Impact of Continuous Infusion Ketamine Compared to Continuous Infusion Benzodiazepines on Delirium in the Intensive Care Unit

Author:

Vollmer Nicholas J.1ORCID,Wieruszewski Erin D.12ORCID,Nei Andrea M.1ORCID,Mara Kristin C.3,Rabinstein Alejandro A.4,Brown Caitlin S.12

Affiliation:

1. Department of Pharmacy, Mayo Clinic Hospital, Rochester, MN, USA

2. Department of Emergency Medicine, Mayo Clinic Hospital, Rochester, MN, USA

3. Department of Quantitative Health Sciences, Mayo Clinic Hospital, Rochester, MN, USA

4. Department of Neurology, Mayo Clinic Hospital, Rochester, MN, USA

Abstract

Purpose: The purpose of this study was to evaluate rates of delirium or coma-free days between continuous infusion sedative-dose ketamine and continuous infusion benzodiazepines in critically ill patients. Materials and Methods: In this single-center, retrospective cohort adult patients were screened for inclusion if they received continuous infusions of either sedative-dose ketamine or benzodiazepines (lorazepam or midazolam) for at least 24 h, were mechanically ventilated for at least 48 h and admitted to the intensive care unit of a large quaternary academic center between 5/5/2018 and 12/1/2021. Results: A total of 165 patients were included with 64 patients in the ketamine group and 101 patients in the benzodiazepine group (lorazepam n = 35, midazolam n = 78). The primary outcome of median (IQR) delirium or coma-free days within the first 28 days of hospitalization was 1.2 (0.0, 3.7) for ketamine and 1.8 (0.7, 4.6) for benzodiazepines (p = 0.13). Patients in the ketamine arm spent a significantly lower proportion of time with RASS −3 to +4, received significantly higher doses and longer durations of propofol and fentanyl infusions, and had a significantly longer intensive care unit length of stay. Conclusions: The use of sedative-dose ketamine had no difference in delirium or coma-free days compared to benzodiazepines.

Publisher

SAGE Publications

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