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. 2024 Mar 6;11(5):ofae126.
doi: 10.1093/ofid/ofae126. eCollection 2024 May.

All-cause and Infection-attributable Mortality Amongst Adults With Bloodstream Infection-a Population-based Study

Affiliations

All-cause and Infection-attributable Mortality Amongst Adults With Bloodstream Infection-a Population-based Study

Jonathan Underwood et al. Open Forum Infect Dis. .

Abstract

Background: Bloodstream infections (BSIs) are common, life-threatening infections. However, it remains unclear whether deaths following BSIs are primarily from uncontrolled infection or underlying comorbidities. We aimed to determine the overall mortality, infection-attributable mortality, and causes of death for four leading BSI pathogens.

Methods: This retrospective cohort study was conducted within the Secure Anonymized Information Linkage Databank, containing anonymized population-scale electronic health record data for Wales, UK. We included adults with Escherichia coli, Klebsiella spp, Pseudomonas aeruginosa, and Staphylococcus aureus BSI between 2010 and 2022 using linked data from Public Health Wales and the Office for National Statistics. Thirty-day all-cause and sepsis-specific mortality, as a proxy for infection-attributable mortality, were compared using Cox proportional hazards and competing risk regression, respectively.

Results: We identified 35 691 adults with BSI (59.6% E coli). Adjusted analyses revealed that all organisms had a higher 30-day mortality versus E coli with Pseudomonas aeruginosa the highest (hazard ratio, 1.96 [1.76-2.17], P < .001). Cancer was the leading cause of death following BSIs for all organisms, particularly deaths occurring between 30 and 90 days (35.9%). A total of 25.5% of deaths within 30 days involved sepsis. Methicillin-resistant Staphylococcus aureus was associated with the highest sepsis mortality versus E coli (hazard ratio, 2.56 [2.10-3.12], P < .001). Peak C-reactive protein was positively associated with increased sepsis mortality (P < .001).

Conclusions: This population-level study challenges the assumption that most deaths following BSIs are directly attributable to uncontrolled infection, particularly subacutely more than 30 days from BSI. Our findings underscore the need for reevaluating clinical trial design and developing better preventive strategies for BSIs.

Keywords: bloodstream infection; cause of death; inflammation; mortality; sepsis.

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Conflict of interest statement

Potential conflicts of interest. The authors nor their institutions have not received any payments or services in the past 36 months from a third party that could be perceived to influence, or give the appearance of potentially influencing, the submitted work. All authors: No reported conflicts.

Figures

Figure 1.
Figure 1.
Mortality following bloodstream infection—stratified by organism. Abbreviations: MRSA, methicillin-resistant Staphylococcus aureus; MSSA, methicillin-sensitive Staphylococcus aureus; PsA, Pseudomonas aeruginosa.
Figure 2.
Figure 2.
Underlying cause of death by organism. Red bars indicate infective causes. Causes with fewer than 5 deaths not displayed for SAIL information governance reasons.

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