Wang Mengqin, Liu Xiao, Tian Zhaoxing
Emergency Department, JiShuiTan Hospital, Beijing, China.
Trop Med Int Health. 2023 Apr;28(4):315-323. doi: 10.1111/tmi.13866. Epub 2023 Mar 23.
Both linezolid and vancomycin are approved by USFDA and IDSA guidelines for the management of nosocomial pneumonia due to methicillin-resistant Staphylococcus aureus (MRSA) in clinical practice. Baseline creatinine clearance is the criterion for prescribing vancomycin or linezolid for hospital-acquired pneumonia in our institution. However, patients with renal function impairment are far more difficult to manage in intensive care. Thus, the objectives of the study were to compare the clinical efficacy and safety of 600 mg of fixed-dose linezolid with intermittent dose-optimised vancomycin in hospital-acquired pneumonia due to MRSA and to evaluate parameters of clinical cure.
Analysis of a review of patients' charts. Patients with creatinine clearance <80 ml/min received 600 mg linezolid/12 h (n = 139, LN cohort), and patients with creatinine clearance ≥80 ml/min received intravenous 15 mg/kg vancomycin/12 h for 1-2 weeks consecutively or 3 weeks in case of bacteremia (n = 152, VC cohort) for management of hospital-acquired pneumonia due to MRSA.
A 59% of patients from the LN cohort and 47% of patients from the VC cohort were clinically cured. Administration of systemic steroids (p = 0.0412) and ≥ 80 ml/min creatinine clearance (p = 0.0498) were the independent parameters for the clinical cure of patients. Nephrotoxicity was higher among patients of the VC cohort than the LN cohort (p = 0.0464). Treatment failed in 41% of patients from the LN cohort and in 53% of patients from the VC cohort (p = 0.0200).
A 600 mg of fixed-dose linezolid is an ideal alternative to intermittent dose-optimised vancomycin for better clinical outcomes for patients with hospital-acquired pneumonia due to MRSA, especially for patients with renal impairment.
在临床实践中,利奈唑胺和万古霉素均获美国食品药品监督管理局(USFDA)及美国感染病学会(IDSA)指南批准,用于治疗耐甲氧西林金黄色葡萄球菌(MRSA)所致的医院获得性肺炎。在我们机构中,基线肌酐清除率是为医院获得性肺炎患者开具万古霉素或利奈唑胺的标准。然而,在重症监护中,肾功能受损的患者更难管理。因此,本研究的目的是比较600mg固定剂量利奈唑胺与间歇剂量优化万古霉素治疗MRSA所致医院获得性肺炎的临床疗效和安全性,并评估临床治愈参数。
对患者病历进行回顾性分析。肌酐清除率<80ml/min的患者接受600mg利奈唑胺/12小时(n = 139,LN队列),肌酐清除率≥80ml/min的患者连续1 - 2周接受静脉注射15mg/kg万古霉素/12小时,若发生菌血症则接受3周治疗(n = 152,VC队列),以治疗MRSA所致的医院获得性肺炎。
LN队列中59%的患者和VC队列中47%的患者临床治愈。全身使用类固醇(p = 0.0412)和肌酐清除率≥80ml/min(p = 0.0498)是患者临床治愈的独立参数。VC队列患者的肾毒性高于LN队列(p = 0.0464)。LN队列中41%的患者和VC队列中53%的患者治疗失败(p = 0.0200)。
对于MRSA所致医院获得性肺炎患者,尤其是肾功能受损患者,600mg固定剂量利奈唑胺是间歇剂量优化万古霉素的理想替代药物,可带来更好的临床结局。