Application of plasma metagenomic next-generation sequencing improves prognosis in hematology patients with neutropenia or hematopoietic stem cell transplantation for infection

被引:3
作者
Chen, Yuhui [1 ]
Wang, Jinjin [1 ]
Gan, Xinai [1 ]
Li, Meng [1 ]
Liao, Yi [1 ]
Zhou, Yongzhao [2 ]
Niu, Ting [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Hematol, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Integrated Care Management Ctr, Chengdu, Peoples R China
关键词
metagenomic next-generation sequencing; infection; hematology patients; diagnosis; prognosis; FEBRILE NEUTROPENIA; PEDIATRIC-PATIENTS; DIAGNOSIS; CANCER; DISEASES; FEVER;
D O I
10.3389/fcimb.2024.1338307
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Metagenomic next-generation sequencing (mNGS) is a novel technique for detecting pathogens. This retrospective study evaluated the diagnostic value of mNGS using plasma for infections in hematology patients and its impact on clinical treatment and prognosis in different subgroups of hematology patients. Methods A total of 153 hematology patients with suspected infection who underwent mNGS using plasma were enrolled in the study. Their clinical histories, conventional microbiological test (CMT) results, mNGS results, treatment and prognosis were retrospectively analyzed. Results In 153 plasma samples, mNGS yielded a higher positivity rate than CMT (total: 88.24% vs. 40.52%, P<0.001; bacteria: 35.95% vs. 21.57%, P < 0.01; virus: 69.93% vs. 21.57%, P<0.001; fungi: 20.26% vs. 7.84%, P<0.01). mNGS had a higher positivity rate for bacteria and fungi in the neutropenia group than in the non-neutropenia group (bacteria: 48.61% vs. 24.69%, P<0.01; fungi: 27.78% vs. 13.58%, P<0.05). mNGS demonstrated a greater advantage in the group of patients with hematopoietic stem cell transplantation (HSCT). Both the 3-day and 7-day efficacy rates in the HSCT group were higher than those in the non-HSCT group (3-day: 82.22% vs. 58.65%, P < 0.01; 7-day: 88.89% vs. 67.31%, P < 0.01), and the 28-day mortality rate was lower in the HSCT group than in the non-HSCT group (6.67% vs. 38.89%, P < 0.000). The neutropenia group achieved similar efficacy and mortality rates to the non-neutropenia group (7-day efficiency rate: 76.39% vs. 71.43%, P > 0.05; mortality rate: 29.17% vs. 29.63%, P > 0.05) with more aggressive antibiotic adjustments (45.83% vs. 22.22%, P < 0.01). Conclusion mNGS can detect more microorganisms with higher positive rates, especially in patients with neutropenia. mNGS had better clinical value in patients with hematopoietic stem cell transplantation (HSCT) or neutropenia, which had a positive effect on treatment and prognosis.
引用
收藏
页数:12
相关论文
共 42 条
[1]   Cell-free DNA next-generation sequencing successfully detects infectious pathogens in pediatric oncology and hematopoietic stem cell transplant patients at risk for invasive fungal disease [J].
Armstrong, Amy E. ;
Rossoff, Jenna ;
Hollemon, Desiree ;
Hong, David K. ;
Muller, William J. ;
Chaudhury, Sonali .
PEDIATRIC BLOOD & CANCER, 2019, 66 (07)
[2]   European guidelines for empirical antibacterial therapy for febrile neutropenic patients in the era of growing resistance: summary of the 2011 4th European Conference on Infections in Leukemia [J].
Averbuch, Diana ;
Orasch, Christina ;
Cordonnier, Catherine ;
Livermore, David M. ;
Mikulska, Malgorzata ;
Viscoli, Claudio ;
Gyssens, Inge C. ;
Kern, Winfried V. ;
Klyasova, Galina ;
Marchetti, Oscar ;
Engelhard, Dan ;
Akova, Murat .
HAEMATOLOGICA, 2013, 98 (12) :1826-1835
[3]  
Cai L J, 2023, Zhonghua Xue Ye Xue Za Zhi, V44, P479, DOI 10.3760/cma.j.issn.0253-2727.2023.06.006
[4]  
Chinese Society of Hematology Chinese Medical Association, 2020, Zhonghua Xue Ye Xue Za Zhi, V41, P969, DOI 10.3760/cma.j.issn.0253-2727.2020.12.001
[5]   Impact of time to antibiotic on hospital stay, intensive care unit admission, and mortality in febrile neutropenia [J].
Daniels, Lisa M. ;
Durani, Urshila ;
Barreto, Jason N. ;
O'Horo, John C. ;
Siddiqui, Mustaqeem A. ;
Park, John G. ;
Tosh, Pritish K. .
SUPPORTIVE CARE IN CANCER, 2019, 27 (11) :4171-4177
[6]   Overview of Infections in the Immunocompromised Host [J].
Dropulic, Lesia K. ;
Lederman, Howard M. .
MICROBIOLOGY SPECTRUM, 2016, 4 (04)
[7]   Effects of viral infection and microbial diversity on patients with sepsis: A retrospective study based on metagenomic next-generation sequencing [J].
Duan, Li-wei ;
Qu, Jin-long ;
Wan, Jian ;
Xu, Yong-hua ;
Shan, Yi ;
Wu, Li-xue ;
Zheng, Jin-hao ;
Jiang, Wei-wei ;
Chen, Qi-tong ;
Zhu, Yan ;
Zhou, Jian ;
Yu, Wen-bo ;
Pei, Lei ;
Song, Xi ;
Li, Wen-fang ;
Lin, Zhao-fen .
WORLD JOURNAL OF EMERGENCY MEDICINE, 2021, 12 (01) :29-35
[8]   Clinical metagenomic sequencing of plasma microbial cell-free DNA for febrile neutropenia in patients with acute leukaemia [J].
Feng, Sizhou ;
Rao, Guanhua ;
Wei, Xudong ;
Fu, Rong ;
Hou, Ming ;
Song, Yongping ;
Xu, Chunhui ;
Han, Peng ;
Gong, Benfa ;
Chen, Xin ;
Wang, Yihao ;
Dong, Xiaoyuan ;
Jiang, Zhi ;
Wang, Jianxiang .
CLINICAL MICROBIOLOGY AND INFECTION, 2024, 30 (01) :107-113
[9]  
Freifeld AG, 2011, CLIN INFECT DIS, V52, pE56, DOI 10.1093/cid/cir073
[10]   Metagenomic Next-Generation Sequencing in the Diagnosis of Infectious Fever During Myelosuppression Among Pediatric Patients with and Diseases [J].
Fu, Yang ;
Zhu, Xiaohua ;
Cao, Ping ;
Shen, Chen ;
Qian, Xiaowen ;
Miao, Hui ;
Yu, Yi ;
Wang, Hongsheng ;
Zhai, Xiaowen .
INFECTION AND DRUG RESISTANCE, 2022, 15 :5425-5434