Castagnola Elio, Caviglia Ilaria, Pescetto Luisa, Bagnasco Francesca, Haupt Riccardo, Bandettini Roberto
Infectious Diseases Unit, Istituto Giannina Gaslini, Genoa, Italy.
Future Microbiol. 2015;10(3):357-64. doi: 10.2217/fmb.14.144.
Monotherapy is recommended as the first choice for initial empirical therapy of febrile neutropenia, but local epidemiological and antibiotic susceptibility data are now considered pivotal to design a correct management strategy.
To evaluate the proportion of Gram-negative rods isolated in bloodstream infections in children with cancer resistant to antibiotics recommended for this indication.
MATERIALS & METHODS: The in vitro susceptibility to ceftazidime, piperacillin-tazobactam, meropenem and amikacin of Gram-negatives isolated in bacteremic episodes in children with cancer followed at the Istituto "Giannina Gaslini", Genoa, Italy in the period of 2001-2013 was retrospectively analyzed using the definitions recommended by EUCAST in 2014. Data were analyzed for any single drug and to the combination of amikacin with each β-lactam. The combination was considered effective in absence of concomitant resistance to both drugs, and not evaluated by means of in vitro analysis of antibiotic combinations (e.g., checkerboard).
A total of 263 strains were evaluated: 27% were resistant to piperacillin-tazobactam, 23% to ceftazidime, 12% to meropenem and 13% to amikacin. Concomitant resistance to β-lactam and amikacin was detected in 6% of strains for piperacillin-tazobactam, 5% for ceftazidime and 5% for meropenem. During the study period there was a nonsignificant increase in the proportions of strains resistant to β-lactams indicated for monotherapy, and also increase in the resistance to combined therapies.
in an era of increasing resistance to antibiotics guideline-recommended monotherapy could be not appropriate for initial empirical therapy of febrile neutropenia. Strict local survey on etiology and antibiotic susceptibility is mandatory for a correct management of this complication in cancer patients.
单药治疗被推荐作为发热性中性粒细胞减少症初始经验性治疗的首选,但目前认为当地的流行病学和抗生素敏感性数据对于设计正确的管理策略至关重要。
评估在癌症患儿血流感染中分离出的革兰氏阴性杆菌对推荐用于该适应症的抗生素耐药的比例。
回顾性分析2001年至2013年期间在意大利热那亚的“吉安尼娜·加斯利尼”研究所接受治疗的癌症患儿菌血症发作中分离出的革兰氏阴性菌对头孢他啶、哌拉西林-他唑巴坦、美罗培南和阿米卡星的体外敏感性,采用2014年欧盟CAST推荐的定义。对每种单一药物以及阿米卡星与每种β-内酰胺类药物的联合用药的数据进行了分析。如果不存在对两种药物的同时耐药,则认为联合用药有效,并且未通过抗生素联合用药的体外分析(例如棋盘法)进行评估。
共评估了263株菌株:27%对哌拉西林-他唑巴坦耐药,23%对头孢他啶耐药,12%对美罗培南耐药,13%对阿米卡星耐药。在6%的菌株中检测到对哌拉西林-他唑巴坦的β-内酰胺类和阿米卡星同时耐药,对头孢他啶为5%,对美罗培南为5%。在研究期间,推荐用于单药治疗的β-内酰胺类耐药菌株的比例有不显著增加,联合治疗的耐药性也有所增加。
在抗生素耐药性不断增加的时代,指南推荐的单药治疗可能不适用于发热性中性粒细胞减少症的初始经验性治疗。对于癌症患者这种并发症的正确管理,必须进行严格的当地病因和抗生素敏感性调查。