Cortegiani Andrea, Russotto Vincenzo, Graziano Giorgio, Geraci Daniela, Saporito Laura, Cocorullo Gianfranco, Raineri Santi Maurizio, Mammina Caterina, Giarratano Antonino
Department of Biopathology and Medical Biotechnologies (DIBIMED), Section of Anesthesia, Analgesia, Intensive Care and Emergency, Policlinico P. Giaccone, University of Palermo, Via del Vespro 129, 90127, Palermo, Italy.
Department of Sciences for Health Promotion and Mother-Child Care, University of Palermo, Palermo, Italy.
PLoS One. 2016 Aug 4;11(8):e0160643. doi: 10.1371/journal.pone.0160643. eCollection 2016.
Early institution of effective antibiotic therapy and source control are pivotal to improve survival of abdominal septic patients. Xpert® Carba-R is a real time polymerase chain reaction assay for rapid detection and differentiation of five genes (blaKPC, blaVIM, blaOXA-48, blaIMP-1, blaNDM) responsible for carbapenem resistance. We performed an observational study investigating the clinical usefulness and applicability of Xpert® Carba-R to detect carbapenem resistance in abdominal septic patients admitted to intensive care unit. We compared the results of Xpert® Carba-R with standard microbiological culture. We collected a set of two rectal/stomia swabs and two swabs from abdominal drainage fluid for each patient. We included 20 patients for a total of 45 comparisons between the two methods. In our clinical setting, the overall performance of Xpert® Carba-R for detection of carbapenem resistance in the presence of genes detectable and non-detectable by the method was: sensitivity 50% (95% CI 24.6-75.3); specificity 93.1% (95% CI 77.2-99.1); positive predictive value (PPV) 80% (95% CI 44.4-97.5); negative predictive value (NPV) 77.1% (95% CI 56.9-89.6). The inter-rater agreement was 0.47 (SE 0.14; 95% CI 0.20-0.74). When considering the only 5 mechanisms of resistance detected by both methods, the overall diagnostic performance was: sensitivity 100% (95% CI 69.1-100), specificity 94.2 (95% CI 80.8-99.3), PPV 83.3 (95% CI 59.6-97.9) and NPV 100% (95% CI 89.4-100). The inter-rater agreement was 0.88 (SE 0.08; 95% CI 0.71-1). Xpert® Carba-R may be considered an additional diagnostic tool for early diagnosis of carbapenem resistance in abdominal septic patients. Clinicians should be aware of their epidemiology before its introduction in the diagnostic protocol of their intensive care units.
尽早开始有效的抗生素治疗和源头控制对于提高腹部脓毒症患者的生存率至关重要。Xpert® Carba - R是一种实时聚合酶链反应检测方法,用于快速检测和区分导致碳青霉烯类耐药的五个基因(blaKPC、blaVIM、blaOXA - 48、blaIMP - 1、blaNDM)。我们进行了一项观察性研究,调查Xpert® Carba - R在检测入住重症监护病房的腹部脓毒症患者碳青霉烯类耐药方面的临床实用性和适用性。我们将Xpert® Carba - R的结果与标准微生物培养结果进行了比较。我们为每位患者收集了一组两份直肠/造口拭子和两份腹部引流液拭子。我们纳入了20名患者,两种方法之间总共进行了45次比较。在我们的临床环境中,对于该方法可检测和不可检测基因存在时,Xpert® Carba - R检测碳青霉烯类耐药的总体性能为:敏感性50%(95%置信区间24.6 - 75.3);特异性93.1%(95%置信区间77.2 - 99.1);阳性预测值(PPV)80%(95%置信区间44.4 - 97.5);阴性预测值(NPV)77.1%(95%置信区间56.9 - 89.6)。评分者间一致性为0.47(标准误0.14;95%置信区间0.20 - 0.74)。当仅考虑两种方法都检测到的5种耐药机制时,总体诊断性能为:敏感性100%(95%置信区间69.1 - 100),特异性94.2(95%置信区间80.8 - 99.3);PPV 83.3(95%置信区间59.6 - 97.9)和NPV 100%(95%置信区间89.4 - 100)。评分者间一致性为0.88(标准误0.08;95%置信区间0.71 - 1)。Xpert® Carba - R可被视为腹部脓毒症患者碳青霉烯类耐药早期诊断的一种额外诊断工具。临床医生在将其引入重症监护病房的诊断方案之前应了解其流行病学情况。