decisionhealth Newsletters, Coder Pink Sheets - 2005 Issue 3 (March)
Visudyne wastage: Under new code, question is not whether Medicare will pay, but how to bill carriers
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Article Overview
This article explains a Medicare billing change affecting Visudyne and why providers were seeking clarification from CMS, carriers, and the drug manufacturer. It is relevant to ophthalmology billing staff, coders, and compliance teams who need to understand general carrier-level guidance, discarded drug reporting, and documentation expectations under the updated supply code framework.
Why This Topic Matters
The topic matters because billing practices for a drug can change when coding units change, and unclear carrier instructions can lead to denials, inconsistent claims handling, and documentation disputes. The article helps readers understand the general reimbursement and reporting issues that arise when a single-use drug is administered partially and some amount is discarded.
Article Sections
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Billing confusion under the updated Visudyne supply code
Introduces the coding and billing uncertainty created by the updated supply code and unit change. It describes the national-versus-carrier guidance issue affecting ophthalmology practices.
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Claims handling approaches being discussed
Summarizes the general claim-format approaches that were being considered for the drug under the new billing structure. It notes that carrier instructions may differ and were not yet fully published.
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Medicare guidance on discarded drugs and biologicals
Reviews the broader Medicare framework for discarded drugs, including the distinction between single-use and multi-use vials. It also references supporting manual guidance cited in the article.
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Carrier and manufacturer commentary
Describes statements from the manufacturer, carrier communications, and CMS-related responses about how providers were expected to document and report the service. It also notes the role of ophthalmology organizations in seeking clarification.
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Additional billing updates and documentation expectations
Covers later carrier updates and comments about documentation, storage, and reuse limitations. The section focuses on general billing process issues rather than detailed clinical administration guidance.
What You Will Learn
- How a drug supply code change can affect billing workflows
- Why carrier-level instructions may matter when national guidance is limited
- What general Medicare guidance says about discarded drugs
- Why documentation and claim presentation become important in wastage situations
- How manufacturer and carrier communications can influence billing practices
Who Should Read This
- Medical coders
- Billing staff
- Ophthalmology practices
- Compliance teams
- Revenue cycle professionals
Codes Discussed
Code Ranges Discussed
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