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Durability of the benefit of vagus nerve stimulation in markedly treatment-resistant major depression: a RECOVER trial report

Title: Durability of the benefit of vagus nerve stimulation in markedly treatment-resistant major depression: a RECOVER trial report
Authors: Conway, Charles R; Rush, Augustus John; Aaronson, Scott T; Bunker, Mark T; Gordon, Charles; George, Mark S; Riva-Posse, Patricio; Allen, Rebecca M; Nahas, Ziad; Kriedt, Christopher L; Zajecka, John; Dunner, David L; Quevedo, João; Sheline, Yvette; Duffy, Walter; Mickey, Brian J; Stedman, Mary; Alva, Gustavo; Manu, Lucian; Tran, Quyen; Zorumski, Charles F; Macaluso, Matthew; Banov, Michael; Cusin, Cristina; Bennett, Jeffrey I; Brown, Hunter; Way, Jeffrey; Shy, Olivia; Lee, Ying-Chieh (Lisa); McAllister-Williams, Richard Hamish; McIntyre, Roger S; Sackeim, Harold A
Contributors: LivaNova; PLC; Centers for Medicare & Medicaid Services
Source: International Journal of Neuropsychopharmacology ; volume 29, issue 1 ; ISSN 1461-1457 1469-5111
Publisher Information: Oxford University Press (OUP)
Publication Year: 2026
Description: Importance Greater levels of treatment resistance in major depressive disorder (MDD) are associated with lower rates of initial benefit and higher rates of relapse (lower durability). Objective Characterize depressive symptoms, function, and quality of life (QoL) over 24 months of adjunctive vagus nerve stimulation (VNS) in participants with markedly treatment-resistant depression. Design Prospective, open-label, single-arm, long-term extension study (RECOVER) conducted from September 2019 to April 2025. Setting Outpatient. Participants Adults with moderate–severe MDD with ≥ 4 failed antidepressant trials in the current episode, randomized to blinded, adjunctive VNS for 12 months, who subsequently received open-label, adjunctive VNS for 12 additional months (n = 214). Interventions Vagus nerve stimulation and concomitant psychotropic medications and interventional psychiatric modalities (electroconvulsive therapy, transcranial magnetic stimulation, and ketamine/esketamine) were characterized over the 12-month extension. Main Outcomes and Measures The durability of benefit achieved at 12 months was assessed at 18 and 24 months for depressive symptoms (3 scales), daily function, QoL, a tripartite composite of all 3 domains, and the Clinical Global Impression–Improvement (CGI-I) scale (overall improvement). Loss of benefit and relapse were assessed, along with the emergence of meaningful benefit in participants without benefit at 12 months. Substantial benefit (at least 50% symptom reduction from baseline; CGI-I of 1 or 2; tripartite measures with at least 2 of 3 subscales evidencing benefit) and meaningful benefit thresholds for symptoms (at least 30% reduction from baseline), function, QoL, CGI-I, and the tripartite measure were set a priori. Results Most participants with substantial benefit maintained their benefit (18-month median = 78.8%; 24-month median = 79.0% across 5 measures), as did participants with at least meaningful benefit at 12 months (18-month median = 83.1%; 24-month median = 81.3% ...
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/ijnp/pyaf080
Availability: https://doi.org/10.1093/ijnp/pyaf080; https://academic.oup.com/ijnp/article-pdf/29/1/pyaf080/66383204/pyaf080.pdf
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.41DB11A6
Database: BASE