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哌拉西林/他唑巴坦在儿童和青少年接受高剂量放化疗及自体干细胞移植后的耐受性

Tolerability of piperacillin/tazobactam in children and adolescents after high dose radio-/chemotherapy and autologous stem cell transplantation.

作者信息

Nürnberger W, Bönig H, Burdach S, Göbel U

机构信息

Klinik für Pädiatrische Hämatologie und Onkologie, Heinrich-Heine-Universität, Düsseldorf, Germany.

出版信息

Infection. 1998 Jan-Feb;26(1):65-7. doi: 10.1007/BF02768763.

DOI:10.1007/BF02768763
PMID:9505187
Abstract

The combination of piperacillin with tazobactam (PIP/TAZ) extends the activity of piperacillin against gram-positive, gram-negative, and anaerobic bacteria. The broad-spectrum of this formulation, together with its low degree of organ toxicity observed in adults, makes PIP/TAZ a tempting choice for children with radio-/chemotherapy-induced neutropenia. However, the use of PIP/TAZ is not yet approved for children under 12 years of age. The tolerability of PIP/TAZ was assessed in 19 children and adolescents between 2 and 18 years of age who developed a fever during aplasia after high dose radio-/chemotherapy and autologous stem cell transplantation (HD-SCT) for primary multifocal or relapsed solid tumours. Treatment with PIP/TAZ was initiated on average 3 days after HD-SCT, and the treatment was continued for approximately 10 days. Both clinical observation and laboratory studies showed no relevant alterations that would have been attributable to PIP/TAZ treatment. These results indicate that PIP/TAZ appears to be well tolerated in children during the acute phase of HD-SCT.

摘要

哌拉西林与他唑巴坦联合使用(PIP/TAZ)可扩大哌拉西林对革兰氏阳性菌、革兰氏阴性菌及厌氧菌的抗菌活性。该制剂的广谱抗菌特性,以及在成人中观察到的低器官毒性,使得PIP/TAZ成为患有放疗/化疗所致中性粒细胞减少症儿童的诱人选择。然而,PIP/TAZ在12岁以下儿童中的使用尚未获得批准。对19名年龄在2至18岁之间的儿童和青少年进行了PIP/TAZ耐受性评估,这些儿童和青少年因原发性多灶性或复发性实体瘤接受高剂量放疗/化疗及自体干细胞移植(HD-SCT)后在造血再生障碍期出现发热。PIP/TAZ治疗平均在HD-SCT后3天开始,持续约10天。临床观察和实验室研究均未显示出与PIP/TAZ治疗相关的显著改变。这些结果表明,在HD-SCT急性期,儿童对PIP/TAZ的耐受性似乎良好。

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引用本文的文献

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Piperacillin-tazobactam in pediatric cancer patients younger than 25 months: a retrospective multicenter survey.哌拉西林-他唑巴坦在25个月以下儿童癌症患者中的应用:一项回顾性多中心调查。
Eur J Clin Microbiol Infect Dis. 2007 Nov;26(11):801-6. doi: 10.1007/s10096-007-0382-5.
2
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Support Care Cancer. 2004 Oct;12(10):720-4. doi: 10.1007/s00520-004-0641-2.

本文引用的文献

1
Humoral coagulation and early complications after allogeneic bone marrow transplantation.异基因骨髓移植后的体液凝固与早期并发症
Klin Padiatr. 1997 Jul-Aug;209(4):209-15. doi: 10.1055/s-2008-1043952.
2
The chemistry, pharmacokinetics and tissue distribution of piperacillin/tazobactam.哌拉西林/他唑巴坦的化学、药代动力学及组织分布
J Antimicrob Chemother. 1993 Jan;31 Suppl A:39-60. doi: 10.1093/jac/31.suppl_a.39.
3
Safety profile of piperacillin/tazobactam in phase I and III clinical studies.
J Antimicrob Chemother. 1993 Jan;31 Suppl A:113-24. doi: 10.1093/jac/31.suppl_a.113.
4
Interactions of tazobactam and clavulanate with inducibly- and constitutively-expressed Class I beta-lactamases.他唑巴坦和克拉维酸与诱导型和组成型表达的I类β-内酰胺酶的相互作用。
J Antimicrob Chemother. 1990 Feb;25(2):199-208. doi: 10.1093/jac/25.2.199.