Difference between revisions of "Platelet Abnormalities"

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[[Image:LH_Platelet_Histology.jpg|right|thumb|175px|<center><p>'''Platelets'''</p><sup>©RVC 2008</sup></center>]]
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{{unfinished}}
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==Introduction==
 
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[[Platelet|Platelets]] (or thrombocytes) are responsible for primary haemostasis by the formation of a temporary platelet plug that initially seals any breach to a blood vessel wall.  These breaches are then sealed more completely by the formation of a fibrin clot induced by the coagulation factor cascade. 
 
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===Terminology===
 
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*'''Thrombocytopaenia''' refers to low absolute numbers of platelets. Infections, neoplasia and [[Immune Mediated Thrombocytopaenia|immune-mediated thrombocytopaenia]] (ITP) are common causes of thrombocytopaenia, which is frequently a secondary disease. 
 
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*'''Thrombocytopathia''' refers to platelets that are unable to function adequately.
 
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*'''Thrombocytosis''' refers to an increase in the blood platelet concentration above the normal level.
 
  
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Thrombocytopaenia and thrombocytopathia lead to disorders of primary haemostasis but, in general, this is less serious than the disorders of secondary haemostasis caused by deficiencies in the [[Coagulation Factor Deficiency|coagulation factors]].
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==Description==
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Platelets (or thrombocytes) are responsible for primary haemostasis, the formation of a temporary platelet plug that initially seals any breach to a blood vessel wall.  Bleeding disorders may occur if platelets are deficient ('''thrombocytopaenia''') or if the platelets are unable to function adequately ('''thrombocytopathia''').  Thrombocytopaenia may be a '''primary disease''' due to disease of the bone marrow that reduces the production of platelets or it may occur '''secondary''' to another insult.
  
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==Thrombocytopaenia==
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===Primary Thrombocytopaenic Disease===
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Thrombocytopaenia is a common haematological abnormality as platelet numbers are subject to fluctuation in a number of diseases. Care should be taken, however to ensure that this finding is not caused by an artefact of sampling where platelet clumps have formed.  The normal blood platelet concentration of the dog is 175-500x10^9; a tendency to bleed following an insult such as venepuncture can be observed if levels fall below 50x10^9 and spontaneous haemorrhage is observed when levels fall below 30x10^9. Acute thrombocytopenia is more likley to give rise to clinical signs than more chronically developed low platelet numbers.
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The aetiology of primary thrombocytopenic disease is often uncertain and it is therefore also known as '''idiopathic''' thrombocytopaenia.  Some cases of primary thrombocytopaenia may occur due to autoimmune responses directed at platelets and, although the [[Bone Marrow - Anatomy & Physiology|bone marrow]] may contain adequate normal megakaryocytes, this disease results in a reduced peripheral blood thrombocyte count. [[Immune Mediated Thrombocytopaenia|Immune-mediated thrombocytopaenia]] occurs most commonly in young animals.
  
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Reductions in platelet numbers may be caused by a failure to produce adequate amounts in the bone marrow during [[Thrombopoiesis|megakaryopoiesis]], or an increased destruction of existing platelets or sequestration of platelets outside of the circulation.   
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===Secondary Thrombocytopaenic Disease===
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Secondary thrombocyopaenic disease is fairly common in adult domestic animals and it may be associated with diseases that depress the production of platelets or increase their consumption or sequestration:
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*Diseases that cause '''[[Bone Marrow - Anatomy & Physiology|bone marrow]] suppression'''
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**'''Aplastic anaemia''' caused by ingestion of bracken, administration of oestrogens or of [[Chloramphenicol|chloramphenicol]] or [[Sulphonamides|sulphonamide]] antibiotics.  Prolonged use of phenylbutazone or salicylate may cause the same disease.
 +
**'''Myelophthisis''', the displacement of the normal tissues of the bone marrow by another cell or tissue type may also reduce the function of the megakaryocytes.  Possible diseases include '''myelofibrosis''' and '''immunoprliferative''' or '''myeloproliferative''' neoplastic disease.
 +
**'''Radiotherapy''' or myelosuppressive '''chemotherapy''' may cause reversible bone marrow suppression.
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*Diseases that cause '''increased destruction of platelets'''
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*Diseases that cause '''sequestration of platelets''' usually involve some enlargement to the spleen as this is the major organ where platelets are stored outside of the circulation.  Examples include:
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**[[Haemangiosarcoma]] of the spleen and liver
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**Splenic enlargement under general anaesthesia with certain agents such as barbiturates and phenothiazines
  
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===Causes of bone marrow suppression===
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* Associated with diseases which cause [bone marrow]] depression.   
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*'''Aplastic anaemia''' which can be caused by the ingestion of bracken or administration of oestrogens, [[Chloramphenicol|chloramphenicol]] or [[Sulphonamides|sulphonamide]] antibiotics.  Prolonged use of [[NSAIDs#Phenylbutazone|phenylbutazone]] or salicylates may cause the same disease.
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* The [[Bone Marrow - Anatomy & Physiology|bone marrow]] is depleted or devoid of megakaryocytes, and there is a nil or markedly reduced peripheral blood thrombocyte count. 
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*'''Infectious diseases''' that reduce stem cell function include [[Distemper|canine distemper]], [[Canine Parvovirus|canine parvovirus]] and [[Feline Panleucopaenia|feline panleucopaenia virus]].
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* Secondary thrombocyopenic disease is seen in the following conditions:
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*'''Myelophthisis''' is the displacement of the normal cell lines of the bone marrow by another cell or tissue type which may also reduce the function of the megakaryocytes. Diseases in this category include '''myelofibrosis''' and '''immunoproliferative''' or '''myeloproliferative''' neoplastic disease.
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*# Severe viral infections.
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*'''Radiotherapy''' or myelosuppressive '''chemotherapy''' may cause reversible bone marrow suppression.
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*#* For examople, ICH, feline panleucopenia, [[Bovine Viral Diarrhoea Virus|mucosal disease]], [[Classical Swine Fever|swine fever]].
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*# Severe protozoal infections.
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*#* For example, in the UK, Haemobartonella may be a cause.
  
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===Causes of increased platelet destruction===
 
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*'''Infectious diseases''' that cause destruction of platelets include [[Bovine Viral Diarrhoea Virus|bovine viral diarrhoea (BVD)]], [[Classical Swine Fever|classical swine fever]] and [[Infectious Canine Hepatitis|infectious canine hepatitis]].  The parasites [[Ehrlichia platys|''Anaplasma platys'']], [[Ehrlichia phagocytophila|''Anaplasma phagocytophilum'']] and ''[[Ehrlichia canis]]'' may also cause infectious thrombocytopaenia.  Any severe bacterial infection, including those caused by [[:Category:Staphylococcus species|''Staphylococci'']] and the Gram negative bacteria that produce endotoxins (e.g. [[:Category:Pseudomonas and Burkholderia species|''Pseudomonas sp.'']] or [[Salmonella|''Salmonella sp.'']]) may also result in the destruction of platelets.
 
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*'''[[Immune Mediated Thrombocytopaenia|Immune-mediated thrombocytopaenia]]''' is an autoimmune disease that leads to the production of antibodies against platelets and their subsequent destruction by cells of the [[Monocytes|monocyte]] phagocyte system (MPS). Platelet numbers can be very low in animals with this condition, but infection and neoplasias are more common causes of thrombocytopaenia.
 
  
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===Causes of platelet sequestration===
 
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Diseases that cause '''sequestration of platelets''' usually involve some enlargement of the spleen, as this is the major organ where platelets are stored outside of the circulation.  A common example would be [[Haemangiosarcoma|haemangiosarcoma]] of the spleen and liver. Splenic enlargement under general anaesthesia maintained with agents such as [[Barbiturates|barbiturates]] and [[Phenothiazines|phenothiazines]] can also lead to sequestration of platelets.
 
  
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===Artefactual or spurious thrombocytopaenia===
 
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*'''Cavalier King Charles spaniels''' have a genetic abnormality which produces a small number of giant platelets (macrothrombocytes) in the circulation with a corresponding reduction in free platelets; they do not suffer from bleeding disorders as they maintain a similar total platelet mass as do dogs of other breeds. Automated blood counts will include the macrothrombocytes in the white or red cell count and the apparent thrombocytopenia will be exaggerated.
 
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*'''Greyhounds''' and other sight hounds frequently have platelet counts at the lowest end of the reference range (as well as increased haematocrit, mild neutropaenia and reduced T4 levels) but this is a normal finding for this breed.
 
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*If venepuncture is traumatic (using small viens with excessive suction or patient agitation) '''platelet clumps''' may form and these will not be counted by automated machines.  The presence of clumps can be investigated by making a blood smear and examining the feathered edge for large agglomerations of platelets. Time, temperature and contact with glass can also cause clumping of platelets once the sample has been taken.
 
  
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==Thrombocytopathia==
 
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Defects in platelet function may be congenital or acquired in association with a number of diseases.  Congenital thrombocytopathias are rare inherited diseases which are characterised by defects in platelet adhesiveness, aggregation or factor release.  The defects are usually associated with particular breeds, such as '''Chediak-Higashi syndrome''' in blue smoke Persian cats.
 
  
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Causes of acquired thrombocytopathia include:
 
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*Infection with ''[[Angiostrongylus vasorum]]'', the canine lungworm, which also causes a consumptive coagulopathy.
 
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*'''Hypergammaglobulinaemia''' as occurs with multiple myeloma and some forms of (B-cell) lymphoma may affect platelet function.
 
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*Administration of large volumes of some '''[[Colloids|colloid solutions]]'''.
 
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*Administration of certain '''pharmaceutical products''', including [[NSAIDs|non-steroidal anti-inflammatory drugs]] and [[Cephalosporins|cephalosporins]].
 
  
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==Thrombocytosis==
 
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Increased platelet number above normal levels may occur due to physiological or pathological processes. 
 
  
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Physiological causes include:
 
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*'''Splenic contraction''' which pushes sequestered platelets into the circulation.  This phenomenon is especially marked in '''horses''' which have a muscular splenic capsule. 
 
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*'''Splenectomy''' prevents the sequestration of platelets in the spleen, resulting in consistently increased levels of platelets.
 
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*As part of a response to [[Regenerative and Non-Regenerative Anaemias|anaemia]] a '''reactive thrombocytosis''' is often documented and this may precede signs of regeneration.
 
  
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Pathological
 
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*'''Essential thrombocythaemia''' is a rare myeloproliferative disease that results in the excessive production of platelets which function abnormally.  Affected animals suffer from bouts of spontaneous haemorrhage.
 
  
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==Clinical Significance==
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*# Other miscellaneous causes.
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Other than essential thrombocythaemia, thrombocytosis has no clinical importance except as an indicator of another disease process.  Thrombocytopaenia and thrombocytopathia both result in reductions in the effectiveness of primary haemostasis, producing bleeding disorders. Since bleeding points are usually sealed by a fibrin clot, disorders of primary haemostasis tend to be less severe than those caused by deficiencies of the coagulation factors.  Common signs of a disorder of primary haemostasis include:
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*#* Severe bacterial infections.
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*Petechial or ecchymotic [[Haemorrhage|haemorrhages]] on the skin or mucous membranes.
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*#** For example,  [[:Category:Staphylococcus species|''Staphylococci'']], and those Gram -ve bacteria producing endotoxins (e.g. [[:Category:Pseudomonas and Burkholderia species|''Pseudomonas'']] or [[Salmonella|''Salmonella'']] spp.).
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*[[Haemorrhage|Haemorrhages]] from the mucous membranes, producing haematuria, haematochezia, haematemesis, haemoptysis and melaena.
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*#* [[Liver - Anatomy & Physiology|Liver]] disease.
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*[[Regenerative and Non-Regenerative Anaemias|Anaemia]] with a reactive [[Neutrophilia|neutrophilia]] and [[Monocytosis|monocytosis]] if the haemorrhage is severe.
 
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Severe platelet deficiencies may be managed with transfusions of whole blood or, in the USA, with transfusions of platelet cryoprecipitate - this helps to control the anaemia which occurs as a consequence of haemorrhage and which is the life threatening sympton that required correction (rather than the thrombocytopenia). With both techniques however, it is likely that the transfused platelets have only a short half life in the recipient. 
 
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The use of Vincristine (a drug also used in chemotherapy for neoplasia) has been advocated in cases of thrombocytopaenia as it increases the rate of fragmentation of megakaryocytes and decreases the descruction of platelets by macrophages. A single intravenous dose is usually given.
 
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{{Learning
 
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|literature search = [http://www.cabdirect.org/search.html?q=title%3A%28thrombocytopenia%29+OR+title%3A%28thrombocytopaenia%29&fq=sc%3A%22ve%22 Thrombocytopaenia publications]
 
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[http://www.cabdirect.org/search.html?q=title%3A%28thrombocytopathia%29+ Thrombocytopathia publications]
 
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[http://www.cabdirect.org/search.html?q=title%3A%28thrombocytosis%29&fq=sc%3A%22ve%22 Thrombocytosis publications]
 
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|flashcards = [[Small Animal Emergency and Critical Care Medicine Q&A 21]]
 
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}}
 
  
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====Thrombocytopathia====
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{{unfinished}}
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Von Willebrands, Angiostrongylus, colloids, granule disease.
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* A rare inherited condition.
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* Recorded in the dog. 
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* Characterised by defective thrombocyte formation.
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** Poor adhesiveness.
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** Poor aggregations.
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** Poor platelet factor release.
  
 
[[Category:Haemorrhagic Diseases]]
 
[[Category:Haemorrhagic Diseases]]
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[[Category:Haematology Changes]]
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[[Category:To Do - James]]
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[[Category:Lymphoreticular and Haematopoietic Diseases - Dog]]
 
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[[Category:Cardiology Section]]
 

Revision as of 14:07, 17 August 2010


 This article is still under construction.


Description

Platelets (or thrombocytes) are responsible for primary haemostasis, the formation of a temporary platelet plug that initially seals any breach to a blood vessel wall. Bleeding disorders may occur if platelets are deficient (thrombocytopaenia) or if the platelets are unable to function adequately (thrombocytopathia). Thrombocytopaenia may be a primary disease due to disease of the bone marrow that reduces the production of platelets or it may occur secondary to another insult.

Primary Thrombocytopaenic Disease

The aetiology of primary thrombocytopenic disease is often uncertain and it is therefore also known as idiopathic thrombocytopaenia. Some cases of primary thrombocytopaenia may occur due to autoimmune responses directed at platelets and, although the bone marrow may contain adequate normal megakaryocytes, this disease results in a reduced peripheral blood thrombocyte count. Immune-mediated thrombocytopaenia occurs most commonly in young animals.

Secondary Thrombocytopaenic Disease

Secondary thrombocyopaenic disease is fairly common in adult domestic animals and it may be associated with diseases that depress the production of platelets or increase their consumption or sequestration:

  • Diseases that cause bone marrow suppression
    • Aplastic anaemia caused by ingestion of bracken, administration of oestrogens or of chloramphenicol or sulphonamide antibiotics. Prolonged use of phenylbutazone or salicylate may cause the same disease.
    • Myelophthisis, the displacement of the normal tissues of the bone marrow by another cell or tissue type may also reduce the function of the megakaryocytes. Possible diseases include myelofibrosis and immunoprliferative or myeloproliferative neoplastic disease.
    • Radiotherapy or myelosuppressive chemotherapy may cause reversible bone marrow suppression.
  • Diseases that cause increased destruction of platelets
  • Diseases that cause sequestration of platelets usually involve some enlargement to the spleen as this is the major organ where platelets are stored outside of the circulation. Examples include:
    • Haemangiosarcoma of the spleen and liver
    • Splenic enlargement under general anaesthesia with certain agents such as barbiturates and phenothiazines
  • Associated with diseases which cause [bone marrow]] depression.
  • The bone marrow is depleted or devoid of megakaryocytes, and there is a nil or markedly reduced peripheral blood thrombocyte count.
  • Secondary thrombocyopenic disease is seen in the following conditions:
    1. Severe viral infections.
    2. Severe protozoal infections.
      • For example, in the UK, Haemobartonella may be a cause.





Thrombocytopathia


 This article is still under construction.


Von Willebrands, Angiostrongylus, colloids, granule disease.

  • A rare inherited condition.
  • Recorded in the dog.
  • Characterised by defective thrombocyte formation.
    • Poor adhesiveness.
    • Poor aggregations.
    • Poor platelet factor release.
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