Hasibi Mehrdad, Jafari Sirous, Manshadi Seyyed Ali, Asadollahi Marjan, Salehi Mohammadreza, Zarch Varasteh Vakili, Kouhi Ali
Department of Infectious Diseases, Amir-Alam Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Ear Nose Throat J. 2017 Feb;96(2):E18-E22. doi: 10.1177/014556131709600214.
Amphotericin B deoxycholate (ABD) is the best therapeutic agent available for the treatment of most systemic fungal infections. However, some untoward adverse effects such as nephrotoxicity may limit its appropriate therapeutic use. We conducted a randomized, controlled trial ofthe infusion of fat emulsion (Intralipid) shortly after the infusion of ABD to evaluate its effects on reducing ABD-associated nephrotoxicity. Our patient population was made up of 31 patients who were randomized into two groups: an intervention group (n = 16) and a control group (15 patients). There were no statistically significant differences between the two groups in demographic or clinical variables. All patients received 1mg/kg/day of ABD in dextrose 5%. In addition, the patients in the intervention arm received Intralipid 10%, which was started as soon as possible within 1 hour after the infusion of ABD. ABD-associated nephrotoxicity was defined as a minimum 50% increase in baseline serum creatinine to a minimum of 2mg/dl. We also measured daily serum creatinine changes during the first 2 weeks of treatment, and we compared some other relevant indices of renal function, as well as ABD-related hypokalemia. We found no statistically significant differences between the two treatments in terms of ABD-associated nephrotoxicity or any of the other indices. We conclude that the administration of Intralipid 10% early after infusion of ABD in dextrose 5% does not have any effect in decreasing ABD-associated nephrotoxicity or hypokalemia.
两性霉素B去氧胆酸盐(ABD)是治疗大多数全身性真菌感染的最佳可用治疗药物。然而,一些不良副作用,如肾毒性,可能会限制其适当的治疗应用。我们进行了一项随机对照试验,在输注ABD后不久输注脂肪乳剂(英脱利匹特),以评估其对降低ABD相关肾毒性的影响。我们的患者群体由31名患者组成,他们被随机分为两组:干预组(n = 16)和对照组(15名患者)。两组在人口统计学或临床变量方面没有统计学上的显著差异。所有患者均接受1mg/kg/天的ABD溶于5%葡萄糖溶液中。此外,干预组的患者接受10%的英脱利匹特,在输注ABD后1小时内尽快开始输注。ABD相关肾毒性定义为基线血清肌酐至少增加50%,至至少2mg/dl。我们还测量了治疗前2周内每日血清肌酐的变化,并比较了其他一些相关的肾功能指标以及与ABD相关的低钾血症。我们发现两种治疗方法在ABD相关肾毒性或任何其他指标方面没有统计学上的显著差异。我们得出结论,在5%葡萄糖溶液中输注ABD后早期给予10%的英脱利匹特对降低ABD相关肾毒性或低钾血症没有任何作用。