Simple risk models to predict cardiovascular death in patients with stable coronary artery disease

Author:

Ford Ian1ORCID,Robertson Michele1,Greenlaw Nicola1,Bauters Christophe2,Lemesle Gilles2,Sorbets Emmanuel34567ORCID,Ferrari Roberto8,Tardif Jean-Claude9ORCID,Tendera Michal10,Fox Kim34ORCID,Steg Philippe Gabriel3456,

Affiliation:

1. Robertson Centre for Biostatistics, University of Glasgow, Level 11, Boyd Orr Building, Glasgow G12 8QQ, UK

2. Cardiology Department, Institut Coeur Poumon, CHU, Université de Lille, Bd du Professeur Jules Leclercq, 59000 Lille, France

3. National Heart and Lung Institute, Imperial College, Dovehouse Street London SW3 6LY, UK

4. Royal Brompton Hospital, Sydney St, London SW3 6NP, UK

5. FACT (French Alliance for Cardiovascular Trials), Université de Paris, and AP-HP, Hopital Bichat, INSERM U1148, 46 rue Henri Huchard 75018 Paris, France

6. Université de Paris 13, Sorbonne Paris Cité, AP-HP, Hôpital Avicenne, Bobigny, France

7. Université de Paris, AP-HP, Hôtel-Dieu, Centre de Diagnostic et de thérapeutique, 1 rue de la Cité, 75004 Paris, France

8. Centro Cardiologico Universitario di Ferrara, University of Ferrara, Maria Cecilia Hospital, GVM Care & Research, Via Corriera, 1 48010 Cotignola, Ravenna, Italy

9. Montreal Heart Institute, 5000 Belanger Street, Montreal, H1T1C8, Université de Montréal, Canada

10. Department of Cardiology and Structural Heart Disease, Medical School in Katowice, Medical University of Silesia, Ziolowa Str. 45/47, 40-635 Katowice, Poland

Abstract

Abstract Aims Risk estimation is important to motivate patients to adhere to treatment and to identify those in whom additional treatments may be warranted and expensive treatments might be most cost effective. Our aim was to develop a simple risk model based on readily available risk factors for patients with stable coronary artery disease (CAD). Methods and results Models were developed in the CLARIFY registry of patients with stable CAD, first incorporating only simple clinical variables and then with the inclusion of assessments of left ventricular function, estimated glomerular filtration rate, and haemoglobin levels. The outcome of cardiovascular death over ∼5 years was analysed using a Cox proportional hazards model. Calibration of the models was assessed in an external study, the CORONOR registry of patients with stable coronary disease. We provide formulae for calculation of the risk score and simple integer points-based versions of the scores with associated look-up risk tables. Only the models based on simple clinical variables provided both good c-statistics (0.74 in CLARIFY and 0.80 or over in CORONOR), with no lack of calibration in the external dataset. Conclusion Our preferred model based on 10 readily available variables [age, diabetes, smoking, heart failure (HF) symptom status and histories of atrial fibrillation or flutter, myocardial infarction, peripheral arterial disease, stroke, percutaneous coronary intervention, and hospitalization for HF] had good discriminatory power and fitted well in an external dataset. Study registration The CLARIFY registry is registered in the ISRCTN registry of clinical trials (ISRCTN43070564).

Funder

RHU iVASC

French National Research Agency

Fédération Française de Cardiologie

Servier

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Health Policy

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