Abstract

BackgroundTo compare illness characteristics, treatment history, response and durability, and suicidality scores over a 5-year period in patients with treatment-resistant bipolar depression participating in a prospective, multicenter, open-label registry and receiving Vagus Nerve Stimulation Therapy (VNS Therapy) plus treatment-as-usual (VNS + TAU) or TAU alone.MethodsResponse was defined as ≥ 50% decrease from baseline Montgomery–Åsberg Depression Rating Scale (MADRS) total score at 3, 6, 9, or 12 months post-baseline. Response was retained while MADRS score remained ≥ 40% lower than baseline. Time-to-events was estimated using Kaplan–Meier (KM) analysis and compared using log-rank test. Suicidality was assessed using the MADRS Item 10 score.ResultsAt baseline (entry into registry), the VNS + TAU group (N = 97) had more episodes of depression, psychiatric hospitalizations, lifetime suicide attempts and higher suicidality score, more severe symptoms (based on MADRS and other scales), and higher rate of prior electroconvulsive therapy than TAU group (N = 59). Lifetime use of medications was similar between the groups (a mean of 9) and was consistent with the severe treatment-resistant nature of their depression. Over 5 years, 63% (61/97) in VNS + TAU had an initial response compared with 39% (23/59) in TAU. The time-to-initial response was significantly quicker for VNS + TAU than for TAU (p < 0.03). Among responders in the first year after implant, the KM estimate of the median time-to-relapse from initial response was 15.2 vs 7.6 months for VNS + TAU compared with TAU (difference was not statistically significant). The mean reduction in suicidality score across the study visits was significantly greater in the VNS + TAU than in the TAU group (p < 0.001).ConclusionsThe patients who received VNS + TAU included in this analysis had severe bipolar depression that had proved extremely difficult to treat. The TAU comparator group were similar though had slightly less severe illnesses on some measures and had less history of suicide attempts. Treatment with VNS + TAU was associated with a higher likelihood of attaining a response compared to TAU alone. VNS + TAU was also associated with a significantly greater mean reduction in suicidality.LimitationsIn this registry study, participants were not randomized to the study treatment group, VNS Therapy stimulation parameters were not controlled, and there was a high attrition rate over 5 years.Trial registration ClinicalTrials.gov NCT00320372. Registered 3 May 2006, https://clinicaltrials.gov/ct2/show/NCT00320372 (retrospectively registered)

Highlights

  • To compare illness characteristics, treatment history, response and durability, and suicidality scores over a 5-year period in patients with treatment-resistant bipolar depression participating in a prospective, multicenter, open-label registry and receiving Vagus Nerve Stimulation Therapy (VNS Therapy) plus treatment-as-usual (VNS + TAU) or TAU alone

  • In this report—using the 5-year VNS treatment-resistant depression (TRD) registry discussed above—we examine the pre-treatment clinical characteristics and the clinical outcomes in a subgroup of TRD patients with treatment-resistant bipolar depression (TRBD) comparing VNS + TAU versus TAU alone based on the following areas of interest: I

  • To be eligible to participate in the VNS TRD Registry, participants had to be over 18 years of age, experiencing an active major depressive episode of 2 years or longer in duration, or had a history of at least 3 major depressive episodes, including the current depressive episode, and a history of inadequate response to 4 or more adequate antidepressant treatments, which could include electroconvulsive therapy (ECT)

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Summary

Introduction

Treatment history, response and durability, and suicidality scores over a 5-year period in patients with treatment-resistant bipolar depression participating in a prospective, multicenter, open-label registry and receiving Vagus Nerve Stimulation Therapy (VNS Therapy) plus treatment-as-usual (VNS + TAU) or TAU alone. The UK National Institute for Health and Social Care (NICE) guidelines for the management of bipolar depression list just 3 treatments that are supported by replicated randomized controlled trials: lamotrigine, quetiapine, and olanzapine (with or without fluoxetine) (National Institute for Health and Care Excellence 2014). Since publication of the NICE guidelines, additional evidence has emerged from randomized controlled trials supporting the efficacy of lurasidone for the acute treatment of bipolar depression (Loebel et al 2014a, b). This limited number of treatment options for bipolar depression is further compromised as quetiapine and olanzapine are often poorly tolerated due to weight gain and sedation (Calabrese et al 2005; Tohen et al 2003). TRBD is the major contributor to the enormous burden of disease associated with bipolar disorder (Ferrari et al 2016)

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