Table 5.
Multivariate Analysis of Factors Associated with SVR12
| Group I vs group II | Group I vs group III | |||
|---|---|---|---|---|
| OR (95% CI) | p-value | OR (95% CI) | p-value | |
| CPT (A vs B) | 6.8 (1.5–30) | 0.01 | - | - |
| HTA (no vs yes) | 3.86 (0.5–27) | 0.1 | 2.0 (0.33–12) | 0.4 |
| RBV (no vs yes) | 0.2 (0.55–27) | 0.1 | 0.18 (0.03–0.98) | 0.02 |
| Diabetes (no vs yes) | - | - | 2.6 (0.41–16) | 0.3 |
| Naïve (yes vs no) | - | - | 5.3 (1.2–23) | 0.02 |
Group I, daclatasvir (DCV) + sofosbuvir (SOF) without ribavirin (RBV); group II, DCV/SOF with RBV flat dose of 800 mg/dL; group III, DCV/SOF with RBV weight-based dose.
SVR, sustained viral response; SVR12, SVR at 12 weeks; OR, odds ratio; CI, confidence interval; CPT, Child-Pugh-Turcotte; HTA, hypertension.