Evidence map›Paper›PMID 41292644›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Dynamic Risk Trajectories for Sudden Cardiac Arrest: The Role of Recurrent Cardiovascular Events.

Marita Knudsen Pope, Harpriya Chugh, Thien Tan Tri Tai Truyen, Marco Mathias, Audrey Uy-Evanado, Honghuang Lin, Dan Atar, Nichole Bosson, Kyndaron Reinier, Emelia J Benjamin and 1 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Marita Knudsen PopeCenter for Cardiac Arrest Prevention, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0000-0002-3429-1585
Harpriya ChughCenter for Cardiac Arrest Prevention, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0000-0002-6581-4246
Thien Tan Tri Tai TruyenCenter for Cardiac Arrest Prevention, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0000-0001-8129-2532
Marco MathiasCenter for Cardiac Arrest Prevention, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Audrey Uy-EvanadoCenter for Cardiac Arrest Prevention, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0000-0002-1362-9663
Honghuang LinDepartment of Medicine, University of Massachusetts Chan Medical School, Worcester.ORCID 0000-0003-3043-3942
Dan AtarDepartment of Cardiology, Oslo University Hospital, Ullevaal, and the Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Nichole BossonLos Angeles County Emergency Medical Services Agency.ORCID 0000-0001-8356-0772
Kyndaron ReinierCenter for Cardiac Arrest Prevention, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0000-0002-2588-6827
Emelia J BenjaminBoston University and National Heart, Lung, and Blood Institute's Framingham Heart Study, MA.ORCID 0000-0003-4076-2336
Sumeet S ChughCenter for Cardiac Arrest Prevention, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0000-0002-4417-5326

Funding

FRAMINGHAM HEART STUDY - YEAR 5 EXAM75N92019D00031 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · 2019 to 2024
$29.8M
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
FRAMINGHAM HEART STUDY (FHS), TASK AREA B - PROTOCOL DEVELOPMENT AND BASIC EXAMINATION75N92025D00012 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI LLOYD-JONES, DONALD · 2025 to 2025
$8.9M
THE FRAMINGHAM HEART STUDY-N01HC25195-268025195-268025195N01HC025195 · HC · TRUSTEES OF BOSTON UNIVERSITY · PI WOLF, PHILIP A · 2002 to 2006
–
NHLBI NIH HHS 75N92019D00031NHLBI NIH HHS 75N92025D00012NHLBI NIH HHS HHSN268201500001CNHLBI NIH HHS HHSN268201500001INHLBI NIH HHS N01 HC025195NHLBI NIH HHS R01 HL092577
6 · The paper itself

Abstract

Background: Emerging evidence suggests that dynamic risk assessment may enhance sudden cardiac arrest (SCA) risk stratification. While cardiovascular events, including acute coronary syndrome (ACS) and heart failure (HF) hospitalization, are associated with increased SCA risk, the impact of recurrent events on subsequent SCA risk in a contemporary, real-world population is unknown. This study aimed to assess whether patients with a first-time ACS or HF hospitalization who experience a recurrent cardiovascular event have higher risk of SCA compared to those who do not. Methods: The Observational Study of Cardiac Arrest Risk (OSCAR) is a prospective cohort study with adjudicated SCA outcomes. In the current study, patients who survived a first ACS or HF hospitalization were categorized into index ACS or HF cohorts. Participants were followed for recurrent cardiovascular events and SCA. Associations between recurrent events and SCA were assessed using Cox models with recurrent event modeled as a time-dependent variable. Findings were validated in the Framingham Heart Study (FHS). Results: In the OSCAR discovery cohort, 2946 patients experienced an index ACS event. The incidence rate of SCA was higher following a recurrent ACS event than without (3.70 vs 1.28 per 100 patient-years). Recurrent ACS event was associated with a significantly higher risk of SCA (adjusted HR 3.15, 95% CI 2.06-4.83, p<0.0001). A total of 6711 patients experienced an index HF hospitalization, and the incidence rate of SCA was higher following a recurrent HF event than without (1.35 vs 0.97 per 100 patient-years). Recurrent HF hospitalization was associated with a significantly higher risk of SCA (HR 1.81, 95% CI 1.46-2.26, p<0.0001).In the FHS validation cohorts a recurrent event during follow-up was associated with a significantly higher risk of SCA in the ACS cohort (HR 2.85, 95% CI 1.66-4.90, p=0.0002), but the association was not statistically significant in the HF cohort (HR 1.49, 95% CI 0.73-3.03, p=0.27). Conclusion: Recurrent ACS event was associated with more than threefold higher risk of SCA, and a recurrent HF hospitalization with 80% higher risk of SCA. These findings suggest that dynamic clinical trajectories of recurrent cardiovascular events may inform management and prevention of SCA.

Identifiers

PMID41292644
PMCPMC12642720

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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.