Wiskott-Aldrich syndrome is a rare X-linked immunodeficiency disorder characterized by the triad of eczema, recurrent infections, and thrombocytopenia. It is caused by mutations in the WAS gene, leading to impaired immune function and increased susceptibility to infections. Accurate coding with ICD-10 Code D82.0 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate care and resources.
What is ICD-10 Code D82.0 for Wiskott-Aldrich syndrome?
ICD-10 Code D82.0 specifically denotes Wiskott-Aldrich syndrome, a genetic disorder affecting the immune system and blood platelets. This code should be used in clinical documentation and billing when diagnosing patients exhibiting symptoms such as eczema, recurrent infections, and low platelet counts, facilitating accurate treatment and management of the condition.
ICD-10 Code D82.0 – Clinical Definition and Explanation of Wiskott-Aldrich syndrome
Wiskott-Aldrich syndrome is caused by mutations in the WAS gene, leading to a deficiency in immune response and platelet production. The condition progresses with increased risk of infections and bleeding complications, necessitating prompt medical attention and management.
Key Clinical Features:
- Eczema in early childhood
- Recurrent bacterial and viral infections
- Thrombocytopenia with bleeding tendencies
- Increased risk of autoimmune disorders
- Potential development of lymphoid malignancies
ICD-10 Code D82.0 for Wiskott-Aldrich syndrome – SOAP Notes & Clinical Use
ICD-10 Code D82.0 is utilized in SOAP notes to document the patient's symptoms, assessment findings, and treatment plans. It is relevant in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and facilitating continuity of care.
What Does ICD-10 Code D82.0 for Wiskott-Aldrich syndrome Mean in SOAP Notes?
In SOAP notes, ICD-10 Code D82.0 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of Wiskott-Aldrich syndrome. This coding ensures continuity of care, supports accurate billing, and meets EHR documentation standards.
Treatment Options for ICD-10 Code D82.0 – Wiskott-Aldrich syndrome
Wiskott-Aldrich syndrome requires urgent medical intervention due to its complications. Treatment focuses on managing symptoms and preventing infections.
Antibiotic Therapy:
- Intravenous immunoglobulin (IVIG) therapy for infection prevention
- Prophylactic antibiotics such as penicillin for bacterial infections
- Alternative antibiotics may include azithromycin for respiratory infections
- Duration of therapy is based on clinical response and infection history
Supportive Care:
- Management of eczema with topical corticosteroids
- Platelet transfusions for severe thrombocytopenia
- Regular monitoring for infections and autoimmune complications
- Education on infection prevention strategies
Infection Control:
- Strict hygiene practices to prevent infections
- Isolation precautions during outbreaks of infectious diseases
- Vaccination against preventable diseases, avoiding live vaccines
- Regular follow-up with immunology specialists
How to Document Symptoms of Wiskott-Aldrich syndrome (ICD-10 D82.0) in SOAP Notes
Subjective:
- Patient reports recurrent skin rashes and itching
- History of frequent respiratory infections
- Family history of bleeding disorders
- Patient experiences easy bruising and prolonged bleeding
Objective:
- Erythematous, scaly patches noted on skin examination
- Laboratory results show low platelet count
- Signs of infection such as fever or cough
- Physical examination reveals lymphadenopathy
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SOAP Note Guidelines for Diagnosing Wiskott-Aldrich syndrome (ICD-10 Code D82.0)
Assessment:
- Diagnosis: Wiskott-Aldrich syndrome, moderate severity
- ICD-10 Code: D82.0
- Contributing factors include genetic mutation and environmental triggers
- Patient exhibits classic triad of symptoms
Plan:
- Initiate IVIG therapy for immune support
- Schedule regular follow-ups for monitoring platelet levels
- Educate patient on infection prevention and management
- Consider referral to a hematologist for further evaluation
Treatment & Plan Section for ICD-10 Code D82.0 – Wiskott-Aldrich syndrome
- Administer prophylactic antibiotics to prevent infections
- Implement regular monitoring of platelet counts and immune function
- Educate patient on recognizing signs of infection and bleeding
- Schedule follow-up appointments for ongoing management and support
Using ICD-10 Code D82.0 for Wiskott-Aldrich syndrome in Billing & SOAP Note Compliance
- Ensure accurate documentation of symptoms and clinical findings in SOAP notes
- Use D82.0 for all encounters related to Wiskott-Aldrich syndrome
- Align treatment plans with clinical guidelines to support billing
- Include relevant CPT codes that correspond to the services provided
Related ICD-10 Codes Often Used with Wiskott-Aldrich syndrome
- D80.9 – Immunodeficiency, unspecified
ICD-10 Code D82.0 in Medical Billing and Insurance for Wiskott-Aldrich syndrome
ICD-10 Code D82.0 is critical in medical billing, particularly in hospital, ER, or infectious disease care settings.
Billing Notes:
- Document all relevant symptoms and clinical findings to support the diagnosis
- Use D82.0 in conjunction with other codes for comprehensive billing
- Ensure that treatment plans are clearly outlined in the patient's chart
- Include any complications or comorbidities in the documentation
Common CPT Pairings:
| CPT Code | Description |
|---|---|
| 36415 | Collection of venous blood by venipuncture |
| 96365 | IV infusion, for therapy, prophylaxis, or diagnosis |
| 85027 | Complete blood count with automated differential |
| 99214 | Established patient office visit, level 4 |
Frequently Asked Questions
Common Questions About Using ICD-10 Code D82.0 for Wiskott-Aldrich syndrome
What are the common symptoms of Wiskott-Aldrich syndrome?
Common symptoms include eczema, recurrent infections, and low platelet counts leading to easy bruising and bleeding. These symptoms typically manifest in early childhood and require careful monitoring and management.
How is Wiskott-Aldrich syndrome diagnosed?
Diagnosis is based on clinical presentation, family history, and laboratory tests showing low platelet counts and immune deficiencies. Genetic testing can confirm mutations in the WAS gene.
What treatments are available for Wiskott-Aldrich syndrome?
Treatment options include immunoglobulin therapy to boost immune function, prophylactic antibiotics to prevent infections, and supportive care for managing symptoms. In severe cases, hematopoietic stem cell transplantation may be considered.
Is Wiskott-Aldrich syndrome hereditary?
Yes, Wiskott-Aldrich syndrome is an X-linked recessive disorder, meaning it is primarily inherited through the mother. Males are predominantly affected, while females may be carriers.
