Comprehensive comparison of stroke risk score performance: a systematic review and meta-analysis among 6 267 728 patients with atrial fibrillation

Author:

van der Endt Vera H W1ORCID,Milders Jet1ORCID,Penning de Vries Bas B L1ORCID,Trines Serge A2ORCID,Groenwold Rolf H H1ORCID,Dekkers Olaf M1ORCID,Trevisan Marco3ORCID,Carrero Juan J3ORCID,van Diepen Merel1ORCID,Dekker Friedo W1ORCID,de Jong Ype14ORCID

Affiliation:

1. Department of Clinical Epidemiology, Leiden University Medical Center , PO Box 9600, 2333 ZA Leiden , The Netherlands

2. Department of Cardiology, Willem Einthoven Center of Arrhythmia Research and Management, Leiden University Medical Center , 2333 ZA Leiden , The Netherlands

3. Department of Medical Epidemiology and Biostatistics (MEB), Karolinska Institutet , 171 77 Stockholm , Sweden

4. Department of Internal Medicine, Leiden University Medical Center , 2333 ZA Leiden , The Netherlands

Abstract

Abstract Aims Multiple risk scores to predict ischaemic stroke (IS) in patients with atrial fibrillation (AF) have been developed. This study aims to systematically review these scores, their validations and updates, assess their methodological quality, and calculate pooled estimates of the predictive performance. Methods and results We searched PubMed and Web of Science for studies developing, validating, or updating risk scores for IS in AF patients. Methodological quality was assessed using the Prediction model Risk Of Bias ASsessment Tool (PROBAST). To assess discrimination, pooled c-statistics were calculated using random-effects meta-analysis. We identified 19 scores, which were validated and updated once or more in 70 and 40 studies, respectively, including 329 validations and 76 updates—nearly all on the CHA2DS2-VASc and CHADS2. Pooled c-statistics were calculated among 6 267 728 patients and 359 373 events of IS. For the CHA2DS2-VASc and CHADS2, pooled c-statistics were 0.644 [95% confidence interval (CI) 0.635–0.653] and 0.658 (0.644–0.672), respectively. Better discriminatory abilities were found in the newer risk scores, with the modified-CHADS2 demonstrating the best discrimination [c-statistic 0.715 (0.674–0.754)]. Updates were found for the CHA2DS2-VASc and CHADS2 only, showing improved discrimination. Calibration was reasonable but available for only 17 studies. The PROBAST indicated a risk of methodological bias in all studies. Conclusion Nineteen risk scores and 76 updates are available to predict IS in patients with AF. The guideline-endorsed CHA2DS2-VASc shows inferior discriminative abilities compared with newer scores. Additional external validations and data on calibration are required before considering the newer scores in clinical practice. Clinical trial registration ID CRD4202161247 (PROSPERO).

Funder

Dutch Kidney Foundation

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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