Multidisciplinary evaluation and management of obstructive hypertrophic cardiomyopathy in 2020: Towards the HCM Heart Team.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 04 2020
Historique:
received: 05 01 2020
accepted: 10 01 2020
pubmed: 28 1 2020
medline: 15 5 2021
entrez: 28 1 2020
Statut: ppublish

Résumé

Patients with hypertrophic cardiomyopathy (HCM) exhibit a variable phenotype with ventricular hypertrophy as the cardinal manifestation and left ventricular (LV) outflow tract obstruction (LVOTO) as a key pathophysiologic determinant. Patients with severe LVOTO usually present with exertional dyspnea, exertional syncope, and heart failure symptoms, while successful relief of LVOTO by pharmacological or invasive interventions leads to a dramatic improvement in clinical status. Proper management of obstructive HCM remains challenging and poses numerous clinical dilemmas. Since the development of surgical myectomy over half a century ago, progress in the management of LVOTO in HCM has paralleled technological advances in genetic testing, cardiac imaging, arrhythmic prophylaxis, cardiac surgery and interventional cardiology. These changes have been incorporated in dedicated scientific guidelines on both sides of the Atlantic. However, either the 2011 American guidelines or the 2014 European guidelines remain largely based on expert consensus for lack of recommendations with level of evidence A regarding any of the treatment options commonly employed in HCM. Consequently, management of obstructive HCM patients remains largely subjective and dependent on clinical judgment, local expertise, and patient preference. Following the trend that has emerged for other cardiac diseases amenable to invasive interventions, adequate evaluation and management of obstruction in HCM today requires a multidisciplinary team capable of optimizing referral, choosing the best available options, minimizing complications and ensuring state-of-the-art results. The concept of an HCM Heart Team is coming of age. This review aims to provide an update of available pharmacologic and invasive options for the management of LVOTO in HCM, either in adulthood or in childhood, highlighting areas for multidisciplinary integration and future development.

Identifiants

pubmed: 31983465
pii: S0167-5273(20)30095-4
doi: 10.1016/j.ijcard.2020.01.021
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

86-92

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Francesco Pelliccia (F)

Department of Cardiovascular Sciences, University Sapienza of Rome, Rome, Italy. Electronic address: f.pelliccia@mclink.it.

Ottavio Alfieri (O)

Department of Cardiovascular and Thoracic Surgery, San Raffaele University Hospital, Milan, Italy.

Paolo Calabrò (P)

Division of Cardiology, A.O.R.N. 'Sant'Anna e San Sebastiano', Caserta, Italy; Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.

Franco Cecchi (F)

IRCCS Istituto Auxologico Italiano, Department of Cardiovascular, Neural and Metabolic Sciences, San Luca Hospital, Milan, Italy.

Paolo Ferrazzi (P)

Hypertrophic Cardiomyopathy Center, Policlinico di Monza, Monza, Italy.

Felice Gragnano (F)

Division of Cardiology, A.O.R.N. 'Sant'Anna e San Sebastiano', Caserta, Italy; Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.

Juan Pablo Kaski (JP)

Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital, University College London Institute of Cardiovascular Science, London, UK.

Giuseppe Limongelli (G)

Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy; Institute of Cardiovascular Sciences, University College of London, St. Bartholomew's Hospital, London, UK.

Martin Maron (M)

Hypertrophic Cardiomyopathy Center, Division of Cardiology, Tufts Medical Center, Boston, MA, USA.

Claudio Rapezzi (C)

Cardiology, University of Ferrara & Maria Cecilia Hospital, GVM Care and Research, Cotignola, Italy.

Hubert Seggewiss (H)

Klinikum Würzburg Mitte - Standort Juliusspital, Würzburg, Germany.

Magdi H Yacoub (MH)

Heart Science Centre, National Heart and Lung Institute, Imperial College London, London, UK.

Iacopo Olivotto (I)

Cardiomyopathy Unit, Careggi University Hospital, Florence, Italy.

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Classifications MeSH