Augmenting Atrial Fibrillation Risk Prediction Tools – How Does Risk Differ by Prior Stroke Type?
Author(s)
Ciminata G1, Quinn T2, Venson R2, Trotter R3, Pollock KG4, Lister S5, Geue C2
1University of Glasgow, Glasgow, GLG, UK, 2University of Glasgow, Glasgow, UK, 3Pfizer UK, Surrey, UK, 4Bristol Myers Squibb, Uxbridge, UK, 5Bristol-Myers Squibb, Uxbridge, UK
Presentation Documents
OBJECTIVES: To augment the AF risk prediction tools CHA2DS2-VASc and HAS-BLED by adding more detail regarding the stroke event while maintaining the scoring structure of the original scale
METHODS: We linked individual-level hospital and prescribing datasets for all adult patients in Scotland with incident AF (2009 -2017.) Based on presumed differential risk, for CHA2DS2-VASc, we assigned ischaemic stroke two points, TIA one point, and haemorrhage zero points. For HAS-BLED we assigned haemorrhage two points, ischaemic stroke one point, and TIA zero points. We compared prognostic utility of original and augmented tools against outcomes of stroke, bleeding, mortality, and care home admission using discrimination and calibration plots.
RESULTS: We included 117,749 people with AF: mean age 73 years (SD:12.7), 48% female. Original and augmented tools performed similarly, for CHA2DS2-VASc prediction of stroke, AUC original:0.56 (95%CI:0.56-0.57), AUC augmented:0.57 (95%CI:0.56-0.57). For HAS-BLED prediction of bleeding, AUC original:0.53 (95%CI:0.51-0.54), AUC augmented:0.53 (95%CI:0.52-0.54). Patterns were similar for mortality and care-home outcomes.
CONCLUSIONS: It is possible to use routinely-recorded clinical data to augment AF risk prediction tools, However, improvements in prognostic utility were negligible. When applying CHA2DS2-VASc and HAS-BLED, any previous history of stroke is important regardless of pathology.
FUNDING: This study was sponsored and funded by Pfizer and Bristol Myers Squibb.Conference/Value in Health Info
Value in Health, Volume 25, Issue 12S (December 2022)
Code
CO139
Topic
Clinical Outcomes
Topic Subcategory
Clinical Outcomes Assessment
Disease
No Additional Disease & Conditions/Specialized Treatment Areas, SDC: Cardiovascular Disorders (including MI, Stroke, Circulatory)