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Table 1 Demographic and clinical features at switch to dual therapy

From: Biochemical and inflammatory modifications after switching to dual antiretroviral therapy in HIV-infected patients in Italy: a multicenter retrospective cohort study from 2007 to 2015

Variables

From tenofovir/emtricitabine n (%)

(n = 364)

From abacavir/lamivudine n (%)

(n = 65)

p-valuea

Male

249 (68.4)

52 (80.0)

0.060

Age, in years, mean (SD)

48.1 (10.2)

51.0 (10.4)

 

 < 40

65 (17.9)

5 (7.7)

0.093

 40–49

145 (39.8)

26 (40.0)

 

 ≥ 50

154 (42.3)

34 (52.3)

 

Intravenous Drug Use

85 (27.6)

15 (25.9)

0.953

HCV co-infection

134 (36.8)

24 (36.9)

0.987

CD4 cell count, cell/mm3, mean (SD)

631.6 (295.6)

678.1 (342.2)

 

 < 200

15 (4.9)

1 (1.8)

0.674

 200–349

35 (11.4)

8 (14.6)

 

 350–499

51 (16.7)

8 (14.6)

 

 ≥ 500

205 (67.0)

38 (69.1)

 

Positive HIV-RNA, >  37 copies/mL

37 (12.3)

6 (11.3)

0.835

Time (months) in tenofovir/abacavir

110.0 (68.3)

110.4 (78.7)

0.970

Dual regimens:

 Atazanavir/r + 3TC (regimen 1)

121 (33.2)

17 (26.2)

< 0.001

 Darunavir/r + 3TC (regimen 2)

84 (23.1)

14 (21.5)

 

 Lopinavir/r + 3TC (regimen 3)

31 (8.5)

1 (1.5)

 

 Raltegravir/dolutegravir+PI/r (regimen 4)

128 (35.2)

33 (50.8)

 

Number of patients with at least one previous virological failure

79 (21.7)

25 (38.5)

0.004

  1. aWe used Student t-test for comparison of means Chi-squared test for comparition of proportions