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ACSQHC-ARCR-444

Prioritised clinical domain
Neonatal critical care
Abbreviation
ANZ CHD Registry
Registry contact

David Celermajer, Royal Prince Alfred Hospital - Cardiology, David.celermajer@health.nsw.gov.au

Year established
2021
Description

The ANZ CHD Registry is an initiative designed to transform care for congenital heart disease (CHD) patients in Australia and New Zealand. This registry will become a comprehensive resource by enrolling over 70,000 CHD patients, encompassing all age groups. This data will quantify the lifelong impact of CHD and shed light on disease progression, current management strategies, and factors affecting health outcomes. The registry will further enhance estimates of CHD prevalence within the ANZ population and evaluate the effectiveness of CHD interventions. Ultimately, these insights will directly inform advancements in CHD care, resource allocation, patient education, and research priorities, aligning perfectly with the National Strategic Action Plan for CHD. This data-driven approach has the potential to revolutionize CHD care and significantly improve the lives of countless patients across Australia and New Zealand.

Reporting process
  • Feedback to contributing clinicians
  • Shared with consumers
  • Reported in Annual Report
  • Reported in other public reports
  • Other
  • Academic Publication
Patient Reported Outcome Measures (PROMs)

Nil

Patient Reported Experience Measures (PREMs)

Nil

Participating sites

New South Wales

  • John Hunter Hospital Royal Newcastle Centre
  • Royal Prince Alfred Hospital
  • The Children's Hospital at Westmead

Queensland

  • Queensland Children's Hospital
  • The Prince Charles Hospital

South Australia

  • The Royal Adelaide Hospital
  • Women's And Children's Hospital, Adelaide

Victoria

  • Royal Melbourne Hospital - City Campus
  • The Royal Children's Hospital, Melbourne

Western Australia

  • Perth Children’s Hospital
  • Sir Charles Gairdner Hospital
Condition
Congenital heart disease
Name
Australia and New Zealand Congenital Heart Disease Registry
Lead organisation
Congenital Heart Alliance of Australia and New Zealand (CHAANZ)
Ethics approval reference
Ethics Review Committee Royal Prince Alfred Zone of the Sydney Local Health District
Reference: X17-0441 & 2019/ETH07472
Preferred published date
Immediately
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