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Table 1 Baseline patient characteristics

From: Cost analysis of HIV treatment and drug-related adverse events when fixed-dose combinations of antiretrovirals (FDCs) were stopped, versus continuation with FDCs

 

Exposed patients (n = 75)

Non-exposed patients (n = 150)

 

Gender (female)

18 (24%)

38 (25%)

*

Mean age (years)

44

46

*

Weight (kg)

70

72

*

Mechanism of transmission

*

Homosexual

18 (25%)

37 (25%)

*

IVDU

29 (39%)

52 (35%)

*

Heterosexual

19 (25%)

48 (32%)

*

Unknown

7 (9%)

12 (8%)

*

Concomitant pathologies

 

*

AIDS

18 (24%)

46 (30%)

*

HCV

31 (40%)

56 (39%)

*

Psychiatric history

17 (23%)

27 (18%)

*

Methadone consumption

5 (6%)

22 (14%)

*

Use of psychopharmaceuticals

14 (19%)

19 (13%)

*

FDCs

  

*

AtriplaTM

36 (48%)

72 (48%)

*

TruvadaTM

24 (32%)

48 (32%)

*

KivexaTM

7 (9%)

16 (11%)

*

CombivirTM

6 (8%)

14 (9%)

*

TrizivirTM

2 (3%)

0 (0%)

*

NNRTI

15 (20%)

28 (19%)

*

PI

22 (29%)

54 (36%)

*

Integrase

0 (0%)

3 (2%)

*

Exposure time to FDCs (months)

27 (range: 1–121)

24 (range: 3–98)

*

Exposure time to efavirenz (months)

50 (range: 129–1)

61 (range: 126–3)

*

Viral load > 50 copies/mL at visit −1

12 of 74 (16.2%)

8 of 149 (5.4%)

(OR: 3.4; 95%CI: 1.3-8.8; p = 0.02)

Viral load > 50 copies/mL at baseline visit

10 of 74 (13.5%)

10 of 146 (6.8%)

*

CD4 at first visit (cells/μL)

573 (range: 41–1527)

542 (range: 92–1481)

*

  1. IVDU: intravenous drug user; AIDS: acquired immunodeficiency syndrome; HCV: hepatitis C virus; FDCs: fixed-dose antiretroviral combinations; NNRTI: non-nucleoside reverse transcriptase inhibitor; PI: protease inhibitor; CD4: CD4+ lymphocytes; OR: odds ratio; 95%CI: confidence intervals at the 95% level.
  2. *No statistically significant differences.