This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages without signing in

Investigation

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Investigations include:

  • biochemistry
    • damage to adrenal cortex results in mineralocorticoid deficiency causing low serum sodium, and raised serum potassium and H+ (1)
    • serum urea and albumin are raised because of dehydration
    • serum renin is raised due to sodium depletion.
    • in secondary hypoadrenalism, electrolytes are usually normal as aldosterone-secreting cells are normal
  • serum cortisol level (ideally between 8-9 am)
    • random measurements have a low sensitivity for Addison's disease due to the pulsatile nature and diurnal variation of cortisol secretion (2)
    • if level of serum cortisol is
      • <100 nanomol/L - adrenal insufficiency is highly likely ( if the patient is not on oral or inhaled steroids)
      • >400 nanomol/L - adrenal insufficiency is unlikely (diagnosis is not excluded if the patient is acutely unwell at the time since cortisol values may increase during illness)
      • between 100 and 400 nanomol/L - refer to a specialist for further investigations e.g. - synacthen test (1)
  • blood glucose may be low - insulin-induced hypoglycaemia

  • possible ECG findings are detailed - click here

Secondary care investigations carried out to confirm the diagnosis and to find the cause nclude:

  • plasma rennin (1)
  • markedly elevated plasma ACTH - greater than 80 ng per litre - with low or normal serum cortisol on presentation or in the morning after omitting replacement therapy is an early indication of primary hypoadrenalism
  • synacthen test:
    • short test may confirm suspected hypoadrenalism
    • depot test may discriminate primary and secondary causes
  • adreno-cortical antibodies - often present in autoimmune adrenalitis - more common in women - 80% - than men - 10%
  • abdominal film - calcified adrenals of tuberculosis
  • chest radiology - tuberculous lesions, areas of malignancy and calcification
  • clinical or serological evidence of other organ specific autoimmune disease

Reference:


Related pages

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.