Analysis of Discrepancies Between Pulse Oximetry and Arterial Oxygen Saturation Measurements by Race and Ethnicity and Association With Organ Dysfunction and Mortality.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 11 2021
Historique:
entrez: 3 11 2021
pubmed: 4 11 2021
medline: 27 1 2022
Statut: epublish

Résumé

Discrepancies in oxygen saturation measured by pulse oximetry (Spo2), when compared with arterial oxygen saturation (Sao2) measured by arterial blood gas (ABG), may differentially affect patients according to race and ethnicity. However, the association of these disparities with health outcomes is unknown. To examine racial and ethnic discrepancies between Sao2 and Spo2 measures and their associations with clinical outcomes. This multicenter, retrospective, cross-sectional study included 3 publicly available electronic health record (EHR) databases (ie, the Electronic Intensive Care Unit-Clinical Research Database and Medical Information Mart for Intensive Care III and IV) as well as Emory Healthcare (2014-2021) and Grady Memorial (2014-2020) databases, spanning 215 hospitals and 382 ICUs. From 141 600 hospital encounters with recorded ABG measurements, 87 971 participants with first ABG measurements and an Spo2 of at least 88% within 5 minutes before the ABG test were included. Patients with hidden hypoxemia (ie, Spo2 ≥88% but Sao2 <88%). Outcomes, stratified by race and ethnicity, were Sao2 for each Spo2, hidden hypoxemia prevalence, initial demographic characteristics (age, sex), clinical outcomes (in-hospital mortality, length of stay), organ dysfunction by scores (Sequential Organ Failure Assessment [SOFA]), and laboratory values (lactate and creatinine levels) before and 24 hours after the ABG measurement. The first Spo2-Sao2 pairs from 87 971 patient encounters (27 713 [42.9%] women; mean [SE] age, 62.2 [17.0] years; 1919 [2.3%] Asian patients; 26 032 [29.6%] Black patients; 2397 [2.7%] Hispanic patients, and 57 632 [65.5%] White patients) were analyzed, with 4859 (5.5%) having hidden hypoxemia. Hidden hypoxemia was observed in all subgroups with varying incidence (Black: 1785 [6.8%]; Hispanic: 160 [6.0%]; Asian: 92 [4.8%]; White: 2822 [4.9%]) and was associated with greater organ dysfunction 24 hours after the ABG measurement, as evidenced by higher mean (SE) SOFA scores (7.2 [0.1] vs 6.29 [0.02]) and higher in-hospital mortality (eg, among Black patients: 369 [21.1%] vs 3557 [15.0%]; P < .001). Furthermore, patients with hidden hypoxemia had higher mean (SE) lactate levels before (3.15 [0.09] mg/dL vs 2.66 [0.02] mg/dL) and 24 hours after (2.83 [0.14] mg/dL vs 2.27 [0.02] mg/dL) the ABG test, with less lactate clearance (-0.54 [0.12] mg/dL vs -0.79 [0.03] mg/dL). In this study, there was greater variability in oxygen saturation levels for a given Spo2 level in patients who self-identified as Black, followed by Hispanic, Asian, and White. Patients with and without hidden hypoxemia were demographically and clinically similar at baseline ABG measurement by SOFA scores, but those with hidden hypoxemia subsequently experienced higher organ dysfunction scores and higher in-hospital mortality.

Identifiants

pubmed: 34730820
pii: 2785794
doi: 10.1001/jamanetworkopen.2021.31674
pmc: PMC9178439
mid: NIHMS1807963
doi:

Substances chimiques

Creatinine AYI8EX34EU

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2131674

Subventions

Organisme : NIBIB NIH HHS
ID : R01 EB017205
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM139967
Pays : United States

Commentaires et corrections

Type : ErratumIn

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Auteurs

An-Kwok Ian Wong (AI)

Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University, Atlanta, Georgia.
Division of Pulmonary, Allergy, and Critical Care Medicine, Duke University, Durham, North Carolina.

Marie Charpignon (M)

MIT Institute for Data, Systems and Society, Cambridge, Massachusetts.

Han Kim (H)

Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland.

Christopher Josef (C)

Department of Surgery, Emory University, Atlanta, Georgia.

Anne A H de Hond (AAH)

Leiden University Medical Centre, Department of Biomedical Data Sciences, Leiden, the Netherlands.
Leiden University Medical Centre, Department of Information Technology and Digital Innovation, Leiden, the Netherlands.

Jhalique Jane Fojas (JJ)

Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.

Azade Tabaie (A)

Department of Biomedical Informatics, Emory University, Atlanta, Georgia.

Xiaoli Liu (X)

School of Biological Science and Medical Engineering, Beihang University, Beijing, China.

Eduardo Mireles-Cabodevila (E)

School of Biological Science and Medical Engineering, Beihang University, Beijing, China.

Leandro Carvalho (L)

Respiratory Institute, Cleveland Clinic, Cleveland, Ohio.
Sociedade Mineira de Terapia Intensiva, Belo Horizonte, Brazil.

Rishikesan Kamaleswaran (R)

Department of Biomedical Informatics, Emory University, Atlanta, Georgia.

R W M A Madushani (RWMA)

Department of Infectious Diseases, Boston Medical Center, Boston, Massachusetts.

Lasith Adhikari (L)

Connected Care and Personal Health, Philips Research North America, Cambridge, Massachusetts.

Andre L Holder (AL)

Division of Pulmonary, Allergy, Critical Care, and Sleep Medicine, Emory University, Atlanta, Georgia.

Ewout W Steyerberg (EW)

Leiden University Medical Centre, Department of Biomedical Data Sciences, Leiden, the Netherlands.

Timothy G Buchman (TG)

Department of Surgery, Emory University, Atlanta, Georgia.

Mary E Lough (ME)

Medicine-Primary Care and Population Health, Stanford University, California.
Office of Research, Stanford Health Care, Stanford, California.

Leo Anthony Celi (LA)

Massachusetts Institute of Technology, Laboratory for Computational Physiology, Cambridge.
Division of Pulmonary, Critical Care, and Sleep Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

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Classifications MeSH