Venous thrombosis and prothrombotic factors in inflammatory bowel disease

被引:136
作者
Magro, Fernando [1 ,2 ,3 ]
Soares, Joao-Bruno [4 ]
Fernandes, Dalia [4 ,5 ]
机构
[1] Ctr Hosp Sao Joao, Dept Gastroenterol, P-4200319 Oporto, Portugal
[2] Univ Porto, Fac Med, Inst Pharmacol & Therapeut, P-4200319 Oporto, Portugal
[3] Univ Porto, Inst Mol & Cell Biol, IBMC, P-4150180 Oporto, Portugal
[4] Hosp Braga, Dept Gastroenterol, P-4710243 Braga, Portugal
[5] Ctr Hosp Cova da Beira, Dept Gastroenterol, P-6200251 Covilha, Portugal
关键词
Acquired; Genetic; Prothrombotic; Venous thrombosis; Risk of venous thrombosis; Inflammatory bowel disease; FACTOR-V-LEIDEN; C-REACTIVE PROTEIN; ACTIVE ULCERATIVE-COLITIS; FACTOR-XIII POLYMORPHISM; CORONARY-HEART-DISEASE; VASCULAR RISK-FACTORS; TUMOR-NECROSIS-FACTOR; DEEP-VEIN THROMBOSIS; PLATELET P-SELECTIN; SOLUBLE CD40 LIGAND;
D O I
10.3748/wjg.v20.i17.4857
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Patients with inflammatory bowel disease (IBD) may have an increased risk of venous thrombosis (VTE). PubMed, ISI Web of Knowledge and Scopus were searched to identify studies investigating the risk of VTE and the prevalence of acquired and genetic VTE risk factors and prothrombotic abnormalities in IBD. Overall, IBD patients have a two-to fourfold increased risk of VTE compared with healthy controls, with an overall incidence rate of 1%-8%. The majority of studies did not show significant differences in the risk of VTE between Crohn's disease and ulcerative colitis. Several acquired factors are responsible for the increased risk of VTE in IBD: inflammatory activity, hospitalisation, surgery, pregnancy, disease phenotype (e.g., fistuiising disease, colonic involvement and extensive involvement) and drug therapy (mainly steroids). There is also convincing evidence from basic science and from clinical and epidemiological studies that IBD is associated with several prothrombotic abnormalities, including initiation of the coagulation system, downregulation of natural anticoagulant mechanisms, impairment of fibrinolysis, increased platelet count and reactivity and dysfunction of the endothelium. Classical genetic alterations are not generally found more often in IBD patients than in non-IBD patients, suggesting that genetics does not explain the greater risk of VTE in these patients. IBD VTE may have clinical specificities, namely an earlier first episode of VTE in life, high recurrence rate, decreased efficacy of some drugs in preventing further episodes and poor prognosis. Clinicians should be aware of these risks, and adequate prophylactic actions should be taken in patients who have disease activity, are hospitalised, are submitted to surgery or are undergoing treatment. (C) 2014 Baishideng Publishing Group Co., Limited. All rights reserved.
引用
收藏
页码:4857 / 4872
页数:16
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