Ceken Sabahat, Iskender Gulsen, Gedik Habip, Duygu Fazilet, Mert Duygu, Kaya Ali Hakan, Altuntas Fevzi, Ertek Mustafa
Dr Abdurrahman Yurtaslan Oncology Research and Training Hospital, Ankara, Turkey.
Bakırkör Sadi Konuk Research and Training Hospital, Istanbul, Turkey.
J Infect Dev Ctries. 2018 Apr 30;12(4):265-272. doi: 10.3855/jidc.9720.
Bloodstream infection (BSI) caused by Enterobacteriaceae is associated with mortality in cancer patients receiving chemotherapy. The aim of this study is to identify the risk factors and outcomes related to BSIs caused by extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae in cancer patients.
Hematology/oncology patients, who were diagnosed with BSIs caused by Enterobacteriaceae by positive blood cultures were evaluated retrospectively. Patients were divided into two groups by ESBL-positive and ESBL-negative Enterobacteriaceae bacteremia. Patients' demographic features, underlying conditions, comorbidity, neutrophil count, duration of neutropenia, antibiotic use in the previous three months before infection, mechanical ventilation, steroid use, central venous catheter implementation, total parenteral nutrition (TPN), hospitalization in the past three months, stay in intensive care unit, quinolone prophylaxis, and history of infection with ESBL-producing Enterobactericeae were evaluated. Risk factors related to BSIs caused by ESBL-producing Enterobacteriaceae and mortality were assessed.
A total of 122 patients were evaluated retrospectively. Quinolone propyhlaxis, TPN, infection with Extended Spectrum Beta-Lactamase positive ESBL-P Enterobacteriaceae during the previous three months, treatment with piperasillin-tazobactam or carbapenems in the previous three months were found to be independent risk factors for ESBL-P BSIs. Longer duration of neutropenia before BSI and complication at the beginning of BSI were found to be independent risk factors for mortality related to infection.
ESBL-producing Enterobacteriacea should be treated with an appropriate antibiotic that is associated with better outcomes in hematology/oncology patients with BSIs. History of broad-spectrum antibiotic use and stay in hospital in the previous three months should be taken into consideration upon commencing antibiotic therapy.
肠杆菌科细菌引起的血流感染(BSI)与接受化疗的癌症患者的死亡率相关。本研究的目的是确定癌症患者中由产超广谱β-内酰胺酶(ESBL)的肠杆菌科细菌引起的BSI的危险因素及预后情况。
对血液学/肿瘤学患者进行回顾性评估,这些患者通过血培养阳性被诊断为由肠杆菌科细菌引起的BSI。患者按肠杆菌科细菌血症ESBL阳性和ESBL阴性分为两组。评估患者的人口统计学特征、基础疾病、合并症、中性粒细胞计数、中性粒细胞减少持续时间、感染前三个月的抗生素使用情况、机械通气、类固醇使用、中心静脉导管置入、全胃肠外营养(TPN)、过去三个月的住院情况、入住重症监护病房情况、喹诺酮预防用药以及产ESBL肠杆菌科细菌感染史。评估与产ESBL肠杆菌科细菌引起的BSI相关的危险因素及死亡率。
共对122例患者进行了回顾性评估。发现喹诺酮预防用药、TPN、前三个月产超广谱β-内酰胺酶阳性(ESBL-P)的肠杆菌科细菌感染、前三个月使用哌拉西林-他唑巴坦或碳青霉烯类药物治疗是ESBL-P BSI的独立危险因素。BSI前中性粒细胞减少持续时间较长以及BSI开始时出现并发症是与感染相关死亡率的独立危险因素。
对于血液学/肿瘤学BSI患者,产ESBL的肠杆菌科细菌应使用与之预后较好的合适抗生素进行治疗。开始抗生素治疗时应考虑广谱抗生素使用史和过去三个月的住院情况。