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Acute hepatitis C in patients receiving hemodialysis
I Griveas1, G Germanidis, G Visvardis
1Nephrology Department, Papageorgiou General Hospital, Thessaloniki, Greece. giannisgriv@hotmail.com
Insights
Hepatitis C virus (HCV) infection is common in dialysis patients. Acute HCV infection was studied in 17 patients, with two subtypes identified, and treatment outcomes varied.
Area of Science:
- Nephrology
- Virology
- Epidemiology
Background:
- Hepatitis C virus (HCV) infection is prevalent in end-stage renal disease (ESRD) patients on chronic dialysis.
- Prevalence is linked to dialysis duration and blood transfusions, but has decreased due to blood screening.
Purpose of the Study:
- To investigate acute HCV infection in a dialysis unit.
- To determine HCV subtypes and treatment efficacy over a one-year follow-up.
Main Methods:
- Diagnosis using anti-HCV and HCV-RNA detection.
- HCV genotyping and phylogenetic analysis (NS 5B gene).
- One-year follow-up of 17 patients with acute hepatitis C, including treatment with pegylated interferon (Peg-IFNa2a).
Main Results:
- Two HCV subtypes (1b) were identified as responsible for the acute infection.
- Four out of six treated patients responded well to pegylated interferon therapy.
- One patient with very high viral load developed cirrhosis despite treatment.
Conclusions:
- Further research is needed on HCV incidence, prevalence, and risk factors in dialysis patients.
- Development of diagnostic and management algorithms for hepatitis C in ESRD is recommended.
- Routine screening can improve understanding of HCV natural history in this population.
Abstract:
Hepatitis C virus (HCV) infection is frequent in patients with end-stage renal disease treated by chronic dialysis, with a prevalence varying from 10-65% according to the geographical data. The prevalence is significantly associated with the duration of dialysis and the number of transfused blood products[1,2] and has dramatically declined with efficient blood screening.[3] We studied patients with acute HCV infection in a dialysis unit. The diagnosis was based on both anti-HCV detection and HCV-RNA detection. Other virological tools including HCV genotype determination was also used to tailor treatment to the individual patient and determine its efficacy for a one-year follow-up period. Seventeen patients (7 male and 10 female, mean age: 63.7 +/- 11.6 SD) with acute hepatitis C were enrolled to our study. All of them were followed up for a period of one year after the diagnosis was established. Phylogenetic analysis distinguished two separate HCV subtypes 1b, which were both responsible for this acute infection (see Figure 1). These types did not differ in their behavior on the clinical situation of our patients, as confirmed by the fact that in both groups of patients, there was only one patient who presented with acute illness. Six patients of our study group, three months after the acute infection, received pegylated interferon (Peg-IFNa2a) 135 mug for a six-month period. Four of them responded very well to therapy and at the first determination HCV RNA was below the cutoff point. One of our patients with very high HCV levels (HCV RNA > 50,000,000 IU/mL), despite receiving the same therapy, did not respond well and developed cirrhosis. In conclusion, it is clear from our experience that better information is needed about the current incidence, prevalence, and risk factors for HCV infection in dialysis patients. Algorithms for the diagnosis and management of hepatitis C should be developed by academic societies. Routine screening for hepatitis C also would allow for better definition of the natural history of hepatitis C in patients with end stage renal disease. [image omitted]Figure 1. NS 5B gene phylogenetic tree analysis of the acute hepatitis C epidemic.
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