Trending...
- City of Chicago Announces Landmark Global Settlement To Resolve Wrongful Conviction Lawsuits Tied To Ronald Watts - 107
- NEIU College of Business and Technology's bachelor's in Computer Science has been accredited by the Computing Accreditation Commission of ABET
- Counseling Center of New Smyrna Beach Expands Affordable Mental Health Services for Volusia County
The Sepsis ImmunoScore™ is the first-ever AI Sepsis Diagnostic granted marketing authorization by the FDA.
CHICAGO, April 3, 2024 /PRNewswire/ -- Prenosis, Inc., an artificial intelligence company enabling precision medicine in acute care, today announced the U.S. Food and Drug Administration (FDA) has granted marketing authorization for the Sepsis ImmunoScore™ using the De Novo pathway. The Sepsis ImmunoScore™ is an artificial intelligence/machine learning software as a medical device (AI SaMD) to guide rapid diagnosis and prediction of sepsis. This signifies the first-ever FDA marketing authorization of an AI diagnostic tool for sepsis, an extremely complex condition that is difficult to diagnose early and has been a decades-long challenge for the U.S. healthcare system.
Sepsis, which occurs when a person has an overactive response to an infection, costs the U.S. healthcare system billions of dollars and kills millions of people every year – more than all cancers combined.1 Even if someone with sepsis survives an episode, the disease can have catastrophic and often permanent consequences on their quality of life after discharge. Despite the devastating impact, no AI diagnostic for sepsis had previously received marketing authorization from the FDA until now.
Leveraging a combination of biomarkers and clinical data through AI, the Sepsis ImmunoScore™ aids in the risk assessment for presence of or progression to sepsis within 24 hours of patient assessment in the Emergency Department or hospital. By leveraging 22 diverse parameters, the Sepsis ImmunoScore™ holistically evaluates the patient's biological status to output a risk score and four discrete risk categories; it is not an alert system. These risk categories correlate to a patient's risk of deterioration, represented by length of stay in the hospital, in-hospital mortality, and escalation of care within 24 hours (ICU admission, mechanical ventilation placement, and/or vasopressor use). This combination of both diagnostic and predictive information had never previously been available in a legally marketed device for sepsis.
More on illi News
"FDA authorization of a sepsis diagnostic tool with significant predictive power is a landmark event for people that could ever be at risk of sepsis at some point in their lives," said Bobby Reddy, Jr, Ph.D., Prenosis Co-Founder and CEO. "Until now, there was no other FDA authorized AI diagnostic for sepsis, which is why the Sepsis ImmunoScore™ had to be granted marketing authorization through the De Novo pathway. FDA authorization offers yet another important piece of evidence of the potential of the Sepsis ImmunoScore™ to improve care."
The Sepsis ImmunoScore's™ software is integrated directly into hospital Electronic Medical Records, making it easily accessible to clinicians. An intuitive display reveals how each of the individual patient's parameters was used to calculate their final sepsis score. This transparent look into the model is critical to build trust and intuition with clinicians and to enable a true clinician-AI partnership, which facilitates faster treatment decisions, improved outcomes, quality metrics, and better hospital financials.
A solution such as the Sepsis ImmunoScore™ has significant potential to save lives, reduce hospital length of stay, and improve compliance with payer protocols – such as the Center for Medicare and Medicaid Services' SEP-1 bundle. The SEP-1 bundle is expected to have significant financial implications for hospitals across the United States by as early as 2026.
The Sepsis ImmunoScore™ was built using Prenosis' Immunix™ precision medicine platform, a solution enabling precision medicine in acute care. Immunix™ simultaneously empowers the development and validation of new precision medicine tools and the real-time implementation of those tools to improve patient care and outcomes. Through a decade of collaboration with ten partner hospitals across the United States, Prenosis used ImmunixTM to build a proprietary biobank and dataset consisting of more than 100,000 blood samples from over 25,000 patients housed in Prenosis' Biological Safety Level 2 lab in Chicago. Prenosis uses in-house assays in its wet lab to generate critical biological data from these blood samples and merges these data with extensive clinical data extracted from partner hospitals' Electronic Medical Records. This dual biological-clinical dataset, the largest in the world for acute care patients suspected of having serious infections, is used to develop AI algorithms to elucidate patterns in rapid immune response. The ultimate goal is to enable a deep understanding of each person's individual biology, then use this understanding to recommend personalized therapeutics in real time in the acute care environment.
More on illi News
"The Sepsis ImmunoScore™ FDA authorization marks an important step in helping hospital systems provide better care," said Reddy. "Similar to how sequencing technology enabled the precision medicine revolution in cancer, our powerful Immunix™ platform has the potential to unlock valuable insights to enable the creation of precision therapeutics guided by AI diagnostics. To date, this type of approach has been used predominantly in healthcare outside of emergency departments and hospitals. Prenosis seeks to change this by catalyzing a personalized medicine revolution in acute care."
The Sepsis Immunoscore™ is a registered trademark of Prenosis Inc.
About Prenosis
At Prenosis we believe healthcare should be tailored to individual biology. With our data-driven approach to fast-moving biology in acute care environments, we're ushering in a new era of precision medicine in acute care. Our Immunix™ precision medicine platform generates proprietary biological insights to rapidly develop precision medicine products and enables the real-time delivery of optimal precision therapy in acute care. The platform is based on the world's largest and fastest growing biomarker-clinical dataset for rapid immune response. Using Immunix™, we created and validated the Sepsis ImmunoScore™, the first FDA-authorized AI diagnostic for sepsis.
At Prenosis, we enable the healthcare ecosystem to see people differently. More information at: www.prenosis.com
1 Rudd, K. E. et al. Global, regional, and national sepsis incidence and mortality, 1990–2017: analysis for the Global Burden of Disease Study. The Lancet 395, 200–211 (2020).
SOURCE Prenosis
CHICAGO, April 3, 2024 /PRNewswire/ -- Prenosis, Inc., an artificial intelligence company enabling precision medicine in acute care, today announced the U.S. Food and Drug Administration (FDA) has granted marketing authorization for the Sepsis ImmunoScore™ using the De Novo pathway. The Sepsis ImmunoScore™ is an artificial intelligence/machine learning software as a medical device (AI SaMD) to guide rapid diagnosis and prediction of sepsis. This signifies the first-ever FDA marketing authorization of an AI diagnostic tool for sepsis, an extremely complex condition that is difficult to diagnose early and has been a decades-long challenge for the U.S. healthcare system.
Sepsis, which occurs when a person has an overactive response to an infection, costs the U.S. healthcare system billions of dollars and kills millions of people every year – more than all cancers combined.1 Even if someone with sepsis survives an episode, the disease can have catastrophic and often permanent consequences on their quality of life after discharge. Despite the devastating impact, no AI diagnostic for sepsis had previously received marketing authorization from the FDA until now.
Leveraging a combination of biomarkers and clinical data through AI, the Sepsis ImmunoScore™ aids in the risk assessment for presence of or progression to sepsis within 24 hours of patient assessment in the Emergency Department or hospital. By leveraging 22 diverse parameters, the Sepsis ImmunoScore™ holistically evaluates the patient's biological status to output a risk score and four discrete risk categories; it is not an alert system. These risk categories correlate to a patient's risk of deterioration, represented by length of stay in the hospital, in-hospital mortality, and escalation of care within 24 hours (ICU admission, mechanical ventilation placement, and/or vasopressor use). This combination of both diagnostic and predictive information had never previously been available in a legally marketed device for sepsis.
More on illi News
- New Leadership and Renovations Usher in Next Chapter for Sunrise Manor
- Who Will Win the 2025 WNBA Finals? OddsTrader Shares Live Betting Odds and Projections
- Naperville's Annual Public Safety Open House Set for Sept. 27
- Geeks5g Creative Marketing: The Powerhouse Behind Business Growth
- Agemin Unveils Breakthrough AI Model for Biometric Age Estimation, Setting New Standards in Online Child Safety
"FDA authorization of a sepsis diagnostic tool with significant predictive power is a landmark event for people that could ever be at risk of sepsis at some point in their lives," said Bobby Reddy, Jr, Ph.D., Prenosis Co-Founder and CEO. "Until now, there was no other FDA authorized AI diagnostic for sepsis, which is why the Sepsis ImmunoScore™ had to be granted marketing authorization through the De Novo pathway. FDA authorization offers yet another important piece of evidence of the potential of the Sepsis ImmunoScore™ to improve care."
The Sepsis ImmunoScore's™ software is integrated directly into hospital Electronic Medical Records, making it easily accessible to clinicians. An intuitive display reveals how each of the individual patient's parameters was used to calculate their final sepsis score. This transparent look into the model is critical to build trust and intuition with clinicians and to enable a true clinician-AI partnership, which facilitates faster treatment decisions, improved outcomes, quality metrics, and better hospital financials.
A solution such as the Sepsis ImmunoScore™ has significant potential to save lives, reduce hospital length of stay, and improve compliance with payer protocols – such as the Center for Medicare and Medicaid Services' SEP-1 bundle. The SEP-1 bundle is expected to have significant financial implications for hospitals across the United States by as early as 2026.
The Sepsis ImmunoScore™ was built using Prenosis' Immunix™ precision medicine platform, a solution enabling precision medicine in acute care. Immunix™ simultaneously empowers the development and validation of new precision medicine tools and the real-time implementation of those tools to improve patient care and outcomes. Through a decade of collaboration with ten partner hospitals across the United States, Prenosis used ImmunixTM to build a proprietary biobank and dataset consisting of more than 100,000 blood samples from over 25,000 patients housed in Prenosis' Biological Safety Level 2 lab in Chicago. Prenosis uses in-house assays in its wet lab to generate critical biological data from these blood samples and merges these data with extensive clinical data extracted from partner hospitals' Electronic Medical Records. This dual biological-clinical dataset, the largest in the world for acute care patients suspected of having serious infections, is used to develop AI algorithms to elucidate patterns in rapid immune response. The ultimate goal is to enable a deep understanding of each person's individual biology, then use this understanding to recommend personalized therapeutics in real time in the acute care environment.
More on illi News
- Chicago: O'Hare International Airport Sets All-Time Passenger Record in July 2025
- The Hidden Triggers of Foreclosure Most Families Don't See Coming
- Strategic Partnerships with Defiant Space Corp and Emtel Energy USA Powerfully Enhance Solar Tech Leader with NASA Agreements: Ascent Solar $ASTI
- 120% Revenue Surge with Four Straight Profitable Quarters Signal a Breakout in the Multi-Billion Dollar Homebuilding Market: Innovative Designs $IVDN
- Leading Venture Capital Firms Recognize Wzzph Exchange's Technical Architecture and Security Framework as Industry Benchmark
"The Sepsis ImmunoScore™ FDA authorization marks an important step in helping hospital systems provide better care," said Reddy. "Similar to how sequencing technology enabled the precision medicine revolution in cancer, our powerful Immunix™ platform has the potential to unlock valuable insights to enable the creation of precision therapeutics guided by AI diagnostics. To date, this type of approach has been used predominantly in healthcare outside of emergency departments and hospitals. Prenosis seeks to change this by catalyzing a personalized medicine revolution in acute care."
The Sepsis Immunoscore™ is a registered trademark of Prenosis Inc.
About Prenosis
At Prenosis we believe healthcare should be tailored to individual biology. With our data-driven approach to fast-moving biology in acute care environments, we're ushering in a new era of precision medicine in acute care. Our Immunix™ precision medicine platform generates proprietary biological insights to rapidly develop precision medicine products and enables the real-time delivery of optimal precision therapy in acute care. The platform is based on the world's largest and fastest growing biomarker-clinical dataset for rapid immune response. Using Immunix™, we created and validated the Sepsis ImmunoScore™, the first FDA-authorized AI diagnostic for sepsis.
At Prenosis, we enable the healthcare ecosystem to see people differently. More information at: www.prenosis.com
1 Rudd, K. E. et al. Global, regional, and national sepsis incidence and mortality, 1990–2017: analysis for the Global Burden of Disease Study. The Lancet 395, 200–211 (2020).
SOURCE Prenosis
Filed Under: Business
0 Comments
Latest on illi News
- Dental Surgical Center Accepts Sedation Patients with Medicaid for MD, WV, PA and DC
- MooreSuccess Gaming Launches Digi 995: Color Protocol – A Futuristic Coloring Experience
- A New Era in Healthcare Marketing
- Chicago: Mayor Brandon Johnson Signs 'Right to Protest' Executive Order
- Sloan's Lake Dental Launches New Website to Enhance Patient Experience and Access to Modern Dental Care
- Only 3 Weeks Left till the Start of the OpenSSL Conference 2025
- InventHelp Inventor Develops Portable Sit-On-Scale (CLR-320)
- ENTOUCH Completes $50 million Funding Round
- Teaming Agreement with Emtel Energy USA to Advance Thin-Film PV Energy Storage Capabilities; NASA agreements for Solar Space Tech; Ascent Solar $ASTI
- Nebuvex Acknowledges Platform "Too Secure" for Anonymous Traders; Institutional Investors Disagree
- From Tokyo to Berlin: FreeTo.Chat Unites Cultures with the World's First Confession VRX — EmojiStream™
- AZETHIO Launches Multi-Million Dollar User Protection Initiative Following Unprecedented Platform Growth
- Matecrypt Observes South American Cryptocurrency Adoption Surge Amid Economic Shifts
- Assent Uncovers Over 695 Unique PFAS Across Global Supply Chains as Regulations Increase
- Cryptocurrency Quarterly Trading Volume Surpasses $15 Trillion Record High as BrazilNex Acknowledges Industry 'Growing Pains' Amid Market Speculation
- Simpli.fi Earns Finalist Honors in the 2025 AdExchanger Awards
- Cyrus O'Leary's Introduces Cookie Dough Pybrid for Foodservice, Giving Chefs a Blank Canvas for Signature Desserts
- AHRFD Initiates Legal Proceedings Against Anwalt.de for Publishing Defamatory and False Content
- New Analysis Reveals the Complex Forces Driving the 'Great Human Reshuffle'
- Elevate Unveils GroundComm X30 at 2025 International GSE Expo in Las Vegas