Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?

Background: Acyclovir is a hydrophilic drug that is mainly distributed in the lean compartments of the body. Consequently, dosing on total body weight in obese patients may lead to drug overdosing. Inconsistency in clinical guideline recommendations and a lack of clear recommendations in the Summary...

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Main Authors: Bastiaan TGM Sallevelt, Erin H Smeijsters, Toine CG Egberts, Kim CM van der Elst, Tania Mudrikova
Format: Article
Language:English
Published: Elsevier 2020-10-01
Series:Clinical Infection in Practice
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2590170220300339
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author Bastiaan TGM Sallevelt
Erin H Smeijsters
Toine CG Egberts
Kim CM van der Elst
Tania Mudrikova
author_facet Bastiaan TGM Sallevelt
Erin H Smeijsters
Toine CG Egberts
Kim CM van der Elst
Tania Mudrikova
author_sort Bastiaan TGM Sallevelt
collection DOAJ
description Background: Acyclovir is a hydrophilic drug that is mainly distributed in the lean compartments of the body. Consequently, dosing on total body weight in obese patients may lead to drug overdosing. Inconsistency in clinical guideline recommendations and a lack of clear recommendations in the Summary of Product Characteristics on how to dose acyclovir in obese patients can impede safe and effective treatment. Case report: This report describes a 71-year-old obese patient (body mass index 35 kg/m2) with herpes zoster ophthalmicus and meningoencephalitis. The patient had normal renal function and was treated with acyclovir with a dosage based on actual body weight (10 mg/kg q8h intravenously). Supratherapeutic acyclovir concentrations probably induced acute kidney injury (AKI) and neurotoxicity. Results: Due to the severity of the toxic effects, multiple sessions of hemodialysis were necessary, with eventual full recovery of the renal function and neurotoxic symptoms. Low dose haloperidol and lorazepam were not effective in resolving audiovisual hallucinations in our patient. Conclusion: This case report emphasizes the need for adjusted dosing and subsequent close monitoring of obese patients who are treated with hydrophilic drugs, such as acyclovir, to avoid patient harm. We discuss prevention and management strategies for acyclovir toxicity in obese patients based on the current literature.
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spelling doaj.art-13c879c06bfd453090979d0c9b3fd4aa2022-12-21T22:31:18ZengElsevierClinical Infection in Practice2590-17022020-10-017100046Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?Bastiaan TGM Sallevelt0Erin H Smeijsters1Toine CG Egberts2Kim CM van der Elst3Tania Mudrikova4Department of Clinical Pharmacy, University Medical Center Utrecht, Utrecht, the Netherlands; Corresponding author at: University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, the Netherlands.Department of Clinical Pharmacy, University Medical Center Utrecht, Utrecht, the NetherlandsDepartment of Clinical Pharmacy, University Medical Center Utrecht, Utrecht, the NetherlandsDepartment of Clinical Pharmacy, University Medical Center Utrecht, Utrecht, the NetherlandsDepartment of Internal Medicine, University Medical Center Utrecht, Utrecht, the NetherlandsBackground: Acyclovir is a hydrophilic drug that is mainly distributed in the lean compartments of the body. Consequently, dosing on total body weight in obese patients may lead to drug overdosing. Inconsistency in clinical guideline recommendations and a lack of clear recommendations in the Summary of Product Characteristics on how to dose acyclovir in obese patients can impede safe and effective treatment. Case report: This report describes a 71-year-old obese patient (body mass index 35 kg/m2) with herpes zoster ophthalmicus and meningoencephalitis. The patient had normal renal function and was treated with acyclovir with a dosage based on actual body weight (10 mg/kg q8h intravenously). Supratherapeutic acyclovir concentrations probably induced acute kidney injury (AKI) and neurotoxicity. Results: Due to the severity of the toxic effects, multiple sessions of hemodialysis were necessary, with eventual full recovery of the renal function and neurotoxic symptoms. Low dose haloperidol and lorazepam were not effective in resolving audiovisual hallucinations in our patient. Conclusion: This case report emphasizes the need for adjusted dosing and subsequent close monitoring of obese patients who are treated with hydrophilic drugs, such as acyclovir, to avoid patient harm. We discuss prevention and management strategies for acyclovir toxicity in obese patients based on the current literature.http://www.sciencedirect.com/science/article/pii/S2590170220300339AcyclovirPharmacokineticsDrug-related side effects and adverse reactionsDrug monitoringObesity
spellingShingle Bastiaan TGM Sallevelt
Erin H Smeijsters
Toine CG Egberts
Kim CM van der Elst
Tania Mudrikova
Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?
Clinical Infection in Practice
Acyclovir
Pharmacokinetics
Drug-related side effects and adverse reactions
Drug monitoring
Obesity
title Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?
title_full Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?
title_fullStr Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?
title_full_unstemmed Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?
title_short Acute renal and neurotoxicity due to weight-based dosing of intravenous acyclovir: How to dose in obese patients?
title_sort acute renal and neurotoxicity due to weight based dosing of intravenous acyclovir how to dose in obese patients
topic Acyclovir
Pharmacokinetics
Drug-related side effects and adverse reactions
Drug monitoring
Obesity
url http://www.sciencedirect.com/science/article/pii/S2590170220300339
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