Posaconazole-induced hypertension in children with cystic fibrosis

Rachael Marpole1, Daniel K Yeoh2,3, Adelaide L Withers1,4

  • 1Department of Respiratory and Sleep Medicine Perth Children's Hospital Perth Western Australia Australia.

Respirology Case Reports
|August 11, 2021
PubMed

Insights

Posaconazole treatment for allergic bronchopulmonary aspergillosis in cystic fibrosis patients may cause hypertension. This rare side effect, pseudohyperaldosteronism, requires careful monitoring of blood pressure and electrolytes.

Area of Science:

  • Mycology
  • Pharmacology
  • Pediatrics

Background:

  • Posaconazole is a broad-spectrum triazole antifungal used for mould infections.
  • Emerging evidence suggests its efficacy in treating allergic bronchopulmonary aspergillosis (ABPA) in cystic fibrosis (CF) patients.
  • Pseudohyperaldosteronism is a rare adverse effect of posaconazole, characterized by hypertension and electrolyte imbalances.

Observation:

  • Two pediatric cases of cystic fibrosis (CF) with ABPA are presented.
  • Both patients developed hypertension after initiating posaconazole therapy.
  • The hypertension was attributed to drug-induced pseudohyperaldosteronism.

Findings:

  • Posaconazole, used for ABPA in CF, can induce pseudohyperaldosteronism.
  • Hypertension and electrolyte abnormalities are key clinical manifestations.
  • This adverse effect has been observed in non-CF individuals and now in CF children.

Implications:

  • Clinicians should be vigilant for pseudohyperaldosteronism in CF patients treated with posaconazole for ABPA.
  • Regular monitoring of blood pressure and electrolytes is crucial.
  • This highlights the importance of risk-benefit assessment in antifungal therapy for complex pediatric conditions.

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