ANNUAL REPORTS

Annual reports will be generated once the registry has matured. Please return to this section at a later date.

PEER-REVIEWED PUBLICATIONS

Ioannou L JSerpell JDean J, Bendinelli C, Gough J, Lisewski D, Miller J A, Meyer-Rochow W, Sidhu S, Topliss D, Walters D, Zalcberg J, Ahern S. Development of a binational thyroid cancer clinical quality registry: a protocol paper 

PRESENTATIONS

2019

2018

Ioannou, L., Serpell, J., Bendinelli, C., Walters, D., Gough, J., Lisewski, D., Meyer-Rochow, W., Miller, J., Topliss, D., Fleming, B., Farrell, S., Kiu, A., Kollias, J., Sywak, M., Aniss, A., Fenton, L., Ghusn, D., Harper, S., Popadich, A., Stringer, K., Watters, D., Ahern, S. Development of a Core Set of Clinical Indicators to Measure Quality of Care for Thyroid Cancer: A Modified-Delphi Approach. 88th Annual Meeting of the American Thyroid Association (ATA), Washington D.C., United States (3-7 October 2018) (Oral Presentation).

Ioannou, L., Serpell, J., Dean, J., Bendinelli, C., Gough, J., Lisewski, D., Miller, J., Meyer-Rochow, W., Sidhu, S., Topliss, D., Walters, D., Zalcberg, J., Ahern, S. Development of a Bi-National Thyroid Cancer Clinical Quality Registry. Alfred Health Research Week, Melbourne, Australia (June 2018) (Poster Presentation).

Ioannou, L., Serpell, J., Dean, J., Bendinelli, C., Gough, J., Lisewski, D., Miller, J., Meyer-Rochow, W., Sidhu, S., Topliss, D., Walters, D., Zalcberg, J., Ahern, S. Development of a Bi-National Thyroid Cancer Clinical Quality Registry. Victorian Comprehensive Cancer Centre (VCCC) Postdoctoral Symposium, Melbourne, Australia (1 June 2018) (Poster Presentation).

Ioannou, L., Serpell, J., Dean, J., Bendinelli, C., Gough, J., Lisewski, D., Miller, J., Meyer-Rochow, W., Sidhu, S., Topliss, D., Walters, D., Zalcberg, J., Ahern, S. Development of a Bi-National Thyroid Cancer Clinical Quality Registry. Royal Australian College of Surgeons (RACS) Annual Scientific Congress (ASC), Sydney, Australia (7-11 May 2018) (Oral Presentation).

Research Proposals

The ANZTCR can be used as a platform for hypothesis-driven research projects,  clinical planning and quality improvement. Access to ANZTCR data is restricted to ensure that participant privacy is protected.

Researchers or institutions who would like to request aggregate ANZTCR data will be required to complete the following steps:

  1. Contact the ANZTCR Coordinator to discuss your research proposal, the application process and request the data access form.
  2. Submit a completed data access form, with a HREC Approval Certificate and other relevant documentation for review of the ANZTCR Steering Committee

Please note:

  • Clinicians contributing data to the registry, can access and/or request their own data from the ANZTCR Coordinator at no charge
  • Researchers submitting data for external research purposes may be charged a fee.
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