Skip to main content

Table 2 Study outcomes in case and control group

From: The antiretroviral efficacy of highly active antiretroviral therapy and plasma nevirapine concentrations in HIV-TB co-infected Indian patients receiving rifampicin based antituberculosis treatment

Outcomes

HIV+TB

(Cases: n = 63)

HIV+

(Controls: n = 51)

P value

Vital status at 48 week

-Weight

-Hemoglobin

1. 53.2 ± 8.65

ii. (12.9 ± 1.01

55.7 ± 9.12

12.5 ± 1.52

0.32

0.33

Mortality

13 (20.63%)

4 (7.84%)

0.068

Mean increase in CD4 cell

count at 24 weeks

from Baseline

108.3

112.7

0.83

Mean increase in CD4 cell

count at 48 weeks

from Baseline

128.2

148.4

0.69

Viral load suppression at

24 Weeks

(≤ 400 copies/ml)

35 (55.5%)

--

--

Viral load suppression at 48 Weeks (≤ 400 copies/ml)

37 (58.73%)

--

--

Immunological failure

6 (9.5%)

2 (3.9%)

0.313

Virological failure

5 (7.93%)

--

--

Clinical Progression at

48 weeks

6 (9.5%)

2 (3.9%)

0.313