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口服利福平加氧氟沙星治疗葡萄球菌感染的骨科植入物。

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

作者信息

Drancourt M, Stein A, Argenson J N, Zannier A, Curvale G, Raoult D

机构信息

Laboratoire de Microbiologie Clinique, Hôpital La Conception, Marseille, France.

出版信息

Antimicrob Agents Chemother. 1993 Jun;37(6):1214-8. doi: 10.1128/AAC.37.6.1214.

Abstract

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.

摘要

我们研究了口服利福平加氧氟沙星联合用药治疗感染葡萄球菌的人工骨科植入物的有效性和安全性。这项前瞻性队列研究于1985年至1991年在一家提供门诊护理服务的转诊公立医院进行。从骨科植入物中分离出对研究药物敏感的葡萄球菌且无治疗禁忌证的连续患者符合研究条件。所有患者口服利福平,900毫克/天,加氧氟沙星,600毫克/天。髋关节假体感染患者治疗6个月,治疗5个月后如有不稳定假体则予以取出;膝关节假体感染患者治疗9个月,治疗6个月后取出假体;感染骨板患者治疗6个月,如有必要,治疗3个月后取出骨板。每月进行临床评估直至治疗结束及随访,之后在6、12、24、36、48和60个月进行电话访谈。治疗失败通过临床评估、对感染部位进行培养和抗生素活性测定取样以及必要时进行瘘管造影记录。治愈定义为治疗结束6个月后无感染的临床、生物学和放射学证据,治疗失败定义为未治愈,复发定义为由引起原感染的同一葡萄球菌分离株导致的感染再次出现,无论此次继发感染的时间。在纳入研究且可评估安全性的51例患者中,4例出现副作用,无法评估治疗效果;47例患者的总体成功率为74%,髋关节假体组成功率为81%,膝关节假体组为69%,骨固定装置组为69%。8例治疗失败是由于分离出耐药菌。口服利福平加氧氟沙星联合用药是治疗感染葡萄球菌的骨科植入物的传统长期静脉治疗的合适替代方案。

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