Clinical characteristics, risk factors, and outcomes of patients with polymicrobial Pseudomonas aeruginosa bloodstream infections

Author:

Zheng Cheng1,Wang Guangtao23,Qiu Lingling4,Luo Xinhua5,Zhang Xijiang1,Zhong Li6,Zhang Chuming1,Lin Ronghai1,Chen Qingqing7

Affiliation:

1. Department of Critical Care Medicine, Taizhou Municipal Hospital, Taizhou, Zhejiang, China

2. Department of Neurosurgery, Municipal Hospital Affiliated to Taizhou University, Taizhou, Zhejiang, China

3. Department of Neurointensive Care Unit, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China

4. Department of Neurology, Taizhou Municipal Hospital, Taizhou, Zhejiang, China

5. Department of Clinical Microbiology Laboratory, Taizhou Municipal Hospital, Taizhou, Zhejiang, China

6. Department of Critical Care Medicine, Huzhou First People’s Hospital, Huzhou, Zhejiang, China

7. Department of Critical Care Medicine, Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, Taizhou, China

Abstract

Background: Previous studies on polymicrobial Pseudomonas aeruginosa bloodstream infections (Pa-BSIs) are dated, and it is necessary to reanalyze polymicrobial Pa-BSIs. The aim of this study was to investigate clinical characteristics and risk factors for polymicrobial Pa-BSI in comparison with monomicrobial Pa-BSI. Methods: A double-center retrospective observational study was performed between January 1, 2013 and June 30, 2022, in two tertiary hospitals. All patients with Pa-BSI were enrolled, and their clinical data were collected by reviewing electronic medical records. Results: A total of 278 patients with Pa-BSI were enrolled, including 77 patients (27.7%) with polymicrobial Pa-BSI. Compared with monomicrobial Pa-BSI, the main source of polymicrobial Pa-BSI was pneumonia (49.4% vs 31.3%, p < 0.01), whereas the main source of monomicrobial Pa-BSI was primary BSIs (21.9% vs 2.6%, p = 0.04). In multivariate analysis, a history of cerebrovascular accident (CVA) (adjusted odds ratio [OR], 3.62; 95% CI, 1.46-8.92) was independently associated with polymicrobial Pa-BSI. Primary BSI was associated with monomicrobial Pa-BSI (OR, 0.08; 95% CI, 0.02-0.38). Patients with polymicrobial Pa-BSI had a longer intensive care unit (ICU) length of stay after onset of BSI than those with monomicrobial Pa-BSI (2 [2, 16] vs 13 [3.75, 29], p = 0.02). Conclusion: Patients with Pa-BSI and the presence of CVA need to be alert to the possibility of polymicrobial BSI occurrence. Prolonged ICU stay and pneumonia as a source of BSI warrant clinician attention for polymicrobial Pa-BSI, and primary BSIs are likely associated with monomicrobial BSIs.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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