Maseda Emilio, Salgado Patricia, Anillo Víctor, Ruiz-Carrascoso Guillermo, Gómez-Gil Rosa, Martín-Funke Carmen, Gimenez Maria-Jose, Granizo Juan-José, Aguilar Lorenzo, Gilsanz Fernando
Anesthesiology and Surgical Critical Care Dpt., Hospital Universitario La Paz, Madrid, Spain.
Anesthesiology and Surgical Critical Care Dpt., Hospital Universitario La Paz, Madrid, Spain.
Enferm Infecc Microbiol Clin. 2017 Jun-Jul;35(6):333-337. doi: 10.1016/j.eimc.2016.02.017. Epub 2016 Mar 22.
In 2011, a hospital-wide outbreak of OXA-48 producing Klebsiella pneumoniae occurred in our hospital, an epidemiological setting of high ESBL-producing K. pneumoniae rates. This study identifies risk factors for colonization with carbapenemase-producing enterobacteria (CPE) at Surgical Intensive Care Unit (SICU) admission.
A 2-year retrospective study was performed in all patients admitted to the SICU that following routine had a rectal swab collected upon admission.
Of 254 patients admitted, 41 (16.1%) harbored CPE (five showing two carbapenemase-producing isolates). Most frequent carbapenemase-producing isolates and carbapenemases were K. pneumoniae (39/46, 84.8%) and OXA-48 (31/46; 76.1%), respectively. Carriers significantly had higher rates of chronic renal disease, previous digestive/biliary endoscopy, hospitalization, ICU/SICU admission, intraabdominal surgery, and antibiotic intake, as well as higher median values of clinical scores (SOFA, SAPS II and APACHE II). In the multivariate analysis (R=0.309, p<0.001), CPE carriage was associated with prior administration of 3rd-4th generation cephalosporins (OR=27.96, 95%CI=6.88, 113.58, p<0.001), β-lactam/β-lactamase inhibitor (OR=11.71, 95%CI=4.51, 30.43, p<0.001), abdominal surgery (OR=6.33, 95%CI=2.12, 18.89, p=0.001), and prior digestive/biliary endoscopy (OR=3.88, 95%CI=1.56, 9.67, p=0.004).
A strong association between production of ESBLs and carriage of CPE (mainly OXA-48 producing K. pneumoniae) was found. According to the model, the co-selection of β-lactamases by previous exposure to broad-spectrum cephalosporins and β-lactam/β-lactamase inhibitors (with lower relative risk), abdominal surgery and prior digestive/biliary endoscopy were factors associated with CPE carriage.
2011年,我院发生了一次全院范围的产OXA - 48肺炎克雷伯菌暴发,当时医院环境中产超广谱β-内酰胺酶(ESBL)的肺炎克雷伯菌比例很高。本研究确定了外科重症监护病房(SICU)入院时产碳青霉烯酶肠杆菌(CPE)定植的危险因素。
对所有入住SICU的患者进行了一项为期2年的回顾性研究,这些患者在入院时按常规进行了直肠拭子采集。
在254例入院患者中,41例(16.1%)携带CPE(5例有两种产碳青霉烯酶的分离株)。最常见的产碳青霉烯酶分离株和碳青霉烯酶分别是肺炎克雷伯菌(39/46,84.8%)和OXA - 48(31/46;76.1%)。携带者的慢性肾病、既往消化/胆道内镜检查、住院、入住重症监护病房/外科重症监护病房、腹部手术和抗生素使用发生率显著更高,临床评分(序贯器官衰竭评估、简化急性生理学评分II和急性生理与慢性健康状况评分II)的中位数也更高。在多变量分析中(R = 0.309,p < 0.001),CPE携带与先前使用第三代-第四代头孢菌素(比值比[OR]=27.96,95%置信区间[CI]=6.88,113.58,p < 0.001)、β-内酰胺/β-内酰胺酶抑制剂(OR = 11.71,95%CI = 4.51,30.43,p < 0.001)、腹部手术(OR = 6.33,95%CI = 2.12,18.89,p = 0.001)和先前消化/胆道内镜检查(OR = 3.88,95%CI = 1.56,9.67,p = 0.004)相关。
发现ESBL产生与CPE携带(主要是产OXA - 48的肺炎克雷伯菌)之间存在密切关联。根据该模型,先前接触广谱头孢菌素和β-内酰胺/β-内酰胺酶抑制剂(相对风险较低)、腹部手术和先前消化/胆道内镜检查导致的β-内酰胺酶共同选择是与CPE携带相关的因素。