Sickle-cell thalassemia, unspecified, with splenic sequestration is a hematological condition characterized by the presence of both sickle cell disease and thalassemia, leading to abnormal hemoglobin production. This condition can result in splenic sequestration crises, where red blood cells become trapped in the spleen, causing acute splenic enlargement and pain. Accurate coding with ICD-10 Code D57.412 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that healthcare providers can effectively manage and treat affected patients.
ICD-10 Code D57.412 represents sickle-cell thalassemia, unspecified, with splenic sequestration. This code is used to document cases where patients experience complications related to both sickle cell disease and thalassemia, specifically involving splenic sequestration. It should be applied in clinical documentation and billing when patients present with symptoms indicative of splenic sequestration, ensuring accurate representation of their medical condition.
Sickle-cell thalassemia, unspecified, with splenic sequestration is caused by genetic mutations affecting hemoglobin production, leading to the formation of sickle-shaped red blood cells. These abnormal cells can obstruct blood flow, particularly in the spleen, resulting in splenic sequestration crises. This condition requires prompt medical attention to prevent severe complications such as splenic rupture and severe anemia.
ICD-10 Code D57.412 is utilized in SOAP notes to document the clinical presentation, assessment, and treatment of patients with sickle-cell thalassemia and splenic sequestration. This code aids in capturing the patient's symptoms, guiding clinical assessments, and formulating treatment plans in both acute and chronic care settings.
In SOAP notes, ICD-10 Code D57.412 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of sickle-cell thalassemia with splenic sequestration. This code is crucial for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Management of sickle-cell thalassemia with splenic sequestration often necessitates hospitalization due to the risk of severe complications. Treatment focuses on alleviating symptoms and preventing further crises.


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Learn moreICD-10 Code D57.412 is critical in medical billing, particularly in hospital, ER, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 36430 | Transfusion, blood or blood components. |
| 85025 | Complete blood count (CBC) with differential. |
| 99285 | Emergency department visit, high severity. |
| 88305 | Pathology examination of tissue. |
Common Questions About Using ICD-10 Code D57.412 for Sickle-cell thalassemia, unsp, with splenic sequestration
What are the common symptoms of sickle-cell thalassemia with splenic sequestration?
Common symptoms include severe abdominal pain, fatigue, fever, and signs of anemia such as pallor and shortness of breath. Patients may also experience recurrent infections due to splenic dysfunction.
When should ICD-10 Code D57.412 be used?
This code should be used when a patient presents with symptoms indicative of splenic sequestration in the context of sickle-cell thalassemia. It is essential for accurate documentation and billing.
How does splenic sequestration affect treatment decisions?
Splenic sequestration can lead to acute complications requiring immediate intervention, such as hydration, pain management, and possible blood transfusions. Treatment plans must be adjusted based on the severity of the sequestration.
What is the importance of accurate coding for D57.412?
Accurate coding ensures appropriate reimbursement, facilitates continuity of care, and supports public health reporting. It is crucial for healthcare providers to document the condition correctly to reflect the patient's clinical status.
Clinical Notes
SOAP notes
DAP notes
AI medical notes