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Table 1 Pretherapy Characteristics

From: Effectiveness and Safety of Generic Fixed-Dose Combination of Tenofovir/Emtricitabine/Efavirenz in HIV-1-Infected Patients in Western India

Patient Characteristics

ARV-Naive (n = 49)

ARV-Experienced (n = 92)

Age, median (range), y

40 (28–68)

39 (18–74)

Sex

Male (%)

37 (75.5)

71 (77.1)

Female (%)

11 (24.5)

20 (22.9)

WHO stage before initiating current or past ART

Stage I

15 (30.6)

36 (39.1)

Stage II

5 (10.2)

10 (10.9)

Stage III

5 (10.2)

9 (9.9)

Stage IV

24 (49)

37 (40.1)

Duration of HIV infection since diagnosis months, median (range), y

18.5 (3–161)

38 (2–185)

Pretherapy body mass index, median (range)

21.365 (14.36–33.2)

23.04 (12.3–35.16)

Current pretherapy CD4 count, median (range)

104.5 (6–330)

309 (10–1259)

Reasons for substituting

Patients decision (mutually inclusive)

 

47

Stavudine (d4T)-related toxicity

 

5

Zidovudine (ZDV)-related toxicity

 

20

Dual toxicity (d4T and ZDV)

 

29

Convenience

 

34

Other (mostly co-infection with hepatitis B virus)

 

7

Co-infection with HBV

HBsAg-positive

3 (6.1)

4 (4.3)

HBsAg-negative

29 (59.2)

19 (20.7)

Unknown

17 (34.7)

69 (75)

Pretherapy renal function

Serum creatinine (mg/dL), median (range)

1 (0.5–1.9)

1 (0.4–1.8)

Creatinine clearance (mg/min), median (range)

71.9 (38.1–145.5)

87.4 (32.5–151.6)

  1. ARV = antiretroviral agent; HBsAg = hepatitis B virus surface antigen; WHO = World Health Organization