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Joint Survival Model of CD4 Outcome for HIV/TB Coinfected: Data from Kenya AIDS Indicator Survey

机译:HIV / TB合并感染的CD4结果联合生存模型:来自肯尼亚AIDS指标调查的数据

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HIV infection leads to immune deficiency, increasing the risk of TB in people with HIV. HIV/TB co-infection increases the risk of death from TB or other opportunist infections. CD4 cell counts (cells/mm3) along with viral load are measures of treatment failure. This study purposed to apply shared frailty model in analyzing the survival and hazard rates of the TB/HIV co-infected persons. This work is very important because co-morbidity with TB and HIV is a rambling cause of death in Africa. The research employed a bivariate Gamma Frailty model to get the correlation amongst the HIV/TB outcomes to necessitate valid and reliable statistical inferencing. A survival frailty model on the CD4 counts is developed and fitted to factor in the unobserved heterogeneity that might occur in some observations. Ignoring some unobserved or unmeasured effects gives misguided estimates of survival. Thus, correcting these overdispersion or under-dispersion helps adjust these frailties. Frailty model provided a solid statistical analysis to CD4 data accounting for TB/HIV co-infection. The study also carried out some simulations along with the standard errors to compare the true values of the parameters. From the simulation findings, it is evident that precision and coverage improves with increase in sample size. Data used in this paper is from Kenya AIDS Indicator Survey (2012) which comprised of 648 HIV-positive patients, 10978 HIV-negative, and 2094 whose status was unknown. From the results, it is evident that the survival rate for the HIV positive individuals who are TB negative, with CD4 ≤ 310 is higher, at 0.9963 than that of the TB positive persons, at 0.975. The research finding points TB/HIV co-infection as a key factor for predicting immunological failure as measured by CD4 counts. The Kenyan government, and in particular the ministry of health should develop policies that mandate TB diagnosis among the PLHIV and linkage to TB treatment for the positive cases.
机译:HIV感染会导致免疫缺陷,从而增加HIV感染者患结核病的风险。 HIV / TB合并感染会增加因TB或其他机会主义感染而死亡的风险。 CD4细胞计数(细胞/ mm3)以及病毒载量是治疗失败的量度。这项研究旨在将共享的脆弱模型用于分析结核病/艾滋病毒合并感染者的生存率和危险率。这项工作非常重要,因为与结核病和艾滋病毒并存是非洲致死的主要原因。该研究采用双变量Gamma脆弱模型来获得HIV / TB结果之间的相关性,从而需要有效和可靠的统计推断。建立了CD4计数的生存脆弱模型,并将其拟合为某些观察中可能发生的未观察到的异质性。忽略一些未观察到的或无法测量的影响会导致错误的生存估计。因此,校正这些过度分散或分散不足有助于调整这些脆弱性。脆弱模型为CD4数据提供了可靠的统计分析,说明了TB / HIV合并感染。该研究还进行了一些模拟以及标准误差,以比较参数的真实值。从仿真结果中可以看出,随着样本数量的增加,精度和覆盖率也会提高。本文使用的数据来自肯尼亚艾滋病指标调查(2012年),该调查由648名HIV阳性患者,10978名HIV阴性患者和2094名状态不明的患者组成。从结果可以看出,CD4≤310的TB阴性的HIV阳性个体的存活率更高,为0.9963,而TB阳性的人的存活率为0.975。研究发现,TB / HIV合并感染是预测免疫功能衰竭的关键因素,以CD4计数来衡量。肯尼亚政府,特别是卫生部应制定政策,要求在艾滋病毒感染者中进行结核病诊断,并与阳性病例建立结核病治疗联系。

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