首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Ambulatory Treatment of Multidrug-Resistant Staphylococcus-Infected Orthopedic Implants with High-Dose Oral Co-trimoxazole (Trimethoprim-Sulfamethoxazole)
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Ambulatory Treatment of Multidrug-Resistant Staphylococcus-Infected Orthopedic Implants with High-Dose Oral Co-trimoxazole (Trimethoprim-Sulfamethoxazole)

机译:大剂量口服复方新诺明(Trimethoprim-Sulfamethoxazole)动态治疗耐多药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 high-dose oral co-trimoxazole (trimethoprim-sulfamethoxazole) for the treatment of orthopedic implants infected with multidrug-resistant Staphylococcus species. The prospective study was conducted between 1989 and 1997 in a university medical center with ambulatory-care services. Patients eligible for the study consisted of those from whom multidrug-resistant Staphylococcus spp. organisms susceptible only to glycopeptides and co-trimoxazole were isolated from their orthopedic implants and for whom there was no contraindication to the treatment. All patients were treated orally with high-dose co-trimoxazole (trimethoprim, 20 mg/kg of body weight/day; sulfamethoxazole, 100 mg/kg/day). Patients with prosthetic hip infections were treated for 6 months, with removal of any unstable prosthesis after 5 months of treatment; patients with prosthetic knee infections were treated for 9 months, with removal of any unstable prosthesis after 6 months of treatment; and patients with infected osteosynthetic devices were treated for 6 months, with removal of the device after 3 months of treatment, if necessary. Monthly clinical evaluations were conducted until the completion of the treatment, and follow-up examinations were conducted regularly for up to 6 years. The overall treatment success rate was 66.7% (26 of 39 patients), with success rates of 62.5% for patients with prosthetic knee infections, 50% for those with prosthetic hip infections, and 78.9% for those with other device infections. Seventeen of the 28 (60.7%) patients who did not have any orthopedic material removed were cured. Eight patients stopped the treatment because of side effects, and one patient was not compliant. In three patients treatment failed because of the appearance of a resistant bacterium. Long-term oral ambulatory treatment with co-trimoxazole appears to be an effective alternative to the conventional medicosurgical treatment of chronic multidrug-resistant Staphylococcus-infected orthopedic implants which includes long-term intravenous antibiotic therapy combined with surgical debridement and removal of foreign material or its subsequent one- or two-stage replacement.
机译:我们检查了大剂量口服口服三甲唑(trimethoprim-sulfamethoxazole)治疗感染了多药耐药葡萄球菌的整形外科植入物的有效性和安全性。这项前瞻性研究是在1989年至1997年之间在一家提供门诊服务的大学医学中心进行的。符合研究条件的患者包括多重耐药性葡萄球菌属的患者。从骨科植入物中分离出仅对糖肽和复方新诺明敏感的微生物,没有针对该治疗的禁忌症。所有患者均口服大剂量复方新诺明(甲氧苄啶,20 mg / kg体重/天;磺胺甲恶唑,100 mg / kg /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。膝关节假肢感染患者接受了9个月的治疗,治疗6个月后去除了任何不稳定的假体;并已对感染了骨合成装置的患者进行了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,并定期进行长达6年的随访检查。总体治疗成功率为66.7%(39例患者中的26例),膝关节假肢感染患者的成功率为62.5%,髋关节假肢感染患者为50%,其他器械感染患者为78.9%。在未去除任何矫形材料的28例患者中,有17例(60.7%)得以治愈。 8名患者由于副作用而停止了治疗,其中1名患者不依从。在三例患者中,由于出现耐药菌而治疗失败。长期使用联合曲莫唑进行口服门诊治疗似乎是对慢性耐多药葡萄球菌感染的骨科植入物进行常规药物治疗的有效替代方法,其中包括长期静脉内抗生素治疗以及外科手术清创术并清除异物或其随后的一阶段或两阶段更换。

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