Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology W orking G roup on M yocardial and P ericardial D iseases

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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of heart failure 2021-04, Vol.23 (4), p.512-526
Hauptverfasser: Garcia‐Pavia, Pablo, Rapezzi, Claudio, Adler, Yehuda, Arad, Michael, Basso, Cristina, Brucato, Antonio, Burazor, Ivana, Caforio, Alida L.P., Damy, Thibaud, Eriksson, Urs, Fontana, Marianna, Gillmore, Julian D., Gonzalez‐Lopez, Esther, Grogan, Martha, Heymans, Stephane, Imazio, Massimo, Kindermann, Ingrid, Kristen, Arnt V., Maurer, Mathew S., Merlini, Giampaolo, Pantazis, Antonis, Pankuweit, Sabine, Rigopoulos, Angelos G., Linhart, Ales
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 526
container_issue 4
container_start_page 512
container_title European journal of heart failure
container_volume 23
creator Garcia‐Pavia, Pablo
Rapezzi, Claudio
Adler, Yehuda
Arad, Michael
Basso, Cristina
Brucato, Antonio
Burazor, Ivana
Caforio, Alida L.P.
Damy, Thibaud
Eriksson, Urs
Fontana, Marianna
Gillmore, Julian D.
Gonzalez‐Lopez, Esther
Grogan, Martha
Heymans, Stephane
Imazio, Massimo
Kindermann, Ingrid
Kristen, Arnt V.
Maurer, Mathew S.
Merlini, Giampaolo
Pantazis, Antonis
Pankuweit, Sabine
Rigopoulos, Angelos G.
Linhart, Ales
description 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.
doi_str_mv 10.1002/ejhf.2140
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_1002_ejhf_2140</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1002_ejhf_2140</sourcerecordid><originalsourceid>FETCH-LOGICAL-c740-863a1a24cbbabc94b2792cf3d4dbdaca96f8b9ade2bfc71b7a5f1cc6f19856293</originalsourceid><addsrcrecordid>eNo1kLFOwzAYhC0EEqUw8Ab_ypBiO27ijFVbClIRSFRijH47duuSxpUdhrwPD0pC6XSn06c76Qi5Z3TCKOWPZr-zE84EvSAjJvMioVKIy96nUiaFFPya3MS4p5TlPT4iPwuH28ZHFwGbCtpgsD2YpgVvQWOoHGrAQ1d7Vw3QBGZw7E3rfAOxxdac4XZnYPkd_NFgAx9eO9N2Qz4fSnzttx18gg9frtnCCoL_PkJf8QqdP83Uf_vvYII7Bwtw0WA08ZZcWayjufvXMdk8LTfz52T9tnqZz9aJzgVNZJYiQy60Uqh0IRTPC65tWolKVaixyKxUBVaGK6tzpnKcWqZ1Zlkhpxkv0jF5ONXq4GMMxpbH4A4YupLRcni3HN4th3fTX4iicW4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology W orking G roup on M yocardial and P ericardial D iseases</title><source>Wiley Free Content</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Garcia‐Pavia, Pablo ; Rapezzi, Claudio ; Adler, Yehuda ; Arad, Michael ; Basso, Cristina ; Brucato, Antonio ; Burazor, Ivana ; Caforio, Alida L.P. ; Damy, Thibaud ; Eriksson, Urs ; Fontana, Marianna ; Gillmore, Julian D. ; Gonzalez‐Lopez, Esther ; Grogan, Martha ; Heymans, Stephane ; Imazio, Massimo ; Kindermann, Ingrid ; Kristen, Arnt V. ; Maurer, Mathew S. ; Merlini, Giampaolo ; Pantazis, Antonis ; Pankuweit, Sabine ; Rigopoulos, Angelos G. ; Linhart, Ales</creator><creatorcontrib>Garcia‐Pavia, Pablo ; Rapezzi, Claudio ; Adler, Yehuda ; Arad, Michael ; Basso, Cristina ; Brucato, Antonio ; Burazor, Ivana ; Caforio, Alida L.P. ; Damy, Thibaud ; Eriksson, Urs ; Fontana, Marianna ; Gillmore, Julian D. ; Gonzalez‐Lopez, Esther ; Grogan, Martha ; Heymans, Stephane ; Imazio, Massimo ; Kindermann, Ingrid ; Kristen, Arnt V. ; Maurer, Mathew S. ; Merlini, Giampaolo ; Pantazis, Antonis ; Pankuweit, Sabine ; Rigopoulos, Angelos G. ; Linhart, Ales</creatorcontrib><description>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.</description><identifier>ISSN: 1388-9842</identifier><identifier>EISSN: 1879-0844</identifier><identifier>DOI: 10.1002/ejhf.2140</identifier><language>eng</language><ispartof>European journal of heart failure, 2021-04, Vol.23 (4), p.512-526</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c740-863a1a24cbbabc94b2792cf3d4dbdaca96f8b9ade2bfc71b7a5f1cc6f19856293</citedby><cites>FETCH-LOGICAL-c740-863a1a24cbbabc94b2792cf3d4dbdaca96f8b9ade2bfc71b7a5f1cc6f19856293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Garcia‐Pavia, Pablo</creatorcontrib><creatorcontrib>Rapezzi, Claudio</creatorcontrib><creatorcontrib>Adler, Yehuda</creatorcontrib><creatorcontrib>Arad, Michael</creatorcontrib><creatorcontrib>Basso, Cristina</creatorcontrib><creatorcontrib>Brucato, Antonio</creatorcontrib><creatorcontrib>Burazor, Ivana</creatorcontrib><creatorcontrib>Caforio, Alida L.P.</creatorcontrib><creatorcontrib>Damy, Thibaud</creatorcontrib><creatorcontrib>Eriksson, Urs</creatorcontrib><creatorcontrib>Fontana, Marianna</creatorcontrib><creatorcontrib>Gillmore, Julian D.</creatorcontrib><creatorcontrib>Gonzalez‐Lopez, Esther</creatorcontrib><creatorcontrib>Grogan, Martha</creatorcontrib><creatorcontrib>Heymans, Stephane</creatorcontrib><creatorcontrib>Imazio, Massimo</creatorcontrib><creatorcontrib>Kindermann, Ingrid</creatorcontrib><creatorcontrib>Kristen, Arnt V.</creatorcontrib><creatorcontrib>Maurer, Mathew S.</creatorcontrib><creatorcontrib>Merlini, Giampaolo</creatorcontrib><creatorcontrib>Pantazis, Antonis</creatorcontrib><creatorcontrib>Pankuweit, Sabine</creatorcontrib><creatorcontrib>Rigopoulos, Angelos G.</creatorcontrib><creatorcontrib>Linhart, Ales</creatorcontrib><title>Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology W orking G roup on M yocardial and P ericardial D iseases</title><title>European journal of heart failure</title><description>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.</description><issn>1388-9842</issn><issn>1879-0844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNo1kLFOwzAYhC0EEqUw8Ab_ypBiO27ijFVbClIRSFRijH47duuSxpUdhrwPD0pC6XSn06c76Qi5Z3TCKOWPZr-zE84EvSAjJvMioVKIy96nUiaFFPya3MS4p5TlPT4iPwuH28ZHFwGbCtpgsD2YpgVvQWOoHGrAQ1d7Vw3QBGZw7E3rfAOxxdac4XZnYPkd_NFgAx9eO9N2Qz4fSnzttx18gg9frtnCCoL_PkJf8QqdP83Uf_vvYII7Bwtw0WA08ZZcWayjufvXMdk8LTfz52T9tnqZz9aJzgVNZJYiQy60Uqh0IRTPC65tWolKVaixyKxUBVaGK6tzpnKcWqZ1Zlkhpxkv0jF5ONXq4GMMxpbH4A4YupLRcni3HN4th3fTX4iicW4</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Garcia‐Pavia, Pablo</creator><creator>Rapezzi, Claudio</creator><creator>Adler, Yehuda</creator><creator>Arad, Michael</creator><creator>Basso, Cristina</creator><creator>Brucato, Antonio</creator><creator>Burazor, Ivana</creator><creator>Caforio, Alida L.P.</creator><creator>Damy, Thibaud</creator><creator>Eriksson, Urs</creator><creator>Fontana, Marianna</creator><creator>Gillmore, Julian D.</creator><creator>Gonzalez‐Lopez, Esther</creator><creator>Grogan, Martha</creator><creator>Heymans, Stephane</creator><creator>Imazio, Massimo</creator><creator>Kindermann, Ingrid</creator><creator>Kristen, Arnt V.</creator><creator>Maurer, Mathew S.</creator><creator>Merlini, Giampaolo</creator><creator>Pantazis, Antonis</creator><creator>Pankuweit, Sabine</creator><creator>Rigopoulos, Angelos G.</creator><creator>Linhart, Ales</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>202104</creationdate><title>Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology W orking G roup on M yocardial and P ericardial D iseases</title><author>Garcia‐Pavia, Pablo ; Rapezzi, Claudio ; Adler, Yehuda ; Arad, Michael ; Basso, Cristina ; Brucato, Antonio ; Burazor, Ivana ; Caforio, Alida L.P. ; Damy, Thibaud ; Eriksson, Urs ; Fontana, Marianna ; Gillmore, Julian D. ; Gonzalez‐Lopez, Esther ; Grogan, Martha ; Heymans, Stephane ; Imazio, Massimo ; Kindermann, Ingrid ; Kristen, Arnt V. ; Maurer, Mathew S. ; Merlini, Giampaolo ; Pantazis, Antonis ; Pankuweit, Sabine ; Rigopoulos, Angelos G. ; Linhart, Ales</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c740-863a1a24cbbabc94b2792cf3d4dbdaca96f8b9ade2bfc71b7a5f1cc6f19856293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garcia‐Pavia, Pablo</creatorcontrib><creatorcontrib>Rapezzi, Claudio</creatorcontrib><creatorcontrib>Adler, Yehuda</creatorcontrib><creatorcontrib>Arad, Michael</creatorcontrib><creatorcontrib>Basso, Cristina</creatorcontrib><creatorcontrib>Brucato, Antonio</creatorcontrib><creatorcontrib>Burazor, Ivana</creatorcontrib><creatorcontrib>Caforio, Alida L.P.</creatorcontrib><creatorcontrib>Damy, Thibaud</creatorcontrib><creatorcontrib>Eriksson, Urs</creatorcontrib><creatorcontrib>Fontana, Marianna</creatorcontrib><creatorcontrib>Gillmore, Julian D.</creatorcontrib><creatorcontrib>Gonzalez‐Lopez, Esther</creatorcontrib><creatorcontrib>Grogan, Martha</creatorcontrib><creatorcontrib>Heymans, Stephane</creatorcontrib><creatorcontrib>Imazio, Massimo</creatorcontrib><creatorcontrib>Kindermann, Ingrid</creatorcontrib><creatorcontrib>Kristen, Arnt V.</creatorcontrib><creatorcontrib>Maurer, Mathew S.</creatorcontrib><creatorcontrib>Merlini, Giampaolo</creatorcontrib><creatorcontrib>Pantazis, Antonis</creatorcontrib><creatorcontrib>Pankuweit, Sabine</creatorcontrib><creatorcontrib>Rigopoulos, Angelos G.</creatorcontrib><creatorcontrib>Linhart, Ales</creatorcontrib><collection>CrossRef</collection><jtitle>European journal of heart failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garcia‐Pavia, Pablo</au><au>Rapezzi, Claudio</au><au>Adler, Yehuda</au><au>Arad, Michael</au><au>Basso, Cristina</au><au>Brucato, Antonio</au><au>Burazor, Ivana</au><au>Caforio, Alida L.P.</au><au>Damy, Thibaud</au><au>Eriksson, Urs</au><au>Fontana, Marianna</au><au>Gillmore, Julian D.</au><au>Gonzalez‐Lopez, Esther</au><au>Grogan, Martha</au><au>Heymans, Stephane</au><au>Imazio, Massimo</au><au>Kindermann, Ingrid</au><au>Kristen, Arnt V.</au><au>Maurer, Mathew S.</au><au>Merlini, Giampaolo</au><au>Pantazis, Antonis</au><au>Pankuweit, Sabine</au><au>Rigopoulos, Angelos G.</au><au>Linhart, Ales</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology W orking G roup on M yocardial and P ericardial D iseases</atitle><jtitle>European journal of heart failure</jtitle><date>2021-04</date><risdate>2021</risdate><volume>23</volume><issue>4</issue><spage>512</spage><epage>526</epage><pages>512-526</pages><issn>1388-9842</issn><eissn>1879-0844</eissn><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.</abstract><doi>10.1002/ejhf.2140</doi><tpages>15</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1388-9842
ispartof European journal of heart failure, 2021-04, Vol.23 (4), p.512-526
issn 1388-9842
1879-0844
language eng
recordid cdi_crossref_primary_10_1002_ejhf_2140
source Wiley Free Content; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
title Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology W orking G roup on M yocardial and P ericardial D iseases
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T05%3A31%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Diagnosis%20and%20treatment%20of%20cardiac%20amyloidosis.%20A%20position%20statement%20of%20the%20European%20Society%20of%20Cardiology%20W%20orking%20G%20roup%20on%20M%20yocardial%20and%20P%20ericardial%20D%20iseases&rft.jtitle=European%20journal%20of%20heart%20failure&rft.au=Garcia%E2%80%90Pavia,%20Pablo&rft.date=2021-04&rft.volume=23&rft.issue=4&rft.spage=512&rft.epage=526&rft.pages=512-526&rft.issn=1388-9842&rft.eissn=1879-0844&rft_id=info:doi/10.1002/ejhf.2140&rft_dat=%3Ccrossref%3E10_1002_ejhf_2140%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true