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. 2012;7(3):e31786.
doi: 10.1371/journal.pone.0031786. Epub 2012 Mar 6.

Survival from XDR-TB is associated with modifiable clinical characteristics in rural South Africa

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Survival from XDR-TB is associated with modifiable clinical characteristics in rural South Africa

Sheela V Shenoi et al. PLoS One. 2012.

Abstract

Background: Drug-resistant tuberculosis (TB) is a major threat to global public health. Patients with extensively drug-resistant TB (XDR-TB), particularly those with HIV-coinfection, experience high and accelerated mortality with limited available interventions. To determine modifiable factors associated with survival, we evaluated XDR-TB patients from a community-based hospital in rural South Africa where a large number of XDR-TB cases were first detected.

Methodology/principal findings: A retrospective case control study was conducted of XDR-TB patients diagnosed from 2005-2008. Survivors, those alive at 180 days from diagnostic sputum collection date, were compared with controls who died within 180 days. Clinical, laboratory and microbiological correlates of survival were assessed in 69 survivors (median survival 565 days [IQR 384-774] and 73 non-survivors (median survival 34 days [IQR 18-90]). Among 129 HIV+ patients, multivariate analyses of modifiable factors demonstrated that negative AFB smear (AOR 8.4, CI 1.84-38.21), a lower laboratory index of routine laboratory findings (AOR 0.48, CI 0.22-1.02), CD4>200 cells/mm(3) (AOR 11.53, 1.1-119.32), and receipt of antiretroviral therapy (AOR 20.9, CI 1.16-376.83) were independently associated with survival from XDR-TB.

Conclusions/significance: Survival from XDR-TB with HIV-coinfection is associated with less advanced stages of both diseases at time of diagnosis, absence of laboratory markers indicative of multiorgan dysfunction, and provision of antiretroviral therapy. Survival can be increased by addressing these modifiable risk factors through policy changes and improved clinical management. Health planners and clinicians should develop programmes focusing on earlier case finding and integration of HIV and drug-resistant TB diagnostic, therapeutic, and preventive activities.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Selection of Charts for Review.
Figure 2
Figure 2. Modifiable & Non-Modifiable Clinical Characteristics of XDR-TB Patients.
Figure 3
Figure 3. Kaplan-Meier Estimates of XDR-TB Survival in HIV-Infected Patients (Months), n = 129.
a. Probability of survival according to auramine smear status from time of sputum collection b. Probability of survival according to severity of organ dysfunction at sputum collection c. Probability of survival according to baseline CD4 count at sputum collection d. Probability of survival according to use of ART from the time of sputum collection.

References

    1. AIDS Program, Section of Infectious Diseases, Department of Medicine, Yale University, School of Medicine New Haven, Connecticut, United States of America.
    1. Abdool Karim SS, Churchyard G, Karim Q, Lawn S. HIV infection and tuberculosis in South Africa: an urgent need to escalate the public health response. Lancet. 2009;374:921–933. - PMC - PubMed
    1. World Health Organization. Multidrug and extensively drug-resistant TB (M/XDR-TB): 2010 global report on surveillance and response. Geneva: 2010.
    1. Shenoi S, Heysell S, Moll A, Friedland G. Multidrug-resistant and extensively drug-resistant tuberculosis: consequences for the global HIV community. Current Opinion in Infectious Diseases. 2009;22:11–17. - PMC - PubMed
    1. World Health Organization. 2009. Global tuberculosis control: epidemiology, strategy, financing Geneva.

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