Zhou Chaoe, Sun Liying, Li Haixia, Huang Lei, Liu Xinmin
Department of Geriatrics, Peking University First Hospital, Beijing, People's Republic of China.
Department of Clinical Laboratory, Peking University First Hospital, Beijing, People's Republic of China.
Infect Drug Resist. 2023 Oct 20;16:6767-6779. doi: 10.2147/IDR.S431085. eCollection 2023.
Hospital-acquired pneumonia (HAP) caused by carbapenem-resistant (CRKP), especially in elderly patients, results in high morbidity and mortality. Studies on risk factors, mortality, and antimicrobial susceptibility of CRKP pulmonary infection among elderly patients are lacking.
A retrospective case-control study was conducted from January 2019 to December 2021. The elderly inpatients (≥65 years) who were diagnosed with HAP caused by were enrolled. Clinical data were collected. Univariate and multivariate logistic regression analyses were used to identify risk factors. Propensity score matching was used to minimize the effect of potential confounding variables. Kaplan-Meier analysis was used to compare survival.
A total of 115 patients with CRKP infection and 78 patients with carbapenem-susceptible (CSKP) infection were recruited. There were four independent risk factors for CRKP infection: history of intensive care unit (ICU) stays from hospital admission to positive respiratory specimen culture for (odds ratio (OR)=2.530), Charlson comorbidity index score ≥3 (OR = 2.420), prior exposure to carbapenems (OR = 5.280), and prior infection or colonization in the preceding 3 years (OR = 18.529). The all-cause 30-day mortality was 22.3%, the mortality of CRKP and CSKP infection was 28.7% and 12.8%, respectively. Independent risk factors for mortality included: older age (OR = 1.107), immunocompromised patients (OR = 8.632), severe pneumonia (OR = 51.244), quick Sepsis-related Organ Failure Assessment (qSOFA) score ≥2 (OR = 6.187), exposure to tigecycline before infection (OR = 24.702), and prolonged ICU stay (OR = 0.987). Thirty-day mortality was significantly lower in patients receiving ceftazidime-avibactam (CAZ-AVI) containing regimens than patients receiving polymyxin B sulfate (PB) containing regimens (P = 0.048). qSOFA score had a good prognostic effect [area under receiver operating characteristic curve (AUROC) of 0.838].
Active screening of CRKP for the high-risk populations, especially elderly patients, is significant for early detection and successful management of CRKP infection.
耐碳青霉烯类肺炎克雷伯菌(CRKP)引起的医院获得性肺炎(HAP),尤其是在老年患者中,导致高发病率和死亡率。目前缺乏关于老年患者CRKP肺部感染的危险因素、死亡率和抗菌药物敏感性的研究。
进行一项回顾性病例对照研究,时间跨度为2019年1月至2021年12月。纳入诊断为由[未提及具体病原体,原文此处缺失信息]引起的HAP的老年住院患者(≥65岁)。收集临床数据。采用单因素和多因素逻辑回归分析来识别危险因素。使用倾向得分匹配以尽量减少潜在混杂变量的影响。采用Kaplan-Meier分析比较生存率。
共招募了115例CRKP感染患者和78例对碳青霉烯类敏感的肺炎克雷伯菌(CSKP)感染患者。CRKP感染有四个独立危险因素:从入院到呼吸道标本培养阳性期间入住重症监护病房(ICU)的病史(比值比(OR)=2.530)、Charlson合并症指数评分≥3(OR = 2.420)、先前接触过碳青霉烯类药物(OR = 5.280)以及在之前3年内有过[未提及具体病原体,原文此处缺失信息]感染或定植(OR = 18.529)。全因30天死亡率为22.3%,CRKP和CSKP感染的死亡率分别为28.7%和12.8%。死亡率的独立危险因素包括:年龄较大(OR = 1.107)、免疫功能低下患者(OR = 8.632)、重症肺炎(OR = 51.244)、快速序贯器官衰竭评估(qSOFA)评分≥2(OR = 6.187)、感染前使用替加环素(OR = 24.702)以及ICU住院时间延长(OR = 0.987)。接受含头孢他啶-阿维巴坦(CAZ-AVI)方案治疗的患者30天死亡率显著低于接受含硫酸多粘菌素B(PB)方案治疗的患者(P = 0.048)。qSOFA评分具有良好的预后效果[受试者操作特征曲线下面积(AUROC)为0.838]。
对高危人群,尤其是老年患者进行CRKP的主动筛查,对于CRKP感染的早期发现和成功管理具有重要意义。