Evidence map›Paper›PMID 42436241›Full record

ArticleScientific reports2026

Scalable risk stratification of undiagnosed heart failure using routine health data and its association with imaging phenotypes and outcomes.

Yoko M Nakao, Ramesh Nadarajah, Farag Shuweihdi, Christopher J Hayward, Michihiko Goto, Jung-Chi Hsu, Mohammad Haris, Ben Hurdus, Osama Tariq, Temar Habtezghi and 11 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Yoko M Nakao *Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Ramesh Nadarajah *Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. r.nadarajah@leeds.ac.uk.
Farag ShuweihdiLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Christopher J HaywardLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Michihiko GotoDepartment of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Jung-Chi HsuDepartment of Cardiology, National Taiwan University Hospital, Taipei, Taiwan.
Mohammad HarisLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Ben HurdusLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Osama TariqDepartment of Cardiology, Leeds Teaching Hospital NHS Trust, Leeds, UK.
Temar HabtezghiDepartment of Cardiology, Leeds Teaching Hospital NHS Trust, Leeds, UK.
Anna HelbitzLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Ali WahabLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Lan MuWolfson Institute of Population Health, Queen Mary University of London, London, UK.
Kazuhiro NakaoLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Peter SwobodaDepartment of Biomedical Imaging Science, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.
Amitava BanerjeeInstitute of Health Informatics, University College London, London, UK.
Mark C PetrieSchool of Cardiovascular and Metabolic Health, University of Glasgow, British Heart Foundation Glasgow Cardiovascular Research Centre, Glasgow, UK.
Clare J TaylorDepartment of Applied Health Sciences, School of Health Sciences, College of Medicine and Health, University of Birmingham, Birmingham, UK.
Koji KawakamiDepartment of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Kyoto, Japan.
Jianhua WuWolfson Institute of Population Health, Queen Mary University of London, London, UK.
Chris P GaleLeeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Late diagnosis of Heart failure (HF) is associated with worse outcomes. We aimed to develop a scalable tool to identify those at high risk of undiagnosed HF using routine electronic health records (EHR). We developed and internally validated a logistic regression (FIND-HF) model for incident HF diagnosis within one year in United Kingdom primary care EHRs (CPRD-Aurum, n=3 520 186), with good prediction performance (area under the receiver operating characteristic curve (AUC) 0.79), equal to more complex modelling techniques. We externally validated FIND-HF in United Kingdom (CPRD-GOLD, n=570 850, AUC 0.72), Japan (JMDC, n=6 820 694, AUC 0.73), United States of America (Epic Cosmos, n=7 710 398, AUC 0.78), and Taiwan (NTUH, n=170 518, AUC 0.85). In a cohort who had undergone HF diagnostics an optimised FIND-HF threshold had a positive predictive value of 21.4% and a negative predictive value of 96.9%. Amongst patients with HF who had undergone cardiac magnetic resonance imaging, high FIND-HF risk compared with low FIND-HF risk as reference, was associated with increased risk of a primary composite outcome of heart failure hospitalisation or cardiovascular death and more advanced adverse remodelling including lower left ventricular ejection fraction. FIND-HF is a scalable EHR-based model which has the potential to help rule out undiagnosed HF in low risk cases, whilst high risk cases are associated with more advanced cardiac dysfunction and worse prognosis.

Indexed as

Electronic health recordsHeart failureMortalityPredictionPreventionScreening

Identifiers

PMID42436241
PMCPMC13658026

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.