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Incidence and predictors of acute kidney injury associated with intravenous polymyxin B therapy
被引:137
作者:
Kubin, Christine J.
[1
,2
]
Ellman, Tanya M.
[1
]
Phadke, Varun
[1
]
Haynes, Laura J.
[2
,3
]
Calfee, David P.
[4
]
Yin, Michael T.
[1
]
机构:
[1] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[2] New York Presbyterian Hosp, Dept Pharm, New York, NY 10032 USA
[3] Hosp Univ Penn, Dept Pharm, Philadelphia, PA 19104 USA
[4] Weill Cornell Med Coll, Dept Med & Publ Hlth, New York, NY 10065 USA
关键词:
Polymyxin B;
Nephrotoxicity;
RIFLE;
CRITICALLY-ILL PATIENTS;
NEGATIVE BACTERIAL-INFECTIONS;
ACUTE-RENAL-FAILURE;
COLISTIN METHANESULFONATE;
PHARMACOKINETICS;
NEPHROTOXICITY;
DEFINITION;
BACTEREMIA;
VANCOMYCIN;
IMPACT;
D O I:
10.1016/j.jinf.2012.01.015
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Background: Increases in multidrug-resistance among gram-negative organisms have necessitated the use of polymyxins. To date, the incidence of acute kidney injury (AKI) associated with polymyxin B has not been evaluated using RIFLE criteria. Methods: Adult patients who received polymyxin B were retrospectively evaluated to determine the incidence of AKI during polymyxin B therapy using RIFLE criteria. Predictors of AKI were identified by comparing characteristics of patients with and without AKI. Results: A total of 73 patients were included. The incidence of AKI was 60%. Ten (14%) patients discontinued therapy due to nephrotoxicity. Median duration of polymyxin B was 11 days with a median cumulative dose of 18 mg/kg. Concomitant nephrotoxins were received in 69 (95%). Patients with AKI had a higher median cumulative dose (1578 mg vs. 800 mg; p = 0.02), a higher body mass index (BMI) (27.2 vs. 24.5 kg/ m(2); p = 0.03), and were more likely to receive vancomycin (82% vs. 55%; p = 0.03) compared to those without AKI. After controlling for polymyxin B duration, independent predictors of AKI were higher BMI and concomitant vancomycin. Conclusions: The incidence of AKI during polymyxin B therapy was 60%. Further studies are needed to define dosing parameters that maximize efficacy and minimize nephrotoxicity. (C) 2012 The British Infection Association. Published by Elsevier Ltd. All rights reserved.
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页码:80 / 87
页数:8
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