iRhythm Gains FDA Clearance for its Clinically Integrated ZEUS System
July 22 2022 - 08:30AM
GlobeNewswire Inc.
iRhythm Technologies, Inc. (NASDAQ:IRTC), a leading digital
healthcare solutions company focused on the advancement of cardiac
care, today announced it received FDA 510(k) clearance for its ZEUS
(Zio ECG Utilization Software) System for the Zio Watch. Produced
in partnership with Verily, an Alphabet precision health company,
the ZEUS System combines deep learned algorithms with a proven and
trusted cardiac arrhythmia service. The ZEUS System is the AI
algorithm and solution component of the Zio® Watch: a sensor-based
wearable for noninvasive, clinical grade, long-term continuous
monitoring for atrial fibrillation (AFib). Verily also received FDA
510(k) clearance for the Zio Watch (Study Watch with Irregular
Pulse Monitor).
The Zio Watch with the ZEUS System is an integrated,
prescription-based solution that addresses clinician workflows,
care pathways and the patient experience. The cleared Zio Watch is
a wrist-worn solution that not only detects AFib, but also
characterizes the amount of AFib over time, thus aiding a clinician
in diagnosis. The Zio Watch uses a continuous photoplethysmography
(PPG), AI-based algorithm to detect AFib and calculate an AFib
burden estimate. A preliminary report is then sent to the patient's
clinician for review, potentially leading to diagnosis and clinical
intervention.
“We are incredibly excited about this important milestone as we
make progress in bringing a new monitoring platform to patients who
can benefit from it. There is a clear need in the market today for
a clinical grade, long-term and noninvasive monitoring solution,”
said Quentin Blackford, CEO and President of iRhythm. “iRhythm is
focused on redefining the standard of care with earlier insight to
predict and prevent disease, and the Zio Watch with ZEUS System
provides clinicians a platform that has the potential to
meaningfully improve patients’ lives.”
“Our partnership with iRhythm advances our shared mission of
delivering more efficient care for patients with AFib,” said Dr.
Jessica Mega, Chief Medical and Scientific Officer and Co-founder
of Verily. “The industry is ripe for a clinical grade wearable to
not only improve how we monitor cardiovascular health, but also
develop precision health interventions that could ultimately
prevent more serious cardiac events before they can occur.”
iRhythm has what is believed to be the world’s largest
repository of labelled ECG data, which it leveraged to develop its
proprietary PPG algorithm. Findings from the Verily Study: Watch
AFib Detection At Home, revealed at HRS, show that interval-level
sensitivity and specificity of the AFib Context Engine (ACE)
algorithm within the ZEUS System were 93.6% and 99.1%
respectively.1 Zio XT was used as a reference for
computing performance. AFib episodes occurred in 30.4% of subjects,
and median AFib burden was 9.3%. The Zio Watch PPG-derived AFib
burden estimate was an accurate measure when compared to the Zio XT
reference. iRhythm's proprietary ACE algorithm utilizes a novel
convolutional neural network architecture designed to operate on a
cloud-enabled system compatible with a battery-constrained device.
The results of ACE are presented in clinical preliminary reports
summarizing AFib presence over the monitoring period. This process
enables clinicians to receive clinically meaningful data on AFib
presence/absence, rather than just a single data point in time.
“We’re proud to introduce a clinical grade wearable that has the
potential to fill an important gap in patient care by enabling the
early detection and long-term monitoring of atrial fibrillation,”
said Mark Day, Chief Technology Officer at iRhythm. “This
technology is fundamental to growing a disruptive new monitoring
platform for iRhythm.”
The Zio Watch will be complementary to Zio monitors by adding a
modality with longer wear times for patients who require long-term
monitoring in order to detect, characterize and manage AFib. The
Zio Watch is designed to be a cost-effective, noninvasive
monitoring solution and will fully integrate with the Zio service.
iRhythm plans to introduce the ZEUS System for a limited market
evaluation in 2023.
Disclaimer: The Zio Watch and the ZEUS System are not yet
commercially available at this time and iRhythm will continue to
build clinical research going into 2023.
About iRhythm Technologies, Inc.iRhythm is a
leading digital healthcare company redefining the way cardiac
arrhythmias are clinically diagnosed. The company combines wearable
biosensor devices worn for up to 14 days and cloud-based data
analytics with powerful proprietary algorithms that distill data
from millions of heartbeats into clinically actionable information.
The company believes improvements in arrhythmia detection and
characterization have the potential to change the clinical
management of patients.
About VerilyVerily is a subsidiary of Alphabet
that is using a data-driven, people-first approach to change the
way people manage their health and the way healthcare is delivered.
Launched from Google X in 2015, Verily’s purpose is to bring the
promise of precision health to everyone, every day. Verily is
focused on generating and activating data from a wide variety of
sources, including clinical, social, behavioral and the real world,
to arrive at the best solutions for a person based on a
comprehensive view of the evidence. Verily uses its recognized
expertise and capabilities in technology, data science and
healthcare to enable the entire healthcare ecosystem to drive
better health outcomes. For more information, please visit
verily.com
Investor Relations Contact:Stephanie
Zhadkevich(919)
452-5430stephanie.zhadkevich@irhythmtech.com
iRhythm Media Contact:Morgan Mathis(310)
528-6306irhythm@highwirepr.com
Verily Media Contact:Steven Cooper(646)
358-2765sjcoop@verily.com
1 A Photoplethysmography-based Approach to Atrial
Fibrillation-burden Estimation in High-Risk Patients. Athill, C. et
al. Heart Rhythm 2022.
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