Evidence map›Paper›PMID 32216909›Full record

Trial reportJournal of the American College of Cardiology2020

Low-Dose Alteplase During Primary Percutaneous Coronary Intervention According to Ischemic Time.

Peter J McCartney, Annette M Maznyczka, Hany Eteiba, Margaret McEntegart, Keith G Oldroyd, John P Greenwood, Neil Maredia, Matthias Schmitt, Gerry P McCann, Timothy Fairbairn and 12 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American College of Cardiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02257294 (A Randomised, Double Blind, Placebo-controlled, Parallel Group Trial of Low-dose Adjunctive alTeplase During prIMary PCI), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 7% 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.

NCT02257294 phase2completednot on this map

A Randomised, Double Blind, Placebo-controlled, Parallel Group Trial of Low-dose Adjunctive alTeplase During prIMary PCI

TypeinterventionalSponsorNHS Greater Glasgow and ClydeRan2016 to 2019Enrolled440ConditionsMyocardial InfarctionArmsAlteplase, Placebo
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Low-dose fibrinolysis during primary percutaneous intervention for preventing no-reflow: stepping back to move forward?EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 11 institutions in 2 countries.

Peter J McCartneyBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom; West of Scotland Heart and Lung Center, Golden Jubilee National Hospital, Clydebank, United Kingdom.
Annette M MaznyczkaBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom; West of Scotland Heart and Lung Center, Golden Jubilee National Hospital, Clydebank, United Kingdom.
Hany EteibaBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom; West of Scotland Heart and Lung Center, Golden Jubilee National Hospital, Clydebank, United Kingdom.
Margaret McEntegartBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom; West of Scotland Heart and Lung Center, Golden Jubilee National Hospital, Clydebank, United Kingdom.
Keith G OldroydWest of Scotland Heart and Lung Center, Golden Jubilee National Hospital, Clydebank, United Kingdom.
John P GreenwoodLeeds University and Leeds Teaching Hospitals National Health Service (NHS) Trust, Leeds, United Kingdom.
Neil MarediaSouth Tees Hospitals NHS Foundation Trust, Middlesbrough, United Kingdom.
Matthias SchmittManchester University NHS Foundation Trust, Manchester, United Kingdom.
Gerry P McCannUniversity of Leicester and the National Institute for Health Research Leicester Biomedical Research Center, Leicester, United Kingdom.
Timothy FairbairnLiverpool Heart and Chest Hospital NHS Foundation Trust, Liverpool, United Kingdom.
Elisa McAlindonNew Cross Hospital, Royal Wolverhampton NHS Trust, Wolverhampton, United Kingdom.
Campbell TaitDepartment of Hematology, Royal Infirmary, Glasgow, United Kingdom.
Paul WelshBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom.
Naveed SattarBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom.
Vanessa OrchardWest of Scotland Heart and Lung Center, Golden Jubilee National Hospital, Clydebank, United Kingdom.
David CorcoranBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom.
Thomas J FordBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom; Department of Cardiology, Gosford Hospital, Gosford, New South Wales, Australia.
Aleksandra RadjenovicBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom.
Ian FordRobertson Centre for Biostatistics, Institute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
Alex McConnachieRobertson Centre for Biostatistics, Institute of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom.
Colin BerryBritish Heart Foundation Glasgow Cardiovascular Research Center, University of Glasgow, Glasgow, United Kingdom; West of Scotland Heart and Lung Center, Golden Jubilee National Hospital, Clydebank, United Kingdom. Electronic address: colin.berry@glasgow.ac.uk.
T-TIME Investigators
British Heart Foundation · GBUniversity of Glasgow · GBGolden Jubilee National Hospital · GBGlasgow Royal Infirmary · GBGosford Hospital · AULiverpool Heart and Chest Hospital NHS Trust · GBManchester University NHS Foundation Trust · GBNational Health Service · GBNew Cross Hospital · GBNIHR Leicester Biomedical Research Centre · GBSouth Tees Hospitals NHS Foundation Trust · GB

Funding

British Heart Foundation FS/16/74/32573Department of HealthMedical Research Council MC_PC_12037Medical Research Council MC_PC_15113
6 · The paper itself

Abstract

backgroundMicrovascular obstruction affects one-half of patients with ST-segment elevation myocardial infarction and confers an adverse prognosis.

objectivesThis study aimed to determine whether the efficacy and safety of a therapeutic strategy involving low-dose intracoronary alteplase infused early after coronary reperfusion associates with ischemic time.

methodsThis study was conducted in a prospective, multicenter, parallel group, 1:1:1 randomized, dose-ranging trial in patients undergoing primary percutaneous coronary intervention. Ischemic time, defined as the time from symptom onset to coronary reperfusion, was a pre-specified subgroup of interest. Between March 17, 2016, and December 21, 2017, 440 patients, presenting with ST-segment elevation myocardial infarction within 6 h of symptom onset (<2 h, n = 107; ≥2 h but <4 h, n = 235; ≥4 h to 6 h, n = 98), were enrolled at 11 U.K. hospitals. Participants were randomly assigned to treatment with placebo (n = 151), alteplase 10 mg (n = 144), or alteplase 20 mg (n = 145). The primary outcome was the amount of microvascular obstruction (MVO) (percentage of left ventricular mass) quantified by cardiac magnetic resonance imaging at 2 to 7 days (available for 396 of 440).

resultsOverall, there was no association between alteplase dose and the extent of MVO (p for trend = 0.128). However, in patients with an ischemic time ≥4 to 6 h, alteplase increased the mean extent of MVO compared with placebo: 1.14% (placebo) versus 3.11% (10 mg) versus 5.20% (20 mg); p = 0.009 for the trend. The interaction between ischemic time and alteplase dose was statistically significant (p = 0.018).

conclusionIn patients presenting with ST-segment elevation myocardial infarction and an ischemic time ≥4 to 6 h, adjunctive treatment with low-dose intracoronary alteplase during primary percutaneous coronary intervention was associated with increased MVO. Intracoronary alteplase may be harmful for this subgroup. (A Trial of Low-Dose Adjunctive Alteplase During Primary PCI [T-TIME]; NCT02257294).

Indexed as

AgedDose-Response Relationship, DrugDouble-Blind MethodFemaleFibrinolytic AgentsHumansMaleMiddle AgedMyocardial IschemiaPercutaneous Coronary InterventionProspective StudiesST Elevation Myocardial InfarctionTime FactorsTissue Plasminogen ActivatorFibrinolytic AgentsTissue Plasminogen Activatorfibrinolysismicrovascular obstructionmyocardial hemorrhageprimary percutaneous coronary interventionST-segment elevation myocardial infarction

Identifiers

PMID32216909
PMCPMC7109518
OpenAlexW3012852116

What OpenQuestion holds

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LicenceCC BY
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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.