Laboratory Question for the Week of January 26, 2026
Why was 87812 established in 2026?
Mounting complexity, confusing new rules, new technologies, and diminishing reimbursements could place laboratory coding and compliance into peril, with lost revenue on the table and potential risk for audits. If you’re involved with coding and billing for molecular pathology, molecular biology, cytogenics or drug-of-abuse testing, you know exactly what we’re talking about! How can you possibly keep up with the continual advances?
Count on the laboratory resources from MedLearn Publishing to ensure compliant coding and billing. You’ll get guidance from leading lab authorities, presented in easy-to-understand terms.
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Why was 87812 established in 2026?
Under what conditions do we report new 2026 code 87494?
Why was code 81354 created in 2026, and when do we report it?
Under what circumstances can code 80051 be reported multiple times?
Equip yourself and your team with actionable solutions to conquer laboratory coding challenges, optimize revenue, and ensure compliance. Join us as we dive into the practical application of the many 2026 code changes  and empower you to achieve coding excellence.
During this exclusive webcast, nationally recognized laboratory and pathology expert Robin Zweifel will walk you through the steps of a due diligence audit, including how to look at revenue trends, test utilization trends, compliance risks, correct CPT® coding and accurate charge capture practices. You will learn the best approaches to work queue management, how to correlate coding guidelines with documentation requirements, validate charge capture processes and more.
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