Clinical features and prognosis of patients co-infected with HIV and tuberculosis in the ICU
© Pecego et al.; licensee BioMed Central Ltd. 2013
Published: 5 November 2013
Despites advances in treatment, tuberculosis (TB) remains a global health threat and is the leading co-infection among Brazilian HIV-infected patients [1–4]. Mortality of TB in the presence of sepsis and shock septic can be as high as 67%, with respiratory failure being the leading cause of ICU admission [2, 3, 5]. Clinical factors that enhance mortality among HIV-TB patients are yet to be explored.
Materials and methods
We retrospectively accessed data of HIV/AIDS critically ill patients from January 2007 until May 2012, at a referral infectious diseases hospital. All patients admitted to the ICU with laboratory-confirmed TB were included in the analysis. Demographic and clinical data were categorized for survivors and nonsurvivors and the results were displayed as frequency (%), median values and interquartile range.
Fifty patients were included. Hospital mortality was 48%. Age was 31.5 years (26.5 to 42.75) in the survivors group versus 33.5 years (30 to 45.25) in nonsurvivors (P = 0.25), and the SAPS II score was 44.5 (37.25 to 55.75) versus 47.25 (38.75 to 54.25) (P = 0.58). The most common TB presentation was disseminated disease (56%) followed by pulmonary (44%), with no difference according to survival. The delta of days between ICU admission and beginning of TB treatment was not different between groups. Rifampicin (94%), pyrazynamide (94%), isoniazide (92%) and ethambutol (76%) were administered in the majority of patients, while fluoroquinolones and aminoglycosides were administered in 64% and 54% respectively. Nonsurvivors presented with more elapsed time since HIV diagnosis (1 (1 to 7) vs. 26 (5 to 72), P = 0.10); lower nadir CD4 cell count (72.5 (27.5 to 133.5) vs. 24 (14.5 to 63), P = 0.03); and HAART initiated within 30 days after admission (62% vs. 29%, P = 0.03, odds ratio 3.9 (95% CI 1.2 to 12.7)). The main reason for ICU admission was respiratory failure (70%). Nonsurvivors needed mechanical ventilation (88% vs. 48%, P = 0.006) and vasopressors (71% vs. 41%, P = 0.05) more frequently. Neurological dysfunction was more common in nonsurvivors (79% vs. 41%, P = 0.01, odds ratio 5.2 (95% CI 1.5 to 18.2)). After multivariate analysis, neurological dysfunction was associated with higher mortality, while HAART in the first 30 days of hospitalization was a protective associated factor.
The disseminated form was the most common presentation of TB in HIV/AIDS critically ill patients. Nonsurvivors were more prone to multiple organ dysfunction syndrome, with neurological dysfunction associated with hospital mortality. The administration of HAART within 30 days of hospitalization was associated with survival.
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