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How low can you go? Use of low- and standard-dose liposomal amphotericin B for treatment of invasive fungal infections

机译:你能走多低?使用小剂量和标准剂量的脂质体两性霉素B治疗侵袭性真菌感染

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Objectives: Recommended doses of liposomal amphotericin B (L-AMB) range from 3 to 6mg/kg/day, but 1mg/kg/day may be equally effective and a lower cost alternative for many indications. The objective of this analysis was to assess indications and clinical outcomes of patients who received low-dose (1mg/kg/day rounded up in 50-mg increments) and standard-dose (>=2mg/kg/day) L-AMB. Methods: This was a retrospective analysis of adult L-AMB recipients with suspected invasive fungal infections (IFI) at a single center from 2006 to 2011. The primary outcome was clinical response at the end of treatment. Secondary outcomes included survival and toxicity. Results were analyzed using Chi-square and descriptive statistics. Results: Of 89 adult L-AMB recipients included, 36 had proven or probable IFIs. Nineteen (53%) received low doses and 17 (47%) received standard doses. Median doses were 1.5 and 3.0mg/kg/day. Cryptococcus was the most common fungal pathogen in the low-dose group (37%), and Candida spp. in the standard-dose group (47%). Forty-seven percent of subjects in both groups improved clinically. Sixty-eight percent of low-dose recipients and 76% of standard-dose recipients survived to discharge. Rates of nephrotoxicity and hypokalemia were comparable. Conclusions: Comparable rates of clinical improvement, survival to discharge, and toxicity were identified among low- and standard-dose L-AMB recipients.
机译:目的:脂质体两性霉素B(L-AMB)的推荐剂量范围为3至6mg / kg /天,但1mg / kg /天可能同样有效,并且在许多适应症中成本较低。该分析的目的是评估接受小剂量L-AMB(1毫克/千克/天,以50毫克为增量四舍五入)和标准剂量(> = 2毫克/千克/天)的患者的适应症和临床结果。方法:这是对2006年至2011年在单个中心对患有疑似侵袭性真菌感染(IFI)的成年L-AMB接受者的回顾性分析。主要结果是治疗结束时的临床反应。次要结果包括生存率和毒性。使用卡方和描述性统计分析结果。结果:在包括89名成人L-AMB接受者中,有36名已证实或可能的IFI。 19例(53%)接受低剂量,17例(47%)接受标准剂量。中位剂量为1.5和3.0mg / kg /天。在低剂量组(37%)和念珠菌属中,隐球菌是最常见的真菌病原体。在标准剂量组中(47%)。两组中有47%的受试者在临床上有所改善。 68%的低剂量接受者和76%的标准剂量接受者存活下来。肾毒性和低钾血症的发生率相当。结论:在低剂量和标准剂量的L-AMB接受者中,临床改善率,出院生存率和毒性均具有可比性。

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