Why the study?
Essential thrombocythemia carries risks of both bleeding from abnormal platelet function and thrombosis from excessive platelet proliferation, creating management dilemmas during antithrombotic therapy.
In patients with essential thrombocythemia undergoing PCI, early de-escalation from DAPT to single antiplatelet therapy may be a viable option to manage excessive bleeding risk without causing stent thrombosis.
DAPT may precipitate alveolar hemorrhage in ET patients with MI; this case leaves open optimal antithrombotic strategies.
BACKGROUND Essential thrombocythemia (ET) is a risk factor both for bleeding caused by abnormal platelet function and for thrombus formation caused by excessive platelet proliferation. We present a rare case of alveolar hemorrhage after dual antiplatelet therapy (DAPT), a serious bleeding complication of antithrombotic therapy, in a patient with an acute myocardial infarction complicated by ET. CASE REPORT A 75-year-old man was treated for ET. He experienced an acute myocardial infarction, and an emergent percutaneous coronary intervention was subsequently performed. DAPT was started just before stent implantation. Because a left ventricular thrombus was suspected in spite of DAPT, anticoagulant therapy with heparin was added. On day 7, a large amount of hemoptysis was observed, and alveolar hemorrhage was diagnosed. Although the antithrombotic treatment was de-escalated from DAPT to single antiplatelet therapy, no stent thrombosis or recurrence of alveolar hemorrhage was observed. CONCLUSIONS In ET patients, reduced platelet function due to thrombocytosis and strong antithrombotic therapy may cause an excessive bleeding risk. Switching from DAPT to antiplatelet monotherapy at the early stage of stent implantation is a treatment option in situations in which excessive bleeding risk is a concern.
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Ishikura et al. (2021) studied this question.
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