真性红细胞增多症和原发性血小板增多症患者复发性静脉血栓形成

Valerio De Stefano , Tommaso Za , Elena Rossi , Elena Elli , Alessandro M. Vannucchi , Marco Ruggeri , Caterina Micò , Nicola Vianelli , Rossella R. Cacciola , Alessia Tieghi , Cristina Santoro , Enrico M. Pogliani , Paola Guglielmelli , Lisa Pieri , Francesca Scognamiglio , Francesco Rodeghiero , Guido Finazzi , Luigi Gugliotta , Giuseppe Leone , Tiziano Barbui
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引用次数: 0

摘要

目的真性红细胞增多症和原发性血小板增多症患者再次发生静脉血栓栓塞(VTE)的风险尚不清楚,首次发生深静脉血栓形成(DVT)后是否应推荐长期口服抗凝药物或乙酰水杨酸治疗尚不清楚。这项多中心队列研究旨在评估真性红细胞增多症或原发性血小板增多症患者的静脉血栓栓塞复发率,并与既往静脉血栓栓塞且无肿瘤疾病的对照组进行比较。患者和方法回顾性分析了79例骨髓增生性疾病(MPDs;真性红细胞增多症/原发性血小板增多症,45/34),既往近端有深静脉血栓。患者分为两组。第一组包括41名患者,在口服抗凝治疗6个月后接受乙酰水杨酸治疗。第二组38例患者长期口服抗凝治疗,不含乙酰水杨酸。大多数患者接受细胞毒性药物治疗。结果与176例既往近端深静脉血栓患者短期口服抗凝治疗后的复发情况进行了比较。结果真性红细胞增多症和原发性血小板增多症患者中,乙酰水杨酸组DVT复发率(32%)高于口服抗凝治疗组(16%),但差异无统计学意义。接受乙酰水杨酸治疗的MPD患者DVT复发率与未患癌症的患者相当(33%)。静脉血栓栓塞复发的累积概率表明,长期口服抗凝药物治疗的MPD患者的静脉血栓栓塞事件有减少的趋势。在MPDs患者中,口服抗凝治疗或乙酰水杨酸期间大出血的发生率分别为1%和0.5%患者-年(观察年)。结论:本回顾性分析建议真性红细胞增多症和原发性血小板增多症患者首次DVT后长期口服抗凝治疗。然而,应权衡这一适应症与重大出血事件的风险,似乎较低的长期预防乙酰水杨酸。因此,一项前瞻性临床试验比较乙酰水杨酸在真性红细胞增多症和原发性血小板增多症患者中与口服抗凝治疗在预防静脉血栓栓塞复发方面的作用是有必要的。
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Recurrent Venous Thrombosis in Patients with Polycythemia Vera and Essential Thrombocythemia

Purpose

The risk of recurrent venous thromboembolism (VTE) in patients with polycythemia vera and essential thrombocythemia has been scarcely addressed, and whether long-term oral anticoagulant treatment or acetylsalicylic acid should be recommended after first occurrence of deep venous thrombosis (DVT) is unknown. This multicenter cohort study was aimed to assess the rate of recurrent VTE in patients with polycythemia vera or essential thrombocythemia in comparison with a control group of individuals with previous VTE and without neoplastic diseases.

Patients and Methods

We retrospectively estimated the rate of recurrence in 79 patients with myeloproliferative disorders (MPDs; polycythemia vera/essential thrombocythemia, 45/34) and with a previous proximal DVT. Patients were divided into 2 groups. The first comprised 41 patients who received acetylsalicylic acid after 6 months of oral anticoagulant treatment. The second group was composed of 38 patients given long-term oral anticoagulant treatment without acetylsalicylic acid. The majority of patients were treated with cytotoxic drugs. The results were compared with the recurrences seen in 176 patients without cancer with previous proximal DVT given short-term oral anticoagulant treatment.

Results

In the patients with polycythemia vera and essential thrombocythemia, the rate of recurrent DVT was higher in the group receiving acetylsalicylic acid (32%) compared with the group on oral anticoagulant treatment (16%), although not statistically significant. The rate of recurrent DVT in MPD cases receiving acetylsalicylic acid was quite similar to that of patients without cancer (33%). The cumulative probability of recurrent VTE indicated a trend of fewer events in the MPD cases on long-term oral anticoagulant treatment. In the patients with MPDs, the incidence of major bleeding during oral anticoagulant treatment or acetylsalicylic acid was 1% and 0.5% patient-years (years of observation), respectively.

Conclusion

This retrospective analysis would suggest a long-term oral anticoagulant treatment after a first DVT in patients with polycythemia vera and essential thrombocythemia. However, this indication should be weighed against the risk of major hemorrhagic events that seems lower during long-term prophylaxis with acetylsalicylic acid. Therefore, a prospective clinical trial comparing acetylsalicylic acid in patients with polycythemia vera and essential thrombocythemia with oral anticoagulant treatment in the prevention of recurrent VTE is warranted.

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