Department of Medicine, Hospital for Special Surgery, Weill-Cornell Medical School, New York, NY.
Division of Infectious Diseases, Department of Medicine, NYU School of Medicine, New York, NY.
J Arthroplasty. 2019 May;34(5):954-958. doi: 10.1016/j.arth.2019.01.025. Epub 2019 Jan 17.
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.
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.
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).
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.
类风湿关节炎患者在关节置换术后发生假体周围关节感染的风险增加。原因是多方面的。金黄色葡萄球菌鼻腔定植是一个可改变的危险因素;RA 患者的携带率尚不清楚。本研究的目的是确定接受生物制剂治疗的 RA 患者、接受传统疾病修饰抗风湿药物(DMARDs)治疗的 RA 患者和骨关节炎患者的金黄色葡萄球菌鼻腔携带率。
从 2017 年 4 月至 2018 年 5 月,前瞻性纳入接受生物制剂(±DMARDs)治疗的 RA 患者、接受非生物 DMARDs 治疗的 RA 患者或骨关节炎患者。每个组确定 123 名患者以显示携带率的差异。患者进行鼻腔拭子检查并回答问题以确定其他危险因素。对金黄色葡萄球菌阳性拭子进一步进行 spa 分型。在控制已知危险因素后,采用 logistic 回归评估各组之间金黄色葡萄球菌定植的相关性。
接受生物制剂治疗的 RA 患者(其中 70%接受 DMARDs 治疗)金黄色葡萄球菌定植率(37%)明显高于仅接受 DMARDs 治疗的 RA 患者(24%)或骨关节炎患者(20%)(总体 P=.01)。在控制糖皮质激素、抗生素使用、近期住院和糖尿病后,接受生物制剂治疗的 RA 患者金黄色葡萄球菌鼻腔定植的风险显著增加(优势比 1.80,95%置信区间 1.00-3.22,P=.047)。
与未接受生物制剂治疗的 RA 患者和骨关节炎患者相比,接受生物制剂治疗的 RA 患者金黄色葡萄球菌定植风险增加。金黄色葡萄球菌定植增加了手术部位感染的风险;对于这个高风险患者群体,在进行全关节置换术前应解决这个可改变的危险因素。