BMC2 PCI Risk Calculator for Death, Transfusion, and CIN

Age of patient at the time of care.
Indicate the patient's weight in kilograms.
Indicate the patient's height in centimeters.
Diabetes Mellitus
Any occurrence between birth and arrival at this facility.
Indicate the most aggressive therapy the patient presented with.
Chronic Lung Disease
Any occurrence between birth and arrival at this facility.
Heart Failure w/in 2 Weeks
Indicate if there is physician documentation or report that the patient has been in a state of heart failure within the past 2 weeks.
The highest value between 2 weeks prior to current procedure and current procedure
Indicate the status of the PCI. The status is determined at the time the operator decides to perform a PCI.
Indicate the reason the PCI is being performed.
Indicate the patient’s coronary artery disease (CAD) presentation. Choose the worst status.
The highest value between 2 weeks prior to current procedure and current procedure
Code the best estimate of current left ventricular ejection fraction.
%
Indicate if the left bventricular ejection fraction is not known.
Indicate the most recent hemoglobin level in g/dL.
Indicate if the pre-procedure HGB was not drawn, or not drawn at your facility, or drawn at your facility using point-of-care (bedside) testing.
Indicate the pre-procedure CK-MB baseline that was drawn at your facility. Exclude point-of-care (bedside) testing. (ng/mL)
Indicate if the pre-procedure CK baseline was not drawn, or not drawn at your facility, or drawn at your facility using point-of-care (bedside) testing.
Indicate the pre-procedure Troponin I baseline, in ng/mL, if drawn at your facility. Exclude point-of-care (bedside) testing.
Indicate if the pre-procedure Troponin I baseline was not drawn, not drawn at your facility, or drawn at your facility using point-of-care (bedside) testing.
Indicate the pre-procedure Troponin T baseline, in ng/mL, if drawn at your facility. Exclude point-of-care (bedside) testing.
Indicate if the pre-procedure Troponin T baseline was not drawn, not drawn at your facility, or drawn at your facility using point-of-care (bedside) testing.
Indicate the patient's most recent creatinine level in mg/dL.
Indicate if the pre-procedure creatinine was not drawn, or not drawn at your facility, or drawn at your facility using point-of-care (bedside) testing.
Cardiogenic shock
Any occurrence between 24 prior to through the start of PCI
Cardiac arrest w/in 24 hours
Indicate if the patient has had an episode of cardiac arrest within 24 hours of procedure.
Preprocedural vasopressor use
Pre-PCI administration of a vasopressor.
Pre-procedural atrial fibrilation