HOME | CHAANZ

المسح الوطني لأمراض القلب الخلقية

تم إغلاق الاستبيان الآن ونشرت النتائج في مجلة Heart Lung Circulation. لمزيد من المعلومات حول نتائج هذا المشروع ، اتبع الرابط.

نتائج

أهلا بك

مرحبًا بكم في الموقع الإلكتروني لتحالف أمراض القلب الخلقية في أستراليا ونيوزيلندا (CHAANZ).

CHAANZ هو اتحاد من الباحثين في أمراض القلب الخلقية من أستراليا ونيوزيلندا. والغرض منها هو تسهيل البحث المركز في أمراض القلب الخلقية ، وتعزيز الحاجة إلى موارد أكبر والمساعدة في الخدمات لجميع الأشخاص المصابين بأمراض القلب الخلقية.

دراسة على مستوى أستراليا لنتائج وعبء أمراض القلب الخلقية على مدار الحياة

في يوليو 2020 ، تم منح التمويل لـ CHAANZ من منح صندوق الأبحاث الطبية المستقبلية لأمراض القلب الخلقية. يهدف هذا المشروع إلى فهم أعباء ونتائج أمراض القلب الخلقية.

اقرأ أكثر

Aotearoa New Zealand

The Paediatric and Congenital Cardiac Service based at Starship/Auckland City Hospitals is very pleased to contribute to the CHAANZ Registry collaboration and grateful for the support and endorsement of Heart Kids New Zealand for this project.

At this time, it is only possible to enrol and contribute data from patients from Aotearoa New Zealand who have received inpatient or outpatient care in Te Toka Tumai Auckland (Starship, Greenlane and Auckland Hospitals).

Survey Results The National Congenital Heart Disease survey is now closed and the results have been published in Heart Lung Circulation. Thank you to everyone who participated in this important study. You can read more about the results here.	ANZ Congenital Heart Disease Registry The National Congenital Heart Disease survey is the first step towards addressing current research questions and developing solutions to help all patients with congenital heart disease, irrespective of where they sit on the disease continuum.	Outcomes & Burdens for CHD In addition to providing increased resources for the development of the ANZ Congenital Heart Disease Registry, the MRFF funding will also allow CHAANZ to expand its research in to the burdens and outcomes of congenital heart disease.	National CHD Survey The National Congenital Heart Disease Online Survey was a voluntary online survey to help understand experiences and needs of people with congenital heart disease.
ANZ Epidemiology Research Epidemiology research in congenital heart disease is currently underway in New Zealand and Queensland. Both studies are investigating the burden of disease in each region. More information on these studies can be found here.	Our Research A call for a National Congenital Heart Disease Registry was advised after an extensive review of CHD management across Australia, published in the HeartKids Australia White paper.

المسح الوطني لأمراض القلب الخلقية

أهلا بك

دراسة على مستوى أستراليا لنتائج وعبء أمراض القلب الخلقية على مدار الحياة

Aotearoa New Zealand

ابحاثنا

Survey Results

The National Congenital Heart Disease survey is now closed and the results have been published in Heart Lung Circulation. Thank you to everyone who participated in this important study. You can read more about the results here.

ANZ Congenital Heart Disease Registry

The National Congenital Heart Disease survey is the first step towards addressing current research questions and developing solutions to help all patients with congenital heart disease, irrespective of where they sit on the disease continuum.

Outcomes & Burdens for CHD

In addition to providing increased resources for the development of the ANZ Congenital Heart Disease Registry, the MRFF funding will also allow CHAANZ to expand its research in to the burdens and outcomes of congenital heart disease.

National CHD Survey

The National Congenital Heart Disease Online Survey was a voluntary online survey to help understand experiences and needs of people with congenital heart disease.

ANZ Epidemiology Research

Epidemiology research in congenital heart disease is currently underway in New Zealand and Queensland. Both studies are investigating the burden of disease in each region. More information on these studies can be found here.

Our Research

A call for a National Congenital Heart Disease Registry was advised after an extensive review of CHD management across Australia, published in the HeartKids Australia White paper.

يتم دعم أبحاثنا بسخاء من خلال: