Evidence map›Paper›PMID 35574948›Full record

Trial reportJournal of the American Heart Association2022

Gradual Versus Abrupt Reperfusion During Primary Percutaneous Coronary Interventions in ST-Segment-Elevation Myocardial Infarction (GUARD).

Murat Sezer, Javier Escaned, Christopher J Broyd, Berrin Umman, Zehra Bugra, Ilke Ozcan, Mehmet Rasih Sonsoz, Alp Ozcan, Adem Atici, Emre Aslanger and 4 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American Heart Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.8field-weighted citation impact, top 8% 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.

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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Effects of reperfusion grade and reperfusion strategy on the clinical outcome: Insights from ESCAPE-NA1 trial.Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences · 2024
    Trial
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 9 institutions in 6 countries.

Murat SezerDepartment of Cardiology Istanbul Faculty of Medicine Istanbul University Istanbul Turkey.ORCID 0000-0001-9614-1614
Javier EscanedHospital Clínico San CarlosInstituto de Investigación Sanitaria San CarlosUniversidad Complutense de Madrid Madrid Spain.ORCID 0000-0003-4932-0112
Christopher J BroydThe Prince Charles Hospital Chermside Brisbane Australia.ORCID 0000-0002-6220-2949
Berrin UmmanDepartment of Cardiology Istanbul Faculty of Medicine Istanbul University Istanbul Turkey.
Zehra BugraDepartment of Cardiology Istanbul Faculty of Medicine Istanbul University Istanbul Turkey.
Ilke OzcanDepartment of Cardiovascular Medicine Mayo Clinic Rochester MN.ORCID 0000-0003-2006-3431
Mehmet Rasih SonsozDepartment of Cardiology Istanbul Faculty of Medicine Istanbul University Istanbul Turkey.ORCID 0000-0002-1535-5168
Alp OzcanDepartment of Cardiology Istanbul Faculty of Medicine Istanbul University Istanbul Turkey.
Adem AticiDepartment of Cardiology Istanbul Faculty of Medicine Istanbul University Istanbul Turkey.
Emre AslangerMarmara UniversitySchool of Medicine Istanbul Turkey.
Z Irem SezerAcibadem Atakent Hastanesi, Halkali Istanbul Turkey.
Justin E DaviesHammersmith Hospital Imperial College London London United Kingdom.
Niels van RoyenRadboud University Medical Center Nijmegen Netherlands.ORCID 0000-0001-6136-8640
Sabahattin UmmanDepartment of Cardiology Istanbul Faculty of Medicine Istanbul University Istanbul Turkey.
Istanbul University · TRAcıbadem University · TRAcıbadem University Atakent Hospital · TRHammersmith Hospital · GBMarmara University · TRMayo Clinic · USPrince Charles Hospital · AURadboud University Nijmegen · NLUniversidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Intramyocardial edema and hemorrhage are key pathological mechanisms in the development of reperfusion-related microvascular damage in ST-segment-elevation myocardial infarction. These processes may be facilitated by abrupt restoration of intracoronary pressure and flow triggered by primary percutaneous coronary intervention. We investigated whether pressure-controlled reperfusion via gradual reopening of the infarct-related artery may limit microvascular injury in patients undergoing primary percutaneous coronary intervention. Methods and Results A total of 83 patients with ST-segment-elevation myocardial infarction were assessed for eligibility and 53 who did not meet inclusion criteria were excluded. The remaining 30 patients with totally occluded infarct-related artery were randomized to the pressure-controlled reperfusion with delayed stenting (PCRDS) group (n=15) or standard primary percutaneous coronary intervention with immediate stenting (IS) group (n=15) (intention-to-treat population). Data from 5 patients in each arm were unsuitable to be included in the final analysis. Finally, 20 patients undergoing primary percutaneous coronary intervention who were randomly assigned to either IS (n=10) or PCRDS (n=10) were included. In the PCRDS arm, a 1.5-mm balloon was used to achieve initial reperfusion with thrombolysis in myocardial infarction grade 3 flow and, subsequently, to control distal intracoronary pressure over a 30-minute monitoring period (MP) until stenting was performed. In both study groups, continuous assessment of coronary hemodynamics with intracoronary pressure and Doppler flow velocity was performed, with a final measurement of zero flow pressure (primary end point of the study) at the end of a 60-minute MP. There were no complications associated with IS or PCRDS. PCRDS effectively led to lower distal intracoronary pressures than IS over 30 minutes after reperfusion (71.2±9.37 mm Hg versus 90.13±12.09 mm Hg,

Indexed as

Myocardial InfarctionPercutaneous Coronary InterventionST Elevation Myocardial InfarctionCreatine Kinase, MB FormHumansMicrocirculationReperfusionTreatment OutcomeCreatine Kinase, MB Formcoronary microvascular resistanceintramyocardial hemorrhagemicrovascular injurymyocardial edemaprimary PCIreperfusion injuryST‐segment–elevation myocardial infarction

Identifiers

PMID35574948
PMCPMC9238546
OpenAlexW4280550548

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.