Percutaneous coronary intervention for cardiogenic shock in the SHOCK trial
John G. Webb, MD, FACC*,*,
April M. Lowe, MS ,
Timothy A. Sanborn, MD, FACC ,
Harvey D. White, DSc ,
Lynn A. Sleeper, ScD ,
Ronald G. Carere, MD, FACC*,
Christopher E. Buller, MD, FACC||,
S. Chiu Wong, MD, FACC¶,
Jean Boland, MD#,
Vlad Dzavik, MD**,
Mark Porway, MD, FACC ,
Gordon Pate, MB*,
Geoffrey Bergman, MD, FACC¶,
Judith S. Hochman, MD, FACC for the SHOCK Investigators
* St. Paul's Hospital, Vancouver, Canada
New England Research Institutes, Watertown, Massachusetts, USA
Evanston Northwestern Healthcare, Evanston, Illinois, USA
Green Lane Hospital, Auckland, New Zealand
|| Vancouver General Hospital, Vancouver, Canada
¶ New York Presbyterian, New York, New York, USA
# CHR Citadelle, Liege, Belgium
** Toronto General Hospital, Toronto, Canada
 Baystate Medical Center, Springfield, Massachusetts, USA
 Division of Cardiology, New York University School of Medicine, New York, New York, USA

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Figure 1 Flowchart of SHOCK Trial patients. CABG = coronary artery bypass graft surgery; PCI = percutaneous coronary intervention.
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Figure 2 Relationship of stent implantation in the culprit artery and one-year survival in SHOCK trial patients assigned to early revascularization and undergoing percutaneous coronary intervention.
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Figure 3 Relationship of final angiographic culprit artery Thrombolysis In Myocardial Infarction (TIMI) flow grade after percutaneous coronary intervention and 30-day survival in SHOCK trial patients assigned to early revascularization.
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Figure 4 Time trends in the interventional management of cardiogenic shock and one-year survival. A significant increase in the use of multivessel percutaneous coronary intervention (PCI) (p = 0.018), stents, and glycoprotein IIb/IIIa antagonists (both <0.001) was observed. One-year survival and PCI success rates were similar over time (p = 0.889 for survival and p = 0.128 for success).
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