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哌拉西林/他唑巴坦在化疗后合并血液系统恶性肿瘤和发热性中性粒细胞减少症的癌症患者中的药代动力学。

Pharmacokinetics of piperacillin/tazobactam in cancer patients with hematological malignancies and febrile neutropenia after chemotherapy.

机构信息

(GREICAH): Grupo de Investigación en Enfermedades Infecciosas en Cáncer y alteraciones hematológicas, Bogotá, Colombia.

出版信息

BMC Pharmacol Toxicol. 2013 Nov 28;14:59. doi: 10.1186/2050-6511-14-59.

Abstract

INTRODUCTION

Patients with febrile neutropenia (FN) exhibit changes in extracellular fluid that may alter the plasma concentrations of beta-lactams and result in therapeutic failure or toxicity. We evaluated the pharmacokinetics of piperacillin/tazobactam in patients with hematological malignancies and FN after receiving chemotherapy at a primary public cancer center.

METHODS

This was an open, nonrandomized, observational, descriptive, and prospective study. Samples from 15 patients with hematological malignancies and FN were evaluated after the administration of chemotherapy. Five blood samples were taken from each patient when the antibiotic level was at steady-state 10, 60, 120, 180, and 350 min after each dose. Antibiotic concentrations were measured using gel diffusion with Bacillus subtilis. All study participants provided written informed consent.

RESULTS

We investigated the pharmacokinetics of piperacillin in 14 patients between the ages of 18 years and 59 years and with a mean absolute neutrophil count of 208 cells per mm³ (standard deviation (SD) ± 603.2). The following pharmacokinetic measurements were obtained: maximum concentration, 94.1-1133 mg/L; minimum concentration, 0.47-37.65 mg/L; volume of distribution, 0.08-0.65 L/kg (mean, 0.34 L/kg); drug clearance (CL), 4.42-27.25 L/h (mean, 9.93 L/h); half-life (t(1/2)), 0.55-2.65 h (mean, 1.38 h); and area under the curve, 115.12-827.16 mg · h/L.

CONCLUSION

Patients with FN after receiving chemotherapy exhibited significant variations in the pharmacokinetic parameters of piperacillin compared with healthy individuals; specifically, FN patients demonstrated an increase in t1(/2) and decreased CL.

摘要

简介

患有发热性中性粒细胞减少症(FN)的患者会出现细胞外液的变化,这可能会改变β-内酰胺类抗生素的血浆浓度,导致治疗失败或毒性。我们在一家主要的公立癌症中心评估了接受化疗后患有血液恶性肿瘤和 FN 的患者的哌拉西林/他唑巴坦药代动力学。

方法

这是一项开放、非随机、观察性、描述性和前瞻性研究。在接受化疗后,对 15 名患有血液恶性肿瘤和 FN 的患者的样本进行了评估。在每个剂量后稳态时的 10、60、120、180 和 350 分钟,从每位患者中抽取 5 个血样。使用枯草芽孢杆菌凝胶扩散法测量抗生素浓度。所有研究参与者均提供了书面知情同意书。

结果

我们调查了 14 名年龄在 18 岁至 59 岁之间且绝对中性粒细胞计数为 208 个细胞/mm³(标准差(SD)±603.2)的患者的哌拉西林药代动力学。获得了以下药代动力学测量值:最大浓度,94.1-1133mg/L;最小浓度,0.47-37.65mg/L;分布容积,0.08-0.65L/kg(平均,0.34L/kg);药物清除率(CL),4.42-27.25L/h(平均,9.93L/h);半衰期(t1/2),0.55-2.65h(平均,1.38h);曲线下面积,115.12-827.16mg·h/L。

结论

与健康个体相比,接受化疗后患有 FN 的患者的哌拉西林药代动力学参数存在显著差异;具体而言,FN 患者的 t1/2 增加,CL 降低。

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