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Table 1 Summary of data collection

From: A platform in the use of medicines to treat chronic hepatitis C (PLATINUM C): protocol for a prospective treatment registry of real-world outcomes for hepatitis C

Data type

Information recorded

Time point

Demographics

Age, gender, postcode, Indigenous status

Enrolment

Lifestyle

Self-reported injecting drug use, self-reported alcohol in-take, self-reported housing status, self-reported reuse of a needle/syringe, self-reported prescribed opioid substitution therapy, risk of treatment disruption (including imprisonment)

Enrolment

Clinical

Hepatitis C history, previous treatment, comorbidities, HCV genotype and RNA level, liver function tests, liver fibrosis assessment

Treatment prescription

Treatment

DAA therapy and duration prescribed, treatment setting, type of prescriber, concurrent medication, other concurrent HCV management interventions

Treatment prescription

Medication adherence

Self-reported adherence to therapy

Weekly during treatment course

Quality of life

Self-reported quality of life (QoL) score (EQ-5D-5L)

0, 3, 6, 12 and 24 months after treatment initiation

Outcomes

HCV RNA PCR, all re-collected laboratory and imaging results, self-reported injecting drug use,

3 months after treatment completion