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During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
Patients on maintenance hemodialysis (MHD) have higher prevalence and worse outcomes from chronic viral hepatitis (HBV/HCV). New direct-acting antivirals (DAAs) achieve high cure (SVR) rates for HCV including in CKD/ESRD, and oral nucleos(t)ide analogues (entecavir, tenofovir variants) form the backbone of HBV therapy; dosing and safety considerations differ in dialysis populations and must be followed. Recent guideline updates support use of many SOF-containing regimens and pangenotypic DAAs in ESRD, and recommend long-term entecavir or tenofovir for HBV with renal dose considerations.
In this 24-month prospective cohort, 60 adult CLD patients on MHD (HCV = 34, HBV = 18, coinfected = 8) were followed in a public-sector dialysis program. Direct-acting antivirals (glecaprevir/pibrentasvir or sofosbuvir/velpatasvir) were used for HCV; entecavir or tenofovir alafenamide/disoproxil for HBV with renal dosing. Outcomes included mortality, sustained virologic response (SVR12), HBV DNA suppression, seroconversion, and nosocomial sero-transmission. Predictors of mortality were assessed by Cox regression
DAA therapy achieved SVR12 in 93.3% of treated HCV patients (28/30). HBV DNA suppression occurred in 66.7% (10/15) and HBsAg loss in 5.6%. Overall 24-month mortality was 20%. Independent mortality predictors were serum albumin < 3.5 g/dL (aHR 2.50, p = 0.045) and cirrhosis (aHR 2.75, p = 0.048). Antiviral therapy showed a protective trend (aHR 0.55). Annual HBV vaccination (89.5% seroprotection) and strict segregation reduced incident infections to zero in segregated units.
Low albumin and cirrhosis predicted mortality in HBV/HCV-positive CLD patients on MHD. Vaccination, segregation, and timely antiviral therapy were safe, feasible, and associated with improved virologic and survival outcomes in resource-limited dialysis settings.