Evidence map›Paper›PMID 33752439›Full record

ArticleCirculation2021

High-Sensitivity Cardiac Troponin on Presentation to Rule Out Myocardial Infarction: A Stepped-Wedge Cluster Randomized Controlled Trial.

Atul Anand, Kuan Ken Lee, Andrew R Chapman, Amy V Ferry, Phil D Adamson, Fiona E Strachan, Colin Berry, Iain Findlay, Anne Cruikshank, Alan Reid and 15 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Circulation, 2021. 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 71 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 4 pooled it
–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.

NCT03005158 nacompletednot on this map

High-Sensitivity Cardiac Troponin On Presentation to Rule Out Myocardial Infarction (HiSTORIC): A Stepped Wedge Cluster Randomized Trial

TypeinterventionalSponsorUniversity of EdinburghRan2014 to 2021Enrolled31,492ConditionsAcute Coronary Syndrome, Myocardial InfarctionArmsValidation Phase, Randomization Phase, Implementation Phase
NCT05748691 completednot on this map

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

71 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

Atul Anand *BHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Kuan Ken Lee *BHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Andrew R Chapman *BHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Amy V FerryBHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Phil D AdamsonBHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Fiona E StrachanBHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Colin BerryInstitute of Cardiovascular and Medical Sciences (C.B.), University of Glasgow, United Kingdom.
Iain FindlayDepartment of Cardiology, Royal Alexandra Hospital, Paisley, United Kingdom (I.F.).
Anne CruikshankDepartment of Biochemistry, Queen Elizabeth University Hospital, Glasgow, United Kingdom (A.C., A.R.).
Alan ReidDepartment of Biochemistry, Queen Elizabeth University Hospital, Glasgow, United Kingdom (A.C., A.R.).
Paul O CollinsonDepartments of Clinical Blood Sciences and Cardiology, St. George's University Hospitals NHS Trust and St. George's University of London, United Kingdom (P.O.C.).
Fred S AppleDepartment of Laboratory Medicine and Pathology, Hennepin Healthcare & University of Minnesota School of Medicine, Minneapolis (F.S.A.).
David A McAllisterInstitute of Health and Wellbeing (D.A.M.), University of Glasgow, United Kingdom.
Donogh MaguireEmergency Medicine Department, Glasgow Royal Infirmary, United Kingdom (D.M.).
Keith A A FoxBHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
David E NewbyBHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Chris TuckEdinburgh Clinical Trials Unit (C.T., R.H., C.K., C.J.W., R.A.P.), University of Edinburgh, United Kingdom.
Ronald HarkessEdinburgh Clinical Trials Unit (C.T., R.H., C.K., C.J.W., R.A.P.), University of Edinburgh, United Kingdom.
Catriona KeerieEdinburgh Clinical Trials Unit (C.T., R.H., C.K., C.J.W., R.A.P.), University of Edinburgh, United Kingdom.
Christopher J WeirEdinburgh Clinical Trials Unit (C.T., R.H., C.K., C.J.W., R.A.P.), University of Edinburgh, United Kingdom.
Richard A ParkerEdinburgh Clinical Trials Unit (C.T., R.H., C.K., C.J.W., R.A.P.), University of Edinburgh, United Kingdom.
Alasdair GrayUsher Institute (A.G., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.
Anoop S V ShahBHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
Nicholas L MillsBHF Centre for Cardiovascular Science (A.A., K.K.L., A.R.C., A.V.F., P.D.A., F.E.S., K.A.A.F., D.E.N., A.S.V.S., N.L.M.), University of Edinburgh, United Kingdom.s.
HiSTORIC Investigators†

Funding

British Heart Foundation CH/09/002/26360British Heart Foundation CH/F/21/90010British Heart Foundation FS/16/14/32023British Heart Foundation FS/18/25/33454British Heart Foundation FS/19/17/34172British Heart Foundation PG/15/51/31596British Heart Foundation RE/18/5/34216British Heart Foundation RE/18/6134217British Heart Foundation RG/20/10/34966British Heart Foundation SP/12/10/29922Medical Research Council MR/V007017/1Medical Research Council MR/W000598/1Wellcome Trust WT103782AIA
6 · The paper itself

Abstract

backgroundHigh-sensitivity cardiac troponin assays enable myocardial infarction to be ruled out earlier, but the safety and efficacy of this approach is uncertain. We investigated whether an early rule-out pathway is safe and effective for patients with suspected acute coronary syndrome.

methodsWe performed a stepped-wedge cluster randomized controlled trial in the emergency departments of 7 acute care hospitals in Scotland. Consecutive patients presenting with suspected acute coronary syndrome between December 2014 and December 2016 were included. Sites were randomized to implement an early rule-out pathway where myocardial infarction was excluded if high-sensitivity cardiac troponin I concentrations were <5 ng/L at presentation. During a previous validation phase, myocardial infarction was ruled out when troponin concentrations were <99th percentile at 6 to 12 hours after symptom onset. The coprimary outcome was length of stay (efficacy) and myocardial infarction or cardiac death after discharge at 30 days (safety). Patients were followed for 1 year to evaluate safety and other secondary outcomes.

resultsWe enrolled 31 492 patients (59±17 years of age [mean±SD]; 45% women) with troponin concentrations <99th percentile at presentation. Length of stay was reduced from 10.1±4.1 to 6.8±3.9 hours (adjusted geometric mean ratio, 0.78 [95% CI, 0.73-0.83];

conclusionsImplementation of an early rule-out pathway for myocardial infarction reduced length of stay and hospital admission. Although noninferiority for the safety outcome was not demonstrated at 30 days, there was no increase in cardiac events at 1 year. Adoption of this pathway would have major benefits for patients and health care providers. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03005158.

Indexed as

AdultAgedBiomarkersElectrocardiographyFemaleFollow-Up StudiesHumansLength of StayMaleMiddle AgedMyocardial InfarctionOdds RatioPatient DischargeRandomized Controlled Trials as TopicRisk FactorsTreatment OutcomeBiomarkersTroponin Ibiomarkerschest painmyocardial infarctionrandomized controlled trialtroponin

Identifiers

PMID33752439
PMCPMC8177493

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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.