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慢性肝病中血小板减少症的管理:聚焦药物治疗策略

Management of Thrombocytopenia in Chronic Liver Disease: Focus on Pharmacotherapeutic Strategies.

作者信息

Maan Raoel, de Knegt Robert J, Veldt Bart J

机构信息

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center Rotterdam, 's Gravendijkwal 230, Room Ha 206, 3015 CE, Rotterdam, The Netherlands.

出版信息

Drugs. 2015 Nov;75(17):1981-92. doi: 10.1007/s40265-015-0480-0.

Abstract

Thrombocytopenia (platelet count <150 × 10(9)/L) often complicates chronic liver disease, impeding optimal management of these patients. The prevalence of this manifestation ranges from 6% among non-cirrhotic patients with chronic liver disease to 70% among patients with liver cirrhosis. It has also been shown that the severity of liver disease is associated with both prevalence and level of thrombocytopenia. Its development is often multifactorial, although thrombopoietin is thought to be a major factor. The discovery of and ability to clone thrombopoietin led to new treatment opportunities for this clinical manifestation. This review discusses data on the three most important thrombopoietin receptor agonists: eltrombopag, avatrombopag, and romiplostim. Currently, only eltrombopag is approved for usage among patients with thrombocytopenia and chronic hepatitis C virus infection in order to initiate and maintain interferon-based antiviral treatment. Nevertheless, the optimal management of hematologic abnormalities among patients with chronic liver disease, and its risk for bleeding complications, is still a matter of discussion. Thrombocytopenia definitely contributes to hemostatic defects but is often counterbalanced by the enhanced presence of procoagulant factors. Therefore, a thorough assessment of the patient's risk for thrombotic events is essential when the use of thrombopoietin receptor agonists is considered among patients with chronic liver disease and thrombocytopenia.

摘要

血小板减少症(血小板计数<150×10⁹/L)常使慢性肝病复杂化,妨碍对这些患者的最佳管理。这种表现的患病率在慢性肝病非肝硬化患者中为6%,在肝硬化患者中为70%。研究还表明,肝病的严重程度与血小板减少症的患病率和程度均相关。其发生通常是多因素的,不过血小板生成素被认为是一个主要因素。血小板生成素的发现及克隆能力为这一临床表现带来了新的治疗机会。本文综述了三种最重要的血小板生成素受体激动剂的数据:艾曲泊帕、阿伐曲泊帕和罗米司亭。目前,仅艾曲泊帕被批准用于血小板减少症和慢性丙型肝炎病毒感染患者,以启动和维持基于干扰素的抗病毒治疗。然而,慢性肝病患者血液学异常的最佳管理及其出血并发症风险仍是一个有待讨论的问题。血小板减少症肯定会导致止血缺陷,但通常会被促凝血因子的增加所抵消。因此,在考虑对慢性肝病合并血小板减少症患者使用血小板生成素受体激动剂时,全面评估患者的血栓形成事件风险至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf47/4642582/87e11ee50389/40265_2015_480_Fig1_HTML.jpg

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