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Browsing by Author "Emdin, Michele (7005694410)"

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    Publication
    Beta-blockers: A real antidote for cocaine-related heart disease?
    (2019)
    Barison, Andrea (24597524200)
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    Aquaro, Giovanni Donato (35279306300)
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    Seferović, Petar M. (6603594879)
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    Emdin, Michele (7005694410)
    [No abstract available]
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    Cardiac remodelling – Part 1: From cells and tissues to circulating biomarkers. A review from the Study Group on Biomarkers of the Heart Failure Association of the European Society of Cardiology
    (2022)
    González, Arantxa (57191823224)
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    Richards, A. Mark (7402299599)
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    de Boer, Rudolf A. (8572907800)
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    Thum, Thomas (57195743477)
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    Arfsten, Henrike (57192299905)
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    Hülsmann, Martin (7006719269)
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    Falcao-Pires, Inês (12771795000)
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    Díez, Javier (7201552601)
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    Foo, Roger S.Y. (14419910700)
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    Chan, Mark Y. (23388249600)
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    Aimo, Alberto (56112889900)
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    Anene-Nzelu, Chukwuemeka G. (36717287000)
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    Abdelhamid, Magdy (57069808700)
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    Adamopoulos, Stamatis (55399885400)
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    Anker, Stefan D. (56223993400)
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    Belenkov, Yuri (7006528098)
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    Gal, Tuvia B. (7003448638)
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    Cohen-Solal, Alain (57189610711)
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    Böhm, Michael (35392235500)
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    Chioncel, Ovidiu (12769077100)
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    Delgado, Victoria (24172709900)
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    Emdin, Michele (7005694410)
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    Jankowska, Ewa A. (21640520500)
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    Gustafsson, Finn (7005115957)
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    Hill, Loreena (56572076500)
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    Jaarsma, Tiny (56962769200)
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    Januzzi, James L. (7003533511)
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    Jhund, Pardeep S. (6506826363)
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    Lopatin, Yuri (59263990100)
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    Lund, Lars H. (7102206508)
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    Metra, Marco (7006770735)
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    Milicic, Davor (56503365500)
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    Moura, Brenda (6602544591)
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    Mueller, Christian (57638261900)
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    Mullens, Wilfried (55916359500)
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    Núñez, Julio (57201547451)
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    Piepoli, Massimo F. (7005292730)
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    Rakisheva, Amina (57196007935)
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    Ristić, Arsen D. (7003835406)
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    Rossignol, Patrick (7006015976)
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    Savarese, Gianluigi (36189499900)
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    Tocchetti, Carlo G. (6507913481)
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    Van Linthout, Sophie (6602562561)
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    Volterrani, Maurizio (7004062259)
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    Seferovic, Petar (6603594879)
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    Rosano, Giuseppe (7007131876)
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    Coats, Andrew J.S. (35395386900)
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    Bayés-Genís, Antoni (7004094140)
    Cardiac remodelling refers to changes in left ventricular structure and function over time, with a progressive deterioration that may lead to heart failure (HF) development (adverse remodelling) or vice versa a recovery (reverse remodelling) in response to HF treatment. Adverse remodelling predicts a worse outcome, whilst reverse remodelling predicts a better prognosis. The geometry, systolic and diastolic function and electric activity of the left ventricle are affected, as well as the left atrium and on the long term even right heart chambers. At a cellular and molecular level, remodelling involves all components of cardiac tissue: cardiomyocytes, fibroblasts, endothelial cells and leucocytes. The molecular, cellular and histological signatures of remodelling may differ according to the cause and severity of cardiac damage, and clearly to the global trend toward worsening or recovery. These processes cannot be routinely evaluated through endomyocardial biopsies, but may be reflected by circulating levels of several biomarkers. Different classes of biomarkers (e.g. proteins, non-coding RNAs, metabolites and/or epigenetic modifications) and several biomarkers of each class might inform on some aspects on HF development, progression and long-term outcomes, but most have failed to enter clinical practice. This may be due to the biological complexity of remodelling, so that no single biomarker could provide great insight on remodelling when assessed alone. Another possible reason is a still incomplete understanding of the role of biomarkers in the pathophysiology of cardiac remodelling. Such role will be investigated in the first part of this review paper on biomarkers of cardiac remodelling. © 2022 European Society of Cardiology.
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    Cardiac remodelling – Part 2: Clinical, imaging and laboratory findings. A review from the Study Group on Biomarkers of the Heart Failure Association of the European Society of Cardiology
    (2022)
    Aimo, Alberto (56112889900)
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    Vergaro, Giuseppe (23111620200)
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    González, Arantxa (57191823224)
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    Barison, Andrea (24597524200)
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    Lupón, Josep (57214510665)
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    Delgado, Victoria (24172709900)
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    Richards, A Mark (7402299599)
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    de Boer, Rudolf A. (8572907800)
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    Thum, Thomas (57195743477)
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    Arfsten, Henrike (57192299905)
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    Hülsmann, Martin (7006719269)
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    Falcao-Pires, Inês (12771795000)
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    Díez, Javier (7201552601)
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    Foo, Roger S.Y. (14419910700)
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    Chan, Mark Yan Yee (23388249600)
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    Anene-Nzelu, Chukwuemeka G. (36717287000)
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    Abdelhamid, Magdy (57069808700)
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    Adamopoulos, Stamatis (55399885400)
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    Anker, Stefan D. (56223993400)
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    Belenkov, Yuri (7006528098)
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    Gal, Tuvia B. (7003448638)
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    Cohen-Solal, Alain (57189610711)
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    Böhm, Michael (35392235500)
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    Chioncel, Ovidiu (12769077100)
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    Jankowska, Ewa A. (21640520500)
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    Gustafsson, Finn (7005115957)
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    Hill, Loreena (56572076500)
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    Jaarsma, Tiny (56962769200)
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    Januzzi, James L. (7003533511)
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    Jhund, Pardeep (6506826363)
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    Lopatin, Yuri (59263990100)
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    Lund, Lars H. (7102206508)
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    Metra, Marco (7006770735)
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    Milicic, Davor (56503365500)
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    Moura, Brenda (6602544591)
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    Mueller, Christian (57638261900)
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    Mullens, Wilfried (55916359500)
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    Núñez, Julio (57201547451)
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    Piepoli, Massimo F. (7005292730)
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    Rakisheva, Amina (57196007935)
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    Ristić, Arsen D. (7003835406)
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    Rossignol, Patrick (7006015976)
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    Savarese, Gianluigi (36189499900)
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    Tocchetti, Carlo G. (6507913481)
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    van Linthout, Sophie (6602562561)
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    Volterrani, Maurizio (7004062259)
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    Seferovic, Petar (6603594879)
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    Rosano, Giuseppe (7007131876)
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    Coats, Andrew J.S. (35395386900)
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    Emdin, Michele (7005694410)
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    Bayes-Genis, Antoni (7004094140)
    In patients with heart failure, the beneficial effects of drug and device therapies counteract to some extent ongoing cardiac damage. According to the net balance between these two factors, cardiac geometry and function may improve (reverse remodelling, RR) and even completely normalize (remission), or vice versa progressively deteriorate (adverse remodelling, AR). RR or remission predict a better prognosis, while AR has been associated with worsening clinical status and outcomes. The remodelling process ultimately involves all cardiac chambers, but has been traditionally evaluated in terms of left ventricular volumes and ejection fraction. This is the second part of a review paper by the Study Group on Biomarkers of the Heart Failure Association of the European Society of Cardiology dedicated to ventricular remodelling. This document examines the proposed criteria to diagnose RR and AR, their prevalence and prognostic value, and the variables predicting remodelling in patients managed according to current guidelines. Much attention will be devoted to RR in patients with heart failure with reduced ejection fraction because most studies on cardiac remodelling focused on this setting. © 2022 European Society of Cardiology.
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    Congestion in heart failure: a circulating biomarker-based perspective. A review from the Biomarkers Working Group of the Heart Failure Association, European Society of Cardiology
    (2022)
    Núñez, Julio (57201547451)
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    de la Espriella, Rafael (57219980090)
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    Rossignol, Patrick (7006015976)
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    Voors, Adriaan A. (7006380706)
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    Mullens, Wilfried (55916359500)
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    Metra, Marco (7006770735)
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    Chioncel, Ovidiu (12769077100)
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    Januzzi, James L. (7003533511)
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    Mueller, Christian (57638261900)
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    Richards, A. Mark (7402299599)
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    de Boer, Rudolf A. (8572907800)
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    Thum, Thomas (57195743477)
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    Arfsten, Henrike (57192299905)
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    González, Arantxa (57191823224)
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    Abdelhamid, Magdy (57069808700)
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    Adamopoulos, Stamatis (55399885400)
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    Anker, Stefan D. (57783017100)
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    Gal, Tuvia Ben (7003448638)
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    Biegus, Jan (6506094842)
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    Cohen-Solal, Alain (57189610711)
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    Böhm, Michael (35392235500)
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    Emdin, Michele (7005694410)
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    Jankowska, Ewa A. (21640520500)
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    Gustafsson, Finn (7005115957)
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    Hill, Loreena (56572076500)
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    Jaarsma, Tiny (56962769200)
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    Jhund, Pardeep S. (6506826363)
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    Lopatin, Yuri (59263990100)
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    Lund, Lars H. (7102206508)
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    Milicic, Davor (56503365500)
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    Moura, Brenda (6602544591)
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    Piepoli, Massimo F. (7005292730)
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    Ponikowski, Piotr (7005331011)
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    Rakisheva, Amina (57196007935)
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    Ristic, Arsen (7003835406)
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    Savarese, Gianluigi (36189499900)
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    Tocchetti, Carlo G. (6507913481)
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    Van Linthout, Sophie (6602562561)
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    Volterrani, Maurizio (7004062259)
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    Seferovic, Petar (6603594879)
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    Rosano, Giuseppe (7007131876)
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    Coats, Andrew J.S. (35395386900)
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    Bayes-Genis, Antoni (7004094140)
    Congestion is a cardinal sign of heart failure (HF). In the past, it was seen as a homogeneous epiphenomenon that identified patients with advanced HF. However, current evidence shows that congestion in HF varies in quantity and distribution. This updated view advocates for a congestive-driven classification of HF according to onset (acute vs. chronic), regional distribution (systemic vs. pulmonary), compartment of distribution (intravascular vs. extravascular), and clinical vs. subclinical. Thus, this review will focus on the utility of circulating biomarkers for assessing and managing the different fluid overload phenotypes. This discussion focused on the clinical utility of the natriuretic peptides, carbohydrate antigen 125 (also called mucin 16), bio-adrenomedullin and mid-regional pro-adrenomedullin, ST2 (also known as interleukin-1 receptor-like 1), cluster of differentiation 146, troponin, C-terminal pro-endothelin-1, and parameters of haemoconcentration. The utility of circulation biomarkers on top of clinical evaluation, haemodynamics, and imaging needs to be better determined by dedicated studies. Some multiparametric frameworks in which these tools contribute to management are proposed. © 2022 European Society of Cardiology.
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    Head-to-head comparison between recommendations by the ESC and ACC/AHA/HFSA heart failure guidelines
    (2022)
    Bayés-Genís, Antoni (7004094140)
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    Aimo, Alberto (56112889900)
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    Metra, Marco (7006770735)
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    Anker, Stefan (56223993400)
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    Seferovic, Petar (6603594879)
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    Rapezzi, Claudio (7005883289)
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    Castiglione, Vincenzo (57200260361)
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    Núñez, Julio (57201547451)
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    Emdin, Michele (7005694410)
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    Rosano, Giuseppe (7007131876)
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    Coats, Andrew J.S. (35395386900)
    Recommendations represent the core messages of guidelines, and are particularly important when the body of scientific evidence is rapidly growing, as in the case of heart failure (HF). The main messages from two latest major HF guidelines, endorsed by the European Society of Cardiology (ESC) and the American College of Cardiology/American Heart Association/Heart Failure Society of America (ACC/AHA/HFSA), are partially overlapping, starting from the four pillars of treatment for HF with reduced ejection fraction. Some notable differences exist, in part related to the timing of recent publications (most notably, the Universal Definition of HF paper and the EMPEROR-Preserved trial), and in part reflecting differing views of the natural history of HF (with a clear differentiation between stages A and B HF in the ACC/AHA/HFSA guidelines). Different approaches are proposed to specific issues such as risk stratification and implantable cardioverter defibrillator use for primary prevention in HFrEF patients with non-ischaemic aetiology. The ACC/AHA/HFSA guidelines put a greater emphasis on some issues that are particularly relevant to the US setting, such as the cost-effectiveness of therapies and the impact of health disparities on HF care. A comparison between guideline recommendations may give readers a deeper understanding of the ESC and ACC/AHA/HFSA guidelines, and help them apply sensible approaches to their own practice, wherever that may be in the world. A comparison may possibly also help further harmonization of recommendations between future guidelines, by identifying why some areas have led to conflicting recommendation, even when ostensibly reviewing the same published evidence. © 2022 European Society of Cardiology.
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    Integration of imaging and circulating biomarkers in heart failure: a consensus document by the Biomarkers and Imaging Study Groups of the Heart Failure Association of the European Society of Cardiology
    (2021)
    Moura, Brenda (6602544591)
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    Aimo, Alberto (56112889900)
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    Al-Mohammad, Abdallah (57191218762)
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    Flammer, Andreas (13007159300)
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    Barberis, Vassilis (55890808700)
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    Bayes-Genis, Antoni (7004094140)
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    Brunner-La Rocca, Hans-Peter (7003352089)
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    Fontes-Carvalho, Ricardo (23097322300)
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    Grapsa, Julia (57204441798)
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    Hülsmann, Martin (7006719269)
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    Ibrahim, Nasrien (56392489500)
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    Knackstedt, Christian (6506839019)
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    Januzzi, James L. (7003533511)
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    Lapinskas, Tomas (57203632017)
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    Sarrias, Axel (55624945200)
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    Matskeplishvili, Simon (6602403114)
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    Meijers, Wouter C. (56085653000)
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    Messroghli, Daniel (6603344046)
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    Mueller, Christian (57638261900)
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    Pavo, Noemi (14065082800)
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    Simonavičius, Justas (57188701168)
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    Teske, Arco J. (22235274900)
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    van Kimmenade, Roland (6508222707)
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    Seferovic, Petar (6603594879)
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    Coats, Andrew J.S. (35395386900)
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    Emdin, Michele (7005694410)
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    Richards, A. Mark (7402299599)
    Circulating biomarkers and imaging techniques provide independent and complementary information to guide management of heart failure (HF). This consensus document by the Heart Failure Association (HFA) of the European Society of Cardiology (ESC) presents current evidence-based indications relevant to integration of imaging techniques and biomarkers in HF. The document first focuses on application of circulating biomarkers together with imaging findings, in the broad domains of screening, diagnosis, risk stratification, guidance of treatment and monitoring, and then discusses specific challenging settings. In each section we crystallize clinically relevant recommendations and identify directions for future research. The target readership of this document includes cardiologists, internal medicine specialists and other clinicians dealing with HF patients. © 2021 European Society of Cardiology
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    The ‘Peptide for Life’ Initiative: a call for action to provide equal access to the use of natriuretic peptides in the diagnosis of acute heart failure across Europe
    (2021)
    Bayes-Genis, Antoni (7004094140)
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    Januzzi, James L. (7003533511)
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    Richards, A. Mark (7402299599)
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    Arfsten, Henrike (57192299905)
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    de Boer, Rudolf A. (8572907800)
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    Emdin, Michele (7005694410)
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    González, Arantxa (57191823224)
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    Jaarsma, Tiny (56962769200)
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    Jhund, Pardeep S. (6506826363)
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    Mueller, Christian (57638261900)
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    Núñez, Julio (57201547451)
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    Rossignol, Patrick (7006015976)
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    Milinkovic, Ivan (51764040100)
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    Rosano, Giuseppe M.C. (7007131876)
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    Coats, Andrew (35395386900)
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    Seferovic, Petar (6603594879)
    [No abstract available]
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    Treatment of cardiac transthyretin amyloidosis: An update
    (2019)
    Emdin, Michele (7005694410)
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    Aimo, Alberto (56112889900)
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    Rapezzi, Claudio (7005883289)
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    Fontana, Marianna (16306839900)
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    Perfetto, Federico (7006428492)
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    Seferović, Petar M (6603594879)
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    Barison, Andrea (24597524200)
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    Castiglione, Vincenzo (57200260361)
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    Vergaro, Giuseppe (23111620200)
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    Giannoni, Alberto (24490709200)
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    Passino, Claudio (56868372700)
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    Merlini, Giampaolo (7006059649)
    Transthyretin (TTR) is a tetrameric protein synthesized mostly by the liver. As a result of gene mutations or as an ageing-related phenomenon, TTR molecules may misfold and deposit in the heart and in other organs as amyloid fibrils. Cardiac involvement in TTR-related amyloidosis (ATTR) manifests typically as left ventricular pseudohypertrophy and/or heart failure with preserved ejection fraction. ATTR is an underdiagnosed disorder as well as a crucial determinant of morbidity and mortality, thus justifying the current quest for a safe and effective treatment. Therapies targeting cardiac damage and its direct consequences may yield limited benefit, mostly related to dyspnoea relief through diuretics. For many years, liver or combined heart and liver transplantation have been the only available treatments for patients with mutations causing ATTR, including those with cardiac involvement. The therapeutic options now include several pharmacological agents that inhibit hepatic synthesis of TTR, stabilize the tetramer, or disrupt fibrils. Following the positive results of a phase 3 trial on tafamidis, and preliminary findings on patisiran and inotersen in patients with ATTR-related neuropathy and cardiac involvement, we provide an update on this rapidly evolving field, together with practical recommendations on the management of cardiac involvement. © 2019 Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2019. For permissions, please email: journals.permissions@oup.com.

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