2024 Australia–New Zealand Expert Consensus Statement on Cardiac Amyloidosis - 01/05/24
, Diane Fatkin, BSc(Med), FRACP, FSCANZ a, James Gunton, MBBS, PhD b, James L. Hare, PhD, FRACP c, Dariusz Korczyk, FRACP, FCSANZ, DDU d, Fiona Kwok, PhD, FRACP e, Kaitlyn Lam, MBBS, PhD f, David Russell, BMedSci, FRACP, FCSANZ g, Hasib Sidiqi, MBBS, PhD h, Tim Sutton, FRACP, FCSANZ i, Simon D.J. Gibbs, FRACP, FRCPA j, Peter Mollee, MMedSc, FRACP, FRCPA k, Liza Thomas, MBBS, PhD l, ⁎ 
Abstract |
Over the past 5 years, early diagnosis of and new treatments for cardiac amyloidosis (CA) have emerged that hold promise for early intervention. These include non-invasive diagnostic tests and disease modifying therapies. Recently, CA has been one of the first types of cardiomyopathy to be treated with gene editing techniques. Although these therapies are not yet widely available to patients in Australia and New Zealand, this may change in the near future. Given the rapid pace with which this field is evolving, it is important to view these advances within the Australian and New Zealand context. This Consensus Statement aims to update the Australian and New Zealand general physician and cardiologist with regards to the diagnosis, investigations, and management of CA.
Le texte complet de cet article est disponible en PDF.Keywords : Amyloidosis, Cardiac, Transthyretin, Hereditary, Heart failure with preserved ejection fraction, Heart failure, Genetics
Plan
| Address for reprints: A/Prof Nicole Bart, Department of Cardiology, St Vincent’s Hospital, Sydney, NSW 2145, Australia Email: nicole.bart@svh.org.au |
Vol 33 - N° 4
P. 420-442 - avril 2024 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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