icd 10 code for thomboytopenia

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 code for hemorrhagic thrombocythemia?

2018/2019 ICD-10-CM Diagnosis Code D47.3. Essential (hemorrhagic) thrombocythemia. 2016 2017 2018 2019 Billable/Specific Code. D47.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

What is the ICD 10 code for mastocytosis?

Code annotations containing back-references to D47.3: Code Also: D47.02, I27.29 ICD-10-CM Diagnosis Code D47.02. Systemic mastocytosis 2018 - New Code 2019 Billable/Specific Code Type 1 Excludes: D69, D69 ICD-10-CM Diagnosis Code D69. Purpura and other hemorrhagic conditions 2016 2017 2018 2019 Non-Billable/Non-Specific Code

What is the ICD 10 code for neoplasm?

This is the American ICD-10-CM version of D47.3 - other international versions of ICD-10 D47.3 may differ. All neoplasms are classified in this chapter, whether they are functionally active or not.

What does thrombocytopenia mean?

Listen to pronunciation. (THROM-boh-sy-toh-PEE-nee-uh) A condition in which there is a lower-than-normal number of platelets in the blood. It may result in easy bruising and excessive bleeding from wounds or bleeding in mucous membranes and other tissues.

What is the ICD-10 code for thrombocytopenia due to chemotherapy?

Other secondary thrombocytopenia The 2022 edition of ICD-10-CM D69. 59 became effective on October 1, 2021. This is the American ICD-10-CM version of D69. 59 - other international versions of ICD-10 D69.

What are the two types of thrombocytopenia?

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 the ICD-10 code for personal history of thrombocytopenia?

Z86. 2 - Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | ICD-10-CM.

How do you code 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 2022 edition of ICD-10-CM D69. 6 became effective on October 1, 2021.

What is the difference between pancytopenia and thrombocytopenia?

Pancytopenia occurs when you have a combination of three different blood disorders: Anemia is when you have too few red blood cells. Leukopenia is when you have too few white blood cells. Thrombocytopenia is when you have too few platelets.

What are the main causes of thrombocytopenia?

What causes thrombocytopenia?Alcohol use disorder and alcoholism.Autoimmune disease which causes ITP. ... Bone marrow diseases, including aplastic anemia, leukemia, certain lymphomas and myelodysplastic syndromes.Cancer treatments like chemotherapy and radiation therapy.More items...•

What causes thrombocytopenic disorder?

Thrombocytopenia might occur as a result of a bone marrow disorder such as leukemia or an immune system problem. Or it can be a side effect of taking certain medications. It affects both children and adults.

What platelet count is thrombocytopenia?

A normal platelet count ranges from 150,000 to 450,000 platelets per microliter of blood. Having more than 450,000 platelets is a condition called thrombocytosis; having less than 150,000 is known as thrombocytopenia.

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).

What ICD-10 covers PT PTT?

NCD - Partial ThromboplastinTime (PTT) (190.16)

What is the ICD-10 code for thrombocytosis?

Essential (hemorrhagic) thrombocythemia The 2022 edition of ICD-10-CM D47. 3 became effective on October 1, 2021.

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).

What are the four mechanisms of thrombocytopenia?

There are four primary causes of thrombocytopenia: hypoproliferation (lack of production), sequestration, consumption (utilization), and destruction. Sampling or laboratory artifact may also lead to falsely low platelet counts.

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 differential diagnosis of thrombocytopenia?

Important differential diagnoses in patients with severe thrombocytopenia are: acute leukemia, thrombotic thrombocytopenic purpura, autoimmune thrombocytopenia and drug-dependent thrombocytopenia. Multifactorial causes are thrombocytopenia associated with pregnancy, chronic alcohol abuse, and liver cirrhosis.

What is the code for a primary malignant neoplasm?

A primary malignant neoplasm that overlaps two or more contiguous (next to each other) sites should be classified to the subcategory/code .8 ('overlapping lesion'), unless the combination is specifically indexed elsewhere.

What is the table of neoplasms used for?

The Table of Neoplasms should be used to identify the correct topography code. In a few cases, such as for malignant melanoma and certain neuroendocrine tumors, the morphology (histologic type) is included in the category and codes. Primary malignant neoplasms overlapping site boundaries.

What is a chronic myeloproliferative neoplasm?

A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterized by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocytes in the bone marrow, and episodes of thrombosis and/or hemorrhage. The cause is unknown.

What are the two most common diseases that result in thrombosis in microvasculature?

Diseases that result in thrombosis in microvasculature. The two most prominent diseases are purpura, thrombotic thrombocytopenic; and hemolytic-uremic syndrome. Multiple etiological factors include vascular endothelial cell damage due to shiga toxin; factor h deficiency; and aberrant von willebrand factor formation.

What is a microangiopathic hemolytic anemia?

A disorder characterized by the presence of microangiopathic hemolytic anemia, thrombocytopenic purpura, fever, renal abnormalities and neurological abnormalities such as seizures, hemiplegia, and visual disturbances. It is an acute or subacute condition.