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Table 2 Outcomes for the 84 virologically suppressed HIV-infected patients entered in this study

From: Efficacy and safety of switching from nevirapine immediate-release twice daily to nevirapine extended-release once daily in virologically suppressed HIV-infected patients: a retrospective cohort study in Taiwan

 

All

NVP-XR

NVP-IR

P

N = 84

N = 35

N = 49

Ability to maintain a virological response, n (%)

71 (84.5)

29 (82.9)

42 (85.7)

0.72

Reason for treatment failure

 Death, n (%)

0 (0.0)

0 (0.0)

0 (0.0)

 

 Switch to other cART due to adverse effect or other cause, n (%)

4 (4.8)

2 (5.7) a

2 (4.1)

1.00

 Virological failure, n (%)

2 (2.4)

1 (2.9)

1 (2.0)

1.00

 Loss to follow-up, n (%)

6 (7.1)

3 (8.6)

4 (8.1)

1.00

Virological blip, n (%)

6 (7.1)

4 (11.4)

2 (4.1)

0.23

Change from baseline in CD4 T-cells, mean cells/mm3 (± SD)

14 (122)

23 (171)

76 (127)

0.33

  1. cART combined antiretroviral therapy, NVP nevirapine, SD standard deviation
  2. aOne patient in the NVP-XR group discontinued NVP-XR because of insufficient supply of the drug