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Continuous infusion vs intermittent vancomycin in neurosurgical intensive care unit patients

Abstract Purpose Target plasma level achievement has remained a challenge in neurosurgical intensive care unit patients receiving intravenous vancomycin. We evaluated continuous infusion (CI) and intermittent vancomycin dosing strategies in these patients. Methods This retrospective cohort compared...

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Published in:Journal of critical care 2015-10, Vol.30 (5), p.1153.e1-1153.e6
Main Authors: Hong, Lisa T., PharmD, BCPS, Goolsby, Tiffany A., PharmD, BCPS (AQ-ID), Sherman, Deborah S., PharmD, Mueller, Scott W., PharmD, BCPS, Reynolds, Paul, PharmD, BCPS, Cava, Luis, MD, Neumann, Robert, MD, Kiser, Tyree H., PharmD, FCCM, FCCP, BCPS
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Language:English
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Summary:Abstract Purpose Target plasma level achievement has remained a challenge in neurosurgical intensive care unit patients receiving intravenous vancomycin. We evaluated continuous infusion (CI) and intermittent vancomycin dosing strategies in these patients. Methods This retrospective cohort compared CI vancomycin (target random levels, 20-30 mg/L) to intermittent vancomycin (target troughs, 15-20 mg/L) in regards to achievement of target plasma levels, nephrotoxicity, pharmacodynamic target attainment, and cost savings in 130 patients. Results Continuous infusion resulted in greater achievement of goal plasma concentrations at the first steady-state level (40 vs 21.5%, P = .02), more rapid achievement of goal plasma concentrations (2.04 vs 3.76 days, P < .0001), and increased time within therapeutic range (55% vs 34%, P < .0001) but no significant difference in nephrotoxicity (15.4% vs 21.5%, P = .5). Continuous infusion improved pharmacodynamic target attainment (92.3% vs 30.8%, P < .0001) and also reduced levels drawn (3.8 vs 5.7, P = .0007), dose adjustments (1.4 vs 2.4, P = .0006), days of therapy (10.4 vs 14.1, P = .01), and mean total daily dose requirements (33 vs 35.7 mg/kg, P < .0001) per patient. Conclusions Continuous infusion appears beneficial for improving attainment of target plasma concentrations, pharmacodynamic goals, and financial burden, without increasing risk of acute kidney injury.
ISSN:0883-9441
1557-8615
DOI:10.1016/j.jcrc.2015.06.012