We conducted a national retrospective survey on hospital practitioners to evaluate the magnitude of erythropoietin (EPO) or granulocyte colony-stimulating factor (G-CSF) prescriptions in patients treated for chronic hepatitis C. Four hundred seventy-one questionnaires were sent, and 274 practitioners (58.2%) responded. Forty-six percent of practitioners used EPO, and 31% used G-CSF. The total number of HCV-infected patients receiving antiviral therapy per year was estimated at 6,630 patients, of whom 8.8% and 4% received EPO and G-CSF, respectively. EPO- was the main EPO molecule prescribed at a median dose of 30,000 IU/wk (range: 2,000-80,000). The indications for prescribing EPO varied greatly, including "fragile patients" (34%), "low" Hb level (8-11 g/dL) (19%), "rapid decline" in Hb level (2-5 g/dL during the first month of therapy) (12%), and symptomatic anemic patients (7%). G-CSF was mainly prescribed for a "low" level of neutrophils ranging from 400 to 750 neutrophils/mm 3 . In multivariate analysis, independent predictors of EPO and G-CSF prescription were age of practitioner less than 45 years (EPO: OR ؍ H epatitis C virus infection is a major cause of morbidity and mortality, affecting 170 million people worldwide 1,2 and a total of 368,000 people in France in 2004, of whom 221,000 were RNA positive. 3 Persistent infection over many years is associated with an increased risk of complications including cirrhosis, hepatic decompensation, and hepatocellular carcinoma. The current and more effective treatment for HCV infection consists of a combination of pegylated interferon with ribavirin, providing a sustained virological response rate of 40% to 45% in patients with HCV genotype 1 and of 80% in patients with HCV genotypes 2 or 3 in randomized controlled trials. 4,5 However, the sustained viral response rate decreases dramatically when adherence to treatment is not optimal. 6 Patients may not comply with the treatment regularly because of the multiple side effects encountered, especially a dose-limiting hemolytic anemia with ribavirin that often results in early withdrawal. Neutropenia is another concern, but to a lesser extent. Adverse hematological events may require treatment disruption or result in a 10% to 20% reduction in virological response. 4,5,7 Because the primary goal of