亚马逊地区某卫生单位艾滋病毒/艾滋病患者巨细胞病毒感染情况,Belém, Parô,巴西

Silva Dfl, Arruda Lmf, Silva Nf, Sagica Fes, Moraes Mm, Jr Jlsa, Santos Tvr, Medeiros Rs
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摘要

导语:随着世界范围内HIV/AIDS患病率的上升,由于HIV引起的免疫缺陷和TCD4+细胞的减少,CMV感染成为一个严重的公共卫生问题。目的:对巴西贝伦-帕拉亚马逊地区一家公立医院收治的患者进行临床流行病学和实验室方面的评估。方法:采用问卷调查法和病历法收集临床和流行病学资料,全血ELISA法检测抗巨细胞病毒抗体;实时聚合酶链反应(qPCR)检测病毒载量的方法。结果:社会经济数据显示,基础教育水平不全的个体占35.3%,收入较低的个体占57.7%。通过病历发现重要的合并症;以肺结核(19.9%)、弓形虫病(19.5%)、肺外结核(14.5%)和腹泻综合征(14.1%)居多。根据血清学分析,只有2.1例患者具有急性感染特征(IgG+IgM+),而qPCR中超过50%的患者具有高病毒载量(M =107,479.48拷贝/ ml)。在本研究中,49例患者死亡,63.3%的患者同时感染了分子检测的HIV/CMV。当TCD4淋巴细胞<100cells/mm3时,cmv感染者发生率最高。分子数据与血清学结果差异有统计学意义(Z=12.98, p<0.0001)。结论:分子方法是临床诊断免疫缺陷患者继发性巨细胞病毒感染最合适的方法,CD4+<100/mm³细胞减少是HIV/AIDS患者发生机会性感染的重要危险因素。
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Cytomegalovirus Infections in Patients with HIV/AIDS in a Unit of Healthof the Amazonian Region, Belém, Pará, Brazil
Introduction: With the increase in prevalence of HIV/AIDS in the world, infection by CMV became a serious public health problem because of the immunodeficiency caused by HIV and the reduction of TCD4+ cells. Objective: Clinical-epidemiological and laboratory aspects of patients were evaluated, which were admitted in a public hospital in the Amazon Region, Belem-Para, Brazil. Methods: We collected clinical and epidemiological data by questionnaires and medical records, and whole blood for detection of anti-CMV antibodies by ELISA; and the method of Polymerase Chain Reaction in Real Time (qPCR) for detecting viral load. Results: The socioeconomic data indicated high frequency of individuals with incomplete level of basic education (35.3%) and low income (57.7%). Important comorbidities were found by using medical records; pulmonary tuberculosis (19.9%), toxoplasmosis (19.5%), extrapulmonary tuberculosis (14.5%) and diarrheal syndrome (14.1%) occurred more frequently. According to the serological analysis it was observed that only 2.1 of patients had acute infection profile ( IgG+IgM+), while in qPCR more than 50% of patients had high viral load (M =107,479.48 copies/ ml). During this study, 49 patients died, 63.3% were co-infected by HIV/CMV detected using molecular method. It was observed the highest occurrence of CMV-infected individuals when the TCD4 lymphocytes were <100cells/mm3. There were significant differences between molecular data and serological results (Z=12.98, p<0.0001). Conclusions: Molecular methods are the most appropriate technique to help in the clinical diagnosis of secondary CMV infection in immunodeficiencies and the reduction of CD4+<100/mm³ cells is an important risk factor that predisposes people with HIV/AIDS to opportunistic infections.
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