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脑脊液多重聚合酶链反应检测在疑似中枢神经系统感染患者中的诊断准确性:阿联酋的一项多中心研究

Diagnostic Accuracy of Cerebrospinal Fluid Multiplex Polymerase Chain Reaction Panel Testing in Patients With Suspected Central Nervous System Infections: A Multi-Center Study in the United Arab Emirates.

作者信息

Ghoweba Yousra, Safizadeh Shabestari Seyed Ali, Malik Zainab A

机构信息

Pediatrics, Mohammed Bin Rashid University Of Medicine and Health Sciences, Dubai, ARE.

Medicine, Mohammed Bin Rashid University Of Medicine and Health Sciences, Dubai, ARE.

出版信息

Cureus. 2024 Jan 8;16(1):e51906. doi: 10.7759/cureus.51906. eCollection 2024 Jan.

DOI:10.7759/cureus.51906
PMID:38333447
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10851033/
Abstract

Background Delays in diagnosis and treatment of central nervous system (CNS) infections can lead to significant morbidity and mortality among children and adults. Prior antibiotic treatment is a major hurdle to accurate diagnosis due to falsely negative cerebrospinal fluid (CSF) cultures in partially treated patients. Increasingly, molecular diagnostic methods using multiplex polymerase chain reaction (mPCR) testing on CSF samples are being utilized in clinical practice for timely and accurate diagnosis. However, there is no data regarding the diagnostic accuracy or clinical impact of CSF mPCR testing in the Middle East region. We sought to compare the diagnostic accuracy of an automated mPCR CSF panel with routine CSF culture, the current gold standard, in the United Arab Emirates (UAE).  Methods This single-gated, multi-center, diagnostic accuracy study included patients from birth onwards who were admitted to any of the three participating hospitals with an initial diagnosis of meningitis or encephalitis, between January 2017 and March 2021, and had CSF samples collected for mPCR and culture. Sociodemographic, clinical, and molecular data were collected for all. Results A total of 353 CSF samples were collected from patients from 0-90 years old hospitalized for suspected CNS infection. Children constituted 51% of the study population, and males were slightly over-represented (55.2%). Pathogens were detected by mPCR in 78 (22%) CSF samples, of which 19 (24%) were bacteria and 59 (76%) were viruses. No fungal pathogens were detected. Enteroviruses were the most prevalent CNS pathogen among our cohort (40%), followed by (HSV-2) (12.5%). Children constituted 69% of positive samples for enterovirus, while HSV-2 was exclusively detected among adults. Using CSF culture as the diagnostic gold standard, the mPCR panel demonstrated high specificity (100%) and sensitivity (96.3%) in diagnosing CNS infection among all age groups. mPCR testing demonstrated a high overall percentage of agreement (OPA) with CSF culture (98.9%). Patients with bacterial meningitis had a significantly longer hospitalization (p=0.004) and duration of antibiotic therapy (p=0.001) compared to those with viral meningitis. Three CSF samples were negative on mPCR testing but positive on culture. These pathogens included: methicillin-sensitive (MSSA)and (MTB). In addition, 13 patients had negative CSF cultures but tested positive on CSF mPCR. These pathogens included (seven patients), (three patients), (two patients), and (one patient). All discordant results were confirmed by reviewing the patient's clinical presentation, CSF analysis, clinical course, and final diagnosis. Conclusion CSF mPCR panel is a highly sensitive and specific diagnostic tool for the diagnosis of CNS infections among all age groups in the UAE. Routine use of CSF mPCR panels can decrease healthcare costs by reducing the length of stay and can also aid antibiotic stewardship efforts by reducing antibiotic overuse in patients with viral CSF infections. CSF culture and mPCR complement each other by identifying CNS pathogens in patients with prior antibiotic exposure who would otherwise be missed if relying on CSF culture alone. However, concomitant CSF culture samples should be sent to avoid missing unusual CNS pathogens.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/f7b28a737424/cureus-0016-00000051906-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/ebcd80c0acee/cureus-0016-00000051906-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/5976a73fe441/cureus-0016-00000051906-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/ab15d4db9ae1/cureus-0016-00000051906-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/f7b28a737424/cureus-0016-00000051906-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/ebcd80c0acee/cureus-0016-00000051906-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/5976a73fe441/cureus-0016-00000051906-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/ab15d4db9ae1/cureus-0016-00000051906-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cad/10851033/f7b28a737424/cureus-0016-00000051906-i04.jpg
摘要

背景 中枢神经系统(CNS)感染的诊断和治疗延迟可导致儿童和成人出现显著的发病率和死亡率。由于部分接受治疗的患者脑脊液(CSF)培养结果呈假阴性,先前的抗生素治疗成为准确诊断的主要障碍。越来越多的临床实践中开始使用对脑脊液样本进行多重聚合酶链反应(mPCR)检测的分子诊断方法来实现及时、准确的诊断。然而,中东地区尚无关于脑脊液mPCR检测的诊断准确性或临床影响的数据。我们试图在阿拉伯联合酋长国(阿联酋)比较自动化mPCR脑脊液检测板与常规脑脊液培养(当前的金标准)的诊断准确性。

方法 这项单门、多中心诊断准确性研究纳入了2017年1月至2021年3月期间因初步诊断为脑膜炎或脑炎而入住三家参与研究医院中任何一家的从出生起的患者,并采集了用于mPCR和培养的脑脊液样本。收集了所有患者的社会人口统计学、临床和分子数据。

结果 共从0至90岁因疑似中枢神经系统感染住院的患者中采集了353份脑脊液样本。儿童占研究人群的51%,男性略多(55.2%)。通过mPCR在78份(22%)脑脊液样本中检测到病原体,其中19份(24%)为细菌,59份(76%)为病毒。未检测到真菌病原体。肠道病毒是我们队列中最常见的中枢神经系统病原体(40%),其次是单纯疱疹病毒2型(HSV - 2)(12.5%)。肠道病毒阳性样本中儿童占69%,而HSV - 2仅在成人中检测到。以脑脊液培养作为诊断金标准,mPCR检测板在诊断所有年龄组的中枢神经系统感染时显示出高特异性(100%)和敏感性(96.3%)。mPCR检测与脑脊液培养显示出较高的总体一致性百分比(OPA)(98.9%)。与病毒性脑膜炎患者相比,细菌性脑膜炎患者的住院时间(p = 0.004)和抗生素治疗持续时间(p = 0.001)明显更长。3份脑脊液样本mPCR检测为阴性但培养为阳性。这些病原体包括:甲氧西林敏感金黄色葡萄球菌(MSSA)和结核分枝杆菌(MTB)。此外,13例患者脑脊液培养为阴性但脑脊液mPCR检测为阳性。这些病原体包括:肠道病毒(7例患者)、单纯疱疹病毒1型(HSV - 1)(3例患者)、巨细胞病毒(CMV)(2例患者)和EB病毒(1例患者)。所有不一致的结果均通过回顾患者的临床表现、脑脊液分析、临床病程和最终诊断得以确认。

结论 在阿联酋,脑脊液mPCR检测板是诊断所有年龄组中枢神经系统感染的高度敏感和特异的诊断工具。常规使用脑脊液mPCR检测板可通过缩短住院时间降低医疗成本,还可通过减少病毒性脑脊液感染患者的抗生素过度使用来助力抗生素管理工作。脑脊液培养和mPCR相互补充,可识别先前接受过抗生素治疗患者中的中枢神经系统病原体,否则仅依靠脑脊液培养会导致这些病原体漏诊。然而,应同时送检脑脊液培养样本以避免遗漏不常见的中枢神经系统病原体。

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