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[哌拉西林联合舒巴坦单药治疗并可能序贯万古霉素在实体瘤发热性中性粒细胞减少症中的价值]

[Value of mono-antibiotic therapy using piperacillin associated with sulbactam and possibly followed by vancomycin in febrile neutropenia in solid tumors].

作者信息

Abs L, Kattan J, Culine S, Bekradda M, Farhat F, Droz J P

机构信息

Département de médecine, institut Gustave-Roussy, Villejuif, France.

出版信息

Bull Cancer. 1994 Oct;81(10):871-6.

PMID:7734770
Abstract

We evaluated the efficacy and safety of a monotherapy by piperacillin and sulbactam potentially associated to vancomycin as an empiric antimicrobial therapy in febrile neutropenic patients treated with nephrotoxic chemotherapy for solid tumors. Twenty-three patients were treated during 32 episodes with piperacillin 4 g i.v. every 8 hours and sulbactam 1 g IV every 8 hours. If the patient remained febrile after 48 hours, 1 g of vancomycin i.v. was added every 12 hours as indicated by our study design. The mean duration of neutropenia was 5.5 days (2-13 days). In ten episodes, the granulocyte nadir was < 100/mm3. Infection was microbiologically documented in seven episodes (22%) with six Gram negative bacilli and 3 Gram positive cocci. There were 19 apyrexia with piperacillin and sulbactam (59%) and further seven were resolved by the addition of vancomycin (total success: 81%). Failure was observed in six episodes consecutive to germ resistance (one episode), clinical deterioration (one episode), relapsing fever related to Pseudomonas infection (one episode), persistent fever despite withdrawal of neutropenia and no microbiological documentation (two episodes) and protocol violation (one episode). Neither septic death nor toxicity were observed. We conclude that this empirical treatment is active and safe in short period febrile neutropenic episodes in patients heavily treated with nephrotoxic chemotherapy for solid tumors.

摘要

我们评估了哌拉西林和舒巴坦单一疗法的疗效和安全性,该疗法可能与万古霉素联合用于实体瘤肾毒性化疗的发热性中性粒细胞减少患者的经验性抗菌治疗。23例患者在32个疗程中接受治疗,静脉注射哌拉西林4g,每8小时一次,静脉注射舒巴坦1g,每8小时一次。根据我们的研究设计,如果患者在48小时后仍发热,则每12小时静脉注射1g万古霉素。中性粒细胞减少的平均持续时间为5.5天(2 - 13天)。在10个疗程中,粒细胞最低点<100/mm³。7个疗程(22%)有微生物学记录的感染,其中6例为革兰氏阴性杆菌,3例为革兰氏阳性球菌。使用哌拉西林和舒巴坦后有19例退热(59%),另外7例通过添加万古霉素后退热(总成功率:81%)。在6个疗程中观察到治疗失败,原因分别为细菌耐药(1个疗程)、临床恶化(1个疗程)、与铜绿假单胞菌感染相关的复发性发热(1个疗程)、尽管中性粒细胞减少已消除但仍持续发热且无微生物学记录(2个疗程)以及违反方案(1个疗程)。未观察到败血症死亡或毒性反应。我们得出结论,这种经验性治疗对于接受实体瘤肾毒性化疗的重症患者短期发热性中性粒细胞减少发作是有效且安全的。

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