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ORIGINAL RESEARCH article

Front. Psychiatry, 30 January 2024
Sec. Neurostimulation
This article is part of the Research Topic Treatment Resistant Depression (TRD): epidemiology, clinic, burden and treatment View all 14 articles

Vagus nerve stimulation allows to cease maintenance electroconvulsive therapy in treatment-resistant depression: a retrospective monocentric case series

Oumaima Aboubakr,Oumaima Aboubakr1,2Philippe Domenech,Philippe Domenech3,4Isabelle HeurtebiseIsabelle Heurtebise5Raphaël Gaillard,Raphaël Gaillard3,6Aurore Guy-RubinAurore Guy-Rubin7Romain Carron,Romain Carron8,9Philibert Duriez,Philibert Duriez10,11Philip Gorwood,Philip Gorwood10,11Fabien Vinckier,&#x;Fabien Vinckier4,5Johan Pallud,&#x;Johan Pallud1,2Marc Zanello,
Marc Zanello1,2*
  • 1Department of Neurosurgery, GHU Paris Psychiatrie et Neurosciences, Site Sainte-Anne, Paris, France
  • 2Université Paris Cité, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Paris, France
  • 3Department of Psychiatry, Service Hospitalo-Universitaire, GHU Paris Psychiatrie et Neurosciences, Site Sainte-Anne, Paris, France
  • 4Institut du Cerveau, Inserm U1127, CNRS UMR7225 Sorbonne Université, Paris, France
  • 5Cardiology Department Centre Hospitalier de Bourges, Bourges, France
  • 6Motivation, Brain, and Behavior (MBB) Lab, Paris Brain Institute (ICM) Hôpital Pitié-Salpêtrière, Paris, France
  • 7Clinique Villa Montsouris, Paris, France
  • 8Department of Functional and Stereotactic Neurosurgery, Timone University Hospital, Marseille, France
  • 9Aix Marseille Univ, APHM, INSERM, INS, Inst Neurosci Syst, Timone Hospital, Epileptology Department, Marseille, France
  • 10CMME Psychiatry Department, GHU PARIS Sainte-Anne, Paris, France
  • 11Laboratoire de Physiopathologie des Maladies Psychiatriques, Institute of Psychiatry and Neuroscience of Paris INSERM, Paris, France

Context: The use of vagus nerve stimulation (VNS) to reduce or stop electroconvulsive therapy (ECT) in treatment-resistant depression seems promising. The aim of this study was to investigate the efficacy of VNS on the reduction of ECT sessions and mood stabilization.

Methods: We conducted a monocentric retrospective case series of patients who suffered from treatment-resistant depression, treated with ECT and referred to our center for VNS. We investigated the number and the frequency of ECT sessions before and after VNS implantation. Secondary criteria consisted in the Montgomery Åsberg Depression Rating Scale (MADRS) score, number of medical treatments, dosage of the main treatment and length of hospital stays before and after VNS. Additionally, we sent an anonymous survey to psychiatrists and other physicians in our institution to investigate their knowledge and perception of VNS therapy to treat treatment-resistant depression.

Results: Seven patients benefited from VNS: six (86%) were female (mean age of 51.7 +/− 16.0 years at surgery), and five (71%) suffered from bipolar depression (three type I and two type II). All patients were followed up at least 2 years post-implantation (range: 27–68 months). Prior to VNS, six patients were treated by maintenance ECT. After VNS, three (43%) patients did not require maintenance ECT anymore, and three (43%) patients required less frequent ECT session with a mean 14.7 +/− 9.8 weeks between sessions after VNS vs. 2.9 +/− 0.8 weeks before VNS. At last follow-up, 4 (57%) patients had stopped ECT. Five (71%) patients implanted with VNS were good responders (50% decrease relative to baseline MADRS). According to the survey, psychiatrists had a significantly better perception and knowledge of ECT, but a worse perception and knowledge of VNS compared to other physicians.

Conclusion: VNS is a good option for treatment-resistant depression requiring maintenance ECT dependence. Larger on-going studies will help broaden the implanted patients while strengthening psychiatrists’ knowledge on this therapy.

Introduction

According to the World Health Organization (WHO), over 300 million people are estimated to suffer from depression, equivalent to 4.4% of the world’s population (1). Approximately 30% of depressive patients are treatment-resistant (2, 3). Electroconvulsive therapy (ECT) is the standard treatment for treatment-resistant depression (4). It is recognized as efficient for mood stabilization but is associated with several issues, such as its long-term side effects (headaches, memory loss), a poor acceptability, and a high rate of relapse after ECT interruption (58). The necessity for maintenance ECT is challenging in terms of hospital resources and costs. More recently, Abrupt discontinuation of maintenance ECT during COVID-19 pandemic lead to relapses and highlighted the need for alternative therapy (911).

Vagus Nerve Stimulation (VNS) has been approved by the FDA as a treatment option for treatment-resistant depression since 2005 in the US and long-term follow-up of large cohorts revealed its efficacy in treatment-resistant depression (12). It is possible to perform ECT while having a VNS device and a previous case series described VNS as a potential relay to progressively cease maintenance ECT (13).

In France, VNS is still not recommended for treatment-resistant depression: it remains only offered to a few patients in tertiary care centers based on humanitarian exemptions. The referral of potential candidates to VNS remains a challenge, which makes VNS hardly accessible to most patient suffering treatment resistant depression (14). The main goal of this study was to assess the efficacy of VNS on maintenance ECT weaning and on depressive mood stabilization in treatment-resistant depression. The GHU PARIS Hospital (Paris, France) was born after the merger of the Sainte Anne Hospital, the Maison Blanche Hospital, and the Perray-Vaucluse Hospital in 2019. Due to its large coverage of the Ile de France region (representing approximatively 20% of the French population), GHU PARIS Hospitals takes care of approximatively 1 people on 40 in that region. If there is a large majority of psychiatrists, the GHU PARIS hospital medical population also includes general care practitioners, intensive care specialists, neurologists, neuroradiologists, specialists of physical and functional rehabilitation, and neurosurgeons with a tradition of multidisciplinary dialogue (15).

The main objective of the study was to retrospectively collected data concerning efficacy and safety of VNS for treatment-resistant depression after maintenance ECT. The second objective was to review psychiatrists and non-psychiatrists’ knowledge and perception of ECT and VNS as treatment options for depression using an anonymous online survey, in order to understand the low number of patients referred to VNS surgery after maintenance ECT.

Methods

Study design – settings and timeframes

This study is a retrospective, monocentric case series (tertiary care center, GHU PARIS Hospital, France). One investigator (O.A) collected clinical, imaging, surgical, treatment-related and follow-up data for all patients who underwent VNS surgery for treatment-resistant depression using a protocol designed for this study. This case series has been reported in line with the Preferred Reporting Of CasE Series in Surgery (PROCESS) Guidelines (16). The period of interest was from January 2015 to January 2020. Post January 2020, the COVID pandemic stopped these compassionate surgeries. The GHU PARIS Hospital (France) is a tertiary care center with a dedicated functional neurosurgery team and a dedicated psychiatry team.

Participants – registration

Inclusion criteria were: (1) patients older than 18 at surgery; (2) treatment resistant depression (unipolar or bipolar); (3) implantation with a VNS system; (4) available data. Exclusion criteria were: (1) patients lost to follow-up (no contact with the medical team from GHU PARIS Sainte Anne during the last year); (2) follow-up shorter than 2 years.

The collected data included patient demographics (sex, profession, age at diagnosis, personal and family medical history), clinical characteristics (symptoms at diagnosis, number and severity of episodes, hospital stays, suicide attempts), imaging data when available, medical treatment details in particular dosage of main therapy, ECT details, surgical and post operative data.

All patients filled a signed informed consent concerning the use of their de-identified data for scientific purpose. The study was conducted in accordance with the Declaration of Helsinki. The local institutional review board approved the study protocol (IRB00011687).

Intervention

Patients who were referred by their psychiatry team to a functional neurosurgeon for a neuromodulation treatment option were assessed and implanted with a VNS device (Demi-Pulse®, LivaNova, United States) on the left side. The surgical technique was previously described (17). Briefly, the patients were under general anesthesia on supine position, the vagus nerve dissection and placing the helical coils around the nerve were performed under optical magnification. Stimulation was activated between 1- to 16 weeks after the operation at the standard parameters used for treatment resistant epilepsy. The intensity of stimulation was gradually increased to maximize its efficacy while minimizing sides effects.

Follow-up and efficacy assessment

Follow-up was conducted jointly by the psychiatry and the neurosurgery team through clinical consultations. Patients were followed between 2 and 5 years post-operatively with repeated measurements of the MontgomeryÅsberg Depression Rating Scale (MADRS). It is a ten-item diagnostic scale for depression, designed to be sensitive to treatment effect, validated in several languages including French and widely used (18, 19).

The interruption or reduction of ECT sessions after VNS activation was the primary outcome. Secondary outcomes were: 2/difference between MADRS scores obtained in the month preceding VNS activation and at last follow-up; 3/the number of medications and changes in dosage of the main treatment in the month preceding VNS activation and at last follow-up; 4/length of hospitalization in a psychiatric Department before and since VNS activation (measured in days) until last follow-up.

Survey

An anonymous survey was sent to psychiatrists and other physicians (general practitioners, neurologists, neurosurgeons, and intensive care specialists) working at GHU PARIS Hospital via Google Forms. This 13-items questionnaire was designed by a multidisciplinary team including 2 senior neurosurgeons, and 3 senior psychiatrists (see Supplementary Table S1). A paired Likert score ensured proper comparability between answers. A scale ranging from 1 to 4 was used, with 1 corresponding to “Very good,” and 4 “Bad.” There was no neutral proposition (forced answers). The questionnaire included: 5 items concerning individual participants and local organization (specialization of the participants, awareness of the multidisciplinary meeting, etc.), 8 items concerning the neuromodulation procedure (knowledge and perception) dealing with ECT, VNS but also repetitive trans magnetic stimulation (rTMS) and deep brain stimulation (DBS). A free comment section was provided at the end of the questionnaire. Answers were binarized into positive answers for 1 & 2 (“very good” and “good,” respectively) and negative answers for 3 & 4 (“mediocre” and “bad,” respectively).

The questionnaire was sent by e-mail to 587 physicians working at GHU PARIS Hospital. Reminder e-mails were sent 2 weeks and 4 weeks after the initial email.

Measurements and analysis

Categorical variables were described as number and percentages. Continuous variables were described as mean ± standard deviation. Univariate analyses were carried out using the chi-square test after converting Likert’s scale data into binary variables when required. A value of p of less than 0.05 was considered significant. Analyses were performed using Jamovi (20).

Results

Patients’ characteristics

Table 1 summarizes patients’ characteristics.

Table 1
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Table 1. Patients’ characteristics.

Since March 2017, seven patients were implanted with VNS for treatment-resistant depression (five bipolar and two unipolar) at GHU PARIS Hospital’s Neurosurgery department. Patients’ characteristics are detailed in Table 1. Six patients were female, the mean age at implantation was 51 years (range 22–74). Three patients were also diagnosed with other psychiatric conditions (anorexia, generalized anxiety disorder and substance abuse disorder). Five patients have a close family history of psychiatric disorder (mood disorders, substance abuse disorder, suicide). Four patients have attempted suicide at least once. One patient happens to also have epilepsy (VNS surgery for treatment-resistant depression only).

The median delay to surgery was equal to 13 years (range 5–23 years) between diagnosis and referral for VNS. At surgery, all patients had received several medical treatments consisting in antidepressants, mood regulators and neuroleptics (four out of seven had received more than 10 different drugs). Two patients had received a treatment by clozapine and three patients had tried ketamine intravenous perfusions. As for non-pharmaceutical treatments, all patients had received ECT, and two patients had also received repetitive rTMS. Six patients were on maintenance ECT at the time of surgery.

All patients were followed up at least 2 years post-implantation (mean: 43.9 +/− 14.3 months, range: 27–68 months). After VNS implantation, one patient experienced a short-term complication (transitory voice alteration) and two patients experienced long term complications (Supplementary Figures S3, S4; Supplementary Video 1): sternocleidomastoid muscle contraction likely caused by the involuntary stimulation of the superior root of the ansa cervicalis (21), and severe sinus bradycardia, a rare complication of VNS (2225), respectively. Muscle contraction disappeared after a revision surgery with lead replacement for the first patient whereas the implantation of a pacemaker allowed to restart VNS for the second one. The median activation period was 36 months (range 12–64). At last follow-up, six VNS devices were still activated. The only deactivated stimulator was deactivated at the patient’s request (chest discomfort without dyspnea).

Efficacy of VNS on decreasing the use of ECT

Figure 1 presents the results of VNS on several efficacy criteria.

Figure 1
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Figure 1. Efficacy of VNS on mood stabilization in the case of 7 patients stimulated at GHU PARIS Hospital. (A) Number of ECT sessions in the 2 years before VNS activation and in the 2 years after VNS activation. Patients 1, 2, 3, 4, 6, and 7 required less ECT sessions in the 2 years after VNS activation. Only patient 5 received 19 sessions in the 2 years after VNS versus 0 in the 2 years before. (B) MADRS score before VNS activation and at last follow-up. Patients 1, 2, 3, 4, and 7 show a reduction of their MADRS score and are in remission (MADRS ≤9). Clinically, patients 1, 2, 4, and 7 are in remission and patient 3 is experiencing a mild depressive episode. Patients 5 and 6 show a higher MADRS score at last follow-up than before VNS. Clinically, they are hospitalized in a psychiatry ward for a recurrent depressive episode. (C) Number of medications prescribed before VNS activation and at last follow-up. Patient 7 has been consistently prescribed 2 medications and all the other patients take less medications at last follow-up. (D) Number of days per year spent in a psychiatric ward in the 2 years before and after VNS activation. Of note, patient 7 has never been admitted to psychiatry. Patients 1 to 4 show a tendency towards less hospitalizations since VNS activation. Patients 5 and 6 are currently hospitalized in a psychiatry ward.

Since all patients received ECT before being referred to neurosurgery for VNS, we documented the number of sessions they received in the 2 years before VNS and in the 2 years following VNS activation (Figure 1A).

Three (43%) patients did not require any ECT in the 2 years following VNS activation. Three (43%) patients could reduce ECT frequency in the 2 years following VNS activation with a mean 14.9 +/− 9.8 weeks between ECT sessions vs. 2.9 +/− 0.8 weeks in the 2 years before VNS. Only one patient received 19 ECT sessions in the 2 years following VNS activation vs. 0 in the 2 years before VNS: it was the patient suffering from the severe sinus bradycardia with a deactivated VNS. At last follow-up, 4 (67%) patients had stopped ECT and the patient requiring a pacemaker implantation showed a favorable evolution after VNS activation. No adverse effect occurred during ECT sessions after VNS implantation.

Efficacy of VNS on mood stabilization

Regarding VNS efficacy based on MADRS score, five patients showed a positive response with a reduction of their MADRS score (Figure 1B). Four patients (1, 2, 4, and 7) are currently in clinical remission (MADRS ≤4), euthymic and living at home. Patient 3 is receiving outpatient intravenous ketamine perfusions for a mild recurrent depressive episode (MADRS = 8 vs. 36 before VNS). Patients 5 and 6 are hospitalized in a psychiatry Department for a recurrent depressive episode.

We observed a reduction of the total number of medications prescribed for all but one patient who has been consistently prescribed 2 medications (Theralite and Carbamazepine) before and after VNS activation (Figure 1C). The mean reduction was of 1.4 +/− 0.8 treatment with a decrease in dosage of the main treatment of 38.3% +/− 35.1 (4 patients took Lithium, 2 anti-psychotic medications, and 1 a dopamine agonist).

There was a general trend towards less hospitalized days in a psychiatric department after the VNS activation in comparison with the baseline period (Figure 1D), but with important individual variations: for instance, patient 1 spent 36 days hospitalized after VNS surgery vs. 176 before whereas patient 3 was hospitalized 135 days after VNS surgery vs. 136 before.

There were no suicide following VNS activation and one episode of self-harm in a patient suffering from numerous self-harm episodes prior to VNS activation.

GHU PARIS medical population survey: psychiatrists and other physicians’ knowledge and perception of ECT and VNS

Figure 2 summarize the results of survey analysis.

Figure 2
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Figure 2. Results of the anonymous survey sent to psychiatrists and other physicians working at GHU PARIS Hospital, assessing their knowledge and perception of neuromodulation treatments for depression (ECT and VNS). 94% of psychiatrists vs. 10% of other physicians report a good (very good + good) knowledge of ECT (p < 0.001) and 96% of psychiatrists have a good perception of ECT vs. 79% of physicians (p = 0.027). 28% of psychiatrists vs. 42% of physicians report a good knowledge of VNS (p = 0.268) whereas 46% of psychiatrists vs. 89% of physicians have a good perception of VNS (p = 0.007). Psychiatrists have a significantly worse knowledge of VNS compared to ECT (p < 0.001). Their perception of VNS was the worse among the four investigated neuromodulation techniques (p < 0.001 vs. ECT).

Response rate to the survey was 13.5% 50 psychiatrists and 19 other physicians (2 general practitioners, 2 intensive care specialists, 7 neurologists, and 8 neurosurgeons).

Regarding ECT, 94% of psychiatrists vs. 10% of other physicians reported a good (very good + good) knowledge of the procedure (p < 0.001) and 96% of psychiatrists had a good perception of ECT vs. 79% of other physicians (p = 0.027). By contrast, 72% of psychiatrists vs. 58% of other physicians reported a bad (mediocre + bad) knowledge of VNS and 54% of psychiatrists had a bad perception of VNS vs. 11% of other physicians (p < 0.001). Psychiatrists had a significantly poorer knowledge of VNS compared to ECT (p < 0.001). Their perception of VNS was the worse among the four investigated neuromodulation techniques (p < 0.001 vs. ECT). The results for deep brain stimulation (DBS) and repetitive trans magnetic (rTMS) are reported in Supplementary Figure S5.

Discussion

Key results

This study showed that: 1/VNS could contribute to cease or reduce the frequency of maintenance ECT, 2/after VNS, the majority of patients had fewer medications and/or fewer recurrences and/or shorter hospital stays, 3/VNS in treatment-resistant depression, unipolar or bipolar, was successful in mood stabilization according to MADRS, 4/psychiatrists at a tertiary care center had a poor knowledge and perception of VNS and in general of invasive neuromodulation therapies.

Interpretation

About 50% of patients with major depression relapse within 1 year of treatment with ECT but maintenance ECT remains discussed, due to neurocognitive adverse effects of ECT (26, 27). During COVID-19 pandemic, nearly 60% of the patients requiring maintenance ECT relapsed after abrupt discontinuation (911). It has been reported that VNS can help to decrease frequency or to stop maintenance ECT (13, 28, 29). Our results were in line with these results: all the patients with the VNS activated at least 2 years after the implantation performed less ECT session than before VNS implantation and 4 out 5 totally stopped maintenance ECT. Moreover, maintenance ECT has a significant cost: reducing the frequency of ECT session at the cost of a VNS implantation is economically sound (28). As previously described, none complication occurred during ECT session after VNS implantation: it is another argument to propose VNS in front of an ECT dependence (29, 30).

The link between maintenance ECT and VNS is not evident. Mechanisms of action of both techniques are not fully understood (31, 32). Some directions could be: the role of the neuro-endocrine system as ECT and VNS both exert an effect on it (31, 33); the need to disturb causal depression network as VNS is known to perturb epileptic aberrant network (34, 35); the effect of neurogenesis with an increase in hippocampal volume after VNS or after ECT (36, 37). It is probably the conjunction of several mechanisms of action that explained the therapeutic effect of both techniques.

This cases series was another step towards the confirmation of VNS efficacy for treatment resistant depression: five patients had favorable outcomes after VNS activation despite being considered after the failure of more than 4 different medications and the bad tolerance, non-response, exhaustion, reliance on ECT treatment. Apart from MADRS score, length of hospitalization, number of medication and number of ECT sessions were globally reduced. This is in line with other studies and should be confirmed by larger studies (12, 3842). There were no suicide following VNS activation and one episode of self-harm in a patient suffering from numerous self-harm episodes prior to VNS activation. The other complications rate was higher compared to previous literature, probably due to the small sample size (12). It should be stressed that the VNS efficacy and tolerance was correct in a population mainly made up of patients suffering from bipolar disorder, making VNS a potential treatment of choice for this subpopulation (12).

The paucity of patients suffering from treatment-resistant depression referred to VNS surgery was in line with previous results (43, 44). Beside the difficult definition of treatment-resistance in psychiatry, several reasons could be provided: the psychiatrists’ residency offers only limited contact with neuromodulation, only few hospitals have enough resources to take care of treatment-resistant psychiatric patients, perception of medical invasiveness is highly variable, psychiatrists have little knowledge on current neurosurgical procedures, and literature is not straightforward (4547). The anonymous survey provided additional evidence that psychiatrists working at a tertiary care center did not have enough knowledge on invasive neuromodulation such as VNS whereas ECT was well-known. There was a significant difference between psychiatrists and other physicians in term of invasive neuromodulation perception, even if their knowledge was not significantly different. There is a need for better teaching of psychiatric neurosurgery for both residents and seniors physicians (46, 48, 49).

Limitations

These findings should be interpreted with caution, given the retrospective and monocentric design, the lack of a control group, all limiting the generalizability of the results. The specific medical population and the low response rate weaken the survey analysis. Further confirmatory analyses are required to reproduce the present results.

Conclusion

This case series adds to the growing literature concerning VNS usefulness in case of maintenance ECT. VNS did not preclude to perform ECT sessions after the implantation but help to reduce the frequency or even to stop maintenance ECT. Large ongoing studies, such as the RECOVER study, on VNS in treatment-resistant depression will help to precise the appropriate place of VNS in the treatment algorithm for treatment-resistant depression and will ease the referral of patients to surgery (50).

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving humans were approved by Campus de Neurochirurgie – IRB00011687. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and institutional requirements.

Author contributions

OA: Data curation, Investigation, Writing – original draft, Writing – review & editing. PDo: Data curation, Investigation, Validation, Writing – original draft, Writing – review & editing. IH: Data curation, Investigation, Writing – original draft, Writing – review & editing. RG: Conceptualization, Data curation, Formal analysis, Writing – original draft, Writing – review & editing. AG-R: Formal analysis, Investigation, Writing – original draft, Writing – review & editing. RC: Data curation, Formal analysis, Writing – original draft, Writing – review & editing. PDu: Methodology, Writing – original draft, Writing – review & editing. PG: Formal analysis, Writing – original draft, Writing – review & editing. FV: Investigation, Writing – original draft, Writing – review & editing. JP: Data curation, Formal analysis, Investigation, Methodology, Project administration, Writing – original draft, Writing – review & editing. MZ: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Supervision, Validation, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

MZ reports a relationship with LivaNova PLC that includes: travel reimbursement. RC reports a relationship with LivaNova PLC that includes: speaking and lecture fees and travel reimbursement. PDo reports a relationship with LivaNova PLC that includes: speaking and lecture fees and travel reimbursement.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpsyt.2023.1305603/full#supplementary-material

References

1. World Health Organization. Depression and other common mental disorders: Global Health estimates. Geneva: World Health Organization (2017). Available at: https://iris.who.int/bitstream/handle/10665/254610/WHO-MSD-MER-2017.2-eng.pdf?sequence=1 (Accessed November 26, 2023).

Google Scholar

2. Voineskos, D, Daskalakis, ZJ, and Blumberger, DM. Management of Treatment-Resistant Depression: challenges and strategies. Neuropsychiatr Dis Treat. (2020) 16:221–34. doi: 10.2147/NDT.S198774

PubMed Abstract | Crossref Full Text | Google Scholar

3. Fava, M. Diagnosis and definition of treatment-resistant depression. Biol Psychiatry. (2003) 53:649–59. doi: 10.1016/S0006-3223(03)00231-2

Crossref Full Text | Google Scholar

4. The UK ECT Review Group.Efficacy and safety of electroconvulsive therapy in depressive disorders: a systematic review and meta-analysis. Lancet. (2003) 361:799–808. doi: 10.1016/S0140-6736(03)12705-5

PubMed Abstract | Crossref Full Text | Google Scholar

5. Andrade, C, Arumugham, SS, and Thirthalli, J. Adverse effects of electroconvulsive therapy. Psychiatr Clin North Am. (2016) 39:513–30. doi: 10.1016/j.psc.2016.04.004

Crossref Full Text | Google Scholar

6. Moksnes, KM, and Ilner, SO. Electroconvulsive therapy – efficacy and side-effects. Tidsskr Den Nor Legeforening. (2010) 130:2460–4. doi: 10.4045/tidsskr.09.1102

Crossref Full Text | Google Scholar

7. MacQueen, G, Parkin, C, Marriott, M, Bégin, H, and Hasey, G. The long-term impact of treatment with electroconvulsive therapy on discrete memory systems in patients with bipolar disorder. J Psychiatry Neurosci. (2007) 32:241–9.

PubMed Abstract | Google Scholar

8. Petrides, G, Tobias, KG, Kellner, CH, and Rudorfer, MV. Continuation and maintenance electroconvulsive therapy for mood disorders: review of the literature. Neuropsychobiology. (2011) 64:129–40. doi: 10.1159/000328943

PubMed Abstract | Crossref Full Text | Google Scholar

9. Lambrichts, S, Vansteelandt, K, Crauwels, B, Obbels, J, Pilato, E, and Denduyver, J. Relapse after abrupt discontinuation of maintenance electroconvulsive therapy during the COVID-19 pandemic. Acta Psychiatr Scand. (2021) 144:230–7. doi: 10.1111/acps.13334

PubMed Abstract | Crossref Full Text | Google Scholar

10. Martínez-Amorós, E, Serra, P, Bassa, A, Palao, DJ, and Cardoner, N. Discontinuation of maintenance electroconvulsive therapy: lessons learned from the COVID-19 pandemic. Rev Psiquiatr Salud Ment. (2022) 15:154–5. doi: 10.1016/j.rpsm.2021.07.005

PubMed Abstract | Crossref Full Text | Google Scholar

11. Van de Velde, N, Geerts, P-J, Tandt, H, Vanderhasselt, M-A, and Titeca, K. Discontinuation of continuation or maintenance electroconvulsive therapy caused by the COVID-19 pandemic: a naturalistic study investigating relapse in patients with major depressive disorder. J ECT. (2021) 37:230–7. doi: 10.1097/YCT.0000000000000785

Crossref Full Text | Google Scholar

12. Aaronson, ST, Sears, P, Ruvuna, F, Bunker, M, Conway, CR, and Dougherty, DD. A 5-year observational study of patients with treatment-resistant depression treated with Vagus nerve stimulation or treatment as usual: comparison of response, remission, and suicidality. Am J Psychiatry. (2017) 174:640–8. doi: 10.1176/appi.ajp.2017.16010034

PubMed Abstract | Crossref Full Text | Google Scholar

13. Aaronson, ST, Goldwaser, EL, Kutzer, DJ, McAllister-Williams, RH, and Sackeim, HA. Vagus nerve stimulation in patients receiving maintenance therapy with electroconvulsive therapy: a series of 10 cases. J ECT. (2021) 37:84. doi: 10.1097/YCT.0000000000000724

PubMed Abstract | Crossref Full Text | Google Scholar

14. McAllister-Williams, RH, Bulmer, S, Newton, K, Heath, K, Cousins, DA, and Currie, A. Assessment for vagus nerve stimulation in patients with difficult-to-treat depression: a model from the Newcastle regional affective disorders service (RADS). J Affect Disord. (2021) 280:315–8. doi: 10.1016/j.jad.2020.11.020

PubMed Abstract | Crossref Full Text | Google Scholar

15. Zanello, M, Pallud, J, Baup, N, Peeters, S, Turak, B, and Krebs, MO. History of psychosurgery at Sainte-Anne hospital, Paris, France, through translational interactions between psychiatrists and neurosurgeons. Neurosurg Focus. (2017) 43:E9. doi: 10.3171/2017.6.FOCUS17250

PubMed Abstract | Crossref Full Text | Google Scholar

16. Agha, RA, Fowler, AJ, Rajmohan, S, Barai, I, and Orgill, DP. Preferred reporting of case series in surgery; the PROCESS guidelines. Int J Surg Lond Engl. (2016) 36:319–23. doi: 10.1016/j.ijsu.2016.10.025

PubMed Abstract | Crossref Full Text | Google Scholar

17. Hamdi, H, Spatola, G, Lagarde, S, McGonigal, A, Paz-Paredes, A, and Bizeau, A. Use of polyvinyl alcohol sponge cubes for vagal nerve stimulation: a suggestion for the wrapping step. Oper Neurosurg Hagerstown. (2020) 18:487–95. doi: 10.1093/ons/opz227

PubMed Abstract | Crossref Full Text | Google Scholar

18. Montgomery, SA, and Åsberg, M. A new depression scale designed to be sensitive to change. Br J Psychiatry. (1979) 134:382–9. doi: 10.1192/bjp.134.4.382

Crossref Full Text | Google Scholar

19. Huijbrechts, IP, Haffmans, PMJ, Jonker, K, Van, DA, and Hoencamp, E. A comparison of the Hamilton rating scale for depression and the Montgomery-Asberg depression rating scale. Acta Neuropsychiatr. (1999) 11:34–7. doi: 10.1017/S0924270800036358

Crossref Full Text | Google Scholar

20. The jamovi project. Jamovi (version 2.3) [computer software], (2023), Available at: https://www.jamovi.org

Google Scholar

21. Gopalakrishnan, CV, Kestle, JRW, and Connolly, MB. The “vagal ansa”: a source of complication in vagus nerve stimulation. J Neurosurg Pediatr. (2015) 15:535–8. doi: 10.3171/2014.10.PEDS14259

PubMed Abstract | Crossref Full Text | Google Scholar

22. Clark, AJ, Kuperman, RA, and Auguste, KI, Sun PP. Intractable episodic bradycardia resulting from progressive lead traction in an epileptic child with a vagus nerve stimulator: a delayed complication. J Neurosurg Pediatr (2012) 9:389–393. doi: 10.3171/2011.12.PEDS11124

PubMed Abstract | Crossref Full Text | Google Scholar

23. Iriarte, J, Urrestarazu, E, Alegre, M, Macías, A, Gómez, A, and Amaro, P. Late-onset periodic asystolia during vagus nerve stimulation. Epilepsia. (2009) 50:928–32. doi: 10.1111/j.1528-1167.2008.01918.x

PubMed Abstract | Crossref Full Text | Google Scholar

24. Shankar, R, Olotu, VO, Cole, N, Sullivan, H, and Jory, C. Case report: vagal nerve stimulation and late onset asystole. Seizure. (2013) 22:312–4. doi: 10.1016/j.seizure.2012.12.011

Crossref Full Text | Google Scholar

25. Ratajczak, T, Blank, R, Parikh, A, and Wase, A. Late-onset asystolic episodes in a patient with a vagal nerve stimulator. Hear Case Rep. (2018) 4:314–7. doi: 10.1016/j.hrcr.2018.04.004

PubMed Abstract | Crossref Full Text | Google Scholar

26. Sackeim, HA, Prudic, J, Fuller, R, Keilp, J, and Lavori, PW. The cognitive effects of electroconvulsive therapy in community settings. Neuropsychopharmacology. (2007) 32:244–54. doi: 10.1038/sj.npp.1301180

PubMed Abstract | Crossref Full Text | Google Scholar

27. Jelovac, A, Kolshus, E, and McLoughlin, DM. Relapse following successful electroconvulsive therapy for major depression: a Meta-analysis. Neuropsychopharmacology. (2013) 38:2467–74. doi: 10.1038/npp.2013.149

PubMed Abstract | Crossref Full Text | Google Scholar

28. Warnell, RL, and Elahi, N. Introduction of vagus nerve stimulation into a maintenance electroconvulsive therapy regimen: a case study and cost analysis. J ECT. (2007) 23:114–9. doi: 10.1097/YCT.0b013e3180616647

PubMed Abstract | Crossref Full Text | Google Scholar

29. Burke, MJ, and Husain, MM. Concomitant use of vagus nerve stimulation and electroconvulsive therapy for treatment-resistant depression. J ECT. (2006) 22:218–22. doi: 10.1097/01.yct.0000230364.04240.52

PubMed Abstract | Crossref Full Text | Google Scholar

30. Santermans, L, Vanderbruggen, N, Zeeuws, D, and Baeken, C. Successful ECT treatment after relapse during VNS therapy. Psychiatr Danub. (2010) 22:S166.

Google Scholar

31. Carron, R, Roncon, P, Lagarde, S, Dibué, M, Zanello, M, and Bartolomei, F. Latest views on the mechanisms of action of surgically implanted cervical vagal nerve stimulation in epilepsy. Neuromodulation J Int Neuromodulation Soc. (2022) 26:498–506. doi: 10.1016/j.neurom.2022.08.447

PubMed Abstract | Crossref Full Text | Google Scholar

32. Bolwig, TG. How does electroconvulsive therapy work? Theories on its mechanism. Can J Psychiatry Rev Can Psychiatr. (2011) 56:13–8. doi: 10.1177/070674371105600104

PubMed Abstract | Crossref Full Text | Google Scholar

33. Haskett, RF. Electroconvulsive Therapy’s mechanism of action: neuroendocrine hypotheses. J ECT. (2014) 30:107. doi: 10.1097/YCT.0000000000000143

Crossref Full Text | Google Scholar

34. Bartolomei, F, Bonini, F, Vidal, E, Trébuchon, A, Lagarde, S, and Lambert, I. How does vagal nerve stimulation (VNS) change EEG brain functional connectivity? Epilepsy Res. (2016) 126:141–6. doi: 10.1016/j.eplepsyres.2016.06.008

Crossref Full Text | Google Scholar

35. Siddiqi, SH, Schaper, FLWVJ, Horn, A, Hsu, J, Padmanabhan, JL, and Brodtmann, A. Brain stimulation and brain lesions converge on common causal circuits in neuropsychiatric disease. Nat. Hum Behav. (2021) 5:1707–16. doi: 10.1038/s41562-021-01161-1

PubMed Abstract | Crossref Full Text | Google Scholar

36. Argyelan, M, Deng, Z-D, Ousdal, OT, Oltedal, L, Angulo, B, and Baradits, M. Electroconvulsive therapy-induced volumetric brain changes converge on a common causal circuit in depression. Mol Psychiatry. (2023) 2:1–9. doi: 10.1038/s41380-023-02318-2

PubMed Abstract | Crossref Full Text | Google Scholar

37. Perini, GI, Toffanin, T, Pigato, G, Ferri, G, Follador, H, and Zonta, F. Hippocampal gray volumes increase in treatment-resistant depression responding to Vagus nerve stimulation. J ECT. (2017) 33:160. doi: 10.1097/YCT.0000000000000424

PubMed Abstract | Crossref Full Text | Google Scholar

38. George, MS, Rush, AJ, Marangell, LB, Sackeim, HA, Brannan, SK, and Davis, SM. A one-year comparison of Vagus nerve stimulation with treatment as usual for treatment-resistant depression. Biol Psychiatry. (2005) 58:364–73. doi: 10.1016/j.biopsych.2005.07.028

PubMed Abstract | Crossref Full Text | Google Scholar

39. Conway, CR, Kumar, A, Xiong, W, Bunker, M, Aaronson, ST, and Rush, AJ. Chronic Vagus nerve stimulation significantly improves quality of life in treatment-resistant major depression. J Clin Psychiatry. (2018) 79:22269. doi: 10.4088/JCP.18m12178

Crossref Full Text | Google Scholar

40. Christmas, D, Steele, JD, Tolomeo, S, Eljamel, MS, and Matthews, K. Vagus nerve stimulation for chronic major depressive disorder: 12-month outcomes in highly treatment-refractory patients. J Affect Disord. (2013) 150:1221–5. doi: 10.1016/j.jad.2013.05.080

PubMed Abstract | Crossref Full Text | Google Scholar

41. Schlaepfer, TE, Frick, C, Zobel, A, Maier, W, Heuser, I, and Bajbouj, M. Vagus nerve stimulation for depression: efficacy and safety in a European study. Psychol Med. (2008) 38:651–61. doi: 10.1017/S0033291707001924

PubMed Abstract | Crossref Full Text | Google Scholar

42. Aaronson, ST, Carpenter, LL, Conway, CR, Reimherr, FW, Lisanby, SH, and Schwartz, TL. Vagus nerve stimulation therapy randomized to different amounts of electrical charge for treatment-resistant depression: acute and chronic effects. Brain Stimulat. (2013) 6:631–40. doi: 10.1016/j.brs.2012.09.013

PubMed Abstract | Crossref Full Text | Google Scholar

43. Ramasubbu, R, Golding, S, Williams, K, Mackie, A, MacQueen, G, and Kiss, ZHT. Recruitment challenges for studies of deep brain stimulation for treatment-resistant depression. Neuropsychiatr Dis Treat. (2021) 17:765–75. doi: 10.2147/NDT.S299913

PubMed Abstract | Crossref Full Text | Google Scholar

44. Filkowski, MM, Mayberg, HS, and Holtzheimer, PE. Considering eligibility for studies of deep brain stimulation for treatment-resistant depression: insights from a clinical trial in unipolar and bipolar depression. J ECT. (2016) 32:122–6. doi: 10.1097/YCT.0000000000000281

PubMed Abstract | Crossref Full Text | Google Scholar

45. Bluhm, R, Cortright, M, Achtyes, ED, and Cabrera, LY. They are invasive in different ways: stakeholders perceptions of the invasiveness of psychiatric electroceutical interventions. AJOB Neurosci. (2021) 14:1. doi: 10.1080/21507740.2021.1958098

PubMed Abstract | Crossref Full Text | Google Scholar

46. Cormier, J, Iorio-Morin, C, Mathieu, D, and Ducharme, S. Psychiatric neurosurgery: a survey on the perceptions of psychiatrists and residents. Can J Neurol Sci. (2019) 46:303–10. doi: 10.1017/cjn.2019.5

PubMed Abstract | Crossref Full Text | Google Scholar

47. Brem, A-K, and Lehto, SM. Stuck between bench and bedside: why non-invasive brain stimulation is not accessible to depressed patients in Europe. Front Hum Neurosci. (2017) 11:39. doi: 10.3389/fnhum.2017.00039

PubMed Abstract | Crossref Full Text | Google Scholar

48. LY, C, GR, N, AM, MC, E, A, and R, B. A qualitative study of key stakeholders’ perceived risks and benefits of psychiatric electroceutical interventions. Health Risk Soc. (2021) 23:217–35. doi: 10.1080/13698575.2021.1979194

PubMed Abstract | Crossref Full Text | Google Scholar

49. Naesström, M, Blomstedt, P, Hariz, M, and Bodlund, O. Deep brain stimulation for obsessive-compulsive disorder: knowledge and concerns among psychiatrists, psychotherapists and patients. Surg Neurol Int. (2017) 8:298. doi: 10.4103/sni.sni_19_17

PubMed Abstract | Crossref Full Text | Google Scholar

50. Kennedy, SH, Milev, R, Giacobbe, P, Ramasubbu, R, Lam, RW, and Parikh, SV. Canadian network for mood and anxiety treatments (CANMAT) clinical guidelines for the management of major depressive disorder in adults: IV. Neurostimulation therapies. J Affect Disord. (2009) 117:S44–53. doi: 10.1016/j.jad.2009.06.039

Crossref Full Text | Google Scholar

Keywords: drug resistance, electric stimulation therapy, treatment outcome, safety, perception

Citation: Aboubakr O, Domenech P, Heurtebise I, Gaillard R, Guy-Rubin A, Carron R, Duriez P, Gorwood P, Vinckier F, Pallud J and Zanello M (2024) Vagus nerve stimulation allows to cease maintenance electroconvulsive therapy in treatment-resistant depression: a retrospective monocentric case series. Front. Psychiatry. 14:1305603. doi: 10.3389/fpsyt.2023.1305603

Received: 02 October 2023; Accepted: 11 December 2023;
Published: 30 January 2024.

Edited by:

Andrea Fiorillo, University of Campania Luigi Vanvitelli, Italy

Reviewed by:

Delfina Janiri, Sapienza University of Rome, Italy
Wen-Wang Rao, McGill University, Canada

Copyright © 2024 Aboubakr, Domenech, Heurtebise, Gaillard, Guy-Rubin, Carron, Duriez, Gorwood, Vinckier, Pallud and Zanello. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Marc Zanello, zanello.marc@gmail.com

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.