2022
DOI: 10.1007/s40261-022-01193-z
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Efficacy and Safety of Subcutaneous Esketamine in the Treatment of Suicidality in Major Depressive Disorder and Bipolar Depression

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Cited by 9 publications
(3 citation statements)
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“…The majority of the studies discussed are open-label involving small cohorts, underscoring the need for more comprehensive research through large-scale RCTs with extended follow-up durations. Presented research also suggest ketamine's antisuicidal properties with only one study reporting worsening in this symptomatic dimension (17,23,32,35). The risk of the affective switch seems low, and transient self-limiting adverse effects like drowsiness, dizziness, blurred vision, nausea, dissociative symptoms, and headaches confirm the good safety profile of ketamine in BD (12).…”
Section: Discussionmentioning
confidence: 73%
See 1 more Smart Citation
“…The majority of the studies discussed are open-label involving small cohorts, underscoring the need for more comprehensive research through large-scale RCTs with extended follow-up durations. Presented research also suggest ketamine's antisuicidal properties with only one study reporting worsening in this symptomatic dimension (17,23,32,35). The risk of the affective switch seems low, and transient self-limiting adverse effects like drowsiness, dizziness, blurred vision, nausea, dissociative symptoms, and headaches confirm the good safety profile of ketamine in BD (12).…”
Section: Discussionmentioning
confidence: 73%
“…Reported side effects (i.e., feeling dizzy, cognitive impairment, dissociation, nausea, headache, odd sensations, flatulence, and blurred vision) were transient. The cases of discontinuation were rare (14, 16,18,19,21,23,24,32,35). One report of increased suicidality was described above and seems an isolated event (17).…”
Section: Ketamine Safety and Tolerability In Bipolar Depressionmentioning
confidence: 98%
“…In 2019, the United States Food and Drug Administration (FDA) approved the S-enantiomer form of ketamine, esketamine (brand name Spravato), for use in patients with Treatment-Resistant Depression (TRD) and Major Depressive Disorder (MDD) with suicidal ideation. Spravato's efficacy has been demonstrated in numerous follow-on studies in a variety of populations ( 5 , 7 13 ). While Spravato's efficacy and the need for new mental health treatments has driven significant growth, a major limitation to more rapid and accessible uptake is the monitoring requirements necessary during and after Spravato dosing as a part of its FDA-mandated Risk Evaluation and Mitigation Strategy (REMS) program ( 14 , 15 ).…”
Section: Introductionmentioning
confidence: 99%