Georg Fuernau1,2,3, Karl Fengler4, Steffen Desch5,6, Ingo Eitel5,6, Franz-Josef Neumann7, Hans-Georg Olbrich8, Antoinette de Waha9, Suzanne de Waha5,6, Gert Richardt10, Marcus Hennersdorf11, Klaus Empen12, Rainer Hambrecht13, Christian Jung14, Michael Böhm15, Janine Pöss5,6, Ruth H Strasser16, Steffen Schneider17, Taoufik Ouarrak17, Gerhard Schuler4, Karl Werdan18, Uwe Zeymer17, Holger Thiele5,6. 1. Medical Clinic II (Cardiology/Angiology/Intensive Care Medicine), University Heart Center Lübeck, University Hospital Schleswig-Holstein, Ratzeburger Allee 160, Lübeck, 23538, Germany. georg.fuernau@uksh.de. 2. Department of Internal Medicine/Cardiology, University of Leipzig Heart Center, Leipzig, Germany. georg.fuernau@uksh.de. 3. German Centre for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Lübeck, Germany. georg.fuernau@uksh.de. 4. Department of Internal Medicine/Cardiology, University of Leipzig Heart Center, Leipzig, Germany. 5. Medical Clinic II (Cardiology/Angiology/Intensive Care Medicine), University Heart Center Lübeck, University Hospital Schleswig-Holstein, Ratzeburger Allee 160, Lübeck, 23538, Germany. 6. German Centre for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Lübeck, Germany. 7. Department of Cardiology, Bad Krozingen Heart Center, University of Freiburg, Bad Krozingen, Germany. 8. Department of Internal Medicine I, Hospital Langen, Langen, Germany. 9. Department of Cardiology, German Heart Center Munich, Munich, Germany. 10. Department of Cardiology/Angiology, Bad Segeberg Heart Center, Bad Segeberg, Germany. 11. Department of Internal Medicine I, Klinikum am Gesundbrunnen, Heilbronn, Germany. 12. Department of Internal Medicine B, University of Greifswald, Greifswald, Germany. 13. Department of Cardiology/Angiology, Klinikum Links der Weser, Bremen, Germany. 14. Division of Cardiology, Pulmonology and Vascular Medicine, Department of Internal Medicine, Heinrich-Heine-University, Düsseldorf, Germany. 15. Department of Internal Medicine III, University of Homburg, Homburg/Saar, Germany. 16. Clinic for Internal Medicine/Cardiology, University of Dresden-Heart Center, Dresden, Germany. 17. Institut für Herzinfarktforschung, Ludwigshafen, Germany. 18. Department of Internal Medicine III, Martin-Luther-University Halle-Wittenberg, Halle/Saale, Germany.
Abstract
BACKGROUND: In myocardial infarction without cardiogenic shock (CS), the affected coronary vessel has significant influence on the final infarct size and patient prognosis. CS data on this relation are scarce. The objective of this study was to determine the prognostic relevance of the culprit lesion location in patients with CS complicating acute myocardial infarction. METHODS: In the Intraaortic Balloon Pump in Cardiogenic Shock II (IABP-SHOCK II) trial patients with CS were randomized to therapy with intraaortic balloon pump or control. Additional CS patients not eligible for the randomized trial were included in a registry. We compared the location of the culprit lesions in these patients with regard to the affected coronary vessel [left main (LM), left anterior descending (LAD), left circumflex (LCX) and right coronary artery (RCA)] and location within the vessel (proximal, mid or distal) regarding short- and long-term outcome. RESULTS: Of 758 patients, the majority had the culprit lesion in the LAD (44 %) compared to RCA (27 %), LCX (19 %) or LM (10 %). Proximal lesions were more frequent than mid or distal culprit lesions (60 vs. 27 vs. 13 %, p < 0.001). No differences were observed for mortality with respect to either culprit vessel (log-rank p value = 0.54). In contrast, a higher mortality was observed for patients with distal culprit lesions after 1 year (log-rank p value = 0.04). This difference persisted after multivariable adjustment (hazard ratio for distal lesions 1.40; 95 % confidential interval 1.03-1.90; p = 0.03). CONCLUSION: For patients with CS complicating myocardial infarction, the culprit vessel seems to be unrelated with mortality whereas distal culprit lesions may have a worse outcome.
RCT Entities:
BACKGROUND: In myocardial infarction without cardiogenic shock (CS), the affected coronary vessel has significant influence on the final infarct size and patient prognosis. CS data on this relation are scarce. The objective of this study was to determine the prognostic relevance of the culprit lesion location in patients with CS complicating acute myocardial infarction. METHODS: In the Intraaortic Balloon Pump in Cardiogenic Shock II (IABP-SHOCK II) trial patients with CS were randomized to therapy with intraaortic balloon pump or control. Additional CS patients not eligible for the randomized trial were included in a registry. We compared the location of the culprit lesions in these patients with regard to the affected coronary vessel [left main (LM), left anterior descending (LAD), left circumflex (LCX) and right coronary artery (RCA)] and location within the vessel (proximal, mid or distal) regarding short- and long-term outcome. RESULTS: Of 758 patients, the majority had the culprit lesion in the LAD (44 %) compared to RCA (27 %), LCX (19 %) or LM (10 %). Proximal lesions were more frequent than mid or distal culprit lesions (60 vs. 27 vs. 13 %, p < 0.001). No differences were observed for mortality with respect to either culprit vessel (log-rank p value = 0.54). In contrast, a higher mortality was observed for patients with distal culprit lesions after 1 year (log-rank p value = 0.04). This difference persisted after multivariable adjustment (hazard ratio for distal lesions 1.40; 95 % confidential interval 1.03-1.90; p = 0.03). CONCLUSION: For patients with CS complicating myocardial infarction, the culprit vessel seems to be unrelated with mortality whereas distal culprit lesions may have a worse outcome.
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