Management of venous thrombo-embolism: an update

被引:69
作者
Konstantinides, Stavros [1 ,2 ]
Torbicki, Adam [3 ]
机构
[1] Univ Med Ctr Mainz, CTH, D-55131 Mainz, Germany
[2] Democritus Univ Thrace, Dept Cardiol, Thrace, Greece
[3] ECZ Otwock, Ctr Postgrad Med Educ, Dept Pulm Circulat & Thromboembol Dis, Otwock, Poland
关键词
Venous thrombo-embolism; Pulmonary embolism; Prognosis; Management; Risk assessment; Anticoagulants; Thrombolysis; Chronic thrombo-embolic pulmonary hypertension; ACUTE PULMONARY-EMBOLISM; RIGHT-VENTRICULAR DYSFUNCTION; ASSESSING CLINICAL PROBABILITY; NON-INFERIORITY TRIAL; DEEP-VEIN THROMBOSIS; NORMOTENSIVE PATIENTS; RISK-ASSESSMENT; PROGNOSTIC MODEL; ORAL RIVAROXABAN; SEVERITY INDEX;
D O I
10.1093/eurheartj/ehu243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Venous thrombo-embolism is the third most frequent acute cardiovascular syndrome after myocardial infarction and stroke. Recently published landmark trials paved the way for significant progress in the management of the disease and provided the evidence for the ESC Pulmonary Embolism (PE) Guidelines 2014 update. Risk stratification strategies for non-high-risk PE continue to evolve, with an increasing emphasis on clinical prediction rules and right ventricular (RV) assessment on computed tomographic pulmonary angiography. In the field of anticoagulation treatment, pharmacogenetic testing for vitamin K antagonists on top of clinical parameters was not found to offer a significant benefit during the initiation phase; on the other hand, dosing based on the patient's clinical data seems superior to fixed loading regimens. The phase 3 trial programme of new oral anticoagulants in the treatment of venous thrombo-embolism has been completed, and the results indicate that these agents are at least as effective and probably cause less major bleeding than currently standard treatment. A multicentre prospective phase 4 trial will determine whether early discharge and out-of-hospital treatment of low-risk PE with the oral factor Xa inhibitor rivaroxaban is feasible, effective, and safe. For intermediate-risk PE defined on the basis of imaging tests and laboratory biomarkers, the bleeding risks of full-dose thrombolytic treatment appear too high to justify its use, unless clinical signs of haemodynamic decompensation appear. Patients in whom PE has resulted in chronic thrombo-embolic pulmonary hypertension and who are not suitable for pulmonary endarterectomy, may be expected to benefit from emerging pharmaceutical and interventional treatment options.
引用
收藏
页码:2855 / U21
页数:12
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