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宏基因组下一代测序(mNGS)检测细菌性脑膜脑炎的诊断准确性:一项系统评价和荟萃分析

Diagnostic accuracy of the metagenomic next-generation sequencing (mNGS) for detection of bacterial meningoencephalitis: a systematic review and meta-analysis.

作者信息

Kanaujia Rimjhim, Biswal Manisha, Angrup Archana, Ray Pallab

机构信息

Department of Medical Microbiology PGIMER, Chandigarh, India.

出版信息

Eur J Clin Microbiol Infect Dis. 2022 Jun;41(6):881-891. doi: 10.1007/s10096-022-04445-0. Epub 2022 Apr 26.

Abstract

The early diagnosis of bacterial meningoencephalitis (BM/E) is difficult, and delay in diagnosis can cause complications leading to neurological impairment/death. In cases of unexplained BM/E, the metagenomic NGS (mNGS) offers an advantage over conventional methods, especially when a rare pathogen is implicated or the patient is on antibiotics. This study aims to evaluate and compare the diagnostic efficacy of mNGS for the diagnosis of BM/E using cerebrospinal fluid (CSF) specimens versus a composite reference standard (CRS). The electronic databases (Embase, PubMed, and Web of Science) were searched up to 15 June 2021. Studies such as cohort, case-control, prospective, or retrospective studies that assessed the diagnostic efficacy of mNGS in suspected bacterial meningitis/encephalitis cases were included. Ten studies met the inclusion criteria, including three retrospective and seven prospective studies. The sensitivity of mNGS for diagnosis of BM/E from CSF samples ranged from 33 (95% CI: 13-62) to 98% (95% CI: 76-99). The specificity of mNGS ranged from 67 (95% CI: 55-78) to 98% (95% CI: 95-99). The estimated AUC (area under curve) by hierarchical summary receiver operating characteristic (HSROC) of the studies being analyzed was 0.912. The meta-regression analysis demonstrated that the different types of studies (single-center vs. multi-center) had an effect on the specificity of mNGS for BM/E compared with CRS (90% vs. 96%, meta-regression P < 0.05). The current analysis revealed moderate diagnostic accuracy of mNGS. This approach can be helpful, especially in cases of undiagnosed BM/E by identification of organism and subsequently accelerating the patient management.

摘要

细菌性脑膜脑炎(BM/E)的早期诊断较为困难,诊断延迟可导致并发症,进而引起神经功能损害或死亡。在不明原因的BM/E病例中,宏基因组二代测序(mNGS)相较于传统方法具有优势,尤其是在涉及罕见病原体或患者正在使用抗生素的情况下。本研究旨在评估和比较mNGS使用脑脊液(CSF)标本诊断BM/E与复合参考标准(CRS)的诊断效能。检索了截至2021年6月15日的电子数据库(Embase、PubMed和Web of Science)。纳入了评估mNGS在疑似细菌性脑膜炎/脑炎病例中诊断效能的队列研究、病例对照研究、前瞻性研究或回顾性研究等。十项研究符合纳入标准,包括三项回顾性研究和七项前瞻性研究。mNGS诊断CSF样本中BM/E的敏感性范围为33%(95%CI:13%-62%)至98%(95%CI:76%-99%)。mNGS的特异性范围为67%(95%CI:55%-78%)至98%(95%CI:95%-99%)。所分析研究的分层汇总接受者操作特征(HSROC)估计的曲线下面积(AUC)为0.912。meta回归分析表明,与CRS相比,不同类型的研究(单中心与多中心)对mNGS诊断BM/E的特异性有影响(90%对96%,meta回归P<0.05)。当前分析显示mNGS具有中等诊断准确性。这种方法可能会有所帮助,尤其是在未确诊的BM/E病例中,通过识别病原体并随后加快患者管理。

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