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Ep 31 – Diagnosing and managing Addison’s disease in primary care

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Posted 13 Aug 2021

Dr Kevin Fernando

In this episode, Kevin discusses the case of Louise, a 19-year-old who has been living with type 1 diabetes for the last 12 years and hypothyroidism for the last 8 years. She presents to us in primary care with a history of recurring unexplained hypoglycaemic episodes despite proactive adjustments to her insulin regimen. In addition to her insulin, she is taking levothyroxine 150 μg/day. She has not recently made significant changes to her diet or daily physical activity. Louise has also been experiencing light-headedness when rising from a sitting position. She has a BMI of 19 kg/m2, and a recent HbA1c value was 63 mmol/mol (7.9%). You record her sitting blood pressure as 119/67 mmHg and her standing value as 99/72 mmHg. You notice some patches of vitiligo on her face. What should we do next?

 


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Key take-home messages from the episode:

  • If there is recurrent unexplained hypoglycaemia or diabetic ketoacidosis in a person living with type 1 diabetes (T1D), think Addison’s disease.
  • An unexplained reduction of total insulin dose >15–20% (due to frequent hypoglycaemia) in a person living with T1D should also raise suspicion of Addison’s disease.
  • Abnormal pigmentation in those with T1D warrants further investigation of adrenocortical function.
  • Electrolyte abnormalities are often not present until an advanced stage; 20–30% of individuals do not have hyponatraemia or hyperkalaemia at any time.
  • The diagnosis of adrenocortical insufficiency also requires simultaneous investigation of thyroid function and thyroid autoantibodies: 25% of those with Addison’s disease also have hypothyroidism.
  • As a "rule of thumb", double the hydrocortisone dose during illness until recovery and add 5–10 mg to the usual regimen before any strenuous exercise.
  • A random cortisol is of limited clinical value when testing for cortisol excess.
  • Deficiency is highly unlikely if 9am cortisol >400–475 nmol/L. However, levels of 150–400 nmol/L require further investigation; and levels <150 nmol/L require urgent discussion with, or referral to, endocrinology.

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