Sickle-cell/Hb-C disease with crisis with other complications is a hematological disorder characterized by the presence of abnormal hemoglobin, leading to sickle-shaped red blood cells. This condition can result in painful vaso-occlusive crises and various complications, including infections and organ damage. Accurate coding with ICD-10 Code D57.218 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and resources.
ICD-10 Code D57.218 represents Sickle-cell/Hb-C disease with crisis with other complications. This code is used when a patient experiences a crisis related to their sickle-cell disease, which may involve additional complications such as acute chest syndrome or splenic sequestration. It is crucial for clinical documentation and billing to accurately reflect the severity and nature of the patient's condition.
Sickle-cell/Hb-C disease with crisis with other complications arises from genetic mutations affecting hemoglobin structure, leading to sickle-shaped erythrocytes. These abnormal cells can obstruct blood flow, causing pain and potential organ damage. Prompt medical attention is necessary to manage crises and prevent severe complications.
ICD-10 Code D57.218 is utilized in SOAP notes to document the patient's symptoms, assessment, and treatment plan. It is relevant in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and guiding appropriate management strategies.
In SOAP notes, ICD-10 Code D57.218 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis. This code is essential for ensuring continuity of care, supporting accurate billing, and meeting EHR documentation standards.
Management of Sickle-cell/Hb-C disease with crisis with other complications often requires hospitalization for acute episodes. Treatment focuses on pain relief, hydration, and prevention of complications.


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Learn moreICD-10 Code D57.218 is critical in medical billing, particularly in hospital, ER, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 99285 | Emergency department visit for high severity. |
| 36415 | Collection of venous blood by venipuncture. |
| 36430 | Transfusion of blood products. |
| 85027 | Complete blood count with automated differential. |
Common Questions About Using ICD-10 Code D57.218 for Sickle-cell/Hb-C disease with crisis with oth complication
What are the common complications associated with Sickle-cell/Hb-C disease?
Common complications include vaso-occlusive crises, acute chest syndrome, infections, and stroke. These complications can significantly impact the patient's health and require prompt medical intervention.
When should ICD-10 Code D57.218 be used?
ICD-10 Code D57.218 should be used when a patient with Sickle-cell/Hb-C disease experiences a crisis accompanied by other complications, ensuring accurate documentation and billing.
How does Sickle-cell disease affect patient management?
Sickle-cell disease requires comprehensive management strategies, including pain control, hydration, and monitoring for complications. Regular follow-ups are essential to manage chronic symptoms and prevent crises.
Is Sickle-cell disease hereditary?
Yes, Sickle-cell disease is an inherited condition caused by mutations in the hemoglobin gene. It is passed from parents to children in an autosomal recessive pattern.
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