Division of Infectious Diseases, Far-Eastern Memorial Hospital, New Taipei City, Taiwan.
Division of Infectious Diseases, Far-Eastern Memorial Hospital, New Taipei City, Taiwan; School of Medicine, National Yang-Ming University, Taipei, Taiwan.
J Microbiol Immunol Infect. 2020 Dec;53(6):909-915. doi: 10.1016/j.jmii.2020.08.004. Epub 2020 Aug 14.
Methicillin-resistant Staphylococcus aureus (MRSA)-associated central nervous system infections are potentially devastating. Linezolid has good penetration into cerebrospinal fluid and brain tissue. In clinical practice, linezolid may be used to treat central nervous system infections caused by MRSA resulting from glycopeptide intolerance or treatment failure. However, the clinical experience of linezolid in treating MRSA related central nervous system infections is scarce.
From 2006 to 2016, patients aged ≥20 years who had central nervous system infections caused by MRSA treated with linezolid for more than 24 hours were retrospectively included from two medical centers. The demographic details, treatment response, side effects, and relapse of infection were reviewed.
Sixty-six patients with proven CNS infection caused by MRSA were treated with linezolid. The mean age was 53.3 years. The diagnoses in this cohort consisted of brain abscesses (n = 19, 28.8%), spinal epidural abscess (n = 18, 27.3%), meningitis only (n = 12, 18.2%), meningitis with brain epidural abscess (n = 9, 13.6%), and spine device-related infection (n = 5, 7.6%). The main reasons to prescribe linezolid were glycopeptide treatment failure (51.5%) and glycopeptide allergy (48.5%). Ninety-one percent of patients were treated with linezolid for more than 14 days. The in-hospital mortality rate was 13.6%. The relapse rate after treatment was 16.7%. Drug-related adverse events (mainly cytopenia) were observed in 27.3% of patients, but none of the adverse events was fatal.
In our retrospective study, linezolid demonstrated promising effect as a salvage therapy for central nervous system infection caused by MRSA, whether due to drug allergy or glycopeptide treatment failure.
耐甲氧西林金黄色葡萄球菌(MRSA)相关的中枢神经系统感染具有潜在的破坏性。利奈唑胺对脑脊液和脑组织有良好的穿透性。在临床实践中,利奈唑胺可能用于治疗因糖肽类不耐受或治疗失败导致的由 MRSA 引起的中枢神经系统感染。然而,利奈唑胺治疗 MRSA 相关中枢神经系统感染的临床经验有限。
本研究回顾性纳入了 2006 年至 2016 年期间在两个医疗中心接受利奈唑胺治疗超过 24 小时的由 MRSA 引起的中枢神经系统感染患者。对患者的人口统计学资料、治疗反应、不良反应和感染复发情况进行了回顾性分析。
66 例经证实由 MRSA 引起的中枢神经系统感染患者接受了利奈唑胺治疗。患者的平均年龄为 53.3 岁。该队列的诊断包括脑脓肿(n=19,28.8%)、脊柱硬膜外脓肿(n=18,27.3%)、单纯脑膜炎(n=12,18.2%)、脑膜炎合并脑硬膜外脓肿(n=9,13.6%)和脊柱器械相关感染(n=5,7.6%)。应用利奈唑胺的主要原因是糖肽类治疗失败(51.5%)和糖肽类过敏(48.5%)。91%的患者接受利奈唑胺治疗的时间超过 14 天。住院期间的死亡率为 13.6%。治疗后复发率为 16.7%。27.3%的患者出现与药物相关的不良反应(主要为血细胞减少症),但无任何不良反应导致死亡。
在本回顾性研究中,利奈唑胺作为一种治疗 MRSA 引起的中枢神经系统感染的补救治疗方法,无论是由于药物过敏还是糖肽类治疗失败,均显示出良好的疗效。