[Fever and neutropenia in children with cancer: a new therapeutic proposal].

A S Petrilli, R Melaragno, A Bianchi, E Kusano, K V Barros, A A Silva
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Abstract

Based on our previous experience treating children with cancer, fever and neutropenia we selected two different empirical regimens: Ceftriaxone once a day, for patients with solid tumors and lymphomas I-II (Low Risk group--LR) and Imipenem for patients with leukemias and lymphomas III-IV (High Risk group--HR). From Oct 1988 to Nov 1989, 121 episodes of fever (F+) and granulocytopenia (G+) in LR Group and 119 in HR Group were studied: the HR had 51.3% documented infections and the LR 58.7%. In the HR Group the following organisms were isolated from the blood cultures: Gram + 52%, Gram - 20% and fungal 28%. In the LR Group 78% of the organisms were Gram+. Positive blood cultures was 21% for the HR Group and 8.3% for the LR Group. There were 23.5% superinfections in the HR Group vs 5.7% in the LR. The mean time and the median time of granulocytopenia was 11.5 and 8 days (HR) and 6.9 and 6.0 days (LR), respectively. There were 14.5% (LR) and 45.4% (HR) modifications to the initial empirical antibiotic regimen (Amphotericin B, Vancomycin and Amikacin). The overall success rate was 97.6% (LR) and 94.2% (HR) and for documented infection the success rate was 95.7% (LR) and 91.8% (HR). We conclude that: a) The allocation of patients to two risk groups aiming to use distinguished therapy, allowed us to delineate two different populations, predominantly based on time of granulocytopenia, disappearance of fever, rate of superinfection, causative organisms and need of additional drugs to the initial scheme.(ABSTRACT TRUNCATED AT 250 WORDS)

[发烧和中性粒细胞减少症的儿童癌症:一个新的治疗建议]。
根据我们以前治疗儿童癌症、发热和中性粒细胞减少症的经验,我们选择了两种不同的经验方案:头孢曲松每天一次,用于实体瘤和淋巴瘤I-II(低风险组-LR),亚胺培南用于白血病和淋巴瘤III-IV(高风险组-HR)。1988年10月至1989年11月,我们对121例发热(F+)和粒细胞减少症(G+)病例进行了研究,其中HR组和HR组分别有119例和51.3%和58.7%的病例。HR组血培养分离出革兰氏阳性菌52%,革兰氏阴性菌20%,真菌28%。LR组78%的微生物为Gram+。HR组血培养阳性21%,LR组血培养阳性8.3%。HR组有23.5%的重复感染,而LR组有5.7%。粒细胞减少的平均时间和中位时间分别为11.5和8 d (HR)和6.9和6.0 d (LR)。对初始经验抗生素方案(两性霉素B、万古霉素和阿米卡星)的修改分别为14.5% (LR)和45.4% (HR)。总成功率为97.6% (LR)和94.2% (HR),记录感染的成功率为95.7% (LR)和91.8% (HR)。我们的结论是:a)将患者分配到两个风险组,旨在使用不同的治疗方法,使我们能够主要根据粒细胞减少的时间,发烧消失,重复感染率,致病生物体和初始方案的额外药物需求来描绘两个不同的人群。(摘要删节250字)
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