Interestingly I’ve taken Ketamine for Pain Management but not for my Bipolar Disorder. When I spoke with my doctor about years ago he said that the percentage of people with my level of depression experiencing high results was low. The key to remember is everyone is different. The treatment is nothing like Electro Convulsive Therapy. It’s given in an IV and can take an hour to an hour and a half. During my treatments, I felt like I was on an LSD trip and stayed grounded by listening to calming music. If you let yourself fight the effect of the drug I can see where some would get anxious. Ask your doctor before the treatment of the ways to have the best experience.
August 10, 2020
In adult patients with major depressive disorder (MDD) or bipolar disorder (BD), the use of intravenous (IV) ketamine is generally well tolerated and safe when administered mainly as an acute treatment, according to a study published in the journal Expert Opinion on Drug Safety.
In the current analysis, retrospective data derived from a post hoc analysis (ClinicalTrials.gov identifier:NCT04209296) from the Canadian Rapid Treatment of Excellence (CRTCE), conducted in Mississauga, Ontario, Canada, were examined. Individuals who had been referred to the CRTCE by primary care physicians, psychiatrists, or nurse practitioners for treatment-resistant depression (TRD)—that is, MDD or BP—were enrolled. Individuals with posttraumatic stress disorder or obsessive-compulsive disorder were also eligible for enrollment, provided the presence of a depressive episode was their main complaint. Patients with dementia, psychosis, and/or active substance or alcohol use disorder were excluded from this study.
Data were analyzed from a total of 203 patients with TRD who were treated with repeat-dose IV ketamine. The participants received 723 IV ketamine infusions at the CRCTE between July 2018 and December 2019. Safety was evaluated as hemodynamic changes. Tolerability was assessed via the reporting of adverse events and dissociation symptom severity, which were calculated with use of the Clinician-Administered Dissociative States Scale (CADSS).
IV ketamine was administered adjunctively with patients’ current, concomitant medications, in order to try to increase participants’ acceptability and feasibility of treatment. In an attempt to minimize the likelihood of hazardous drug-drug interactions, the participants were instructed not to take any medications for 6 hours prior to the infusion and for 4 hours after the infusion. The participants received a total of 4 infusions over a period of 1 to 2 weeks.Today’s Top Picks for You on Psychiatry AdvisorPsychosocial Factors Linked to the Development of MDD in Adults With Type 2 DiabetesCord Blood Does Not Improve Socialization Skills in AutismLow Dose Ketamine Accelerates Onset of Antidepressant Effect for Electroconvulsive Therapy
Overall, approximately 40% (81 of 203) of participants did not have a dose optimization and received all 4 infusions at the index dose (ie, 0.5 mg/kg). In contrast, approximately 60% (123 of 203) of participants received 2 doses at the index dose and then received 2 optimized doses (ie, 0.75 mg/kg). In fact, a total of 203 infusions were received by the participants at the optimized dose.
Significant transient increases in patients’ mean blood pressure and heart rate were reported during the infusion. Overall, 44.3% of participants fulfilled criteria for treatment-emergent hypertension (ie, blood pressure ≥165/100 mm Hg), with 12% of the patients reporting hypertension that necessitated pharmacologic intervention. In particular, systolic blood pressure increased by 17.9 ± 13.4 mm Hg, diastolic blood pressure by 12.9 ± 10.3 mm Hg, and heart rate by 8.4 ± 10.1 beats per minute (P <.0001). Blood pressure and heart rate began to decrease, however, once the infusion had been completed. In fact, at 20 minutes postinfusion, most of the participants’ cardiovascular measures had returned to within 10% of their baseline values.
Results of the study demonstrated that ketamine was well tolerated, with <5% of participants withdrawing from the study because of tolerability issues. The adverse events most often reported included drowsiness in 56.4% of participants, dizziness in 45.2%, dissociation in 35.6%, and nausea in 13.3%. Additionally, the severity of dissociation was significantly diminished following the initial infusion but plateaued with subsequent infusions.
Limitations of the study include the nature of retrospective analysis of outpatients without a control group, and lack of data on long-term exposure. Furthermore, the CADSS was not developed primarily as a safety measure for ketamine treatment, and therefore may underestimate the extent of dissociation experience with ketamine.
The investigators concluded that the use of IV ketamine in this patient population was safe and well tolerated, with no participants exhibiting psychosis, mania, or new-onset suicidality. The researchers support the use of multidisciplinary treatments at the point of care, in order to guarantee the safe and skillful administration of IV ketamine.
Rodrigues NB, McIntyre RS, Lipsitz O, et al. Safety and tolerability of IV ketamine in adults with major depressive or bipolar disorder: results from the Canadian rapid treatment center of excellence [published online June 15, 2020]. Expert Opin Drug Saf. doi: 10.1080/14740338.2020.1776699