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ICD-10 Code D89.82 | Autoimmune lymphoproliferative syndrome [ALPS] Symptoms, Diagnosis, Billing

Autoimmune lymphoproliferative syndrome (ALPS) is a rare genetic disorder characterized by the abnormal proliferation of lymphocytes due to defective apoptosis. This condition can lead to lymphadenopathy, splenomegaly, and autoimmune manifestations. Accurate coding with ICD-10 Code D89.82 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 D89.82 for Autoimmune lymphoproliferative syndrome [ALPS]?

ICD-10 Code D89.82 represents Autoimmune lymphoproliferative syndrome (ALPS), a disorder resulting from mutations affecting lymphocyte apoptosis. This code should be used in clinical documentation and billing when diagnosing patients with ALPS, particularly when they present with symptoms such as lymphadenopathy, splenomegaly, and autoimmune complications.

ICD-10 Code D89.82 – Clinical Definition and Explanation of Autoimmune lymphoproliferative syndrome [ALPS]

Autoimmune lymphoproliferative syndrome (ALPS) is primarily caused by genetic mutations that impair the normal process of programmed cell death (apoptosis), leading to an accumulation of lymphocytes. This condition can progress to severe autoimmune disorders and requires prompt medical attention to manage symptoms and prevent complications.

Key Clinical Features:

  • Lymphadenopathy (swollen lymph nodes)
  • Splenomegaly (enlarged spleen)
  • Autoimmune cytopenias (e.g., hemolytic anemia, thrombocytopenia)
  • Increased susceptibility to infections
  • Family history of autoimmune diseases

ICD-10 Code D89.82 for Autoimmune lymphoproliferative syndrome [ALPS] – SOAP Notes & Clinical Use

ICD-10 Code D89.82 is utilized in SOAP notes to document the presence of Autoimmune lymphoproliferative syndrome (ALPS). It plays a crucial role in capturing patient symptoms, assessments, and treatment plans, relevant in both acute and chronic care settings.

What Does ICD-10 Code D89.82 for Autoimmune lymphoproliferative syndrome [ALPS] Mean in SOAP Notes?

In SOAP notes, ICD-10 Code D89.82 connects subjective patient-reported symptoms and objective clinical findings to a formal diagnosis of Autoimmune lymphoproliferative syndrome (ALPS). This ensures continuity of care, supports accurate billing, and meets EHR documentation standards.

Treatment Options for ICD-10 Code D89.82 – Autoimmune lymphoproliferative syndrome [ALPS]

Management of Autoimmune lymphoproliferative syndrome (ALPS) often requires hospitalization due to potential complications. Treatment focuses on controlling symptoms and preventing autoimmune manifestations.

Antibiotic Therapy:

  • Not applicable as ALPS is not an infectious condition.

Supportive Care:

  • Corticosteroids to manage autoimmune symptoms
  • Immunosuppressive therapy for severe cases
  • Regular monitoring of blood counts and lymphocyte levels

Infection Control:

  • Implement standard precautions to prevent infections
  • Educate patients on hygiene practices
  • Monitor for signs of infection due to immunosuppression

How to Document Symptoms of Autoimmune lymphoproliferative syndrome [ALPS] (ICD-10 D89.82) in SOAP Notes

Subjective:

  • Patient reports persistent lymphadenopathy.
  • History of recurrent infections.
  • Complaints of fatigue and weakness.
  • Family history of autoimmune disorders.

Objective:

  • Physical examination reveals enlarged lymph nodes.
  • Splenomegaly noted on palpation.
  • Laboratory tests show elevated lymphocyte counts.
  • Complete blood count indicates anemia.
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SOAP Note Guidelines for Diagnosing Autoimmune lymphoproliferative syndrome [ALPS] (ICD-10 Code D89.82)

Assessment:

  • Diagnosis: Autoimmune lymphoproliferative syndrome (ALPS), moderate severity.
  • ICD-10 Code: D89.82.
  • Triggers: Genetic predisposition and environmental factors.
  • Complications: Risk of autoimmune cytopenias.

Plan:

  • Initiate corticosteroid therapy to reduce lymphocyte proliferation.
  • Educate patient on signs of infection and when to seek care.
  • Schedule follow-up appointments for monitoring blood counts.
  • Consider referral to a hematologist for specialized care.

Treatment & Plan Section for ICD-10 Code D89.82 – Autoimmune lymphoproliferative syndrome [ALPS]

  • First-line pharmacologic treatments include corticosteroids and immunosuppressants.
  • Non-pharmacologic strategies involve patient education on infection prevention.
  • Monitoring practices include regular blood tests to assess lymphocyte levels.
  • Follow-up appointments should be scheduled every 3-6 months.

Using ICD-10 Code D89.82 for Autoimmune lymphoproliferative syndrome [ALPS] in Billing & SOAP Note Compliance

  • Select appropriate ICD-10 code based on clinical findings and patient history.
  • Document symptoms clearly under Subjective (S) and Objective (O) sections.
  • Ensure treatment plans align with clinical guidelines to support justified billing.
  • Include relevant CPT codes that correspond to the services provided.

ICD-10 Code D89.82 in Medical Billing and Insurance for Autoimmune lymphoproliferative syndrome [ALPS]

ICD-10 Code D89.82 is critical for billing purposes in hospital, ER, or infectious disease care settings.

Billing Notes:

  • Ensure accurate documentation of patient history and clinical findings.
  • Use the code in settings where ALPS is diagnosed or treated.
  • Include key chart elements such as lab results and treatment plans.

Common CPT Pairings:

CPT CodeDescription
99214Established patient office visit, moderate complexity.
85025Complete blood count with differential.
36415Collection of venous blood by venipuncture.

Frequently Asked Questions

Common Questions About Using ICD-10 Code D89.82 for Autoimmune lymphoproliferative syndrome [ALPS]

What are the common symptoms of ALPS?

Common symptoms of Autoimmune lymphoproliferative syndrome (ALPS) include swollen lymph nodes, an enlarged spleen, fatigue, and recurrent infections due to immune dysregulation.

How is ALPS diagnosed?

ALPS is diagnosed through clinical evaluation, family history assessment, and laboratory tests that show elevated lymphocyte counts and autoimmune manifestations.

What treatments are available for ALPS?

Treatment for ALPS may include corticosteroids, immunosuppressive therapy, and supportive care to manage symptoms and prevent complications.

Is ALPS a hereditary condition?

Yes, Autoimmune lymphoproliferative syndrome (ALPS) is often hereditary, typically caused by mutations in genes involved in lymphocyte apoptosis.

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