Abstract
Objectives: This study sought to determine frequency, associated factors, and impact of bleeding in infarct-related cardiogenic shock. Background: Early revascularization is associated with improved survival in patients with acute myocardial infarction complicated by cardiogenic shock. On the downside, invasive treatment and accompanying antithrombotic therapies are associated with an increased bleeding risk. Prospective data assessing the incidence, severity, risk factors, and prognostic implication of bleeding in patients with cardiogenic shock are scarce. Methods: As a pre-defined subanalysis of the CULPRIT-SHOCK (PCI Strategies in Patients with Acute Myocardial Infarction and Cardiogenic Shock) randomized trial, we examined distribution of bleeding events in 684 patients with infarct-related cardiogenic shock and compared patients with any bleeding to those without. Results: A total of 21.5% patients experienced at least 1 bleeding event until 30 days after randomization. The vast majority of bleeding (57%) occurred within the first 2 days of hospitalization. Patients with bleeding had prolonged catecholamine treatment and mechanical ventilation and there was a significant association with sepsis, peripheral ischemic complications, new atrial fibrillation, and ventricular fibrillation. In multivariable analysis, bleeding was associated with a significantly higher mortality (hazard ratio: 2.11; 95% confidence interval: 1.63 to 2.75; p < 0.0001). Treatment with active mechanical support by extracorporeal membrane oxygenation or Impella emerged as the major risk factor for bleeding. Conclusions: Risk of bleeding in infarct-related cardiogenic shock is high and associated with increased mortality.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | JACC: Cardiovascular Interventions |
| Jahrgang | 13 |
| Ausgabenummer | 10 |
| Seiten (von - bis) | 1182-1193 |
| Seitenumfang | 12 |
| ISSN | 1936-8798 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 25.05.2020 |
Fördermittel
?Drs. Thiele and Desch contributed equally to this work. This work was supported by the European Union and the German Centre for Cardiovascular Research. Dr. Montalescot has received institutional research grants or consulting/lecture fees from Abbott, Amgen, Actelion, the American College of Cardiology Foundation, AstraZeneca, Axis-Sant?, Bayer, Boston Scientific, Boehringer Ingelheim, Bristol-Myers Squibb, Beth Israel Deaconess Medical, Brigham Women's Hospital, China Heart House, Daiichi-Sankyo, Idorsia, Elsevier, Europa, F?d?ration Fran?aise de Cardiologie, ICAN, Lead-Up, Medtronic, Menarini, MSD, Novo Nordisk, Partners, Pfizer, Quantum Genomics, Sanofi, Servier, and WebMD. Dr. Windecker has received research, educational, and training grant support from Amgen, Abbott, Bayer, Bristol-Myers Squibb, Boston Scientific, Biotronik, Medtronic, Edwards Lifesciences, Sinomed, and Polares. Dr. Zeymer has received grants and personal fees from Bristol-Myers Squibb, Novartis, and AstraZeneca; personal fees from Boehringer Ingelheim, MSD, Sanofi, Trommsdorf, and Amgen; and grants and personal fees from Pfizer and Bayer, outside the submitted work. Dr. Ouarrak has received institutional research grants from the German Centre for Cardiovascular Research. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
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