医学
血栓形成
静脉血栓形成
乌斯特基努马
不利影响
托法替尼
内科学
维多利祖马布
溃疡性结肠炎
炎症性肠病
胃肠病学
疾病
阿达木单抗
肿瘤坏死因子α
类风湿性关节炎
作者
Virginia Solitano,Gionata Fiorino,Ferdinando D’Amico,Laurent Peyrin‐Biroulet,Silvio Danese
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2020-12-31
卷期号:22 (1): 126-136
被引量:12
标识
DOI:10.2174/1389450121666200902164240
摘要
Patients with inflammatory bowel diseases (IBD) have an increased risk of thrombosis. The interaction between inflammation and coagulation has been extensively studied. It is well-known that some drugs can influence the haemostatic system, but several concerns on the association between therapies and increased risk of thrombosis remain open. While biologics seem to have a protective role against thrombosis via their anti-inflammatory effect, some concerns about an increased risk of thrombosis with JAK inhibitors have been raised. We conducted a literature review to assess the association between biologics/small molecules and venous/arterial thrombotic complications. An increased risk of venous and arterial thrombosis was found in patients treated with corticosteroids, whereas anti-TNF were considered protective agents. No thromboembolic adverse event was reported with vedolizumab and ustekinumab. In addition, thromboembolic events rarely occurred in patients with ulcerative colitis (UC) after therapy with tofacitinib. The overall risk of both venous and arterial thrombosis was not increased based on the available evidence. Finally, in the era of JAK inhibitors, treatment should be individualized by evaluating the pre-existing potential thrombotic risk balanced with the intrinsic risk of the medication used.
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