Table 2.
Data extraction
| Study design | |
| • Study name, author and year of publication • Study design • Study period • Inclusion/exclusion criteria • Country • Settings • HCV treatment regimen • Definition of cirrhosis detection • HCV RNA quantification limit • Population analysed • Attrition and selection bias |
|
| Trial characteristics | |
| • Type of publication • Type of study • Treatment regimen • Treatment duration • Ribavirin |
|
| Patient characteristics | |
| • Proportion of men • Ethnicity (Caucasian/Asian) • Body-mass index • GT3 sample size at baseline • Treatment-naïve patients • CKD stages • Dialysis • Renal transplantation • Concomitant treatment with proton pump inhibitor (PPI) |
|
| Disease characteristics | |
| • HCV RNA • Baseline resistance-associated variants/substitutions (RAV) • Human immunodeficiency virus (HIV) co-infection • Liver transplantation • Cirrhosis (compensated/decompensated) • MELD score • Child-Pugh score • Liver disease severity (F0/F1/F2/F3/F4) |
|
| Treatment outcomes | |
| • Rates of SVR (SVR4, SVR12, SVR24 and/or unspecified SVR) • 95% confidence interval (calculated from SVR data, where reported) • Rates of relapse after treatment • Type of relapse • Treatment discontinuation • Serious adverse events (SAEs) |
CKD chronic kidney disease, GT3 genotype 3, HCV hepatitis C virus, MELD model for end-stage liver disease, SVR sustained virological response