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.
ICD-10-CM Diagnosis Code D69.3 [convert to ICD-9-CM] Immune thrombocytopenic purpura. Acute idiopathic thrombocytopenic purpura; Chronic idiopathic thrombocytopenic purpura; Idiopathic thrombocytopenia purpura (itp); Idiopathic thrombocytopenic purpura; Idiopathic thrombocytopenic purpura, chronic; Purpura, idiopathic thrombocytopenia, ...
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism D69.59 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 D69.59 became effective on October 1, 2021.
Z86.2 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 Z86.2 became effective on October 1, 2021. This is the American ICD-10-CM version of Z86.2 - other international versions of ICD-10 Z86.2 may differ. D60-D64 Aplastic and other anemias and other bon...
Adult chronic immune thrombocytopenic purpura (chronic ITP) is an autoimmune disorder in which patients produce antiplatelet autoantibodies and specialized white blood cells that destroy their blood platelets and, in some cases, damage their megakaryocytes (the cells that produce platelets in the bone marrow), causing ...
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.
Though the abbreviation “ITP” remains the same, it now refers to immune thrombocytopenia, which can be either primary or secondary. ITP is defined as a platelet count of less than 100 × 109/L (100,000/μL) with no evidence of leukopenia or anemia.
ICD-10 code: D69. 6 Thrombocytopenia, unspecified | gesund.bund.de.
ICD-10-CM Code for Thrombocytopenia, unspecified D69. 6.
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).
Immune thrombocytopenia usually happens when your immune system mistakenly attacks and destroys platelets, which are cell fragments that help blood clot. In adults, this may be triggered by infection with HIV , hepatitis or H. pylori — the type of bacteria that causes stomach ulcers.
The incidence (how many people are diagnosed each year) of adult ITP in the USA is roughly estimated to be 3.3 per 100,000/year. The prevalence (how many have ITP at any time) is 9.5 per 100,000.
Summary. Idiopathic thrombocytopenic purpura (ITP) is a rare autoimmune disorder, in which a person's blood doesn't clot properly, because the immune system destroys the blood-clotting platelets.
ICD-10 | Thrombocytopenia, unspecified (D69. 6)
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 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...•
For most children and adults, ITP is not a serious condition. Acute ITP in children often goes away on its own within a few weeks or months and does not return. For a small number of children, ITP does not go away on its own, and the child may need treatment.
Key points about immune thrombocytopenic purpura ITP may happen suddenly and go away in about 6 months. Or it may be ongoing (chronic) and last for years. Treatment options include medicines that can reduce platelet destruction or help the body make more platelets. In some cases, surgery to remove the spleen is needed.
To diagnose immune thrombocytopenia, your doctor is likely to order further blood tests that require drawing a small amount of blood from a vein in an arm. He or she may also refer you to a specialist in blood diseases (hematologist).
ITP is known to be a diagnosis of exclusion and acute leukaemia happens to be a strong differential diagnosis. Other causes of thrombocytopaenia include myelophthisic marrow infiltration, myelodysplasia, aplastic anaemia, adverse drug reaction, systemic lupus erythematosus, HIV and other viral infections etc.
Clinical Information. 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.
The 2022 edition of ICD-10-CM D69.6 became effective on October 1, 2021.
A decrease in the number of platelets in the blood that may result in easy bruising and excessive bleeding from wound s or bleeding in mucous membranes and other tissues. A finding based on laboratory test results that indicate a decrease in number of platelets in a blood specimen. A subnormal level of blood platelets.
The 2022 edition of ICD-10-CM D69.59 became effective on October 1, 2021.
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
A type 2 excludes note represents "not included here". A type 2 excludes note indicates that the condition excluded is not part of the condition it is excluded from but a patient may have both conditions at the same time. When a type 2 excludes note appears under a code it is acceptable to use both the code ( D75.83) and the excluded code together.
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
D75.83 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism 1 Z00-Z99#N#2021 ICD-10-CM Range Z00-Z99#N#Factors influencing health status and contact with health services#N#Note#N#Z codes represent reasons for encounters. A corresponding procedure code must accompany a Z code if a procedure is performed. Categories Z00-Z99 are provided for occasions when circumstances other than a disease, injury or external cause classifiable to categories A00 -Y89 are recorded as 'diagnoses' or 'problems'. This can arise in two main ways:#N#(a) When a person who may or may not be sick encounters the health services for some specific purpose, such as to receive limited care or service for a current condition, to donate an organ or tissue, to receive prophylactic vaccination (immunization), or to discuss a problem which is in itself not a disease or injury.#N#(b) When some circumstance or problem is present which influences the person's health status but is not in itself a current illness or injury.#N#Factors influencing health status and contact with health services 2 Z77-Z99#N#2021 ICD-10-CM Range Z77-Z99#N#Persons with potential health hazards related to family and personal history and certain conditions influencing health status#N#Code Also#N#any follow-up examination ( Z08 - Z09)#N#Persons with potential health hazards related to family and personal history and certain conditions influencing health status 3 Z86#N#ICD-10-CM Diagnosis Code Z86#N#Personal history of certain other diseases#N#2016 2017 2018 2019 2020 2021 Non-Billable/Non-Specific Code#N#Code First#N#any follow-up examination after treatment ( Z09)#N#Personal history of certain other diseases
The 2022 edition of ICD-10-CM Z86.2 became effective on October 1, 2021.
Z77-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status
CPT codes, descriptions and other data only are copyright 2021 American Medical Association. All Rights Reserved. Applicable FARS/HHSARS apply.
This article gives guidance for billing, coding, and other guidelines in relation to local coverage policy DL38268-Immune Thrombocytopenia (ITP) Therapy.
Contractors may specify Bill Types to help providers identify those Bill Types typically used to report this service. Absence of a Bill Type does not guarantee that the article does not apply to that Bill Type.
Contractors may specify Revenue Codes to help providers identify those Revenue Codes typically used to report this service. In most instances Revenue Codes are purely advisory. Unless specified in the article, services reported under other Revenue Codes are equally subject to this coverage determination.