What is the protocol for a fludrocortisone (Florinef) suppression test to diagnose primary aldosteronism?

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Fludrocortisone Suppression Test Protocol for Primary Aldosteronism

The fludrocortisone suppression test (FST) protocol involves administering fludrocortisone 0.1 mg every 6 hours for 4 days along with oral salt loading, followed by measurement of upright plasma aldosterone levels to confirm primary aldosteronism when levels fail to suppress below the threshold value. 1

Standard Protocol

The standard fludrocortisone suppression test protocol consists of:

  1. Preparation:

    • Patient should be on a high-sodium diet (200 mEq/day) prior to and during the test 2
    • Potassium levels should be monitored and supplemented as needed to maintain normal range
  2. Administration:

    • Fludrocortisone dose: 0.1 mg orally every 6 hours (total 0.4 mg daily) for 4 days 1, 3
    • Concurrent oral salt loading during the test period
    • Maintain adequate potassium levels throughout testing
  3. Monitoring:

    • Measure baseline plasma aldosterone and renin levels before starting fludrocortisone
    • Monitor blood pressure and serum potassium daily during the test
    • Watch for hypokalemia, which is a common complication requiring supplementation
  4. Sampling and Interpretation:

    • On day 4, measure upright plasma aldosterone levels at 10 AM 4
    • Positive test: Failure of aldosterone to suppress below 165 pmol/L (approximately 6 ng/dL) 4, 3
    • This confirms the diagnosis of primary aldosteronism

Clinical Considerations

  • Medication Adjustments: Medications that affect the renin-angiotensin-aldosterone system should be discontinued before testing:

    • Spironolactone, eplerenone: at least 4-6 weeks prior
    • ACE inhibitors, ARBs, diuretics: at least 2 weeks prior
    • Beta-blockers, central alpha-2 agonists: at least 1 week prior
  • Safety Precautions:

    • Regular monitoring of blood pressure is essential as sodium loading may exacerbate hypertension
    • Potassium levels must be checked daily and supplemented aggressively if low
    • The test should be performed in an inpatient setting for patients with severe hypertension or heart failure
  • Alternative Testing:

    • If FST is not feasible, seated saline suppression testing (SSST) offers a reliable alternative with high sensitivity (87%) and specificity (94%) 3
    • SSST is less complicated and less expensive than FST while maintaining diagnostic accuracy 3

Comparative Effectiveness

  • FST is generally considered the gold standard confirmatory test for primary aldosteronism 1, 5
  • Seated saline suppression testing (SSST) has emerged as a reliable alternative with comparable diagnostic accuracy 3
  • SSST is more sensitive than recumbent saline suppression testing (RSST), particularly for posture-responsive forms of primary aldosteronism 4, 3

Potential Complications

  • Hypokalemia (most common) - requires close monitoring and supplementation
  • Worsening hypertension due to salt loading
  • Fluid retention and edema
  • Headache and dizziness

The fludrocortisone suppression test remains an important diagnostic tool for confirming primary aldosteronism, particularly in cases where the diagnosis remains uncertain after initial screening with aldosterone-to-renin ratio.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Seated saline suppression testing for the diagnosis of primary aldosteronism: a preliminary study.

The Journal of clinical endocrinology and metabolism, 2014

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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