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Printed Date: 9/22/2015
Dosage of erythropoietin stimulating agent has been reduced and maintained in response to hematocrit or hemoglobin level.
This modifier is used for national claims monitoring for ESAs administered in Medicare renal dialysis facilities, so therefore, is not applicable to Part B.
Reference: CMS Medicare Claims Processing Manual (Pub. 100-04), Chapter 8, Section 60.4 (PDF, 1.82 MB).
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Last Updated: 05/03/2019