Coronary disease & ACS

Prepercutaneous coronary intervention Zalunfiban dose-response relationship to target vessel blood flow at initial angiogram in st-elevation myocardial infarction – A post hoc analysis of the cel-02 phase IIa study

Am Heart JPublished Post hoc analysis of an open-label phase IIa study

Authors' conclusion

This post hoc analysis found that higher doses of zalunfiban administered in the cardiac catheterization lab prior to vascular access were associated with greater coronary and myocardial perfusion, and lower thrombus burden at initial angiogram in patients with STEMI undergoing primary percutaneous coronary intervention.

Study context

Population
ST-elevation myocardial infarction (STEMI) patients; zalunfiban given in cath lab before vascular access, ∼10 to 15 minutes before initial angiogramTwentyfour evaluable for angiography
Participants
27 patients
Comparison
Zalunfiban 0.075 vs 0.090 vs 0.110 mg/kg
  • 0.075 mg/kgn = 7
  • 0.090 mg/kgn = 9
  • 0.110 mg/kgn = 8
Primary endpoint
Dose-dependent association with infarct-related artery (IRA) angiographic indices (coronary and myocardial blood flow, thrombus burden)
Follow-up
Initial angiogram
Methodological detailsblinded independent core laboratory, All angiographic data analysed by a blinded, independent, core laboratory
  • Blinded independent core laboratory
  • All angiographic data analysed by a blinded, independent, core laboratory

Primary result

As reported in the abstract

TIMI flow grade 2 or 3

0.075 mg/kg

1 of 7

events

0.090 mg/kg

6 of 9

events

0.110 mg/kg

7 of 8

events

P for trend = 0.004

TIMI myocardial perfusion grade 3 more frequent with higher dose
P for trend = 0.005
TIMI thrombus ≥4 grade inversely related to dose
P for trend = 0.02

Original publication

Prepercutaneous coronary intervention Zalunfiban dose-response relationship to target vessel blood flow at initial angiogram in st-elevation myocardial infarction – A post hoc analysis of the cel-02 phase IIa study. Am Heart J. Published 22 April 2023. doi:10.1016/j.ahj.2023.04.009

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.