European Physician Survey Characterizing the Clinical Pathway and Treatment Patterns of Patients Post-Myocardial Infarction.


Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 16 08 2022
accepted: 29 09 2022
pubmed: 27 10 2022
medline: 25 1 2023
entrez: 26 10 2022
Statut: ppublish

Résumé

The 2019 European Society of Cardiology and European Atherosclerosis Society (2019 ESC/EAS) guidelines stress the importance of managing low-density lipoprotein cholesterol (LDL-C) after myocardial infarction (MI) to reduce the risk of cardiovascular events. Information on guideline implementation is limited. The aim of this survey was to describe current clinical practice regarding LDL-C management in the first year post-MI across Europe, improving understanding of the role of ESC/EAS guidelines on clinical practice. A qualitative web-based cross-sectional physician survey about the patient pathway and LDL-C management post-MI was conducted in 360 physicians from France, Italy, Germany, The Netherlands, Spain, and the UK (n = 60/country) between December 2019 and June 2020. Secondary and primary care physicians (SCPs/PCPs) described their experiences treating patients post-MI over the preceding 2 months. Physicians reported that on average 90.7% of patients not prescribed lipid-lowering therapy (LLT) before an MI initiated LLT as inpatients; for patients already taking LLT, treatment was intensified for 64.7% of inpatients post-MI. SCPs reported prescribing higher-intensity statins and/or ezetimibe for between 72.3% (Italy) and 88.6% (UK) of patients post-MI. More than 80.0% of SCPs and 51.2% of PCPs stated that they would initiate a change in LLT immediately if patients did not achieve their LDL-C treatment goal by 12 weeks post-MI; 82.0% of SCPs and 55.1% of PCPs reported referring to 2019 ESC/EAS guidelines for management of patients post-MI. Barriers to initiating PCSK9 inhibitors (PCSK9is) included prior prescription of a maximally tolerated dose of statin (49.4%) and/or ezetimibe (38.9%), requirement to reach threshold LDL-C levels (44.9%), and pre-authorization requirements (30.4%). Differences in clinical practice post-MI were reported across the countries surveyed, including divergence between 2019 ESC/EAS and local guidelines. Increased use of innovative medicines to achieve LDL-C goals should reduce risk of subsequent cardiovascular events in very high-risk patients post-MI.

Identifiants

pubmed: 36289145
doi: 10.1007/s12325-022-02344-6
pii: 10.1007/s12325-022-02344-6
pmc: PMC9859915
doi:

Substances chimiques

Anticholesteremic Agents 0
Cholesterol, LDL 0
Ezetimibe EOR26LQQ24
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Types de publication

Journal Article

Langues

eng

Pagination

233-251

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

Nadeem Qureshi (N)

University of Nottingham, Nottingham, UK.

Sotiris Antoniou (S)

Barts Health NHS Trust, London, UK.

Jan H Cornel (JH)

Radboud University Medical Center, Nijmegen, The Netherlands.

Francois Schiele (F)

Regional University Hospital Jean Minjoz, Besancon, France.

Pasquale Perrone-Filardi (P)

Department of Advanced Biomedical Sciences, Federico II University and Mediterranea Cardiocentro, Naples, Italy.

Johannes Brachmann (J)

REGIOMED-KLINIKEN, Coburg, Germany.

Eduard Sidelnikov (E)

Amgen (Europe) GmbH, Suurstoffi 22, 6343, Rotkreuz, Switzerland. eduards@amgen.com.

Guillermo Villa (G)

Amgen (Europe) GmbH, Suurstoffi 22, 6343, Rotkreuz, Switzerland.

Samara Ferguson (S)

PRMA Consulting, Fleet, UK.

Christina Rowlands (C)

PRMA Consulting, Fleet, UK.

José R González-Juanatey (JR)

Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, CIBERCV, Santiago, Spain.

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