小儿肿瘤患者万古霉素适宜剂量的确定

E. Suzuki, Jun Nishijo, Mami Oguchi, Katsuyuki Hori, Takemi Murai, Kisei Minami
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摘要

由于病理生理和抗癌药物的不良反应,儿童癌症与感染的高风险相关。虽然万古霉素(VCM)常用于治疗癌症相关感染,但关于儿童癌症中万古霉素剂量的研究有限。因此,我们回顾性地研究了长野儿童医院给儿童癌症患者的VCM剂量。将剂量谷值与药师治疗药物监测(TDM)干预和修订后的抗菌TDM指南进行比较。在2011年4月至2017年3月期间,接受VCM治疗的1-12岁儿童癌症患者参加了这项研究。比较两组患者的日剂量、给药次数、VCM波谷值及给药开始和结束时血清肌酐水平。29例1-6岁患者的平均日剂量从治疗开始时的45.8 mg/kg/天显著增加到治疗结束时的61.8 mg/kg/天。剂量从每天3次显著增加到4次。VCM波谷值由5.0 μg/mL显著升高至10.0 μg/mL。血清肌酐水平从0.21 mg/dL维持到0.20 mg/dL。在9例7-12岁的患者中,日剂量从46.1 mg/kg/天增加到60.0 mg/kg/天。剂量数量保持不变,每天4次。波谷值由6.5 μg/mL显著升高至10.2 μg/mL。然而,血清肌酐水平从0.24 mg/dL到0.25 mg/dL保持不变。在儿童癌症患者中,根据修订后的指南,1-6岁儿童的VCM剂量为61.8 mg/kg/天(15.5 mg/kg,每6小时),7-12岁儿童的VCM剂量为60.0 mg/kg/天(15.0 mg/kg,每6小时),以达到谷浓度10 μg/mL或更高的目标。通过进一步的TDM, VCM可能达到目标波谷值。
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Determination of the Appropriate Dose of Vancomycin for Pediatric Patients with Cancer
Childhood cancers are associated with a high risk of infection due to the pathophysiology and adverse effects of anticancer drugs. Although vancomycin (VCM) is often used for treating cancer-associated infections, there are limited studies on VCM dosing in childhood cancers. Therefore, we retrospectively investigated VCM dosing administered to pediatric patients with cancer at Nagano Children’s Hospital. The trough values of the dose were compared with pharmacists’ therapeutic drug monitoring (TDM) intervention and the revised antimicrobial TDM guidelines. Between April 2011 and March 2017, pediatric patients with cancer aged 1-12 years who were administered VCM were enrolled in the study. The daily dose, number of doses, trough value of VCM, and serum creatinine level at the start and end of VCM administration were compared. The average daily doses significantly increased from 45.8 mg/kg/day at the beginning to 61.8 mg/kg/day at the end of therapy in 29 patients aged 1-6 years. The number of doses significantly increased from 3 to 4 times daily. The trough value of VCM significantly increased from 5.0 μg/mL to 10.0 μg/mL. The serum creatinine level remained unchanged from 0.21 mg/dL to 0.20 mg/dL. In nine patients aged 7-12 years, the daily dose increased from 46.1 mg/kg/day to 60.0 mg/kg/day. The number of doses remained unchanged 4 times a day. The trough value increased significantly from 6.5 μg/mL to 10.2 μg/mL. However, the serum creatinine level remained unchanged from 0.24 mg/dL to 0.25 mg/dL. In pediatric patients with cancer, VCM doses to reach the target value of a trough concentration of 10 μg/mL or more were started with an administration of 61.8 mg/kg/day (15.5 mg/kg, every 6 h) for children aged 1-6 years and 60.0 mg/kg/day (15.0 mg/kg, every 6 h) according to the revised guidelines for those aged 7-12 years. VCM might reach the target trough value by further TDM.
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