In this webinar, Jondavid  Klipp (Laboratory Economics) and the NovoPath team unpack what 2026 will look like for pathology labs: Medicare fee schedule changes, looming clinical lab cuts, and, most importantly, the disconnect between real digital pathology adoption and the tiny 1.1% utilization CMS currently “sees.” You’ll learn why reporting digital pathology add-on codes matters, why it’s so hard today, and how NovoPath’s LIS-led approach automates reporting so labs can accelerate toward future reimbursement and AI-enabled efficiency.

Highlights

Bottom line: If you want Medicare and other payers to eventually reimburse for digitizing slides and AI-enabled workflows, your lab needs to both adopt and report digital pathology—and your LIS/RCM stack must actively help you do it.

What this webinar covers

NovoPath’s core perspective: “Your LIS should not just store data, it should actively help you prove digital adoption to CMS and payers without burning out your staff.”

In the webinar, NovoPath outlines how it tackles this unique problem:

The webinar also highlights current ROI for digital pathology, even without direct reimbursement for digitization:

Commercial edge: Labs with end-to-end digital pathology often gain marketing, sales, and differentiation advantages in their markets.

Who should watch this webinar?

This session is especially relevant for:

LIS / IT leaders responsible for integrating digital viewers, scanners, and revenue cycle systems

Frequently Asked Questions (addressed in the webinar)

 A: On average, ~0.6% increase for pathology services, with specific updates for key codes like CPT 88305 and significant increases for certain flow cytometry technical components (88184, 88185). The impact will vary by lab and geography due to local adjustments.

A: Approximately 800 tests on the Medicare Clinical Laboratory Fee Schedule are currently scheduled for cuts of up to 15% starting Feb 1, 2026, subject to legislative changes. The webinar explains the 30-day delay and ongoing advocacy by ACLA, CAP, and others.

 A: CMS first wants to see meaningful utilization of digital pathology documented through the 43 digital add-on codes. Current reported utilization (~1.1%) is too low to trigger reimbursement policy changes, and that low number is driven largely by under-reporting, not lack of real-world adoption.

A: Key reasons:

  • Reporting is technically hard: requires LIS upgrades, digital viewer integration, and RCM alignment.
  • There is no immediate payment for digital add-on codes, so labs see little short-term financial incentive.
  • Manual workflows (reading reports, adding codes by hand) aren’t scalable for busy coding and billing teams.

 

A: CMS has not published a specific target (e.g., 5%, 10%). The webinar discussion suggests it likely needs to be meaningfully higher than 1%—perhaps in the 5–10%+ range—before CMS seriously considers permanent, reimbursed Category 1 digital pathology codes.

 A: NovoPath:

  • Integrates with major digital slide viewers to detect digitally read cases.
  • Automatically applies corresponding digital add-on CPT codes based on the base pathology CPT.
  • Sends structured data to RCM systems, reducing manual coding and billing work.
  • Acts as a consultative partner, helping labs design digital workflows, understand regulations, and scale reporting.

 

 A: Yes. Labs already see value from:

  • AI-assisted workflows that increase productivity and case throughput
  • Remote reading flexibility for pathologists (work-from-home days)
  • Competitive differentiation in their market and better recruitment/retention of pathologists