Immune thrombocytopenic purpura (ITP) is an autoimmune disorder characterized by a decrease in platelet count, leading to increased bleeding and bruising. The condition arises when the immune system mistakenly targets and destroys platelets. Accurate coding with ICD-10 Code D69.3 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and resources.
ICD-10 Code D69.3 represents Immune thrombocytopenic purpura, a condition where the immune system produces antibodies against platelets, resulting in thrombocytopenia. This code should be used in clinical documentation and billing when diagnosing patients with ITP, particularly when they present with symptoms such as easy bruising, petechiae, or prolonged bleeding.
Immune thrombocytopenic purpura is primarily caused by the immune system's inappropriate response, leading to the destruction of platelets. The condition can be acute or chronic and may require medical intervention to prevent serious complications such as hemorrhage. Prompt diagnosis and treatment are crucial.
ICD-10 Code D69.3 is utilized in SOAP notes to document the patient's symptoms, assessment findings, and treatment plans. It is relevant in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and facilitating appropriate management.
In SOAP notes, ICD-10 Code D69.3 connects subjective reports of symptoms with objective clinical findings, leading to a formal diagnosis of Immune thrombocytopenic purpura. This code supports continuity of care, accurate billing, and compliance with EHR documentation standards.
Management of Immune thrombocytopenic purpura may require hospitalization, especially in severe cases. Treatment focuses on addressing the underlying immune response and managing symptoms.


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Learn moreICD-10 Code D69.3 is critical in medical billing, particularly in hospital, ER, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 36415 | Collection of venous blood by venipuncture. |
| 85027 | Complete blood count (CBC) with automated differential. |
| 96372 | Therapeutic, prophylactic, or diagnostic injection. |
Common Questions About Using ICD-10 Code D69.3 for Immune thrombocytopenic purpura
What are the common symptoms of Immune thrombocytopenic purpura?
Common symptoms include easy bruising, petechiae, prolonged bleeding from cuts, and fatigue. Patients may also experience nosebleeds or bleeding gums.
How is Immune thrombocytopenic purpura diagnosed?
Diagnosis typically involves a complete blood count (CBC) to assess platelet levels, along with a review of the patient's medical history and symptoms.
What treatments are available for Immune thrombocytopenic purpura?
Treatment options include corticosteroids, intravenous immunoglobulin (IVIG), and in severe cases, platelet transfusions or splenectomy.
Is Immune thrombocytopenic purpura a contagious condition?
No, Immune thrombocytopenic purpura is not contagious. It is an autoimmune disorder where the body mistakenly attacks its own platelets.
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