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dc.contributor.authorJobson, Dale
dc.contributor.authorRoffey, Benjamin
dc.contributor.authorBest, Renee
dc.contributor.authorButton-Sloan, Alison
dc.contributor.authorCossio, Danica
dc.contributor.authorEvans, Sue
dc.contributor.authorShang, Catherine
dc.contributor.authorMoore, Julie
dc.contributor.authorArnold, Christopher
dc.contributor.authorMann, Graham
dc.contributor.authorShackleton, Mark
dc.contributor.authorSoyer, H Peter
dc.contributor.authorMorton, Rachael L
dc.contributor.authorZalcberg, John
dc.contributor.authorMar, Victoria
dc.date.accessioned2023-03-21T02:20:50Z
dc.date.available2023-03-21T02:20:50Z
dc.date.issued2022en
dc.identifier.urihttps://hdl.handle.net/2123/30259
dc.description.abstractIntroduction Australia has the highest incidence of melanoma in the world with variable care provided by a diverse range of clinicians. Clinical quality registries aim to identify these variations in care and provide anonymised, benchmarked feedback to clinicians and institutions to improve patient outcomes. The Australian Melanoma Clinical Outcomes Registry (MelCOR) aims to collect population-wide, clinical-level data for the early management of cutaneous melanoma and provide anonymised feedback to healthcare providers. Methods and analysis A modified Delphi process will be undertaken to identify key clinical quality indicators for inclusion in the MelCOR pilot. MelCOR will prospectively collect data relevant to these quality indicators, initially for all people over the age of 18 years living in Victoria and Queensland with a melanoma diagnosis confirmed by histopathology, via a two-stage recruitment and consent process. In stage 1, existing State-based cancer registries contact the treating clinician and provide an opportunity for them to opt themselves or their patients out of direct contact with MelCOR. After stage 1, re-identifiable clinical data are provided to the MelCOR under a waiver of consent. In stage 2, the State-based cancer registry will approach the patient directly and invite them to opt in to MelCOR and share identifiable data. If a patient elects to opt in, MelCOR will be able to contact patients directly to collect patient-reported outcome measures. Aggregated data will be used to provide benchmarked, comparative feedback to participating institutions/clinicians. Ethics and dissemination Following the successful collection of pilot data, the feasibility of an Australia-wide roll out will be evaluated. Key quality indicator data will be the core of the MelCOR dataset, with additional data points added later. Annual reports will be issued, first to the relevant stakeholders followed by the public. MelCOR is approved by the Alfred Ethics Committee (58280/127/20).en
dc.language.isoenen
dc.publisherBMJ Openen
dc.rightsCreative Commons Attribution-NonCommercial 4.0en
dc.subjectAustralian Melanomaen
dc.subjectclinical outcomesen
dc.subjectprotocolen
dc.titleDeveloping an Australian Melanoma Clinical Outcomes Registry (MelCOR): a protocol paperen
dc.typeArticleen
dc.identifier.doi10.1136/bmjopen-2022-062139
dc.type.pubtypePublisher's versionen
usyd.facultyFaculty of Medicine and Healthen
usyd.departmentNHMRC Clinical Trials Centreen
workflow.metadata.onlyNoen


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