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Cangrelor Induces More Potent Platelet Inhibition without Increasing Bleeding in Resuscitated Patients
Florian Prüller1, Lukasz Bis2, Oliver Leopold Milke3
1Clinical Institute of Medical and Chemical Laboratory Diagnostics, University Hospital Graz, Graz 8036, Austria. florian.prueller@klinikum-graz.at.
Insights
Intravenous cangrelor provided stronger P2Y12-inhibition than oral agents in myocardial infarction (MI) patients undergoing therapeutic hypothermia (TH). This effective antiplatelet therapy did not increase bleeding risk, showing feasibility in this critical patient group.
Area of Science:
- Cardiology
- Pharmacology
- Critical Care Medicine
Background:
- Dual antiplatelet therapy is standard for myocardial infarction (MI) patients after resuscitation and therapeutic hypothermia (TH).
- Comparing intravenous cangrelor with oral P2Y12-inhibitors is crucial for optimizing antiplatelet effects and bleeding risk in this population.
Purpose of the Study:
- To prospectively compare the antiplatelet efficacy and bleeding risk of intravenous cangrelor versus oral P2Y12-inhibitors.
- To evaluate cangrelor's feasibility and effectiveness in patients with MI receiving TH.
Main Methods:
- Prospective comparison of two matched patient cohorts: CANGRELOR (NCT03445546) and ORAL P2Y12 (NCT02914795).
- Platelet function testing using light-transmittance aggregometry monitored over 4 days.
- Assessment of bleeding events using TIMI and BARC criteria, along with blood transfusion rates and hematological parameters.
Main Results:
- Stronger P2Y12-inhibition was observed with cangrelor compared to oral P2Y12-inhibitors at day 1 (ADP AUC: 26.0 vs. 160.9).
- This difference diminished as patients transitioned from cangrelor to oral agents.
- No significant differences in bleeding events (TIMI, BARC), blood transfusions, or changes in Hb/Hct were noted between groups.
Conclusions:
- Intravenous cangrelor is feasible and effective in resuscitated MI patients treated with TH.
- Cangrelor demonstrates superior platelet inhibition compared to oral P2Y12-inhibitors without elevating bleeding risk.
- This suggests cangrelor as a viable option for potent antiplatelet therapy in this high-risk cohort.
Abstract:
Dual antiplatelet therapy is the standard of care for patients with myocardial infarction (MI), who have been resuscitated and treated with therapeutic hypothermia (TH). We compare the antiplatelet effect and bleeding risk of intravenous cangrelor to oral P2Y12-inhibitors in patients with MI receiving TH in a prospective comparison of two matched patient cohorts. Twenty-five patients within the CANGRELOR cohort were compared to 17 patients receiving oral P2Y12-inhibitors. CANGRELOR group (NCT03445546) and the ORAL P2Y12 Group (NCT02914795) were registered at clinicaltrials.gov. Platelet function testing was performed using light-transmittance aggregometry and monitored for 4 days. P2Y12-inhibition was stronger in CANGRELOR compared to ORAL P2Y12 (adenosine diphosphate (ADP) (area under the curve (AUC)) 26.0 (5.9⁻71.6) vs. 160.9 (47.1⁻193.7)) at day 1. This difference decreased over the following days as more patients were switched from CANGRELOR to oral P2Y12-inhibitor treatment. There was no difference in the effect of aspirin between the two groups. We did not observe significant differences with respect to thrombolysis in myocardial infarction (TIMI) or Bleeding Academic Research Consortium (BARC) classified bleedings, number of blood transfusions or drop in haemoglobin B (Hb) or hematocrit (Hct) over time. Cangrelor treatment is not only feasible and effective in resuscitated patients, but also inhibited platelet function more effectively than orally administered P2Y12-inhibitors without an increased event rate for bleeding.
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