Idiopathic thrombocytopenic purpura (ITP) - NYSORA

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Idiopathic thrombocytopenic purpura (ITP)

Idiopathic thrombocytopenic purpura (ITP)

Learning objectives

  • Definition of idiopathic thrombocytopenia purpura (ITP)
  • Treatment and perioperative management of ITP

Definitions and mechanisms

  • Idiopathic thrombocytopenic purpura (ITP) is an autoimmune disease characterized by a low platelet count, purpura, and hemorrhagic episodes
  • Resulting in easy or excessive bruising and bleeding due to unusually low levels of platelets
  • The immune system produces antibodies against platelets 
    • Most often against platelet membrane glycoproteins IIB-IIIa or Ib-IX
  • Normal platelet count is between 150.000 and 450.000, the platelet count is less than 10.000 with ITP
  • Pregnant women with ITP have an increased incidence of fetal loss, a low fetal birth rate, and a higher incidence of premature births
  • Two types:
    • Acute thrombocytopenic purpura
      • Affects young children between 2-6 years, often following a coral infection
      • Starts suddenly and symptoms usually disappear in less than 6 months, often within a few weeks
      • Most common form and resolves spontaneously
    • Chronic thrombocytopenic purpura
      • Onset can happen at any age
      • Symptoms can last a minimum of 6 months to several years or a lifetime
      • More common in adults and in females
      • Requires continual follow-up care

Signs and symptoms

  • Easy or excessive bruising
  • Petechiae
  • Bleeding from the gums or nose
  • Blood in urine or stools
  • Unusually heavy menstrual flow

Complications

  • Subarachnoid or intracerebral hemorrhage
  • Lower gastrointestinal bleeding

Causes

  • Medication (the medication absorbs the platelet cell membrane)
  • Infection: the virus that causes chickenpox, hepatitis C, and AIDS
  • Pregnancy
  • Immune disorders: rheumatoid arthritis, lupus
  • Cancer: low-grade lymphomas and leukemia
  • The cause is sometimes unknown

Diagnosis

  • Complete blood count
  • Low platelet count, usually <40×10^9/L for over three months
  • Bleeding time
  • Blood and urine tests to detect a possible infection
  • Antiplatelet antibody test
  • Bone marrow examination shows an increased number of megakaryocytes

Management

Idiopathic thrombocytopenic purpura (ITP), platelet transfusion, IV immunoglobulin, ccorticosteroids, prednisone, splenectomy, rituximab, dapsone, anti-RhD globulin, plasmapheresis,

Suggested reading

  • Toyomasu Y, Shimabukuro R, Moriyama H, et al. Successful perioperative management of a patient with idiopathic thrombocytopenic purpura undergoing emergent appendectomy: Report of a case. Int J Surg Case Rep. 2013;4(10):898-900.
  • Ramalingam, G., Jones, N., Besser, M., 2016. Platelets for anaesthetists—part 1: physiology and pathology. BJA Education 16, 134–139.
  • Warrier R, Chauhan A. Management of immune thrombocytopenic purpura: an update. Ochsner J. 2012;12(3):221-227.
  • Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy. 2003. British Journal of Haematology 120, 574–596.

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