@article{975f1f7ba1a147d891748821ab5e57a9,
title = "Establishing a hepatitis C continuum of care among HIV/hepatitis C virus-coinfected individuals in EuroSIDA",
abstract = "Objectives: The aim of the study was to establish a methodology for evaluating the hepatitis C continuum of care in HIV/hepatitis C virus (HCV)-coinfected individuals and to characterize the continuum in Europe on 1 January 2015, prior to widespread access to direct-acting antiviral (DAA) therapy. Methods: Stages included in the continuum were as follows: anti-HCV antibody positive, HCV RNA tested, currently HCV RNA positive, ever HCV RNA positive, ever received HCV treatment, completed HCV treatment, follow-up HCV RNA test, and cure. Sustained virological response (SVR) could only be assessed for those with a follow-up HCV RNA test and was defined as a negative HCV RNA result measured > 12 or 24 weeks after stopping treatment. Results: Numbers and percentages for the stages of the HCV continuum of care were as follows: anti-HCV positive (n = 5173), HCV RNA tested (4207 of 5173; 81.3%), currently HCV RNA positive (3179 of 5173; 61.5%), ever HCV RNA positive (n = 3876), initiated HCV treatment (1693 of 3876; 43.7%), completed HCV treatment (1598 of 3876; 41.2%), follow-up HCV RNA test to allow SVR assessment (1195 of 3876; 30.8%), and cure (629 of 3876; 16.2%). The proportion that achieved SVR was 52.6% (629 of 1195). There were significant differences between regions at each stage of the continuum (P < 0.0001). Conclusions: In the proposed HCV continuum of care for HIV/HCV-coinfected individuals, we found major gaps at all stages, with almost 20% of anti-HCV-positive individuals having no documented HCV RNA test and a low proportion achieving SVR, in the pre-DAA era.",
keywords = "continuum of care, Europe, HIV/HCV coinfection, sustained virological response, treatment",
author = "{the EuroSIDA study group} and S. Amele and L. Peters and M. Sluzhynska and A. Yakovlev and A. Scherrer and P. Domingo and J. Gerstoft and Viard, {J. P.} and M. Gisinger and R. Flisiak and S. Bhaghani and M. Ristola and C. Leen and E. Jablonowska and G. Wandeler and H. Stellbrink and K. Falconer and {D'Arminio Monforte}, A. and A. Horban and Rockstroh, {J. K.} and Lundgren, {J. D.} and A. Mocroft and M. Losso and M. Kundro and B. Schmied and R. Zangerle and I. Karpov and A. Vassilenko and Mitsura, {V. M.} and D. Paduto and N. Clumeck and {De Wit}, S. and M. Delforge and E. Florence and L. Vandekerckhove and V. Hadziosmanovic and J. Begovac and L. Machala and D. Jilich and D. Sedlacek and G. Kronborg and T. Benfield and T. Katzenstein and C. Pedersen and Johansen, {I. S.} and L. Ostergaard and L. Wiese and Moller, {N. F.} and Nielsen, {L. N.} and B. Rozentale",
note = "Funding Information: Financial disclosure: EuroSIDA was supported by the European Union{\textquoteright}s Seventh Framework Programme for research, technological development and demonstration under EuroCoord grant agreement n˚ 260694. Current support includes unrestricted grants from ViiV Healthcare LLC, GlaxoSmithKline R&D Limited, Janssen Scientific Affairs, Janssen R&D, Bristol-Myers Squibb Company, Merck Sharp & Dohme Corp, and Gilead Sciences. The participation of centres from Switzerland was supported by The Swiss National Science Foundation (grant 148522). The study is also supported by a grant (grant number DNRF126) from the Danish National Research Foundation and by the International Cohort Consortium of Infectious Disease (RESPOND). Funding Information: SA, LP, JKR, JDL and AM conceived the project, designed the analysis, interpreted the findings, and conceptualized the main messages. SA executed the analysis and wrote and revised the first and subsequent drafts of the manuscript. LP and AM reviewed and commented on the first and subsequent drafts of the manuscript. MS, AY, AS, PD, JG, JV, MG, RF, SB, MR, CL, EJ, GW, HS, KF, ADM and AH reviewed and commented on the final draft of the manuscript and were involved in the interpretation of findings. Financial disclosure: EuroSIDA was supported by the European Union's Seventh Framework Programme for research, technological development and demonstration under EuroCoord grant agreement n? 260694. Current support includes unrestricted grants from ViiV Healthcare LLC, GlaxoSmithKline R&D Limited, Janssen Scientific Affairs, Janssen R&D, Bristol-Myers Squibb Company, Merck Sharp & Dohme Corp, and Gilead Sciences. The participation of centres from Switzerland was supported by The Swiss National Science Foundation (grant 148522). The study is also supported by a grant (grant number DNRF126) from the Danish National Research Foundation and by the International Cohort Consortium of Infectious Disease (RESPOND). Publisher Copyright: {\textcopyright} 2019 British HIV Association",
year = "2019",
month = apr,
doi = "10.1111/hiv.12711",
language = "English",
volume = "20",
pages = "264--273",
journal = "HIV Medicine",
issn = "1464-2662",
publisher = "Wiley-Blackwell Publishing Ltd",
number = "4",
}