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An Evaluation of Hepatotoxicity and Nephrotoxicity of Liposomal Amphotericin B (L-AMB)

机译:脂质体两性霉素B(L-AMB)的肝毒性和肾毒性评估

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Hepatic and renal functions are important considerations when selecting antifungal therapy. This investigation of liposomal amphotericin B (L-AMB) was conducted to determine the incidence and factors associated with the development of hepatotoxicity and nephrotoxicity. A retrospective chart review was conducted of 100 consecutive patients receiving L-AMB at doses of 1, 3, and 5 mg/kg. Hepatotoxicity was defined as an increase of bilirubin greater than 1.5 mg/dl or AST and ALT greater than three times the normal range. Nephrotoxicity was defined as an increase in serum creatinine of 0.5 mg/dl or an increase of 50% from baseline. Patients were included if they were 18 years of age or older. Patients were excluded if they had developed hepatic or renal dysfunction prior to L-AMB administration. Seventy-five patients were included based upon the predefined inclusion/exclusion criteria. Twenty-one percent (16/75) developed hepatotoxicity based upon the predefined criteria. There were no additive correlates for this adverse effect. Overall, 56% (42/75) of patients developed nephrotoxicity. Seventy-four percent (31/42) were exposed to IV contrast, and 90% (38/42) were receiving nephrotoxins concurrently. Age, cumulative dose, concomitant nephrotoxins, and IV contrast exposure were associated with increased nephrotoxicity (p 0.001). The development of hepatotoxicity was observed; however, no correlates (age, dose escalation, or cumulative dose) were significantly associated with its occurrence. Overall nephrotoxicity with L-AMB was common and often multifactorial. Lipid amphotericin B products are associated with lower rates of nephrotoxicity than conventional amphotericin; however, in this analysis, L-AMB was associated with a high incidence of nephrotoxicity.
机译:选择抗真菌治疗时,肝和肾功能是重要的考虑因素。进行了脂质体两性霉素B(L-AMB)的研究,以确定与肝毒性和肾毒性发展相关的发生率和因素。回顾性图表回顾了100名连续接受L,AMB,1、3和5 mg / kg剂量的患者。肝毒性定义为胆红素增加超过1.5 mg / dl或AST和ALT超过正常范围三倍。肾毒性定义为血清肌酐增加0.5 mg / dl或较基线增加50%。如果患者年满18岁,则包括在内。如果患者在服用L-AMB之前已出现肝或肾功能障碍,则将其排除在外。根据预定义的纳入/排除标准,纳入了75名患者。根据预定标准,有21%(16/75)发生肝毒性。没有与此不良反应相关的添加剂。总体而言,有56%(42/75)的患者出现了肾毒性。 74%(31/42)的患者接受了静脉造影,而90%(38/42)的患者同时接受了肾毒素。年龄,累积剂量,伴随的肾毒素和静脉内造影剂暴露与肾毒性增加相关(p <0.001)。观察到肝毒性的发展;但是,没有相关性(年龄,剂量递增或累积剂量)与其发生率显着相关。 L-AMB的总体肾毒性很常见,而且通常是多因素的。与传统的两性霉素相比,脂质两性霉素B产品与较低的肾毒性有关。然而,在该分析中,L-AMB与肾毒性的高发生有关。

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