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Development of a binational thyroid cancer clinical quality registry: a protocol paper
INTRODUCTION: The occurrence of thyroid cancer is increasing throughout the developed world and since the 1990s has become the fastest increasing malignancy. In 2014, a total of 2693 Australians and 302 New Zealanders were diagnosed with thyroid cancer, with this number projected to rise to 3650 in...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352782/ https://www.ncbi.nlm.nih.gov/pubmed/30782713 http://dx.doi.org/10.1136/bmjopen-2018-023723 |
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author | Ioannou, Liane J Serpell, Jonathan Dean, Joanne Bendinelli, Cino Gough, Jenny Lisewski, Dean Miller, Julie A Meyer-Rochow, Win Sidhu, Stan Topliss, Duncan Walters, David Zalcberg, John Ahern, Susannah |
author_facet | Ioannou, Liane J Serpell, Jonathan Dean, Joanne Bendinelli, Cino Gough, Jenny Lisewski, Dean Miller, Julie A Meyer-Rochow, Win Sidhu, Stan Topliss, Duncan Walters, David Zalcberg, John Ahern, Susannah |
author_sort | Ioannou, Liane J |
collection | PubMed |
description | INTRODUCTION: The occurrence of thyroid cancer is increasing throughout the developed world and since the 1990s has become the fastest increasing malignancy. In 2014, a total of 2693 Australians and 302 New Zealanders were diagnosed with thyroid cancer, with this number projected to rise to 3650 in 2018. The purpose of this protocol is to establish a binational population-based clinical quality registry with the aim of monitoring and improving the quality of care provided to patients diagnosed with thyroid cancer in Australia and New Zealand. METHODS AND ANALYSIS: The Australian and New Zealand Thyroid Cancer Registry (ANZTCR) aims to capture clinical data for all patients over the age of 16 years with thyroid cancer, confirmed by histopathology report, who have been diagnosed, assessed or treated at a contributing hospital. A multidisciplinary steering committee was formed which, with operational support from Monash University, established the ANZTCR in early 2017. The pilot phase of the registry is currently operating in Victoria, New South Wales, Queensland, Western Australia and South Australia, with over 20 sites expected to come on board across Australia in 2018. A modified Delphi process was undertaken to determine the clinical quality indicators to be reported by the registry, and a minimum data set was developed comprising information regarding thyroid cancer diagnosis, pathology, surgery and 90-day follow-up. FUTURE PLANS: The establishment of the ANZTCR provides the opportunity for Australia and New Zealand to further understand current practice in the treatment of thyroid cancer and identify variation in outcomes. The engagement of endocrine surgeons in supporting this initiative is crucial. While the pilot registry has a focus on early clinical outcomes, it is anticipated that future collection of longer term outcome data particularly for patients with poor prognostic disease will add significant further value to the registry. |
format | Online Article Text |
id | pubmed-6352782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-63527822019-03-10 Development of a binational thyroid cancer clinical quality registry: a protocol paper Ioannou, Liane J Serpell, Jonathan Dean, Joanne Bendinelli, Cino Gough, Jenny Lisewski, Dean Miller, Julie A Meyer-Rochow, Win Sidhu, Stan Topliss, Duncan Walters, David Zalcberg, John Ahern, Susannah BMJ Open Health Services Research INTRODUCTION: The occurrence of thyroid cancer is increasing throughout the developed world and since the 1990s has become the fastest increasing malignancy. In 2014, a total of 2693 Australians and 302 New Zealanders were diagnosed with thyroid cancer, with this number projected to rise to 3650 in 2018. The purpose of this protocol is to establish a binational population-based clinical quality registry with the aim of monitoring and improving the quality of care provided to patients diagnosed with thyroid cancer in Australia and New Zealand. METHODS AND ANALYSIS: The Australian and New Zealand Thyroid Cancer Registry (ANZTCR) aims to capture clinical data for all patients over the age of 16 years with thyroid cancer, confirmed by histopathology report, who have been diagnosed, assessed or treated at a contributing hospital. A multidisciplinary steering committee was formed which, with operational support from Monash University, established the ANZTCR in early 2017. The pilot phase of the registry is currently operating in Victoria, New South Wales, Queensland, Western Australia and South Australia, with over 20 sites expected to come on board across Australia in 2018. A modified Delphi process was undertaken to determine the clinical quality indicators to be reported by the registry, and a minimum data set was developed comprising information regarding thyroid cancer diagnosis, pathology, surgery and 90-day follow-up. FUTURE PLANS: The establishment of the ANZTCR provides the opportunity for Australia and New Zealand to further understand current practice in the treatment of thyroid cancer and identify variation in outcomes. The engagement of endocrine surgeons in supporting this initiative is crucial. While the pilot registry has a focus on early clinical outcomes, it is anticipated that future collection of longer term outcome data particularly for patients with poor prognostic disease will add significant further value to the registry. BMJ Publishing Group 2019-01-28 /pmc/articles/PMC6352782/ /pubmed/30782713 http://dx.doi.org/10.1136/bmjopen-2018-023723 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 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, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Health Services Research Ioannou, Liane J Serpell, Jonathan Dean, Joanne Bendinelli, Cino Gough, Jenny Lisewski, Dean Miller, Julie A Meyer-Rochow, Win Sidhu, Stan Topliss, Duncan Walters, David Zalcberg, John Ahern, Susannah Development of a binational thyroid cancer clinical quality registry: a protocol paper |
title | Development of a binational thyroid cancer clinical quality registry: a protocol paper |
title_full | Development of a binational thyroid cancer clinical quality registry: a protocol paper |
title_fullStr | Development of a binational thyroid cancer clinical quality registry: a protocol paper |
title_full_unstemmed | Development of a binational thyroid cancer clinical quality registry: a protocol paper |
title_short | Development of a binational thyroid cancer clinical quality registry: a protocol paper |
title_sort | development of a binational thyroid cancer clinical quality registry: a protocol paper |
topic | Health Services Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6352782/ https://www.ncbi.nlm.nih.gov/pubmed/30782713 http://dx.doi.org/10.1136/bmjopen-2018-023723 |
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