首页> 外文期刊>Pediatric Hematology and Oncology >Randomized comparison of piperacillin-tazobactam plus amikacin versus cefoperazone-sulbactam plus amikacin for management of febrile neutropenia in children with lymphoma and solid tumors
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Randomized comparison of piperacillin-tazobactam plus amikacin versus cefoperazone-sulbactam plus amikacin for management of febrile neutropenia in children with lymphoma and solid tumors

机译:哌拉西林他唑巴坦加阿米卡星与头孢哌酮舒巴坦加阿米卡星治疗淋巴瘤和实体瘤患儿发热性中性粒细胞减少症的随机比较

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The objective of this study was to compare the effectiveness of piperacillin-tazobactam (PIP/TAZO) plus amikacin (AMK) (PIP/TAZO+AMK) versus cefoperazone-sulbactam (CS) plus AMK (CS+AMK) for the treatment of febrile neutropenia (FN) in children with cancer. The study was designed prospectively and randomized in 0-to 18-year-old children with lymphoma or solid tumor who were hospitalized with FN diagnosis. Consecutively randomized patients received either PIP/TAZO 360 mg/kg/day in 4 doses plus AMK 15 mg/kg/day in 3 doses or CS 100 mg/kg/day in 3 doses plus AMK 15 mg/kg/day in 3 doses intravenously. Treatment modification was defined as any change in the initial empirical antibiotic therapy. A total of 116 FN episodes were managed in 46 patients (26 boys and 20 girls) with a median age of 6.5 years (range .8-17.0) during the study period. Success rates without modification of therapy were 47.5% and 52.6% in PIP/TAZO+AMK group and CS+AMK group, respectively (P >.05). No statistical difference was found between treatment groups in terms of durations of neutropenia, fever, and hospitalization. The overall success rate in all groups was 97.4%. No major side effect was observed in either group during the course of the study. Our study is the first to compare the effectiveness of PIP/TAZO+AMK and CS+AMK therapies. Both combinations were effective and safe as empirical therapy for febrile neutropenic patients.
机译:这项研究的目的是比较哌拉西林-他唑巴坦(PIP / TAZO)加阿米卡星(AMK)(PIP / TAZO + AMK)与头孢哌酮舒巴坦(CS)加AMK(CS + AMK)的疗效儿童患中性粒细胞减少症(FN)。这项研究是前瞻性设计的,并被随机分入FN诊断住院的0至18岁淋巴瘤或实体瘤患儿。连续随机分组的患者接受4剂PIP / TAZO 360 mg / kg /天,3剂AMK 15 mg / kg /天,3剂CS 100 mg / kg /天,3剂量以及3剂AMK 15 mg / kg /天静脉注射。治疗修改定义为最初的经验性抗生素治疗中的任何变化。在研究期间,共对46位患者(26位男孩和20位女孩)进行了116次FN发作,中位年龄为6.5岁(范围为0.8-17.0)。 PIP / TAZO + AMK组和CS + AMK组未经治疗修改的成功率分别为47.5%和52.6%(P> .05)。在中性粒细胞减少症,发热和住院时间方面,各治疗组之间无统计学差异。所有组的总成功率为97.4%。在研究过程中,两组均未观察到重大副作用。我们的研究是第一个比较PIP / TAZO + AMK和CS + AMK疗法有效性的研究。两种组合作为高热中性粒细胞减少症患者的经验疗法都是有效和安全的。

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