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Diagnostic Evaluation of Pneumocystis Pneumonia by Metagenomic Next-Generation Sequencing in Immunosuppressive Patients Undergoing Mechanical Ventilation in the Intensive Care Unit

34 Pages Posted: 17 Jul 2023

See all articles by Yin Xi

Yin Xi

Guangzhou Medical University

Sibei Chen

Guangzhou Medical University

Lingbo Nong

Guangzhou Medical University

Weibo Liang

Guangzhou Medical University

Yuheng Yu

Guangzhou Medical University

Jing Zhou

Guangzhou Medical University

Zhimin Lin

Guangzhou Medical University

Fanlin Meng

CapitalBio Technology Inc.

Wenyan Qin

CapitalBio Technology Inc.

Chun Yang

Guangzhou Medical University

Dongdong Liu

Guangzhou Medical University

Yonghao Xu

Guangzhou Medical University

Jie Zhang

Guangzhou Medical University

Rong Zhang

Guangzhou Medical University

Xuesong Liu

Guangzhou Medical University

Yuanda Xu

Guangzhou Medical University

Yimin Li

Guangzhou Medical University

Xiaoqing Liu

Guangzhou Medical University

Weiqun He

Guangzhou Medical University

Ling Sang

Guangzhou Medical University - Department of Critical Care Medicine

More...

Abstract

Background: Pneumocystis jirovecii is an opportunistic pathogen which can cause fatal Pneumocystis
pneumonia (PCP). The precise diagnosis of PCP remains challenging for its heterogeneity of clinical presentation.


Methods:
 We performed a retrospective cohort study of patients in ICU from March 2018 to May 2020. All cases were immunosuppressed due to organ transplantation, cancer or autoimmune diseases, and performed metagenomic next-generation sequencing (mNGS) for pathogen identification.

Results: A total of 46 immunocompromised cases were enrolled in this study. 17 of 46 cases were diagnosed with PCP by combining with imaging examination and other clinical detection methods. The LDH level and the positive rate of β-D-glucan assay were higher in PCP group than non-PCP group, 594(506~733) vs. 456(342~576), p = 0.006;
14/17(82.4%) vs. 10/29(34.5%), p = 0.005. APACHE II score of PCP group was lower
than Non-PCP group, 20(16~26) vs. 25(19~30), p = 0.039. The sensitivity and specificity of mNGS for the diagnosis of PCP were both 100%, while those of β-D-glucan assay combined with LDH were 41.2% and 86.2%, respectively. If we assume that positive result of Β-D-glucan assay, LDH >255 U/L, APACHE II score ≤ 27 as
the screening standard, compared with mNGS method, the specificity and sensitivity for the diagnosis of PCP are 82.4% and 86.2% respectively.


Conclusionsm: NGS could be a promising technology to diagnose PCP and detect mixed infections
in pulmonary infection in immunosuppressed patients, Combined APACHE II/BG/LDH with mNGS might be a rapid screening method for PCP diagnosis.

Funding: This study was funded by National Key Research and Development Program of China (2022YFC0869400), National Natural Science Foundation of China (Grant No. 82270081), Emergency Key Program of Guangzhou Laboratory (Grant No. EKPG21- 17), National Natural Science Foundation of China (Grant No. 81870069), Selfdetermined Project of GIRH (2019GIRHQ05) , Natural Science Foundation of Guangdong Province (2020A1515011459) and Zhongnanshan Medical Fundation of Guangdong Province(2020B1111340017).

Declaration of Interest: All authors declare that they have no competing interests.

Ethical Approval: The study was approved by the Institutional Ethics Committee of the First Affiliated Hospital of Guangzhou Medical University (No.2020K-42). Informed consent was waived by the ethics committee due to the retrospective nature of study design.

Keywords: PCP, mNGS, Dignosis, ICU, LDH, Pneumocystis jirovecii

Suggested Citation

Xi, Yin and Chen, Sibei and Nong, Lingbo and Liang, Weibo and Yu, Yuheng and Zhou, Jing and Lin, Zhimin and Meng, Fanlin and Qin, Wenyan and Yang, Chun and Liu, Dongdong and Xu, Yonghao and Zhang, Jie and Zhang, Rong and Liu, Xuesong and Xu, Yuanda and Li, Yimin and Liu, Xiaoqing and He, Weiqun and Sang, Ling, Diagnostic Evaluation of Pneumocystis Pneumonia by Metagenomic Next-Generation Sequencing in Immunosuppressive Patients Undergoing Mechanical Ventilation in the Intensive Care Unit. Available at SSRN: https://ssrn.com/abstract=4508432 or http://dx.doi.org/10.2139/ssrn.4508432

Yin Xi

Guangzhou Medical University ( email )

Sibei Chen

Guangzhou Medical University ( email )

Lingbo Nong

Guangzhou Medical University ( email )

Weibo Liang

Guangzhou Medical University ( email )

Yuheng Yu

Guangzhou Medical University ( email )

Jing Zhou

Guangzhou Medical University ( email )

Zhimin Lin

Guangzhou Medical University ( email )

Fanlin Meng

CapitalBio Technology Inc. ( email )

Wenyan Qin

CapitalBio Technology Inc. ( email )

Chun Yang

Guangzhou Medical University ( email )

Dongdong Liu

Guangzhou Medical University ( email )

Yonghao Xu

Guangzhou Medical University ( email )

Jie Zhang

Guangzhou Medical University ( email )

Rong Zhang

Guangzhou Medical University ( email )

Xuesong Liu

Guangzhou Medical University ( email )

Yuanda Xu

Guangzhou Medical University ( email )

Yimin Li

Guangzhou Medical University ( email )

Xiaoqing Liu

Guangzhou Medical University ( email )

Weiqun He

Guangzhou Medical University ( email )

Ling Sang (Contact Author)

Guangzhou Medical University - Department of Critical Care Medicine ( email )

195 Dongfeng W Rd
Yuexiu Qu
Guangzhou Shi, Guangdong Sheng 510080
China

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