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CMS gives InVision dedicated Medicare payment for cardiac amyloidosis AI

2 hours ago
By AI, Created 18:33 UTC, Aug 05, 2026, AGP -

CMS finalized a New Technology Add-on Payment for InVision’s AI software that detects cardiac amyloidosis from echocardiograms, creating a Medicare reimbursement path for inpatient use starting Oct. 1, 2026. The decision gives the company payment coverage across inpatient, outpatient and physician-office settings for a disease that is often missed until late.

Why it matters: - CMS approval gives InVision a dedicated Medicare payment path for Precision Cardiac Amyloid in inpatient care. - The add-on payment can reduce a reimbursement barrier that may slow adoption of AI tools in hospital echo labs. - Cardiac amyloidosis is often underdiagnosed and diagnosed late, when outcomes worsen. - The coverage now extends across inpatient, hospital outpatient and physician-office settings.

What happened: - CMS finalized a New Technology Add-on Payment for InVision Precision Cardiac Amyloid in the FY 2027 Inpatient Prospective Payment System final rule. - The inpatient payment takes effect for discharges on or after Oct. 1, 2026. - Eligible inpatient cases can receive up to $2,275.00 per stay on top of the standard MS-DRG payment. - InVision said Category III CPT code 0932T has been active for hospital outpatient and physician-office studies since Jan. 1, 2025. - The company said the Medicare payment pathway is now defined across both inpatient and outpatient settings.

The details: - Precision Cardiac Amyloid is FDA-cleared AI software that analyzes routine transthoracic echocardiography. - The software looks at apical four-chamber and parasternal long-axis views to flag patients at high risk for cardiac amyloidosis. - The underlying algorithm was published in JAMA Cardiology in 2022. - In a head-to-head evaluation published in JACC Advances in 2025, the product delivered twice the positive predictive value of a comparator algorithm, which translates into fewer false positives and fewer unnecessary confirmatory workups. - InVision said the technology is the first AI echocardiography product to receive a dedicated Medicare add-on payment for cardiac amyloidosis. - InVision said it is also the only echocardiography technology approved for an NTAP in FY 2027 under the alternative pathway. - The technology received FDA 510(k) clearance on May 21, 2025. - The product had previously earned FDA Breakthrough Device Designation. - The indication covers adult patients age 65 and older undergoing cardiovascular assessment with echocardiography when used by an interpreting physician. - Hospitals seeking the inpatient add-on payment will use ICD-10-PCS code XEZZXLC, which stands for "Computer-aided detection and notification for imaging abnormalities in echocardiography, new technology group 12." - The ICD-10-PCS code is effective for dates of service on or after Oct. 1, 2026. - Health systems can find NTAP and CPT coding guidance at reimbursement guidance.

Between the lines: - The Medicare decision turns an AI detection tool into something that can be billed in routine care, not just tested in specialized settings. - For InVision, payment coverage may matter as much as regulatory clearance because hospitals often weigh reimbursement before adopting new technology. - The company is positioning echocardiography as an early screening point for a disease that can hide inside common heart-failure evaluations. - The claims about improved clinical access and broader adoption are forward-looking and depend on hospital implementation.

What's next: - Hospitals can begin preparing for inpatient use tied to XEZZXLC before the Oct. 1, 2026 effective date. - Health systems can use the existing outpatient CPT code 0932T for studies performed in hospital outpatient and physician-office settings. - InVision is likely to push implementation support as providers evaluate whether to add the software to echo workflows.

The bottom line: - CMS has now created a full Medicare payment path for InVision’s cardiac amyloidosis AI, removing a key barrier to broader use in routine echocardiography.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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