Navigating the No Surprises Act

Navigating the No Surprises Act: The Hidden Costs of Ineligible Arbitration Disputes 

The No Surprises Act, enacted in 2020 as part of the Consolidated Appropriations Act, was hailed as a landmark consumer protection measure. By shielding patients from unexpected out-of-network medical billsparticularly for emergency services, air ambulances, and non-emergency care at in-network facilitiesit aimed to curb the predatory practices of surprise billing that plagued the U.S. healthcare system. Central to this framework is the Independent Dispute Resolution (IDR) process, a baseball-style arbitration where insurers and providers submit payment offers, and a neutral arbiter selects one as binding. 

Yet, five years on, the system is buckling under its own weight. A 2024 survey by America’s Health Insurance Plans (AHIP) and the Blue Cross Blue Shield Association (BCBSA)representing 25 health plans covering 154 million Americansreveals a stark reality: 39% of claims submitted to IDR were ineligible for arbitration. Alarmingly, arbiters flagged only about 17% of these as improper, allowing the rest to proceed to binding determinations that often favor providers. 

This discrepancy isn't just procedural; it's a financial black hole. With providers winning the majority of disputes and securing reimbursements three to four times higher than in-network rates, ineligible claims are inflating premiums, employer costs, and ultimately, patient out-of-pocket expenses. As Mike Tuffin, AHIP’s president and CEO, noted, “The same private equity-backed outfits that created the surprise billing business model have turned to arbitration abuse as their new strategy to gouge consumers and employers.” 

This article dissects the survey’s findings, analyzes their systemic implications, and offers practical strategies for stakeholders to mitigate the fallout. 

The IDR Process: A Double-Edged Sword 

When negotiations fail, parties have 30 business days to initiate IDR after the initial payment determination. The arbiter evaluates factors like the Qualifying Payment Amount (QPA)—a median in-network ratethe provider’s experience, market rates, and patient acuity. The “baseballrule ensures no middle-ground compromise; it’s all-or-nothing, a design that has led to contentious litigation from providers alleging bias toward insurerslower QPAs. 

Since the IDR portal’s April 2022 launch, filings have surged far beyond projectionshundreds of thousands per year, totaling over one million disputes through 2024–2025. Federal data show that a small number of large, private-equity-backed groups, such as Radiology Partners and TeamHealth, dominate dispute volume, accounting for a disproportionate share of resolutions in 2023–2024. 

The AHIP/BCBSA survey exposes a critical bottleneck: eligibility screening. Plans identified 33% of emergency, 45% of non-emergency, and 23% of air ambulance claims as ineligiblemore than double the shares caught by arbiters (15%, 19%, and 10%, respectively). This gap resulted in an estimated 184,500 improper disputes advancing in 2024, contributing to $2–$2.5 billion in wasteful spending. 

Unpacking the Ineligibility Epidemic 

Why are so many claims slipping through? The survey highlights recurring issues: untimely submissions, incomplete documentation, conflicts with state surprise-billing laws, and services outside the Act’s scope (such as routine ground ambulances or elective procedures). These are not technicalitiesthey’re safeguards meant to ensure IDR addresses genuinesurprisescenarios. 

The incentives are asymmetric. Providers, facing tight margins in fee-for-service medicine, view IDR as a high-stakes lottery with favorable odds. Multiple analyses show providers prevail in a majority of determinations, with median prevailing offers roughly 300–450% of the QPA. Insurers, by contrast, characterize the process as pay-to-play, where filing volume outweighs merit. Private equity magnifies this distortion by acquiring specialty practices, keeping them out-of-network, and flooding IDR with disputes, betting on arbiter leniency and regulatory backlog. 

The fallout is multifaceted: 

  • Economically, it erodes the Act’s cost-containment goals. Analyses suggest that IDR-driven reimbursements exert upward pressure on commercial premiums, though the exact impact varies. 

  • Operationally, ineligible disputes clog the IDR portal, delaying legitimate cases and straining CMS resourcescompounded by temporary staff furloughs during the 2025 federal shutdown, which paused implementation of the pending 2023 eligibility-review rule. 

  • Ethically, it undermines trust: patients, shielded from direct bills, still pay indirectly through rising insurance costs. 

Providers counter that insurerslow initial offers, often pegged to opaque QPAs, force defensive filings. The American Medical Association and others argue CMS undervalues provider inputs. Yet, data show patterns of repeat offendersa small number of groups account for most disputes, echoing pre-Act surprise-billing behaviors. 

Practical Strategies for Stakeholders 

For Health Plans and Insurers 

  • Enhance Pre-IDR Triage: Deploy AI-assisted claim audits to flag ineligible submissions earlycross-check timestamps, documentation, and state-law applicability. AHIP data indicate plans already detect twice as many ineligible disputes as arbiters; scaling this through shared consortia could cut improper payouts by 20–30%. 

  • Strategic Negotiations: Prioritize batch or bundled negotiations with high-volume providers. Offer good-faithin-network contracts with upside incentives (e.g., 110% of QPA for quality metrics) to dissuade arbitration abuse. Track and escalate repeat filers to regulators. 

  • Advocacy and Data Sharing: Collaborate on AHIP/BCBSA-style surveys to build transparency and pressure CMS for real-time eligibility APIs. Support emergency funding to finalize the stalled 2023 rule introducing automated ineligibility gates. 

For Providers and Practice Groups 

  • Compliance Discipline: Maintain detailed submission checklistsverify the 30-day window, include complete acuity documentation, and confirm state-law applicability. For PE-backed entities, conduct monthly random audits (≈10%) to withdraw ineligible filings proactively. 

  • Value-Based Alternatives: Transition from volume-driven IDR reliance toward value-based or capitation models. When using IDR, emphasize patient-outcome data (e.g., via EHR integrations like Epic’s acuity modules) to justify higher offers without excess. 

  • Balanced Litigation: Engage in advocacy for QPA transparency but pair this with self-regulatory pledgespublicly disclosing out-of-network rationales can bolster credibility. 

For Policymakers and Regulators 

  • Streamline Oversight: Finalize the 2023 CMS rule mandating pre-screening by certified vendors and scalable filing fees for serial abusers. Consider a fast-trackchannel for disputes under $1,000. 

  • Data-Driven Reforms: Require annual CMS reports identifying high-volume filers exceeding 5% of total disputes for audit review. Strengthen state-federal data sharing to harmonize eligibility standards. 

  • Consumer Safeguards: Launch HHS educational campaigns detailing patientsrights and how to report suspected abuse. 

For Employers and Consumers 

  • Employers: Audit plan exposure to IDR disputes; negotiate premium guarantees and rate-stability clauses. 

  • Consumers: Review Explanation of Benefits (EOB) documents for required QPA disclosures and appeal questionable charges through state regulators. Resources like Healthcare Bluebook can provide fair-price benchmarks. 

Reforming for Resilience 

The No Surprises Act’s IDR process, once a beacon of reform, now illustrates how well-intentioned policy can be subverted by volume and loopholes. With nearly 40% of disputes deemed ineligible and billions wasted, the system risks amplifying the very costs it sought to contain. 

But the crisis is solvable. Through vigilant compliance, data transparency, and technological modernization, stakeholders can restore balance. Policymakers must act decisivelyfinalizing portal upgrades and refining QPA methodology could halve inefficiencies by 2027. Until then, the AHIP/BCBSA survey should serve not as indictment, but as blueprint: for insurers, a call to fortify triage; for providers, a nudge toward sustainable contracting; and for policymakers, a reminder that true surprise-billing protection demands shared accountability. 

Limitations & Methodological Notes 

All quantitative findings are drawn from publicly available sources (AHIP/BCBSA survey 2024–2025; CMS IDR portal data; Georgetown CHIR analyses; KFF issue briefs). Estimates of cost impact and eligibility rates derive from insurer-reported data and should be interpreted as indicative, not exhaustive. Independent audits and CMS validation may refine these figures in future releases. 

Sources 

  1. AHIP. New AHIP/BCBSA Survey Shows Nearly 40% of ProvidersSurprise Billing Disputes Are Ineligible Under No Surprises Act. Oct 2025. https://www.ahip.org/news/press-releases/new-ahip-bcbsa-survey-shows-nearly-40-of-providers-surprise-billing-disputes-are-ineligible-under-no-surprises-act 

  1. Healthcare Dive. High Volume of Surprise Billing Disputes Are Ineligible for Arbitration, Insurers Allege. Oct 2025. https://www.healthcaredive.com/news/surprise-billing-disputes-ineligible-survey-ahip-bcbsa/803785/ 

  1. Georgetown University Center on Health Insurance Reforms. The Substantial Costs of the No Surprises Act Arbitration Process. Sept 2025. https://chir.georgetown.edu/the-substantial-costs-of-the-no-surprises-act-arbitration-process/ 

  1. KFF. The No Surprises Act: Implementation and Ongoing Challenges. 2024. https://www.kff.org/health-costs/issue-brief/the-no-surprises-act-implementation-and-challenges/ 

  1. CMS. No Surprises Act Independent Dispute Resolution Portal Data Updates. Accessed Oct 2025. https://www.cms.gov/nosurprises/independent-dispute-resolution 

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