Difference between revisions of "Coagulation Factor Deficiency"
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− | + | '''Factor deficiencies''' are often the result of congenital deficiency in one or more of the coagulation factors. | |
− | + | ** Gives ineffective blood clotting and development of a disease syndrome characterized by excessive bleeding. S | |
− | + | *** Such bleeding is usually detected following trauma or surgery. | |
− | + | **** May occasionally be spontaneous (e.g. into alimentary or urinary tracts). | |
+ | ** Often seen as familial inherited problems. | ||
+ | *** E.g. haemophilia | ||
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− | == | + | ===Diseases associated with coagulation factor defects=== |
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− | + | * Most cases of "factor disease" in animals are similar to those studied in man. | |
− | + | ** Congenital. | |
− | + | ** Based on familial occurence. | |
+ | ** Clotting biochemistry is similar in man and animals. | ||
+ | * Most investigations have been carried out in the dog. | ||
+ | * Haemophilia (factor VIII deficiency) is probably the best understood condition. | ||
− | == | + | ====Von Willebrand's Disease==== |
− | |||
− | + | * Seen in the dog. | |
− | + | ** Most common in Scottish Terriers and Chesapeake Bay Retrievers. | |
+ | ** Has been seen more recently in Dobermanns, Setters and German Shepherd dogs. | ||
+ | ** A similar disease has been recorded in the pig. | ||
+ | * Von Willebrand's Disease is an inherited autosomal recessive trait. | ||
+ | ** It is incompletely dominant, so there is variable expression. | ||
+ | * '''Presentation''' | ||
+ | ** Purpura. | ||
+ | ** Prolonged bleeding time. | ||
+ | ** Reduced platelet adhesiveness. | ||
+ | ** Low Factor XIII levels. | ||
+ | * The disease can be assessed by the measurement of Von Willebrand Factor protein levels. | ||
+ | ** A Factor VIII-related protein. | ||
+ | ** Synthesised in endothelial cells and megakaryocytes. | ||
+ | ** Stored in platelets. | ||
+ | ** Levels are low in affected animals. | ||
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− | + | '''Deficiency states of other factors have been recorded sporadically as follows:''' | |
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− | ==Factor | + | ====Factor I ==== |
− | |||
− | + | * Factor 1 is fibrinogen. | |
− | + | * '''Hyperfibrinogenaemia''' occurs in | |
+ | ** Pregnancy | ||
+ | ** Acute infections | ||
+ | ** Post-operative states | ||
+ | ** Pyometra | ||
+ | * '''Hypofibrinogenaemia''' is seen in | ||
+ | ** Liver disease. | ||
+ | ** Depletion by intravascular coagulation. | ||
− | + | ====Factor II ==== | |
− | [[Category:Coagulation Defects]][[Category: | + | * Factor II is part of the prothrombin complex. |
+ | * '''Hypoprothrombinaemia''' | ||
+ | ** A depression of the components of the prothrombin complex. | ||
+ | *** I.e. Factors II, VII, IX, X | ||
+ | ** May be caused by dicoumarol and its derivatives, for example sweet clover and warfarin. | ||
+ | *** Competitively inhibits Vitamin K in the liver, where the above Factors are synthesised. | ||
+ | |||
+ | ====Factor IV ==== | ||
+ | |||
+ | * Factor IV is calcium. | ||
+ | ** Necessary at several stages of coagulation. | ||
+ | * '''Hypocalcaemia''' at a level sufficient to impair haemostasis is incompatible with life. | ||
+ | ** There is therefore no bleeding defect associated with hypocalcaemia. | ||
+ | |||
+ | ====Factor VII==== | ||
+ | |||
+ | * Factor VII is Proconvertin. | ||
+ | * Deficiencies do not appear to impair the formation of haemostatic plug. | ||
+ | ** The bleeding defect is normally mild. | ||
+ | * Newborn pups have a very low plasma level of Factor VII. | ||
+ | ** Spontaneous and inherited deficiencies have been reported in Beagle colonies. | ||
+ | * Deficiencies may also occur associated with [[Liver - Anatomy & Physiology|liver]] disease and in dicoumarol poisoning. | ||
+ | |||
+ | ====Factor VIII ==== | ||
+ | |||
+ | * Factor VIII is known as antihaemophilic factor (AHF). | ||
+ | * Deficiency of this factor causes '''haemophilia A'''. | ||
+ | ** The primary thrombocyte plug is abnormal. | ||
+ | *** More vascular channels than usual. | ||
+ | *** Less fibrin-collagen contact around the edges. | ||
+ | ** Plugs are therefore easily dislodged. | ||
+ | *** Results in rebleeding. | ||
+ | *** Secondary plugs only form with difficulty. | ||
+ | * Haemophilia is reported in horses and in around 20 breeds of dogs. | ||
+ | * Haemophilia is as a sex-linked recessive condition. | ||
+ | ** Associated with the X chromosome. | ||
+ | ** Affects males only. | ||
+ | * The severity of the disease correlates with the Factor VIII levels. | ||
+ | * Haematomas and haemarthrosis are common lesions. | ||
+ | |||
+ | ====Factor IX ==== | ||
+ | |||
+ | * Factor IX is Christmas Factor. | ||
+ | * Deficiency causes '''haemophilia B'''. | ||
+ | ** Seen in Cairn Terriers and Black and Tan Hounds. | ||
+ | ** A sex-linked (X chromosome) recessive. | ||
+ | ** Results in a deficient haemostatic plug. | ||
+ | *** Similar to Factor VIII deficiency. | ||
+ | |||
+ | ====Factor XI==== | ||
+ | |||
+ | * Factore XI is Plasma Thromboplastin Antecedent. | ||
+ | * Deficiency has been reported in a cow, and reduced levels in the horse. | ||
+ | |||
+ | ====Factor XII==== | ||
+ | |||
+ | * Factor XII is Hageman Factor. | ||
+ | * Low plasma levels had been reported in cats and horses. | ||
+ | |||
+ | [[Category:Coagulation Defects]][[Category:Dog]][[Category:Cat]][[Category:Cattle]][[Category:Horse]] | ||
[[Category:Haemorrhagic Diseases]] | [[Category:Haemorrhagic Diseases]] | ||
− | [[Category: | + | [[Category:To Do - James]] |
Revision as of 09:58, 29 September 2010
This article is still under construction. |
Factor deficiencies are often the result of congenital deficiency in one or more of the coagulation factors.
- Gives ineffective blood clotting and development of a disease syndrome characterized by excessive bleeding. S
- Such bleeding is usually detected following trauma or surgery.
- May occasionally be spontaneous (e.g. into alimentary or urinary tracts).
- Such bleeding is usually detected following trauma or surgery.
- Often seen as familial inherited problems.
- E.g. haemophilia
- Gives ineffective blood clotting and development of a disease syndrome characterized by excessive bleeding. S
Diseases associated with coagulation factor defects
- Most cases of "factor disease" in animals are similar to those studied in man.
- Congenital.
- Based on familial occurence.
- Clotting biochemistry is similar in man and animals.
- Most investigations have been carried out in the dog.
- Haemophilia (factor VIII deficiency) is probably the best understood condition.
Von Willebrand's Disease
- Seen in the dog.
- Most common in Scottish Terriers and Chesapeake Bay Retrievers.
- Has been seen more recently in Dobermanns, Setters and German Shepherd dogs.
- A similar disease has been recorded in the pig.
- Von Willebrand's Disease is an inherited autosomal recessive trait.
- It is incompletely dominant, so there is variable expression.
- Presentation
- Purpura.
- Prolonged bleeding time.
- Reduced platelet adhesiveness.
- Low Factor XIII levels.
- The disease can be assessed by the measurement of Von Willebrand Factor protein levels.
- A Factor VIII-related protein.
- Synthesised in endothelial cells and megakaryocytes.
- Stored in platelets.
- Levels are low in affected animals.
Deficiency states of other factors have been recorded sporadically as follows:
Factor I
- Factor 1 is fibrinogen.
- Hyperfibrinogenaemia occurs in
- Pregnancy
- Acute infections
- Post-operative states
- Pyometra
- Hypofibrinogenaemia is seen in
- Liver disease.
- Depletion by intravascular coagulation.
Factor II
- Factor II is part of the prothrombin complex.
- Hypoprothrombinaemia
- A depression of the components of the prothrombin complex.
- I.e. Factors II, VII, IX, X
- May be caused by dicoumarol and its derivatives, for example sweet clover and warfarin.
- Competitively inhibits Vitamin K in the liver, where the above Factors are synthesised.
- A depression of the components of the prothrombin complex.
Factor IV
- Factor IV is calcium.
- Necessary at several stages of coagulation.
- Hypocalcaemia at a level sufficient to impair haemostasis is incompatible with life.
- There is therefore no bleeding defect associated with hypocalcaemia.
Factor VII
- Factor VII is Proconvertin.
- Deficiencies do not appear to impair the formation of haemostatic plug.
- The bleeding defect is normally mild.
- Newborn pups have a very low plasma level of Factor VII.
- Spontaneous and inherited deficiencies have been reported in Beagle colonies.
- Deficiencies may also occur associated with liver disease and in dicoumarol poisoning.
Factor VIII
- Factor VIII is known as antihaemophilic factor (AHF).
- Deficiency of this factor causes haemophilia A.
- The primary thrombocyte plug is abnormal.
- More vascular channels than usual.
- Less fibrin-collagen contact around the edges.
- Plugs are therefore easily dislodged.
- Results in rebleeding.
- Secondary plugs only form with difficulty.
- The primary thrombocyte plug is abnormal.
- Haemophilia is reported in horses and in around 20 breeds of dogs.
- Haemophilia is as a sex-linked recessive condition.
- Associated with the X chromosome.
- Affects males only.
- The severity of the disease correlates with the Factor VIII levels.
- Haematomas and haemarthrosis are common lesions.
Factor IX
- Factor IX is Christmas Factor.
- Deficiency causes haemophilia B.
- Seen in Cairn Terriers and Black and Tan Hounds.
- A sex-linked (X chromosome) recessive.
- Results in a deficient haemostatic plug.
- Similar to Factor VIII deficiency.
Factor XI
- Factore XI is Plasma Thromboplastin Antecedent.
- Deficiency has been reported in a cow, and reduced levels in the horse.
Factor XII
- Factor XII is Hageman Factor.
- Low plasma levels had been reported in cats and horses.