Literature DB >> 26824940

Prospective, Controlled Study of Acyclovir Pharmacokinetics in Obese Patients.

R Brigg Turner1, Aaron Cumpston2, Michael Sweet1, Frank Briggs1, Douglas Slain3, Sijin Wen4, Michael Craig4, Mehdi Hamadani4, William Petros4.   

Abstract

The current recommendations for intravenous (i.v.) acyclovir dosing in obese patients suggest using ideal body weight (IBW) rather than total body weight (TBW). To our knowledge, no pharmacokinetic analysis has validated this recommendation. This single-dose pharmacokinetic study was conducted in an inpatient oncology population. Enrollment was conducted by 1:1 matching of obese patients (>190% of IBW) to normal-weight patients (80 to 120% of IBW). All patients received a single dose of i.v. acyclovir, 5 mg/kg, infused over 60 min. Consistent with current recommendations, IBW was used for obese patients and TBW for normal-weight patients. Serial plasma concentrations were obtained and compared. Seven obese and seven normal-weight patients were enrolled, with mean body mass indexes of 45.0 and 22.5 kg/m(2), respectively. Systemic clearance was substantially higher in the obese than normal-weight patients (mean, 19.4 ± 5.3 versus 14.3 ± 5.4 liters/h; P = 0.047). Area under the concentration-time curve was lower in the obese patients (15.2 ± 2.9 versus 24.0 ± 9.4 mg · h/liter; P = 0.011), as was maximum concentration (5.8 ± 0.9 versus 8.2 ± 1.3 mg/liter; P = 0.031). Utilization of IBW for dose calculation of i.v. acyclovir in obese patients leads to lower systemic exposure than dosing by TBW in normal-weight patients. While not directly evaluated in this study, utilization of an adjusted body weight for dose determination appears to more closely approximate the exposure seen in normal-weight patients. (This study has been registered at ClinicalTrials.gov under registration no. NCT01714180.).
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

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Year:  2016        PMID: 26824940      PMCID: PMC4775958          DOI: 10.1128/AAC.02010-15

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  16 in total

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Authors:  S L Spruance; S K Tyring; B DeGregorio; C Miller; K Beutner
Journal:  Arch Intern Med       Date:  1996 Aug 12-26

2.  Acyclovir for treatment of postherpetic neuralgia: efficacy and pharmacokinetics.

Authors:  E P Acosta; H H Balfour
Journal:  Antimicrob Agents Chemother       Date:  2001-10       Impact factor: 5.191

3.  A double-blind, randomized study assessing the equivalence of valacyclovir 1000 mg once daily versus 500 mg twice daily in the episodic treatment of recurrent genital herpes. Genival Study Group.

Authors:  P Saiag; D Praindhui; C Chastang
Journal:  J Antimicrob Chemother       Date:  1999-10       Impact factor: 5.790

4.  Single-dose pharmacokinetics of acyclovir.

Authors:  S A Spector; J D Connor; M Hintz; R P Quinn; M R Blum; R E Keeney
Journal:  Antimicrob Agents Chemother       Date:  1981-04       Impact factor: 5.191

5.  A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group.

Authors:  A S Levey; J P Bosch; J B Lewis; T Greene; N Rogers; D Roth
Journal:  Ann Intern Med       Date:  1999-03-16       Impact factor: 25.391

Review 6.  Overview of acyclovir pharmacokinetic disposition in adults and children.

Authors:  M R Blum; S H Liao; P de Miranda
Journal:  Am J Med       Date:  1982-07-20       Impact factor: 4.965

7.  Valaciclovir for the suppression of recurrent genital herpes simplex virus infection: a large-scale dose range-finding study. International Valaciclovir HSV Study Group.

Authors:  M Reitano; S Tyring; W Lang; C Thoming; A M Worm; S Borelli; L O Chambers; J M Robinson; L Corey
Journal:  J Infect Dis       Date:  1998-09       Impact factor: 5.226

8.  Pharmacokinetics of the acyclovir pro-drug valaciclovir after escalating single- and multiple-dose administration to normal volunteers.

Authors:  S Weller; M R Blum; M Doucette; T Burnette; D M Cederberg; P de Miranda; M L Smiley
Journal:  Clin Pharmacol Ther       Date:  1993-12       Impact factor: 6.875

9.  Pharmacokinetics and tolerance of acyclovir, a new anti-herpesvirus agent, in humans.

Authors:  O L Laskin; J A Longstreth; R Saral; P de Miranda; R Keeney; P S Lietman
Journal:  Antimicrob Agents Chemother       Date:  1982-03       Impact factor: 5.191

10.  DALI: defining antibiotic levels in intensive care unit patients: are current β-lactam antibiotic doses sufficient for critically ill patients?

Authors:  Jason A Roberts; Sanjoy K Paul; Murat Akova; Matteo Bassetti; Jan J De Waele; George Dimopoulos; Kirsi-Maija Kaukonen; Despoina Koulenti; Claude Martin; Philippe Montravers; Jordi Rello; Andrew Rhodes; Therese Starr; Steven C Wallis; Jeffrey Lipman
Journal:  Clin Infect Dis       Date:  2014-01-14       Impact factor: 9.079

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Journal:  J Neurol       Date:  2022-01-31       Impact factor: 4.849

2.  Impact of Obesity on Acyclovir-Induced Nephrotoxicity.

Authors:  Katie E Barber; Jamie L Wagner; Kayla R Stover
Journal:  Open Forum Infect Dis       Date:  2019-03-07       Impact factor: 3.835

  2 in total

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