2015
DOI: 10.1016/j.jhep.2015.06.006
|View full text |Cite
|
Sign up to set email alerts
|

The long-term benefits of nucleos(t)ide analogs in compensated HBV cirrhotic patients with no or small esophageal varices: A 12-year prospective cohort study

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

3
52
1
2

Year Published

2016
2016
2022
2022

Publication Types

Select...
6
4

Relationship

1
9

Authors

Journals

citations
Cited by 75 publications
(58 citation statements)
references
References 52 publications
(86 reference statements)
3
52
1
2
Order By: Relevance
“…All chronic hepatitis and cirrhosis patients in the present study were considered for anti-HBV treatment and, in accordance with the current national guidelines [13, 37, 38], some were left untreated and some were treated with either peginterferon α-2a or nucleos(t)ide analogues, with results similar to those observed for the local Italian population [3942]. …”
Section: Discussionmentioning
confidence: 96%
“…All chronic hepatitis and cirrhosis patients in the present study were considered for anti-HBV treatment and, in accordance with the current national guidelines [13, 37, 38], some were left untreated and some were treated with either peginterferon α-2a or nucleos(t)ide analogues, with results similar to those observed for the local Italian population [3942]. …”
Section: Discussionmentioning
confidence: 96%
“…The additional impact of long-term HBV viral control through the dual activity of nucleos(t)ide analogs would be expected to reduce complications related to chronic HBV infection. HBV suppression has been shown to reduce liver-related outcomes in HBV monoinfection [32,33] and to reduce hepatic decompensation in triply infected patients [34]. However, there are little long-term data on the impact of HBV DNA suppression on liver disease progression in HIV coinfection.…”
Section: Discussionmentioning
confidence: 99%
“…It therefore represents the cornerstone endpoint of all our current therapeutic attempts. 1,25,[34][35][36][37][38][39][40] The level of HBV DNA suppression that should be attained in order to achieve these benefits is not well defined, but inferred that the lower, the better. Treatment-induced HBeAg loss and seroconversion to antiHBe characterises the induction of a partial immune control often leading to a low replicative phase of the chronic HBV infection.…”
Section: Recommendationsmentioning
confidence: 99%