mayra.zambrano
Contributor
I have a feeling that we are missing information when we are billing skin substitutes to Medicare. I have a patient who we either gets denials for the product itself or for the application fee. Denial states that the reason this is being denied is because it does not qualify per LCD guidelines. Patient's wound is on the chest and LCD only covers lower extremities. Pharm rep has told the provider that this product is covered as long as we can prove medical necessity. He has also stated that the reason the claim may be denying is because we have included a CLIA number to the claim. Patient has been receiving the product for over a year. My question is this, is there something I need to add to the claim in order to indicate that the the patient has received the product? When will Medicare stop covering this product? lastly does the anatomical site of the application matter when it comes to reimbursement?