Impact of the 2021 European Society for Cardiology prevention guideline’s stepwise approach for cardiovascular risk factor treatment in patients with established atherosclerotic cardiovascular disease

Author:

Holtrop Joris1ORCID,Bhatt Deepak L2ORCID,Ray Kausik K3,Mach François4,Smulders Yvo M5,Carballo David4ORCID,Steg Philippe Gabriel6,Visseren Frank L J1,Dorresteijn Jannick A N1ORCID

Affiliation:

1. Department of Vascular Medicine, University Medical Centre Utrecht , Heidelberglaan 100, Utrecht, 3584 CX , The Netherlands

2. Mount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai Health System , New York, NY , USA

3. Imperial Centre for Cardiovascular Disease Prevention, ICTU-Global, Imperial College London , London , UK

4. Division of Cardiology, Faculty of Medicine, Geneva University Hospitals , Geneva , Switzerland

5. Department of Internal Medicine, VU University Medical Center , Amsterdam , The Netherlands

6. Department of Cardiology, Université Paris-Cité, FACT (French Alliance for Cardiovascular Trials) NSERM1148/LVTS, AP-HP, Hôpital Bichat , Paris , France

Abstract

Abstract Aims This study aimed to evaluate the stepwise approach for cardiovascular (CV) risk factor treatment as outlined by the European Society for Cardiology 2021 guidelines on CV disease (CVD) prevention in patients with established atherosclerotic CVD (ASCVD). Methods and results In patients with ASCVD, included in UCC-SMART (n = 8730) and European parts of the REACH registry (n = 18 364), the 10-year CV risk was estimated using SMART2. Treatment effects were derived from meta-analyses and trials. Step 1 recommendations were LDL cholesterol (LDLc) < 1.8 mmol/L, systolic blood pressure (SBP) < 140 mmHg, using any antithrombotic medication, sodium–glucose co-transporter 2 (SGLT2) inhibition, and smoking cessation. Step 2 recommendations were LDLc < 1.4 mmol/L, SBP < 130 mmHg, dual-pathway inhibition (DPI, aspirin plus low-dose rivaroxaban), colchicine, glucagon-like peptide (GLP)-1 receptor agonists, and eicosapentaenoic acid. Step 2 was modelled accounting for Step 1 non-attainment. With current treatment, residual CV risk was 22%, 32%, and 60% in the low, moderate, and pooled (very) high European risk regions, respectively. Step 2 could prevent up to 198, 223 and 245 events per 1000 patients treated, respectively. Intensified LDLc reduction, colchicine, and DPI could be applied to most patients, preventing up to 57, 74, and 59 events per 1000 patients treated, respectively. Following Step 2, the number of patients with a CV risk of <10% could increase from 20%, 6.4%, and 0.5%, following Step 1, to 63%, 48%, and 12%, in the respective risk regions. Conclusion With current treatment, residual CV risk in patients with ASCVD remains high across all European risk regions. The intensified Step 2 treatment options result in marked further reduction of residual CV risk in patients with established ASCVD. Key findings Guideline-recommended intensive treatment of patients with cardiovascular disease could prevent additional 198–245 new cardiovascular events for every 1000 patients treated.

Funder

University Medical Centre Utrecht

Sanofi-Aventis and Bristol-Myers Squibb

World Heart Federation

Publisher

Oxford University Press (OUP)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Editorial comments: focus on cardiovascular risk estimation and prevention;European Journal of Preventive Cardiology;2024-04

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