decisionhealth Newsletters, Part B News - 2018 Issue 9 (September)
Avoid specimen validity, drug screen codes on same day except in rare cases
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Article Overview
This article explains recent CMS, OIG, and related guidance affecting billing for urine drug testing and specimen validity testing. It is intended for coders, billers, compliance staff, laboratories, and physician practices that report these services and need to understand when same-day reporting may be scrutinized, how bundled services are treated, and what broad circumstances may support separate reporting.
Why This Topic Matters
The topic matters because these claims have been targeted in audits and edits, and incorrect reporting can lead to denials or improper payments. Understanding the scope of the guidance helps organizations reduce compliance risk and review payer-specific policies.
Article Sections
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CMS and OIG guidance on specimen validity testing
Introduces the compliance concern, the role of CMS and OIG, and the overall billing issue involving urine drug screening and specimen validity testing.
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When same-day reporting may be considered
Describes the narrow circumstances in which specimen-related testing may be viewed as part of a separate diagnostic service rather than only a drug-screening service.
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Examples and payer policy considerations
Provides a general illustration of documentation context and notes the importance of local Medicare coverage policy and contractor-level review.
What You Will Learn
- How CMS and OIG describe the relationship between urine drug screening and specimen validity testing
- What broad situations may support separate reporting of related laboratory services
- Why audits, edits, and local payer policies matter for these claims
- Which kinds of providers and staff should review this guidance
Who Should Read This
- Medical coders
- Medical billers
- Compliance professionals
- Laboratory staff
- Physician practice administrators
- Revenue cycle teams
Codes Discussed
Code Ranges Discussed
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