Laboratory Medicine ›› 2023, Vol. 38 ›› Issue (12): 1173-1176.DOI: 10.3969/j.issn.1673-8640.2023.12.012

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Analysis of Mycobacterium infection in HIV/AIDS patients

DAI Fangfang1, LU Xinxin2, YU Yanhua1, CHEN Ming1, SUN Guizhen1()   

  1. 1. Department of Clinical Laboratory,Beijing Youan Hospital,Capital Medical University,Beijing 100069,China
    2. Department of Clinical Laboratory,Beijing Tongren Hospital,Capital Medical University,Beijing 100176,China
  • Received:2022-06-03 Revised:2023-06-12 Online:2023-12-30 Published:2024-02-20

Abstract:

Objective To analyze the determination of Mycobacterium infection in human immunodeficiency virus(HIV)/acquired immune deficiency syndrome(AIDS)patients. Methods Totally,1 379 Mycobacterium acid-fast staining specimens,1 975 Mycobacterium culture specimens,1 406 Mycobacterium tuberculosis(MTB)-polymerase chain reaction(PCR) specimens and 522 interferon-gamma release assay(IGRA) specimens were collected from HIV/AIDS patients from January 2018 to December 2021 Beijing Youan Hospital of Capital Medical University. The results of these specimens by the 4 methods were analyzed and compared retrospectively. Results The positive rates of acid-fast staining,culture,MTB-PCR and IGRA were 3.41%,5.47%,5.83% and 11.49%,respectively. The positive rates of acid-fast staining and culture were improved,when they were determined with MTB-PCR or IGRA. The positive rate was high when the 4 methods were used simultaneously,and it was easy to distinguish MTB from non-tuberculous Mycobacterium(NTM). MTB-PCR and IGRA were the specific methods for the identification of MTB,and their identification results were consistent. Conclusions In HIV/AIDS patients with Mycobacterium infection,the positive rates of acid-fast staining and culture are low. MTB-PCR and IGRA can distinguish MTB from NTM. When HIV/AIDS patients are suspected with Mycobacterium infection,it is recommended to combine multiple determination methods.

Key words: Human immunodeficiency virus, Mycobacterium, Acid-fast staining, Culture, Polymerase chain reaction, Interferon-gamma release assay

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