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Managing hepatitis C Bacon BRAm J Manag Care 2004[Mar]; 10 (2 Suppl): S30-40Availability of a drug regimen that eradicates the hepatitis C virus (HCV) in more than half of treated patients provides the medical community with a powerful new weapon to diminish the anticipated future wave of HCV-related liver disease and cancer. Clinicians must understand the benefits, risks, and costs associated with the combination of peginterferon alfa and ribavirin. Major clinical trials with this new standard of HCV therapy have demonstrated sustained virologic responses of 54% and 56% with 48 weeks of combination therapy. Response is highest in those with genotype 2/3, with early virologic response by week 12, in patients with high adherence, and in patients receiving weight-appropriate ribavirin dosages. The most common side effects are manageable and include fatigue, headache, myalgia, rigors, fever, nausea, insomnia, and depression. Neutropenia associated with interferon and anemia associated with ribavirin are more serious side effects that can cause discontinuation or dose reduction. Clinicians can maximize results and reduce costs with a regimen of peginterferon alfa plus ribavirin by choosing patients carefully, educating patients thoroughly, stopping therapy early in those patients who do not respond by week 12 of therapy, and enhancing adherence by managing side effects with appropriate dose reductions and/or selective use of antidepressants or hematopoietic colony stimulators.|*Interferon-alpha/administration & dosage/*therapeutic use[MESH]|*Polyethylene Glycols[MESH]|Antiviral Agents/administration & dosage/*therapeutic use[MESH]|Drug Therapy, Combination[MESH]|Hepatitis C/*drug therapy/economics[MESH]|Humans[MESH]|Interferon alpha-2[MESH]|Liver Diseases/prevention & control[MESH]|Liver Neoplasms/prevention & control[MESH]|Practice Patterns, Physicians'[MESH]|Randomized Controlled Trials as Topic[MESH]|Recombinant Proteins[MESH]|Ribavirin/administration & dosage/*therapeutic use[MESH]|United States[MESH] |
