Platelet survival study
CPT 78191 is the billing code for a platelet survival study, a nuclear medicine test that uses a small amount of radioactive material to track how long platelets (blood cells that help clotting) survive in your bloodstream. This specialized test helps doctors diagnose bleeding disorders and problems with platelet production or destruction.
This calculator gives a typical-case estimate using standard Medicare modifier rules. Actual payment depends on payer policies, documentation, code-specific CMS status indicators, and locality. Verify before billing.
RVU breakdown
Conversion factor: 32.3465 · Source: CMS MPFS RVU25A · Confidence: High
NCCI bundling edits
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Billing tips
Bill 78191 as a global service unless there is a contractual split between technical and professional components
Impact: Ensures full $120.65 reimbursement rather than risking underpayment from incomplete component billing
Document all serial blood sampling dates and times (typically 5-10 samples over 7-10 days) with corresponding radioactivity measurements in the medical record
Impact: Prevents denials for insufficient documentation; serial sampling is inherent to the procedure and must be evident to justify the 3.73 RVU assignment
Include specific radiopharmaceutical used (Indium-111 oxine or Chromium-51) and dosage in documentation, as this is not separately billable under OPPS
Impact: Radiopharmaceutical cost is bundled into the $120.65 payment; separate billing will result in denial and potential compliance issues
Verify medical necessity by documenting failed or inconclusive conventional platelet studies and specific clinical questions that only platelet survival can answer
Impact: Reduces denial risk for this specialized test; many payers require prior authorization and clear justification beyond simple thrombocytopenia
Do not unbundle blood drawing, processing, or imaging components as these are included in the platelet survival study code
Impact: Attempting to bill venipuncture (36415) or blood handling separately will trigger bundling edits and delay payment of the primary $120.65 claim
Submit claims after the complete study is finished (typically 7-10 days post-injection), not on the day of radiopharmaceutical administration
Billing prematurely may result in requests for refund if the study is not completed; wait until final calculations are documented to ensure the 3.73 RVUs are earned
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