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Review article

The Safety and Efficacy of Repetitive Transcranial Magnetic Stimulation in the Treatment of Major Depression Among Children and Adolescents: A Systematic Review


Major depression is a chronic debilitating condition affecting people of all ages and is rising over the past decade. Major depression among children and adolescents is often resistant to traditional treatments, thus necessitating the exploration of novel strategies. Repetitive transcranial magnetic stimulation (rTMS) is gaining increasing attention as a useful tool in treating various conditions and has received the US Food and Drug Administration (FDA) approval to treat depression and obsessive-compulsive disorder among adults. Favorable outcomes among adults generated interest in using it among children. Until recently, the existing literature lacked randomized sham-controlled trials on this topic among children and adolescents. The newest additions in the literature necessitated another in-depth look at the data to explore the safety and efficacy of rTMS in the context of depression among children and adolescents. We searched the Medline and Cochrane databases and included 18 articles for our systematic review. Our systematic review indicates level 1 evidence that rTMS is safe but failed to show its superiority to placebo as a stand-alone treatment for resistant depression among children and adolescents. However, there is level 2 evidence favoring add-on rTMS to treat major depression among children and adolescents. The study subjects appear to tolerate the rTMS treatment well with some minor and mostly self-limited side effects. Risks of treatment-emergent hypomanic symptoms and seizure appear to be very low. There is no evidence of worsening of suicidal ideation or cognitive decline during rTMS treatment.

Introduction & Background

The rate of major depression has increased from 8.7% in 2005 to 11.3% in 2014 in adolescents [1]. Major depression in childhood is often associated with school dropout, unemployment, and unwanted pregnancy [2]. The Treatment for Adolescents with Depression Study showed that a combination of fluoxetine and cognitive-behavioral therapy was associated with a higher remission rate in adolescent depression than either treatment alone [3]. Nevertheless, almost 30-40% of depressed adolescents fail to respond to traditional treatment [4,5]. There are also concerns about treatment-emergent side effects, such as suicidality with the use of antidepressants [6,7]. The practice parameter of the American Association of Child and Adolescent Psychiatry recommends electroconvulsive therapy (ECT) for adolescents in resistant cases of major depression [8]. However, ECT is less frequently used [4,9] due to cognitive side effects, prolonged seizure, and anesthetic complications [4,10]. As a result, there is an increasing interest in novel treatment approaches for major depression.

Repetitive transcranial magnetic stimulation (rTMS) is a relatively new treatment modality that is gaining attention in the treatment of various conditions afflicting adults [11-13]. Three large, multi-site, randomized, sham-controlled trials amongst medication-free depressed adults who failed to respond to antidepressant trials have demonstrated its efficacy in major depression [14-16]. A recent systematic review indicates a better response rate among adults with fewer previous failed antidepressant trials [17]. The response rate can be as high as 95.5% and a remission rate of 68.2% in the first episode [18].

The US FDA approved the use of rTMS for major depression and obsessive-compulsive disorder among adults who failed to respond to medications [13,19]. Adult literature indicates that the most common side-effects of rTMS are scalp tenderness and headache [11,20]. Serious side-effects such as seizure and treatment-emergent mania or hypomania are rare [20,21]. The adult literature generated a growing interest in investigating its role in depression among children and adolescents. The current systematic review explores the safety and efficacy of rTMS in the case of major depression among children and adolescents.



The systematic review aimed to collate various open-label studies, randomized controlled trials (RCTs), case reports, case series investigating the safety and efficacy of rTMS in treating major depression among children and adolescents (age≤18). Studies that included children and adults but focused on adults or did not present data of children and adolescents separately were not included. We searched the Medline and Cochrane databases and kept various MeSH keywords such as “pediatric,” “adolescent,” “depression,” “rTMS” in varying combinations. Additionally, we searched the reference lists of various articles and reviews using the same search engine and contacted other researchers to gather additional information about their published papers. We included literature in the English language published until November 2020. We excluded studies whose primary diagnosis was not major depression and those who used other variety of TMS. We have utilized the Joanna Briggs Institute quality appraisal tool to assess the quality of the included studies [22]. One of the authors (PM), in consultation with two other authors (SB and TP), selected the articles for the systematic review and followed the PRISMA guideline (Figure 1). We did not attempt a quantitative synthesis with the data due to the heterogeneity of studies and outcome parameters/assessment methods.


Using the various combinations of keywords, we retrieved 457 articles. Removal of duplicates resulted in 300 publications. All these 300 articles were screened based upon the titles and abstracts. We excluded 186 articles due to various reasons (as shown in Figure 1). We retrieved 114 full texts for eligibility amongst which, 96 were excluded based on relevance (N 10), involving adults (N 60), reviews (N 17), different diagnosis (N 4), unable to access (N 1), secondary analysis (N 3), and could not differentiate pediatric data from adult data (N 1). Finally, 18 articles, including 13 multi-subject trials and 5 case reports, were incorporated in this systematic review. We identified another three studies [24-26] that incorporated data from previous studies already included in this systematic review. We have discussed their findings.

Characteristics of the Studies

Tables 1 and 2 summarized the characteristics of the studies. The studies include open-label trials [27-32], case reports [33-37], case series [38-41], naturalistic studies [42], and randomized sham-controlled trial [43]. One study used emailed questionnaires to a Worldwide pool of rTMS centers [44]. The majority of the studies are from the USA [28-31,33-35,40,43]. The rest of the studies were from China [37,38,42], Israel [32], Finland [36], Canada [27,39], Australia [41], and across multiple nations [44]. The lowest age of the recipient of rTMS was ten [40,42,43], but most of the patients were above 12.

Author Study design Rating scales N (age) Number of sessions Session duration (Sec per train, sec per duration) Intensity %MT Reported side effects Efficacy/effectiveness
Croarkin et al. [43] Randomized, sham-controlled HAM-D, MADRS, CDRS-R, CGI-S, QIDS-A-17-SR, CSSR-S, YMRS 103 (12–22) rTMS group-48 sham-controlled group-55 30 75 trains, 10 pulses per second over 4 seconds, intertrain interval of 26 seconds, 10 Hz, 3000 pulses per session 120 Suicidal ideation, classified as not related to rTMS headache, nausea, facial twitching Response rate is 41.7% (remission rate 29.2%) in the active treatment group and 36.4% (remission rate 29%) in sham-controlled group
Zhang et al. [42] Naturalistic study HAM-D, HAM-A 42 adolescents vs. 75 adults (10–80) 11–20 80 trains, 30 pulses per train, 10Hz, 12 seconds intertrain-interval, 2400 pulses per session 120 Transient headache, musculoskeletal discomfort All age groups showed improvement in both anxiety and depression. Symptom improvement more among adolescents. Significant time-effect was seen 94.1% of adolescents responded, and 88.2% achieved remission at the end of 4 weeks
MacMaster et al. [27] Open level K-SADS-PL, CDRS-R, HAM-D, HAM-A, BDI HAM-D, Pediatric TMS safety and tolerability measure 32 (13–21) 15 40 pulses over 4 seconds, 10 Hz; intertrain interval, 26 s; 75 trains; 3000 pulses 120 Headache, mild neck pain, unpleasant tingling, nausea, lightheadedness 56% responders responded and 44% achieved remission
Pan et al. [38] Case series from a previous double-blind sham-controlled study SCID BSI-CV MADRS 3 (16, 17, 15) 7 120 trains of 5 seconds dura­tion at 10 Hz with intertrain intervals of 15 seconds (i.e., 6000 pulses per session 100 Sleepiness, hypomanic symptoms 40-100% improvement in BSI-CV score, and 14.63–47.83% improvement in MADRS score of all three patients. Remission of suicidal thought of one of the patients
Wall et al. [28] Open level study KSADS-PL, CDRS-R, QIDS-A17-SR, CSSR-S, CGI-S, CGI-I 10 (13.9–17.4) 30 4-second stimulus trains, 10 HZ separated by 26-second intertrain intervals, with 3000 magnetic pulses per session 120 Scalp pain, worsening of depression, headaches, dizziness, musculoskeletal discomfort, neck stiffness, eye twitching, and nausea 60% of participants responded. The total mean score of CDRS-R, QIDS-A17-SR, and CGI-S significantly improved at 20, 30, and at 6-month follow-up
Croarkin et al. [29] Open level K-SADS, SCID, CDRS-R, ATHF 10 (13–17) 30 Six completed 30, and one each completed 1, 5, 17, and 29 sessions 4-second stimulus trains, 10 Hz separated by 26-seconds intertrain intervals, with 3000 magnetic pulses per session 120 Unspecified ~33.5% improvement in CDRS-R score post-treatment, and almost 45.6% improvement at 6 months post-treatment
Yang et al. [39] Case series KSADS, HAMD, BDI, HAMA 6 (15–21) 15 4 seconds stimulus, intertrain interval 26 seconds, 10 Hz, 3000 pulses per treatment 120% Mild scalp discomfort, headache 66% responded 68% decrease in HAMD score and 84% reduction in BDI score 78% reduction of HAMA score
Wall et al. [30] Open level, prospective, multi-center KSADS-PL, CDRS-R, ATHF, CAVLT-2, D-KEFS, trail-making test 18 (13.9–17.8) 14 completed treatment 30 4 seconds stimulus duration, intertrain interval of 26 seconds, 10 Hz, 3000 stimuli per session 120%   Substantial improvement in depressive symptoms
Wall et al. [31] Open level, perspective K-SADS-PL, CDRS-R, QIDS-A17, CGI-S and CGI-I, CSSR-S, Subjective Reactive Questionnaire, Adverse Event Monitoring form 8 (14.6–17.8) 30 4 seconds stimulus duration, 10 Hz, intertrain interval 26 seconds, 75 trains, 3000 stimulations per session 120 Scalp pain Almost 50% decrease in the mean baseline CDRS and QIDS A17 from baseline to at treatment 30
Croarkin et al. [40] Case series K-SADS-PL, CDRS- R 2 cases* (10 and 17) Unspecified Unspecified Up to 40 Scalp pain Unspecified
Bloch et al. [32] Open level study SCID, BDI, CDRS, CGI-S, SIQ, SCARED, CNTA 9 (16–18) 14 2-second trains, 10 Hz, intertrain interval 58 seconds, 20 stimuli, 400 stimuli per session 80% Headache Subjects had lower depression, anxiety, and no cognitive changes or suicidal ideation
Loo et al. [41] First two cases from double-blind sham-controlled trial MDRAS, BDI, CGI-S, CES- DC, RAVLT, Weschler digit span forward and backward, TMT A and B, COWAT 2 (16) Case 1 - 29 Case 2 - 27 5 seconds, 10 Hz, 25 seconds intertrain interval, 40 trains, 2000 stimuli per session 110% None No cognitive changes
Walter et al. [44] Emailed questionnaire to a worldwide pool of rTMS centers HAMD, BQ 3 (16, 17, 17) 10 One case with - 2 seconds stimulus duration, 10 Hz, intertrain interval 28 seconds, 40 trains, 1600 stimulations per session. Two other cases - 8 seconds stimulus duration, 10 Hz, intertrain interval 52 seconds, 20 trains, 1600 stimulus per session      
Author Rating scales Age (years) Number of sessions Session duration (second per train, second per duration) Intensity %MT Reported side effects Efficacy/effectiveness
Cullen et al. [33] None 17 8 2-second trains, 18 Hz, 55, total 1980 pulses 85–120 Scalp pain Generalized, tonic-clonic seizure Unspecified
Cristancho et al. [34] No rating scale used 15 10 at RDLPFC 26 at LDLPFC 1 Hz, 10 seconds on, and 10–15 seconds off. The pulse increased from 150 PPS and increased to 300 PPS by the second week over RDLPFC and then 300–600 PPS by the fourth week over LDLPFC 90 Mild headaches, jaw twitch, and transient dizziness Improvement in mood, less tearfulness
Segev et al. [35] BDI-II, CDRS-R 17 20 4-second stimulus, intertrain interval 30 seconds, 10 Hz, 1680 pulses per treatment 100 Headache, scalp pain, and scalp burning Improvement in anxiety from 46 to 25 score in SCARED. No improvement in BDI-II and CDRS-R scores. SIQ score improved transiently. 
Chiramberro et al. [36] SCID 16 12 5-second stimulus duration, 10 Hz, 60 trains, intertrain interval - 25 seconds, 3000 stimuli per session Unspecified Seizure Unspecified
Hu et al. [37]   15 1 4-second stimulus duration, 10 Hz, intertrain interval 26 seconds, 20 trains per session, the cumulative number of daily pulses 800 80 The generalized tonic-clonic seizure followed by hypomanic symptoms lasting for 8-9 hours Unspecified

The sample size ranged from 1 (case reports) to 103 [43]. The case series by Croarkin et al. presented three cases [40]. However, one of the three cases was a healthy control. So, we have included two out of these three cases in this systematic review. Similarly, the case series by Walter et al. presented seven cases. However, we included three of them as the other four subjects had other primary diagnoses such as bipolar disorder and schizophrenia [44]. All the multi-subject trials allowed comorbid anxiety disorder, dysthymia, attention deficit hyperactivity disorder (ADHD) but excluded schizophrenia, bipolar disorder, substance use disorder, post-traumatic stress disorder (PTSD), intellectual disability, pervasive developmental disorders, and eating disorders. One study included comorbid substance abuse [32], and another one allowed the inclusion of bipolar type II [42]. Zhang et al. included “mood or anxiety disorder” and thus, incorporated other diagnoses such as bipolar type II, dysthymia, generalized anxiety disorder [42]. No change in psychotherapy was allowed a few weeks before and during the trial [30-32]. Some studies have excluded patients with suicide attempts in the previous six months [28,31] or with “suicidal propensity” [42].

Most of the studies included treatment-resistant depression [25-32,39,43] and established the diagnosis by Kiddie Schedule for Affective Disorder and Schizophrenia [27-31,39,40]. Others utilized Structured Clinical Interviews based on the Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM-IV) [32,36,38]; clinical interviews [35,42,43], Mini International Neuropsychiatric Interview for children, or Mini Neuropsychiatric Interview [43]. One of the studies used the World Health Organization International Classification of Disease - version 10 [37].

The outcomes were measured using Hamilton Depression Rating Scale (HAM-D) and Hamilton Anxiety Rating Scale (HAM-A) [27,39,42], HAM-D [43], Montgomery-Asberg Depression Rating Scale [38,41,43], Children’s Depression Rating Scale, Revised [28,29,31,32,35,43], Quick Inventory for Depressive Symptomatology Adolescent Seventeen Item Self Report [28,31,43], Clinical Global Impressions-Severity [28,31,32,41,43], Screen for Child Anxiety-Related Disorders questionnaire [32,35], Beck Depression Inventory [32,35,39,41], Beck Scale for Suicide Ideation-Chinese Version [38], Columbia Suicide Severity Rating Scale [28,31,43], Suicidal Ideation Questionnaire [32,35], Mini International Neuropsychiatric Interview [43], Mini International Neuropsychiatric Interview for Children [43], and Young Mania Rating Scale [43].

Antidepressant Use Among the Included Studies

The antidepressant use of the included studies is summarized in Tables 3 and 4. All the studies, except Croarkin et al., allowed antidepressant medications [43]. The studies have included patients with a history of one [27-30,39], two [32] to several failed antidepressant trials [28,33,40,43]. Pan et al. included either drug naïve or patients not taking antidepressants for nearly two weeks [38]. The majority of the studies have specified no change in antidepressant dosages during the trial [28-32,42]. Participants of some studies did not take any antipsychotics, mood stabilizers, benzodiazepines, stimulants, tricyclic antidepressants, or bupropion during TMS treatment [28,31].

Author Antidepressant use Previous treatment failure Psychosocial intervention used Change of dosages allowed
Croarkin et al. [43] None Yes No change in psychosocial interventions N/A
Zhang et al. [42] All used one type of antidepressant treatment during rTMS along with other medications Unspecified but excluded patients who were taking more than one antidepressant Unspecified No
MacMaster et al. [27] Psychotropic medications use were allowed if stable for 6 weeks 31.25% were not on psychotropics At least two previous failed medication trials Unspecified No unless medically necessary
Pan et al. [38] Either drug naïve or was not taking antidepressants for 2 weeks prior to the study All three patients took an antidepressant in the past for an unspecified dose and duration Unspecified N/A
Wall et al. [28] All used either SSRI or SNRI At least one prior medication trial failure as defined by ATHF. Study participants had a mean of 4.0 prior failed medication trial (SD 2.1). No change in psychotherapy treatment was allowed within the last 4 weeks of treatment No
Croarkin et al. [29] All were on antidepressants At least one prior failed medication trials Unspecified No
Yang et al. [39] Unspecified At least one failed trial Unspecified Unspecified
Wall et al. [30] All were on antidepressants At least one prior failed trial No change in psychotherapy or therapist No
Wall et al. [31] Yes Yes - at least two failed trials No change in psychotherapy or therapist in 4 weeks prior to rTMS No
Croarkin et al. [40] Case 1 - none; Case 2 - yes Case 1 - none; case 2 - multiple Unspecified No
Bloch et al. [32] Yes Failure of one course of psychotherapy and two courses of medication trials 8 weeks each, with at least one of the antidepressants being Fluoxetine No change in therapy within 5 weeks before starting of rTMS No 
Loo et al. [41] Case 1 - unspecified; case 2 - yes Case 1 - failure of one course of psychotherapy; case 2 - one course of psychotherapy, two medication trials Unspecified Case 1 - unspecified; Case 2 - no
Walter et al. [44] No Unspecified Unspecified Unspecified
Author Antidepressant use Previous treatment failure Psychosocial intervention used Change of dosages allowed
Cullen et al. [33] None Multiple failed trials Unspecified N/A
Cristancho et al. [34] Yes Multiple failed trials Unspecified N/A
Segev et al. [35] Yes Yes Unspecified Unspecified
Chiramberro et al. [36] Yes Yes Unspecified Unspecified
Hu et al. [37] Yes on sertraline Unspecified Unspecified Unspecified

Administration of rTMS

All studies delivered rTMS over the left dorsolateral prefrontal cortex (LDLPFC), except one study by Cristancho et al. that delivered it in both right and left DLPFC [34]. Most of them utilized the “5 cm rule” for localization of LDLPFC. Most of the studies used a figure of eight coil [27,34-39,41,42], and others used circular coil [32] or H1 coil [33]. The number of sessions varied from 1 [37,40] to 30 [28-31,43]. Most of the studies delivered rTMS at a frequency of 10 Hz, except two studies, Cullen et al. (18 Hz) and Cristancho et al. (1 Hz) [33,34]. Seven studies delivered 3000 stimuli per session [27-31,36,39,43]. The majority of the studies used 120% of motor threshold (MT) [27-31,39,42,43] and others varied from 40% to 120%, such as 100% [35,38], 90% [34], 80% [37], 80% [32], 110% [41], and 90-110% [44].


The majority of the studies found that rTMS is a safe and effective add-on treatment for child and adolescent depression [27-32,34,38,39,42]. The improvement started as early as one [32,38] to two weeks [28,42]. Treatment benefits were noted at six months [28-31] to one year [32] post-trials. Croarkin et al. reported an improvement of 33.5% in CDRS-R scores and almost 45.6% improvement at six months post-treatment [29]. A similar rate of improvement (33%) was reported by Bloch et al. [32]. Wall et al. noted improvement among 60% of the study subjects [28]. Zhang et al. compared 42 adolescents with 75 adults and found a response rate of 94.1% and a remission rate of 88.2% among adolescents [42]. The older group had a less impressive improvement, higher baseline depression and anxiety scores, and shorter follow-up. A secondary analysis by Zhang et al. indicated that add-on rTMS improved depression and somatic and psychic anxiety among adolescents [24]. Sonmez et al. pooled data from three previous studies [28,30,31] and found that rTMS may improve hypersomnia in addition to its antidepressant action [26].

Side Effects

The majority of the studies reported mild side-effects such as scalp tenderness and headache [27,28,31-35,39,42-44], musculoskeletal discomfort [28,42], neck-pain and stiffness [27,28]. The other side effects that were reported include eye-twitching [28], eye pain [43], facial twitch [43], jaw-twitching [34], nausea [27,28,43], tingling sensation [27], and lightheadedness/dizziness [27,28,34]. There are three case reports of treatment-emergent seizures [33,36,37] and one case series of intolerable headaches [40] leading to the termination of the procedure. There is one case report of emergent hypomanic symptoms [38]. No cognitive decline was reported [30,31].

Suicidal Ideation

Several studies have assessed suicidal behavior and found no worsening of symptoms during rTMS. Croarkin et al. reported that 4 out of 103 patients developed suicidal ideation, but none were related to rTMS treatment [43]. Wall et al. reported 8 out of 10 subjects had suicidal ideation before the study, two subjects experienced worsening suicidal thoughts during the trial [28]. One subject had self-injurious behavior at six months follow up. In another study, subjects with suicidal thoughts at baseline reported improvement with treatment [31]. At the end of six months, one patient had self-mutilating behavior, and another patient needed hospitalization, which was unrelated to rTMS. In a pooled data analysis of the above studies [28,31], the suicidal ideation at baseline and at the end of the study period was 63.16% and 16.67%, respectively [25]. In another case series by Pan et al., one out of three subjects experienced remission of suicidal ideation during rTMS [38]. Segev et al. reported a case where suicidality was transiently improved, followed by deterioration, and finally plateaued [35]. Bloch et al. also found out that suicidal ideation was not affected by the stage of rTMS treatment [32].


To the best of our knowledge, our systematic review is the only one that has incorporated the data of more than 250 patients. Our findings support the results of the previous systematic reviews on the topic [45,46]. Previous systematic reviews on this topic have been criticized for lacking a controlled group in the included studies and the relatively smaller number of total subjects in the included studies [45,46]. In our systematic review, the addition of the only available RCT with a sham-control group improved the quality of the evidence of efficacy by utilizing a comparison group that approximates a placebo group [47]. Our systematic review included the three recent studies with larger sample sizes than previous articles [27,42,43]. Although better quality studies are still needed, there is a strong indication that rTMS is a safe and useful add-on, but not a stand-alone treatment for child and adolescent depression that has not responded to at least one antidepressant treatment. Twelve out of 18 included studies found out that rTMS could be an effective treatment for major depression among children and adolescents.

Studies showing reduced depressive symptoms have most commonly delivered rTMS in 10 Hz frequency, 120% MT, four seconds train, and 3000 stimuli per session for 30 sessions. One of the significant advantages of rTMS is that the patient can be monitored multiple times a week. Moreover, the side- effects are mild and self-limiting. Suicidality and treatment-emergent manic or hypomanic symptoms appear to be rare with rTMS in this age group. The side effects reported in the majority of the studies are mild and self-limiting. Out of the three case reports demonstrating the development of seizure spells in the context of rTMS, one delivered rTMS in a somewhat different protocol from the other studies, such as they used two-second trains (instead of the usual four-second trains used by other authors), used 18 Hz frequency instead of 10 Hz frequency, and delivered a total of 1980 pulses per session [33]. The other case report of seizure spell involved the use of 75 mg olanzapine (which was later corrected by the author as 7.5 mg) and a blood alcohol concentration of 0.20% at the time of the seizure episode [36]. The only one case report of the emergence of hypomanic symptoms has used 6000 pulses per session [38]. Such a low occurrence of significant side effects has also been reported in other non-invasive brain stimulation studies involving children and adolescents [48-50].

According to the University of Oxford Centre for Evidence-Based Medicine published criteria to determine the evidence levels, the sham-controlled RCT demonstrated level 1 evidence that rTMS is safe but is not better than placebo as a stand-alone treatment for resistant depression among children and adolescents [23]. Nevertheless, 41.7% responded, and 29.2% achieved remission with rTMS [43]. Seven open-label studies showed level 2 evidence for efficacy [27-32,42]. Multiple case series and case reports showed a level 4 degree of evidence of efficacy [34-41,44]. The study's treatment response rate by Zhang et al. seems to be an outlier. It could be because of the naturalistic study design or having a somewhat different inclusion and exclusion criteria [42]. Further, the study's comparison groups were different from each other in significant parameters such as the course of illness, baseline HAM-D score [42]. The studies that did not find rTMS as a useful tool for the treatment of depression have either used it as a stand-alone treatment [43] or comprise of only case reports demonstrating side-effects that led to premature termination of treatment [36,37,40].

We have used Joanna Briggs Institute Critical Appraisal Tools to assess the quality of the included studies (see Appendix) [22]. The overall quality of the studies is average except for Croarkin et al. which seems to have high [43]. rTMS can still be considered a relatively novel treatment option for minors and could have contributed to the included studies’ relatively small sample sizes. Moreover, almost all the studies have used well-validated diagnostic tools and rating scales to provide objective data of the treatment response. All the studies attempted to use rTMS only in the context of previous treatment failures. Still, the existing database's main drawbacks are the studies' limited sample size and mostly open-label study designs. The overall quality of the existing studies is low. The other limitations are heterogeneity in the inclusion criteria, the number of previously failed antidepressant trials, various parameters, and the number of rTMS sessions. The heterogeneity mentioned above could explain some varied treatment responses in the reported studies. There is a strong need to conduct RCTs involving large study subjects to explore the efficacy of rTMS as an add-on treatment in child and adolescent major depression. There is a need to explore the stage of treatment of Major Depression when the addition of rTMS to antidepressant treatment could lead to the best possible treatment outcome in terms of its utility as an add-on agent for treatment. This is especially true given the favorable side effects reported in the previously published studies. Although it is challenging to draw a sweeping conclusion at this time, rTMS has a strong potential in treating depression among children and adolescents, particularly among adolescents.


Major depression among children and adolescents is associated with a high non-response rate with traditional treatment. rTMS can be a useful add-on treatment for child and adolescent major depression, not responding to at least one antidepressant. The existing database is limited by the limited number of RCTs. Despite limitations, most of the studies indicate that rTMS is generally safe among children and adolescents and carries a minimal risk of seizure and treatment-emergent hypomanic symptoms. rTMS is not more effective than placebo as a stand-alone treatment of resistant major depression among children and adolescents.


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  Q1 Q2 Q3 Q4 Q5 Q6 Q7 Q8
Cullen et al. [33] - - - + - - + +
Cristancho et al. [34] + + + - + - + +
Segev et al. [35] + + + + + + + +
Chiramberro et al. [36] - + + + + - + -
Hu et al. [37] - - - - + + + +
  Q1 Q2 Q3 Q4 Q5 Q6 Q7 Q8 Q9
Zhang et al. [42] + - + - + + + + +
MacMaster et al. [27] + + + - + + + + +
Wall et al. [28] + + + - + + + + +
Croarkin et al. [29] + + + - + + + + +
Wall et al. [30] + + + - + + + + +
Wall et al. [31] + + + - + + + + +
Bloch, 2008 [32] + + + - + + + + +
  Q1 Q2 Q3 Q4 Q5 Q6 Q7 Q8 Q9 Q10 Q11 Q12 Q13
Croarkin et al. [43] + + + + + + + + ? + + + +
  Q1 Q2 Q3 Q4 Q5 Q6 Q7 Q8 Q9 Q10
Pan et al. [38] + + + - - - + + - NA
Yang et al. [39] + + + ? + - - + - +
Croarkin et al. [40] - + + - - - + + - NA
Loo et al. [41] + + + + - - + + - ?
Walter et al. [44] - + + - - - - + - -

Review article

The Safety and Efficacy of Repetitive Transcranial Magnetic Stimulation in the Treatment of Major Depression Among Children and Adolescents: A Systematic Review

Author Information

Pradipta Majumder Corresponding Author

Psychiatry, WellSpan, York, USA

Sabish Balan

Psychiatry, Harlem Hospital, New York, USA

Vikas Gupta

Psychiatry, South Carolina Department of Mental Health, Columbia, USA

Roopma Wadhwa

Psychiatry and Behavioral Sciences, South Carolina Department of Mental Health, South Carolina, USA

Tarique D. Perera

Psychiatry and Behavioral Sciences, Contemporary Care, Greenwich, USA

Ethics Statement and Conflict of Interest Disclosures

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: Dr. Pradipta Majumder is an rTMS provider. However, this has not have influenced the outcome ot the systematic review. Dr. Perera is an rTMS provider. However, this has not have influenced the outcome of the systematic review. No conflict of interest relevant for other authors.


We are indebted to Dr. Paul Croarkin, D.O., M.S. for his timely support in providing additional materials and full-texts of some published papers.

Review article

The Safety and Efficacy of Repetitive Transcranial Magnetic Stimulation in the Treatment of Major Depression Among Children and Adolescents: A Systematic Review

Figures etc.


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