Fouyssac F, Salmon A, Mansuy L, Schmitt C, Bordigoni P, Chastagner P
Service d'hémato-oncologie pédiatrique, hôpital d'Enfants, CHU de Nancy, 54500 Vandoeuvre-lès-Nancy, France.
Med Mal Infect. 2005 Jun;35(6):357-62. doi: 10.1016/j.medmal.2005.04.004.
The authors had for aim to assess the effectiveness and toxicity of a piperacillin-tazobactam-netilmicin combination, and the possibility of avoiding using glycopeptide, in children with febrile neutropenic episodes induced by chemotherapy.
A retrospective study was made, including children treated for a febrile neutropenic episode (absolute neutrophile count < 0.5 x 10(9)/l) by a piperacillin-tazobactam-netilmicin combination. If fever persisted 48 hours after the beginning of antibiotic therapy, a glycopeptide could be added. The responses to the treatment were defined as follows: 1) total success (no fever or documented infection) at 48 hours and at 72 hours following the beginning of treatment; 2) partial success (apyrexia beyond 72 hours without any therapeutic change); 3) failure (persistent infectious signs 48 hours after the introduction of glycopeptide).
Sixty-nine episodes were assessable, corresponding to 41 patients, treated for a solid tumour (29), an acute leukaemia in remission (11), or a metabolic disease (1). The febrile episodes were divided into fever of unknown origin (71%), microbiologically documented fever (12%), and clinically documented fever (17%). No death occurred, no toxicity was reported. With this antibiotic therapy, total success at 72 hours was observed in 72% in case of fever of unknown origin and 45% in case of documented infections. The success rate reached 84% when a glycopeptide was added (30% of the cases).
The piperacillin-tazobactam-netilmicin combination is very effective and well tolerated in probabilistic treatment of febrile neutropenia induced by chemotherapy, but does not allow to decreasing the frequency of glycopeptide administration.
作者旨在评估哌拉西林-他唑巴坦-奈替米星联合用药的有效性和毒性,以及在化疗引起的发热性中性粒细胞减少发作的儿童中避免使用糖肽类药物的可能性。
进行了一项回顾性研究,纳入了因发热性中性粒细胞减少发作(绝对中性粒细胞计数<0.5×10⁹/L)接受哌拉西林-他唑巴坦-奈替米星联合治疗的儿童。如果在抗生素治疗开始后48小时仍有发热,可加用糖肽类药物。治疗反应定义如下:1)治疗开始后48小时和72小时时完全成功(无发热或有记录的感染);2)部分成功(72小时后无热且无任何治疗改变);3)失败(加用糖肽类药物48小时后仍有持续感染体征)。
69例发作可评估,对应41例患者,治疗的疾病包括实体瘤(29例)、缓解期急性白血病(11例)或代谢性疾病(1例)。发热发作分为不明原因发热(71%)、微生物学证实的发热(12%)和临床证实的发热(17%)。无死亡病例,未报告毒性反应。采用这种抗生素治疗,不明原因发热患者72小时时的完全成功率为72%,有记录感染患者为45%。加用糖肽类药物时成功率达到84%(占病例的30%)。
哌拉西林-他唑巴坦-奈替米星联合用药在化疗引起的发热性中性粒细胞减少的概率性治疗中非常有效且耐受性良好,但不能降低糖肽类药物的给药频率。