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ICD-10-CM Codes
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D50-D89
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D65-D69
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D69-
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2023 ICD-10-CM Diagnosis Code D69.3
2023 ICD-10-CM Diagnosis Code D69.3
Immune thrombocytopenic purpura
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- D69.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM D69.3 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D69.3 - other international versions of ICD-10 D69.3 may differ.
Applicable To- Hemorrhagic (thrombocytopenic) purpura
- Idiopathic thrombocytopenic purpura
- Tidal platelet dysgenesis
The following code(s) above
D69.3 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
D69.3:
Approximate Synonyms
- Acute idiopathic thrombocytopenic purpura
- Chronic idiopathic thrombocytopenic purpura
- Idiopathic thrombocytopenia purpura (itp)
- Idiopathic thrombocytopenic purpura
- Idiopathic thrombocytopenic purpura, chronic
- Purpura, idiopathic thrombocytopenia, acute
Clinical Information
- A condition in which platelets (blood cells that cause blood clots to form) are destroyed by the immune system. The low platelet count causes easy bruising and bleeding, which may be seen as purple areas in the skin, mucous membranes, and outer linings of organs.
- An autoimmune disorder in which the number of circulating platelets is reduced due to their antibody-mediated destruction. Itp is a diagnosis of exclusion and is heterogeneous in origin.
- Bleeding or bruising tendency due to low platelet level
- Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases immunoglobulin g autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms.
ICD-10-CM D69.3 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 813 Coagulation disorders
Convert D69.3 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations containing back-references to D69.3:
- Dysgenesis
- Frank's essential thrombocytopenia D69.3
- Hemorrhage, hemorrhagic (concealed) R58
ICD-10-CM Diagnosis Code R58
Hemorrhage, not elsewhere classified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Type 1 Excludes- hemorrhage included with underlying conditions, such as:
- acute duodenal ulcer with hemorrhage (K26.0)
- acute gastritis with bleeding (K29.01)
- ulcerative enterocolitis with rectal bleeding (K51.01)
- Purpura D69.2
ICD-10-CM Diagnosis Code D69.2
Other nonthrombocytopenic purpura
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Purpura NOS
- Purpura simplex
- Senile purpura
- hemorrhagic, hemorrhagica D69.3
- idiopathic (thrombocytopenic) D69.3
- thrombocytopenic D69.49
ICD-10-CM Diagnosis Code D69.49
Other primary thrombocytopenia
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Megakaryocytic hypoplasia
- Primary thrombocytopenia NOS
- hemorrhagic D69.3
- idiopathic D69.3
- immune D69.3
- immune thrombocytopenic D69.3
- Thrombocytopenia, thrombocytopenic D69.6
ICD-10-CM Diagnosis Code D69.6
Thrombocytopenia, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- primary NEC D69.49
ICD-10-CM Diagnosis Code D69.49
Other primary thrombocytopenia
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Megakaryocytic hypoplasia
- Primary thrombocytopenia NOS
- essential D69.3
- idiopathic D69.3
- Werlhof's disease D69.3
ICD-10-CM Codes Adjacent To D69.3
D68.6 Other thrombophilia
D68.61 Antiphospholipid syndrome
D68.62 Lupus anticoagulant syndrome
D68.8 Other specified coagulation defects
D68.9 Coagulation defect, unspecified
D69 Purpura and other hemorrhagic conditions
D69.1 Qualitative platelet defects
D69.2 Other nonthrombocytopenic purpura
D69.3
Immune thrombocytopenic purpura
D69.4 Other primary thrombocytopenia
D69.42 Congenital and hereditary thrombocytopenia purpura
D69.49 Other primary thrombocytopenia
D69.5 Secondary thrombocytopenia
D69.51 Posttransfusion purpura
D69.59 Other secondary thrombocytopenia
D69.6 Thrombocytopenia, unspecified
D69.8 Other specified hemorrhagic conditions
D69.9 Hemorrhagic condition, unspecified
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.