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万古霉素相关性肾毒性的发生率及预测因素

Incidence and predictors of vancomycin-associated nephrotoxicity.

作者信息

Moh'd Hamzah, Kheir Fayez, Kong Lan, Du Ping, Farag Hosam, Mohamad Ahmad, Zurlo John J

机构信息

From the Department of Medicine, Division of Infectious Diseases and Epidemiology, Penn State Hershey Milton S. Hershey Medical Center, Penn State College of Medicine, Hershey, Pennsylvania, the Department of Medicine, Section of Pulmonary Diseases, Critical Care, and Environmental Medicine, Tulane University Health Sciences Center, New Orleans, Louisiana, the Department of Public Health Sciences, Penn State College of Medicine, Hershey, and the Department of Internal Medicine, Chicago Medical School at Rosalind Franklin University, Chicago, Illinois.

出版信息

South Med J. 2014 Jun;107(6):383-8. doi: 10.14423/01.SMJ.0000450716.84291.59.

Abstract

OBJECTIVES

Earlier studies reported a low incidence of vancomycin-associated nephrotoxicity (VAN); however, recent studies have reported higher incidences exceeding 30%. Predictors of nephrotoxicity are not well defined. In this study we aimed to better estimate the incidence and evaluate predictors of VAN in a cohort of patients predominated by long treatment courses.

METHODS

We conducted a retrospective study on patients treated with vancomycin while in the hospital and who were observed closely through the Outpatient Parenteral Antibiotic Therapy program. Nephrotoxicity was defined as an increase in the serum creatinine level of 0.5 mg/dL or 50% from baseline on at least two consecutive readings while taking vancomycin. We compared the patients who developed nephrotoxicity with those who did not with regard to vancomycin dosing, trough levels, baseline serum creatinine, underlying infection, residence in the critical care unit, comorbid conditions, concurrent nephrotoxic treatments, and baseline characteristics.

RESULTS

Of 579 patients, 154 (26.6%) developed nephrotoxicity. Ninety patients developed VAN within the first 14 days of treatment, whereas 64 patients developed nephrotoxicity after 14 days of treatment. The median time to development of nephrotoxicity was 9 days. Admission to the intensive care unit, concurrent use of loop diuretics, and comorbidity with cirrhosis were independently associated with nephrotoxicity. A higher baseline creatinine value was unexpectedly associated with a lower incidence of nephrotoxicity (P = 0.0016).

CONCLUSIONS

VAN is not an uncommon outcome in both short- and long-term treatment courses. Admission to the intensive care unit while receiving treatment, concurrent treatment with a loop diuretic, an underlying diagnosis of cirrhosis, and the initial trough level appear to be the main risk factors for nephrotoxicity. Unexpectedly, elevated baseline creatinine levels appeared to be protective and this could be the result of careful use of vancomycin among individuals with relatively higher baseline creatinine values.

摘要

目的

早期研究报告万古霉素相关肾毒性(VAN)的发生率较低;然而,近期研究报告的发生率较高,超过了30%。肾毒性的预测因素尚未明确界定。在本研究中,我们旨在更好地估计VAN的发生率,并评估以长疗程治疗为主的一组患者中VAN的预测因素。

方法

我们对住院期间接受万古霉素治疗且通过门诊肠外抗生素治疗项目密切观察的患者进行了一项回顾性研究。肾毒性定义为在服用万古霉素期间,血清肌酐水平至少连续两次读数较基线水平升高0.5mg/dL或升高50%。我们比较了发生肾毒性的患者与未发生肾毒性的患者在万古霉素剂量、谷浓度、基线血清肌酐、潜在感染、入住重症监护病房、合并症、同时进行的肾毒性治疗以及基线特征方面的差异。

结果

579例患者中,154例(26.6%)发生了肾毒性。90例患者在治疗的前14天内发生了VAN,而64例患者在治疗14天后发生了肾毒性。发生肾毒性的中位时间为9天。入住重症监护病房、同时使用袢利尿剂以及合并肝硬化与肾毒性独立相关。较高的基线肌酐值意外地与较低的肾毒性发生率相关(P = 0.0016)。

结论

在短期和长期治疗过程中,VAN并非罕见结果。治疗期间入住重症监护病房、同时使用袢利尿剂、潜在的肝硬化诊断以及初始谷浓度似乎是肾毒性的主要危险因素。出乎意料的是,基线肌酐水平升高似乎具有保护作用,这可能是由于基线肌酐值相对较高的个体谨慎使用万古霉素的结果。

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