At-home blood oxygen monitoring devices less accurate on people with darker skin

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Photo by Mufid Majnun on Unsplash
Photo by Mufid Majnun on Unsplash

Fingertip pulse oximeters are more likely to miss dangerously low oxygen in darker skinned people, a new study shows. UK researchers conducted the largest study so far on this topic, involving over 900 critically ill adults in ICUs. They had both "gold-standard" blood gas measurements from the hospital machines, and measurements using the at-home fingertip devices. A special camera was also used to measure patients' skin tones. The study found that for patients with darker skin, pulse oximeters more commonly missed the low oxygen levels that require medical or emergency help, but were less likely to wrongly show a too-low oxygen level. An accompanying editorial notes that early evidence of this inequity was reported more than 30 years ago. The authors' recommendations include regulations to require monitoring and sharing information on the devices' performance, and education and awareness for clinicians using pulse oximeters to avoid perpetuating inequalities.

News release

From: BMJ Group

Home fingertip oxygen monitors less accurate for people with darker skin tones

Largest study on this topic suggests that measurement errors lead to potential delays in care and contribute to health disparities

Fingertip monitors known as pulse oximeters that can be used at home to detect low blood oxygen levels (hypoxaemia) give higher readings for patients with darker than lighter skin tones, finds the largest study on this topic published by The BMJ today.

This means that low blood oxygen levels may be missed in patients with darker skin tones, potentially delaying care, while patients with lighter skin tones may get unnecessary treatment.

Pulse oximeters use light to measure the amount of oxygen in the blood (SpO2). For most people, a normal pulse oximeter reading is between 95% and 100%, with readings below 90-92% generally considered low and requiring medical attention.

They are known to be affected by several factors, including skin tone, as pigment in darker skin can absorb more light, making the device “think” there's more oxygen than there is. But so far, studies have been unable to draw any firm conclusions about the impact of skin tone on diagnostic accuracy.

To address this, researchers set out to test the measurement and diagnostic accuracy of five fingertip pulse oximeters provided by the NHS for use at home in the NHS England COVID oximetry @home scheme.

They drew on data from 903 critically ill adults (average age 56 years; 67% male) on 24 NHS intensive care units in England between June 2022 and August 2024.

Although the fingertip pulse oximeters tested were those used at home, intensive care units were used as the test laboratory as patients have lower blood oxygen values and routinely have their blood oxygen accurately measured using hospital machines.

For each patient, skin tone was measured objectively using a spectrophotometer (a type of camera that measures colour). The researchers then compared pulse oximetry blood oxygen values (SpO2) with “gold-standard” arterial blood gas measurements (SaO2).

SpO2 values were assessed at two thresholds in line with current guidance either to seek medical help (94% or lower) or to attend the emergency department (92% or lower).

A total of 11,018 paired SpO2-SaO2 measurements were analysed. All five pulse oximeters returned higher SpO2 values for patients with darker skin tones than patients with lighter skin tones, at any given level of SaO2 measurement.

SpO2 readings were, on average, 0.6-1.5 percentage points higher for patients with darker than lighter skin tone.

At both SpO2 thresholds assessed, false negative rates (low oxygen missed by the pulse oximeter when present) increased with darker skin tones, while false positive rates (low oxygen indicated by the pulse oximeter when absent) decreased with darker skin tone.

And while absolute differences in readings were small, “they can result in substantially higher rates of false negatives and lower rates of false positives in the diagnosis of hypoxaemia,” note the researchers.

This is an observational study, so no definitive conclusions can be drawn about cause and effect. And the authors acknowledge that the study was conducted in critically ill patients, which may limit the generalisability of the findings.

However, they say this was a large study using sophisticated statistical modelling to assess the performance of the pulse oximeters across multiple domains of both measurement and diagnostic accuracy.

As such, they conclude: “SpO2 readings should be interpreted in the context of other clinical information and trends in SpO2 values given greater importance than single readings, particularly in patients with darker skin tones.”

They add: “Healthcare systems should develop guidance to inform and aid practitioners, patients and the public, particularly in settings where additional clinical readings from other medical measurement devices would not be available.”

In a linked editorial, researchers agree that clinicians must recognise the limitations of current devices and interpret readings for patients with darker skin with care and caution, and they say regulation must now catch up with science to mitigate harm.

“The goal is not to abandon pulse oximetry but to understand its limits and make it equitable, ensuring that the technology designed to measure oxygen does not itself perpetuate inequalities in those who receive it,” they conclude.

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Research BMJ Group, Web page URL will go live when the embargo lifts
Editorial / Opinion BMJ Group, Web page URL will go live when the embargo lifts
Journal/
conference:
The BMJ
Research: Link to Paper 1 | Paper 2
Organisation/s: University of Plymouth (UK) - research paper, University of Colorado (USA) - editorial
Funder: This study was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (NIHR135577). WNC was funded by an NIHR Pre-doctoral Fellowship in Epidemiology (NIHR302788) during this study. The funder of the study had no role in the study design, the collection, analysis and interpretation of data, the writing of the report, or the decision to submit the article for publication. All authors are independent of the funders. All authors had full access to all of the data (including statistical reports and tables) in the study and can take responsibility for the integrity of the data and the accuracy of the data analysis.
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