CULPRIT-SHOCK: Multivessel PCI in cardiogenic shock
American College of Cardiology News Nov 03, 2017
Patients with multivessel coronary artery disease and acute myocardial infarction with cardiogenic shock that underwent culprit lesion only percutaneous coronary intervention (PCI) had a lower 30-day risk of death or severe renal failure compared to those who had immediate multivessel PCI, said researchers presented results of CULPRIT-SHOCK trial at Transcatheter Cardiovascular Therapeutics (TCT 2017) meeting.
The trial randomized 706 patients to either culprit lesion only PCI, with the option of staged revascularization, or immediate multivessel PCI. The primary efficacy endpoint was 30-day mortality or severe renal failure requiring renal replacement therapy. Safety endpoints included assessment of bleeding and stroke. Roughly half of enrolled patients had been resuscitated prior to randomization, 62% presented with STEMI, and 28% received some form of hemodynamic support.
Results, which were also published in the New England Journal of Medicine, showed the rate of the primary composite endpoint was significantly lower in patients assigned to culprit lesion only PCI compared to immediate multivessel PCI (45.9% vs 55.4%). There was a significant difference between study groups with respect to all-cause mortality (43.3% vs 51.5%), while the difference in the rates of renal replacement therapy was not statistically significant (11.6% vs 16.4%). Additionally, researchers noted no significant differences in the time to hemodynamic stabilization, length of intensive care unit stay, or requirement for and duration of catecholamine therapy.
"Cardiogenic shock during myocardial infarction is a relatively rare, but extremely dangerous condition, in which the heart is unable to pump enough blood to meet the body's needs," said Holger Thiele, MD, director of the Heart Center Leipzig - University Hospital in Leipzig, Germany. "Not only is CULPRIT-SHOCK the largest randomized trial in cardiogenic shock, it is also the first randomized trial to assess a strategy of multivessel PCI versus culprit vessel only PCI with the option of staged revascularization in this patient population. Based on these 30-day results, culprit vessel only PCI reduces mortality or severe renal failure."
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The trial randomized 706 patients to either culprit lesion only PCI, with the option of staged revascularization, or immediate multivessel PCI. The primary efficacy endpoint was 30-day mortality or severe renal failure requiring renal replacement therapy. Safety endpoints included assessment of bleeding and stroke. Roughly half of enrolled patients had been resuscitated prior to randomization, 62% presented with STEMI, and 28% received some form of hemodynamic support.
Results, which were also published in the New England Journal of Medicine, showed the rate of the primary composite endpoint was significantly lower in patients assigned to culprit lesion only PCI compared to immediate multivessel PCI (45.9% vs 55.4%). There was a significant difference between study groups with respect to all-cause mortality (43.3% vs 51.5%), while the difference in the rates of renal replacement therapy was not statistically significant (11.6% vs 16.4%). Additionally, researchers noted no significant differences in the time to hemodynamic stabilization, length of intensive care unit stay, or requirement for and duration of catecholamine therapy.
"Cardiogenic shock during myocardial infarction is a relatively rare, but extremely dangerous condition, in which the heart is unable to pump enough blood to meet the body's needs," said Holger Thiele, MD, director of the Heart Center Leipzig - University Hospital in Leipzig, Germany. "Not only is CULPRIT-SHOCK the largest randomized trial in cardiogenic shock, it is also the first randomized trial to assess a strategy of multivessel PCI versus culprit vessel only PCI with the option of staged revascularization in this patient population. Based on these 30-day results, culprit vessel only PCI reduces mortality or severe renal failure."
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