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DOI 10.1186/1471-2334-10-83

Медицинская библиотека · BMC infectious diseases · 2010

Clinical deterioration during antituberculosis treatment in Africa: incidence, causes and risk factors.

Pepper Dominique J, Marais Suzaan, Wilkinson Robert J, Bhaijee Feriyl, Maartens Gary, McIlleron Helen, De Azevedo Virginia, Cox Helen, McDermid Cheryl, Sokhela Simiso, Patel Janisha, Meintjes Graeme

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПоддержка правительства СШАПеревод в очереди

Аннотация

BACKGROUND

HIV-1 and Mycobacterium tuberculosis cause substantial morbidity and mortality. Despite the availability of antiretroviral and antituberculosis treatment in Africa, clinical deterioration during antituberculosis treatment remains a frequent reason for hospital admission. We therefore determined the incidence, causes and risk factors for clinical deterioration.

METHODS

Prospective cohort study of 292 adults who initiated antituberculosis treatment during a 3-month period. We evaluated those with clinical deterioration over the following 24 weeks of treatment.

RESULTS

Seventy-one percent (209/292) of patients were HIV-1 infected (median CD4+: 129 cells/microL [IQR:62-277]). At tuberculosis diagnosis, 23% (34/145) of HIV-1 infected patients qualifying for antiretroviral treatment (ART) were receiving ART; 6 months later, 75% (109/145) had received ART. Within 24 weeks of initiating antituberculosis treatment, 40% (117/292) of patients experienced clinical deterioration due to co-morbid illness (n = 70), tuberculosis related illness (n = 47), non AIDS-defining HIV-1 related infection (n = 25) and AIDS-defining illness (n = 21). Using HIV-1 uninfected patients as the referent group, HIV-1 infected patients had an increasing risk of clinical deterioration as CD4+ counts decreased [CD4+>350 cells/microL: RR = 1.4, 95% CI = 0.7-2.9; CD4+:200-350 cells/microL: RR = 2.0, 95% CI = 1.1-3.6; CD4+<200 cells/microL: RR = 3.0, 95% CI = 1.9-4.7]. During follow-up, 26% (30/117) of patients with clinical deterioration required hospital admission and 15% (17/117) died. Fifteen deaths were in HIV-1 infected patients with a CD4+<200 cells/microL.

CONCLUSIONS

In multivariate analysis, HIV-1 infection and a low CD4+ count at tuberculosis diagnosis were significant risk factors for clinical deterioration and death. The initiation of ART at a CD4+ count of <350 cells/microL will likely reduce the high burden of clinical deterioration.

Для цитирования: Pepper Dominique J, Marais Suzaan, Wilkinson Robert J, Bhaijee Feriyl, Maartens Gary, McIlleron Helen, De Azevedo Virginia, Cox Helen, McDermid Cheryl, Sokhela Simiso, Patel Janisha, Meintjes Graeme. Clinical deterioration during antituberculosis treatment in Africa: incidence, causes and risk factors.. BMC infectious diseases. 2010. DOI: 10.1186/1471-2334-10-83.

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