Workpackage 02: Prospective CULPRIT-SHOCK registry

Workpackage leader

The main objective of workpackage 02 is:

To set-up a multinational European collaborative network of tertiary care centres for enrolment of patients with AMI and cardiogenic shock qualifying for the registry
To obtain ethical approval for all participating centres according to the respective laws and rules in all participating countries for registry patients
To include patients not eligible for randomization (WP01) into the registry
To describe the reasons for inclusion into the registry and the 30-day outcome of patients with cardiogenic shock after AMI non-eligible for the randomized CULPRIT-SHOCK trial
To perform intermediate and long-term follow-up at 6 and 12 months to further define the outcome of patients with cardiogenic shock in the registry