对接受体外心肺复苏的院内心脏骤停患者进行早期 mNGS 检测,以诊断和预测早发肺炎。

IF 4.6 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2024-11-08 eCollection Date: 2024-01-01 DOI:10.3389/fcimb.2024.1382273
Rui-Ming Guo, Xing-Xing Li, Yi-Heng Zhou, Yi-Juan Liu, Jun Li, Guo-Wei Fu, Hui Zhao, Xin Zhang, Yang-Chao Zhao
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引用次数: 0

摘要

目的:元基因组下一代测序(mNGS)作为一种新型诊断技术正逐渐被应用于各种感染性疾病的诊断中;然而,对其在院内心脏骤停(IHCA)后接受体外心肺复苏(ECPR)患者早发肺炎(EOP)的病原学诊断中应用的研究还很有限,早期mNGS在预测ECPR后IHCA患者短期预后中的临床意义仍不明确:这项回顾性研究纳入了2018年1月至2022年12月在郑州大学第一附属医院接受ECPR的76例IHCA患者。收集并统计分析了所有患者住院期间的基线特征和病因学数据。本研究的主要结果是EOP的诊断,次要结果包括体外膜肺氧合(ECMO)的成功断流和出院时的存活率。此外,通过分析 mNGS 结果和培养结果,比较了这些患者支气管肺泡灌洗液(BALF)菌群的特征:结果:采用多变量逻辑回归分析了 ECMO 断流失败、出院死亡率和 EOP 发生率的预测因素。最终,入院时 SOFA 评分较低的患者[OR (95%CI):1.447 (1.107-1.890),p=0.007]和在 ECPR 后 48 小时内接受早期 mNGS 检测的患者[OR (95%CI):0.273 (0.086-0.865),p=0.027]成功断开 ECMO 的概率较高。入院时 SOFA 评分较高 [OR (95%CI):2.404 (1.422-4.064),p=0.001] 和乳酸水平升高 [OR (95%CI):1.176 (1.017-1.361),p=0.029] 的患者出院时死亡的可能性增加。此外,早期检测到 mNGS [OR (95%CI):0.186 (0.035-0.979),p=0.047] 和较低的 CRP 水平(ECMO 后 48 小时至 7 天)[OR (95%CI):1.011 (1.003-1.019),p=0.006] 与 EOP 发生率降低有关。此外,ECPR 后 48 小时内 mNGS 检测到的病原体主要是口腔定植细菌和病毒,其中病毒占多数,而所有 BALF 培养均为阴性。相反,在 ECPR 后 48 小时至 7 天内,所有 EOP 患者的 BALF 培养均呈阳性:结论:早期通过 mNGS 检测确定微生物菌群有助于及时调整抗生素方案,从而降低 EOP 的发生率,改善 IHCA 后接受 ECPR 患者的短期预后。
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Early mNGS testing for diagnose and prognostic prediction of early onset pneumonia among in-hospital cardiac arrest patients undergoing extracorporeal cardiopulmonary resuscitation.

Objectives: Metagenomic next-generation sequencing (mNGS) is emerging as a novel diagnostic technology for various infectious diseases; however, limited studies have investigated its application in etiological diagnosis of early onset pneumonia (EOP) among patients undergoing extracorporeal cardiopulmonary resuscitation (ECPR) following in-hospital cardiac arrest (IHCA), The clinical significance of early mNGS in predicting short-term prognosis of IHCA patients after ECPR remains unclear.

Methods: This retrospective study included 76 patients with IHCA who underwent ECPR at the First Affiliated Hospital of Zhengzhou University from January 2018 to December 2022. Baseline characteristics and etiological data of all patients during their hospitalization were collected and statistically analyzed. The primary outcome of this study was the diagnosis of EOP, while the secondary outcomes included successful extracorporeal membrane oxygenation (ECMO) weaning and survival at discharge. Additionally, the characteristics of bronchoalveolar lavage fluid (BALF) flora in these patients were compared by analyzing both mNGS results and culture results.

Results: Multivariate logistic regression were employed to analyze the predictors of ECMO weaning failure, mortality at discharge, and the incidence of EOP. Ultimately, patients with lower SOFA scores on admission [OR (95%CI): 1.447 (1.107-1.890), p=0.007] and those who underwent early mNGS testing within 48 hours after ECPR [OR (95%CI): 0.273 (0.086-0.865), p=0.027] demonstrated a higher probability of successful weaning from ECMO. Patients with higher SOFA scores on admission [OR (95%CI): 2.404 (1.422-4.064), p=0.001], and elevated lactate levels [OR (95%CI): 1.176 (1.017-1.361), p=0.029] exhibited an increased likelihood of mortality at discharge. Furthermore, early mNGS detection [OR (95%CI): 0.186 (0.035-0.979), p=0.047], and lower CRP levels (48h-7d after ECMO) [OR (95%CI):1.011 (1.003-1.019), p=0.006] were associated with a reduced incidence of EOP. In addition, the pathogens detected by mNGS within 48 hours after ECPR were mainly oral colonizing bacteria and viruses, and viruses were in the majority, while all BALF cultures were negative. In contrast, between 48 hours and 7 days after ECPR, BALF cultures were positive in all EOP patients.

Conclusions: Early mNGS testing to identify microbial flora facilitates timely adjustment of antibiotic regimens, thereby reducing the incidence of EOP and improving short-term prognosis in patients undergoing ECPR following IHCA.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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