A hospital-based observational study on HIV-TB co-infection.

Access microbiology Pub Date : 2025-08-06 eCollection Date: 2025-01-01 DOI:10.1099/acmi.0.000787.v4
Akansha Soni, Vimala Venkatesh, Parul Jain, Amita Jain, D Himanshu Reddy, Neetu Gupta, Ritu Tandon
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Abstract

Background. Human immunodeficiency virus (HIV) is the major cause of failure to reach targets of tuberculosis (TB) control in settings with high HIV loads. TB, on the other hand, enhances the progression of HIV infection to AIDS. This study was done to understand the epidemiological and clinical profile of HIV-TB co-infected patients and to study the impact of TB on the recovery of CD4 counts. Methodology. An observational study was conducted in which of the 573 patients newly diagnosed with HIV infection and enrolled at the antiretroviral therapy (ART) centre, King George's Medical University, Lucknow, between May 2021 and June 2022, 80 patients who also had newly diagnosed TB were included. These HIV-TB co-infected patients were analysed for demographic factors. Also, clusters of differentiation 4 (CD4) counts were done at the time of enrolment on ART and then later, ~6 to 8 months of recieving ART and anti-tubercular treatment (ATT) initiation. For comparison, of the 493 HIV-only patients, 50 age- and gender-matched consecutive patients for whom baseline and follow-up CD4 counts were available were enrolled as controls. The change from baseline CD4 count was calculated using a paired t-test and Wilcoxon signed rank test. Results. In the present study, among HIV-TB co-infected patients, baseline CD4 levels were 194.52±162.27, and follow-up CD4 levels were 285.09±170.33. A statistically significant increment of 90.57±165.60 in mean CD4 levels was observed (t=4.019; P<0.001). Likewise, in only HIV-positive patients, a statistically significant increment of 125.26±191.48 (35.75%) cells in mean CD4 levels was observed (t=4.626; P<0.001). The increase in CD4 counts in HIV only population was significantly higher than that observed in HIV-TB co0infected patients. Conclusion. Though significant rise in CD4 counts was observed in both HIV-TB co-infected patients and HIV-only patients after 6 to 8 months of appropriate therapy, the rise was significantly higher among the HIV-only group as compared to the HIV-TB co-infected group.

Abstract Image

一项基于医院的HIV-TB合并感染的观察性研究。
背景。人类免疫缺陷病毒(HIV)是在艾滋病毒载量高的环境中无法达到结核病控制目标的主要原因。另一方面,结核病加速了艾滋病毒感染向艾滋病的发展。本研究旨在了解HIV-TB合并感染患者的流行病学和临床概况,并研究结核病对CD4计数恢复的影响。方法。进行了一项观察性研究,在2021年5月至2022年6月期间,在勒克诺乔治国王医科大学抗逆转录病毒治疗中心登记的573名新诊断为艾滋病毒感染的患者中,包括80名新诊断为结核病的患者。对这些HIV-TB合并感染患者进行人口统计学因素分析。此外,在ART入组时进行CD4细胞计数,然后在ART和抗结核治疗(ATT)开始后的6至8个月进行计数。为了比较,在493名hiv患者中,50名年龄和性别匹配的连续患者作为对照,这些患者的基线和随访CD4计数都是可用的。使用配对t检验和Wilcoxon符号秩检验计算基线CD4计数的变化。结果。本研究中,HIV-TB合并感染患者的基线CD4水平为194.52±162.27,随访CD4水平为285.09±170.33。两组患者CD4平均水平增加90.57±165.60,差异有统计学意义(t=4.019;Pt = 4.626;PConclusion。虽然经过6至8个月的适当治疗后,HIV-TB合并感染患者和HIV-TB合并感染患者的CD4计数均显著上升,但与HIV-TB合并感染组相比,HIV-TB合并感染组的CD4计数明显上升。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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