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Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology 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, 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, 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), Ramat Gan, Israel.
  • Burazor I; Heart Failure Institute, Leviev Heart Centre, Sheba Hospital and Sackler School of Medicine, Tel Aviv University, Tel Aviv, 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, and Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua, Padua, Italy.
  • Eriksson U; Department of Biomedical and Clinical Sciences, University of Milan, Fatebenefratelli Hospital, Milan, Italy.
  • Fontana M; Belgrade University School of Medicine, Cardiology, Institute for Rehabilitation, Belgrade, Serbia.
  • Gillmore JD; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart.
  • Gonzalez-Lopez E; Cardiology, Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua, Padua, Italy.
  • Grogan M; French Referral Centre for Cardiac Amyloidosis, Amyloidosis Mondor Network, GRC Amyloid Research Institute, CHU Henri Mondor, Créteil, France.
  • Heymans S; GZO - Zurich Regional Health Centre, Wetzikon & Cardioimmunology, Centre for Molecular Cardiology, University of Zurich, Zurich, Switzerland.
  • Imazio M; National Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, UK.
  • Kindermann I; National Amyloidosis Centre, Division of Medicine, University College London, Royal Free Hospital, London, UK.
  • Kristen AV; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro Majadahonda, CIBERCV, Madrid, Spain.
  • Maurer MS; European Reference Network for Rare, Low Prevalence and Complex Diseases of the Heart-ERN GUARD-Heart.
  • Merlini G; Cardiac Amyloid Clinic, Division of Circulatory Failure, Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA.
  • Pantazis A; Department of Cardiology, Maastricht University, CARIM School for Cardiovascular Diseases, Maastricht, The Netherlands.
  • Pankuweit S; Centre for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
  • Rigopoulos AG; ICIN-Netherlands Heart Institute, Holland Heart House, Utrecht, The Netherlands.
  • Linhart A; University Cardiology, Cardiovascular and Thoracic Department, AOU Città della Salute e della Scienza di Torino, Turin, Italy.
Eur J Heart Fail ; 23(4): 512-526, 2021 04.
Article em En | MEDLINE | ID: mdl-33826207
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiologia / Cardiopatias / Insuficiência Cardíaca / Amiloidose / Cardiomiopatias Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiologia / Cardiopatias / Insuficiência Cardíaca / Amiloidose / Cardiomiopatias Idioma: En Ano de publicação: 2021 Tipo de documento: Article