D-dimer

The biomarker of choice to aid the diagnosis of venous thromboembolism

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Fast results
High NPV
Reduced imaging*

D-dimer testing in the emergency department (ED)

Point-of-care D-dimer testing* gives the possibility to rapidly test patients for venous thromboembolism (VTE), thus leading to a potential decrease in overcrowding in urgent care facilities [1].

Patients who present with signs and symptoms that may be caused by VTE require objective evaluation to exclude or confirm the diagnosis of a thrombus [2].

For patients at low or intermediate VTE risk, using D-dimer* as the initial test reduces the need for diagnostic imaging [3]. Imaging is associated with several disadvantages, e.g. radiation exposure, complications related to the administration of intravenous contrast and high healthcare costs [4].

*When used in combination with clinical assessment.

Immunoassay products and solutions

βhCG (Human chorionic gonadotropin)

D-dimer

NT-proBNP

PCT (Procalcitonin)

Troponin I

CRP (C-reactive protein)

D-dimer is produced as the end product of fibrinolysis

The presence of D-dimer indicates that the in vivo coagulation system has been activated, forming a thrombus (blood clot) that initially stops a bleeding. D-dimer is the end product of the degradation that occurs in the healing process [5].

Venous thromboembolism

The most common presentation of VTE are deep vein thrombosis (DVT) and pulmonary embolism (PE). The causes can be multifactorial and both inherited or acquired [6].

VTE is a condition that can have potentially serious and even life-threatening consequences [3].

Therefore, a fast decision has to be made on whether to exclude VTE by a negative D-dimer test or confirm by sending the patient for imaging.

Venous thromboembolism

Testing D-dimer on the AQT90 FLEX analyser

The AQT90 FLEX analyser delivers lab-standard quantitative results on the D-dimer assay in less than 21 minutes, accelerating DVT and PE diagnosis in the ED to support rapid clinical decision making.

High negative predictive value (NPV) allows you to trust the D-dimer* results and help avoid sending ill patients home [5]. A high specificity means a lower number of false positive results. This minimises unnecessary imaging on healthy persons, which is a benefit for the healthy person as well as for the healthcare system [5].

* In combination with clinical probability assessment.

The AQT90 FLEX immunoassay analyser is a benchtop analyser that brings rapid biomarker assessment capabilities right to the patient’s bedside.

Its closed tube system makes D-dimer testing easy: the operator simply inserts the sample tube into the tube holder in the sample port and the analyser performs all assay steps automatically. There is no need for sample preparation.

All necessary reagents are included in the test cartridges, which remain stable onboard the analyser for 31 days ensuring maximum availability and uptime.

Key benefits of D-dimer on the AQT90 FLEX analyser

No blood exposure: closed system
No sample or assay preparation
Specimen types: venous whole blood
No presence of hook effect or carry-over
Hemolysis, lipemia, icteria and biotin* show no interference with the assay
Sample tubes: fit most 13 × 75 mm standard tubes

* No interference was observed with biotin up to 2.6 mg/L (2,600 ng/mL)

Clinical performance and method comparison

D-dimer assay specifics

Turnaround time:

< 21 min.

CV % (plasma): Within-lab CV% at conc. 572 μg/L: 12.8%

95th percentile*: < 50 years/whole blood 630 μg/L
> 50 years/whole blood 654 μg/L

Traceability: Hytest, 8D710

* These values should only be used as an example. Each laboratory should establish its own decision threshold level.

References

1. Favresse J, Lippi G, Roy PM, et al. D-dimer: Preanalytical, analytical, post-analytical variables, and clinical applications. Crit Rev Clin Lab Sci. 2018; 55,8
2. CLSI. Quantitative D-dimer for the Exclusion of Venous Thromboembolic Disease; Approved Guideline. CLSI document H59-A. Wayne, PA: Clinical and Laboratory Standards Institute; 2011.
3. Konstantinides SV et al. 2019 ESC Guidelines for the diagnosis and management of acute pulmonary embolism developed in collaboration with the EuropeanRespiratory Society (ERS). Eur Heart J. 2020; 41: 543-603.
4. Van der Hulle T, Dronkers CEA, Klok FA, Huisman MV. Recent developments in the diagnosis and treatment ofpulmonary embolism. JOIM 2015
5. Strandberg K. The clinical use of a D-dimer assay. acutecaretesting.org 2017
6. Lijfering WM, Rosendaal FR, Cannegieter. Risk factors for venous thrombosis - current understanding from an epidemiological point of view. Br J Haematol. 2010; 149, 6.
7. Stokes N, Dietz,B,and Liang J,Cardiopulmonary laboratory biomarkers in the evaluation of acute dyspnea, Open Access Emerg Med. 2016; 8: 35–45. page 10.
8. Lusky, Karen. One-two Punch in Evaluating PE Risk. Cap Today. Modified November 2006. http://www.captodayonline.com/Archives/feature_stories/1106pe_risk.html.
9.Sidelmann JJ, Gram J, Larsen A, Overgaard K, Jespersen J. Analytical and clinical validation of a new point-of-care testing system for determination of D-Dimer in human blood. Thrombosis Research 126 (2010) 524–530