Analysis-Wanted: an oxygen monitor reliable for all races
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[November 02, 2022]
By Nancy Lapid
(Reuters) - Medical device makers and
scientists are working on new technologies to improve widely-used
devices that assess potential heart and respiratory problems given
mounting evidence that current ones could lead to inadequate healthcare
for patients with darker skin.
Doctors have long known that pulse oximeters are less accurate in
estimating blood oxygen levels in non-white patients, but the
discrepancies were considered insignificant. The COVID-19 pandemic
exposed some of the real dangers of these flaws, as the devices gave
falsely high oxygen readings in patients with dark skin.
As a result, some patients faced COVID treatment delays or were denied
treatment, and some were discharged from emergency rooms instead of
receiving care, researchers found, adding to the litany of healthcare
disparities experienced by non-white populations.
Expert advisers to the U.S. Food and Drug Administration met virtually
on Tuesday to discuss improvements in standards for pulse oximeters.
The devices, which clip to a fingertip, pass red and infrared light
through the skin and measure how much light is absorbed by
oxygen-carrying hemoglobin. Melanin pigment in darker skin also absorbs
the light, however, and current devices do not adjust for that effect.
To address the problem, some researchers are testing devices that use
other wavelengths of light not absorbed by melanin.
Among the furthest along in development is a sensor from Rockley
Photonics Holdings that uses spectrophotometers and laser instruments on
chips to emit a broad spectrum of light, which the company says more
accurately monitors not only blood oxygen but also hydration, blood
pressure and other biomarkers.
Rockley Chief Executive Andrew Rickman told Reuters his company plans to
begin shipping the product next month to companies that would package it
into wearable and other devices. Customers include Medtronic Plc, a
major manufacturer of oximeters, which announced a partnership with
Rockley in March. It is not clear when the new devices will become
available.
At Brown University, researchers Kimani Toussaint and Rutendo Jakachira
are experimenting with light at wavelengths insensitive to melanin.
Valencia Koomson of Tufts University is developing a device that takes
into account a patient's skin tone and presence of melanin to better
adjust oxygen level estimates.
All agree that more accurate pulse oximeters are long overdue.
Imarc Group market research firm forecast the global pulse oximeter
market reaching $3.25 billion by 2027.
'ENORMOUS' PROBLEM
In recent years, studies have shown that low oxygen levels more often go
undetected in Black adults and infants, and that Black patients receive
less supplemental oxygen than similarly ill white patients due to pulse
oximeter inaccuracies.
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A medical worker (R) puts a pulse
oximeter on a woman's finger to check her oxygen level during a
door-to-door survey for the coronavirus disease (COVID-19) amidst
its spread in Ahmedabad, India June 26, 2020. REUTERS/Amit Dave/File
Photo
COVID amplified those risks. The
coronavirus can cause dangerously low oxygen levels even before a
patient feels out of breath or appears to be in distress, making
healthcare providers even more dependent on accurate oximeter
readings.
Pulse oximeter problems "suddenly became enormous" during the
pandemic, said Dr. Philip Bickler, director of the University of
California, San Francisco's (UCSF) Hypoxia Research & Pulse Oximeter
Test Facility.
Bickler, whose laboratory analyzes pulse oximeter accuracy for
manufacturers, said he believes industry leaders "are all working to
address the devices' shortcomings."
Experts say the FDA needs to strengthen its criteria for approving
new devices. Current rules require that pulse oximeters be tested in
a minimum of just 10 subjects, only two of whom must be
"darkly-pigmented."
When more than 10 subjects are involved, only 15% must be non-white,
although some manufacturers do test in larger, more
racially-balanced groups. The agency does not require a standardized
assessment for classifying skin pigmentation, tools that would be
critical in evaluating inaccuracies.
FDA staff speaking at Tuesday's meeting acknowledged that although
variables in sick patients affect accuracy, pulse oximeters are
tested under "ideal" laboratory conditions in healthy individuals.
Pediatric devices are tested in small adults rather than children or
infants.
In advance of the meeting, some pulse oximeter manufacturers
appeared open to discussing improvements while maintaining that
their devices worked well.
Medtronic told Reuters it "looks forward to sharing perspectives and
recommending ways we can collaborate with other industry members,
standards organizations, clinicians, researchers and academics to
continue to strengthen these technologies."
Medical technology company Masimo Corp said its equipment does not
have "a bias problem between Black and white subjects." Still, the
company told Reuters, "we will continue to improve our pulse
oximeters."
For now, Tufts' Koomson said, devices that are less accurate on dark
skin and in sicker individuals will remain in wide use.
The first step to ensure appropriate access to care requires raising
awareness about the potential inaccuracies, especially among
healthcare providers, she said.
While the devices are still useful, UCSF's Bickler said, doctors
"should not base patient care only on pulse oximeter findings."
(Reporting by Nancy Lapid and Shawana Alleyne-Morris; Editing by
Michele Gershberg and Bill Berkrot)
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