哌拉西林/他唑巴坦在恶性血液病伴发热性中性粒细胞减少患者化疗后的药代动力学研究。

IF 2.9 3区 医学 Q2 Medicine BMC Pharmacology & Toxicology Pub Date : 2013-11-28 DOI:10.1186/2050-6511-14-59
José C Álvarez, Sonia I Cuervo, Javier R Garzón, Julio C Gómez, Jorge Augusto Díaz, Edelberto Silva, Ricardo Sánchez, Jorge A Cortés
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引用次数: 9

摘要

发热性中性粒细胞减少症(FN)患者表现出细胞外液的变化,可能改变β -内酰胺的血浆浓度,导致治疗失败或毒性。我们评估了哌拉西林/他唑巴坦在原发性公共癌症中心接受化疗的血液恶性肿瘤和FN患者中的药代动力学。方法:这是一项开放、非随机、观察性、描述性和前瞻性研究。对15例血液恶性肿瘤和FN患者进行化疗后的样本进行评估。在每次给药后10、60、120、180和350分钟的稳定状态下,从每位患者采集5份血液样本。用枯草芽孢杆菌凝胶扩散法测定抗生素浓度。所有研究参与者都提供了书面知情同意书。结果:我们研究了14例年龄在18岁至59岁之间,平均绝对中性粒细胞计数为208个细胞/ mm³(标准差(SD)±603.2)的患者哌西林的药代动力学。获得了以下药代动力学测量值:最大浓度为94.1 ~ 1133 mg/L;最低浓度0.47 ~ 37.65 mg/L;分布容积0.08-0.65 L/kg(平均值0.34 L/kg);药物清除率(CL) 4.42 ~ 27.25 L/h(平均9.93 L/h);半衰期(t(1/2)), 0.55-2.65 h(平均1.38 h);曲线下面积为115.12 ~ 827.16 mg·h/L。结论:FN患者化疗后哌拉西林药动学参数与健康人相比存在显著差异;具体而言,FN患者表现出t1(/2)增加和CL降低。
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Pharmacokinetics of piperacillin/tazobactam in cancer patients with hematological malignancies and febrile neutropenia after chemotherapy.

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.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACY-TOXICOLOGY
CiteScore
4.40
自引率
0.00%
发文量
0
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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