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Increased Staphylococcus aureus Nasal Carriage Rates in Rheumatoid Arthritis Patients on Biologic Therapy.

Authors :
Goodman SM
Nocon AA
Selemon NA
Shopsin B
Fulmer Y
Decker ME
Grond SE
Donlin LT
Figgie MP
Sculco TP
Russell LA
Henry ME
Bass AR
Miller AO
Sculco PK
Source :
The Journal of arthroplasty [J Arthroplasty] 2019 May; Vol. 34 (5), pp. 954-958. Date of Electronic Publication: 2019 Jan 17.
Publication Year :
2019

Abstract

Background: Rheumatoid arthritis patients are at increased risk for periprosthetic joint infection after arthroplasty. The reason is multifactorial. Nasal colonization with Staphylococcus aureus is a modifiable risk factor; carriage rates in RA patients are unknown. The goal of this study is to determine the S aureus nasal carriage rates of RA patients on biologics, RA patients on traditional disease-modifying anti-rheumatic drugs (DMARDs), and osteoarthritis.<br />Methods: Consecutive patients with RA on biologics (±DMARDs), RA on non-biologic DMARDs, or OA were prospectively enrolled from April 2017 to May 2018. One hundred twenty-three patients were determined necessary per group to show a difference in carriage rates. Patients underwent a nasal swab and answered questions to identify additional risk factors. S aureus positive swabs were further categorized using spa typing. Logistic regression evaluated the association with S aureus colonization between the groups after controlling for known risk factors.<br />Results: RA patients on biologics, 70% of whom were on DMARDs, had statistically significant increase in S aureus colonization (37%) compared to RA on DMARDs alone (24%), or OA (20%) (P = .01 overall). After controlling for glucocorticoids, antibiotic use, recent hospitalization, and diabetes, RA on biologics had a significant increased risk of S aureus nasal colonization (Odds ratio 1.80, 95% confidence interval 1.00-3.22, P = .047).<br />Conclusion: S aureus colonization risk was increased for RA on biologics compared to RA not on biologics and OA. Nasal S aureus carriage increases the risk of surgical site infection; this modifiable risk factor should be addressed prior to total joint arthroplasty for this higher risk patient group.<br /> (Copyright © 2019 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1532-8406
Volume :
34
Issue :
5
Database :
MEDLINE
Journal :
The Journal of arthroplasty
Publication Type :
Academic Journal
Accession number :
30733073
Full Text :
https://doi.org/10.1016/j.arth.2019.01.025