Confirmatory testing in primary aldosteronism: extensive medication switching is not needed in all patients
Language English Country Great Britain, England Media print-electronic
Document type Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
PubMed
22253400
PubMed Central
PMC3315831
DOI
10.1530/eje-11-0914
PII: EJE-11-0914
Knihovny.cz E-resources
- MeSH
- Aldosterone blood MeSH
- Algorithms MeSH
- Mineralocorticoid Receptor Antagonists administration & dosage therapeutic use MeSH
- Antihypertensive Agents administration & dosage therapeutic use MeSH
- Diagnostic Techniques, Endocrine * MeSH
- Diuretics administration & dosage therapeutic use MeSH
- Adult MeSH
- Hyperaldosteronism diagnosis drug therapy epidemiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Drug Substitution statistics & numerical data MeSH
- Needs Assessment statistics & numerical data MeSH
- Renin-Angiotensin System drug effects physiology MeSH
- Aged MeSH
- Validation Studies as Topic * MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Aldosterone MeSH
- Mineralocorticoid Receptor Antagonists MeSH
- Antihypertensive Agents MeSH
- Diuretics MeSH
OBJECTIVE: Confirmatory testing of suspected primary aldosteronism (PA) requires an extensive medication switch that can be difficult for patients with severe complicated hypertension and/or refractory hypokalemia. For this reason, we investigated the effect of chronic antihypertensive medication on confirmatory testing results. To allow the results to be interpreted, the reproducibility of confirmatory testing was also evaluated. DESIGN AND METHODS: The study enrolled 114 individuals with suspected PA who underwent two confirmatory tests. The patients were divided into two groups. In Group A, both tests were performed on the guidelines-recommended therapy, i.e. not interfering with the renin-angiotensin-aldosterone system. In Group B, the first test was performed on chronic therapy with the exclusion of thiazides, loop diuretics, and aldosterone antagonists; and the second test was performed on guidelines-recommended therapy. Saline infusion, preceded by oral sodium loading, was used to suppress aldosterone secretion. RESULTS: Agreement in the interpretation of the two confirmatory tests was observed in 84 and 66% of patients in Groups A and B respectively. For all 20 individuals in Group A who ever had end-test serum aldosterone levels ≥240 pmol/l, aldosterone was concordantly nonsuppressible during the other test. Similarly, for all 16 individuals in Group B who had end-test serum aldosterone levels ≥240 pmol/l on modified chronic therapy, aldosterone remained nonsuppressible with guidelines-recommended therapy. CONCLUSION: Confirmatory testing performed while the patient is on chronic therapy without diuretics and aldosterone antagonists can confirm the diagnosis of PA, provided serum aldosterone remains markedly elevated at the end of saline infusion.
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