Evidence map›Paper›PMID 40842283›Full record

ArticleEuropean heart journal. Cardiovascular Imaging2026

Associations and prognostic implications of myocardial tissue injury stages in ST-elevation myocardial infarction using the Canadian Cardiovascular Society classification.

Ivan Lechner, Jaclyn Carberry, Thomas Stiermaier, Christina Tiller, Magdalena Holzknecht, Fritz Oberhollenzer, Alex Kaser, Johannes Mair, Agnes Mayr, Hans-Josef Feistritzer and 9 more

Abstract read
In one paragraph

Article in European heart journal. Cardiovascular Imaging, 2026. 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

19 authors.

Ivan LechnerUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.ORCID 0000-0003-1379-3233
Jaclyn CarberryBritish Heart Foundation Glasgow Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.ORCID 0000-0002-4184-0714
Thomas StiermaierUniversity Heart Centre Lübeck, Medical Clinic II (Cardiology/Angiology/Intensive Care Medicine), University Hospital Schleswig-Holstein, Lübeck, Germany.ORCID 0000-0003-1957-3741
Christina TillerUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.
Magdalena HolzknechtUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.ORCID 0000-0003-2415-8622
Fritz OberhollenzerUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.ORCID 0000-0002-5979-2108
Alex KaserUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.
Johannes MairUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.ORCID 0000-0003-1706-5962
Agnes MayrUniversity Clinic of Radiology, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0001-9363-873X
Hans-Josef FeistritzerDepartment of Internal Medicine/Cardiology, Heart Centre Leipzig at Leipzig University and Leipzig Heart Science, Leipzig, Germany.
David CarrickBritish Heart Foundation Glasgow Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
Clemens DlaskaUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.ORCID 0000-0002-8798-0827
Axel BauerUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.
Holger ThieleDepartment of Internal Medicine/Cardiology, Heart Centre Leipzig at Leipzig University and Leipzig Heart Science, Leipzig, Germany.ORCID 0000-0002-0169-998X
Ingo EitelUniversity Heart Centre Lübeck, Medical Clinic II (Cardiology/Angiology/Intensive Care Medicine), University Hospital Schleswig-Holstein, Lübeck, Germany.ORCID 0000-0002-6442-246X
Bernhard MetzlerUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.
Colin BerryBritish Heart Foundation Glasgow Cardiovascular Research Centre, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.ORCID 0000-0002-4547-8636
Martin ReindlUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.ORCID 0000-0002-8414-9552
Sebastian J ReinstadlerUniversity Clinic of Internal Medicine III, Cardiology and Angiology, Medical University of Innsbruck, Anichstr. 35, Innsbruck 6020, Austria.ORCID 0000-0002-7700-1357

Funding

Austrian Science Fund KLI 772-BAustrian Society of CardiologyBritish Heart Foundation RE/18/6134217University of Leipzig-Heart Centre
6 · The paper itself

Abstract

aimsThe recently proposed Canadian Cardiovascular Society (CCS) classification categorizes post-infarction tissue injury into four stages, potentially improving risk stratification and guiding cardioprotective strategies. Its clinical and prognostic relevance in ST-elevation myocardial infarction (STEMI) remains unclear. We aimed to compare clinical characteristics across CCS stages and validate their prognostic implications in STEMI. METHODS AND

resultsWe analysed 1109 STEMI patients included in three prospective studies. Cardiac magnetic resonance (CMR) imaging was performed 3 (interquartile range 2-5) days after myocardial infarction (MI) and patients were classified as follows: Stage 1 (aborted MI), Stage 2 (MI with necrosis and absence of microvascular injury), Stage 3 (MI with necrosis and microvascular obstruction), and Stage 4 (MI with necrosis and intramyocardial haemorrhage). This analysis revealed distinct patterns of clinical presentation, biomarker profiles, and cardiac function across the different CCS stages. There were differences in adverse clinical event rates and mortality between CCS stages [major adverse cardiovascular event (MACE): 0.7%, 3.4%, 3.1%, and 15.7%, P < 0.001 and mortality: 0.7%, 1.7%, 0.9%, and 6.3%, P < 0.001]. The CCS stage had a moderate to good predictive value for MACE and mortality [area under the curve (AUC) 0.74 (95% CI: 0.68-0.80), P < 0.001 and AUC 0.71 (95% CI: 0.61-0.80), P < 0.001] at 12 months, respectively. CCS stages were independently associated with MACE in multivariable Cox regression [hazard ratio: 2.18 (95% CI: 1.70-2.78), P < 0.001].

conclusionThis study describes clinical characteristics across CCS stages and provides insights into their prognostic implications in a large cohort of STEMI patients reperfused by percutaneous coronary intervention. These data should inform the use of CCS stages in future trial designs.

Indexed as

Magnetic Resonance Imaging, CineST Elevation Myocardial InfarctionAgedCanadaFemaleHumansMaleMiddle AgedPrognosisProspective StudiesRisk AssessmentSeverity of Illness IndexSocieties, Medicalcardiac magnetic resonancemicrovascular injuryprognosisST-segment elevation myocardial infarction

Identifiers

PMID40842283
PMCPMC13021278

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.