REACH-C REACH-C online formPlease fill out patient and doctor details below to have data reviewed by a specialist. Patient data is de-identified and collected for the REACH-C Study. We will contact you via email to provide the approval to treat. We will also contact via email when your patient has reached SVR12 (HCV RNA testing 12-weeks post-treatment) to confirm that they are cured. * Indicates required field Date of request* DD slash MM slash YYYY Patient Initials* Prescriber informationPrescriber name* Prescriber phone number (mobile)* Prescriber phone number (surgery) Prescriber email address* Please use personal work email if available (not general reception email).Prescriber type* General practitioner Nurse practitioner Prescriber postcode* Patient demographicsDate of birth* DD slash MM slash YYYY Gender* Male Female Transgender Aboriginal and/or Torres Strait Islander* Yes No Unknown Clinical informationCurrent opioid substitution therapy:* Yes No Unknown Injecting drug use (any in last 6 months)* Yes No Unknown Cirrhosis:* Yes No Unknown FibroScan score (if available) AST (U/L)Please enter a number greater than or equal to 0.Upper limit of normal (AST)Please enter a number from 0 to 99.ALT (U/L):Please enter a number greater than or equal to 0.Platelets (10^9/L)Please enter a number greater than or equal to 0.eGFR (mL/minBSAc):Please enter a number greater than or equal to 0.APRIHBsAg* Yes No Unknown HIV infection* Yes No Unknown HCV genotype 1a 1b 2 3 4 5 6 HCV RNA level < 6 million IU/mL > 6 million IU/mL Unknown HCV therapyPrevious HCV treatment* No Yes, interferon-containing Yes, interferon-free Planned HCV regimen* Sofosbuvir/velpatasvir (Epclusa®) Glecaprevir/pibrentasvir (Maviret®) Sofosbuvir/velpatasvir/voxilaprevir (Vosevi®) Planned duration* 8 weeks 12 weeks 16 weeks 24 weeks Date of authority prescription:* DD slash MM slash YYYY If unknown, proposed dateYou will be contacted by the REACH-C study team to collect the 12 week post-treatment outcome and adherence for this patient.Information required for specialist approvalThe following information is required for specialist approval but will not be collected for REACH-C studyPatient Body weight* if weight is <100kg, add a 0 in frontEtOH current (g/day)*Please enter a number from 0 to 99.List of current comorbiditiesList of other concurrent medicationDrug-drug interactions reviewed*Please check result from HEP Drug Interaction Checker at http://www.hep-druginteractions.org/ Yes No Assessed for adherence*E.g. note any change in medication, dose reduction required Yes No Notes:Additional commentsSPAM protectionHiddenSPECIALIST APPROVALHiddenSpecialist name: HiddenSpecialist sign-off: Hiddenon DD slash MM slash YYYY (dd/mm/yyyy)HiddenResult: Approved Patient requires specialist referral/assessment Needs further data PhoneThis field is for validation purposes and should be left unchanged.