Effects of Ketamine Infusion on Breathing and Encephalography in Spontaneously Breathing ICU Patients

Author:

Suleiman Aiman123,Santer Peter1,Munoz-Acuna Ronny1,Hammer Maximilian1,Schaefer Maximilian S.124,Wachtendorf Luca J.125,Rumyantsev Sandra6,Berra Lorenzo7,Chamadia Shubham7,Johnson-Akeju Oluwaseun78,Baedorf-Kassis Elias N.9,Eikermann Matthias510ORCID

Affiliation:

1. Department of Anesthesia, Critical Care & Pain Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA

2. Center for Anesthesia Research Excellence (CARE), Beth Israel Deaconess Medical Center, Boston, MA, USA

3. Department of Anesthesia and Intensive Care, Faculty of Medicine, University of Jordan, Amman, Jordan

4. Department of Anesthesiology, Duesseldorf University Hospital, Germany

5. Department of Anesthesiology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, USA

6. Pharmacy, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA

7. Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

8. McCance Center for Brain Health, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

9. Department of Medicine, Division of Pulmonary and Critical Care, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA

10. Klinik für Anästhesiologie und Intensivmedizin, Universität Duisburg-Essen, Essen, Germany

Abstract

Background Preclinical studies suggest that ketamine stimulates breathing. We investigated whether adding a ketamine infusion at low and high doses to propofol sedation improves inspiratory flow and enhances sedation in spontaneously breathing critically ill patients. Methods In this prospective interventional study, twelve intubated, spontaneously breathing patients received ketamine infusions at 5 mcg/kg/min, followed by 10 mcg/kg/min for 1 h each. Airway flow, pressure, and esophageal pressure were recorded during a spontaneous breathing trial (SBT) at baseline, and during the SBT conducted at the end of each ketamine infusion regimen. SBT consisted of one-minute breathing with zero end-expiratory pressure and no pressure support. Changes in inspiratory flow at the pre-specified time points were assessed as the primary outcome. Ketamine-induced change in beta-gamma electroencephalogram power was the key secondary endpoint. We also analyzed changes in other ventilatory parameters respiratory timing, and resistive and elastic inspiratory work of breathing. Results Ketamine infusion of 5 and 10 mcg/kg/min increased inspiratory flow (median, IQR) from 0.36 (0.29-0.46) L/s at baseline to 0.47 (0.32-0.57) L/s and 0.44 (0.33-0.58) L/s, respectively ( p = .013). Resistive work of breathing decreased from 0.4 (0.1-0.6) J/l at baseline to 0.2 (0.1-0.3) J/l after ketamine 10 mcg/kg/min ( p = .042), while elastic work of breathing remained unchanged. Electroencephalogram beta-gamma power (19-44 Hz) increased compared to baseline ( p < .01). Conclusions In intubated, spontaneously breathing patients receiving a constant rate of propofol, ketamine increased inspiratory flow, reduced inspiratory work of breathing, and was associated with an “activated” electroencephalographic pattern. These characteristics might facilitate weaning from mechanical ventilation.

Funder

Jeffrey and Judy Buzen

Publisher

SAGE Publications

Subject

Critical Care and Intensive Care Medicine

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