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Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases.
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.
Afiliação
  • Garcia-Pavia P; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro Majadahonda, CIBERCV, Manuel de Falla, 2, 28222 Madrid, Spain.
  • Rapezzi C; Universidad Francisco de Vitoria (UFV), Pozuelo de Alarcon, Spain.
  • Adler Y; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart.
  • Arad M; Cardiologic Centre, University of Ferrara, Italy.
  • Basso C; Maria Cecilia Hospital, GVM Care & Research, Cotignola, Italy.
  • Brucato A; Leviev Heart Centre, Chaim Sheba Medical Centre (affiliated to Tel Aviv University), Israel.
  • Burazor I; Heart Failure Institute, Leviev Heart Centre, Sheba Hospital and Sackler School of Medicine, Tel Aviv University, Israel.
  • Caforio ALP; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart.
  • Damy T; Cardiovascular Pathology Unit, University Hospital, Padua, Italy.
  • Eriksson U; Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua, Padua, Italy.
  • Fontana M; Dipartimento di Scienze Biomediche e Cliniche, Università degli Studi d Milano, Ospedale Fatebenefratelli, Italy.
  • Gillmore JD; Belgrade University School of Medicine, Cardiology, Institute for Rehabilitation, Belgrade, Serbia.
  • Gonzalez-Lopez E; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart.
  • Grogan M; Cardiology, Department of Cardiac Thoracic Vascular Sciences and Public Health, University of Padova, Padova, Italy.
  • Heymans S; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart.
  • Imazio M; French Referral Centre for Cardiac Amyloidosis, Amyloidosis Mondor Network, GRC Amyloid Research Institute, CHU Henri Mondor, Créteil, France.
  • Kindermann I; GZO-Zurich Regional Health Centre, Wetzikon & Cardioimmunology, Centre for Molecular Cardiology, University of Zurich, Switzerland.
  • Kristen AV; National Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, UK.
  • Maurer MS; National Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, UK.
  • Merlini G; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro Majadahonda, CIBERCV, Manuel de Falla, 2, 28222 Madrid, Spain.
  • Pantazis A; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart.
  • Pankuweit S; Cardiac Amyloid Clinic, Division of Circulatory Failure, Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA.
  • Rigopoulos AG; Department of Cardiology, Maastricht University, CARIM School for Cardiovascular Diseases, Maastricht, Netherlands.
  • Linhart A; Centre for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
Eur Heart J ; 42(16): 1554-1568, 2021 04 21.
Article em En | MEDLINE | ID: mdl-33825853
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiopatias / Amiloidose / Cardiomiopatias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiopatias / Amiloidose / Cardiomiopatias Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Espanha