Abstract

BackgroundTuberculosis infection still places a great burden on HIV-infected individuals in China and other developing countries. Knowledge of the survival of HIV-infected patients with pulmonary tuberculosis (PTB) would provide important insights for the clinical management of this population, which remains to be well described in current China.MethodsHIV-infected patients with PTB admitted to Shanghai Public Health Clinical Center from January 2011 to December 2015 were retrospectively enrolled. In this cohort, the survival prognosis was estimated by the Kaplan-Meier method, while univariate and multivariate Cox proportional hazards models were used to determine the risk factors affecting mortality.ResultsAfter reviewing 4914 admitted patients with HIV infection, 359 PTB cases were identified. At the time of PTB diagnosis, the patients’ median CD4+ T cell count was 51 /mm3 (IQR: 23–116), and 27.30% of patients (98/359) were on combination antiretroviral therapy (cART). For the 333 cases included in the survival analysis, the overall mortality was 15.92% (53/333) during a median 27-month follow-up. The risk factors, including age older than 60 years (HR: 3.18; 95% CI: 1.66–6.10), complication with bacterial pneumonia (HR: 2.64; 95% CI: 1.30–5.35), diagnosis delay (HR: 2.60; 95% CI: 1.42–4.78), CD4+ T cell count less than 50/mm3 (HR: 2.38; 95% CI: 1.27–4.43) and pulmonary atelectasis (HR: 2.20; 95% CI: 1.05–4.60), might independently contribute to poor survival. Among patients without cART before anti-TB treatment, the later initiation of cART (more than 8 weeks after starting anti-TB treatment) was found to increase the mortality rate (OR: 4.33; 95% CI: 1.22–15.36), while the initiation of cART within 4–8 weeks after starting anti-TB treatment was associated with the fewest deaths (0/14).ConclusionsThe subjects in this study conducted in the cART era were still characterized by depressed immunological competence and low rates of cART administration, revealing possible intervention targets for preventing TB reactivation in HIV-infected individuals under current circumstances. Furthermore, our study indicated that the timely diagnosis of PTB, prevention of secondary bacterial pneumonia by prophylactic management and optimization of the timing of cART initiation could have significant impacts on decreasing mortality among HIV/PTB co-infected populations. These findings deserve further prospective investigations to optimize the management of HIV/PTB-co-infected patients.Trial registrationNCT01344148, Registered September 14, 2010.

Highlights

  • Tuberculosis infection still places a great burden on human immunodeficiency virus (HIV)-infected individuals in China and other developing countries

  • The subjects in this study conducted in the combination antiretroviral therapy (cART) era were still characterized by depressed immunological competence and low rates of cART administration, revealing possible intervention targets for preventing TB reactivation in HIV-infected individuals under current circumstances

  • Our study indicated that the timely diagnosis of pulmonary tuberculosis (PTB), prevention of secondary bacterial pneumonia by prophylactic management and optimization of the timing of cART initiation could have significant impacts on decreasing mortality among HIV/PTB co-infected populations

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Summary

Introduction

Tuberculosis infection still places a great burden on HIV-infected individuals in China and other developing countries. In developing countries with limited medical resources, TB is one of the most common opportunistic infections in acquired immunodeficiency syndrome (AIDS) patients [3,4,5] Both TB and HIV drastically affect the host’s immune system because they can evade immune surveillance and clearance, the mechanism is not fully understood [6]. With TB infection, the cytokines induced by immune responses could enhance the replication of HIV and accelerate AIDS progression [9]. For this reason, TB infection has been one of the most common causes of death in HIV-infected patients, accounting for 26% of AIDSrelated deaths [7, 10], almost (99%) of which occurred in developing countries [6]

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