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. Author manuscript; available in PMC: 2010 Jun 24.
Published in final edited form as: Aliment Pharmacol Ther. 2008 Aug 1;28(3):289–293. doi: 10.1111/j.1365-2036.2008.03718.x

Table 2. Subject treatment characteristics by co-infection status.

Total (n=180) HCV mono (n=136) HCV/HIV coinfected (n=41) Significance OR (95%)

First HCV treatment n (%) 129 (72) 97 (71) 32 (78) p = 0.47 1.4 (0.6-3.1)

Interferon alfa-2a n (%) 144 (80) 104 (76) 40 (98) P = 0.00 11.2(1.5-84.6)

HCV Genotype n (%)
Type 1 127 (71) 96 (71) 31 (76)
Type 2 26 (14) 18 (13) 8 (20)
Type 3 16 (9) 14 (10) 2 (5)
Type 4 4 (2) 4 (3) 0 (0) p = 0.38

Self-injects IFN n (%) 155 (86) 121 (89) 34 (83) p = 0.50 0.7 (0.3-1.9)

Ribavirin dose n (%)
800mg or < 45 (25) 34 (25) 11 (27)
1000mg 44 (24) 36 (26) 8 (20)
1200mg or > 65 (36) 47 (35) 18 (44) p = 0.52

Time on treatment in weeks mean (sd) 19.3 (13.4) 19.2 (12.8) 19.6 (15.5) p = 0.88

In clinical trial n (%) 27 (15) 22 (16) 5 (12) p = 0.57 0.7 (0.3-2.1)

On anti-depressant n (%) 60 (33) 35 (26) 25 (61) p = 0.00 4.5 (2.1-9.5)

Meds for anemia n (%) 67 (37) 46 (34) 21 (51) p = 0.53 2.0 (1.0-4.1)

Mood mean (sd) 6.4 (2.2) 6.5 (2.1) 6.3 (2.6) p = 0.74

Energy mean (sd) 5.4 (2.5) 5.4 (2.5) 5.5 (2.5) p = 0.76

Side Effects mean (sd) 4.6 (2.6) 4.8 (2.7) 4.2 (2.7) p = 0.26