Evidence map›Paper›PMID 42532518›Full record

ArticleActa psychiatrica Scandinavica2026

Transcranial Magnetic Stimulation Retreatment for Recurrent Depression: A Large Real-World Multisite Cohort Study.

Stanley Lyndon, Jason B Gibbons, Loreen Straub, Meekang Sung, Jacob C Jameson, David B Hathaway, Denise H Mulcahy, Cason Elliott, Rachel Wood, Matthew Ruble and 6 more

Abstract read
In one paragraph

Article in Acta psychiatrica Scandinavica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Stanley LyndonHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-2651-9754
Jason B GibbonsHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-1724-6897
Loreen StraubHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-2623-2726
Meekang SungHarvard Medical School, Boston, Massachusetts, USA.
Jacob C JamesonHarvard University, Boston, Massachusetts, USA.ORCID https://orcid.org/0009-0000-6980-2982
David B HathawayHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-7271-0018
Denise H MulcahyDiscovery Behavioral Health, Irvine, California, USA.
Cason ElliottDiscovery Behavioral Health, Irvine, California, USA.
Rachel WoodDiscovery Behavioral Health, Irvine, California, USA.ORCID https://orcid.org/0009-0006-8597-0509
Matthew RubleDiscovery Behavioral Health, Irvine, California, USA.ORCID https://orcid.org/0009-0005-8589-8263
Alejandro G SzmulewiczHarvard Medical School, Boston, Massachusetts, USA.
Jie YangHarvard Medical School, Boston, Massachusetts, USA.
Rajendra AldisHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-8252-4964
Richard WyssHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0009-0007-6832-5900
Philip S WangHarvard Medical School, Boston, Massachusetts, USA.
Shan H SiddiqiHarvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-0967-9289

Funding

Dynamic Decision Support Tools for Precision Treatment-Resistant Depression CareUG3MH141096 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI ALDIS, RAJENDRA, SIDDIQI, SHAN · 2025 to 2025
$1.7M
NIMH NIH HHS 1UG3MH141096-01NIMH NIH HHS UG3 MH141096
6 · The paper itself

Abstract

introductionWhen depressive symptoms return after an initial response to transcranial magnetic stimulation (TMS), evidence to guide use of a second acute course is strikingly limited. We aimed to estimate how often and how quickly patients with recurrent major depressive disorder benefit from a second course of transcranial magnetic stimulation after they previously improved with TMS.

methodsA retrospective cohort study across 20 outpatient centres included 259 patients who received ≥ 2 TMS courses between January 1, 2023 and October 1, 2025, and had clinically significant depressive symptoms at the start of course 2; 177 prior responders formed the primary cohort. Treatment used standard 10-Hz left dorsolateral prefrontal cortex TMS. Response and remission were assessed using the PHQ-9 and/or BDI-II; response was defined as a ≥ 50% reduction and remission as PHQ-9 ≤ 4 and/or BDI-II ≤ 9. Symptom change from baseline to end of course 2 and time to first response by session were compared between courses.

resultsAmong past responders, 146 of 177 patients (82.5%; 95% CI, 76.1%-87.8%) responded again during course 2 and 96 of 177 (54.2%; 95% CI, 46.6%-61.7%) achieved remission. PHQ-9 scores decreased by a median of 65.0% (p < 0.001), and BDI-II scores decreased by a mean of 12.0 points (95% CI, -14.0 to -10.0; p < 0.001). Among responders, the first session meeting response criteria occurred earlier during retreatment than during the initial course on both PHQ-9 (median session, 12 vs. 16; hazard ratio = 1.40, 95% CI, 1.14-1.72; p = 0.001) and BDI-II (13.5 vs. 22.5; hazard ratio = 1.46, 95% CI, 1.07-2.00; p = 0.018).

conclusionsMost patients who previously benefited from acute TMS improved again when symptoms recurred, and among responders, the first session meeting response criteria often occurred earlier during retreatment than during the initial course.

Indexed as

major depressive disordermeasurement‐based carereal‐world cohortremissionresponse timingretreatmenttranscranial magnetic stimulation

Identifiers

PMID42532518
PMCPMC13505613

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.