A clinical model to predict incident AF achieved an AUROC of 84.1%, which improved to 86.5% (95% CI 84.5-88.5%; p<0.001) with NT-proBNP, and was cost-effective compared to no screening.
Cohort (n=23,830)
Sí
Does universal or model-guided atrial fibrillation screening improve quality-adjusted life years and reduce costs compared to no screening in people with no prior atrial fibrillation?
23,830 people with no prior atrial fibrillation from the Generation Scotland study (externally validated in UK Biobank), mean age 47.0 years, 59% female.
Atrial fibrillation screening (either universal screening or screening guided by a clinical prediction model incorporating age, weight, ischemic heart disease, heart failure, and NT-proBNP).
No screening.
Incident atrial fibrillation (for model development) and cost-effectiveness (quality-adjusted life years gained and cost reduction per person).
A clinical prediction model can effectively guide atrial fibrillation screening, and both universal and model-guided screening strategies are cost-effective compared to no screening.
Estimación del efecto: AUROC (95% CI 84.5-88.5)
Tasa de eventos absoluta: 86.5% vs 84.1%
valor p: p=<0.001
Abstract Background and aims Atrial fibrillation (AF) causes ischaemic stroke but population AF screening is not recommended. We developed and externally validated a model to guide AF screening and assessed health economic impact. Methods We analysed clinical demographics, NT-proBNP concentrations and artificial intelligence analysis of ECG data from people with no prior AF in the Generation Scotland study, with external validation in UK Biobank. Record linkage identified people with AF during follow-up. A clinical model for incident AF was developed using penalised logistic regression with Lasso modelling (80:20 training/testing). We assessed incorporating NT-proBNP or ECG data by De Long’s test. A decision-analytic model assessed cost-effectiveness of screening everyone or using the clinical model to guide AF screening, compared with no screening. Results We analysed 23,830 people: 14,061 (59%) female and mean (SD) age 47.0 (15.3) years. AF was diagnosed in 901 people (3.8%). The clinical model included age (OR 1.20, 1.13-1.28), age2 (OR 0.99, 0.99-1.00), weight (OR 1.03, 1.02-1.03), ischaemic heart disease (OR 1.63, 1.31-2.02) and heart failure (OR 3.78, 2.03-7.03). AUROC was 84.1% (82.1-86.1%) in test data and 75.4% (75.1-75.6%) in external validation. Model performance improved with logeNT-proBNP (86.5%, 84.5-88.5%; p0.001) but not ECG data (84.5%, 82.2-86.5%; p=0.76). The quality-adjusted life years (QALYs) gained and cost reduction per-person was 0.05 years and £656 for screening everyone; and 0.04 and £548 for the clinical model to guide screening. Conclusions A clinical model could guide AF screening to prevent stroke and can be augmented by NT-proBNP. Screening everyone and using a clinical model is cost-effective. Conflict of interest
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Cameron et al. (Fri,) conducted a cohort in Atrial fibrillation (n=23,830). Clinical model augmented with NT-proBNP vs. Clinical model alone was evaluated on Incident AF prediction (AUROC) (AUROC, 95% CI 84.5-88.5, p=<0.001). A clinical model to predict incident AF achieved an AUROC of 84.1%, which improved to 86.5% (95% CI 84.5-88.5%; p<0.001) with NT-proBNP, and was cost-effective compared to no screening.
synapsesocial.com/papers/69fd7fb8bfa21ec5bbf08423 — DOI: https://doi.org/10.1093/esj/aakag023.1901
Alan Cameron
University of Glasgow
Robert Heggie
University of Glasgow
Heather Fraser
University of Glasgow
European Stroke Journal
University of Glasgow
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