2010
DOI: 10.1016/j.brs.2010.07.003
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Durability of clinical benefit with transcranial magnetic stimulation (TMS) in the treatment of pharmacoresistant major depression: assessment of relapse during a 6-month, multisite, open-label study

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Cited by 130 publications
(88 citation statements)
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“…12,18 The report by Mantovani and colleagues 18 followed a cohort of patients (N = 50) for 3 months who had remitted (HDRS-24 score ≤ 10) following acute TMS in either an earlier multisite randomized trial 14 or an open-label follow-up study, 35 in which patients were tapered off TMS and transitioned to maintenance medications. At 3 months, 29 of 50 patients (58.0%) remained in remission (HDRS-24 score < 11), with an overall relapse rate of 13.5% (HDRS-24 score ≥ 20).…”
Section: Discussionmentioning
confidence: 99%
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“…12,18 The report by Mantovani and colleagues 18 followed a cohort of patients (N = 50) for 3 months who had remitted (HDRS-24 score ≤ 10) following acute TMS in either an earlier multisite randomized trial 14 or an open-label follow-up study, 35 in which patients were tapered off TMS and transitioned to maintenance medications. At 3 months, 29 of 50 patients (58.0%) remained in remission (HDRS-24 score < 11), with an overall relapse rate of 13.5% (HDRS-24 score ≥ 20).…”
Section: Discussionmentioning
confidence: 99%
“…[4][5][6][7][8][9][10][11] Transcranial magnetic stimulation (TMS) is a safe, effective, and well-tolerated alternative to pharmacotherapy for MDD. [12][13][14][15][16][17][18] Cumulative data in the last decade support that benefit of acute TMS appears sustained over periods of weeks to months. 12,[18][19][20][21][22][23][24] Upon symptom reemergence, reintroduction of TMS often results in restoration of acute benefit.…”
mentioning
confidence: 99%
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“…Also, Aguirre et al (2011) have shown that the rates of response and remission 4 weeks post-treatment increased from 33.3-38.9% (ie, from 6-7 subjects) and from 5.5-16.7% (ie, from 1-3 subjects) for the LF-rTMS group, respectively, and were maintained at the same initial level for the sham rTMS group. Encouragingly, a recent 6-month follow-up study with over 90 depressed subjects has shown that the therapeutic benefits of highfrequency rTMS are durable, and that it can be used for precluding impending relapse (Janicak et al, 2010). Nevertheless, it is clear that future RCTs on rTMS should include longer follow-up periods (eg, 46-12 months), especially considering the labor-intensive and time-consuming nature of rTMS (Wassermann and Zimmermann, 2012).…”
Section: Limitationsmentioning
confidence: 99%
“…A recent RCT [20] that described the time course of continued benefit after 6 weeks of highfrequency TMS to left DLPFC by using as maintenance antidepressant monotherapy, found a relapse rate of 10.1%. These results are comparable to ours, with the difference that in our study the follow-up was mostly naturalistic in nature and shorter.…”
Section: Discussionmentioning
confidence: 99%