Murat Altinay1, Harish Karne1, Amit Anand1. 1. Altinay, MD, Karne, BS, Anand, MD, Center for Behavioral Health, Cleveland Clinic, Cleveland, ohio.
Abstract
Introduction and Background: Patients with depression who fail to respond to at least two antidepressants in their current episode are considered to have Treatment Resistant Depression (TRD). ECT is an effective treatment of TRD but cognitive side effects limit its use. Ketamine elicits a rapid antidepressant response in sub-anesthetic repeated doses. ECT and ketamine may be modulating the glutamate system, therefore when administered in an interleaved fashion, they could have a synergistic effect. Methods: 15 TRD patients were recruited and 12 were included in the analysis. Patients were randomly assigned to an ECT + iv. ketamine or ECT + iv. placebo (midazolam). At baseline and before each infusion, depression severity scales were administered. At baseline, halfway through and at the end of the study, cognitive tests were administered. Results: There was no difference between the ketamine and placebo arms, per change in 17-item Hamilton Depression Scores (HAM-D), Young Mania Rating Scores or cognitive tests. Per HAMD scores, 3 ECT +ketamine subjects (42%) showed early remission (HAMD < 8) and maintained euthymia for 3 additional visits. None of the ECT +midazolam subjects (0%) achieved early remission. This difference showed a trend level significance (Chi square P-Value = 0.0910). Conclusion: The results of the study were limited due to the small sample size. However, a trend level difference in rates of early remission was seen, suggesting that ketamine + ECT may lead to a faster symptom relief. A larger sample size is needed for statistical confirmation.
RCT Entities:
Introduction and Background: Patients with depression who fail to respond to at least two antidepressants in their current episode are considered to have Treatment Resistant Depression (TRD). ECT is an effective treatment of TRD but cognitive side effects limit its use. Ketamine elicits a rapid antidepressant response in sub-anesthetic repeated doses. ECT and ketamine may be modulating the glutamate system, therefore when administered in an interleaved fashion, they could have a synergistic effect. Methods: 15 TRD patients were recruited and 12 were included in the analysis. Patients were randomly assigned to an ECT + iv. ketamine or ECT + iv. placebo (midazolam). At baseline and before each infusion, depression severity scales were administered. At baseline, halfway through and at the end of the study, cognitive tests were administered. Results: There was no difference between the ketamine and placebo arms, per change in 17-item Hamilton Depression Scores (HAM-D), Young Mania Rating Scores or cognitive tests. Per HAMD scores, 3 ECT +ketamine subjects (42%) showed early remission (HAMD < 8) and maintained euthymia for 3 additional visits. None of the ECT +midazolam subjects (0%) achieved early remission. This difference showed a trend level significance (Chi square P-Value = 0.0910). Conclusion: The results of the study were limited due to the small sample size. However, a trend level difference in rates of early remission was seen, suggesting that ketamine + ECT may lead to a faster symptom relief. A larger sample size is needed for statistical confirmation.
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