Investigation of invasive fungal infection in tuberculosis/human immunodeficiency virus co-infected patients

肺结核 共感染 医学 人类免疫缺陷病毒(HIV) 免疫学 艾滋病相关机会性感染 微生物学 病毒学 生物 西达 病毒性疾病 病理
作者
Rejane Roncaglio,Dienefer Venske Bierhals,Emília Ferreira Andrade,Bianca dos Santos Blan,Romina Buffarini,Andréa von Groll,Rossana Patrícia Basso,Pedro Eduardo Almeida da Silva,Melissa Orzechowski Xavier,Ivy Bastos Ramis
出处
期刊:Medical Mycology [Oxford University Press]
卷期号:63 (6)
标识
DOI:10.1093/mmy/myaf045
摘要

Tuberculosis (TB) and human immunodeficiency virus (HIV) represent important public health problems. Suppression of the immune system, due to both diseases, predisposes to the development of opportunistic infections, such as invasive fungal infections (IFI). The aims of this study were to determine the frequency of investigation of IFI in TB/HIV co-infected patients, identify the most frequent IFI and evaluate the clinical-epidemiological characteristics of TB/HIV/IFI patients. A descriptive and retrospective study was conducted including patients assisted at Hospital Dr. Miguel Riet Corrêa Jr. (HU-FURG/Ebserh), in Rio Grande City, southern Brazil. All patients diagnosed with TB/HIV from 2017 to 2022 were included, and databases were analyzed for data regarding mycological exams for fungal disease investigation. Of the 194 TB/HIV co-infected patients, 77.8% (n = 151) were investigated for at least one IFI. Co-infection was confirmed in 13.9% (21/151), being 52.4% (n = 11) of the patients diagnosed with cryptococcosis, followed by histoplasmosis (47.6%; n = 10) and probable invasive aspergillosis (IA) (9.6%; n = 2). Furthermore, some patients presented more than one fungal co-infection (9.5%; n = 2). CD4 T cell count < 200 cells/mm3 represented a risk factor for the development of IFI (P = 0.006) and the outcome death was higher in the TB/HIV/IFI group, as well as 38% of patients died. Even without a systematic investigation for IFI in TB/HIV patients, a high rate of co-infection was shown. Therefore, it is necessary to investigate TB and IFI concomitantly, in people living with HIV, due to the worsening of the outcome when these infections are associated.
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