Key result
Warfarin sodium administered at 0.04-0.08 mg/kg daily increased prothrombin time by 33-50% in miniature swine, with doses >0.08 mg/kg resulting in fatal intoxication.
Why the study?
Does warfarin sodium effectively increase prothrombin time in an atherosclerotic miniature swine model?
Does warfarin sodium effectively increase prothrombin time in an atherosclerotic miniature swine model?
Warfarin sodium can effectively anticoagulate miniature swine when dosed at 0.06 mg/kg daily with careful twice-weekly prothrombin time monitoring to avoid fatal intoxication.
Answers are grounded in this paper and cite their sources.
Enables anticoagulation studies in miniature swine; leaves open translation to human atherosclerotic models.
Warfarin sodium (Coumadin) has been used as an effective anticoagulating agent in human medicine for many years, although careful monitoring of its effects are necessary to avoid excessive anticoagulation. Previous experience with this drug for chronic anticoagulation therapy in miniature swine has been limited. The effect of warfarin sodium was studied by measuring prothrombin time in twelve 8-month-old Hanford miniature swine. The pigs had been fed a high-cholesterol diet and had undergone a prior coronary artery abrasion procedure for development of an atherosclerotic coronary disease model. Atherosclerosis was induced by feeding a high-cholesterol diet. Baseline prothrombin time ranged from 12.8 to 15.0 s (13.7 s mean). Prothrombin time was determined daily for the first 5 days of treatment and at least twice weekly thereafter until the animals were sacrificed. Animals received warfarin for 37-41 days. Prothrombin time could be increased 33-50% by once daily oral administration of warfarin 0.04-0.08 mg/kg. Oral administration of more than 0.08 mg/kg as a maintenance dose resulted in the death of two pigs. Most animals responded well to 0.08 mg/kg for the first 3 days of treatment followed by a maintenance dose of 0.06 mg/kg. Dosage was adjusted periodically when prothrombin times exceeded 50% above baseline. It is our experience that monitoring prothrombin time at least twice weekly and adjusting the maintenance dose can eliminate death losses due to warfarin intoxication.
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Cromeens et al. (1990) studied Atherosclerotic coronary disease model (n=12). Warfarin sodium was evaluated on Prothrombin time. Warfarin sodium administered at 0.04-0.08 mg/kg daily increased prothrombin time by 33-50% in miniature swine, with doses >0.08 mg/kg resulting in fatal intoxication.
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