Bleeding diathesis: Difference between revisions
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== Overview == | == Overview == | ||
Bleeding diathesis is unusual susceptibility to bleed due to coagulopathies. These diseases can occur due to a disorder of homeostasis, localized process (tissue injury), or medications. Bleeding diathesis can be resulted from vessel wall injury, platelet disorders, and coagulation factor disorders. Clinical manifestation of bleeding disorders can have a wide range of symptoms from no symptom to massive symptomatic and life threatening bleeding. Platelet disorders mostly have skin manifestations such as petechiae, and ecchymoses. In order to find the cause of coagulopathy, there are established laboratory tests that might be used. These laboratory tests such as peripheral blood smear, platelet count and platelet function analysis, coagulation factor deficiencies and inhibitors, fibrinolysis tests (eg. D-dimer level), bleeding time, prothrombin time, activated partial thromboplastin time, thrombin time and reptilase time. | |||
== Classification == | == Classification == |
Revision as of 13:29, 30 August 2018
Bleeding diathesis main page |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Mehrian Jafarizade, M.D [2] Nazia Fuad M.D.
Overview
Bleeding diathesis is unusual susceptibility to bleed due to coagulopathies. These diseases can occur due to a disorder of homeostasis, localized process (tissue injury), or medications. Bleeding diathesis can be resulted from vessel wall injury, platelet disorders, and coagulation factor disorders. Clinical manifestation of bleeding disorders can have a wide range of symptoms from no symptom to massive symptomatic and life threatening bleeding. Platelet disorders mostly have skin manifestations such as petechiae, and ecchymoses. In order to find the cause of coagulopathy, there are established laboratory tests that might be used. These laboratory tests such as peripheral blood smear, platelet count and platelet function analysis, coagulation factor deficiencies and inhibitors, fibrinolysis tests (eg. D-dimer level), bleeding time, prothrombin time, activated partial thromboplastin time, thrombin time and reptilase time.
Classification
Differential Diagnosis
Category | Sub-category | Diseases | History | Clinical manifestation | Laboratory testing | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Petechiae | Ecchymoses | Menorrhagia | Hematomas | Hemarthrosis | platelet count | Bleeding time (BT) | Prothrombin time (PT) | Platelet count activated partial thromboplastin time (aPTT) | Thrombin time (TT) | ||||
Platelet disorders | Thrombocytopenia | Infection-Induced Thrombocytopenia | + | + | ↓ | N | N | ||||||
Medications-Induced Thrombocytopenia | History of medications | + | + | ↓ | N | N | |||||||
Heparin-Induced Thrombocytopenia | Trombosis and unexplained thrombocytopenia up to 3 weeks after the end of heparin therapy | + | + | ↓ | |||||||||
Immune Thrombocytopenic Purpura (ITP) | + | + | ↓ | ↑ | N | N | |||||||
Inherited Thrombocytopenia | ↓ | ↑ | N | N | |||||||||
Thrombotic Thrombocytopenic Purpura (TTP) | ↑ | ||||||||||||
Hemolytic Uremic Syndrome | N | N | |||||||||||
Thromobcytosis | Digital pain
Headache Paresthesias Transient ischemic attacks |
− | − | − | + | + | ↑ | ɴormal or slightly prolonged | ɴ | ɴ | |||
Qualitative Disorders of Platelet Function | Inherited Disorders of Platelet Function | ||||||||||||
Acquired Disorders of Platelet Function | |||||||||||||
Von Willebrand Disease | Easy bruising
Oral cavity bleeding Bleeding after dental extraction/surgery |
+ | + | + | + | + | ↑ | Ν | ↑ | ||||
Vessel wall disorders | Metabolic and Inflammatory Disorders | ||||||||||||
Inherited Disorders of the Vessel Wall | |||||||||||||
Coagulation disorders | Fibrinogen deficiency | ||||||||||||
Prothrombin deficiency | |||||||||||||
Factor V deficiency | |||||||||||||
Factor VII deficiency | |||||||||||||
Factor VIII deficiency | |||||||||||||
Factor IX deficiency | |||||||||||||
Factor X deficiency | |||||||||||||
Factor XI deficiency | |||||||||||||
Factor XII deficiency | |||||||||||||
HK deficiency | |||||||||||||
Prekallikrein deficiency | |||||||||||||
Factor XIII deficiency | |||||||||||||
Hemophilia | Type A deficiency | Eeasy bruising Inadequate clotting in trauma or mild injury spontaneous hemorrhage. hemarthrosis, epistaxis, gingival bleeding | _ | _ | + | + | + | Unaffected | Unaffected | Unaffected | Prolonged | N | |
Type B deficiency | Neonatal bleeding
trauma-related soft-tissue hemorrhage hemarthrosis and hematomas |
_ | _ | + | + | + | Unaffected | N | N | ↑ | N | ||
Type C deficiency | Family history of bleeding disorder,
bleeding after surgry or injury |
_ | _ | + | Rare | Rare | N | N | N | ↑ | N | ||
Rare diseases | Disseminated Intravascular Coagulation | Trauma, burn, crush
Sepsis Malignancy Obstetric complication: abruption, amniotic fluid embolism Hemolytic anemia |
+ | + | _ | + | + | ↓ | ↑ | ↑ | ↑ | ||
Vitamin K Deficiency | Bleeding after trauma, epistaxis, hematoma, gastrointestinal bleeding, menorrhagia, hematuria, gum bleeding, and oozing from venipuncture sites and easy bruisability | + | + | + | + | + | N | ↑ | ↑ | Normal or mildly prolonged | |||
Coagulation Disorders Associated with Liver Failure | |||||||||||||
Acquired Inhibitors of Coagulation Factors |