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Corrigendum to ‘Utility of plasma cell-free DNA next-generation sequencing for diagnosis of infectious diseases in patients with hematological disorders’ [Journal of Infection Volume 86 Issue 1 (2023) pages 14–23]

  • Chunhui Xu
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China

    Microbiology Laboratory, Tianjin Union Precision Medical Diagnostic Co., Ltd, Tianjin 301617, China
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  • Xin Chen
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Guoqing Zhu
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Huiming Yi
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Shulian Chen
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Yuetian Yu
    Affiliations
    Department of Critical Care Medicine, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
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  • Erlie Jiang
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Yizhou Zheng
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Fengkui Zhang
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Jianxiang Wang
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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  • Sizhou Feng
    Correspondence
    Corresponding author.
    Affiliations
    State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China
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Open AccessPublished:January 17, 2023DOI:https://doi.org/10.1016/j.jinf.2023.01.011
      The authors regret an error was included in the published funding information for this article. The correct funding information is:
      This work was supported by the CAMS Innovation Fund for Medical Sciences (CIFMS) [2021-I2M-1-017] & [2021-I2M-C&T-B-080], Tianjin Municipal Science and Technology Commission Grant (21JCZDJC01170) and Haihe Laboratory of Cell Ecosystem Innovation Fund [HH22KYZX0036].
      Table S3 was also included in the supplementary material in error.
      The authors would like to apologize for any inconvenience caused.

      Linked Article

      • Utility of plasma cell-free DNA next-generation sequencing for diagnosis of infectious diseases in patients with hematological disorders
        Journal of InfectionVol. 86Issue 1
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          Neutropenia is an independent risk factor for infection in patients with hematological disorders who have undergone hematopoietic stem cell transplantation (HSCT) and received cytotoxic chemotherapy or immunosuppressive therapy.1-3 Infection is one of the most common complications for patients with neutropenia and can lead to high mortality if inappropriate empirical antibiotic treatment is administered.4, 5 Accurate and timely pathogen detection is critical in optimizing antibiotic use; however, it is challenging in patients with neutropenia because of nonspecific clinical symptoms, signs, and the low positivity rate of conventional microbiological tests (CMT).
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