2003
DOI: 10.7326/0003-4819-138-9-200305060-00007
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Comparison of 10-mg and 5-mg Warfarin Initiation Nomograms Together with Low-Molecular-Weight Heparin for Outpatient Treatment of Acute Venous Thromboembolism

Abstract: The 10-mg warfarin initiation nomogram is superior to the 5-mg nomogram because it allows more rapid achievement of a therapeutic INR.

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Cited by 196 publications
(145 citation statements)
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“…4 There is conflicting evidence as to the optimal dose with which to initiate warfarin therapy. 53,54 An initial randomized trial found a 5-mg initial daily dose of warfarin as effective as 10 mg daily in achieving a therapeutic international normalized prothrombin time ratio within 5 days, with less tendency toward excessive anticoagulation. 53 In a more recent trial, involving only outpatients with VTE, 54 a 10-mg daily initial dose was more effective than 5 mg daily in achieving therapeutic anticoagulation (international normalized prothrombin time ratio 2.0 to 3.0) by the fifth day of therapy without excessive anticoagulation.…”
Section: Initiation Of Oral Anticoagulant Therapymentioning
confidence: 99%
“…4 There is conflicting evidence as to the optimal dose with which to initiate warfarin therapy. 53,54 An initial randomized trial found a 5-mg initial daily dose of warfarin as effective as 10 mg daily in achieving a therapeutic international normalized prothrombin time ratio within 5 days, with less tendency toward excessive anticoagulation. 53 In a more recent trial, involving only outpatients with VTE, 54 a 10-mg daily initial dose was more effective than 5 mg daily in achieving therapeutic anticoagulation (international normalized prothrombin time ratio 2.0 to 3.0) by the fifth day of therapy without excessive anticoagulation.…”
Section: Initiation Of Oral Anticoagulant Therapymentioning
confidence: 99%
“…Dosing algorithm was highly variable. 24,[31][32][33][34][35][36][37][38] Percentage TTR All studies but one 30 reported on this outcome, and all the studies except one used a standard linear interpolation method between successive INR values to calculate % TTR. 21 Hillman et al 25 did not report on the method used to calculate this variable.…”
Section: Description Of Included Studiesmentioning
confidence: 99%
“…VTEs were diagnosed using previously published criteria. 34 The primary safety outcome was the occurrence of a major bleeding event (defined according to the International Society on Thrombosis and Haemostasis 35 ) during the period of administration of a nonheparin anticoagulant and up to 2 days after its discontinuation. We attempted to assess nonmajor bleeding events (defined as overt bleeding that did not meet the criteria for a major bleed, but were documented by any health professional); however, due to improper documentation, we were unable to do this.…”
Section: Study Outcomesmentioning
confidence: 99%