Physician perceptions, attitudes, and strategies towards implementing guideline-directed medical therapy in heart failure with reduced ejection fraction. A survey of the Heart Failure Association of the ESC and the ESC Council for Cardiology Practice.

Guideline‐directed medical therapy Heart failure with reduced ejection fraction Treatment implementation

Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
22 Mar 2024
Historique:
revised: 14 02 2024
received: 13 01 2024
accepted: 13 03 2024
medline: 22 3 2024
pubmed: 22 3 2024
entrez: 22 3 2024
Statut: aheadofprint

Résumé

Recent guidelines recommend four core drug classes (renin-angiotensin system/angiotensin receptor-neprilysin inhibitor [RASi/ARNi], beta-blocker, mineralocorticoid receptor antagonist [MRA], and sodium-glucose cotransporter 2 inhibitor [SGLT2i]) for the pharmacological management of heart failure (HF) with reduced ejection fraction (HFrEF). We assessed physicians' perceived (i) comfort with implementing the recent HFrEF guideline recommendations; (ii) status of guideline-directed medical therapy (GDMT) implementation; (iii) use of different GDMT sequencing strategies; and (iv) barriers and strategies for achieving implementation. A 26-question survey was disseminated via bulletin, e-mail and social channels directed to physicians with an interest in HF. Of 432 respondents representing 91 countries, 36% were female, 52% were aged <50 years, and 90% mainly practiced in cardiology (30% HF). Overall comfort with implementing quadruple therapy was high (87%). Only 12% estimated that >90% of patients with HFrEF without contraindications received quadruple therapy. The time required to initiate quadruple therapy was estimated at 1-2 weeks by 34% of respondents, 1 month by 36%, 3 months by 24%, and ≥6 months by 6%. The average respondent favoured traditional drug sequencing strategies (RASi/ARNi with/followed by beta-blocker, and then MRA with/followed by SGLT2i) over simultaneous initiation or SGLT2i-first sequences. The most frequently perceived clinical barriers to implementation were hypotension (70%), creatinine increase (47%), hyperkalaemia (45%) and patient adherence (42%). Although comfort with implementing all four core drug classes in patients with HFrEF was high among physicians, a majority estimated implementation of GDMT in HFrEF to be low. We identified several important perceived clinical and non-clinical barriers that can be targeted to improve implementation.

Identifiants

pubmed: 38515385
doi: 10.1002/ejhf.3214
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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Auteurs

Gianluigi Savarese (G)

Division of Cardiology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Heart, Vascular and Neuro Theme, Karolinska University Hospital, Stockholm, Sweden.

Felix Lindberg (F)

Division of Cardiology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

Ruxandra M Christodorescu (RM)

Department V Internal Medicine, University of Medicine and Pharmacy V. Babes Timisoara, Institute of Cardiology Research Center, Timișoara, Romania.

Marc Ferrini (M)

Department of Cardiology and Vascular Pathology, CH Saint Joseph and Saint Luc, Lyon, France.

Thomas Kumler (T)

Department of Cardiology, Herlev-Gentofte University Hospital, Copenhagen, Denmark.
Steno Diabetes Center Copenhagen, Denmark.

Konstantinos Toutoutzas (K)

First Department of Cardiology, Medical School, National and Kapodistrian University of Athens, 'Hippokration' General Hospital of Athens, Athens, Greece.

Giuseppe Dattilo (G)

Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.

Antoni Bayes-Genis (A)

Institut del Cor, Hospital Universitari Germans Trias I Pujol, Barcelona, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV; Departamento de Medicina, Universitat Autònoma de Barcelona), Barcelona, Spain.

Brenda Moura (B)

Armed Forces Hospital, Faculty of Medicine of the University of Porto, Porto, Portugal.

Offer Amir (O)

Heart Institute, Hadassah Medical Center & Faculty of Medicine, Hebrew University, Jerusalem, Israel.

Mark C Petrie (MC)

Institute of Cardiovascular and Medical Sciences, The University Court of the University of Glasgow, Glasgow, UK.

Petar Seferovic (P)

University Medical Center, Medical Faculty University of Belgrade, Serbian Academy of Sciences and Arts, Belgrade, Serbia.

Ovidiu Chioncel (O)

Emergency Institute for Cardiovascular Diseases 'Prof. C.C. Iliescu', Bucharest, Romania.
University of Medicine Carol Davila, Bucharest, Romania.

Marco Metra (M)

Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.

Andrew J S Coats (AJS)

Heart Research Institute, Sydney, Australia.

Giuseppe M C Rosano (GMC)

Cardiovascular Clinical Academic Group, St George's University Hospital, London, UK.
Cardiology, IRCCS San Raffaele, Rome, Italy.

Classifications MeSH