Service des Maladies Infectieuses et Tropicales, Hospices Civils de Lyon, Lyon, France.
Antimicrob Agents Chemother. 2014;58(2):746-55. doi: 10.1128/AAC.02032-13. Epub 2013 Nov 18.
Prolonged antimicrobial therapy is recommended for methicillin-susceptible Staphylococcus aureus (MSSA) bone and joint infections (BJI), but its safety profile and risk factors for severe adverse events (SAE) in clinical practice are unknown. We addressed these issues in a retrospective cohort study (2001 to 2011) analyzing antimicrobial-related SAE (defined according to the Common Terminology Criteria for Adverse Events) in 200 patients (male, 62%; median age, 60.8 years [interquartile range {IQR}, 45.5 to 74.2 years]) with MSSA BJI admitted to a reference regional center with acute (66%) or chronic arthritis (7.5%), osteomyelitis (9.5%), spondylodiscitis (16%), or orthopedic device-related infections (67%). These patients received antistaphylococcal therapy for a median of 26.6 weeks (IQR, 16.8 to 37.8 weeks). Thirty-eight SAE occurred in 30 patients (15%), with a median time delay of 34 days (IQR, 14.75 to 60.5 days), including 10 patients with hematologic reactions, 9 with cutaneomucosal reactions, 6 with acute renal injuries, 4 with hypokalemia, and 4 with cholestatic hepatitis. The most frequently implicated antimicrobials were antistaphylococcal penicillins (ASP) (13 SAE/145 patients), fluoroquinolones (12 SAE/187 patients), glycopeptides (9 SAE/101 patients), and rifampin (7 SAE/107 patients). Kaplan-Meier curves and stepwise binary logistic regression analyses were used to determine the risk factors for the occurrence of antimicrobial-related SAE. Age (odds ratio [OR], 1.479 for 10-year increase; 95% confidence interval [CI], 1.116 to 1.960; P = 0.006) appeared to be the only independent risk factor for SAE. In patients receiving ASP or rifampin, daily dose (OR, 1.028; 95% CI, 1.006 to 1.051; P = 0.014) and obesity (OR, 8.991; 95% CI, 1.453 to 55.627; P = 0.018) were associated with the occurrence of SAE. The high rate of SAE and their determinants highlighted the importance of the management and follow-up of BJI, with particular attention to be paid to older persons, especially for ASP dosage, and to rifampin dose adjustment in obese patients.
建议对耐甲氧西林金黄色葡萄球菌(MSSA)骨和关节感染(BJI)进行延长抗菌治疗,但在临床实践中,其安全性概况和严重不良事件(SAE)的风险因素尚不清楚。我们通过一项回顾性队列研究(2001 年至 2011 年)来解决这些问题,该研究分析了在被转诊至一个参考区域中心的 200 名 MSSA BJI 患者(男性占 62%;中位年龄为 60.8 岁[四分位距{IQR},45.5 至 74.2 岁])中,与抗菌治疗相关的 SAE(根据不良事件通用术语标准定义),这些患者患有急性(66%)或慢性关节炎(7.5%)、骨髓炎(9.5%)、脊椎炎(16%)或骨科器械相关感染(67%)。这些患者接受抗葡萄球菌治疗的中位数时间为 26.6 周(IQR,16.8 至 37.8 周)。30 名患者(15%)发生了 38 例 SAE,中位时间延迟为 34 天(IQR,14.75 至 60.5 天),包括 10 例血液学反应、9 例皮肤黏膜反应、6 例急性肾损伤、4 例低钾血症和 4 例胆汁淤积性肝炎。最常涉及的抗菌药物是抗葡萄球菌青霉素(ASP)(13 例 SAE/145 例患者)、氟喹诺酮类(12 例 SAE/187 例患者)、糖肽类(9 例 SAE/101 例患者)和利福平(7 例 SAE/107 例患者)。Kaplan-Meier 曲线和逐步二元逻辑回归分析用于确定与抗菌相关 SAE 发生相关的风险因素。年龄(比值比[OR],每增加 10 岁为 1.479;95%置信区间[CI],1.116 至 1.960;P = 0.006)似乎是 SAE 的唯一独立危险因素。在接受 ASP 或利福平治疗的患者中,每日剂量(OR,1.028;95%CI,1.006 至 1.051;P = 0.014)和肥胖(OR,8.991;95%CI,1.453 至 55.627;P = 0.018)与 SAE 的发生相关。高发生率的 SAE 和其决定因素突出了 BJI 管理和随访的重要性,尤其需要关注老年人,尤其是 ASP 剂量,以及肥胖患者利福平剂量的调整。