Hemophagocytic lymphohistiocytosis is a severe systemic inflammatory syndrome characterized by excessive activation of the immune system, leading to hemophagocytosis. It can be triggered by infections, malignancies, or autoimmune diseases. Accurate coding with ICD-10 Code D76.1 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring appropriate management and resource allocation.
ICD-10 Code D76.1 represents Hemophagocytic lymphohistiocytosis, a condition where the body's immune system becomes overly activated, leading to the destruction of blood cells. This code should be used when documenting cases of hemophagocytic lymphohistiocytosis, particularly in relation to underlying diseases or complications, to ensure accurate clinical documentation and billing.
Hemophagocytic lymphohistiocytosis is caused by an uncontrolled immune response, often triggered by infections, malignancies, or autoimmune disorders. It can progress rapidly, leading to multi-organ failure and requires immediate medical attention.
ICD-10 Code D76.1 is utilized in SOAP notes to document the clinical presentation, assessment, and treatment of hemophagocytic lymphohistiocytosis. It is relevant in both acute and chronic care settings, facilitating comprehensive patient management.
In SOAP notes, ICD-10 Code D76.1 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of hemophagocytic lymphohistiocytosis, ensuring continuity of care and supporting accurate billing.
Hemophagocytic lymphohistiocytosis often necessitates hospitalization for intensive management. Treatment focuses on addressing the underlying cause and may include specific therapies.


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Learn moreICD-10 Code D76.1 is crucial for billing in hospital, ER, or infectious disease care settings, ensuring accurate reimbursement for services rendered.
| CPT Code | Description |
|---|---|
| 36415 | Collection of venous blood by venipuncture. |
| 85025 | Complete blood count with automated differential. |
| 96365 | Intravenous infusion, for therapy, prophylaxis, or diagnosis. |
Common Questions About Using ICD-10 Code D76.1 for Hemophagocytic lymphohistiocytosis
What are the common causes of Hemophagocytic lymphohistiocytosis?
Common causes include viral infections, autoimmune diseases, and certain malignancies. Identifying the underlying cause is crucial for effective treatment.
How is Hemophagocytic lymphohistiocytosis diagnosed?
Diagnosis is based on clinical presentation, laboratory findings, and imaging studies. Key indicators include cytopenias and elevated ferritin levels.
What is the treatment for Hemophagocytic lymphohistiocytosis?
Treatment typically involves corticosteroids and supportive care. Addressing any underlying conditions is also essential for management.
Is Hemophagocytic lymphohistiocytosis contagious?
Hemophagocytic lymphohistiocytosis itself is not contagious; however, underlying infections that may trigger it can be.
Clinical Notes
SOAP notes
DAP notes
AI medical notes