Evidence map›Paper›PMID 39549261›Full record

ArticleCirculation. Heart failure2025

Natural Language Processing to Adjudicate Heart Failure Hospitalizations in Global Clinical Trials.

Pablo M Marti-Castellote, Christopher Reeder, Brian Claggett, Pulkit Singh, Emily S Lau, Shaan Khurshid, Puneet Batra, Steven A Lubitz, Mahnaz Maddah, Orly Vardeny and 9 more

Abstract read
In one paragraph

Article in Circulation. Heart failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
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  9. The potential of artificial intelligence in clinical trials.European journal of clinical investigation · 2026
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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

19 authors.

Pablo M Marti-CastelloteDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0003-0252-5831
Christopher ReederCardiovascular Disease Initiative (P.M.M.-C., C.R., P.S., E.S.L., S.K., P.B., S.A.L., M.M., P.T.E., J.E.H., J.W.C.), Broad Institute of Harvard University and the Massachusetts Institute of Technology, Cambridge.
Brian ClaggettDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0002-4215-9218
Pulkit SinghCardiovascular Disease Initiative (P.M.M.-C., C.R., P.S., E.S.L., S.K., P.B., S.A.L., M.M., P.T.E., J.E.H., J.W.C.), Broad Institute of Harvard University and the Massachusetts Institute of Technology, Cambridge.
Emily S LauDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0001-9361-6397
Shaan KhurshidDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0002-2840-4539
Puneet BatraCardiovascular Disease Initiative (P.M.M.-C., C.R., P.S., E.S.L., S.K., P.B., S.A.L., M.M., P.T.E., J.E.H., J.W.C.), Broad Institute of Harvard University and the Massachusetts Institute of Technology, Cambridge.ORCID 0000-0001-6822-0593
Steven A LubitzDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0002-9599-4866
Mahnaz MaddahCardiovascular Disease Initiative (P.M.M.-C., C.R., P.S., E.S.L., S.K., P.B., S.A.L., M.M., P.T.E., J.E.H., J.W.C.), Broad Institute of Harvard University and the Massachusetts Institute of Technology, Cambridge.ORCID 0000-0002-9837-6000
Orly VardenyCenter for Care Delivery and Outcomes Research, Minneapolis VA Hospital, University of Minnesota (O.V.).
Eldrin F LewisDivision of Cardiovascular Medicine, Stanford University School of Medicine, Palo Alto, CA (E.F.L.).
Marc PfefferDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0003-3876-7568
Pardeep JhundBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, United Kingdom (P.J., J.J.V.M.).ORCID 0000-0003-4306-5317
Akshay S DesaiDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0002-1443-0701
John J V McMurrayBritish Heart Foundation Cardiovascular Research Centre, University of Glasgow, United Kingdom (P.J., J.J.V.M.).ORCID 0000-0002-6317-3975
Patrick T EllinorCardiovascular Disease Initiative (P.M.M.-C., C.R., P.S., E.S.L., S.K., P.B., S.A.L., M.M., P.T.E., J.E.H., J.W.C.), Broad Institute of Harvard University and the Massachusetts Institute of Technology, Cambridge.ORCID 0000-0002-2067-0533
Jennifer E HoCardiovascular Disease Initiative (P.M.M.-C., C.R., P.S., E.S.L., S.K., P.B., S.A.L., M.M., P.T.E., J.E.H., J.W.C.), Broad Institute of Harvard University and the Massachusetts Institute of Technology, Cambridge.ORCID 0000-0002-7987-4768
Scott D SolomonDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0003-3698-9597
Jonathan W CunninghamDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA (P.M.M.-C., B.C., M.P., A.S.D., S.D.S., J.W.C.).ORCID 0000-0003-4481-7867

Funding

IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVALR01HL092577 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2009 to 2025
$20.6M
Endothelial Cell Health Across the Spectrum of Cardiometabolic DiseaseR01HL168889 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Naomi Miriam Hamburg, Jennifer E Ho · 2023 to 2026
$3.1M
Long-Term Endothelial Effects of COVID-19 in ObesityR01HL160003 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI HAMBURG, NAOMI MIRIAM, HO, JENNIFER E · 2022 to 2025
$2.8M
Mentoring in Arrhythmia ResearchK24HL105780 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2011 to 2020
$1.2M
HFpEF Susceptibility in Women: The Role of InflammationK23HL159243 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Emily Lau · 2022 to 2026
$1.1M
Electrocardiogram-based deep learning and decision analysis to improve atrial fibrillation risk estimationK23HL169839 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Shaan Khurshid · 2023 to 2026
$860k
Mentoring in Patient-Oriented and Translational HFpEF ResearchK24HL153669 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Jennifer E Ho · 2020 to 2026
$744k
Effect of Neprilysin Inhibition on Myocardial Interstitial FibrosisK23HL168163 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Jonathan Woo Cunningham · 2024 to 2026
$586k
NHLBI NIH HHS K23 HL159243NHLBI NIH HHS K23 HL168163NHLBI NIH HHS K23 HL169839NHLBI NIH HHS K24 HL105780NHLBI NIH HHS K24 HL153669NHLBI NIH HHS R01 HL092577NHLBI NIH HHS R01 HL160003NHLBI NIH HHS R01 HL168889
6 · The paper itself

Abstract

backgroundMedical record review by a physician clinical events committee is the gold standard for identifying cardiovascular outcomes in clinical trials, but is labor-intensive and poorly reproducible. Automated outcome adjudication by artificial intelligence (AI) could enable larger and less expensive clinical trials but has not been validated in global studies.

methodsWe developed a novel model for automated AI-based heart failure adjudication (Heart Failure Natural Language Processing) using hospitalizations from 3 international clinical outcomes trials. This model was tested on potential heart failure hospitalizations from the DELIVER trial (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure), a cardiovascular outcomes trial comparing dapagliflozin with placebo in 6063 patients with heart failure with mildly reduced or preserved ejection fraction. AI-based adjudications were compared with adjudications from a clinical events committee that followed Food and Drug Administration-based criteria.

resultsAI-based adjudication agreed with the clinical events committee in 83% of events. A strategy of human review for events that the AI model deemed uncertain (16%) would have achieved 91% agreement with the clinical events committee while reducing the adjudication workload by 84%. The estimated effect of dapagliflozin on heart failure hospitalization was nearly identical with AI-based adjudication (hazard ratio, 0.76 [95% CI, 0.66-0.88]) compared with clinical events committee adjudication (hazard ratio, 0.77 [95% CI, 0.67-0.89]). The AI model extracted symptoms, signs, and treatments of heart failure from each medical record in tabular format and quoted sentences documenting them.

conclusionsAI-based adjudication of clinical outcomes has the potential to improve the efficiency of global clinical trials while preserving accuracy and interpretability.

Indexed as

Artificial IntelligenceClinical Trials as TopicHeart FailureHospitalizationNatural Language ProcessingBenzhydryl CompoundsElectronic Health RecordsFemaleGlucosidesHumansMaleReproducibility of ResultsSodium-Glucose Transporter 2 InhibitorsStroke VolumeBenzhydryl CompoundsdapagliflozinGlucosidesSodium-Glucose Transporter 2 Inhibitorsartificial intelligencedapagliflozinheart failureNatural Language ProcessingUnited States Food and Drug Administration

Identifiers

PMID39549261
PMCPMC11910182

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Registered trials

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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.