Risk Factors for Recurrent Staphylococcus aureus Bacteremia

Author:

Choi Seong-Ho12,Dagher Michael1,Ruffin Felicia1,Park Lawrence P13,Sharma-Kuinkel Batu K1,Souli Maria14,Morse Alison M56,Eichenberger Emily M1,Hale Lauren1,Kohler Celia1,Warren Bobby1,Hansen Brenda17,Medie Felix Mba1,McIntyre Lauren M56,Fowler Vance G14

Affiliation:

1. Department of Medicine, Duke University Medical Center, Durham, North Carolina, USA

2. Division of Infectious Diseases, Department of Internal Medicine, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, South Korea

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

4. Duke Clinical Research Institute, Durham, North Carolina, USA

5. Departments of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida, USA

6. University of Florida Genetics Institute University of Florida, Gainesville Florida, USA

7. Pediatric Gastroenterology, University of North Carolina, Chapel Hill, North Carolina, USA

Abstract

Abstract Background To understand the clinical, bacterial, and host characteristics associated with recurrent Staphylococcus aureus bacteremia (R-SAB), patients with R-SAB were compared to contemporaneous patients with a single episode of SAB (S-SAB). Methods All SAB isolates underwent spa genotyping. All isolates from R-SAB patients underwent pulsed-field gel electrophoresis (PFGE). PFGE-indistinguishable pairs from 40 patients underwent whole genome sequencing (WGS). Acute phase plasma from R-SAB and S-SAB patients was matched 1:1 for age, race, sex, and bacterial genotype, and underwent cytokine quantification using 25-analyte multiplex bead array. Results R-SAB occurred in 69 (9.1%) of the 756 study patients. Of the 69 patients, 30 experienced relapse (43.5%) and 39 reinfection (56.5%). Age, race, hemodialysis dependence, presence of foreign body, methicillin-resistant Staphyloccus aureus, and persistent bacteremia were individually associated with likelihood of recurrence. Multivariate risk modeling revealed that black hemodialysis patients were nearly 2 times more likely (odds ratio [OR] = 9.652 [95% confidence interval [CI], 5.402–17.418]) than white hemodialysis patients (OR = 4.53 [95% CI, 1.696–10.879]) to experience R-SAB. WGS confirmed PFGE interpretations in all cases. Median RANTES (regulated on activation, normal T cell expressed and secreted) levels in acute phase plasma from the initial episode of SAB were higher in R-SAB than in matched S-SAB controls (P = .0053, false discovery rate < 0.10). Conclusion This study identified several risk factors for R-SAB. The largest risk for R-SAB is among black hemodialysis patients. Higher RANTES levels in R-SAB compared to matched controls warrants further study.

Funder

National Institutes of Health

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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