Why the study?
Managing patients with immune thrombocytopenic purpura and severe thrombocytopenia presenting with acute coronary syndrome is challenging due to bleeding and thrombotic risks during invasive management.
Does steroid pretreatment to improve platelet counts allow safe PCI and dual antiplatelet therapy in patients with ACS and severe thrombocytopenia secondary to ITP?
Case Report (n=1)
Does steroid pretreatment to improve platelet counts allow safe PCI and dual antiplatelet therapy in patients with ACS and severe thrombocytopenia secondary to ITP?
High-dose steroids can safely improve platelet counts in stable patients with ITP and ACS, enabling successful PCI and dual antiplatelet therapy.
Managing patients with immune thrombocytopenic purpura (ITP) and thrombocytopenia is challenging when they present with acute coronary syndrome (ACS). They are at high risk of thrombotic events; however, antiplatelet medications may further lower the platelet count and predispose them to significant bleeding events, especially if undergoing percutaneous coronary intervention (PCI). We present a case of a man in his 70s, previously diagnosed with adult-onset ITP, admitted with ACS and severe thrombocytopenia. He was treated with a single antiplatelet and commenced on high-dose steroids. Once platelet levels had improved, he was started on second antiplatelet and underwent successful PCI with drug-eluting stent. He was safely discharged with dual antiplatelets for 1 month and then lifelong clopidogrel without any immediate complications. Our case shows that such patients, if stable, can be safely and successfully treated with steroids to improve platelet count before proceeding to invasive management and dual antiplatelet medications.
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Shah et al. (2022) conducted a case report in NSTEMI and severe thrombocytopenia secondary to adult-onset ITP (n=1). High-dose steroids and PCI was evaluated on Clinical outcome (successful PCI and discharge).
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