icd code 10 for itp

What is the ICD10 code for idiopathic thrombocytopenic purpura?

ICD10 codes matching "Idiopathic Thrombocytopenic Purpura" Codes: = Billable. D69.3 Immune thrombocytopenic purpura

What is the ICD 10 code for thrombocytopenia?

Thrombocytopenia, unspecified. D69.6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2020 edition of ICD-10-CM D69.6 became effective on October 1, 2019.

What is the ICD 10 version of platelet count?

This is the American ICD-10-CM version of D69.3 - other international versions of ICD-10 D69.3 may differ. A condition in which platelets (blood cells that cause blood clots to form) are destroyed by the immune system.

How many terms are there in the ICD-10-CM alphabetical index?

The ICD-10-CM Alphabetical Index is designed to allow medical coders to look up various medical terms and connect them with the appropriate ICD codes. There are 135 terms under the parent term 'Anemia And Thrombocytopenia' in the ICD-10-CM Alphabetical Index .

What is the ICD-10 code for History of ITP?

Immune thrombocytopenic purpura D69. 3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM D69. 3 became effective on October 1, 2021.

What are the two types of ITP?

There are two forms of ITP:Acute thrombocytopenic purpura. This usually affects young children, ages 2 to 6 years old. ... Chronic thrombocytopenic purpura. The onset of the disorder can happen at any age, and the symptoms can last a minimum of 6 months, several years, or a lifetime.

What is ITP syndrome?

Overview. Immune thrombocytopenia (ITP) is a disorder that can lead to easy or excessive bruising and bleeding. The bleeding results from unusually low levels of platelets — the cells that help blood clot.

What is the ICD-10 code for low platelets?

ICD-10-CM Code for Thrombocytopenia, unspecified D69. 6.

What is the difference between thrombocytopenia and ITP?

A healthy person usually has a platelet count of 150,000 to 400,000. You have thrombocytopenia if your number falls under 150,000. If you're wondering what the long name means, here's how it breaks down: "Thrombocytes" are your platelets, and "penia" means you don't have enough of something.

What is the main cause of ITP?

The cause of ITP is not known, but it is thought that some kinds of viral infection may cause the immune system to malfunction and start producing antibodies that attack platelets. Treatment options for ITP include ongoing monitoring of platelet levels, medications, and surgical removal of the spleen in severe cases.

Is ITP an autoimmune disease?

Immune thrombocytopenia (ITP) is an autoimmune bleeding disorder characterized by abnormally low levels of blood cells called platelets, a situation which is referred to as thrombocytopenia.

How ITP is diagnosed?

Blood smear: For this test, some of your blood is put on a slide. A microscope is used to look at your platelets. Bone marrow tests: These tests check whether your bone marrow is healthy. You may need this test to confirm that you have ITP and not another platelet disorder, especially if your treatment is not working.

What is ITP and how is it treated?

Most adults with ITP will eventually need treatment, as the condition often becomes severe or long term (chronic). Treatment may include a number of approaches, such as medications to boost your platelet count or surgery to remove your spleen (splenectomy).

What is a low platelet count called?

Thrombocytopenia is a condition in which you have a low blood platelet count. Platelets (thrombocytes) are colorless blood cells that help blood clot. Platelets stop bleeding by clumping and forming plugs in blood vessel injuries.

What is considered severe thrombocytopenia?

Degrees of thrombocytopenia can be further subdivided into mild (platelet count 100,000 to 150,000/microL), moderate (50,000 to 99,000/microL), and severe (<50,000/microL) [1].

What is the difference between primary and secondary thrombocytopenia?

The ITP Syndrome ITP is an autoimmune bleeding disorder caused by various etiologies, which is characterized by increased platelet destruction and impaired production, resulting in a decreased platelet count. Primary ITP is idiopathic, whereas secondary ITP is linked to an underlying condition (1).