Splenic rupture complicating periinterventional glycoprotein IIb/IIIa antagonist therapy for myocardial infarction in polycythemia vera.

E B Friedrich, M Kindermann, A Link, M Böhm
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引用次数: 11

Abstract

Polycythemia vera is a myeloproliferative disorder predisposing to thromboembolic and bleeding complications. We report the case of a patient with polyglobuly, leukocytosis, and thrombocytosis, who suffered from acute ST-segment elevation myocardial infarction due to thrombotic high-grade pre-stent stenosis two months after percutaneous coronary intervention for complex coronary one vessel disease. Following re-PTCA and stent implantation in conjunction with periinterventional GP IIb/IIIa antagonist treatment, the patient was initially symptom free for about two hours before rapidly developing signs of a hemorrhagic shock. An abdominal CT scan showed splenic rupture with massive intraabdominal hemorrhage as a consequence of secondary bleeding into multiple pre-existing splenic infarctions. The patient's condition stabilized after emergency splenectomy. Subsequent bone marrow biopsy revealed the presence of polycythemia vera. Post-operatively, the patient was treated with the anti-platelet agents aspirin and clopidogrel to prevent subacute stent thrombosis. Additionally, cyto-reductive therapy with hydroxyurea was initiated because of a further increase in the platelet count. In patients with polycythemia vera, the indication for treatment with GP IIb/IIIa antagonists should be carefully weighed against the potentially serious bleeding complications. Should treatment be established, a risk stratification using abdominal sonography and bleeding time testing is recommended, while during treatment red blood count, platelet count, coagulation tests, and hemodynamic parameters should be closely monitored.

真性红细胞增多症患者脾破裂并发介入周糖蛋白IIb/IIIa拮抗剂治疗心肌梗死。
真性红细胞增多症是一种骨髓增生性疾病,易导致血栓栓塞和出血并发症。我们报告一例患有多球蛋白、白细胞增多和血小板增多症的患者,在复杂冠状动脉单支血管疾病经皮冠状动脉介入治疗两个月后,由于血栓性支架前高级别狭窄而发生急性st段抬高型心肌梗死。在重新ptca和支架植入以及围介入治疗GP IIb/IIIa拮抗剂治疗后,患者最初无症状约2小时,但迅速出现失血性休克迹象。腹部CT扫描显示脾破裂伴大量腹内出血,这是多次脾梗塞继发性出血的结果。急诊脾切除术后患者病情稳定。随后骨髓活检显示真性红细胞增多症的存在。术后给予抗血小板药物阿司匹林和氯吡格雷预防亚急性支架血栓形成。此外,由于血小板计数进一步增加,开始使用羟基脲进行细胞减少治疗。真性红细胞增多症患者,应仔细权衡GP IIb/IIIa拮抗剂治疗的适应症与潜在的严重出血并发症。如果确定治疗,建议使用腹部超声和出血时间检测进行风险分层,同时在治疗期间应密切监测红细胞计数、血小板计数、凝血试验和血流动力学参数。
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