Thromb Haemost 1989; 62(04): 1043-1045
DOI: 10.1055/s-0038-1647113
Original Article
Clinical Studies
Schattauer GmbH Stuttgart

Is Quantitative Determination of Fibrin(ogen) Degradation Products and Thrombin-Antithrombin III Complexes Useful to Diagnose Deep Venous Thrombosis in Outpatients?

Paul F M M van Bergen
1   The Center for Clinical Decision Making/Department of Internal Medicine II, University Hospital “Dijkzigt”, Rotterdam, The Netherlands
,
Eduard A R Knot
1   The Center for Clinical Decision Making/Department of Internal Medicine II, University Hospital “Dijkzigt”, Rotterdam, The Netherlands
,
Jan J C Jonker
2   The Thrombosis Service Center Rotterdam, Rotterdam, The Netherlands
,
Auke C de Boer
3   The Department of Internal Medicine, Bergweg Municipal Hospital, Rotterdam, The Netherlands
,
Moniek P M de Maat
1   The Center for Clinical Decision Making/Department of Internal Medicine II, University Hospital “Dijkzigt”, Rotterdam, The Netherlands
› Author Affiliations
Further Information

Publication History

Received 02 January 1989

Accepted after revision 22 August 1989

Publication Date:
24 July 2018 (online)

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Summary

We studied the diagnostic value of recently introduced ELISA’s for the determination of thrombin-antithrombin III (TAT) complexes, fibrin degradation products (FbDP), fibrinogen degradation products (FgDP) and total degradation products (TDP) for deep venous thrombosis (DVT) in plasma of 239 consecutive outpatients, suspected for DVT by their family doctor. DVT was confirmed by impedance plethysmography in 60 patients. Using the 95th percentile range of 42 healthy volunteers the sensitivity for the detection of DVT was: 37% for TAT, 95% for TDP, 92% for FbDP and 90% for FgDP. Specificity was: 88% for TAT, 16% for TDP, 20% for FbDP and 25% for FgDP.

We conclude that these assays are of little value in the diagnosis of DVT in outpatients.