Evidence map›Paper›PMID 31623760›Full record

Trial reportJournal of the American College of Cardiology2019

Sex-Specific Thresholds of High-Sensitivity Troponin in Patients With Suspected Acute Coronary Syndrome.

Kuan Ken Lee, Amy V Ferry, Atul Anand, Fiona E Strachan, Andrew R Chapman, Dorien M Kimenai, Steven J R Meex, Colin Berry, Iain Findlay, Alan Reid and 14 more

2 registry-linked trialsOpen access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American College of Cardiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 59 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 3 pooled it
8.9field-weighted citation impact, top 2% of its field
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.

NCT01852123 nacompletednot on this map

High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syndrome: A Randomized Controlled Trial

TypeinterventionalSponsorUniversity of EdinburghRan2013 to 2017Enrolled48,282ConditionsAcute Coronary Syndrome, Myocardial InfarctionArmsHigh-sensitivity troponin I assay
NCT05748691 completednot on this mapstarted 2020, after this paper: background citation

Trial of Switching High-sensitivity Cardiac Troponin Assays in Suspected Acute Coronary Syndrome: an Interrupted Time Series Analysis (TWITCH-ED Study)

TypeobservationalSponsorUniversity of EdinburghRan2020 to 2023Enrolled26,000ConditionsAcute Coronary Syndrome, Acute Myocardial Infarction, Acute Myocardial Ischemia, Myocardial InjuryArmsClinical implementation of hs-cTnT
3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 3 syntheses or guidelines pooled it, 124 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Pooled it
  4. Trial
  5. Review
  6. Article
  7. Review
  8. Review
  9. Observational
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Harnessing Artificial Intelligence for Innovation in Interventional Cardiovascular Care.Journal of the Society for Cardiovascular Angiography & Interventions · 2025
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 12 institutions in 3 countries.

Kuan Ken LeeBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Amy V FerryBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Atul AnandBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Fiona E StrachanBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Andrew R ChapmanBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Dorien M KimenaiCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, the Netherlands; Central Diagnostic Laboratory, Maastricht University Medical Center, Maastricht, the Netherlands.
Steven J R MeexCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, the Netherlands; Central Diagnostic Laboratory, Maastricht University Medical Center, Maastricht, the Netherlands.
Colin BerryInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.
Iain FindlayDepartment of Cardiology, Royal Alexandra Hospital, Paisley, United Kingdom.
Alan ReidDepartment of Biochemistry, Queen Elizabeth University Hospital, Glasgow, United Kingdom.
Anne CruickshankDepartment of Biochemistry, Queen Elizabeth University Hospital, Glasgow, United Kingdom.
Alasdair GrayEmergency Medicine Research Group Edinburgh, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom.
Paul O CollinsonDepartments of Clinical Blood Sciences and Cardiology, St. George's, University Hospitals NHS Trust and St. George's University of London, London, United Kingdom.
Fred S AppleDepartment of Laboratory Medicine and Pathology, Hennepin County Medical Center & University of Minnesota, Minneapolis, Minnesota.
David A McAllisterInstitute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
Donogh MaguireEmergency Medicine Department, Glasgow Royal Infirmary, Glasgow, United Kingdom.
Keith A A FoxBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
David E NewbyBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom.
Chris TuckEdinburgh Clinical Trials Unit, University of Edinburgh, Edinburgh, United Kingdom.
Catriona KeerieEdinburgh Clinical Trials Unit, University of Edinburgh, Edinburgh, United Kingdom.
Christopher J WeirEdinburgh Clinical Trials Unit, University of Edinburgh, Edinburgh, United Kingdom.
Anoop S V ShahBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, United Kingdom.
Nicholas L MillsBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, United Kingdom. Electronic address: nick.mills@ed.ac.uk.
High-STEACS Investigators
University of Edinburgh · GBBritish Heart Foundation · GBQueen Elizabeth University Hospital · GBUniversity of Glasgow · GBEdinburgh Royal Infirmary · GBGlasgow Royal Infirmary · GBMaastricht University · NLRoyal Alexandra Hospital · GBSt George's, University of London · GBHennepin County Medical Center · USSt George’s University Hospitals NHS Foundation Trust · GBUniversity of Minnesota · US

Funding

British Heart Foundation CH/09/002/26360British Heart Foundation FS/16/14/32023British Heart Foundation FS/16/75/32533British Heart Foundation FS/18/25/33454
6 · The paper itself

Abstract

backgroundMajor disparities between women and men in the diagnosis, management, and outcomes of acute coronary syndrome are well recognized.

objectivesThe aim of this study was to evaluate the impact of implementing a high-sensitivity cardiac troponin I assay with sex-specific diagnostic thresholds for myocardial infarction in women and men with suspected acute coronary syndrome.

methodsConsecutive patients with suspected acute coronary syndrome were enrolled in a stepped-wedge, cluster-randomized controlled trial across 10 hospitals. Myocardial injury was defined as high-sensitivity cardiac troponin I concentration >99th centile of 16 ng/l in women and 34 ng/l in men. The primary outcome was recurrent myocardial infarction or cardiovascular death at 1 year.

resultsA total of 48,282 patients (47% women) were included. Use of the high-sensitivity cardiac troponin I assay with sex-specific thresholds increased myocardial injury in women by 42% and in men by 6%. Following implementation, women with myocardial injury remained less likely than men to undergo coronary revascularization (15% vs. 34%) and to receive dual antiplatelet (26% vs. 43%), statin (16% vs. 26%), or other preventive therapies (p < 0.001 for all). The primary outcome occurred in 18% (369 of 2,072) and 17% (488 of 2,919) of women with myocardial injury before and after implementation, respectively (adjusted hazard ratio: 1.11; 95% confidence interval: 0.92 to 1.33), compared with 18% (370 of 2,044) and 15% (513 of 3,325) of men (adjusted hazard ratio: 0.85; 95% confidence interval: 0.71 to 1.01).

conclusionsUse of sex-specific thresholds identified 5 times more additional women than men with myocardial injury. Despite this increase, women received approximately one-half the number of treatments for coronary artery disease as men, and outcomes were not improved. (High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syndrome [High-STEACS]; NCT01852123).

Indexed as

Sex FactorsAcute Coronary SyndromeAgedCardiologyFemaleHumansMaleMiddle AgedProportional Hazards ModelsRecurrenceReference ValuesRisk AssessmentTreatment OutcomeTroponin ITroponin Iacute coronary syndromehigh-sensitivity cardiac troponinmyocardial infarctionsex-specific threshold

Identifiers

PMID31623760
PMCPMC6876271
OpenAlexW2979396815

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.