Please use this identifier to cite or link to this item: https://swslhd.intersearch.com.au/swslhdjspui/handle/1/13109
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dc.contributor.authorGoh, B.-
dc.contributor.authorBhaskar, S. M. M.-
dc.date.accessioned2024-12-11T00:34:10Z-
dc.date.available2024-12-11T00:34:10Z-
dc.date.issued2024-
dc.identifier.issn20754418 (ISSN)-
dc.identifier.urihttps://swslhd.intersearch.com.au/swslhdjspui/handle/1/13109-
dc.description.abstractBackground/Objective: Atrial fibrillation (AF) complicates the management of acute ischemic stroke (AIS), necessitating precise predictive models to enhance clinical outcomes. This meta-analysis evaluates the efficacy of machine learning (ML) models in three key areas: stroke prognosis in AF patients, stroke prediction in AF patients, and AF prediction in stroke patients. The study aims to assess the accuracy and variability of ML models in forecasting AIS outcomes and detecting AF in stroke patients, while exploring the clinical benefits and limitations of integrating these models into practice. Methods: We conducted a systematic search of PubMed, Embase, and Cochrane databases up to June 2024, selecting studies that evaluated ML accuracy in stroke prognosis and prediction in AF patients and AF prediction in stroke patients. Data extraction and quality assessment were performed independently by two reviewers, with random-effects modeling applied to estimate pooled accuracy metrics. Results: The meta-analysis included twenty-four studies comprising 7,391,645 patients, categorized into groups for stroke prognosis in AF patients (eight studies), stroke prediction in AF patients (thirteen studies), and AF prediction in stroke patients (three studies). The pooled AUROC was 0.79 for stroke prognosis and 0.68 for stroke prediction in AF, with higher accuracy noted in short-term predictions. The mean AUROC across studies was 0.75, with models such as Extreme Gradient Boosting (XGB) and Random Forest (RF) showing superior performance. For stroke prognosis in AF, the mean AUROC was 0.78, whereas stroke prediction yielded a mean AUROC of 0.73. AF prediction post-stroke had an average AUROC of 0.75. These findings indicate moderate predictive capability of ML models, underscoring the need for further refinement and standardization. The absence of comprehensive sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) metrics limited the ability to conduct full meta-analytic modeling. Conclusions: While ML models demonstrate potential for enhancing stroke prognosis and AF prediction, they have yet to meet the clinical standards required for widespread adoption. Future efforts should focus on refining these models and validating them across diverse populations to improve their clinical utility. � 2024 by the authors.-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.subjectacute ischemic stroke artificial intelligence atrial fibrillation machine learning prediction prognosis stroke angiotensin receptor antagonist antiarrhythmic agent anticoagulant agent antiinflammatory agent antithrombocytic agent antiulcer agent antivitamin K beta adrenergic receptor blocking agent calcium channel blocking agent corticosteroid dipeptidyl carboxypeptidase inhibitor diuretic agent hydroxymethylglutaryl coenzyme A reductase inhibitor proton pump inhibitor serotonin uptake inhibitor adult aged Article clinical outcome Cochrane Library data extraction diagnostic accuracy Embase female human male Medline meta analysis multicenter study (topic) performance indicator predictive value Preferred Reporting Items for Systematic Reviews and Meta-Analyses prevalence quality control random forest risk factor sensitivity and specificity stroke patient systematic review-
dc.titleEvaluating Machine Learning Models for Stroke Prognosis and Prediction in Atrial Fibrillation Patients: A Comprehensive Meta-Analysis-
dc.typeJournal Article-
dc.description.affiliatesGlobal Health Neurology Lab, Sydney, 2150, NSW, Australia UNSW Medicine and Health, University of New South Wales (UNSW), South West Sydney Clinical Campuses, Sydney, 2170, NSW, Australia Clinical Sciences Stream, Ingham Institute for Applied Medical Research, Liverpool, 2170, NSW, Australia NSW Brain Clot Bank, NSW Health Pathology, Sydney, 2170, NSW, Australia Department of Neurology & Neurophysiology, Liverpool Hospital, South Western Sydney Local Health District, Liverpool, 2170, NSW, Australia Department of Neurology, Division of Cerebrovascular Medicine and Neurology, National Cerebral and Cardiovascular Center (NCVC), Osaka, Suita, 564-8565, Japan-
dc.identifier.doi10.3390/diagnostics14212391-
dc.type.studyortrialArticle-
dc.identifier.journaltitleDiagnostics-
Appears in Collections:South Western Sydney Local Health District

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