Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases
European Heart Journal

Abstract
Cardiac amyloidosis is a serious and progressive infiltrative disease that is caused by the deposition of amyloid fibrils at the cardiac level. It can be due to rare genetic variants in the hereditary forms or as a consequence of acquired conditions. Thanks to advances in imaging techniques and the possibility of achieving a non-invasive diagnosis, we now know that cardiac amyloidosis is a more frequent disease than traditionally considered. In this position paper the Working Group on Myocardial and Pericardial Disease proposes an invasive and non-invasive definition of cardiac amyloidosis, addresses clinical scenarios and situations to suspect the condition and proposes a diagnostic algorithm to aid diagnosis. Furthermore, we also review how to monitor and treat cardiac amyloidosis, in an attempt to bridge the gap between the latest advances in the field and clinical practice.
Contributors

Claudio Rapezzi
Author

Yehuda Adler
Author

Michael Arad
Author

Cristina Basso
Author

Ivana Burazor
Author

Urs Eriksson
Author

Marianna Fontana
Author

Esther Gonzalez-Lopez
Author

Martha Grogan
Author

Stephane Heymans
Author

Ingrid Kindermann
Author

Arnt V Kristen
Author

Mathew S Maurer
Author

Giampaolo Merlini
Author

Antonis Pantazis
Author

Sabine Pankuweit
Author

Angelos G Rigopoulos
Author

Ales Linhart
Author






