Petrilli A S, Melaragno R, Bianchi A, Kusano E, Barros K V, Silva A A
Dep. de Oncol. Pediát. do Hosp. A.C. Camargo.
AMB Rev Assoc Med Bras. 1991 Oct-Dec;37(4):173-80.
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)
根据我们以往治疗儿童癌症、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性治疗方案:对于实体瘤和Ⅰ - Ⅱ期淋巴瘤患者(低风险组 - LR),每日使用一次头孢曲松;对于白血病和Ⅲ - Ⅳ期淋巴瘤患者(高风险组 - HR),使用亚胺培南。从1988年10月至1989年11月,对低风险组的121例发热(F +)和粒细胞减少(G +)发作以及高风险组的119例进行了研究:高风险组有51.3%的确诊感染病例,低风险组为58.7%。在高风险组中,从血培养中分离出以下微生物:革兰氏阳性菌52%,革兰氏阴性菌20%,真菌28%。在低风险组中,78%的微生物为革兰氏阳性菌。高风险组血培养阳性率为21%,低风险组为8.3%。高风险组的二重感染率为23.5%,低风险组为5.7%。粒细胞减少的平均时间和中位数时间在高风险组分别为11.5天和8天,在低风险组分别为6.9天和6.0天。初始经验性抗生素方案(两性霉素B、万古霉素和阿米卡星)的调整率在低风险组为14.5%,在高风险组为45.4%。总体成功率在低风险组为97.6%,在高风险组为94.2%;对于确诊感染,成功率在低风险组为95.7%,在高风险组为91.8%。我们得出结论:a)将患者分为两个风险组以采用不同的治疗方法,使我们能够区分出两个不同的群体,主要依据是粒细胞减少的时间、发热消退情况、二重感染率、致病微生物以及初始方案中是否需要添加其他药物。(摘要截选至250字)