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Acute hepatic injury with amphotericin B deoxycholate in an immunocompetent patient
Jamie L Wagner1, Allison M Bell1
1Department of Pharmacy Practice, University of Mississippi School of Pharmacy, Jackson, Mississippi, USA.
Abstract:
Amphotericin B deoxycholate (AmBd) is rarely used due to its adverse effect profile, which includes nephrotoxicity, infusion-related reactions, and hepatotoxicity. The incidence of hepatotoxicity related to AmBd is 18-23%, but the reports of this adverse effect are mainly in immunocompromised patients receiving chemotherapy. We report a case of AmBd-related acute hepatic injury in an immunocompetent male with multiple medical problems. The patient initially had acute hepatic injury likely caused by poor nutritional status and a diagnosis of failure to thrive, but was recovering. He was also diagnosed with bilateral renal fungal mycetomas and received systemic treatment initially with micafungin and then fluconazole after urine cultures returned with the growth of Candida glabrata. Therapy was expanded to systemic AmBd when the fungal balls persisted. The patient subsequently developed hepatic re-injury with 1 dose of AmBd, and the therapy was discontinued. Caution should be exerted when utilizing AmBd in treating patients with previous hepatic injury.
Insights
Amphotericin B deoxycholate can cause liver injury, even in immunocompetent patients. This case highlights the risk of hepatic re-injury with Amphotericin B deoxycholate, especially in those with prior liver issues.
Area of Science:
- Medical Mycology
- Hepatology
- Clinical Pharmacology
Background:
- Amphotericin B deoxycholate (AmBd) is associated with significant adverse effects, including hepatotoxicity (18-23% incidence), primarily reported in immunocompromised patients.
- Fungal mycetomas, particularly those caused by Candida glabrata, necessitate systemic antifungal treatment.
- Prior hepatic injury or compromised nutritional status may increase susceptibility to drug-induced liver injury.
Observation:
- A case report details an immunocompetent male with multiple comorbidities and bilateral renal fungal mycetomas.
- The patient experienced initial hepatic injury, likely multifactorial, but was recovering before antifungal treatment.
- Systemic treatment with micafungin and fluconazole was initiated for Candida glabrata, followed by Amphotericin B deoxycholate due to persistent fungal balls.
Findings:
- The patient developed acute hepatic re-injury shortly after receiving a single dose of Amphotericin B deoxycholate.
- Amphotericin B deoxycholate therapy was discontinued due to the observed hepatotoxicity.
- This event underscores the potential for Amphotericin B deoxycholate to cause severe liver injury, even in non-chemotherapy patients.
Implications:
- Clinicians should exercise caution when prescribing Amphotericin B deoxycholate to patients with a history of hepatic injury.
- Further investigation into the specific mechanisms of Amphotericin B deoxycholate-induced hepatotoxicity in diverse patient populations is warranted.
- Risk-benefit assessment is crucial when considering Amphotericin B deoxycholate for fungal infections, particularly in patients with pre-existing liver conditions.
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