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Exogenous Cushing syndrome with inhaled fluticasone in a child receiving lopinavir/ritonavir
Nasreen A Bhumbra1, Eric G Sahloff, Sandra J Oehrtman
1Department of Pediatrics, College of Medicine, University of Toledo, Toledo, OH, USA.
Insights
A child developed Cushing syndrome due to an interaction between inhaled fluticasone propionate and lopinavir/ritonavir. This highlights potential adverse effects in pediatric patients using these medications concurrently.
Area of Science:
- Pediatric Endocrinology
- Pharmacology
- HIV Medicine
Background:
- Cushing syndrome can arise from exogenous corticosteroid use.
- Protease inhibitors (PIs) like lopinavir/ritonavir inhibit CYP3A4, increasing concentrations of metabolized drugs.
- Inhaled corticosteroids (ICS) are crucial for managing asthma in children, but drug interactions are a concern.
Observation:
- A 9-year-old boy with HIV and asthma developed Cushing syndrome symptoms (moon facies, hirsutism, weight gain) while on inhaled fluticasone propionate, nasal mometasone, and lopinavir/ritonavir.
- Laboratory tests indicated adrenal suppression.
- Symptoms resolved after discontinuing fluticasone propionate.
Findings:
- The Naranjo scale suggested a probable interaction between lopinavir/ritonavir and fluticasone propionate, leading to adrenal suppression.
- Concurrent use of PIs and CYP3A4-metabolized ICS can result in elevated ICS levels and toxicity.
- This interaction is well-documented in adults but less so in pediatric cases.
Implications:
- Clinicians should be aware of potential drug interactions between PIs and ICS in pediatric HIV patients.
- Monitoring for Cushing syndrome is recommended in children receiving concurrent lopinavir/ritonavir and fluticasone propionate.
- This case underscores the importance of considering drug metabolism pathways when managing comorbidities in HIV-infected children.
Objective:
To describe a case of Cushing syndrome in a child during concurrent use of inhaled fluticasone propionate, nasal mometasone, and a highly active antiretroviral regimen including lopinavir/ritonavir.
Case Summary:
A 9-year-old boy with HIV infection and asthma developed moon facies, increased facial hair, and increased weight after fluticasone propionate inhalation (1 puff; 220 microg) therapy was begun. His antiretroviral regimen contained the protease inhibitor combination lopinavir/ritonavir at a dose of 216/54 mg twice daily, and he had been stable for the previous 5 years. He had also been receiving intranasal mometasone for 11 months for the management of allergic rhinitis. Serum cortisol and adrenocorticotropic hormone levels were consistent with adrenal suppression. These physical findings and symptoms and laboratory values normalized after discontinuation of the fluticasone propionate. The Naranjo probability scale indicated that a probable interaction occurred between lopinavir/ritonavir and fluticasone propionate, leading to subsequent adrenal suppression.
Discussion:
Protease inhibitors are associated with numerous drug interactions due to inhibition of the CYP3A4 isoenzyme. Pharmaceutical agents used to treat comorbidities in HIV-infected individuals often can interact with protease inhibitors, leading to toxic drug concentrations or untoward effects. Inhaled corticosteroids such as fluticasone propionate are often necessary to treat asthma in young children and are metabolized by CYP3A4. Interactions between protease inhibitors and inhaled fluticasone propionate have been reported in the adult population, but reports are limited in the pediatric literature.
Conclusions:
This case raises awareness of the interaction between fluticasone propionate and lopinavir/ritonavir and adverse effects in children receiving both medications.
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