STOCK TITAN

American Medical Association (AMA) Grants Cardio Diagnostics a Dedicated CPT PLA Reimbursement Code for Epi+Gen CHD, an AI-powered Test for Assessing the Probability of a Heart Attack or Coronary Heart Disease Event

Rhea-AI Impact
(Moderate)
Rhea-AI Sentiment
(Neutral)
Tags
AI
Rhea-AI Summary
Cardio Diagnostics Holdings, an AI-driven precision cardiovascular medicine company (Nasdaq: CDIO), has received a dedicated CPT PLA code, 0439U, from the American Medical Association for its AI-powered coronary heart disease event risk assessment test, Epi+Gen CHD. This milestone will accelerate reimbursement from federal and private payers, increasing access to precision cardiovascular medicine.
Positive
  • None.
Negative
  • None.

The assignment of a dedicated CPT PLA code by the AMA for Cardio Diagnostics Holdings' Epi+Gen CHD test represents a pivotal development for the company's financial trajectory. This coding is crucial for the billing process, allowing healthcare providers to bill federal and private payers for the use of the test. The ability to secure reimbursement is often a gatekeeper for widespread clinical adoption, which in turn can significantly impact a company's revenue streams. The code's effective date in 2024 provides a clear timeline for potential revenue growth and market penetration.

The precision cardiovascular medicine market is rapidly evolving and the integration of AI in diagnostics is a competitive edge that can lead to increased market share. The financial implications for stakeholders include not only the potential for increased sales but also the impact on health insurance companies as they adjust to new billing codes and possibly higher volumes of testing. Long-term benefits might include reduced overall healthcare costs if the test proves effective in preventing heart attacks, but this will need to be balanced against the test's cost-effectiveness and reimbursement rates provided by payers.

The Epi+Gen CHD test's ability to integrate genetic and epigenetic markers to assess CHD event risk represents a significant advancement in precision medicine. The test's predictive capabilities for heart attack risk within a three-year window can lead to better patient outcomes through targeted prevention strategies. For stakeholders in the healthcare sector, this translates to a value proposition that could shift standard care practices towards more personalized approaches.

However, the success of such a test depends on its clinical validation and acceptance within the medical community. The AMA's recognition through the CPT PLA code is a step towards legitimacy, but peer-reviewed studies and real-world data will be crucial in determining the test's efficacy and adoption rate. Long-term, the test could set a new standard for cardiovascular risk assessment, influencing research and development strategies across the industry.

The AMA's decision to grant a CPT PLA code is not only a win for Cardio Diagnostics Holdings but also a reflection of the healthcare industry's move towards precision medicine and AI integration. This move has policy implications, as it indicates a willingness to embrace innovative technologies that promise improved patient outcomes. For payers, including Medicare and private insurers, the new code will necessitate the evaluation of cost versus benefit, which could influence future policy decisions regarding coverage of AI-powered tests.

Looking ahead, the adoption of the Epi+Gen CHD test could serve as a case study for policy makers in assessing the impact of AI on healthcare costs and outcomes. The balance between innovation and affordability will be critical and this test could become a benchmark for future policy on reimbursement for AI-driven diagnostic tools.

This is the second CPT PLA code the American Medical Association (AMA) granted for the Company’s AI-powered coronary heart disease tests. This significant milestone enables the acceleration of reimbursement for the Epi+Gen CHD test from federal and private payers, while increasing access to this precision cardiovascular medicine test.

CHICAGO--(BUSINESS WIRE)-- Cardio Diagnostics Holdings, Inc. (Nasdaq: CDIO), an AI-driven precision cardiovascular medicine company, today announced that the American Medical Association (AMA) has granted and assigned a dedicated Current Procedural Terminology (CPT®) Proprietary Laboratory Analysis (PLA) code, 0439U, for the company’s AI-driven coronary heart disease (CHD) event risk assessment test, Epi+Gen CHD.

Receipt of this new CPT PLA code, which will be effective on April 1, 2024, is a significant step toward payer billing and payment, facilitating broader adoption of the first and only AI-powered integrated genetic-epigenetic clinical blood test for evaluating the likelihood of a patient experiencing a CHD event, mainly a heart attack, within the next three years.

Primary Prevention of Heart Attacks: The Clinical and Economic Benefits of Epi+Gen CHD

Every year, about 805,000 people in the United States have a heart attack, with someone experiencing a heart attack every 40 seconds. Heart disease is the leading cause of death for both men and women. In 2021, heart disease was responsible for the deaths of more than 695,000 Americans. Of those deaths, 310,661 occurred in women, which represents one in every five female deaths.

There are challenges in detecting women’s heart disease because, according to Johns Hopkins Medicine, women’s heart disease symptoms and signs can be atypical, which delays understanding of their risks for a heart attack. Epi+Gen CHD evaluates an individual’s unique genetic and epigenetics to predict their risk for a heart attack or sudden cardiac death associated with CHD with unrivaled personalized insights driven by the company’s groundbreaking epigenetic-genetic technology. By leveraging the power of AI, the company’s technology can provide patient-specific epigenetic and genetic drivers of CHD to help guide preventive care and potentially save lives.

In peer-reviewed studies, Epi+Gen CHD was more cost-effective and more sensitive for assessing heart attack risk compared to standard lipid-based risk calculators. Specifically, in a validation study conducted with Intermountain Healthcare, Epi+Gen CHD was shown to be, on average, about twice as sensitive in detecting risk for a CHD event in women than lipid-based calculators.

Enhancing Employer Risk Mitigation Strategies with Epi+Gen CHD

For employers, the financial burden of heart attacks includes direct costs related to diagnosing, managing and treating heart disease, as well as indirect costs such as lost productivity due to employee absenteeism and short-term disability. Employee absenteeism and short-term disability resulting from cardiovascular disease can cost employers about $1,119 more in the first month following a cardiovascular event. The cardiovascular health of U.S. employees costs $363 billion annually, including $216 billion in direct medical costs and nearly $147 billion in indirect costs.

Uniquely, Cardio Diagnostics combines the ability to offer employees the advanced Epi+Gen CHD heart attack risk test with aggregated risk data for employers to help inform their benefits offerings. Cardio Diagnostics’ Employer Risk IntelligenceTM platform provides employers and brokers with the first-of-its-kind cardiovascular employee population health intelligence backed by a clinical test and layered insights in a compliant manner.

“Cardio Diagnostics is committed to driving widespread adoption of our solutions, and obtaining a reimbursement code for Epi+Gen CHD is a critical milestone in our commercialization strategy and for gaining reimbursement from federal and private payers,” said Meesha Dogan, Ph.D., CEO and Co-Founder of Cardio Diagnostics.

For employers, this means potentially greater access to a technology that enables a healthier workforce and significant savings in healthcare costs related to heart disease. Cardio Diagnostics continues to lead the way in precision cardiovascular medicine, leveraging the power of AI and epigenetics to help prevent heart attacks. The company's commitment to making heart disease risk assessment, detection, and management more accessible, personalized, and precise is key to winning the fight against the leading cause of death in the United States.

About Cardio Diagnostics

Cardio Diagnostics is an artificial intelligence-powered precision cardiovascular medicine company that makes cardiovascular disease prevention, detection, and management more accessible, personalized, and precise. The Company was formed to further develop and commercialize clinical tests by leveraging a proprietary Artificial Intelligence (AI)-driven Integrated Genetic-Epigenetic Engine (“Core Technology”) for cardiovascular disease to become one of the leading medical technology companies for improving prevention, detection, and treatment of cardiovascular disease. For more information, please visit www.cardiodiagnosticsinc.com.

Forward-Looking Statements

Certain statements and information included in this press release constitute "forward-looking statements" within the meaning of the Private Securities Litigation Act of 1995. When used in this press release, the words or phrases “will”, "will likely result," "expected to," "will continue," "anticipated," "estimate," "projected," "intend," “goal,” or similar expressions are intended to identify "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements are subject to certain risks, known and unknown, and uncertainties, many of which are beyond the control of the Company. Such uncertainties and risks include but are not limited to, our ability to successfully execute our growth strategy, changes in laws or regulations, economic conditions, dependence on management, dilution to stockholders, lack of capital, the effects of rapid growth upon the Company and the ability of management to effectively respond to the growth and demand for products and services of the Company, newly developing technologies, the Company’s ability to compete, regulatory matters, protection of technology, the effects of competition and the ability of the Company to obtain future financing. An extensive list of factors that can affect future results are discussed in the Current Report on Form 10-K for the period ended December 31, 2022 and Form 10-Q for the period ended March 31, 2023 under the heading “Risk Factors” in Part I, Item IA thereof, and other documents filed from time to time with the Securities and Exchange Commission. Such factors could materially adversely affect the Company's financial performance and could cause the Company's actual results for future periods to differ materially from any opinions or statements expressed within this press release.

Investors:

Gene Mannheimer

Investor Relations

855-226-9991

investors@cardiodiagnosticsinc.com

Media & Public Relations:

Khullani Abdullahi

855-226-9991

pr@cardiodiagnosticsinc.com

Source: Cardio Diagnostics Holdings, Inc.

FAQ

What is the significance of the CPT PLA code 0439U granted to Cardio Diagnostics Holdings?

The CPT PLA code 0439U granted by the American Medical Association for Epi+Gen CHD test will accelerate reimbursement from federal and private payers, increasing access to precision cardiovascular medicine.

When will the CPT PLA code 0439U be effective for Cardio Diagnostics Holdings?

The CPT PLA code 0439U will be effective on April 1, 2024 for Cardio Diagnostics Holdings.

What is the Epi+Gen CHD test by Cardio Diagnostics Holdings?

Epi+Gen CHD is the first and only AI-powered integrated genetic-epigenetic clinical blood test for evaluating the likelihood of a patient experiencing a coronary heart disease event, mainly a heart attack, within the next three years.

What are the clinical and economic benefits of Epi+Gen CHD test?

Epi+Gen CHD test provides primary prevention of heart attacks and offers clinical and economic benefits by evaluating the likelihood of a patient experiencing a heart attack within the next three years.

Cardio Diagnostics Holdings Inc.

NASDAQ:CDIO

CDIO Rankings

CDIO Latest News

CDIO Stock Data

6.69M
23.94M
16.01%
7.57%
1.2%
Biotechnology
In Vitro & in Vivo Diagnostic Substances
Link
United States of America
CHICAGO