Acute cardiac care & resuscitationRandomised controlled trial

Impact of tocilizumab on endothelial function following out-of-hospital cardiac arrest: a substudy of the IMICA randomized controlled trial

Eur Heart J Acute Cardiovasc CarePublished

  • randomized controlled trial
  • substudy

Authors' conclusion

Plasma syndecan-1 decline was less pronounced in comatose OHCA patients treated with tocilizumab, without affecting sTM or PECAM-1. This contrasts with previous IMICA findings of reduced systemic inflammation, vasopressor use, and myocardial injury, suggesting a complex relationship between inflammation and endothelial injury. Finally, PECAM-1 levels already at hospital admission had a moderate predictive value for mortality.

Study context

Population
Comatose resuscitated out-of-hospital cardiac arrest (OHCA) patientscomatose OHCA patients randomized in the IMICA trial
Participants
80 participants
Comparison
tocilizumab or placebo

Primary result

As reported in the abstract

Syndecan-1 concentrations · 0 h, 24, 48, and 72 h

Syndecan-1 concentrations declined over time in both groups; reduction significantly less in the tocilizumab group

all P < 0.003

Further findings

Soluble thrombomodulin (sTM) and PECAM-1

No significant between-group differences

Prediction of 30-day mortality by baseline biomarkers

baseline PECAM-1 AUROC
0.71 (95% CI 0.59-0.83)
Syndecan-1 AUROC (no predictive value)
0.61
sTM AUROC (no predictive value)
0.53

Original publication

Impact of tocilizumab on endothelial function following out-of-hospital cardiac arrest: a substudy of the IMICA randomized controlled trial. Eur Heart J Acute Cardiovasc Care. Published 10 March 2026. doi:10.1093/ehjacc/zuag034

Summarised from the published abstract; every number is checked against it