D60.1 ICD-10-CM Code: Transient acquired pure red cell aplasia
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FY 2026 Apr update / Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89) / Aplastic and other anemias and other bone marrow failure syndromes (D60-D64)
D60.1
Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidanceTransient acquired pure red cell aplasia
A temporary condition where the bone marrow temporarily stops producing red blood cells, usually resolving on its own within weeks.

Buddy Insight
Transient acquired pure red cell aplasia is a temporary cessation of red blood cell production by the bone marrow that typically resolves spontaneously within weeks.
CMS-HCC V28
00
RAF 0
CMS-HCC V24
MappedHCC 46
RAF 0.666
ACA/HHS
00
RAF 0
ESRD/PACE
MappedHCC 46
RAF 0.0
RXHCC
MappedHCC 96
RAF 0.0
Code Trumping
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Code Book Path
Inclusion Terms
OfficialICD-10-CM does not list inclusion terms for D60.1 in this effective period.
Excludes 2
OfficialICD-10-CM does not list Excludes 2 notes for D60.1 in this effective period.
Related Child Codes
Includes
Official- red cell aplasia (acquired) (adult) (with thymoma)
Excludes 1
Official- congenital red cell aplasia (D61.01)
Code First
OfficialICD-10-CM does not list Code First sequencing instructions for D60.1 in this effective period.
Use Additional
OfficialICD-10-CM does not list Use Additional Code instructions for D60.1 in this effective period.
Code Also
OfficialICD-10-CM does not list Code Also instructions for D60.1 in this effective period.
Buddy Documentation Tip
MEAT Support
Audit Caution
Common Mistakes
Last updated: FY2026 ICD-10-CM Apr update, Apr 1, 2026 through Sep 30, 2026. CMS-HCC V28 is 100% phased in for payment year 2026.
Is D60.1 an HCC code?
Yes. D60.1 maps to Severe Hematological Disorders under the V24 model but is not retained in V28.
HCC Category Mapping
RAF weights shown are the community, non-dual, aged base weights from the CMS risk adjustment model file. Actual per-patient RAF contribution depends on member segment, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains in use during the transition and for historical data.
Work D60.1 in the Code Book — tabular path, V28 RAF, and MEAT checklist →
MEAT Criteria for D60.1
For D60.1to count as a valid HCC diagnosis in a given encounter, the provider's documentation must show MEAT: Monitor, Evaluate, Assess, or Treat. A diagnosis from a prior year does not carry forward automatically, it has to be re-documented and supported each calendar year.
- MMonitor: signs, symptoms, disease progression, or lab trending documented in the note
- EEvaluate: test results, medication response, or physical findings reviewed by the provider
- AAssess: explicit mention in the assessment or plan with acknowledgment of status
- TTreat: medication, referral, procedure, therapy, or counseling tied to the diagnosis
Only one of M/E/A/T is required to support the code, but the documentation must be specific enough to show that the provider actually addressed D60.1 during that encounter, not just copy-forwarded from a problem list.
Coder workflow notes
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What This Code Means
D60.1 is the ICD-10-CM diagnosis code for transient acquired pure red cell aplasia. A temporary condition where the bone marrow temporarily stops producing red blood cells, usually resolving on its own within weeks. D60.1 sits in the ICD-10-CM chapter for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (d50-d89), within the section covering aplastic and other anemias and other bone marrow failure syndromes (d60-d64).
Under the older CMS-HCC V24 model, D60.1 maps to Severe Hematological Disorders (HCC 46) with a community, non-dual, aged base RAF weight of 0.666. V28 is the CMS-HCC risk adjustment model that reached 100% phase-in for payment year 2026, replacing V24 which was used during the PY2024–PY2025 transition.
Verify documentation confirms the temporary nature and expected resolution of the condition. Because D60.1 maps to a payment HCC, the provider's documentation must satisfy MEAT criteria (Monitor, Evaluate, Assess, or Treat) for the encounter to count toward the patient's Medicare Advantage risk adjustment score. When documentation is ambiguous, coders should issue a provider query rather than assume the highest-specificity variant.
HCC Buddy maintains structured V28 and V24 mapping, RAF weights, and MEAT documentation criteria for D60.1 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.
Coding Tips
Clinical Significance
Transient acquired pure red cell aplasia is a temporary cessation of red blood cell production by the bone marrow that typically resolves spontaneously within weeks. The most common cause is parvovirus B19 infection, which directly infects and destroys erythroid precursor cells, producing a transient aplastic crisis especially dangerous in patients with pre-existing hemolytic anemias who depend on compensatory increased red cell production. Other causes include certain medications and acute viral infections that temporarily suppress erythropoiesis.
Documentation Requirements
- ✓Document the temporary nature of the red cell aplasia with expected or actual resolution timeline.
- ✓Record parvovirus B19 serologies (immunoglobulin M for acute infection) or polymerase chain reaction when infection-associated.
- ✓Include hemoglobin values, reticulocyte count showing near-zero production, and normal white blood cell and platelet counts.
- ✓Document any causative agent or triggering event.
- ✓Record transfusion support provided during the aplastic episode and evidence of recovery.
Commonly Confused Codes
- •D60.0 (Chronic acquired pure red cell aplasia) is for persistent conditions lasting beyond the expected transient period.
- •D61.01 (Constitutional pure red blood cell aplasia) is congenital Diamond-Blackfan anemia.
- •D60.9 (Acquired pure red cell aplasia, unspecified) does not specify whether the condition is transient or chronic.
- •D64.9 (Anemia, unspecified) is far less specific and should not be used when pure red cell aplasia is documented.