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Oral rifampin plus ofloxacin for treatment of Staphylococcus-infected orthopedic implants.

机译:口服利福平加氧氟沙星治疗葡萄球菌感染的骨科植入物。

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摘要

We examined the effectiveness and safety of the combination of rifampin plus ofloxacin given orally for treating prosthetic orthopedic implants infected with staphylococci. The prospective cohort study was conducted in a referral public hospital with ambulatory care services between 1985 and 1991. Consecutive patients from whom Staphylococcus organisms susceptible to the study drugs were isolated from their orthopedic implants and who had no contraindication to the treatment were eligible for the study. All patients were treated orally with rifampin, 900 mg/day, plus ofloxacin, 600 mg/day. Patients with hip prosthesis infection were treated for 6 months, with removal of any unstable prostheses after 5 months of treatment; patients with knee prosthesis infection were treated for 9 months, with removal of the prosthesis after 6 months of treatment; and patients with infected bone plates were treated for 6 months, with removal of the plate after 3 months of treatment, if necessary. Monthly clinical evaluations were conducted until the completion of the treatment and follow-up or telephone interviews were conducted at 6, 12, 24, 36, 48, and 60 months thereafter. Treatment failures were documented by clinical evaluation, sampling of the infected site for culture and antibiotic activity measurement, and fistulography, if possible. Cure was defined as the absence of clinical, biological, and radiological evidence of infection 6 months after the completion of treatment, treatment failure was defined as the absence of cure, and relapse was defined as the reappearance of infection caused by the same Staphylococcus isolate that caused the original infection, regardless of the timing of this secondary infection. Among 51 patients included in the study and evaluable for safety, 4 patients had side effects and were not evaluable for treatment effectiveness; the overall success rate was 74% among 47 patients, with a success rate of 81% for the hip prosthesis group, 69% for the knee prosthesis group, and 69% for the osteosynthesis device group. Eight treatment failures were relaxed to the isolation of a resistant bacterium. The combination of rifampin administered orally plus ofloxacin is a suitable alternative to the conventional long-term intravenous therapy for treatment of orthopedic implants infected with staphylococci.
机译:我们研究了利福平联合氧氟沙星口服联合使用对治疗感染葡萄球菌的假体骨科植入物的有效性和安全性。这项前瞻性队列研究是在1985年至1991年之间由转诊的公立医院提供门诊服务进行的。从该患者的骨科植入物中分离出对本研究药物敏感的葡萄球菌生物体且无治疗禁忌症的连续患者。所有患者均口服利福平900毫克/天,氧氟沙星600毫克/天。髋关节假体感染患者接受了6个月的治疗,治疗5个月后去除了任何不稳定的假体;膝关节假体感染患者接受了9个月的治疗,治疗6个月后移除了假体;并对感染了骨板的患者进行了6个月的治疗,必要时在3个月的治疗后将其取出。每月进行临床评估直至治疗结束,并在之后的6、12、24、36、48和60个月进行随访或电话访谈。通过临床评估,感染部位取样进行培养和抗生素活性测量以及瘘管造影记录治疗失败。治愈是指治疗结束后6个月没有临床,生物学和放射学上的感染证据,治疗失败的定义是没有治愈,复发的定义是由相同的葡萄球菌分离物引起的感染再次出现导致最初的感染,而不考虑这种继发感染的时间。在纳入研究的51例患者中,有安全性可评估,其中4例有副作用且治疗效果无法评估。 47例患者的总体成功率为74%,其中髋关节假体组为81%,膝关节假体组为69%,骨合成器械组为69%。八种治疗失败被轻松分离出抗性细菌。口服利福平与氧氟沙星的组合是常规长期静脉疗法的合适替代方案,可用于治疗感染葡萄球菌的骨科植入物。

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