Black and White Patients With Staphylococcus aureus Bacteremia Have Similar Outcomes but Different Risk Factors

Author:

Ruffin Felicia1,Dagher Michael1,Park Lawrence P12,Wanda Lisa34,Hill-Rorie Jonathan5,Mohnasky Michael3,Marshall Julia1,Souli Maria16,Lantos Paul1,Sharma-Kuinkel Batu K1,Maskarinec Stacey A1,Eichenberger Emily M1,Muiruri Charles7,Broadnax Brittney1,Fowler Vance G16ORCID

Affiliation:

1. Division of Infectious Diseases, Duke University , Durham, North Carolina , USA

2. Duke Global Health Institute, Duke University , Durham, North Carolina , USA

3. University of North Carolina School of Medicine , Chapel Hill, North Carolina , USA

4. University of North Carolina Gillings School of Global Public Health , Chapel Hill, North Carolina , USA

5. Fenway Institute at Fenway Health , Boston, Massachusetts , USA

6. Duke Clinical Research Institute, Duke University , Durham, North Carolina , USA

7. Department of Population Health Sciences, Duke University , Durham, North Carolina , USA

Abstract

Abstract Background Staphylococcus aureus bacteremia (SAB) disproportionately affects Black patients. The reasons for this disparity are unclear. Methods We evaluated a prospectively ascertained cohort of patients with SAB from 1995 to 2020. Clinical characteristics, bacterial genotypes, and outcome were compared among Black and White patients with SAB. Multivariable logistic regression models were used to determine factors independently associated with the outcomes. Results Among 3068 patients with SAB, 1107 (36%) were Black. Black patients were younger (median, 56 years vs 63 years; P < .001) and had higher rates of diabetes (47.5% vs 34.5%, P < .001), hemodialysis dependence (40.0% vs 7.3%, P < .001), and human immunodeficiency virus (6.4% vs 0.6%, P < .001). Black patients had higher rates of methicillin-resistant S. aureus (49.3% vs 44.9%, P = .020), including the USA300 hypervirulent clone (11.5% vs 8.4%, P = .007). White patients had higher rates of corticosteroid use (22.4% vs 15.8%, P < .0001) and surgery in the preceding 30 days (28.1% vs 18.7%, P < .001). Although the median Acute Physiology Score (APS) at the time of initial SAB diagnosis was significantly higher in Black patients (median APS, 9; interquartile range [IQR], 5–14 vs median APS, 7; IQR, 4–12; P < .001), race was not associated with 90-day mortality (risk ratio, 1.02; 95% confidence interval, .93–1.12), and rates of metastatic infection were lower among Black patients (37.2% vs 41.3% White, P = .029). Conclusions Despite differences in Black patients' higher APS on presentation and more risk factors, including a 5 times higher risk of hemodialysis dependence, 90-day mortality among Black and White patients with SAB was similar.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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