Zheng Hongfei, Peng Pei, Wang Shaofei, Zhang Bo, Yang Linying, Wang Yaoyao, Li Lejun, Pang Guifen
Department of Respiratory and Critical Care Medicine, Affiliated Hospital of Chengde Medical College, Chengde, 67000, People's Republic of China.
Shanghai Biotecan Pharmaceuticals Co., Ltd, Shanghai, 201204, People's Republic of China.
Infect Drug Resist. 2025 Mar 1;18:1223-1236. doi: 10.2147/IDR.S462358. eCollection 2025.
Community-acquired pneumonia (CAP) presents a significant public health concern, necessitating timely and precise diagnosis. Metagenomic next-generation sequencing (mNGS) has shown promise as a powerful tool for pathogen identification in infectious diseases. This study aimed to evaluate the diagnostic efficacy and clinical applicability of mNGS for immunocompromised patients with CAP compared to the culture method.
This study included 168 patients. We used both mNGS and conventional culture methods to identify the pathogen spectrum and evaluate diagnostic performance. Treatment regimens and clinical outcomes were meticulously documented.
The sensitivity of mNGS was greater than that of the culture method across all samples (79.05% vs 16.03%; < 0.001). mNGS identified pathogens missed by culture in 59.52% of patients and detected polymicrobial infections that were not detected by culture in 47.62% of patients. , and at classification level emerged as the predominant pathogens identified in CAP patients through mNGS. When examining the mNGS results between groups, the proportions of immunocompromised patients with bacterial ( < 0.001), fungal ( < 0.001), viral ( < 0.05), and mixed infections ( < 0.001) were all significantly higher than those in immunocompetent patients. Treatment adjustments guided by mNGS were observed in 73.21% of patients. Specifically, a beneficial clinical effect was observed in 50.60% (85/168) of patients, treatment confirmation in 22.62% (38/168) of patients, and no clinical benefit in 26.80% (45/168) of patients based on mNGS-guided antibiotic treatment adjustments.
These findings highlight the diagnostic performance of mNGS for identifying pathogens, particularly in immunocompromised patients vulnerable to infections, offering valuable insights for clinical decision-making.
社区获得性肺炎(CAP)是一个重大的公共卫生问题,需要及时、准确的诊断。宏基因组下一代测序(mNGS)已显示出作为传染病病原体鉴定的强大工具的前景。本研究旨在评估mNGS与培养方法相比,对免疫功能低下的CAP患者的诊断效能和临床适用性。
本研究纳入了168例患者。我们使用mNGS和传统培养方法来确定病原体谱并评估诊断性能。精心记录治疗方案和临床结果。
在所有样本中,mNGS的敏感性高于培养方法(79.05%对16.03%;P<0.001)。mNGS在59.52%的患者中鉴定出培养未发现的病原体,在47.62%的患者中检测到培养未发现的混合感染。在分类水平上,[此处原文缺失具体病原体信息]成为通过mNGS在CAP患者中鉴定出的主要病原体。在比较各组的mNGS结果时,免疫功能低下患者的细菌感染(P<0.001)、真菌感染(P<0.001)、病毒感染(P<0.05)和混合感染(P<0.001)比例均显著高于免疫功能正常患者。73.21%的患者根据mNGS进行了治疗调整。具体而言,基于mNGS指导的抗生素治疗调整,50.60%(85/168)的患者观察到有益的临床效果,22.62%(38/168)的患者治疗得到确认,26.80%(45/168)的患者未观察到临床益处。
这些发现突出了mNGS在鉴定病原体方面的诊断性能,特别是在易感染的免疫功能低下患者中,为临床决策提供了有价值的见解。