Key result
Abciximab and heparin during PCI linked to acute profound thrombocytopenia within 9 hours.
Case Report (n=1)
This case highlights the critical need for routine platelet monitoring 2-4 hours post-abciximab infusion to rapidly identify acute profound thrombocytopenia.
Alerts clinicians to early thrombocytopenia risk after abciximab; leaves open whether routine monitoring improves PCI outcomes.
Abciximab (c7E3 Fab) is one of the three potent intravenous glycoprotein IIb/IIIa receptor inhibitors (along with eptifibatide and tirofiban) that have shown significant positive outcomes when used in patients with intracoronary thrombus. However, major side effects have been reported with its use including hypotension, major bleeding and thrombocytopenia. This case is a 53-year-old man presenting with acute chest pain diagnosed with non-ST-elevation myocardial infarction, who underwent percutaneous coronary intervention with abciximab and heparin infusion and developed acute profound thrombocytopenia (platelet count <20,000/L) within 9 hours of infusion. This case demonstrates the importance of routinely monitoring the platelet count prior to and 2-4 hours following abciximab infusion and differentiating other causes of acute profound thrombocytopenia, particularly pseudothrombocytopenia and heparin-induced thrombocytopenia.
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Golden et al. (2017) conducted a case report in Non-ST-elevation myocardial infarction (NSTEMI) (n=1). Abciximab and heparin infusion was evaluated on Acute profound thrombocytopenia (platelet count <20,000/L). A 53-year-old man developed acute profound thrombocytopenia (platelet count <20,000/L) within 9 hours of receiving abciximab and heparin infusion during PCI for NSTEMI.
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