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Do DanGer-SHOCK-like patients benefit from VA-ECMO treatment in infarct-related cardiogenic shock? results of an individual patient data meta-analysis
U. Zeymer, A. Freund, M. Hochadel, P. Ostadal, J. Belohlavek, S. Massberg, S. Brunner, M. Flather, D. Adlam, C. Hassager, JE. Moeller, S. Schneider, S. Desch, H. Thiele
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, metaanalýza
Grantová podpora
Stiftung Institut für Herzinfarktforschung Ludwigshafen
PubMed
39217624
DOI
10.1093/ehjacc/zuae093
Knihovny.cz E-zdroje
- MeSH
- infarkt myokardu * komplikace terapie mortalita MeSH
- kardiogenní šok * terapie mortalita etiologie MeSH
- lidé MeSH
- mimotělní membránová oxygenace * metody MeSH
- randomizované kontrolované studie jako téma MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
AIMS: In a recent meta-analysis of randomized controlled trials, routine use of veno-arterial ECMO (VA-ECMO) did not improve outcomes in patients with acute myocardial infarction-related cardiogenic shock (AMI-CS), while a microaxial flow pump reduced mortality in a selected group of patients with AMI-CS in the DanGer-Shock trial. METHODS AND RESULTS: Individual patient data of patients included in four randomized clinical trials investigating the routine use of VA-ECMO in AMI-CS were centrally analysed. For the purpose of this sub-analysis, DanGer-Shock-like patients were analysed (STEMI only, presumed low likelihood of brain injury). The primary endpoint was 180-day all-cause mortality. A total of 202 patients (106 randomized to VA-ECMO and 96 to control) were included. There were no differences in baseline characteristics, angiographic and interventional features between the two groups. Mortality after 6 months was numerically lower with VA-ECMO between the groups [45% in VA-ECMO group vs. 51% in control group; hazard ratio, 0.84; 95% confidence interval (CI), 0.56-1.26], while major bleeding (OR, 2.24; 95% CI, 1.08-4.64) and peripheral vascular complications (OR, 3.65; 95% CI, 1.15-11.56) were increased with the use of VA-ECMO. CONCLUSION: In this exploratory subgroup analysis in patients with CS, STEMI, and a low likelihood of brain injury, there was no mortality benefit with the routine use of VA-ECMO. However, as indicated by the large confidence intervals, the statistical power was limited to draw definite conclusions.
2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic
Department of Cardiology Heart Center Leipzig at Leipzig University Leipzig Germany
Department of Cardiovascular Sciences and NIHR Leicester Biomedical Research Centre Leicester UK
Institut für Herzinfarktforschung Ludwigshafen Germany
Klinikum Ludwigshafen Medizinische Klinik B Ludwigshafen Germany
Citace poskytuje Crossref.org
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