Hyperaldosteronism: Difference between revisions

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==Management==
==Management==
 
In the Emergency Department:
* Correct hypokalemia (PO or IV potassium)
*
* Avoid ACE inhibitors/ARBs until potassium is corrected
*
* Manage hypertension per usual protocols (IV meds if emergent)
*
* Initiate cardiac monitoring if K⁺ <3.0 mEq/L or if arrhythmia is present


==Disposition==
==Disposition==

Revision as of 23:45, 5 May 2025

Background

Hyperaldosteronism refers to a condition of excess aldosterone secretion, typically leading to sodium retention, potassium excretion, and metabolic alkalosis. It is categorized into:

  • Primary hyperaldosteronism (Conn syndrome) – autonomous overproduction of aldosterone, most commonly from an adrenal adenoma or bilateral adrenal hyperplasia.
  • Secondary hyperaldosteronism – due to increased renin from conditions like renal artery stenosis, heart failure, or cirrhosis.

Primary hyperaldosteronism is an important and potentially reversible cause of secondary hypertension, accounting for 5–10% of hypertensive cases and up to 20% of treatment-resistant hypertension. It is often underdiagnosed in emergency settings.

Clinical Features

  • Hypertension (often severe or resistant)
  • Hypokalemia, which may manifest as:
    • Weakness
    • Fatigue
    • Muscle cramps
    • Constipation
    • Paresthesia
  • Polyuria and polydipsia
  • Metabolic alkalosis (less commonly symptomatic)
  • Headache or nonspecific complaints
  • Asymptomatic in some patients

Differential Diagnosis

  • Essential hypertension
  • Cushing’s syndrome
  • Pheochromocytoma
  • Renal artery stenosis
  • Diuretic or laxative use
  • Liddle syndrome
  • Bartter/Gitelman syndromes
  • Chronic licorice ingestion

Evaluation

Workup

Consider hyperaldosteronism in ED patients with:

  • Severe or refractory hypertension
  • Unexplained hypokalemia
  • Metabolic alkalosis

Recommended ED labs:

  • Electrolytes (noting hypokalemia and alkalosis)
  • Creatinine/BUN
  • ECG (look for U waves, flattened T waves, arrhythmias)
  • ABG or venous blood gas (if alkalosis suspected)
  • Urine potassium (if available)

Diagnosis

Clinical suspicion in setting of hypertension + hypokalemia

Confirmatory outpatient testing with PAC/PRA ratio

Further endocrinology-guided evaluation determines surgical vs. medical management

Management

In the Emergency Department:

  • Correct hypokalemia (PO or IV potassium)
  • Avoid ACE inhibitors/ARBs until potassium is corrected
  • Manage hypertension per usual protocols (IV meds if emergent)
  • Initiate cardiac monitoring if K⁺ <3.0 mEq/L or if arrhythmia is present

Disposition

See Also

External Links

References