Thrombophilia: Difference between revisions

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|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular'''
|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular'''
|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" | • Cerebral vein thrombosis • Acute myocardial infarction • Deep vein thrombophlebitis • Portal vein thrombosis • Pelvic thrombophlebitis
|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" | • Cerebral vein [[thrombosis]] [[Acute myocardial infarction]] [[Deep vein thrombophlebitis]] [[Portal vein thrombosis]] • Pelvic [[thrombophlebitis]]
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| '''Endocrine'''
| '''Endocrine'''
|bgcolor="Beige"| • Hyperosmolar non-ketotic diabetic coma
|bgcolor="Beige"| • [[Hyperosmolar non-ketotic diabetic coma]]
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Gastroenterologic'''
| '''Gastroenterologic'''
|bgcolor="Beige"| • Acute pancreatitis • Portal hypertension
|bgcolor="Beige"| • Acute [[pancreatitis]] [[Portal hypertension]]
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|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Genetic'''
| '''Genetic'''
|bgcolor="Beige"| Congenital Dysfibrinogenemia • Factor II mutation • Hereditary thrombophlebitis • Antithrombin III deficiency • Factor V Leiden mutation • Protein C deficiency • Protein S deficiency • Klippel-Trenaunay syndrome • Klinefelter syndrome • Sickle cell disease • Carbohydrate-deficient glycoprotein syndrome type 1b • Factor XII deficiency • Haemoglobin SC disease • Hyperprothrombinemia 20210G-A • Plasminogen deficiency • Activated protein C resistance • CD59 antigen deficiency • Cystathionine beta-synthase deficiency
|bgcolor="Beige"| Congenital Dysfibrinogenemia • Factor II mutation • Hereditary thrombophlebitis • [[Antithrombin III deficiency]] [[Factor V Leiden mutation]] [[Protein C deficiency]] [[Protein S deficiency]] [[Klippel-Trenaunay syndrome]] [[Klinefelter syndrome]] [[Sickle cell disease]] • Carbohydrate-deficient glycoprotein syndrome type 1b • Factor XII deficiency • Haemoglobin SC disease • Hyperprothrombinemia 20210G-A • Plasminogen deficiency • Activated protein C resistance • CD59 antigen deficiency • Cystathionine beta-synthase deficiency
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|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Hematologic'''
| '''Hematologic'''
|bgcolor="Beige"|  • Polycythemia vera • Essential thrombocythemia • Myeloproliferative disease • Hyperviscosity syndrome • Paroxysmal Nocturnal Hemoglobinuria • Thrombocytosis • Raised homocysteine levels
|bgcolor="Beige"|  • [[Polycythemia vera]] [[Essential thrombocythemia]] [[Myeloproliferative disease]] [[Hyperviscosity]] syndrome • [[Paroxysmal Nocturnal Hemoglobinuria]] [[Thrombocytosis]] • Raised homocysteine levels
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| '''Infectious Disease'''
| '''Infectious Disease'''
|bgcolor="Beige"| • Intraperitoneal abscess • Acute peritonitis • Visceral abscess • Diverticulitis • Intravenous catheter infection
|bgcolor="Beige"| • Intraperitoneal abscess • [[Acute peritonitis]] • Visceral [[abscess]] [[Diverticulitis]] • Intravenous catheter infection
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| '''Nutritional / Metabolic'''
| '''Nutritional / Metabolic'''
|bgcolor="Beige"| • Cystathionuria • Homocystinuria • Methyltetrahydrofolate reductase deficiency • Metabolic Syndrome • Insulin resistance • Folic acid deficiency • Obesity
|bgcolor="Beige"| • Cystathionuria • Homocystinuria • Methyltetrahydrofolate reductase deficiency • [[Metabolic Syndrome]] [[Insulin resistance]] • Folic acid deficiency • [[Obesity]]
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| '''Oncologic'''
| '''Oncologic'''
|bgcolor="Beige"|  • Malignancy • Peritoneal metastasis • Adenocarcinoma of cecum • Adenocarcinoma of colon • Occult malignancy • Leukemia • Pancreatic cancer • Glucagonoma
|bgcolor="Beige"|  • Malignancy • Peritoneal metastasis • Adenocarcinoma of cecum • Adenocarcinoma of colon • Occult malignancy • Leukemia • Pancreatic cancer • [[Glucagonoma]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Renal / Electrolyte'''
| '''Renal / Electrolyte'''
|bgcolor="Beige"| • Chronic renal failure • Paroxysmal Nocturnal Hemoglobinuria • Nephrotic syndrome
|bgcolor="Beige"| • [[Chronic renal failure]] [[Paroxysmal Nocturnal Hemoglobinuria]] [[Nephrotic syndrome]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Rheum / Immune / Allergy'''
| '''Rheum / Immune / Allergy'''
|bgcolor="Beige"|  • Antiphospholipid Syndrome • Circulatin anticoagulant • Heparin induced thrombocytopenia • Inflammatory bowel disease • Crohn's disease • Behcet disease • Hughes-Stovin syndrome • Polyarteritis Nodosa • SLE
|bgcolor="Beige"|  • [[Antiphospholipid Syndrome]] • Circulatin anticoagulant • [[Heparin induced thrombocytopenia]] [[Inflammatory bowel disease]] [[Crohn's]] disease • [[Behcet disease]] • Hughes-Stovin syndrome • [[Polyarteritis Nodosa]] [[SLE]]
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| '''Miscellaneous'''
| '''Miscellaneous'''
|bgcolor="Beige"| • Paraneoplastic syndrome • Hypereosinophilic syndrome • Immobility
|bgcolor="Beige"| • [[Paraneoplastic syndrome]] • Hypereosinophilic syndrome • Immobility
|-
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|}
|}

Revision as of 01:19, 7 May 2012

Thrombophilia
OMIM 188050
DiseasesDB 29080
MeSH D019851

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List of terms related to Thrombophilia

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-In-Chief: Kashish Goel, M.D.

Synonyms and Keywords: Hypercoagulability, coagulability, hypercoagulable state

Overview

Thrombophilia means increased risk of thrombosis (blood clots) in the body, due to an abnormality in the system of coagulation. Thrombophilia can be congenital or acquired. Less than 50% of the cases of thrombosis not diagnosed with un underlying thrombophilia.

Classification

Thrombophilia can be classified in various forms.

  • The most common classification is by the nature of the thrombosis: arterial, venous or combined.
  • Crowther & Kelton (2003) propose to classify the abnormality by the molecular deficiency, type I being the (severe) deficiencies of inhibitors, and type II being the less severe elevation of coagulation factors.[1]
  • Acquired vs. congenital

Pathophysiology

Epidemiology and Demographics

Risk factors

Causes

Common types:

Rare forms:

Differential diagnosis of thrombophilia

(By organ system)

Cardiovascular • Cerebral vein thrombosisAcute myocardial infarctionDeep vein thrombophlebitisPortal vein thrombosis • Pelvic thrombophlebitis
Drug Side Effect • Asparaginase • Bevacizumab • Combined oral contraceptive pill • Cyproterone • Diethylstilboestrol • Drospirenone • Eltrombopag • Erythropoietin • Ethinylestradiol • Fosfestrol • Granulocyte-macrophage colony stimulating factor • Heparin • Hormone replacement therapy • Lenalidomide • Peginesatide • Polyestradiol • Raloxifene • Strontium ranelate • Tamoxifen • Tobacco smoking • Tranexamic acid • Vorinostat
Endocrine Hyperosmolar non-ketotic diabetic coma
Gastroenterologic • Acute pancreatitisPortal hypertension
Genetic Congenital Dysfibrinogenemia • Factor II mutation • Hereditary thrombophlebitis • Antithrombin III deficiencyFactor V Leiden mutationProtein C deficiencyProtein S deficiencyKlippel-Trenaunay syndromeKlinefelter syndromeSickle cell disease • Carbohydrate-deficient glycoprotein syndrome type 1b • Factor XII deficiency • Haemoglobin SC disease • Hyperprothrombinemia 20210G-A • Plasminogen deficiency • Activated protein C resistance • CD59 antigen deficiency • Cystathionine beta-synthase deficiency
Hematologic Polycythemia veraEssential thrombocythemiaMyeloproliferative diseaseHyperviscosity syndrome • Paroxysmal Nocturnal HemoglobinuriaThrombocytosis • Raised homocysteine levels
Iatrogenic Surgical complication
Infectious Disease • Intraperitoneal abscess • Acute peritonitis • Visceral abscessDiverticulitis • Intravenous catheter infection
Musculoskeletal / Ortho • Orthopedic surgeries • Abdominal surgery
Nutritional / Metabolic • Cystathionuria • Homocystinuria • Methyltetrahydrofolate reductase deficiency • Metabolic SyndromeInsulin resistance • Folic acid deficiency • Obesity
Obstetric/Gynecologic • Pregnancy • Puerperium period • Ovarian hyperstimulation syndrome
Oncologic • Malignancy • Peritoneal metastasis • Adenocarcinoma of cecum • Adenocarcinoma of colon • Occult malignancy • Leukemia • Pancreatic cancer • Glucagonoma
Renal / Electrolyte Chronic renal failureParoxysmal Nocturnal HemoglobinuriaNephrotic syndrome
Rheum / Immune / Allergy Antiphospholipid Syndrome • Circulatin anticoagulant • Heparin induced thrombocytopeniaInflammatory bowel diseaseCrohn's disease • Behcet disease • Hughes-Stovin syndrome • Polyarteritis NodosaSLE
Trauma • Trauma • Abdominal trauma
Miscellaneous Paraneoplastic syndrome • Hypereosinophilic syndrome • Immobility

Indications for testing

Searching for a coagulation abnormality is not normally undertaken in patients in whom thrombosis has an obvious other cause. For example, if the thrombosis is due to immobilisation after recent orthopedic surgery, it is unlikely that an underlying cause is found.

Conversely, although thrombosis itself may occur in any person, repeated (two or more) unprovoked episodes of thrombosis and unusual sites and types of thrombosis (e.g. Budd-Chiari syndrome) may point towards a coagulation disorder.

Increasingly, recurrent miscarriage is seen as an indication for thrombophilia screening. [2]

Tests for thrombophilia include prothrombin time and INR, partial thromboplastin time, thrombin time, fibrinogen levels, antiphospholipid antibody levels (IgG- and IgM-anticardiolipin, dilute Russell viper venom time and lupus anticoagulant), protein C, protein S and antithrombin (both levels and activity), activated protein C resistance (APC resistance), factor V Leiden and prothrombin mutation. Many laboratories add on various other tests, depending on local policy and guidelines.

Treatment

References

  1. Crowther MA, Kelton JG (2003). "Congenital thrombophilic states associated with venous thrombosis: a qualitative overview and proposed classification system". Ann. Intern. Med. 138 (2): 128–34. PMID 12529095.
  2. Dawood, F., Farquharson, R., Quenby, S.Recurrent miscarriage. Current Obstetrics & Gynaecology, 2004; 14:247-253.

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