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ICU重症肺炎患者耐碳青霉烯类肺炎克雷伯菌与产超广谱β内酰胺酶大肠埃希菌感染耐药性及危险因素

Analysis of drug resistance and infection-related risk factors of carbapenem-resistant Klebsiella pneumoniae and extended-spectrum β-lactamase-producing Escherichia coli in patients with severe pneumonia in ICU

  • 摘要:
    目的 分析建立人工气道的重症肺炎患者支气管肺泡灌洗液(bronchoalveolar lavage fluid, BALF)中耐碳青霉烯类肺炎克雷伯菌(carbapenem-resistant Klebsiella pneumoniae, CRKP)与产超广谱β内酰胺酶大肠埃希菌(extended-spectrum β-lactamase-producing Escherichia coli, ESBL-E.coli)耐药率及CRKP感染的危险因素。
    方法 选择2022年5月至2025年5月于复旦大学附属金山医院急危重病中心救治的建立人工气道的重症肺炎患者,分离培养BALF中肺炎克雷伯菌(Klebsiella pneumoniae, K. pneumoniae)与大肠埃希菌(Escherichia coli, E.coli)。比较两种细菌对各种抗生素的耐药率。采用多因素logistic回归分析评估CRKP感染的危险因素。
    结果 共纳入患者384例,培养出K. pneumoniae 330株(85.9%)及E.coli 54株(14.1%),K. pneumoniae感染率更高。K. pneumoniae耐药基因表达比例低于E.coli(37.3% vs 57.4%, P<0.01)。CRKP对头孢噻肟、头孢吡肟、氨曲南、亚胺培南的耐药率高于ESBL-E.coliP<0.003)。CRKP及ESBL-E.coli对多粘菌素、替加环素均有较高敏感性。logistic回归分析显示,机械通气时间≥7 d、联用≥2种抗生素超过7 d是感染CRKP的独立危险因素(P<0.01)。
    结论 建立人工气道的ICU重症肺炎患者肺部感染以 K. pneumoniae为主;BALF中CRKP及ESBL-E.coli对各类抗生素呈现不同程度耐药,均有多重耐药特点,且均对多粘菌素、替加环素敏感。对于CRKP感染,尤其应加强危险因素防控。

     

    Abstract:
    Objective To analyze the rates of drug resistance of carbapenem-resistant Klebsiella pneumoniae (CRKP) and extended-spectrum β-lactamase-producing Escherichia coli (ESBL-E.coli) in bronchoalveolar lavage fluid (BALF) of critically ill patients with severe pneumonia and artificial airway and risk factors of CRKP.
    Methods Patients with severe pneumonia and artificial airway treated in the Center of Emergency and Intensive Care Unit, Jinshan Hospital, Fudan University from May 2022 to May 2025 were selected. Klebsiella pneumoniae (K. pneumoniae) and Escherichia coli (E.coli) isolated and cultured from BALF of these patients were analyzed. The drug resistance rates of the two bacteria were compared. The multivariate logistic regression was used to analyze related risk factors for CRKP infection.
    Results A total of 384 patients were included, and 384 strains were cultured, including 330 strains (85.9%) of K. pneumoniae and 54 strains (14.1%) of E.coli. The infection rate of K. pneumoniae was higher. Compared with E.coli, the drug-resistant gene expression rate of K. pneumoniae was lower (37.3% vs 57.4%, P<0.01). The resistance rates of CRKP to cefotaxime, cefepime, aztreonam, and imipenem were higher than those of ESBL-E.coli (P<0.003). Both CRKP and ESBL-E.coli had high sensitivity to polymyxin and tigecycline. Multivariate logistic regression showed duration of mechanical ventilation ≥ 7 days, and combination of ≥ 2 antibiotics for over 7 days were independent risk factors for CRKP infection (P<0.01).
    Conclusions For patients with severe pneumonia and artificial airway in ICU, K. pneumoniae is the main bacterial infection. CRKP and ESBL-E.coli in BALF exhibit different degrees of drug resistance to various antibacterial agents, both have the characteristic of multidrug resistance, and are sensitive to polymyxin and tigecycline. Prevention and control of risk factors related to CRKP should be formulated particularly.

     

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