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Published Online, 28 February 2006, www.theannals.com, DOI 10.1345/aph.1G509.
The Annals of Pharmacotherapy: Vol. 40, No. 3, pp. 553-558. DOI 10.1345/aph.1G509
© 2006 Harvey Whitney Books Company.
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Using Vancomycin Concentrations for Dosing Daptomycin in a Morbidly Obese Patient with Renal Insufficiency

Manjunath P Pai, PharmD

Assistant Professor, College of Pharmacy, University of New Mexico, Albuquerque, NM

Renee-Claude Mercier, PharmD

Associate Professor, College of Pharmacy, University of New Mexico

Sarah E Allen, MD

Clinical Associate Professor, School of Medicine, University of New Mexico

Reprints: Dr. Pai, College of Pharmacy, University of New Mexico, MSC09 5360, Albuquerque, NM 87131-0001, fax 505/272-6749, apai{at}salud.unm.edu

OBJECTIVE: To report a case in which vancomycin clearance was used to determine the daptomycin dosing interval in a morbidly obese patient with renal impairment.

CASE SUMMARY: A 46-year-old man (209 kg; 178 cm) failed a 42 day course of vancomycin therapy for treatment of a methicillin-resistant Staphylococcus aureus-infected wound and cellulitis. The median trough vancomycin concentration was 12.6 µg/mL (range 7.3-24.1) through his course of therapy. Estimation of creatinine clearance (Clcr) was confounded in this clinical scenario, given the patient's weight and a lack of valid equations in this patient population. Daptomycin was administered empirically at 6 mg/kg dosed every 48 hours based on estimated clearance from measured vancomycin concentrations. Steady-state plasma concentrations of daptomycin were determined, and the daptomycin half-life in this patient was more accurately estimated using vancomycin clearance as a surrogate. In addition, a 4 mg/kg dose of daptomycin would have been sufficient based on plasma concentrations. The patient demonstrated rapid clinical improvement and remained free of cellulitis for 6 months after completion of daptomycin and a 12 week course of trimethoprim/sulfamethoxazole.

DISCUSSION: The dosing interval of daptomycin is adjusted based on Clcr. However, estimation of Clcr is difficult in morbidly obese patients with renal impairment, given a lack of valid equations. In this clinical scenario, vancomycin concentrations were used to estimate Clcr and served as a surrogate measure to determine the daptomycin dosing interval. Measured daptomycin concentrations validated this approach and confirmed the inadequacy of commonly used Clcr equations.

CONCLUSIONS: In this clinical scenario, vancomycin concentrations more accurately estimated Clcr, thereby facilitating determination of the daptomycin dosing interval.

Key Words: daptomycin, morbid obesity, renal impairment, vancomycin

Published Online, February 28, 2006. www.theannals.com, DOI 10.1345/aph.1G509


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