Your browser doesn't support javascript.
loading
[Initiation of oral anticoagulant treatment: comparison between different dosage regimens of warfarin and phenprocoumon]. / Initialphase der oralen Antikoagulanzientherapie: Vergleich verschiedener Dosierungen von Warfarin und Phenprocoumon.
Kemkes-Matthes, B; Matzdorff, A; Heidt, M; Winkler, L; Bernardo, A; Bernardo, A.
Afiliación
  • Kemkes-Matthes B; Zentrum für Innere Medizin der Universität Giessen, Klinikstr. 36, 35385 Giessen, Germany. Bettina.Kemkes-Matthes@innere.med.uni-giessen.de
Hamostaseologie ; 22(2): 47-51, 2002 May.
Article en De | MEDLINE | ID: mdl-12193977
ABSTRACT
A high "loading dosage" is often given during initiation of oral anticoagulant treatment in order to reach sufficient anticoagulation within short time. Increased bleeding risk as well as a transient prothrombotic tendency are complications of this treatment schedule. The aim of our study was to find proper dosage regimens of phenprocoumon and warfarin allowing initiation of oral anticoagulant treatment in a short time. For 50% of the patients 7.5 mg warfarin daily resulted in stable INR values within 4 days. Patients receiving higher (10 mg) or lower (5 mg) daily dosages of warfarin or 6 or 9 mg phenprocoumon daily during the first days of therapy reached the therapeutic range significantly later. Furthermore, no significant differences of prothrombin fragment F 1+2 were observed, indicating that no enhanced thrombin formation occurred. Thus, initiation of oral anticoagulant treatment using 7.5 mg warfarin daily is a simple and safe dosage regimen.
Asunto(s)
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenprocumón / Warfarina / Anticoagulantes Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: De Revista: Hamostaseologie Año: 2002 Tipo del documento: Article País de afiliación: Alemania
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenprocumón / Warfarina / Anticoagulantes Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: De Revista: Hamostaseologie Año: 2002 Tipo del documento: Article País de afiliación: Alemania