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Murine Oropharyngeal Aspiration Model of Ventilator-associated and Hospital-acquired Bacterial Pneumonia
Published on: June 28, 2018
Community-acquired bacterial co-infection predicts severity and mortality in influenza-associated pneumonia admitted
Fei Teng1, Xin Liu1, Shu-Bin Guo1
1Emergency Department, Beijing Chao-Yang Hospital, Capital Medical University, Chaoyang District, Beijing 100020, China.
Background:
Influenza is frequently complicated by bacterial co-infection, causing additional hospitalization and mortality. We determined the incidence, risk factors and outcomes of patients with influenza-associated community-acquired bacterial co-infection.
Method:
This was a retrospective, observational study. Influenza was diagnosed using the polymerase chain reaction. Co-infection had to be confirmed using standard bacteriological tests. The primary endpoint was presence of community-acquired co-infection, and the secondary endpoint was in-hospital mortality.
Results:
During the 8 influenza seasons from 2010 to 2018, of the 209 influenza-associated pneumonia admitted patients, 41 (19.6%) were identified with community-acquired bacterial co-infections and Staphylococcus aureus was the predominant strain. Compared with patients without co-infection, patients with co-infection had similar demographic characteristics and co-morbidities, obtained a higher APACHE II score and a higher SOFA score, and had higher ratio of sepsis shock, invasive mechanical ventilation, and ICU requirement. In-hospital mortality independently associated with bacterial co-infection (adjusted hazard ratio (aHR) 2.619; 95%CI 1.252-5.480; p = 0.011); in subgroup S. aureus (aHR 6.267; 95%CI 2.679-14.662; p < 0.001) and other pathogens (aHR 2.964; 95%CI 1.160-7.577; p = 0.023); and in subgroup positive findings in bloodstream (aHR 7.420; 95%CI 2.712-20.302; p < 0.001) and positive findings in other site (aHR 3.427; 95%CI 1.514-7.757; p = 0.003).
Conclusion:
Community-acquired bacterial co-infection was frequent in influenza-associated pneumonia, without risk factor identified yet. Bacterial co-infection was likely to predict severity, and was an independent risk factor for in-hospital mortality. Co-infection of Staphylococcus aureus with influenza was identified as a lethal synergism, and should be targeted when developing clinical antibiotic strategies.
Insights
Bacterial co-infections frequently complicate influenza, increasing severity and mortality. Staphylococcus aureus co-infection with influenza presents a lethal combination requiring targeted antibiotic strategies.
Area of Science:
- Infectious Diseases
- Pulmonology
- Critical Care Medicine
Background:
- Influenza often leads to bacterial co-infections, significantly increasing hospitalization and mortality rates.
- Understanding the incidence, risk factors, and outcomes of these co-infections is crucial for patient management.
Purpose of the Study:
- To determine the incidence, risk factors, and outcomes of community-acquired bacterial co-infections in patients with influenza-associated pneumonia.
- To identify specific pathogens and their impact on patient mortality.
Main Methods:
- Retrospective, observational study analyzing data from 8 influenza seasons (2010-2018).
- Influenza diagnosed via polymerase chain reaction (PCR); bacterial co-infections confirmed by standard bacteriological tests.
- Primary endpoint: presence of community-acquired co-infection; secondary endpoint: in-hospital mortality.
Main Results:
- 19.6% of influenza-associated pneumonia patients had bacterial co-infections, with Staphylococcus aureus being predominant.
- Co-infected patients showed higher severity scores (APACHE II, SOFA) and increased rates of sepsis shock, mechanical ventilation, and ICU admission.
- Bacterial co-infection, particularly with S. aureus, was an independent predictor of in-hospital mortality.
Conclusions:
- Community-acquired bacterial co-infection is common in influenza-associated pneumonia and predicts increased severity and mortality.
- Staphylococcus aureus co-infection with influenza demonstrates a lethal synergistic effect.
- Targeted antibiotic strategies are essential for managing these severe co-infections.
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