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| | Also known as: '''''ITP — Idiopathic Thrombocytopaenic Purpura — [[Evan's syndrome|Evan’s Syndrome]] | | Also known as: '''''ITP — Idiopathic Thrombocytopaenic Purpura — [[Evan's syndrome|Evan’s Syndrome]] |
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| | ==Introduction== | | ==Introduction== |
| − | Immune-mediated thrombocytopaenia (ITP) occurs due to an autoimmune response directed against circulating platelets or megakaryocytes in the bone marrow. The destruction of cells is mediated by antibodies, making ITP a form of '''[[Type II Hypersensitivity|type II hypersensitivity]]'''. The antibodies bind to cells and act as a foundation for the assembly of serum complement components or as opsonins, promoting the uptake and destruction of platelets by cells of the monocyte-phagocyte system (MPS). The destruction of platelets usually results in severe [[Platelet Abnormalities|thrombocytopaenia]] and, if the blood level of platelets fall below approximately 50x10^9/l, the affected animal is at risk of mucosal haemorrhages. | + | Immune-mediated thrombocytopaenia (ITP) occurs due to an autoimmune response directed against circulating platelets or megakaryocytes in the bone marrow. The destruction of cells is mediated by antibodies, making ITP a form of '''[[Type II Hypersensitivity|type II hypersensitivity]]'''. The antibodies bind to surface recptors on the platelets and act as a foundation for the assembly of serum complement components or as opsonins, promoting the uptake and destruction of platelets by cells of the monocyte-phagocyte system (MPS). The destruction of platelets usually results in severe [[Platelet Abnormalities|thrombocytopaenia]] and, if the blood level of platelets fall below approximately 50x10^9/l, the affected animal is at risk of mucosal haemorrhages. |
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| − | ITP may be '''primary''' (with no apparent underlying cause) or '''secondary''' to another disease process, to an infection or as a reaction to some drugs. ITP that occurs concurrently with [[Immune Mediated Haemolytic Anaemia|immune-mediated haemolytic anaemia]] (IMHA) is known as '''Evan’s syndrome'''. | + | ITP may be '''primary''' (with no apparent underlying cause) or '''secondary''' to another disease process; infections, neoplasia, other automimmune diseases, transfusion reactions and drug reactions (particularly antibiotics) are underlying conditions that can cause a secondary ITP . ITP that occurs concurrently with [[Immune Mediated Haemolytic Anaemia|immune-mediated haemolytic anaemia]] (IMHA) is known as '''Evan’s syndrome'''. |
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| | ==Signalment== | | ==Signalment== |
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| | ===Laboratory Tests=== | | ===Laboratory Tests=== |
| − | Haematological analysis of a blood sample will show '''thrombocytopaenia''', often with extremely low platelet counts (e.g. 1-5x10^9/l). There may be a reactive [[Neutrophilia|neutrophilia]] and other features of a stress leucogram. Examination of a blood smear may show evidence of '''microthrombocytes''' (small platelets that have been partially phagocytosed by cells of the MPS, similar to spherocytes in IMHA) or immature '''macrothrombocytes''' (a sign of bone marrow platelet regeneration). The patient may be anaemic in cases of Evan’s syndrome or if significant haemorrhage has occurred. | + | Haematological analysis of a blood sample will show '''thrombocytopaenia''', often with extremely low platelet counts (e.g. 1-5x10^9/l). There may be a reactive [[Neutrophilia|neutrophilia]] and other features of a [[Stress Leucogram|stress leucogram]]. Examination of a blood smear may show evidence of '''microthrombocytes''' (small platelets that have been partially phagocytosed by cells of the MPS, similar to spherocytes in IMHA) or immature '''macrothrombocytes''' (a sign of bone marrow platelet regeneration). The patient may be anaemic in cases of Evan’s syndrome or if significant haemorrhage has occurred. |
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| | ===Other Tests=== | | ===Other Tests=== |
| | Definitive diagnosis relies on the detection of serum anti-platelet antibodies but this test is not widely available. | | Definitive diagnosis relies on the detection of serum anti-platelet antibodies but this test is not widely available. |
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| − | Other tests may also be used to exclude potential infectious causes of thrombocytopaenia such as ''[[Ehrlichia platys]]'' and ''Anaplasma phagocytophilum''. | + | Other tests may also be used to exclude potential infectious causes of thrombocytopaenia such as ''[[Ehrlichia platys]]'' and ''[[Anaplasma phagocytophilum]]''. |
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| | Faecal occult blood tests represent an unreliable way of detecting gastro-intestinal haemorrhage in cases of mild melaena. The animal must be deprived of meat, bismuth subsalicylate and ferrous sulphate for 3 days before the faecal samples are taken for analysis. | | Faecal occult blood tests represent an unreliable way of detecting gastro-intestinal haemorrhage in cases of mild melaena. The animal must be deprived of meat, bismuth subsalicylate and ferrous sulphate for 3 days before the faecal samples are taken for analysis. |
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| | ==Prognosis== | | ==Prognosis== |
| − | Similarly to IMHA, mortality is most likely in the initial stages of the disease and the mortality rate is approximately 30% in this period. Beyond this, the majority of animals recover well although they may require immunosuppressive treatment for several months to completely control the disease. | + | Similarly to IMHA, mortality is most likely in the initial stages of the disease and the mortality rate is approximately 30% in this period. Beyond this, the majority of animals recover well although they usually require tapered immunosuppressive treatment for roughly six months to completely control the disease. Initial responses to treatment are relatively quick, so if no increase in platelet number is seen within 1 week of initiating treatment, investigate further for an underlying cause which requires treatment. |
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| − | ==Literature Search==
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| − | [[File:CABI logo.jpg|left|90px]]
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| | + | {{Learning |
| | + | |literature search = [http://www.cabdirect.org/search.html?q=%28%28+title%3A%28%22Immune+Mediated%22%29++AND++%28+title%3A%28%22Thrombocytopaenia%22%29++OR++title%3A%28%22thrombocytopenia%22%29+%29+%29++OR+++%28+%28+title%3A%28Idiopathic%29+++AND++%28+title%3A%28%22Thrombocytopaenic%22%29+++OR++title%3A%28%22thrombocytopenic%22%29+%29+++AND++title%3A%28Purpura%29+%29+%29%29&fq=sc%3A%22ve%22 Immune Mediated Thrombocytopaenia publications] |
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| − | Use these links to find recent scientific publications via CAB Abstracts (log in required unless accessing from a subscribing organisation).
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| − | [http://www.cabdirect.org/search.html?q=%28%28+title%3A%28%22Immune+Mediated%22%29++AND++%28+title%3A%28%22Thrombocytopaenia%22%29++OR++title%3A%28%22thrombocytopenia%22%29+%29+%29++OR+++%28+%28+title%3A%28Idiopathic%29+++AND++%28+title%3A%28%22Thrombocytopaenic%22%29+++OR++title%3A%28%22thrombocytopenic%22%29+%29+++AND++title%3A%28Purpura%29+%29+%29%29&fq=sc%3A%22ve%22 Immune Mediated Thrombocytopaenia publications]
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| | ==References== | | ==References== |
| | Ettinger, S.J, Feldman, E.C. (2005) '''Textbook of Veterinary Internal Medicine''' (6th edition, volume 2) Elsevier Saunders Company | | Ettinger, S.J, Feldman, E.C. (2005) '''Textbook of Veterinary Internal Medicine''' (6th edition, volume 2) Elsevier Saunders Company |
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| | [[Category:Antibody Mediated Autoimmune Diseases]] | | [[Category:Antibody Mediated Autoimmune Diseases]] |
| − | [[Category:Dog]][[Category:Cat]][[Category:Expert Review]] | + | [[Category:Immunological Diseases - Dog]][[Category:Lymphoreticular and Haematopoietic Diseases - Dog]][[Category:Immunological Diseases - Cat]][[Category:Lymphoreticular and Haematopoietic Diseases - Cat]][[Category:Expert Review - Small Animal]] |