Survival after Amphotericin B Overdose Treated with Plasmapheresis

Author:

Wang George Sam1,Banerji Shireen2,Roussil T Keith3,Heard Kennon J4

Affiliation:

1. George Sam Wang MD, Medical Toxicology Fellow, Rocky Mountain Poison and Drug Center, Denver Health and Hospital, Denver, CO

2. Shireen Banerji PharmD DBAT, Clinical Toxicology Coordinator, Rocky Mountain Poison and Drug Center, Denver Health and Hospital

3. T Keith Roussil BSN RN C-SPI, Certified Specialist in Poison Information, Rocky Mountain Poison and Drug Center, Denver Health and Hospital

4. Kennon J Heard MD, Assistant Director, Rocky Mountain Poison and Drug Center, Denver Health and Hospital; Associate Professor, Department of Emergency Medicine, School of Medicine, University of Colorado, Denver

Abstract

OBJECTIVE: To report a case of accidental amphotericin B overdose that was treated with plasmapheresis. CASE SUMMARY: A 60-year-old woman with a history of kidney transplant 4 years prior to presentation for a congenital abnormality was admitted for a suspected systemic fungal infection. The patient inadvertently received intravenous amphotericin B deoxycholate 250 mg (4.3 mg/kg) over 2 hours instead of prescribed liposomal amphotericin B. The medication error was discovered 16 hours after administration. She had normal vital signs at that time and reported abdominal pain and general malaise. Results of a metabolic panel were significant for a creatinine level of 2.1 mg/dL and CO2 of 17 mg/dL. Her serum amphotericin B concentration 33 hours after the initial dose was 4.9 μg/mL. She subsequently received 5 courses of plasmapheresis and 3 courses of hemodialysis and ultimately did not develop any further renal injury, as well as hemolysis, cardiovascular collapse, dysrhythmias, or severe electrolyte abnormalities. DISCUSSION: The dosing differences between nonliposomal and liposomal preparations of amphotericin B can be as high as 50-fold. Reported adverse events from overdose in both animal models and human case reports include renal insufficiency, hemolysis, thrombocytopenia, electrolyte abnormality, and cardiac dysrhythmias. There have been previous reports of similar errors that have led to death. Furthermore, amphotericin B has been shown to be poorly dialyzable. Our patient's serum amphotericin B concentration decreased after she received plasmapheresis, and she did not develop severe complications. CONCLUSIONS: We describe a patient who survived a 4-fold overdose of amphotericin B because of a medication error. The use of plasmapheresis may have enhanced the elimination of amphotericin B and may have contributed to the positive outcome. However, the role of plasmapheresis in amphotericin overdose is not fully understood.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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1. Effect of amphotericin B‐deoxycholate (Fungizone) on the mitochondria of Wistar rats' renal proximal tubules cells;Journal of Applied Toxicology;2021-03-19

2. The Problem with Amphotericin;Clinical Drug Investigation;2020-06-08

3. Drug Dosing in Patients Undergoing Therapeutic Plasma Exchange;Neurocritical Care;2020-05-22

4. Therapeutic Plasma Exchange;Demystifying Drug Dosing in Renal Dysfunction;2019-05-31

5. The utility of therapeutic plasma exchange for amphotericin B overdose;Transfusion and Apheresis Science;2018-12

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