Trial (year), [reference] |
Parameters |
Participants |
SCAI stage |
Obling et al. (2018), [110] |
Age, stroke, symptom onset to intervention, anterior STEMI, HR/SAP ratio, comatose status after cardiopulmonary resuscitation |
2247 STEMI patients treated by primary PCI |
A-B |
ORBI (2018), [107] |
Age>70 years (2 points), previous stroke/TIA (2 points), cardiac arrest upon admission (3 points), anterior STEMI (1 point), FMC-to-PCI delay>90 min (2 points), Killip class (2-6 points), combination of SAP<125 mmHg and pulse pressure<45 mmHg (4 points), glycemia>10 mmol/L (3 points), culprit lesion in the left main artery (5 points), post-PCI TIMI-flow<3 (5 points) |
6838 patients without CS upon admission and treated by primary PCI |
A-B |
ALKK (2004), [111] |
Left main artery disease, TIMI-flow<3 post-PCI, advanced age, three-vessel disease, long time intervals between symptom onset and PCI |
1333 patients from the ALKK registry |
C-E |
Sutton et al. (2005), [112] |
Previous myocardial infarction, age>70 years, failed reperfusion |
113 patients |
C-E |
ACC-NCDR (2005), [113] |
Age, female gender, serum creatinine>2 mg/dL, total occlusion of the left anterior descending artery, no stent used, no glycoprotein IIb/IIIa inhibitor used |
483 patients from the ACC-NCDR |
C-E |
TRIUMPH (2009), [114] |
SAP, creatinine clearance, number of vasopressors used, norepinephrine dose used |
396 patients from the TRIUMPH trial |
C-E |
SHOCK (2010), [115] |
Clinical score: age, anoxic brain damage, end-organ hypoperfusion, shock upon admission, prior CABG, non-inferior infarction, serum creatinine≥1.9 mg/dL, SAP hemodynamic plus clinical score: stroke work, LVEF<28%, age, anoxic brain damage, end-organ hypoperfusion |
1217 patients from the SHOCK trial and registry |
C-E |
CARD-SHOCK (2014), [103] |
Prior CABG, ACS etiology, confusion, previous infarction, serum lactates, LVEF, age, SAP |
219 patients from a multicenter European registry |
C-E |
IABP-SHOCK II (2017), [106] |
Age>73 years (1 point), previous stroke (2 points), blood glucose>191 mg/dL or 10.6 mmol/L (1 point), serum creatinine>1.5 mg/dL or 132.6 μmol/L(1 point), serum lactates>5 mmol/L (2 points), TIMI-flow<3 post-PCI (2 points) |
600 patients from the IABP-SHOCK II study |
C-E |