Howden Benjamin P, Ward Peter B, Charles Patrick G P, Korman Tony M, Fuller Andrew, du Cros Philipp, Grabsch Elizabeth A, Roberts Sally A, Robson Jenny, Read Kerry, Bak Narin, Hurley James, Johnson Paul D R, Morris Arthur J, Mayall Barrie C, Grayson M Lindsay
Department of Infectious Diseases, Austin Hospital, Heidelberg, Victoria, Australia.
Clin Infect Dis. 2004 Feb 15;38(4):521-8. doi: 10.1086/381202. Epub 2004 Jan 29.
Although infections caused by methicillin-resistant Staphylococcus aureus with reduced vancomycin susceptibility (SA-RVS) have been reported from a number of countries, including Australia, the optimal therapy is unknown. We reviewed the clinical features, therapy, and outcome of 25 patients with serious infections due to SA-RVS in Australia and New Zealand. Eight patients had endocarditis, 9 had bacteremia associated with deep-seated infection, 6 had osteomyelitis or septic arthritis, and 2 had empyema. All patients had received vancomycin before the isolation of SA-RVS, and glycopeptide treatment had failed for 19 patients (76%). Twenty-one patients subsequently received active treatment, which was effective for 16 patients (76%). Eighteen patients received linezolid, which was effective in 14 (78%), including 4 patients with endocarditis. Twelve patients received a combination of rifampicin and fusidic acid. Surgical intervention was required for 15 patients (60%). Antibiotic therapy, especially linezolid with or without rifampicin and fusidic acid, in conjunction with surgical debulking is effective therapy for the majority of patients with serious infections (including endocarditis) caused by SA-RVS.
尽管包括澳大利亚在内的许多国家都报告了由对万古霉素敏感性降低的耐甲氧西林金黄色葡萄球菌(SA-RVS)引起的感染,但最佳治疗方法尚不清楚。我们回顾了澳大利亚和新西兰25例因SA-RVS导致严重感染患者的临床特征、治疗方法及治疗结果。8例患者患有心内膜炎,9例患有与深部感染相关的菌血症,6例患有骨髓炎或化脓性关节炎,2例患有脓胸。所有患者在分离出SA-RVS之前均接受过万古霉素治疗,19例患者(76%)的糖肽类治疗无效。随后21例患者接受了积极治疗,其中16例(76%)有效。18例患者接受了利奈唑胺治疗,其中14例(78%)有效,包括4例心内膜炎患者。12例患者接受了利福平与夫西地酸联合治疗。15例患者(60%)需要手术干预。对于大多数由SA-RVS引起的严重感染(包括心内膜炎)患者,抗生素治疗,尤其是利奈唑胺联合或不联合利福平与夫西地酸,并结合手术减瘤是有效的治疗方法。