Carbapenemase genes and mortality in patients with carbapenem-resistant Enterobacterales, Atlanta, Georgia, 2011–2020

Lucy Witt, Ahmed Babike, Gillian Smith, Sarah Satola, Mary Elizabeth Sexton, Jesse Jacob
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Abstract

Background: Carbapenemase genes in carbapenem-resistant Enterobacterales (CP-CRE) may be transmitted between patients and bacteria. Reported rates of carbapenemase genes vary widely, and it is unclear whether having a carbapenemase gene portends worse outcomes given that all patients with CRE infections have limited treatment options. Methods: Using active population- and laboratory-based active surveillance data collected by the US CDC-funded Georgia Emerging Infections Program from 2011 to 2020, we assessed the frequency of carbapenemase genes in a convenience sample of CRE isolates using whole-genome sequencing (WGS), and we investigated risk factors for carbapenemase positivity. Only the first isolate per patient in a 30-day period was included. We compared characteristics of patients with CP-CRE and non–CP-CRE. Using multivariable log binomial regression, we assessed the association of carbapenemase gene positivity and 90-day mortality. Results: Of 284 CRE isolates, 171 isolates (60.2%) possessed a carbapenemase gene (Table 1), and KPC-3 was the most common carbapenemase gene (80.7%), with only 7 isolates possessing NDM (Table 2). No isolates possessed >1 carbapenemase gene, and most isolates were from urine (82.4%) (Table 1). Carbapenemase gene positivity was associated with lower age, male sex, black race, infection with Klebsiella pneumoniae , polymicrobial infection, having an indwelling medical device, receiving chronic dialysis, and prior stay in a long-term acute-care hospital, long-term care facility, and/or prior hospitalization in the last year. The 90-day mortality rates were similar in patients with non–CP-CRE and CP-CRE: 24.8% versus 25.7% ( P = .86). In multivariable analysis, carbapenemase gene presence was not associated with 90-day mortality (adjusted risk ratio, 0.82; 95% CI, 0.50–1.35) when adjusting for CCI, infection with Klebsiella pneumoniae , and chronic dialysis use. Conclusions: The frequency of CP-CRE among CRE was high in this study, but unlike prior studies, the 90-day mortality rates wer similar in patients with CP-CRE compared to non–CP-CRE. Our results provide novel associations (eg, lower age, male sex, infection with Klebsiella pneumoniae , and indwelling medical devices) that infection preventionists could use to target high-risk patients for screening or isolation prior to CP-CRE detection. Disclosure: None
碳青霉烯耐药肠杆菌患者碳青霉烯酶基因与死亡率,亚特兰大,乔治亚州,2011-2020
背景:碳青霉烯耐药肠杆菌(CP-CRE)碳青霉烯酶基因可能在患者和细菌之间传播。碳青霉烯酶基因的报道率差异很大,考虑到所有CRE感染患者的治疗选择有限,尚不清楚是否有碳青霉烯酶基因预示着更糟糕的结果。方法:利用美国疾病控制与预防中心资助的乔治亚州新发感染项目收集的2011 - 2020年活跃人群和基于实验室的活跃监测数据,利用全基因组测序(WGS)评估CRE分离株便捷样本中碳青霉烯酶基因的频率,并调查碳青霉烯酶阳性的危险因素。仅包括每位患者在30天内的第一个分离株。我们比较了CP-CRE和非CP-CRE患者的特征。使用多变量对数二项回归,我们评估了碳青霉烯酶基因阳性与90天死亡率的关系。结果:284株CRE分离株中,有171株(60.2%)具有碳青霉烯酶基因(表1),KPC-3是最常见的碳青霉烯酶基因(80.7%),仅有7株具有NDM(表2)。碳青霉烯酶基因为1的分离株均不存在,且大多数分离株来自尿液(82.4%)(表1)。碳青霉烯酶基因阳性与年龄较小、男性、黑人、感染肺炎克雷伯菌、多微生物感染、使用留用医疗器械、接受慢性透析治疗,过去一年曾在长期急症医院、长期护理机构和/或住院治疗。非CP-CRE和CP-CRE患者的90天死亡率相似:分别为24.8%和25.7% (P = 0.86)。在多变量分析中,碳青霉烯酶基因的存在与90天死亡率无关(校正风险比,0.82;当调整CCI、肺炎克雷伯菌感染和慢性透析使用时,95% CI, 0.50-1.35)。结论:本研究中,CP-CRE在CRE患者中的发生率很高,但与之前的研究不同的是,CP-CRE患者的90天死亡率与非CP-CRE患者相似。我们的研究结果提供了新的关联(例如,年龄较小,男性,肺炎克雷伯菌感染和留置医疗器械),感染预防学家可以在检测CP-CRE之前针对高危患者进行筛查或隔离。披露:没有
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