Twists and Turns Persist for the No Surprises Act

Twists and Turns Persist for the No Surprises Act

Well, I’ve got a couple of updates for you in the absolute roller coaster that is the No Surprises Act’s Independent Dispute Resolution (IDR) process!

The federal government officially filed their formal notice of an intent to appeal the ruling on the Texas Medical Association’s (TMA’s) third lawsuit, conveniently called TMA III, regarding the calculation of the qualifying payment amount (QPA) in the IDR process.

There isn’t really any supporting documentation of what exactly their argument will be, but this is the first step in the process after the Centers for Medicare & Medicaid Services (CMS) announced their plans to appeal in guidance released early this month citing the outcomes of the most recent TMA cases. 

This appeal is separate from the government’s appeal of TMA II back in the spring, but will be heard in the same court: the U.S. Court of Appeals for the 5th Circuit. In that case, both sides have filed their written briefs, and a hearing will likely be scheduled next.

With all this up in the air, and CMS stating that they did not intend to issue interim guidance about the TMA III ruling, given the fact they planned to appeal, some thought we were more in a holding pattern as those appeals played out; after all, there are no lawsuits still pending in Texas courts at this time.

But very late last Friday afternoon, the government issued a proposed rule making changes to the IDR process; although it does not address the TMA ruling directly, it still features quite a few changes that aim to address many of the criticisms the process has faced over the months.

Take, for example, the backlog in the IDR process, which is partially a result of the unexpectedly high numbers of disputes submitted, as well as those that end up being ineligible. Under this new proposal, an eligibility review process the government can invoke when dispute volumes are high would be created, and payers would be required to include additional information in their initial payment or notice of denial of payment that would hopefully make eligibility easier to determine (and open negotiations more meaningful).

Another concern has been the ease of access to the IDR process. Many providers have expressed concern that the process is not as accessible as it should be, whether due to what they believe to be overly restrictive batching rules or the mandatory administrative fee.

The newly released proposed rule appears to address some of these concerns, because it broadens the batching provisions, allowing batching of claims related to a single patient encounter, those billed under the same service code (or a comparable code on a different system), and for certain specialties like anesthesiology, radiology, and pathology. With the proposed changes, those items and services could be billed under service codes belonging to the same Category/CPT code section.

It also proposes that the administrative fee be collected by the government directly from the disputing parties and that a reduced rate be implemented in certain situations where it would be unfair to charge the full amount.

According to the administration, the proposed rule is meant to “improve communication between payers, providers, and certified IDR entities (and) create a more efficient dispute resolution process, (changing) the administrative fee structure to improve accessibility.” In that early October guidance I mentioned, CMS stated that any proposals regarding the QPA methodology would require a lot of resources and take months rather than weeks, so it’s not entirely unlikely that everyone will be waiting for the resolution of the TMA appeals for the next big changes in guidance.

With how many ups and downs the IDR process has gone through lately, you never know!

Facebook
Twitter
LinkedIn

Cate Brantley, JD

Cate Brantley is a Senior Government Affairs Liaison for Zelis. She has over 9 years of experience in both the public and private sector. Cate is licensed to practice law in the state of Oklahoma.

Related Stories

Leave a Reply

Please log in to your account to comment on this article.

Featured Webcasts

Sepsis: Bridging the Clinical Documentation and Coding Gap to Reduce Denials

Sepsis: Bridging the Clinical Documentation and Coding Gap to Reduce Denials

Sepsis remains one of the most frequently denied and contested diagnoses, creating costly revenue loss and compliance risks. In this webcast, Angela Comfort, DBA, MBA, RHIA, CDIP, CCS, CCS-P, provides practical, real-world strategies to align documentation with coding guidelines, reconcile Sepsis-2 and Sepsis-3 definitions, and apply compliant queries. You’ll learn how to identify and address documentation gaps, strengthen provider engagement, and defend diagnoses against payer scrutiny—equipping you to protect reimbursement, improve SOI/ROM capture, and reduce audit vulnerability in this high-risk area.

September 24, 2025
2026 IPPS Masterclass 3: Master MS-DRG Shifts and NTAPs

2026 IPPS Masterclass Day 3: MS-DRG Shifts and NTAPs

This third session in our 2026 IPPS Masterclass will feature a review of FY26 changes to the MS-DRG methodology and new technology add-on payments (NTAPs), presented by nationally recognized ICD-10 coding expert Christine Geiger, MA, RHIA, CCS, CRC, with bonus insights and analysis from Dr. James Kennedy.

August 14, 2025
2026 IPPS Masterclass Day 2: Master ICD-10-PCS Changes

2026 IPPS Masterclass Day 2: Master ICD-10-PCS Changes

This second session in our 2026 IPPS Masterclass will feature a review the FY26 changes to ICD-10-PCS codes. This information will be presented by nationally recognized ICD-10 coding expert Christine Geiger, MA, RHIA, CCS, CRC, with bonus insights and analysis from Dr. James Kennedy.

August 13, 2025

Trending News

Featured Webcasts

Surviving Federal Audits for Inpatient Rehab Facility Services

Surviving Federal Audits for Inpatient Rehab Facility Services

Federal auditors are zeroing in on Inpatient Rehabilitation Facility (IRF) and hospital rehab unit services, with OIG and CERT audits leading to millions in penalties—often due to documentation and administrative errors, not quality of care. Join compliance expert Michael Calahan, PA, MBA, to learn the five clinical “pillars” of IRF-PPS admissions, key documentation requirements, and real-life case lessons to help protect your revenue.

November 13, 2025
E/M Services Under Intensive Federal Scrutiny: Navigating Split/Shared, Incident-to & Critical Care Compliance in 2025-2026

E/M Services Under Intensive Federal Scrutiny: Navigating Split/Shared, Incident-to & Critical Care Compliance in 2025-2026

During this essential RACmonitor webcast Michael Calahan, PA, MBA Certified Compliance Officer, will clarify the rules, dispel common misconceptions, and equip you with practical strategies to code, document, and bill high-risk split/shared, incident-to & critical care E/M services with confidence. Don’t let audit risks or revenue losses catch your organization off guard — learn exactly what federal auditors are looking for and how to ensure your documentation and reporting stand up to scrutiny.

August 26, 2025
The Two-Midnight Rule: New Challenges, Proven Strategies

The Two-Midnight Rule: New Challenges, Proven Strategies

RACmonitor is proud to welcome back Dr. Ronald Hirsch, one of his most requested webcasts. In this highly anticipated session, Dr. Hirsch will break down the complex Two Midnight Rule Medicare regulations, translating them into clear, actionable guidance. He’ll walk you through the basics of the rule, offer expert interpretation, and apply the rule to real-world clinical scenarios—so you leave with greater clarity, confidence, and the tools to ensure compliance.

June 19, 2025

Trending News

Happy National Doctor’s Day! Learn how to get a complimentary webcast on ‘Decoding Social Admissions’ as a token of our heartfelt appreciation! Click here to learn more →

CYBER WEEK IS HERE! Don’t miss your chance to get 20% off now until Dec. 2 with code CYBER24