dicoumarol/blødning

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Haemorrhagic syndrome of cattle associated with the feeding of sweet vernal (Anthoxanthum odoratum) hay containing dicoumarol.

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An outbreak of a haemorrhagic diathesis in cattle fed home produced hay is described. A similar syndrome was reproduced experimentally in calves by feeding them the hay. The experimental disease was characterised by increased prothrombin and partial thromboplastin times while the leucocyte and

Haemorrhagic manifestations secondary to dicoumarol.

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Dicoumarol drugs and the problem of haemorrhage.

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Haemorrhagic necrosis of the skin during dicoumarol therapy.

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Bilateral adrenal hemorrhage complicating dicoumarol therapy for myocardial infarction.

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[Hemorrhagic complications due to long-term administration of dicoumarol derivatives in coronary artery disease].

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Dicoumarol toxicity in cattle associated with ingestion of silage containing sweet vernal grass (Anthoxanthum odoratum).

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A diagnosis of dicoumarol toxicity in a herd of Friesian cattle was made following investigation of the deaths of three mature cows and eleven yearling heifers. Affected stock had been fed wrapped, bailed silage containing approximately 90% sweet vernal grass (Anthoxanthum odoratum). Sweet vernal

Dicoumarol activates Ca2+-permeable cation channels triggering erythrocyte cell membrane scrambling.

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Dicoumarol, a widely used anticoagulant, may cause anemia, which may result from enhanced erythrocyte loss due to bleeding or due to accelerated erythrocyte death. Erythrocytes may undergo suicidal death or eryptosis, characterized by cell shrinkage and phospholipid scrambling of the cell membrane.

Dicoumarol toxicity in neonatal calves associated with the feeding of sweet vernal (Anthoxanthum odoratum) hay.

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Neonatal calves from a seasonal dairy herd in North Western Tasmania were presented for veterinary care due to mortalities and bleeding from multiple orifices. Necropsy examination revealed free blood throughout the parenchymatous organs, body cavities and connective tissues. There was no history of

[On the history of vitamin K, dicoumarol and warfarin].

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The history of the discovery and development of vitamin K and its antagonists, the oral anticoagulants dicoumarol and warfarin, are fascinating, triumphant landmarks in the annals of medicine. Vitamin K was found by Carl Peter Henrik Dam and Fritz Schønheyder from the University of Copenhagen. The

Anemia in sleep-deprived rats receiving anticoagulants.

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Independent groups of rats were deprived of sleep and treated with the anticoagulant drugs phenylindanedione or dicoumarol for 1 to 8 days. These animals developed an extremely severe anemia which was accelerated by p-chlorophenylalanine. The red cell count and amount of hemoglobin decreased to half

A novel 4-hydroxycoumarin biosynthetic pathway.

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Coumarin forms in melilotoside (trans-ortho-coumaric acid glucoside)-containing plant species upon cell damage. In moldy melilotoside-containing plant material, trans-ortho-coumaric acid is converted by fungi to 4-hydroxycoumarin, two molecules of which spontaneously combine with formaldehyde to

[Subdural hematoma and anticoagulant therapy].

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The authors report a series of 22 cases of subdural hematomas in patients submitted to anticoagulant therapy. A review of the literature finds 150 cases. Subdural hematomas occurs in about one third of the patients presenting hemorrhage of central nervous system related to anticoagulant therapy.

Dosage of i.v. brinase in man based on brinase inhibitor capacity and coagulation studies.

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In 17 patients a total of 148 brinase infusions were given. All patients but two had anticoagulant treatment (dicoumarol or heparin) during the brinase series. Dosage of brinase was based on determination of brinase inhibitor capacity in plasma (azocollagen technique) prior to infusion of the

Warfarin-induced changes in procoagulant and anticoagulant proteins.

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Dicoumarol was found to be the causative agent of a haemorrhagic disease in cattle following the ingestion of spoiled sweet clover. Vitamin K deficiency in chickens caused bleeding. Dicoumarol was later determined to be a vitamin K antagonist. A more potent form of the drug was produced

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