de Maio Carrilho Claudia M D, de Oliveira Larissa Marques, Gaudereto Juliana, Perozin Jamile S, Urbano Mariana Ragassi, Camargo Carlos H, Grion Cintia M C, Levin Anna Sara S, Costa Silvia F
Internal Medicine Department, Londrina State University, Paraná, Brazil.
Microbiologist, Londrina, Brazil.
BMC Infect Dis. 2016 Nov 3;16(1):629. doi: 10.1186/s12879-016-1979-z.
To describe the clinical and microbiological data of carbapenem-resistant Enterobacteriaceae (CRE) infections, the treatment used, hospital- and infection-related mortality, and risk factors for death.
A prospective cohort conducted from March 2011 to December 2012. Clinical, demographic, and microbiological data such as in vitro sensitivity, clonality, carbapenemase gene mortality related to infection, and overall mortality were evaluated. Data were analyzed using Epi Info version 7.0 (CDC, Atlanta, GA, USA) and SPSS (Chicago, IL, USA).
One hundred and twenty-seven patients were evaluated. Pneumonia, 52 (42 %), and urinary tract infections (UTI), 51 (40.2 %), were the most frequent sites of infection. The isolates were polyclonal; the Bla gene was found in 75.6 % of isolates, and 27 % of isolates were resistant to colistin. Mortality related to infection was 34.6 %, and was higher among patients with pneumonia (61.4 %). Combination therapy was used in 98 (77.2 %), and monotherapy in 22.8 %; 96.5 % of them were UTI patients. Shock, age, and dialysis were independent risk factors for death. There was no difference in infection-related death comparing colistin-susceptible and colistin-resistant infections (p = 0.46); neither in survival rate comparing the use of combination therapy with two drugs or more than two drugs (p = 0.32).
CRE infection mortality was higher among patients with pneumonia. Infections caused by colistin-resistant isolates did not increase mortality. The use of more than two drugs on combination therapy did not show a protective effect on outcome. The isolates were polyclonal, and the bla gene was the only carbapenemase found. Shock, dialysis, and age over 60 years were independent risk factors for death.
描述耐碳青霉烯类肠杆菌科细菌(CRE)感染的临床和微生物学数据、所采用的治疗方法、与医院和感染相关的死亡率以及死亡风险因素。
于2011年3月至2012年12月进行一项前瞻性队列研究。评估临床、人口统计学和微生物学数据,如体外敏感性、克隆性、与感染相关的碳青霉烯酶基因死亡率以及总体死亡率。使用Epi Info 7.0版本(美国疾病控制与预防中心,佐治亚州亚特兰大)和SPSS(美国伊利诺伊州芝加哥)对数据进行分析。
共评估了127例患者。肺炎(52例,42%)和尿路感染(UTI,51例,40.2%)是最常见的感染部位。分离株为多克隆;75.6%的分离株中发现了Bla基因,27%的分离株对黏菌素耐药。与感染相关的死亡率为34.6%,肺炎患者中的死亡率更高(61.4%)。98例(77.2%)采用联合治疗,22.8%采用单药治疗;其中96.5%为UTI患者。休克、年龄和透析是死亡的独立危险因素。比较黏菌素敏感和耐药感染的感染相关死亡情况无差异(p = 0.46);比较使用两种或两种以上药物的联合治疗的生存率也无差异(p = 0.32)。
肺炎患者中CRE感染死亡率更高。由耐黏菌素分离株引起的感染并未增加死亡率。联合治疗中使用两种以上药物对结局未显示出保护作用。分离株为多克隆,且Bla基因是唯一发现的碳青霉烯酶。休克、透析和60岁以上年龄是死亡的独立危险因素。