Thromb Haemost 1992; 67(05): 510-513
DOI: 10.1055/s-0038-1648483
Original Articles
Schattauer GmbH Stuttgart

The Use of the D-Dimer Test in Combination with Non-Invasive Testing Versus Serial Non-Invasive Testing Alone for the Diagnosis of Deep-Vein Thrombosis

Harriët Heijboer
1   The Centre for Haemostasis, Thrombosis, Atherosclerosis and Inflammation Research, Academic Medical Centre, Amsterdam, The Netherlands
,
Jeffrey S Ginsberg
2   Department of Medicine, McMaster University, Hamilton, Canada
,
Harry R Büller
1   The Centre for Haemostasis, Thrombosis, Atherosclerosis and Inflammation Research, Academic Medical Centre, Amsterdam, The Netherlands
,
Anthonie W A Lensing
2   Department of Medicine, McMaster University, Hamilton, Canada
,
Louisa P Colly
3   Thrombosis Service, Amsterdam, The Netherlands
,
Jan Wouter ten Cate
1   The Centre for Haemostasis, Thrombosis, Atherosclerosis and Inflammation Research, Academic Medical Centre, Amsterdam, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 30 August 1991

Accepted after revision 10 December 1991

Publication Date:
03 July 2018 (online)

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Summary

We studied the usefulness of the determination of plasma D-dimer levels (using an ELISA) in combination with non-invasive testing with impedance plethysmography (IPG) or real-time ultrasonography (US) for the diagnosis of deep-vein thrombosis (DVT), in outpatients with clinically suspected DVT This combined approach was compared to serial non-invasive testing alone in these patients. The sensitivity of a positive D-dimer test (>300 μg/1) for the presence of DVT was 100% (70/70 patients; 95% C. I.: 95-100%), whereas the specificity was 29% (69/ 239 patients; 95% C. I.: 23-34%). The proportion of patients in which a definitive decision about the presence or absence of DVT could be made on the day of referral, was calculated for both approaches. When applying the combined approach, in 42% of all referred patients the diagnosis of DVT could either be established or refuted on entry, as opposed to only 19% of patients using serial non-invasive testing alone.

Also, the costs per DVT diagnosed were calculated for the two diagnostic approaches. For the diagnosis of DVT the costs using serial IPG were comparable to the costs using the combination of IPG and the D-dimer test. The same conclusion holds for the comparison of serial US with the combination of US and D-dimer testing.

We conclude that for the diagnosis of DVT in symptomatic outpatients the combination of non-invasive testing with the D-dimer test might be preferred over serial non-invasive testing alone, although the safety of such an approach remains to be established in future management studies.