Diferencia entre revisiones de «Adrenal crisis»

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- fever, hypoTN (refractory to fluids), hyperpigmentation by increased ACTH
* Major factor precipitating adrenal crisis is mineralocorticoid, not glucocorticoid, deficiency
* Major clinical problem is hypotension
* Most commonly presents as shock


- cushingoid look by chronic steroid use
==Clinical Manifestations==


- think about in kids with congenital adrenal hyperplasia (CAH) who present with shock


* Hypotension
* Refractory to fluids
* Volume depletion
* Abdominal tenderness
* Usually generalized
* Fever
* Usually caused by infection (source must be identified and treated)
   
   


==Workup==
Lab tests


* Hyperkalemia
* Hyponatremia


labs (istat)
fever, hypoTN (refractory to fluids), hyperpigmentation by increased ACTH


- hypoNa (by increased ADH)
- cushingoid look by chronic steroid use


- hyperK
- think about in kids with congenital adrenal hyperplasia (CAH) who present with shock
 
- azotemia


   
   


==Treatment==
==Workup==




Steroids, Steroids, Steroids
* Chemistry/glucose
* Guides therapy
* Cortisol level
* Confirms diagnosis
* Renin, ACTH
* For evaluating differential diagnosis if cortisol level normal 


2 mg/kg of hydrocortisone
Treatment==


- Fludrocort, not as necessary since hydrocort has glucocorticoid activity


Treat underlying cause
* Do not wait for lab results to start treatment
* Fluids
* Infuse 2-3L of NS or D5NS (to correct hypoglycemia)
* Avoid hypotonic fluids (may worsen hyponatremia)
* Glucocorticoids
* Patient without previous diagnosis of adrenal insufficiency
* Dexamethasone 4mg IV bolus is preferred tx
* Patient with known primary adrenal insufficiency w/ potassium > 6
* Hydrocortisone 100mg IV bolus (preferred due to its mineralcorticoid activity)
* Mineralocorticoids are not indicated in acute management
* Treat underlying cause  
== ==




==Source ==
==Source ==




7/2/09 PANI (Adapted from Mistry)
7/2/09 PANI (Adapted from Mistry), UpToDate





Revisión del 23:38 1 mar 2011

Diagnosis

  • Major factor precipitating adrenal crisis is mineralocorticoid, not glucocorticoid, deficiency
  • Major clinical problem is hypotension
  • Most commonly presents as shock


Clinical Manifestations

  • Hypotension
  • Refractory to fluids
  • Volume depletion
  • Abdominal tenderness
  • Usually generalized
  • Fever
  • Usually caused by infection (source must be identified and treated)


Lab tests

  • Hyperkalemia
  • Hyponatremia


fever, hypoTN (refractory to fluids), hyperpigmentation by increased ACTH

- cushingoid look by chronic steroid use

- think about in kids with congenital adrenal hyperplasia (CAH) who present with shock


Workup

  • Chemistry/glucose
  • Guides therapy
  • Cortisol level
  • Confirms diagnosis
  • Renin, ACTH
  • For evaluating differential diagnosis if cortisol level normal


Treatment==


  • Do not wait for lab results to start treatment
  • Fluids
  • Infuse 2-3L of NS or D5NS (to correct hypoglycemia)
  • Avoid hypotonic fluids (may worsen hyponatremia)
  • Glucocorticoids
  • Patient without previous diagnosis of adrenal insufficiency
  • Dexamethasone 4mg IV bolus is preferred tx
  • Patient with known primary adrenal insufficiency w/ potassium > 6
  • Hydrocortisone 100mg IV bolus (preferred due to its mineralcorticoid activity)
  • Mineralocorticoids are not indicated in acute management
  • Treat underlying cause

Source

7/2/09 PANI (Adapted from Mistry), UpToDate