Transcatheter interventions for left-sided valvular heart disease complicated by cardiogenic shock: a consensus statement from the European Association of Percutaneous Cardiovascular Interventions (EAPCI) in collaboration with the Association for Acute Cardiovascular Care (ACVC) and the ESC Working Group on Cardiovascular Surgery
- PMID: 37624587
- PMCID: PMC10587846
- DOI: 10.4244/EIJ-D-23-00473
Transcatheter interventions for left-sided valvular heart disease complicated by cardiogenic shock: a consensus statement from the European Association of Percutaneous Cardiovascular Interventions (EAPCI) in collaboration with the Association for Acute Cardiovascular Care (ACVC) and the ESC Working Group on Cardiovascular Surgery
Abstract
Valvular heart disease (VHD) is one of the most frequent causes of heart failure (HF) and is associated with poor prognosis, particularly among patients with conservative management. The development and improvement of catheter-based VHD interventions have broadened the indications for transcatheter valve interventions from inoperable/high-risk patients to younger/lower-risk patients. Cardiogenic shock (CS) associated with severe VHD is a clinical condition with a very high risk of mortality for which surgical treatment is often deemed a prohibitive risk. Transcatheter valve interventions might be a promising alternative in this setting given that they are less invasive. However, supportive scientific evidence is scarce and often limited to small case series. Current guidelines on VHD do not contain specific recommendations on how to manage patients with both VHD and CS. The purpose of this clinical consensus statement, developed by a group of international experts invited by the European Association of Percutaneous Cardiovascular Interventions (EAPCI) Scientific Documents and Initiatives Committee, is to perform a review of the available scientific evidence on the management of CS associated with left-sided VHD and to provide a rationale and practical approach for the application of transcatheter valve interventions in this specific clinical setting.
Conflict of interest statement
N. Bonaros reports grants from Edwards Lifesciences and Corcym; and lecture fees from Edwards Lifesciences and Medtronic. P. Carrilho-Ferreira reports lecture fees from AstraZeneca, A. Menarini Diagnostics, Bayer, Biotronik, Medinfar, and Medtronic; and serves on an advisory board for Medtronic. M. Czerny is a consultant for Terumo Aortic, Medtronic, Endospan, and NEOS; and is a shareholder of TEVAR Ltd and Ascense Medical. C. Fraccaro reports support for attending meetings from Medtronic. C. Hassager reports research grants from the Novo Nordisk Foundation and the Lundbeck Foundation; and lecture honorarium from Abiomed. N. Karam reports consulting and lecture fees from Medtronic, Edwards Lifesciences, and Abbott Vascular. W-K. Kim reports lecture fees and honoraria from Abbott, Boston Scientific, Meril Life Sciences, Edwards Lifesciences, Medtronic, and Shockwave Medical. K.A. Krychtiuk reports lecture and/or consulting fees from Amgen, Novartis, and Sanofi. H. Möllmann received speaker honoraria/proctor fees from Abbott, Boston Scientific, Edwards Lifesciences, and Medtronic. J. Pręgowski reports lecture fees from Abbott and Edwards Lifesciences; and contracts from Abbott. G. Tarantini reports lecture fees from Medtronic, Edwards Lifesciences, Abbott Vascular, Boston Scientific, GADA, and Abiomed. J. Ternacle reports consulting fees from Abbott, GE HealthCare, and Philips; and lecture fees from Edwards Lifesciences. The other authors have no conflicts of interest to declare.
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