[Repetitive transcranial magnetic stimulation for treatment-resistant depression in adults: effectiveness, safety and efficiency]
Assaf R, Brabant J, Joyal M, Silva H
Record ID 32018014979
French
Original Title:
Stimulation magnétique transcrânienne répétée pour la dépression réfractaire aux traitements chez l’adulte : efficacité, innocuité et efficience
Authors' objectives:
Repetitive transcranial magnetic stimulation (rTMS) is another neuromodulation
technique, which was approved by Health Canada in 2002. In Quebec, the administration
of rTMS by psychiatrists has been covered by the Quebec health insurance plan since
2013. Nonetheless, its clinical relevance has not been evaluated, and no guidelines are
currently available. In this context, the INESSS was mandated by the Ministry of Health
and Social Services (MSSS) to assess the effectiveness and safety of rTMS and its
various protocols, as well as its efficiency in the Quebec context.
Authors' results and conclusions:
RESULTS: The compilation of data from the rapid review of the scientific and grey literature, along
with information collected from stakeholders, led to several key findings regarding:
• The overall effectiveness of rTMS, as well as that of more specific protocols, in
reducing depressive symptoms in adults with unipolar or bipolar TRD;
• The overall safety of rTMS, as well as that of specific protocols;
• Considerations related to the choice of therapeutic approach and, if applicable,
the selection of the rTMS protocol;
• Organizational and economic considerations associated with the delivery of rTMS
services.
Authors' recommendations:
RECOMMENDATION 1 – CLINICAL RELEVANCE:
Considering its clinical effectiveness and safety, demonstrated efficiency, and the need for
treatment options among individuals with TRD, INESSS recommends that:
rTMS be offered to adults3 experiencing a major depressive episode within a unipolar or
bipolar disorder who are not responding to first-line treatments (e.g., psychotherapy,
antidepressants) to reduce the severity of depression. RECOMMENDATION 2 – CARE PATHWAYS AND SERVICES: rTMS should generally be considered before ECT in the care pathway for individuals with
TRD, primarily due to its safety. rTMS may also be considered prior to ketamine. These
factors can help support shared decision-making. RECOMMENDATION 3 – CONDITIONS OF ADMINISTRATION: When rTMS is delivered, it should be done under the following conditions:
prescribed by a psychiatrist or another authorized healthcare professional with expertise
in rTMS, responsible for assessing contraindications and ensuring appropriate medical
follow-up. RECOMMENDATION 4 – PROTOCOLS: Due to limited available data and the lack of clear clinical effectiveness evidence, further
research is needed to evaluate the effectiveness of the following rTMS protocols for reducing
depression severity in adults with unipolar or bipolar TRD:
High-frequency rTMS applied to the right DLPFC or the right ventrolateral prefrontal
cortex. RECOMMENDATION 5 – SERVICE DELIVERY: Based on the evidence of effectiveness, the economic analysis, and the uneven availability of
services across regions, INESSS recommends improving access to rTMS and implementing
service delivery modalities to more equitably address the needs of Quebec adults with TRD. CONCLUSION: Individuals with TRD and their loved ones face significant challenges due to this condition
and often experience multiple treatment failures. These individuals need access to a
range of treatment options that may improve their condition.
Authors' methods:
This report integrates data collected through a rapid review of scientific and grey
literature, economic analyses and information collected from stakeholders. Effectiveness
and safety data were drawn from 56 scientific articles (13 systematic reviews, one meta-
analyses review, and 42 randomized controlled trials) and 29 grey literature sources,
primarily clinical practice guidelines and health technology assessment reports.
Economic analyses included an efficiency analysis, using data from two economic
evaluations identified in the literature, and a budget impact analysis, based on clinical
and administrative data.
Details
Project Status:
Completed
Year Published:
2026
URL for published report:
https://www.inesss.qc.ca/fileadmin/doc/INESSS/Rapports/ServicesSociaux/SMTr_Avis_INESSS.pdf
English language abstract:
An English language summary is available
Publication Type:
Full HTA
Country:
Canada
Province:
Quebec
MeSH Terms
- Depressive Disorder, Treatment-Resistant
- Depressive Disorder, Major
- Transcranial Magnetic Stimulation
- Adult
Contact
Organisation Name:
Institut national d'excellence en sante et en services sociaux
Contact Address:
L'Institut national d'excellence en sante et en services sociaux (INESSS) , 2021, avenue Union, bureau 10.083, Montreal, Quebec, Canada, H3A 2S9;Tel: 1+514-873-2563, Fax: 1+514-873-1369
Contact Name:
demande@inesss.qc.ca
Contact Email:
demande@inesss.qc.ca
Copyright:
L'Institut national d'excellence en sante et en services sociaux (INESSS)
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.