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采用评分系统决策启动原发性血小板增多症患者的血小板降低治疗:长期结果。

Decisional flow with a scoring system to start platelet-lowering treatment in patients with essential thrombocythemia: long-term results.

机构信息

Department of Cellular Biotechnology and Hematology, University "La Sapienza", Via Benevento 6, 00161, Rome, Italy.

Ematologia, Istituto Regina Elena, Rome, Italy.

出版信息

Int J Hematol. 2009 Nov;90(4):486-491. doi: 10.1007/s12185-009-0401-7. Epub 2009 Aug 22.

DOI:10.1007/s12185-009-0401-7
PMID:19701677
Abstract

We prospectively tested, at diagnosis in essential thrombocythemia (ET) patients with no clear indication to platelet (PLT)-lowering treatment, a scoring system based on age, PLT level, cardiovascular diseases, previous thrombotic events, smoking and dysmetabolic diseases. From 04/92 to 03/98, 168 consecutive patients were enrolled. Hydroxyurea (HU) was started at diagnosis in 32 "symptomatic" patients and in 33 patients aged >70 years. The remaining 103 patients ("asymptomatic" and aged <70 years) were classified according to our scoring system. Thirty-two patients with score > or = 4 started HU early after diagnosis. The remaining 71 patients with score <4 at diagnosis received anti-aggregating agents only; of them, 24 (33.8%) started HU during follow-up after a median time from diagnosis of 28 months, while 47 (66.2%) did not start any PLT-lowering treatment. Thrombotic complications occurred in 9/103 patients (8.7%); in particular, they occurred in 4/32 patients (12.5%) with score > or = 4 receiving HU since diagnosis and in 5/71 (7%) with score <4 under anti-aggregating agents only. This scoring system appears effective to discriminate a different risk of thrombotic events, and could be useful to decide when a PLT-lowering therapy needs to be started.

摘要

我们前瞻性地在没有明确血小板(PLT)降低治疗指征的原发性血小板增多症(ET)患者中进行了测试,该测试基于年龄、PLT 水平、心血管疾病、既往血栓事件、吸烟和代谢紊乱疾病建立了一个评分系统。从 1992 年 4 月至 1998 年 3 月,共纳入了 168 例连续患者。在 32 名“有症状”患者和 33 名年龄>70 岁的患者中,诊断时即开始使用羟基脲(HU)。其余 103 名“无症状”且年龄<70 岁的患者根据我们的评分系统进行分类。32 名评分>或=4 的患者在诊断后不久即开始 HU。其余 71 名诊断时评分<4 的患者仅接受抗血小板药物;其中,24 名(33.8%)在中位时间为 28 个月的诊断后开始 HU,而 47 名(66.2%)未开始任何 PLT 降低治疗。103 例患者中有 9 例(8.7%)发生血栓并发症;特别是,在诊断后开始 HU 的评分>或=4 的 32 例患者中发生了 4 例(12.5%),而在仅接受抗血小板药物的评分<4 的 71 例患者中发生了 5 例(7%)。该评分系统似乎能有效区分不同的血栓事件风险,可能有助于决定何时需要开始 PLT 降低治疗。

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Decisional flow with a scoring system to start platelet-lowering treatment in patients with essential thrombocythemia: long-term results.采用评分系统决策启动原发性血小板增多症患者的血小板降低治疗:长期结果。
Int J Hematol. 2009 Nov;90(4):486-491. doi: 10.1007/s12185-009-0401-7. Epub 2009 Aug 22.
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本文引用的文献

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The presence of the JAK2 V617F mutation is associated with a higher haemoglobin and increased risk of thrombosis in essential thrombocythaemia.JAK2 V617F突变的存在与真性红细胞增多症中较高的血红蛋白水平及血栓形成风险增加相关。
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When and how to treat essential thrombocythemia.何时以及如何治疗原发性血小板增多症。
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10
Practice guidelines for the therapy of essential thrombocythemia. A statement from the Italian Society of Hematology, the Italian Society of Experimental Hematology and the Italian Group for Bone Marrow Transplantation.原发性血小板增多症治疗实践指南。来自意大利血液学会、意大利实验血液学会和意大利骨髓移植小组的声明。
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