Abstract

BackgroundBloodstream infections (BSI) and delirium are frequent in critically ill patients. During systemic inflammatory response to BSI, cytokines may interact with neurotransmitters and neuronal receptors driving acute brain dysfunction. However, prospectively collected data on incidence, prediction and impact of delirium in association with BSI are lacking. This study aimed to determine the incidence and predictors of new-onset delirium and its impact on outcome in critically ill adult patients with BSI.MethodsFrom 2011 to 2014, all consecutive adult patients with BSI treated in the intensive care units of an academic medical care center were identified. Pertinent clinical and microbiological data including the Intensive Care Delirium Screening Checklist (ICDSC) were assessed. Multivariable analysis was performed to identify variables independently associated with ICDSC ≥4.ResultsAmong 240 patients, 145 (60%) had an ICDSC ≥4 (i.e., delirium). In-hospital mortality was 34%. Delirious patients had a higher mortality (40 vs. 23%; p = 0.005), a lower proportion with return to functional baseline (30 vs. 46%; p = 0.012), and a higher proportion with unfavorable outcome in survivors (74 vs. 54%; p = 0.010). Multivariable analyses revealed age (OR 1.04, 95% CI 1.02–1.06), male gender (OR 2.26, 95% CI 1.17–4.36), and the number of catheters and drainages before diagnosis of BSI (OR for every additional catheter = 1.14, 95% CI 1.04–1.25) as independent predictors for delirium (adjusted for SAPS [simplified acute physiology score] II, Riker Sedation-Agitation Scale [SAS], Sequential Organ Failure Assessment [SOFA] score, dementia and/or leukoencephalopathy, and albumin levels).ConclusionsThe incidence of delirium in patients with BSI is high and associated with adverse outcome. The number of catheters and drainages may constitute a useful and readily available predictor of delirium in patients with BSI allowing to identify patients at high risk. Ultimately, reliable identification of patients at increased risk for delirium is key for allocation of specific prevention strategies.

Highlights

  • IntroductionDuring systemic inflam‐ matory response to Bloodstream infections (BSI), cytokines may interact with neurotransmitters and neuronal receptors driving acute brain dysfunction

  • Bloodstream infections (BSI) and delirium are frequent in critically ill patients

  • It seems evident that activation of the immune system can induce acute brain dysfunction and that sepsis, is a major risk factor for delirium, most studies are hampered by the fact that sepsis encompasses a variety of different sources and states of infection and do not focus on the immediate and acute neurological impact of specific infections in critical care settings

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Summary

Introduction

During systemic inflam‐ matory response to BSI, cytokines may interact with neurotransmitters and neuronal receptors driving acute brain dysfunction. Sepsis affects more than 25% [3,4,5], and delirium is present in as many as 80% of mechanically ventilated patients [6,7,8] and in up to 50% of non-mechanically ventilated patients [9,10,11] They often concur, and a number of recent studies provide evidence of complex underlying mechanisms explaining how systemic inflammatory response drives acute brain dysfunction, possibly explaining this association. Bloodstream infections (BSI) belong to the most important, frequent, and clearly defined infections encountered in ICUs, prospective studies regarding the incidence, prediction, and impact of delirium in association with BSI are not yet published

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