Optimizing outcomes in heart failure: 2022 and beyond
- PMID: 37060168
- PMCID: PMC10375115
- DOI: 10.1002/ehf2.14363
Optimizing outcomes in heart failure: 2022 and beyond
Abstract
Although the development of therapies and tools for the improved management of heart failure (HF) continues apace, day-to-day management in clinical practice is often far from ideal. A Cardiovascular Round Table workshop was convened by the European Society of Cardiology (ESC) to identify barriers to the optimal implementation of therapies and guidelines and to consider mitigation strategies to improve patient outcomes in the future. Key challenges identified included the complexity of HF itself and its treatment, financial constraints and the perception of HF treatments as costly, failure to meet the needs of patients, suboptimal outpatient management, and the fragmented nature of healthcare systems. It was discussed that ongoing initiatives may help to address some of these barriers, such as changes incorporated into the 2021 ESC HF guideline, ESC Heart Failure Association quality indicators, quality improvement registries (e.g. EuroHeart), new ESC guidelines for patients, and the universal definition of HF. Additional priority action points discussed to promote further improvements included revised definitions of HF 'phenotypes' based on trial data, the development of implementation strategies, improved affordability, greater regulator/payer involvement, increased patient education, further development of patient-reported outcomes, better incorporation of guidelines into primary care systems, and targeted education for primary care practitioners. Finally, it was concluded that overarching changes are needed to improve current HF care models, such as the development of a standardized pathway, with a common adaptable digital backbone, decision-making support, and data integration, to ensure that the model 'learns' as the management of HF continues to evolve.
Keywords: Clinical practice guidelines; Health technology assessment; Heart failure; Medical decision making; Multidisciplinary management; Pharmacotherapy; Quality improvement.
© 2023 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
Conflict of interest statement
E.A.J., L.H., W.M., C.M., F.K., M.V., and U.S. report no disclosures. T.A. is a full‐time employee of AstraZeneca. C.K.‐A. is an employee of MSD Sharp & Dohme GmbH who owns stock/holds stock options in Merck & Co., Inc., Rahway, NJ, USA. B.B. has received consulting fees from AstraZeneca, Amgen, scPharmaceuticals, Baxter Healthcare Corporation, and Sanofi‐Aventis and serves on the clinical event committee for Abbott, the data safety monitoring committee for LivaNova and Cardurion, and steering committees for Relypsa (Care‐HK trial). O.C. reports support from Boehringer Ingelheim. A.J.S.C. declares no conflicts related to this work. Outside of this work, in the last 3 years, A.J.S.C. declares having received honoraria and/or lecture fees from AstraZeneca, Boehringer Ingelheim, Menarini, Novartis, Servier, Vifor Pharma, Abbott, Actimed, Arena, Cardiac Dimensions, Corvia, CVRx, Enopace, ESN Cleer, Faraday, Impulse Dynamics, Respicardia, and Viatris. L.H.L. reports receiving grants from AstraZeneca, Vifor Pharma, Boston Scientific, Boehringer Ingelheim, and Novartis; consulting fees from Merck, Vifor Pharma, AstraZeneca, Bayer, Pharmacosmos, Medscape, Sanofi, Lexicon, MyoKardia, Boehringer Ingelheim, and Servier; speaker's honoraria from Abbott, Medscape, Radcliffe Cardiology, AstraZeneca, and Novartis; and stock ownership in AnaCardio. T.M. has received honoraria in the last year for advisory boards for Bayer, Boehringer Ingelheim, and Eli Lilly. M.M. received personal fees of minimal amounts in the last 3 years from Actelion, Amgen, LivaNova, Servier, and Vifor Pharma as a member of executive or data monitoring committees of sponsored clinical trials and from AstraZeneca, Abbott Vascular, Bayer, Boehringer Ingelheim, and Edwards Therapeutics for participation at advisory boards and/or speeches at sponsored meetings. S.D.S. has received research grants from Actelion, Alnylam, Amgen, AstraZeneca, Bellerophon, Bayer, BMS, Celladon, Cytokinetics, Eidos, Gilead, GSK, Ionis, Lilly, Mesoblast, MyoKardia, NIH/NHLBI, NeuroTronik, Novartis, Novo Nordisk, Respicardia, Sanofi Pasteur, Theracos, and Us2.ai and has consulted for Abbott, Action, Akros, Alnylam, Amgen, Arena, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, Cardior, Cardurion, Corvia, Cytokinetics, Daiichi Sankyo, GSK, Lilly, Merck, MyoKardia, Novartis, Roche, Theracos, Quantum Genomics, Janssen, Cardiac Dimensions, Tenaya, Sanofi Pasteur, Dinaqor, Tremeau, CellProthera, Moderna, American Regent, Sarepta, Lexicon, AnaCardio, Akros, and PureTech Health. J.J.V.M. has received payments through the University of Glasgow from work on clinical trials, consulting, and other activities from Alnylam, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, BMS, Cardurion, Cytokinetics, DalCor, GSK, Ionis, KBP Biosciences, Novartis, Pfizer, and Theracos and received personal lecture fees from the Corpus, Abbott, Hikma, Sun Pharmaceutical, Medscape/Heart.Org, Radcliffe Cardiology, Servier Director, and Global Clinical Trial Partners (GCTP).
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