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Table 1 Patients' characteristics at inclusion (n = 514).

From: Efficacy, safety and pharmacokinetic of once-daily boosted saquinavir (1500/100 mg) together with 2 nucleos(t)ide reverse transcriptase inhibitors in real life: a multicentre prospective study

Groups

A

n = 50

B

n = 80

C

n = 81

D

n = 303

Age, years

39 (20 - 51)

41 (32 - 66)

41 (25 - 75)

41 (23 - 75)

Male

42 (84%)

62 (77.5%)

50 (61.7%)

223 (73.6%)

Weight, kg

68 (50 - 102)

64 (42 - 98.5)

65.5 (36 - 111)

65.9 (39 - 121)

Risk factor for HIV

    

   IV drug use

23 (46%)

64 (80%)

53 (65.4%)

185 (61.1%)

   Hetero/homosexual

27 (64%)

15 (20%)

26 (32.1%)

110 (36.3%)

   Blood products transfusion

  

1 (1.2%)

3 (1%)

   Unknown

  

1 (1.2%)

5 (1.7%)

Methadone treatment

11 (22%)

36 (45%)

20 (24.7%)

56 (18.5%)

Active illegal drug use

4 (8%)

14 (17.5%)

8 (9.9%)

17 (5.6%)

CD4/μl

140 (4 - 563)

227 (4 - 546)

277 (14 - 923)

475 (27 - 1196)

HIV-RNA log10 cop./ml

5.16 (2.0-6.36)

4.61 (2.05-6.54)

3.52 (2.04-4.64)

< 1.69 (< 1.69-2.45)

Clinical category C

10 (20%)

26 (32.6%)

28 (34.6%)

98 (32.4%)

Nadir CD4/μl

152 (4 - 417)

120 (1 - 476)

120 (1 - 815)

130 (1 - 825)

Previous ART (months)

-

46 (1 - 164)

38 (1 -192)

71 (1 - 269)

Associated NRTIs

    

   TDF + FTC

34 (68%)

46 (57.5%)

28 (34.6%)

110 (36.3%)

   ABV + 3TC

8 (16%)

15 (18.8%)

14 (17.3%)

78 (25.7%)

   ddI + 3TC

5 (10%)

3 (3.8%)

5 (6.2%)

37 (12.2%)

   Others

3 (6%)

16 (20.8%)

34 (41.9%)

78 (25.7%)

Chronic viral hepatitis

22 (44%)

63 (78.8%)

48 (59.3%)

190 (62.7%)

   HCV

21 (42%)

55 (68.8%)

45 (55.5%)

185 (61.0%)

   HBV

1 (2%)

2 (2.5%)

2 (2.5%)

2 (0.7%)

   HCV + HVB

-

2 (2.5%)

1 (1.2%)

3 (1.0%)

Cirrhosis

4 (8%)

4 (5%)

6 (7.4%)

26 (8.6%)

  1. ART: antiretroviral treatment. PIs: protease inhibitors. NNRTIs: non-nucleos(t)ide reverse transcriptase inhibitors. M: median. Group A: naive patients. Group B: patients who restarted antiretroviral therapy after dropping out. Group C: patients with virological failure to a PI- or NNRTI-based regimen. Group D: patients who simplified a PI-based regimen to an once daily regimen or had toxicity to a previous regimen based on PIs or NNRTIs. Variables expressed as no. (%) or median (range).