Thromb Haemost 2003; 90(02): 260-266
DOI: 10.1160/TH02-10-0179
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Comparison of control and stability of oral anticoagulant therapy using acenocoumarol versus phenprocoumon

Stephan D. Fihn
1   Northwest Health Services Research Center of Excellence, Veteran Affairs Puget Sound Health Care System
2   Department of Medicine of the University of Washington, Seattle, Washington, USA
,
Alain A. P. Gadisseur
4   Thrombosis Center of the Leiden University Medical Center
,
Edwin Pasterkamp
3   Department of Clinical Epidemiology and Hemostasis and
,
Felix J. M. van der Meer
4   Thrombosis Center of the Leiden University Medical Center
,
W. G. Mimi Breukink-Engbers
5   Oostgelderland Anticoagulation Clinic, Lichtenvoorde
,
Lya M. Geven-Boere
6   Leeuwarden Anticoagulation Clinic
,
Erik van Meegen
7   Anticoagulation Clinic of the Hague
,
Hanneke de Vries-Goldschmeding
8   Thrombosis Center of the Utrecht Division of the Dutch Red Cross
,
Irma Antheunissen-Anneveld
9   Schiedam Anticoagulation Clinic
,
Annelies R. van’t Hoff
1   Northwest Health Services Research Center of Excellence, Veteran Affairs Puget Sound Health Care System
,
Derk Harderman
1   Northwest Health Services Research Center of Excellence, Veteran Affairs Puget Sound Health Care System
,
Margriet Smink
1   Northwest Health Services Research Center of Excellence, Veteran Affairs Puget Sound Health Care System
,
Frits R. Rosendaal
3   Department of Clinical Epidemiology and Hemostasis and
4   Thrombosis Center of the Leiden University Medical Center
› Institutsangaben
Financial support: This work was supported by a visitors grant from the Nederlandse Organizatsie voor Wetenschappelijk Onderzoek.
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Publikationsverlauf

Received 21. Oktober 2002

Accepted after revision 19. März 2003

Publikationsdatum:
06. Dezember 2017 (online)

Summary

Variability in the control of oral anticoagulant therapy has been associated with a heightened risk of complications. We compared control of anticoagulation between two commonly used coumarins, phenprocoumon and acenocoumarol, and among anticoagulation clinics.

All qualifying patients were managed at six regional anticoagulation clinics in the Netherlands.

This retrospective cohort study compiled data during a three-year period from a computerised dosing and management system. Anticoagulation control was expressed as the percent of time within the therapeutic range and stability expressed as the time-weighted variance in the international normalised ratio (INR). Data were available for 22,178 patients of whom 72% were treated with acenocoumarol. INRs of patients who received phenprocoumon were within the therapeutic range 50% of the time compared with 43% for acenocoumarol (OR 1.32,95% CI 1.24-1.41). Moreover, patients on phenprocoumon required 15% fewer monitoring visits and had more stable INR values. These observations were consistent for all six clinics. There were also sizable differences between the clinics with respect to control and stability of anticoagulation that were stable from year-to-year and were unrelated to the drug used.

With its longer half-life of three to five days, phenprocoumon produces more stable anticoagulation than acenocoumarol and should generally be the drug of choice when these are the available choices. The differences observed among clinics suggest that certain clinics employ policies and practices resulting in better control of anticoagulation.

 
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