Huang Fangfang, Shen Ting, Hai Xin, Xiu Huiqing, Zhang Kai, Huang Tiancha, Chen Juan, Guan Zhihui, Zhou Hongwei, Cai Jiachang, Cai Zhijian, Cui Wei, Zhang Shufang, Zhang Gensheng
Department of Critical Care Medicine, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China.
Department of Critical Care Medicine, Yuyao People's Hospital, Yuyao 315400, China.
Heliyon. 2022 Dec 2;8(12):e11978. doi: 10.1016/j.heliyon.2022.e11978. eCollection 2022 Dec.
To investigate the clinical features and risk factors for methicillin-resistant (MRSA) pneumonia (MP) with secondary MRSA bloodstream infections (MRSA-BSI) (termed MP-BSI) compared with MP alone and to study the incidence of MP-BSI among patients with MP.
This was a retrospective, single-center study with clinical data derived from previous medical records. The cases were divided into groups: MP alone and MP-BSI. The determination of independent risk factors for MP-BSI relied on logistic regression analysis. Additionally, the crude outcomes were compared.
A total of 435 patients with MP were recruited, with 18.9% (82/435) having MP-BSI. The median age was 62 (interquartile range, 51,72) years, and 74.5% of the patients were male. Multivariate analysis revealed that immunosuppression, community-acquired MP (CA-MP), time from initial to targeted antibiotic use, high Sequential Organ Failure Assessment (SOFA) score, increased respiratory rate, and elevated γ-GT level (all p < 0.05) were independent risk factors for MP-BSI, while targeted treatment with linezolid was a protective factor. Patients with MP-BSI had a longer duration of hospitalization (median days, 27.5 vs. 19, p = 0.001), a higher 28-day mortality rate (24.4% vs. 11.0%, p = 0.001), and a higher in-hospital mortality rate (26.8% vs. 14.7%, p = 0.009) than those with MP alone.
Secondary MRSA-BSI among patients with MP is not rare. Immunosuppression, CA-MP, time from initial to targeted antibiotic use, high SOFA score, increased respiratory rate and elevated γ-GT level are all independent risk factors for MP-BSI; however, linezolid, as a targeted antibiotic, is a protective factor. Moreover, patients with MP may have worse clinical outcomes when they develop MRSA-BSI.
研究耐甲氧西林金黄色葡萄球菌(MRSA)肺炎(MP)合并继发性MRSA血流感染(MRSA-BSI)(称为MP-BSI)相较于单纯MP的临床特征及危险因素,并研究MP患者中MP-BSI的发生率。
这是一项回顾性单中心研究,临床数据来源于既往病历。病例分为两组:单纯MP组和MP-BSI组。通过逻辑回归分析确定MP-BSI的独立危险因素。此外,比较了粗略的结果。
共纳入435例MP患者,其中18.9%(82/435)合并MP-BSI。中位年龄为62岁(四分位间距,51,72),74.5%的患者为男性。多变量分析显示,免疫抑制、社区获得性MP(CA-MP)、从初始到靶向抗生素使用的时间、高序贯器官衰竭评估(SOFA)评分、呼吸频率增加和γ-GT水平升高(均p<0.05)是MP-BSI的独立危险因素,而利奈唑胺靶向治疗是一个保护因素。与单纯MP患者相比,MP-BSI患者的住院时间更长(中位天数,27. vs. 19,p = 0.001),28天死亡率更高(24.4% vs. 11.0%,p = 0.001),院内死亡率更高(26.8% vs. 14.7%,p = 0.009)。
MP患者中继发性MRSA-BSI并不罕见。免疫抑制、CA-MP、从初始到靶向抗生素使用的时间、高SOFA评分、呼吸频率增加和γ-GT水平升高均为MP-BSI的独立危险因素;然而,利奈唑胺作为靶向抗生素是一个保护因素。此外,MP患者发生MRSA-BSI时临床结局可能更差。