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D61.1

Billable

Drug-induced aplastic anemia

HCC Category Mapping

V24HCC 46Severe Hematological Disorders
0.666
ESRDHCC 46Severe Hematological Disorders
0.000
RxHCCHCC 96Hemolytic and Aplastic Anemias
0.000

What This Code Means

A serious condition where medications or drugs cause the bone marrow to stop producing blood cells.

Coding Tips

  • Document the specific drug or medication causing the aplastic anemia; link the temporal relationship between drug exposure and symptom onset
  • Include the drug name in the medical record and consider using an additional code for the adverse effect if applicable

Clinical Significance

Drug-induced aplastic anemia is a severe and potentially fatal condition where medication exposure triggers destruction or suppression of hematopoietic stem cells, resulting in pancytopenia (low red cells, white cells, and platelets). Unlike drug-induced cytopenias affecting single cell lines, aplastic anemia represents failure of the entire bone marrow. High-risk medications include chloramphenicol, carbamazepine, phenytoin, sulfonamides, gold compounds, and certain chemotherapy agents. The mechanism may involve direct toxicity or idiosyncratic immune-mediated stem cell destruction.

Documentation Requirements

  • Document the specific causative drug by name with clear temporal relationship between drug exposure and aplastic anemia onset.
  • Record complete blood count showing pancytopenia and bone marrow biopsy demonstrating hypocellularity.
  • Include the severity classification (moderate, severe, or very severe aplastic anemia based on absolute neutrophil count, platelet count, and reticulocyte count).
  • Document treatment with drug discontinuation, immunosuppressive therapy, supportive transfusions, or stem cell transplant.
  • Use external cause codes (T36-T50) to identify the responsible drug.

Use Additional Code

  • code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5)

Commonly Confused Codes

Code Hierarchy

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