Posaconazole Serum Drug Levels Associated With Pseudohyperaldosteronism.

Minh-Vu H Nguyen, Matthew R Davis, Rebecca Wittenberg, Ian Mchardy, John W Baddley, Brian Y Young, Alex Odermatt, George R Thompson

Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2021;70(12):2593-2598

PMID: 31403165

Abstract

BACKGROUND

Posaconazole tablets are well tolerated and efficacious in the prophylaxis and treatment of aspergillosis, mucormycosis, and other invasive fungal infections. There have been case reports of posaconazole-induced pseudohyperaldosteronism (PIPH); however, its occurrence and association with serum posaconazole drug levels have not previously been investigated.

METHODS

In this single-center, retrospective, observational study, we examined the occurrence of PIPH in outpatients newly starting posaconazole and evaluated differences in serum posaconazole concentrations and clinical characteristics between those with and without this syndrome.

RESULTS

Sixty-nine patients receiving posaconazole were included, of whom 16 (23.2%) met the definition of PIPH. Patients with PIPH were significantly older (61.1 vs 44.7 years, P = .007) and more frequently had hypertension prior to starting posaconazole (68.8% vs 32.1%, P = .009). Patients with PIPH had a significantly higher median serum posaconazole level than those without PIPH (3.0 vs 1.2 µg/mL, P ≤ .0001). There was a positive correlation between serum posaconazole levels and changes in systolic blood pressure (r = .37, P = .01), a negative correlation between serum posaconazole levels and changes in serum potassium (r = -.39, P = .006), and a positive correlation between serum posaconazole levels and serum 11-deoxycortisol (r = .69, P < .0001).

CONCLUSIONS

Posaconazole is associated with secondary hypertension and hypokalemia, consistent with pseudohyperaldosteronism, and development is associated with higher serum posaconazole concentrations, older age, and baseline hypertension.

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: [email protected].

Address: Department of Internal Medicine, University of California-Davis Health, Sacramento, California, USA; , Basel, Switzerland.; Department of Pharmacy, University of California-Davis Health, Sacramento, California, USA; , Basel, Switzerland.; Department of Medical Microbiology and Immunology, University of California-Davis Health, Sacramento, California, USA, Basel, Switzerland.; Department of Internal Medicine, Division of Infectious Diseases, University of Alabama-Birmingham, Birmingham, Alabama, USA, Basel, Switzerland.; Department of Internal Medicine, Division of Nephrology, University of California-Davis Health, Sacramento, California, USA; , Basel, Switzerland.; Swiss Centre for Applied Human Toxicology and Division of Molecular and Systems Toxicology, Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland.; Department of Internal Medicine, Division of Infectious Diseases, University of California-Davis Health, Sacramento, California, USA.
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