Published online Sep 8, 2015. doi: 10.4254/wjh.v7.i19.2209
Peer-review started: July 5, 2015
First decision: July 31, 2015
Revised: August 7, 2015
Accepted: August 30, 2015
Article in press: August 31, 2015
Published online: September 8, 2015
Processing time: 71 Days and 13 Hours
Core tip: The recently Food and Drug Administration approved direct-acting antiviral regimens for hepatitis C virus (HCV), ledipasvir/sofosbuvir regimen and the ombitasvir/paritaprevir/ritonavir and dasabuvir regimen, have demonstrated great efficacy, and thus far seem to have short treatment timelines and relatively benign side effect profiles. Depression has not emerged as a side effect of these treatments. With efficacious regimens that include no interferon-alpha and no ribavirin, there may no longer be a need for strong psychosocial assessment and monitoring built into the routine of HCV treatment. Good history-taking, strong pharmaceutical review, and reliable consultative relationships should be adequate for meeting psychosocial needs in HCV treatment.
