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Adrenal insufficiency

Anna Hogarth Met3B Englisch 15 Karten

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  1. 1What are the causes of primary adrenal failure?1) Addison's disease (80% in UK; autoimmune adrenalitis)
    2) TB (most common worldwide)
    3) Adrenal metastasis
    4) Lymphoma
    5) Opportunistic infections in HIV
    6) Adrenal haemmorhage (Waterhouse-Friederichson syndrome)
    7) Late onset congenital hyperplasia
  2. 2What are the causes of secondary adrenal failure? How does the presentation differ to that of primary adrenal insufficiency?1) Iatrogenic - long term steroid use leads to suppression of the HPA axis, only revealed on cessation of the steroids
    2) Hypothalamic-pituitary disease - rare
    No hyperpigmentation (as ACTH is low) and no impact on mineralocorticoid production
  3. 3How does primary adrenal insufficiency present?Mood: depression, psychosis
    GI: Nausea/vomiting/abdominal pain (ALWAYS suspect Addison's in unexplained nausea and vomiting)
    Pigmented palmar creases & buccal mucosa
    Postural hypotension
    Vitiligo (often sign of autoimmunity)
  4. 4How does an Addison's crisis present?1) Shock
    2) Metabolic alkalosis
    3) Hyponatremia and hyperkalemia
  5. 5What blood tests should be done when investigating adrenal insufficiency?1) Low sodium, high potassium
    2) Hypoglycaemia
    3) Uraemia
    4) Hypercalcaemia
    5) Eosinophilia
    6) Anaemia
  6. 6What tests are done to diagnose adrenal insufficiency and find the cause?1) Synacthen - measure cortisol, give tetracosactide 250 mcg IM, measure cortisol at +30 mins. If cortisol is >550 nmol/L, Addison's is excluded
    2) 9am ACTH - to confirm primary adrenal failure
    3) 21 hydroxylase adrenal antibodies (present in 80% of autoimmune disease)
    4) Plasma renin and aldosterone - assess mineralocorticoid status
    AXR/CXR - any signs of TB? If no autoantibodies found, can also perform adrenal CT, TB tests, histoplasma tests, and metastatic disease
  7. 7How is Addison's disease managed?1) ~15-25mg hydrocortisone daily in 2-3 doses, i.e. 10mg on waking, 5mg lunchtime - avoid giving late at night due to problems sleeping
    2) 50-200mcg fludrocortisone daily to correct postural hypertension and electrolyte imbalance, adjust both on clinical grounds.
  8. 8If there is poor response clinical response to treatment to Addison's, what should be done next?Check for associated coeliac disease i.e. thyroid and coeliac serology
  9. 9How much extra hydrocortisone should be taken before strenuous activity/exercise?5-10mg hydrocortisone
  10. 10How should medication doses change in illness, severe stress or injury?Doube dosage
  11. 11If a patient is vomiting, how can they self-manage?100mg injection
  12. 12What does follow up with Addison's patients entail?Yearly BP and U&E checks - also watch for autoimmune disease (e.g. pernicious anaemia)
  13. 13How is an Addisonian crisis managed?Always start treatment before waiting for lab results if clinical diagnosis has been made
    1) Blood tests for U&Es, glucose, cortisol and ACTH. May have high K+ and low Na+, ECG and calcium gluconate if necessary
    2) Hydrocortisone 100mg IM stat
    3) 0.9% saline 500ml bolus to correct hypotension and electrolytes, repeat as necessary
    4) Blood, urine and sputum culture and antibiotics as necessary
  14. 14How is Addison's crisis treatment continued?1) Monitor hypoglycaemia and give glucose as necessary
    2) Give hydrocortisone 100 mg/8h IM as necessary
    3) Change to oral steroids after 72 hours if the patient is well enough
    4) Consider fludrocortisone
  15. 15What are the precipitating factors in Addison's crisis?1) Infection
    2) Trauma
    3) Surgery
    4) Missed medication
    Remember that bilateral adrenal haemorrhage is an important cause (i.e. meningococcemia)

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Met3B (Endocrinology) Karteikarten am Adrenal insufficiency, erstellt von Anna Hogarth am 07/03/2020.
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