MRSA PCR提高了检测新生儿定植的敏感性

Nahid Hiermandi, Catherine Foster, Krystal Purnell, James Dunn, Judith Campbell, Lucila Marquez
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摘要

背景:耐甲氧西林金黄色葡萄球菌(MRSA)定植的新生儿发展为危及生命的MRSA感染的风险很高。由于缺乏证据,国家指南目前没有推荐检测MRSA定植的具体方法。我们假设通过聚合酶链反应(PCR)对MRSA定植的监测优于培养检测定植。方法:在这项回顾性研究中,我们比较了两种方法的MRSA监测结果,培养和PCR,在实施MRSA监测和去菌落方案后,德克萨斯州儿童医院妇女馆,42个床位的新生儿重症监护病房。从2017年6月到2020年12月,通过两种方法评估了MRSA在3个身体部位的定植。所有新生儿在进入新生儿重症监护室时进行MRSA筛查,此后每周进行一次筛查,直到MRSA阳性或出院。拭子标本最初通过PCR (Xpert MRSA NxG,造父变星)进行检测,当MRSA阳性反射到培养中以恢复生物进一步表征。这项研究通过了贝勒医学院机构审查委员会的批准。结果:在研究期间,2,351名新生儿通过PCR检测MRSA定植;81例(3.4%)患儿PCR阳性(图1)。其中57例(70.4%)患儿MRSA PCR与培养结果一致,24例(29.6%)患儿MRSA PCR阳性,但培养中未检出分离物。8份标本PCR无法确定。然而,1名培养阴性但PCR阳性的婴儿发生了MRSA眼眶感染。与PCR相比,MRSA培养的总体敏感性为70.4%(根据年份的不同,范围为57.7%-80.8%)(表1)。结论:在检测新生儿MRSA定植方面,PCR比培养更敏感。利用PCR方法可以更容易地识别MRSA定植的婴儿,并允许迅速启动感染控制干预措施,包括隔离预防措施和去菌落策略。对培养物的反射对于疫情调查期间的菌株表征和额外的药敏试验仍然很重要。未来的研究应进行资源利用和成本效益分析,以影响新生儿重症监护病房控制金黄色葡萄球菌定植和感染的国家指南的变化。披露:没有
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MRSA PCR improves sensitivity of detection of colonization in neonates
Background: Neonates colonized with methicillin-resistant Staphylococcus aureus (MRSA) are at high risk of developing life-threatening MRSA infection. Due to lack of evidence, national guidelines do not currently recommend a specific methodology for detecting MRSA colonization. We hypothesize that surveillance for MRSA colonization via polymerase chain reaction (PCR) is superior to culture for the detection of colonization. Methods: In this retrospective study, we compared results of MRSA surveillance by 2 methodologies, culture and PCR, after implementation of an MRSA surveillance and decolonization protocol in the Texas Children’s Hospital Pavilion for Women, a 42-bed neonatal intensive care unit. MRSA colonization of 3 body sites via the 2 methodologies was assessed from June 2017 through December 2020. All neonates were screened for MRSA upon admission to the NICU and weekly thereafter until MRSA-positive or discharged. Swab specimens were initially tested by PCR (Xpert MRSA NxG, Cepheid) and when MRSA-positive reflexed to culture to recover the organism for further characterization. This study was approved through the Baylor College of Medicine Institutional Review Board. Results: During the study period, 2,351 neonates were assessed for MRSA colonization by PCR; 81 (3.4%) infants were PCR positive (Fig. 1). Of those 81, 57 (70.4%) had concordant MRSA PCR and culture results, and 24 (29.6%) were MRSA PCR positive but no isolate was recovered in culture. Also, 8 specimens were indeterminate by PCR. However, 1 infant who was negative by culture but was PCR positive developed an MRSA orbital infection. Compared to PCR, the overall sensitivity of MRSA culture was 70.4% (range, 57.7%–80.8%, depending on the year) (Table 1). Conclusions: PCR is more sensitive than culture for detecting MRSA colonization in neonates. Utilizing a PCR method enhances the ability to identify MRSA colonized infants more readily and allows for prompt initiation of infection control interventions including isolation precautions and decolonization strategies. Reflex to culture remains important for strain characterization during outbreak investigations and for additional susceptibility testing. Resource utilization and cost–benefit analyses should be done in future studies to influence changes in national guidelines for the control of Staphylococcus aureus colonization and infection in neonatal intensive care units. Disclosures: None
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