoms.


'''<big>See Also</big>'''
===See Also===


'''<big>Authors</big>'''
===Sources===
 
<references/>
[http://www.wikem.org/wiki/User:Dx316gol Babak Missaghi]

Revision as of 13:12, 16 January 2015

Background

  • Autosomal dominant channelopathy[1]
  • Symptoms include muscle weakness or paralysis with associated hypokalemia (though potassium levels can be normal), sometimes painful though often painless. Weakness can be from hand to leg to complete paralysis.
  • Triggered by strenuous exercise, high carbohydrate meal, high sodium meals, sudden changes in temperature or emotional stress
  • Attacks can last several hours to several days
  • Most first attacks happen by age 16

Differential Diagnosis

Treatment

  • Replace potassium appropriately - do not try to correct to normal level as once the muscles release potassium you will likely overcorrect
  • Long Term Treatment: Should be initiated by PMD
    • Avoid exacerbating factors
    • Medications to increase potassium: Acetazolomide, Spironolactone, Potassium tablets,

Disposition

Can be discharged from ED after potassium repletion and resolution of symptoms.

See Also

Sources

  1. June-Bum Kim, MD, PhD. Channelopathies. Korean J Pediatr. 2014 Jan;57(1):1-18 Full Text