PMID- 21924673 OWN - NLM STAT- MEDLINE DCOM- 20120301 LR - 20131121 IS - 1873-5967 (Electronic) IS - 1386-6532 (Linking) VI - 52 IP - 4 DP - 2011 Dec TI - Successful treatment of acute hepatitis C virus in HIV positive patients using the European AIDS Treatment Network guidelines for treatment duration. PG - 367-9 LID - 10.1016/j.jcv.2011.08.020 [doi] AB - BACKGROUND: The incidence of acute hepatitis C virus (HCV) in HIV-positive patients is rising. Recent studies summarized by the European AIDS Treatment Network (NEAT)(1) show that pegylated interferon alpha (PEG-IFNalpha) and ribavirin can lead to a sustained virological response (SVR) in approximately 60-80% of patients. Controversy remains on when to start treatment and whether 24 or 48 weeks of treatment lead to better outcomes. OBJECTIVES: To assess the effectiveness of a treatment strategy for acute HCV infection in HIV-positive patients, in which patients with undetectable HCV RNA at 4 weeks (rapid virological response, RVR) receive 24 weeks, while those without receive 48 weeks of PEG-IFNalpha and ribavirin, as per the NEAT guidelines. STUDY DESIGN: A retrospective cohort study of HIV-positive patients diagnosed with acute HCV infection between December 2006 and May 2010. Those who received acute treatment with PEG-IFNalpha and ribavirin had HCV RNA levels monitored and outcomes evaluated. For patients who did not receive acute treatment, the reason for deferral and most recent available HCV RNA were recorded. RESULTS: Twenty-two patients received acute treatment with PEG-IFNalpha and ribavirin. Twelve patients achieved RVR and had 24 weeks treatment, 10 patients had no RVR and had 48 weeks treatment. Two patients discontinued treatment (due to adverse effects [AEs] and failure to suppress HCV RNA sufficiently at 12 weeks). All 20 patients who completed treatment had SVR. CONCLUSION: Our high SVR rate of 91% supports the new NEAT treatment duration recommendations. CI - Copyright (c) 2011 Elsevier B.V. All rights reserved. FAU - Dorward, Jienchi AU - Dorward J AD - The Grahame Hayton Unit, Barts and the London NHS Trust, Royal London Hospital, Whitechapel, London E1 1BB, United Kingdom. FAU - Garrett, Nigel AU - Garrett N FAU - Scott, Duncan AU - Scott D FAU - Buckland, Matthew AU - Buckland M FAU - Orkin, Chloe AU - Orkin C FAU - Baily, Guy AU - Baily G LA - eng PT - Journal Article DEP - 20110915 PL - Netherlands TA - J Clin Virol JT - Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology JID - 9815671 RN - 0 (Antiviral Agents) RN - 0 (Interferon-alpha) RN - 0 (RNA, Viral) RN - 49717AWG6K (Ribavirin) SB - IM MH - Adult MH - Antiviral Agents/*administration & dosage MH - Cohort Studies MH - Female MH - HIV Infections/*complications MH - Hepatitis C/*drug therapy MH - Humans MH - Interferon-alpha/*administration & dosage MH - Male MH - Middle Aged MH - Practice Guidelines as Topic MH - RNA, Viral/blood MH - Retrospective Studies MH - Ribavirin/*administration & dosage MH - Time Factors MH - Treatment Outcome EDAT- 2011/09/20 06:00 MHDA- 2012/03/02 06:00 CRDT- 2011/09/20 06:00 PHST- 2011/06/30 00:00 [received] PHST- 2011/08/21 00:00 [revised] PHST- 2011/08/22 00:00 [accepted] PHST- 2011/09/20 06:00 [entrez] PHST- 2011/09/20 06:00 [pubmed] PHST- 2012/03/02 06:00 [medline] AID - S1386-6532(11)00357-X [pii] AID - 10.1016/j.jcv.2011.08.020 [doi] PST - ppublish SO - J Clin Virol. 2011 Dec;52(4):367-9. doi: 10.1016/j.jcv.2011.08.020. Epub 2011 Sep 15.