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A data abstraction form was designed for this study to collect the following data: study design, study type, practice setting, collaboration (single vs multicentre) and patient demographics including age, gender, ethnicity, viral load, degree of fibrosis/cirrhosis and (sub) genotype. We also obtained data on treatment outcomes including end of treatment response, SVR at 4 weeks after end of treatment and SVR12, as well as safety and tolerability data on side effects, dose reductions, interruptions and/or withdrawals from treatment.
Copyright and License information: ©2016 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/
This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
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