4.6 Article

Clinical Characteristics and Prognosis of Hospital-Acquired Klebsiella pneumoniae Bacteremic Pneumonia versus Escherichia coli Bacteremic Pneumonia: A Retrospective Comparative Study

Journal

INFECTION AND DRUG RESISTANCE
Volume 16, Issue -, Pages 4977-4994

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IDR.S419699

Keywords

Escherichia coli; Klebsiella pneumoniae; hospital-acquired pneumonia; bacteremic pneumonia; 30-day mortality

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This study aimed to investigate the variations in clinical features and prognosis of HABP caused by E. coli and K. pneumoniae. Among the HABP patients, a higher proportion of males, ICU admission, carbapenem-resistant strains, and other risk factors were observed in the K. pneumoniae group compared to the E. coli group. The 30-day mortality rate was also higher in the K. pneumoniae group. The findings suggest that the clinical features and prognosis of HABP vary depending on the causative bacteria.
Objective: This research aimed to investigate the variations in clinical features and prognosis of HABP caused by E. coli and K. pneumoniae. We also aimed to evaluate the risk variables related to 30-day death in the investigated groups.Methods: A single-center retrospective cohort research lasting four years was performed. A total of 117 patients with HABP were involved in this research. The primary prognosis was 30-day death.Results: Among 117 patients with HABP, 60 patients were infected with K. pneumoniae (KP-HABP), and 57 patients were infected with E. coli (E. coli-HABP). A higher proportion of males, ICU admission, undergoing tracheotomy and trachea cannulation, carbapenem-resistant strains, inappropriate empirical therapy (IET), immune compromise, diabetes mellitus, and sepsis were observed in the patients with KP-HABP (all P < 0.05). Meanwhile, the median SOFA score and Pitt score were significantly (P < 0.001) higher in the KP-HABP group compared to the E. coli-HABP group. The 30-day death was 48.33% in the KP-HABP group and 24.56% in the E. coli-HABP group (P = 0.008). After adjusting for the main covariates, the hazard ratios for 30-day mortality in KP-HABP were 1.58 (95% CI:0.80-3.12), 3.24 (95% CI:1.48-7.06), 5.67 (95% CI:2.00-16.07), and 5.99 (95% CI:2.10-17.06), respectively. Multivariate logistic regression models revealed that IET, hypoproteinaemia, cerebral vascular disease (CVD), and SOFA score > 5.0 were the independent risk variables for 30-day death in KP-HABP. Simultaneously, SOFA score > 4.0 and Pitt score > 2.0 were independent risk factors for 30-day mortality in E. coli-HABP. Conclusion: The clinical features of HABP vary depending on whether it is caused by Escherichia coli or K. pneumoniae. KP-HABP patients have higher 30-day mortality than E. coli-HABP patients. To ensure greater validity, it is necessary to further verify this conclusion using a larger sample size.

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