Literature DB >> 33826207

Diagnosis and treatment of cardiac amyloidosis. A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.

Pablo Garcia-Pavia1,2,3, Claudio Rapezzi4,5, Yehuda Adler6, Michael Arad7, Cristina Basso3,8, Antonio Brucato9, Ivana Burazor10, Alida L P Caforio3,11, Thibaud Damy12, Urs Eriksson13, Marianna Fontana14, Julian D Gillmore14, Esther Gonzalez-Lopez1,3, Martha Grogan15, Stephane Heymans16,17,18, Massimo Imazio19, Ingrid Kindermann20, Arnt V Kristen21,22, Mathew S Maurer23, Giampaolo Merlini24,25, Antonis Pantazis26, Sabine Pankuweit27, Angelos G Rigopoulos28, Ales Linhart29.   

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. © European Society of Cardiology 2021.

Entities:  

Year:  2021        PMID: 33826207     DOI: 10.1002/ejhf.2140

Source DB:  PubMed          Journal:  Eur J Heart Fail        ISSN: 1388-9842            Impact factor:   15.534


  18 in total

1.  Late-Onset Hereditary Transthyretin Amyloidosis Val30Met in an Elderly Person in a Non-Endemic Area.

Authors:  Shun Wang; Jingping Sun; Qun Lu; Hao Li; Yun Zhang
Journal:  Int Med Case Rep J       Date:  2022-06-16

2.  Yield of bone scintigraphy screening for transthyretin-related cardiac amyloidosis in different conditions: Methodological issues and clinical implications.

Authors:  Giacomo Tini; Eugenio Sessarego; Stefano Benenati; Pier Filippo Vianello; Beatrice Musumeci; Camillo Autore; Marco Canepa
Journal:  Eur J Clin Invest       Date:  2021-08-22       Impact factor: 5.722

3.  Clinical Profile and Prognosis of Hereditary Transthyretin Amyloid Cardiomyopathy: A Single-Center Study in South China.

Authors:  Shuai Wang; Wenke Peng; Min Pang; Ling Mao; Daoquan Peng; Bilian Yu; Sha Wu; Die Hu; Yang Yang; Jia He; Mingqi Ouyang
Journal:  Front Cardiovasc Med       Date:  2022-06-27

4.  Pulmonary 99mTc-HMDP uptake correlates with restrictive ventilatory defects and abnormal lung reactance in transthyretin cardiac amyloidosis patients.

Authors:  Astrid Monfort; Alexia Rivas; Rishika Banydeen; Jocelyn Inamo; Karim Farid; Remi Neviere
Journal:  Respir Res       Date:  2022-03-27

Review 5.  Advances in Multimodality Cardiovascular Imaging in the Diagnosis of Heart Failure With Preserved Ejection Fraction.

Authors:  Alberico Del Torto; Andrea Igoren Guaricci; Francesca Pomarico; Marco Guglielmo; Laura Fusini; Francesco Monitillo; Daniela Santoro; Monica Vannini; Alexia Rossi; Giuseppe Muscogiuri; Andrea Baggiano; Gianluca Pontone
Journal:  Front Cardiovasc Med       Date:  2022-03-09

6.  Diagnostic Value of 11C-PIB PET/MR in Cardiac Amyloidosis.

Authors:  Xiao Bi; Baixuan Xu; Jiajin Liu; Guanyun Wang; Jing An; Xiaojun Zhang; Ruimin Wang; Wei Dong; Zhiwei Guan
Journal:  Front Cardiovasc Med       Date:  2022-03-16

7.  Case Report: Systemic Amyloidosis Involving the Heart and Skeletal Muscle.

Authors:  Pinchao Lv; Yuxi Li; Lin Wu; Qiuping Shi; Lingchao Meng; Xiaojuan Yu; Lin Nong; Jianping Li
Journal:  Front Cardiovasc Med       Date:  2022-04-04

8.  Deep Learning Supplants Visual Analysis by Experienced Operators for the Diagnosis of Cardiac Amyloidosis by Cine-CMR.

Authors:  Philippe Germain; Armine Vardazaryan; Nicolas Padoy; Aissam Labani; Catherine Roy; Thomas Hellmut Schindler; Soraya El Ghannudi
Journal:  Diagnostics (Basel)       Date:  2021-12-29

9.  Echocardiographic and clinical predictors of cardiac amyloidosis: limitations of apical sparing.

Authors:  Douglas Kyrouac; Walter Schiffer; Brandon Lennep; Nicole Fergestrom; Kathleen W Zhang; John Gorcsan; Daniel J Lenihan; Joshua D Mitchell
Journal:  ESC Heart Fail       Date:  2021-12-08

10.  Step-by-step typing for the accurate diagnosis of concurrent light chain and transthyretin cardiac amyloidosis.

Authors:  Hidenori Moriyama; Hiroki Kitakata; Jin Endo; Hidehiko Ikura; Motoaki Sano; Masayoshi Tasaki; Shunta Sakai; Mitsuharu Ueda; Keiichi Fukuda
Journal:  ESC Heart Fail       Date:  2022-01-21
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