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Bleeding disorders
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Bleeding disorders

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Coagulopathy

Bleeding disorders are a group of conditions in which there is a problem with the body's blood clotting process. These disorders can lead to heavy and prolonged bleeding after an injury. Bleeding can also begin on its own.

Related problems include:

  • Acquired platelet function defects
  • Congenital platelet function defects
  • Congenital protein C or S deficiency
  • Disseminated intravascular coagulation (DIC)
  • Factor II deficiency
  • Factor V deficiency
  • Factor VII deficiency
  • Factor X deficiency
  • Factor XII deficiency
  • Hemophilia A
  • Hemophilia B 
  • Hemophilia C (Factor XI deficiency)
  • Idiopathic thrombocytopenic purpura (ITP)
  • Von Willebrand's disease (types I, II, and III)

I Would Like to Learn About:

  • Causes


    Blood clotting

    Blood clotting

    Normal blood clotting involves as many as 20 different plasma proteins. These are known as blood clotting or coagulation factors. These factors interact with other chemicals to form a substance called fibrin that stops bleeding.

    Problems can occur when certain coagulation factors are low or missing. Bleeding problems can range from mild to severe.

    Some bleeding disorders are present at birth and are passed through families (inherited). Others develop from:

    • Illnesses such as vitamin K deficiency or severe liver disease
    • Treatments such as the use of drugs to stop blood clots (anticoagulants) or the long-term use of antibiotics

    Bleeding disorders can also result from a problem with the number or function of the blood cells that promote blood clotting (platelets). These disorders can also be either inherited or develop later (acquired). The side effects of certain drugs often lead to the acquired forms.

  • Symptoms

    • ·   Bleeding into joints
    • ·   Excessive bruising
    • ·   Heavy bleeding
    • ·   Heavy menstrual bleeding
    • ·   Nosebleeds
    • ·   Excess bleeding with surgical procedures

    The type of problems that occur depend on the specific bleeding disorder, and how severe it is.

  • Exams and Tests

    • Complete blood count (CBC)
    • Bleeding time
    • Partial thromboplastin time (PTT)
    • Platelet aggregation test
    • Prothrombin time (PT)
  • Treatment

    Treatment depends on the type of disorder. It may include:

    • Factor replacement
    • Fresh frozen plasma transfusion
    • Platelet transfusion
    • Other therapies
  • Outlook (Prognosis)

    The outcome also depends on the disorder. Most primary bleeding disorders can be managed. When the disorders is due to diseases, such as DIC, the outcome will depend on how well the underlying disease can be treated.

  • Possible Complications

    • Bleeding in the brain
    • Severe bleeding (usually from the gastrointestinal tract or injuries)

    Other complications can occur, depending on the disorder.

  • When to Contact a Medical Professional

    Call your health care provider if you notice any unusual or severe bleeding.

  • Prevention

    Prevention depends on the specific disorder.

Related Information

  Vitamin KLiver disease     Vitamins

References

Ragni MV. Hemorrhagic disorders: Coagulation factor deficiencies. In: Goldman L, Schafer AI, eds. Goldman's Cecil Medicine. 24th ed. Philadelphia, PA: Saunders Elsevier; 2011:chap 177.

Gailani D, Neff AT. Rare coagulation deficiencies. In: Hoffman R, Benz EJ Jr, Silberstein LE, Heslop HE, Weitz JI, eds. Hematology: Basic Principles and Practice. 6th ed. Philadelphia, PA: Saunders Elsevier; 2012:chap 139.

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Review Date: 3/3/2013  

Reviewed By: Yi-Bin Chen, MD, Leukemia/Bone Marrow Transplant Program, Massachusetts General Hospital. Also reviewed by A.D.A.M. Health Solutions, Ebix, Inc., Editorial Team: David Zieve, MD, MHA, Bethanne Black, Stephanie Slon, and Nissi Wang.

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