Your browser doesn't support javascript.
loading
Data Resource: Vascular Risk in Adult New Zealanders (VARIANZ) datasets.
Mehta, S; Jackson, R; Exeter, D J; Wu, B P; Wells, S; Kerr, A J.
Afiliação
  • Mehta S; Section of Epidemiology and Biostatistics, School of Population Health, University of Auckland, Auckland, New Zealand.
  • Jackson R; Section of Epidemiology and Biostatistics, School of Population Health, University of Auckland, Auckland, New Zealand.
  • Exeter DJ; Section of Epidemiology and Biostatistics, School of Population Health, University of Auckland, Auckland, New Zealand.
  • Wu BP; Section of Epidemiology and Biostatistics, School of Population Health, University of Auckland, Auckland, New Zealand.
  • Wells S; Section of Epidemiology and Biostatistics, School of Population Health, University of Auckland, Auckland, New Zealand.
  • Kerr AJ; Section of Epidemiology and Biostatistics, School of Population Health, University of Auckland, Auckland, New Zealand.
Int J Popul Data Sci ; 4(1): 1107, 2019 Sep 02.
Article em En | MEDLINE | ID: mdl-34095534
ABSTRACT

INTRODUCTION:

The Vascular Risk in Adult New Zealanders (VARIANZ) datasets contain a range of routinely-collected New Zealand health data relevant to cardiovascular disease (CVD) and related conditions. The datasets enable exploration of cardiovascular-related treatment, service utilisation, outcomes and prognosis. PROCESSES Each dataset is constructed by anonymised individual-level linkage of eight national administrative health databases to identify all New Zealand adults aged ≥20 years who have recorded contact with publicly-funded New Zealand health services during a given year from 2006 onwards, when data quality is considered sufficient. DATA CONTENTS Individual-level data for each VARIANZ dataset can include variables covering demography, dispensing of cardiovascular disease (CVD) preventive medications and prior hospitalisations for atherosclerotic CVD, heart failure, atrial fibrillation and diabetes. If required, VARIANZ datasets can be individually linked to follow-up national routinely collected health data in subsequent years, including all-cause mortality events and fatal/non-fatal CVD events, to create VARIANZ longitudinal cohorts. Bespoke linkage can also be undertaken to include other national and regional administrative health data such as non-CVD related hospitalisations in order to explore CVD comorbidities or novel risk factors. Furthermore, a subset of the VARIANZ datasets based on specific health contacts (such as CVD hospitalisations only) can also be identified, and some data can be requested for years prior to 2006. The New Zealand routinely-collected health databases used to construct the VARIANZ datasets do not capture primary care diagnostic classifications or certain CVD risk factor data such as smoking status, blood pressure or lipid profiles.

CONCLUSION:

The Vascular Risk in Adult New Zealanders (VARIANZ) datasets capture the majority of the New Zealand population in a given year and are available from 2006 onwards, or earlier than 2006 for some datasets based on specific health contacts. VARIANZ data can be used to explore a range of research questions regarding management, outcomes and prognosis for CVD.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Int J Popul Data Sci Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Nova Zelândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Int J Popul Data Sci Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Nova Zelândia
...