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[Screening and management of HCV-positive CKD outpatients]
Giuseppe Gernone1, Francesco Detomaso1, Francesca Partipilo1
1UOSVD di Nefrologia e Dialisi ASL Bari. P.O. "S. Maria degli Angeli" Putignano e "S. Giacomo" Monopoli. Sede Direzionale Putignano.
Insights
Screening nephropathic patients for Hepatitis C Virus (HCV) identified a 3.85% prevalence. Treatment with direct-acting antivirals (DAAs) achieved 100% Sustained Virological Response (SVR 12) and improved kidney function.
Area of Science:
- Nephrology
- Hepatology
- Infectious Diseases
Background:
- Hepatitis C Virus (HCV) infection is a risk factor for Chronic Kidney Disease (CKD) and End-Stage Renal Disease (ESRD).
- HCV is often underdiagnosed and worsens outcomes across all stages of CKD.
- Guidelines recommend screening for renal disease in HCV patients and HCV in CKD patients.
Purpose of the Study:
- To implement systematic screening and management of HCV in nephropathic outpatients.
- To improve Sustained Virological Response 12 weeks after treatment (SVR 12) and renal function (GFR, proteinuria).
Main Methods:
- A prospective observational study of 18 months duration.
- Included 2798 adult outpatients not on dialysis.
- Identified HCV-positive patients and initiated treatment with direct-acting antivirals (DAAs).
Main Results:
- Identified 108 HCV-positive patients (3.85% prevalence).
- 51 patients initiated DAA therapy, with 34 completing treatment, achieving 100% SVR 12.
- Significant improvements observed in estimated Glomerular Filtration Rate (eGFR) and proteinuria post-treatment.
Conclusions:
- Direct-acting antiviral (DAA) therapy for HCV is safe and effective in nephropathic patients.
- Treatment is associated with improved renal function, including GFR and proteinuria.
- Systematic screening of CKD patients for HCV supports the WHO goal of HCV elimination by 2030.
Abstract:
Background: Hepatitis C Virus (HCV) disease, which is commonly underdiagnosed, in addition to the well-known effects on the liver is also a risk factor for Cronic Kidney Disease (CKD) and End Stage Renal Disease (ESRD). It worsens the outcome at every stage of CKD; around 400.000 people worldwide die from HCV-related causes each year. The KDIGO 2018 Guidelines recommend that all patients be evaluated for renal disease when HCV is diagnosed and be screened for HCV when CKD is diagnosed, as the prevalence may be higher than in the general population. Effective screening is therefore necessary in order to establish early treatment. Aims of the study: We ran a systematic program of screening and management of HCV in nephropathic outpatients in order to improve Sustained Virological Response 12 weeks after the end of treatment (SVR 12) and renal functions such as GFR and proteinuria. Materials and methods: We considered outpatients not in dialysis and older than 18. The systematic, prospective observational study of HCV infection run over a period of 18 months. Results: Of 2798 nephropathic outpatients that came to our attention during this period, we identified 108 HCV-positive patients (prevalence: 3.85%). The test for HCV-RNA resulted positive in 78 patients and, after hepatological evaluation and informed consent to treatment, 51 of them underwent therapy with the new direct-acting antivirals (DAAs). 34 patients concluded the treatment during the 18-month period, all of them with 100% SVR 12. The average pre-treatment GFR was 40.5 ml/m'; after treatment resulted equal to 45 ml/m' (p=0.01). The average value of pre-treatment proteinuria was 1.18 g/24 h; it was reduced to 0.79 g/24 (p=0.015). The remaining 17 patients were still under treatment/evaluation at the end of the 18 months. Conclusions: Treatment with the new DAAs has been confirmed safe and effective and is associated with an improvement of renal functions. Systematic screening of nephropathic patients may therefore contribute to achieving the WHO target of eliminating HCV by 2030.
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