To cite this article: Huisman MV, Klok FA. Diagnostic management of acute deep vein thrombosis and pulmonary embolism. J Thromb Haemost 2013; 11: 412-22.Summary. Acute deep vein thrombosis (DVT) and pulmonary embolism (PE) represent two expressions of a similar clinical pathological process, often referred to as venous throm-boembolism (VTE). It has long been recognized that, as clinical signs and symptoms of PE and DVT are not specific for the diagnosis, objective diagnosis in both patients presenting with leg symptoms and those with chest symptoms is mandatory. Since the last review on this subject in this journal in 2009, several large trials have been performed that shed new light on all aspects of the diagnostic management of suspected VTE, especially in the field of simplified clinical decision rules, agedependent D-dimer cut-offs and magnetic resonance imaging. A literature search covering the period 2007-2012 was performed using the Medline/PubMed database to identify all relevant papers regarding the diagnostic management of acute PE and DVT. Established concepts and the latest evidence on this subject will be the main focus of this review.Keywords: clinical decision rule, D-dimer, deep vein thrombosis, diagnostic management, imaging, pulmonary embolism, venous thromboembolism.
Clinical probability assessment and D-dimer testsA certain diagnosis of acute PE or DVT can only be established by means of imaging [1]. On the other hand, ruling out acute VTE can be safely achieved by using a standardized clinical probability assessment and a D-Dimer blood test. The main advantage of such an approach is a reduction in the required number of imaging tests, which are in general time consuming, costly and associated with radiation exposure and other complications.
D-dimerFibrin D-dimer is the final product of the plasmin-mediated degradation of cross-linked fibrin. Its plasma concentration is dependent on fibrin generation and subsequent degradation by the endogenous fibrinolytic system [2]. Ddimer levels are typically elevated in patients with acute venous thrombosis. Accordingly, the sensitivity of an elevated D-dimer concentration for VTE is very high [3]. In contrast, as D-dimer levels can be elevated in other clinical conditions that are associated with enhanced fibrin (e.g. malignancy, trauma, increased age, disseminated intravascular coagulation, inflammation, infection, sepsis, postoperative states and pre-eclampsia), the specificity for acute thrombosis is rather poor [3]. Thus the diagnostic strength of D-dimer tests lies in ruling out DVT or PE.A large variety of assays are available for D-dimer measurement, and they are all based on the use of monoclonal antibodies that recognize epitopes of the D-dimer fragment that are not present on fibrinogen or noncrossed fragments of fibrin [4]. From numerous accuracy and management studies, it has been demonstrated that the sensitivities of the D-dimer enzyme-linked immunofluorescence assay (ELFA) (DVT 96%; PE 97%), microplate enzyme-linked immunosorbent assay (...