Difference between revisions of "Hypercoagulable state (thrombophilia)"

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==Inherited thrombophilias==
 
==Inherited thrombophilias==
 
*Prothrombin gene mutation (G20210A)
 
*Prothrombin gene mutation (G20210A)
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==Acquired thrombophilias and clotting risk factors==
 
==Acquired thrombophilias and clotting risk factors==
*Surgery, foreign bodies such as venous catheters, smoking, obesity, elevated factor VIII, advanced age, male sex, trauma, sedentary state, immobilization, malignancy, myeloproliferative disorders--[[polycythemia vera | polycythemia vera (PV)]], [[Essential thrombocythemia | essential thrombocythemia (ET)]], [[Myelofibrosis | primary myelofibrosis (PMF)]], pregnancy, medications--e.g. [[Bevacizumab (Avastin)]], [[Lenalidomide (Revlimid)]], [[Thalidomide (Thalomid)]], [[Tamoxifen (Nolvadex)]], oral contraceptive use, [[heparin]]--in the case of heparin-induced thrombocytopenia/thrombosis (HIT), congestive heart failure, anatomic/low cardiovascular flow states--e.g. inferior vena cava (IVC) abnormalities, chronic inflammation, inflammatory bowel disease, nephrotic syndrome, [[Paroxysmal nocturnal hemoglobinuria (PNH) | paroxysmal noctural hemoglobinuria (PNH)]]
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*[[Surgery]], foreign bodies such as venous catheters, smoking, obesity, elevated factor VIII, advanced age, male sex, trauma, sedentary state, immobilization, malignancy, myeloproliferative disorders--[[polycythemia vera | polycythemia vera (PV)]], [[Essential thrombocythemia | essential thrombocythemia (ET)]], [[Myelofibrosis | primary myelofibrosis (PMF)]], pregnancy, medications--e.g. [[Bevacizumab (Avastin)]], [[Lenalidomide (Revlimid)]], [[Thalidomide (Thalomid)]], [[Tamoxifen (Nolvadex)]], oral contraceptive use, [[heparin]]--in the case of heparin-induced thrombocytopenia/thrombosis (HIT), congestive heart failure, anatomic/low cardiovascular flow states--e.g. inferior vena cava (IVC) abnormalities, chronic inflammation, inflammatory bowel disease, nephrotic syndrome, [[Paroxysmal_nocturnal_hemoglobinuria | paroxysmal noctural hemoglobinuria (PNH)]]
 
*Prior venous thromboembolism (VTE)
 
*Prior venous thromboembolism (VTE)
 
*Antiphospholipid antibody syndrome (APS)
 
*Antiphospholipid antibody syndrome (APS)
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**Beta 2 glycoprotein 1 (B2GP1) IgG, IgM, IgA
 
**Beta 2 glycoprotein 1 (B2GP1) IgG, IgM, IgA
 
**Sapporo criteria for APS
 
**Sapporo criteria for APS
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==Related pages==
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*[[Antiphospholipid antibody syndrome]]
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*[[Inherited thrombophilia]]
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*[[Venous thromboembolism]]
  
 
==References==
 
==References==
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*[https://pubmed.ncbi.nlm.nih.gov/25724822 Moll S. Thrombophilia: clinical-practical aspects. J Thromb Thrombolysis. 2015 Apr;39(3):367-78.]
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**[https://mobile.twitter.com/THilalMD/status/1183941575300263936 Table of reliability of thrombophilia testing with anticoagulants and in acute thrombosis]
  
 
[[Category:Hematology reference pages]]
 
[[Category:Hematology reference pages]]

Latest revision as of 17:51, 7 September 2023

Inherited thrombophilias

  • Prothrombin gene mutation (G20210A)
  • Factor V Leiden mutation
  • Antithrombin III deficiency
  • Protein C deficiency
  • Protein S deficiency
  • Dysfibrinogenemia

Controversial:

  • Plasminogen deficiency
  • Factor XII deficiency

Acquired thrombophilias and clotting risk factors

Related pages

References