D69.3

Applicable To

• Hemorrhagic thrombocytopenic) purpura

• Idiopathic thrombocytopenic purpura

• Tidal platelet dysgenesis

Approximate Synonyms

• Acute idiopathic thrombocytopenic purpura

• Chronic idiopathic thrombocytopenic purpura

• Idiopathic thrombocytopenia purpura itp)

• Idiopathic thrombocytopenic purpura

• Idiopathic thrombocytopenic purpura, chronic

• Purpura, idiopathic thrombocytopenia, acute

Clinical Information

• A condition in which platelets blood cells that cause blood clots to form) are destroyed by the immune system. The low platelet count causes easy bruising and bleeding, which may be seen as purple areas in the skin, mucous membranes, and outer linings of organs.

• An autoimmune disorder in which the number of circulating platelets is reduced due to their antibody-mediated destruction. Itp is a diagnosis of exclusion and is heterogeneous in origin.

• Bleeding or bruising tendency due to low platelet level

• Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases immunoglobulin g autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute affecting children) and chronic adult) forms.

Details

• D69.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM D69.3 became effective on October 1, 2022.

• This is the American ICD-10-CM version of D69.3 – other international versions of ICD-10 D69.3 may differ.