Icd 10 Coding For Idiopathic Thrombocytopenic Purpura

What is Idiopathic Thrombocytopenic Purpura (ICD-10 D69.3)?

Idiopathic thrombocytopenic purpura (ITP) is a blood disorder characterized by a decrease in the number of platelets in the blood. Platelets are small blood cells that help with blood clotting. In ITP, the immune system mistakenly attacks and destroys platelets, leading to a low platelet count. This can result in easy bruising, bleeding, and in severe cases, life-threatening bleeding.

ICD-10 Code Information for Idiopathic Thrombocytopenic Purpura

Coding Clinic Advice: Immune Thrombocytopenic Purpura and Pancytopenia (Q  204)
Coding Clinic Advice: Immune Thrombocytopenic Purpura and Pancytopenia (Q 204)

The ICD-10 code for idiopathic thrombocytopenic purpura is D69.3. This code is used to classify and code for medical conditions related to ITP in healthcare settings.

Diagnostic Related Groups (MS-DRG) for Idiopathic Thrombocytopenic Purpura

ICD--CM Diagnosis Code D
ICD–CM Diagnosis Code D

In terms of MS-DRG, idiopathic thrombocytopenic purpura falls under DRG 811 – Red blood cell disorders with MCC (major complications or comorbidities) or DRG 812 – Red blood cell disorders without MCC.

Converting ICD-10 Code to ICD-9 Code for Idiopathic Thrombocytopenic Purpura

To convert the ICD-10 code D69.3 for idiopathic thrombocytopenic purpura to an ICD-9 code, you would use the code 287.31. This allows for cross-referencing and compatibility with older code systems.

Code History of Idiopathic Thrombocytopenic Purpura

The ICD-10 code for idiopathic thrombocytopenic purpura, D69.3, was introduced in 2016 as part of the updated coding system. It replaced the previous ICD-9 code 287.31 for the same condition.

Approximate Synonyms for Idiopathic Thrombocytopenic Purpura

Autoimmune thrombocytopenic purpura
Immune thrombocytopenic purpura
Primary thrombocytopenic purpura
Idiopathic thrombocytopenic purpura

Clinical Information on Idiopathic Thrombocytopenic Purpura

Idiopathic thrombocytopenic purpura is caused by the immune system mistakenly attacking platelets in the blood. This can lead to a low platelet count, which can result in symptoms such as easy bruising, nosebleeds, and bleeding gums. Diagnosis is typically made through blood tests and a physical exam.

Causes of Idiopathic Thrombocytopenic Purpura

The exact cause of idiopathic thrombocytopenic purpura is not known, but it is believed to be related to an immune system dysfunction. The immune system mistakenly targets platelets for destruction, leading to a decrease in platelet count.

Symptoms of Idiopathic Thrombocytopenic Purpura

Common symptoms of idiopathic thrombocytopenic purpura include easy bruising, nosebleeds, bleeding gums, and petechiae (small red or purple spots on the skin). In severe cases, individuals may experience life-threatening bleeding.

Diagnosis of Idiopathic Thrombocytopenic Purpura

Diagnosis of idiopathic thrombocytopenic purpura is typically made through blood tests to measure platelet count, as well as a physical exam to check for signs of bleeding or bruising. Additional tests may be ordered to rule out other potential causes of low platelet count.

Treatment for Idiopathic Thrombocytopenic Purpura

Treatment for idiopathic thrombocytopenic purpura can vary depending on the severity of symptoms. Common treatment options include corticosteroids to suppress the immune response, intravenous immunoglobulin (IVIG) to increase platelet count, and in some cases, splenectomy (surgical removal of the spleen).


Idiopathic thrombocyt

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