Conclusions
In critically ill adult patients with respiratory failure or shock or both, we found that the OR for delirium doubled when patients were exposed to a wide group of first-, second-, and third-generation cephalosporins but not to penicillins, carbapenems, cefepime, fluoroquinolones, or macrolides. Future studies need to be conducted to determine the effect of different classes of antimicrobials on delirium and, in particular, of newer antibiotics, whose use has increased in recent years with the development of multidrug-resistant organisms. At this time, clinicians should remain hesitant about reflexively shifting active antimicrobial strategies simply because of the occurrence of delirium.
Abbreviations
BRAIN-ICU: Bringing to Light the Risk Factors and Incidence of Neuropsychological Dysfunction in Intensive Care Unit Survivors; CAM-ICU: Confusion Assessment Method for the intensive care unit; CI: Confidence interval; ICU: Intensive care unit; IQCODE: Short Informant Questionnaire on Cognitive Decline in the Elderly; IQR: Interquartile range; OR: Odds ratio; PAD: Pain, Agitation, and Delirium; SOFA: Sequential Organ Failure Assessment
Acknowledgments
None.
Funding
This work was supported by the National Institutes of Health and its National Institutes on Aging (R01 AG027472 and R01 AG035117 to EWE); the National Heart, Lung, and Blood Institute (R01 HL111111 to PPP); the National Institute of General Medical Sciences (R01 GM120484 to MBP); and the National Center for Advancing Translational Sciences (UL1 TR000445 for REDCap and Vanderbilt Institute for Clinical and Translational Research Grant VR22411). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. EWE is supported by the Veterans Affairs Tennessee Valley Geriatric Research, Education and Clinical Center (Nashville, TN, USA).
Availability of data and materials
The datasets used or analyzed (or both) during the present study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The Vanderbilt University Institutional Review Board approved the study protocol.
Consent for publication
Not applicable.
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Crit Care. 2018;22(337) © 2018 BioMed Central, Ltd.
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