Sunday, January 4, 2015

Primary Hyperaldosteronism



An issue that commonly arises in both the outpatient and inpatient settings is the combination of hypertension and hypokalemia. When should these patients be worked up for primary hyperaldosteronism? How do you work these patients up? Let's discuss the diagnosis and management

  • Primary aldosteronism commonly presents with hypertension and hypokalemia. However, normokalemia is present 50% of patients.
  • The most common causes of primary aldosteronism are aldosterone-producing adenomas (APAs) and bilateral adrenal hyperplasia.
  • Abnormally high release of aldosterone leads to an increased risk of cardiovascular disease and morbidity, including left ventricular hypertrophy, myocardial infarction and stroke.
  • 2008 Endocrine Society Guidelines, test for primary aldosteronism in patients with:
    • Hypertension and hypokalemia (diuretic induced-hypokalemia less than 3 or spontaneous hypokalemia less than 3.5.
    • Severe or resistant hypertension
    • Hypertension and an adrenal incidentaloma
    • Hypertension and a family history of early-onset hypertension or CVA age before the age of 40.
    • Hypertension and first-degree relatives with documented primary aldosteronism
  • The initial evaluation:
    • Measure plasma renin activity (PRA) or plasma renin concentration (PRC) and plasma aldosterone concentration.
    • In primary hyperaldosteronism, PRA and PRC are reduced and the plasma aldosterone concentration (PAC) is inappropriately high (approximately PAC/PRA greater than 20 (550 in SI units).
  • This ratio is not sufficient for a diagnosis. You then need suppression testing.
  • This can be performed with orally administered sodium chloride and measurement of urinary aldosterone excretion. Alternatively, it can be done with IV sodium chloride loading and measurement of the PAC. 

  • Once Primary Hyperaldosteronism is confirmed, adrenal CT is done to distinguish between aldosterone-secreting adenoma and bilateral hyperplasia. Adrenal CT will also help to asses for adrenocortical carcinoma.
  • When the CT scan is normal, shows bilateral abnormalities, or shows a unilateral abnormality but the patient is over age 35 years, adrenal venous sampling is recommended to confirm unilateral disease if the patient would like to pursue surgical management of their primary aldosteronism. 
  • The reason 35 years is a significant cut-off is because patients above this age are more likely to have non-functioning adenomas, so you may not be certain that the detected mass accounts for the elevated hyperaldosteronism.


1 comment:

  1. My Mum who was experiencing weight gain, hair loss and acne, bouts of chest and abdominal pain and several months of unrelenting headaches that no medicine could relieve, In fact, it got worse. saw various doctors they decided that the lab levels indicated nothing much at all, until we met a Doc. who did CT scan, and she was diagnosed with adrenocortical carcinoma. So after one year, A surgeon advice was to remove her tumor, along with her left kidney. she needed to see someone with extensive experience in treating adrenal gland tumors for the next phase of her treatment. Knowing she needed to get an answer once and for all, we looked up on the internet and saw someone who testified about Aryan herbal medicine which she took and she had no more symptoms since then. You can also contact him if interested at
    draryan500@gmail.com

    ReplyDelete