Testing for thrombophilia in mesenteric venous thrombosis - Retrospective original study and systematic review

被引:16
作者
Zarrouk, M. [1 ]
Salim, S. [1 ]
Elf, J. [1 ]
Gottsater, A. [1 ]
Acosta, S. [1 ]
机构
[1] Lund Univ, Skane Univ Hosp, Dept Vasc Dis, S-20502 Malmo, Sweden
关键词
Mesenteric venous thrombosis; Splanchnic vein thrombosis; Thrombophilia; Prothrombotic; Hypercoagulability; JAK2; SPLANCHNIC VEIN-THROMBOSIS; JAK2 V617F MUTATION; RISK-FACTORS; PROTEIN-C; MYELOPROLIFERATIVE NEOPLASMS; JAK2V617F MUTATION; PROGNOSTIC-FACTORS; EARLY-DIAGNOSIS; HIGH PREVALENCE; FAMILIAL RISK;
D O I
10.1016/j.bpg.2016.11.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The aim was to perform a local study of risk factors and thrombophilia in mesenteric venous thrombosis (MVT), and to review the literature concerning thrombophilia testing in MVT. Patients hospitalized for surgical or medical treatment of MVT at our center 2000-2015. A systematic review of observational studies was performed. In the local study, the most frequently identified risk factor was Factor V Leiden mutation. The systematic review included 14 original studies. The highest pooled percentage of any inherited thrombophilic factor were: Factor V Leiden mutation 9% (CI 2.9-16.1), prothrombin gene mutation 7% (CI 2.7-11.8). The highest pooled percentage of acquired thrombophilic factors were JAK2 V617F mutation 14% (CI -1.9-28.1). The wide range of frequency of inherited and acquired thrombophilic factors in different populations indicates the necessity to relate these factors to background population based data in order to estimate their overrepresentation in MVT. There is a need to develop guidelines for when and how thrombophilia testing should be performed in MVT. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:39 / 48
页数:10
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