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EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study

BACKGROUND: Chronic kidney disease (CKD) and diabetes are the major causes of death and disability worldwide. They are associated with high health service utilization persisting over many years. Their slow progression and wide clinical variation make them eminently suitable for study in population-b...

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Autores principales: Foote, Celine, Hockham, Carinna, Sukkar, Louisa, Campain, Anna, Kang, Amy, Young, Tamara, Cass, Alan, Chow, Clara K, Comino, Elizabeth, Gallagher, Martin, Jan, Stephen, Knight, John, Liu, Bette, McNamara, Martin, Peiris, David, Pollock, Carol, Sullivan, David, Wong, Germaine, Zoungas, Sophia, Rogers, Kris, Jun, Min, Jardine, Meg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189250/
https://www.ncbi.nlm.nih.gov/pubmed/32285803
http://dx.doi.org/10.2196/15646
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author Foote, Celine
Hockham, Carinna
Sukkar, Louisa
Campain, Anna
Kang, Amy
Young, Tamara
Cass, Alan
Chow, Clara K
Comino, Elizabeth
Gallagher, Martin
Jan, Stephen
Knight, John
Liu, Bette
McNamara, Martin
Peiris, David
Pollock, Carol
Sullivan, David
Wong, Germaine
Zoungas, Sophia
Rogers, Kris
Jun, Min
Jardine, Meg
author_facet Foote, Celine
Hockham, Carinna
Sukkar, Louisa
Campain, Anna
Kang, Amy
Young, Tamara
Cass, Alan
Chow, Clara K
Comino, Elizabeth
Gallagher, Martin
Jan, Stephen
Knight, John
Liu, Bette
McNamara, Martin
Peiris, David
Pollock, Carol
Sullivan, David
Wong, Germaine
Zoungas, Sophia
Rogers, Kris
Jun, Min
Jardine, Meg
author_sort Foote, Celine
collection PubMed
description BACKGROUND: Chronic kidney disease (CKD) and diabetes are the major causes of death and disability worldwide. They are associated with high health service utilization persisting over many years. Their slow progression and wide clinical variation make them eminently suitable for study in population-based cohorts. However, current understanding of their prevalence, incidence, and progression is largely based on studies conducted in clinical populations. OBJECTIVE: This study aims to establish a novel link between an existing population-based cohort (the 45 and Up Study) and routinely collected laboratory and administrative data to facilitate research across the full disease spectrum of CKD and diabetes. METHODS: In the EXTEND45 Study (EXamining OuTcomEs in chroNic Disease in the 45 and Up Study), baseline questionnaire responses of over 260,000 participants of the 45 and Up Study aged ≥45 years living in New South Wales (NSW), collected between January 2006 and December 2009, are linked to data from laboratory service providers as well as national- and state-based administrative datasets via probabilistic linkage. Routinely collected data were obtained for participants who could be linked between January 2005 and July 2013. Laboratory data will enable the identification of early cases of chronic disease and the assessment of clinically relevant biochemical targets during the disease course. Health administrative datasets will allow for the examination of health service use, pharmacological management, and clinical outcomes. RESULTS: The study received ethics approval from the NSW Population and Health Services Research Ethics Committee in February 2014. Data linkage for 267,153 of the 45 and Up Study participants was completed in June 2016, with congruent linkage achieved for 265,086 (99.23%) individuals. To date, the CKD and diabetes cohorts have been identified (published elsewhere), and a diverse portfolio of research projects relating to disease burden, risk factors, health outcomes, and health service utilization is in development. CONCLUSIONS: The EXTEND45 Study represents an unparalleled opportunity to perform extensive research into diseases of considerable public health and clinical importance. Strengths include the population-based nature of the cohort and the availability of longitudinal information on the complete disease pathway for affected individuals. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR1-10.2196/15646
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spelling pubmed-71892502020-05-01 EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study Foote, Celine Hockham, Carinna Sukkar, Louisa Campain, Anna Kang, Amy Young, Tamara Cass, Alan Chow, Clara K Comino, Elizabeth Gallagher, Martin Jan, Stephen Knight, John Liu, Bette McNamara, Martin Peiris, David Pollock, Carol Sullivan, David Wong, Germaine Zoungas, Sophia Rogers, Kris Jun, Min Jardine, Meg JMIR Res Protoc Protocol BACKGROUND: Chronic kidney disease (CKD) and diabetes are the major causes of death and disability worldwide. They are associated with high health service utilization persisting over many years. Their slow progression and wide clinical variation make them eminently suitable for study in population-based cohorts. However, current understanding of their prevalence, incidence, and progression is largely based on studies conducted in clinical populations. OBJECTIVE: This study aims to establish a novel link between an existing population-based cohort (the 45 and Up Study) and routinely collected laboratory and administrative data to facilitate research across the full disease spectrum of CKD and diabetes. METHODS: In the EXTEND45 Study (EXamining OuTcomEs in chroNic Disease in the 45 and Up Study), baseline questionnaire responses of over 260,000 participants of the 45 and Up Study aged ≥45 years living in New South Wales (NSW), collected between January 2006 and December 2009, are linked to data from laboratory service providers as well as national- and state-based administrative datasets via probabilistic linkage. Routinely collected data were obtained for participants who could be linked between January 2005 and July 2013. Laboratory data will enable the identification of early cases of chronic disease and the assessment of clinically relevant biochemical targets during the disease course. Health administrative datasets will allow for the examination of health service use, pharmacological management, and clinical outcomes. RESULTS: The study received ethics approval from the NSW Population and Health Services Research Ethics Committee in February 2014. Data linkage for 267,153 of the 45 and Up Study participants was completed in June 2016, with congruent linkage achieved for 265,086 (99.23%) individuals. To date, the CKD and diabetes cohorts have been identified (published elsewhere), and a diverse portfolio of research projects relating to disease burden, risk factors, health outcomes, and health service utilization is in development. CONCLUSIONS: The EXTEND45 Study represents an unparalleled opportunity to perform extensive research into diseases of considerable public health and clinical importance. Strengths include the population-based nature of the cohort and the availability of longitudinal information on the complete disease pathway for affected individuals. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR1-10.2196/15646 JMIR Publications 2020-04-14 /pmc/articles/PMC7189250/ /pubmed/32285803 http://dx.doi.org/10.2196/15646 Text en ©Celine Foote, Carinna Hockham, Louisa Sukkar, Anna Campain, Amy Kang, Tamara Young, Alan Cass, Clara K Chow, Elizabeth Comino, Martin Gallagher, Stephen Jan, John Knight, Bette Liu, Martin McNamara, David Peiris, Carol Pollock, David Sullivan, Germaine Wong, Sophia Zoungas, Kris Rogers, Min Jun, Meg Jardine. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 14.04.2020. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on http://www.researchprotocols.org, as well as this copyright and license information must be included.
spellingShingle Protocol
Foote, Celine
Hockham, Carinna
Sukkar, Louisa
Campain, Anna
Kang, Amy
Young, Tamara
Cass, Alan
Chow, Clara K
Comino, Elizabeth
Gallagher, Martin
Jan, Stephen
Knight, John
Liu, Bette
McNamara, Martin
Peiris, David
Pollock, Carol
Sullivan, David
Wong, Germaine
Zoungas, Sophia
Rogers, Kris
Jun, Min
Jardine, Meg
EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study
title EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study
title_full EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study
title_fullStr EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study
title_full_unstemmed EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study
title_short EXamining ouTcomEs in chroNic Disease in the 45 and Up Study (the EXTEND45 Study): Protocol for an Australian Linked Cohort Study
title_sort examining outcomes in chronic disease in the 45 and up study (the extend45 study): protocol for an australian linked cohort study
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189250/
https://www.ncbi.nlm.nih.gov/pubmed/32285803
http://dx.doi.org/10.2196/15646
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