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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5250_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Foreword
- •Preface
- •Contents
- •1.1.2.5 Priming (Guiding) Transcranial Magnetic Stimulation (pTMS)
- •1.1.2.6 Synchronized Transcranial Magnetic Stimulation (sTMS)
- •1.1.2.8 Magnetic Seizure Therapy (MST)
- •1.2.1 Treatment Procedures
- •1.2.2 TMS Treatment Precautions
- •1.2.2.1 Seizure Risk
- •1.2.2.3 Other Precautions
- •1.3.1.1 Membrane Potential Alterations
- •1.4 Effect Factors
- •1.4.1 Stimulation Frequency
- •About the Editors
- •1: Transcranial Magnetic Stimulation
- •1.1 Introduction
- •1.1.2.1 Repetitive Transcranial Magnetic Stimulation (rTMS)
- •1.1.2.2 Prolonged Intermittent Theta Burst Stimulation (piTBS)
- •1.1.2.4 Deep Transcranial Magnetic Stimulation (dTMS)
- •1.4.2 Stimulation Intensity
- •1.4.3 Pulse Duration
- •1.4.5 Interstimulus Interval
- •1.5 Conclusion
- •References
- •2: Transcranial Direct Current Stimulation
- •2.1 Introduction
- •2.3.3 Nonneuronal Mechanisms
- •2.3.4 Others
- •2.4 Effect Factors
- •2.4.1 Stimulus Polarity
- •2.4.2 Duration
- •2.4.3 Current Intensity
- •2.4.4 Others
- •2.5 Summary and Outlook
- •References
- •3: Major Depressive Disorder
- •3.1 Introduction
- •3.2 TMS
- •3.2.1 rTMS
- •3.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.2 Deep TMS
- •3.2.2.1 Efficacy
- •3.2.2.2 Safety
- •3.2.2.3 Treatment Regimen
- •3.2.2.4 Clinical Recommendations
- •3.2.3 Priming rTMS
- •3.2.3.1 Efficacy
- •3.2.3.2 Safety
- •3.2.3.3 Treatment Regimen
- •3.2.3.4 Clinical Recommendations
- •3.2.4 Synchronized rTMS
- •3.2.4.1 Efficacy
- •3.2.4.2 Safety
- •3.2.4.3 Treatment Regimen
- •3.2.4.4 Clinical Recommendations
- •3.2.5 TBS
- •3.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.5.3 Continuous TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •3.2.6 Magnetic Seizure Therapy (MST)
- •3.2.6.1 Efficacy
- •3.2.6.2 Safety
- •3.2.6.3 Treatment Regimen
- •3.2.6.4 Clinical Recommendations
- •3.3 tDCS
- •3.3.1 Conventional tDCS
- •3.3.1.1 Efficacy
- •3.3.1.3 Treatment Regimen
- •3.3.1.4 Clinical Recommendations
- •3.3.2 HD-tDCS
- •3.3.2.1 Efficacy
- •3.3.2.2 Safety
- •3.3.2.3 Treatment Regimen
- •3.3.2.4 Clinical Recommendations
- •3.4 TMS Vs. tDCS
- •3.4.1 Efficacy
- •3.4.2 Safety
- •3.5 Conclusion
- •References
- •3.3.1.2 Safety
- •4: Bipolar Disorder
- •4.1 Introduction
- •4.2 TMS
- •4.2.1 rTMS
- •4.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.2 Deep TMS
- •4.2.2.1 Efficacy
- •4.2.2.2 Safety
- •4.2.2.3 Treatment Regimen
- •4.2.2.4 Clinical Recommendations
- •4.2.3 Priming TMS
- •4.2.3.1 Efficacy
- •4.2.3.2 Safety
- •4.2.3.3 Treatment Regimen
- •4.2.3.4 Clinical Recommendations
- •4.2.4 Synchronized TMS
- •4.2.4.1 Efficacy
- •4.2.4.2 Safety
- •4.2.4.3 Treatment Regimen
- •4.2.4.4 Clinical Recommendations
- •4.2.5 TBS
- •4.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.5.3 Continuous TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •4.2.6 MST
- •4.2.6.1 Efficacy
- •4.2.6.2 Safety
- •4.2.6.3 Treatment Regimen
- •4.2.6.4 Clinical Recommendations
- •4.3 tDCS
- •4.3.1 Conventional tDCS
- •4.3.1.1 Efficacy
- •4.3.1.2 Safety
- •4.3.1.3 Treatment Regimen
- •4.3.1.4 Clinical Recommendations
- •4.3.2 HD-tDCS
- •4.3.2.1 Efficacy
- •4.3.2.2 Safety
- •4.3.2.3 Treatment Regimen
- •4.3.2.4 Clinical Recommendations
- •4.4 TMS vs. tDCS
- •4.4.1 Efficacy
- •4.4.2 Safety
- •4.5 Conclusion
- •References
- •5: Schizophrenia
- •5.1 Schizophrenia
- •5.2 TMS
- •5.2.1 rTMS
- •5.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.2 Deep TMS
- •5.2.2.1 Efficacy
- •5.2.2.2 Safety
- •5.2.2.3 Treatment Regimen
- •5.2.2.4 Clinical Recommendations
- •5.2.3 Priming TMS
- •5.2.3.1 Efficacy
- •5.2.3.2 Safety
- •5.2.3.3 Treatment Regimen
- •5.2.3.4 Clinical Recommendations
- •5.2.4 Synchronized TMS
- •5.2.4.1 Efficacy
- •5.2.4.2 Safety
- •5.2.4.3 Treatment Regimen
- •5.2.4.4 Clinical Recommendations
- •5.2.5 TBS
- •5.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •5.2.6 MST
- •5.2.6.1 Efficacy
- •5.2.6.2 Safety
- •5.2.6.3 Treatment Regimen
- •5.2.6.4 Clinical Recommendations
- •5.3 tDCS
- •5.3.1 Conventional tDCS
- •5.3.1.1 Efficacy
- •5.3.1.2 Safety
- •5.3.1.3 Treatment Regimen
- •5.3.1.4 Clinical Recommendations
- •5.3.2 HD-tDCS
- •5.3.2.1 Efficacy
- •5.3.2.2 Safety
- •5.3.2.3 Treatment Regimen
- •5.3.2.4 Clinical Recommendations
- •5.4 TMS vs. tDCS
- •5.4.1 Efficacy
- •5.4.2 Safety
- •5.5 Conclusion
- •References
- •6: Addictive Disorders
- •6.1 Addictive Disorders
- •6.2 TMS
- •6.2.1 rTMS
- •6.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •6.2.1.2 Bilateral rTMS
- •6.2.1.3 Accelerated rTMS
- •6.2.2 Deep TMS
- •6.2.3 Priming TMS
- •6.2.4 Synchronized TMS
- •6.2.5 TBS
- •6.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •6.2.5.2 Accelerated iTBS
- •6.2.5.3 Continuous TBS
- •6.2.5.4 Bilateral TBS
- •6.2.6 MST
- •6.3 tDCS
- •6.3.1 Conventional tDCS
- •6.3.1.1 Efficacy
- •6.3.1.2 Safety
- •6.3.1.3 Treatment Regimen
- •6.3.1.4 Clinical Recommendations
- •6.3.2 HD-tDCS
- •6.4 TMS vs. tDCS
- •6.4.1 Efficacy
- •6.4.2 Safety
- •6.5 Conclusion
- •References
- •7: Obsessive-Compulsive Disorder
- •7.1 Introduction
- •7.2 TMS
- •7.2.1 rTMS
- •7.2.1.1 Unilateral rTMS
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.2 Deep TMS
- •7.2.2.1 Efficacy
- •7.2.2.2 Safety
- •7.2.2.3 Treatment Regimen
- •7.2.2.4 Clinical Recommendations
- •7.2.3 Priming TMS
- •7.2.3.1 Efficacy
- •7.2.3.2 Safety
- •7.2.3.3 Treatment Regimen
- •7.2.3.4 Clinical Recommendations
- •7.2.4 Synchronized TMS
- •7.2.4.1 Efficacy
- •7.2.4.2 Safety
- •7.2.4.3 Treatment Regimen
- •7.2.4.4 Clinical Recommendations
- •7.2.5 TBS
- •7.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •7.2.6 MST
- •7.2.6.1 Safety
- •7.2.6.2 Treatment Regimen
- •7.2.6.3 Clinical Recommendations
- •7.3 tDCS
- •7.3.1 Conventional tDCS
- •7.3.1.1 Efficacy
- •7.3.1.2 Safety
- •7.3.1.3 Treatment Regimen
- •7.3.1.4 Clinical Recommendations
- •7.3.2 HD-tDCS
- •7.3.2.1 Efficacy
- •7.3.2.2 Safety
- •7.3.2.3 Treatment Regimen
- •7.3.2.4 Clinical Recommendations
- •7.4 TMS vs. tDCS
- •7.4.1 Efficacy
- •7.4.2 Safety
- •7.5 Conclusion
- •References
- •8: Attention Deficit Hyperactivity Disorder
- •8.1 ADHD
- •8.1.2 Therapeutic Method
- •8.2 TMS
- •8.2.1 Single-Pulse TMS (spTMS)
- •8.2.1.1 Efficacy
- •8.2.1.2 Safety
- •8.2.1.3 Treatment Regimen
- •8.2.1.4 Clinical Recommendations
- •8.2.2 Paired-Pulse TMS (ppTMS)
- •8.2.2.1 Efficacy
- •8.2.2.2 Safety
- •8.2.2.3 Treatment Regimen
- •8.2.2.4 Clinical Recommendations
- •8.2.3 rTMS
- •8.2.3.1 Low-Frequency rTMS (LF-rTMS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.2.3.2 High-Frequency rTMS (HF-rTMS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.2.4 TBS
- •8.2.4.1 Intermittent TBS (iTBS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.2.4.2 Continuous iTBS (cTBS)
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •8.3 tDCS
- •8.3.1 Conventional tDCS
- •8.3.1.1 Efficacy
- •8.3.1.2 Safety
- •8.3.1.3 Treatment Regimen
- •8.3.1.4 Clinical Recommendations
- •8.3.2.1 Efficacy
- •8.3.2.2 Safety
- •8.3.2.3 Treatment Regimen
- •8.3.2.4 Clinical Recommendations
- •8.4 TMS vs. tDCS
- •8.4.1 Efficacy
- •8.4.2 Safety
- •8.5 Conclusion
- •References
- •9: Autism Spectrum Disorder
- •9.1 Introduction
- •9.2 rTMS
- •9.2.1 Unilateral rTMS
- •9.2.1.1 Efficacy
- •9.2.1.2 Safety
- •9.2.1.3 Treatment Regimen
- •9.2.1.4 Clinical Recommendations
- •9.2.1.5 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.1.6 Accelerated rTMS
- •9.2.2 Deep TMS
- •9.2.2.1 Efficacy
- •9.2.2.2 Safety
- •9.2.2.3 Treatment Regimen
- •9.2.2.4 Clinical Recommendations
- •9.2.3 Priming TMS
- •9.2.4 Synchronized TMS
- •9.2.5 TBS
- •9.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.5.2 Accelerated iTBS
- •9.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •9.2.6 MST
- •9.3 tDCS
- •9.3.1 Conventional tDCS
- •9.3.1.1 Efficacy
- •9.3.1.2 Safety
- •9.3.1.3 Treatment Regimen
- •9.3.1.4 Clinical Recommendations
- •9.3.2 HD-tDCS
- •9.3.2.1 Efficacy
- •9.3.2.2 Safety
- •9.3.2.3 Treatment Regimen
- •9.3.2.4 Clinical Recommendations
- •9.4 TMS Vs. tDCS
- •9.4.1 Efficacy
- •9.4.1.1 Cognitive Effects
- •9.4.1.3 Biological Effects
- •9.4.2 Safety
- •9.5 Conclusion
- •References
- •10: Anxiety Disorder
- •10.1 Introduction
- •10.2 TMS
- •10.2.1 rTMS
- •10.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.2 Deep TMS
- •10.2.2.1 Efficacy
- •10.2.2.2 Safety
- •10.2.2.3 Treatment Regimen
- •10.2.2.4 Clinical Recommendations
- •10.2.3 Priming TMS
- •10.2.3.1 Efficacy
- •10.2.3.2 Safety
- •10.2.3.3 Treatment Regimen
- •10.2.3.4 Clinical Recommendations
- •10.2.4 Synchronized TMS
- •10.2.4.1 Efficacy
- •10.2.4.2 Safety
- •10.2.4.3 Treatment Regimen
- •10.2.4.4 Clinical Recommendations
- •10.2.5 TBS
- •10.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.5.3 Continuation TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.5.4 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •10.2.6 Magnetic Seizure Therapy (MST)
- •10.3 tDCS
- •10.3.1 Conventional tDCS
- •10.3.1.1 Efficacy
- •10.3.1.2 Safety
- •10.3.1.3 Treatment Regimen
- •10.3.1.4 Clinical Recommendations
- •10.3.2 HD-tDCS
- •10.3.2.1 Efficacy
- •10.3.2.2 Safety
- •10.3.2.3 Clinical Recommendations
- •10.4 TMS versus tDCS
- •10.4.1 Efficacy
- •10.4.2 Safety
- •10.5 Conclusion
- •References
- •11: Post-traumatic Stress Disorder
- •11.1 Introduction
- •11.2 TMS
- •11.2.1 rTMS
- •11.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.1.3 Accelerated rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.2 Deep TMS
- •11.2.2.1 Efficacy
- •11.2.2.2 Safety
- •11.2.2.3 Treatment Regimen
- •11.2.2.4 Clinical Recommendations
- •11.2.3 Priming TMS
- •11.2.3.1 Efficacy
- •11.2.3.2 Safety
- •11.2.3.3 Treatment Regimen
- •11.2.3.4 Clinical Recommendations
- •11.2.4 Synchronized TMS
- •11.2.4.1 Efficacy
- •11.2.4.2 Safety
- •11.2.4.3 Treatment Regimen
- •11.2.4.4 Clinical Recommendations
- •11.2.5 TBS
- •11.2.5.1 iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.5.2 Accelerated iTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.5.3 Bilateral TBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •11.2.6 MST
- •11.2.6.1 Efficacy
- •11.2.6.2 Safety
- •11.2.6.3 Treatment Regimen
- •11.2.6.4 Clinical Recommendations
- •11.3 tDCS
- •11.3.1 Conventional tDCS
- •11.3.1.1 Efficacy
- •11.3.1.2 Safety
- •11.3.1.3 Treatment Regimen
- •11.3.1.4 Clinical Recommendations
- •11.3.2 HD-tDCS
- •11.3.2.1 Efficacy
- •11.3.2.2 Safety
- •11.3.2.3 Treatment Regimen
- •11.3.2.4 Clinical Recommendations
- •11.4 TMS vs. tDCS
- •11.4.1 Efficacy
- •11.4.2 Safety
- •11.5 ECT
- •11.5.1 Efficacy
- •11.5.2 Safety
- •11.5.3 Treatment Regimen
- •11.5.4 Clinical Recommendations
- •11.6 Conclusion
- •References
- •12: Sleep Disorders
- •12.1 Introduction
- •12.2 TMS
- •12.2.1 rTMS
- •12.2.1.1 Unilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •12.2.1.2 Bilateral rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •12.2.1.3 Accelerated rTMS
- •12.2.2 Deep TMS
- •12.2.3 Priming TMS
- •12.2.4 Synchronised TMS
- •12.2.5 TBS
- •12.2.5.1 iTBS
- •12.2.5.2 Accelerated iTBS
- •12.2.5.3 cTBS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •12.2.5.4 Bilateral TBS
- •12.2.6 MST
- •12.3 tDCS
- •12.3.1 Efficacy
- •12.3.2 Safety
- •12.3.3 Treatment Regimen
- •12.3.4 Clinical Recommendations
- •12.4 TMS Combined tDCS
- •12.4.1 Efficacy
- •12.4.2 Safety
- •12.5 Conclusion
- •References
- •13: Neurocognitive Disorders
- •13.1 Introduction
- •13.2 TMS
- •13.2.1 TMS
- •13.2.1.1 Conventional rTMS
- •Efficacy
- •Safety
- •Treatment Regimen
- •Clinical Recommendations
- •13.2.1.2 Accelerated rTMS
- •13.2.2 Deep TMS
- •13.2.2.1 Efficacy
- •13.2.2.2 Safety
- •13.2.2.3 Treatment Regimen
- •13.2.2.4 Clinical Recommendations
- •13.2.3 Priming TMS
- •13.2.4 Synchronized TMS
- •13.2.5 iTBS
- •13.2.5.1 Efficacy
- •13.2.5.2 Safety
- •13.2.5.3 Treatment Regimen
- •13.2.5.4 Clinical Recommendations
- •13.2.6 Magnetic Seizure Therapy
- •13.3.1 Conventional tDCS
- •13.3.1.1 Efficacy
- •13.3.1.2 Safety
- •13.3.1.3 Treatment Regimen
- •13.3.1.4 Clinical Recommendations
- •13.3.2 HD-tDCS
- •13.3.2.1 Efficacy
- •13.3.2.2 Safety
- •13.3.2.3 Treatment Regimen
- •13.3.2.4 Clinical Recommendations
- •13.4 TMS vs. tDCS
- •13.4.1 Efficacy
- •13.4.2 Safety
- •13.5 Conclusion
- •References

5 Schizophrenia
131
5.4 TMS vs. tDCS
5.4.1 Efficacy
NIBS has been proposed as an intervention strategy for mental disorders. NIBS
includes TMS and tDCS [186]. The stimulation frequency of TMS can either
increase or decrease cortical excitability and ranges from 1 to 50Hz. On the other
hand, tDCS is another noninvasive neurostimulation technique that uses direct electrical currents to stimulate specic cortical regions. Anodal tDCS (AtDCS) is generally thought to enhance the function of the underlying cortical areas, while cathodal
tDCS has a suppressive effect. The sustained effects of tDCS are thought to share a
similar neurobiological basis with TMS, involving the induction of long-term
potentiation like plasticity [186, 236, 237].
In patients with schizophrenia, tDCS and TMS show different treatment outcomes in reducing positive symptoms. For auditory hallucinations, tDCS produced
a small but highly heterogeneous positive effect, and TMS produced a negligible but
homogeneous positive effect. However, both TMS and tDCS protocols signicantly
improved negative symptoms with a medium effect size. It should be noted that
there was a high degree of heterogeneity in these results. Some caution is needed in
interpreting the results of NIBS for negative symptoms in schizophrenia. In terms of
the efcacy on cognitive impairments in schizophrenia, active TMS was not superior to sham for cognitive improvement. In contrast, tDCS proved effective in
enhancing attention and working memory in schizophrenia patients [186].
Furthermore, research indicates that tDCS may be more effective than TMS in
enhancing attention/vigilance [187]. In conclusion, it seems that neurostimulation
could be used in patients with schizophrenia, in particular for the negative symptoms and cognitive impairments of the disorder.
5.4.2 Safety
Both TMS and tDCS have been widely reported as safe techniques with minimal
adverse effects [209, 238]. In terms of safety, unilateral rTMS has been shown to be
a safe, NIBS technique with no serious adverse effects other than the well-known
side effects of mild headache and localized scalp discomfort observed in the majority of studies. The general impression is that tDCS is a safe technique, with adverse
effects that are mild and transient [188]. The most common adverse effects are
observed in the active group and include itching, tingling, headache, burning, and
discomfort.

132
H. Deng et al.
5.5 Conclusion
The diverse and complex nature of schizophrenia has hindered the establishment of
consensus regarding the efcacy of novel noninvasive neurostimulation techniques,
specically TMS and tDCS.Despite mixed ndings on their effectiveness, both
TMS and tDCS show promise as treatment options for patients with schizophrenia.
However, additional research is necessary to determine the optimal stimulation
parameters and identify key variables that may impact individual responses to either
TMS or tDCS.In the design of future clinical trials, a priority should be the examination of the efcacy of higher doses of tDCS in schizophrenia. These trials should
entail the administration of stimulation sessions twice, and potentially even three
times, per day or using larger current intensity. Moreover, conducting follow-up
assessments 1, 2, and 3months following the conclusion of treatment is imperative.
Furthermore, there is a need for further exploration into the potential of neuronavigation in conjunction with TMS, as this modication of TMS has shown promise in
the treatment of schizophrenia. It is anticipated that these methods will contribute
signicantly to enhancing our understanding of the underlying pathological mechanisms and treatment of schizophrenia, ultimately leading to the achievement of sustained and effective outcomes.
Acknowledgments None.
Disclosure/Conicts of Interest The authors declare no conicts of interest in conducting this
study or preparing the manuscript.
Financial Support This work was supported by the National Natural Science Foundation of
China, 82301693 and 31900751; the Capital’s Funds for Health Improvement and Research,
CFH2024-4-2132; Beijing Municipal Science & Technology Commission, Z221100007422047.
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
1. Huang Y, Wang Y, Wang H, etal. Prevalence of mental disorders in China: a cross-sectional
epidemiological study. Lancet Psychiatry. 2019;6:211–24.
2. McCutcheon RA, Reis Marques T, Howes OD.Schizophrenia-an overview. JAMA Psychiatry.
2020;77:201–10.
3. Salokangas RKR.Symptom dimensions and outcome in schizophrenia. World Psychiatry.
2003;2:172–8.
4. Bowie CR, Harvey PD. Cognitive decits and functional outcome in schizophrenia.
Neuropsychiatr Dis Treat. 2006;2:531–6.
5. Sun C-H, Mai J-X, Shi Z-M, Zheng W, Jiang W-L, Li Z-Z, Huang X-B, Yang X-H, Zheng
W.Adjunctive repetitive transcranial magnetic stimulation for adolescents with rst-episode
major depressive disorder: a meta-analysis. Front Psych. 2023;14:1200738.
6. Aleman A, Enriquez-Geppert S, Knegtering H, Dlabac-de Lange JJ.Moderate effects of noninvasive brain stimulation of the frontal cortex for improving negative symptoms in schizophrenia: meta-analysis of controlled trials. Neurosci Biobehav Rev. 2018;89:111–8.

5 Schizophrenia
7. Osoegawa C, Gomes JS, Grigolon RB, etal. Non-invasive brain stimulation for negative
symptoms in schizophrenia: an updated systematic review and meta-analysis. Schizophr Res.
2018;197:34–44.
8. Klein E, Kolsky Y, Puyerovsky M, Koren D, Chistyakov A, Feinsod M.Right prefrontal slow
repetitive transcranial magnetic stimulation in schizophrenia: a double-blind sham-controlled
pilot study. Biol Psychiatry. 1999;46:1451–4.
9. Lorentzen R, Nguyen TD, McGirr A, Hieronymus F, Østergaard SD.The efcacy of transcranial magnetic stimulation (TMS) for negative symptoms in schizophrenia: a systematic
review and meta-analysis. Schizophrenia (Heidelb Ger). 2022;8:35.
10. Jiang Y, Guo Z, Xing G, He L, Peng H, Du F, McClure MA, Mu Q.Effects of high-frequency
transcranial magnetic stimulation for cognitive decit in schizophrenia: a meta-analysis.
Front Psych. 2019;10:135.
11. Gan J, Duan H, Chen Z, Shi Z, Gao C, Zhu X, Liang X.Effectiveness and safety of high
dose transcranial magnetic stimulation in schizophrenia with refractory negative symptoms:
a randomized controlled study. Zhonghua Yi Xue Za Zhi. 2015;95:3808–12.
12. Hoffman RE, Gueorguieva R, Hawkins KA, Varanko M, Boutros NN, Wu Y, Carroll
K, Krystal JH. Temporoparietal transcranial magnetic stimulation for auditory hallucinations: safety, efcacy and moderators in a fty patient sample. Biol Psychiatry.
2005;58:97–104.
13. Wang J, Zhou Y, Gan H, Pang J, Li H, Wang J, Li C.Efcacy towards negative symptoms and
safety of repetitive transcranial magnetic stimulation treatment for patients with schizophrenia: a systematic review. Shanghai Arch Psychiatry. 2017;29:61–76.
14. Cole J, Bright K, Gagnon L, McGirr A.A systematic review of the safety and effectiveness
of repetitive transcranial magnetic stimulation in the treatment of peripartum depression. J
Psychiatr Res. 2019;115:142–50.
15. Loo CK, McFarquhar TF, Mitchell PB. A review of the safety of repetitive transcranial
magnetic stimulation as a clinical treatment for depression. Int J Neuropsychopharmacol.
2008;11:131–47.
16. Arumugham SS, Thirthalli J, Andrade C.Efcacy and safety of combining clozapine with
electrical or magnetic brain stimulation in treatment-refractory schizophrenia. Expert Rev
Clin Pharmacol. 2016;9:1245–52.
17. Singh S, Kumar N, Verma R, Nehra A.The safety and efcacy of adjunctive 20-Hz repetitive transcranial magnetic stimulation for treatment of negative symptoms in patients with
schizophrenia: a double-blinded, randomized, sham-controlled study. Indian J Psychiatry.
2020;62:21–9.
18. Tikka SK, Godi SM, Siddiqui MA, Garg S.Evidence from Indian studies on safety and efcacy of therapeutic transcranial magnetic stimulation across neuropsychiatric disorders– a
systematic review and meta-analysis. Indian J Psychiatry. 2023;65:18–35.
19. Chibbaro G, Daniele M, Alagona G, Di Pasquale C, Cannavò M, Rapisarda V, Bella R,
Pennisi G.Repetitive transcranial magnetic stimulation in schizophrenic patients reporting
auditory hallucinations. Neurosci Lett. 2005;383:54–7.
20. Poulet E, Brunelin J, Bediou B, Bation R, Forgeard L, Dalery J, d’Amato T, Saoud M.Slow
transcranial magnetic stimulation can rapidly reduce resistant auditory hallucinations in
schizophrenia. Biol Psychiatry. 2005;57:188–91.
21. Rosa MO, Gattaz WF, Rosa MA, etal. Effects of repetitive transcranial magnetic stimulation
on auditory hallucinations refractory to clozapine. J Clin Psychiatry. 2007;68:1528–32.
22. Saba G, Verdon CM, Kalalou K, Rocamora JF, Dumortier G, Benadhira R, Stamatiadis L,
Vicaut E, Lipski H, Januel D.Transcranial magnetic stimulation in the treatment of schizophrenic symptoms: a double blind sham controlled study. J Psychiatr Res. 2006;40:147–52.
23. Cohen E, Bernardo M, Masana J, etal. Repetitive transcranial magnetic stimulation in the
treatment of chronic negative schizophrenia: a pilot study. J Neurol Neurosurg Psychiatry.
1999;67:129–30.
24. Dlabac-de Lange JJ, Bais L, van Es FD, Visser BGJ, Reinink E, Bakker B, van den Heuvel
ER, Aleman A, Knegtering H.Efcacy of bilateral repetitive transcranial magnetic stimula-
133

134
tion for negative symptoms of schizophrenia: results of a multicenter double-blind randomized controlled trial. Psychol Med. 2015;45:1263–75.
25. Prikryl R, Ustohal L, Prikrylova Kucerova H, Kasparek T, Venclikova S, Vrzalova M,
Ceskova E.A detailed analysis of the effect of repetitive transcranial magnetic stimulation on
negative symptoms of schizophrenia: a double-blind trial. Schizophr Res. 2013;149:167–73.
26. Schneider AL, Schneider TL, Stark H.Repetitive transcranial magnetic stimulation (rTMS)
as an augmentation treatment for the negative symptoms of schizophrenia: a 4-week randomized placebo controlled study. Brain Stimul. 2008;1:106–11.
27. Holi MM, Eronen M, Toivonen K, Toivonen P, Marttunen M, Naukkarinen H. Left prefrontal repetitive transcranial magnetic stimulation in schizophrenia. Schizophr Bull.
2004;30:429–34.
28. Mittrach M, Thünker J, Winterer G, etal. The tolerability of rTMS treatment in schizophrenia
with respect to cognitive function. Pharmacopsychiatry. 2010;43:110–7.
29. Zhao S, Kong J, Li S, Tong Z, Yang C, Zhong H.Randomized controlled trial of four protocols of repetitive transcranial magnetic stimulation for treating the negative symptoms of
schizophrenia. Shanghai Arch Psychiatry. 2014;26:15–21.
30. Li Z, Yin M, Lyu X-L, Zhang L-L, Du X-D, Hung GC-L.Delayed effect of repetitive transcranial magnetic stimulation (rTMS) on negative symptoms of schizophrenia: ndings from
a randomized controlled trial. Psychiatry Res. 2016;240:333–5.
31. Tseng P-T, Zeng B-S, Hung C-M, etal. Assessment of noninvasive brain stimulation interventions for negative symptoms of schizophrenia: a systematic review and network metaanalysis. JAMA Psychiatry. 2022;79:770–9.
32. Wobrock T, Guse B, Cordes J, etal. Left prefrontal high-frequency repetitive transcranial
magnetic stimulation for the treatment of schizophrenia with predominant negative symptoms: a sham-controlled, randomized multicenter trial. Biol Psychiatry. 2015;77:979–88.
33. Wölwer W, Lowe A, Brinkmeyer J, Streit M, Habakuck M, Agelink MW, Mobascher A,
Gaebel W, Cordes J. Repetitive transcranial magnetic stimulation (rTMS) improves facial
affect recognition in schizophrenia. Brain Stimul. 2014;7:559–63.
34. Yi S, Wang Q, Wang W, Hong C, Ren Z.Efcacy of repetitive transcranial magnetic stimulation (rTMS) on negative symptoms and cognitive functioning in schizophrenia: an umbrella
review of systematic reviews and meta-analyses. Psychiatry Res. 2024;333:115728.
35. Paillère-Martinot M-L, Galinowski A, Plaze M, etal. Active and placebo transcranial magnetic stimulation effects on external and internal auditory hallucinations of schizophrenia.
Acta Psychiatr Scand. 2017;135:228–38.
36. Dlabac-de Lange JJ, Liemburg EJ, Bais L, Van De Poel-Mustafayeva AT, De Lange-de Klerk
ESM, Knegtering H, Aleman A.Effect of bilateral prefrontal rTMS on left prefrontal NAA
and Glx levels in schizophrenia patients with predominant negative symptoms: an exploratory study. Brain Stimul. 2017;10:59–64.
37. Liemburg EJ, Dlabac-De Lange JJ, Bais L, Knegtering H, Aleman A.Effects of bilateral
prefrontal rTMS on brain activation during social-emotional evaluation in schizophrenia: a
double-blind, randomized, exploratory study. Schizophr Res. 2018;202:210–1.
38. Barr MS, Farzan F, Tran LC, Fitzgerald PB, Daskalakis ZJ.A randomized controlled trial
of sequentially bilateral prefrontal cortex repetitive transcranial magnetic stimulation in the
treatment of negative symptoms in schizophrenia. Brain Stimul. 2012;5:337–46.
39. Hoffman RE, Wu K, Pittman B, Cahill JD, Hawkins KA, Fernandez T, Hannestad
J. Transcranial magnetic stimulation of Wernicke’s and right homologous sites to curtail
“voices”: a randomized trial. Biol Psychiatry. 2013;73:1008–14.
40. Bais L, Vercammen A, Stewart R, van Es F, Visser B, Aleman A, Knegtering H.Short and
long term effects of left and bilateral repetitive transcranial magnetic stimulation in schizophrenia patients with auditory verbal hallucinations: a randomized controlled trial. PLoS
One. 2014;9:e108828.
41. Kim E-J, Yeo S, Hwang I, Park J-I, Cui Y, Jin H-M, Kim HT, Hwang T-Y, Chung Y-C.Bilateral
repetitive transcranial magnetic stimulation for auditory hallucinations in patients with
H. Deng et al.

5 Schizophrenia
schizophrenia: a randomized controlled, cross-over study. Clin Psychopharmacol Neurosci.
2014;12:222–8.
42. Brunelin J, Galvao F, Mondino M.Twice daily low frequency rTMS for treatment-resistant
auditory hallucinations. Int J Clin Health Psychol. 2023;23:100344.
43. Montagne-Larmurier A, Etard O, Razamandimby A, Morello R, Dollfus S.Two-day treatment of auditory hallucinations by high frequency rTMS guided by cerebral imaging: a 6
month follow-up pilot study. Schizophr Res. 2009;113:77–83.
44. Dollfus S, Jaafari N, Guillin O, et al. High-frequency neuronavigated rTMS in auditory
verbal hallucinations: a pilot double-blind controlled study in patients with schizophrenia.
Schizophr Bull. 2018;44:505–14.
45. Kimura H, Kanahara N, Takase M, Yoshida T, Watanabe H, Iyo M.A randomized, sham-controlled study of high frequency rTMS for auditory hallucination in schizophrenia. Psychiatry
Res. 2016;241:190–4.
46. Levkovitz Y, Rabany L, Harel EV, Zangen A.Deep transcranial magnetic stimulation addon for treatment of negative symptoms and cognitive decits of schizophrenia: a feasibility
study. Int J Neuropsychopharmacol. 2011;14:991–6.
47. Linsambarth S, Jeria A, Avirame K, Todder D, Riquelme R, Stehberg J.Deep transcranial
magnetic stimulation for the treatment of negative symptoms in schizophrenia: beyond an
antidepressant effect. J ECT. 2019;35:e46–54.
48. Rabany L, Deutsch L, Levkovitz Y. Double-blind, randomized sham controlled study of
deep-TMS add-on treatment for negative symptoms and cognitive decits in schizophrenia. J
Psychopharmacol (Oxf Engl). 2014;28:686–90.
49. Ray P, Sinha VK, Tikka SK.Adjuvant low-frequency rTMS in treating auditory hallucinations in recent-onset schizophrenia: a randomized controlled study investigating the effect of
high-frequency priming stimulation. Ann General Psychiatry. 2015;14:8.
50. Blumberger DM, Christensen BK, Zipursky RB, Moller B, Chen R, Fitzgerald PB, Daskalakis
ZJ.MRI-targeted repetitive transcranial magnetic stimulation of Heschl’s gyrus for refractory
auditory hallucinations. Brain Stimul. 2012;5:577–85.
51. Barr MS, Farzan F, Rajji TK, Voineskos AN, Blumberger DM, Arenovich T, Fitzgerald PB,
Daskalakis ZJ.Can repetitive magnetic stimulation improve cognition in schizophrenia? Pilot
data from a randomized controlled trial. Biol Psychiatry. 2013;73:510–7.
52. Fitzgerald PB, Herring S, Hoy K, McQueen S, Segrave R, Kulkarni J, Daskalakis ZJ.A study
of the effectiveness of bilateral transcranial magnetic stimulation in the treatment of the negative symptoms of schizophrenia. Brain Stimul. 2008;1:27–32.
53. Kozak K, Sharif-Razi M, Morozova M, Gaudette EV, Barr MS, Daskalakis ZJ,
Blumberger DM, George TP. Effects of short-term, high-frequency repetitive transcranial magnetic stimulation to bilateral dorsolateral prefrontal cortex on smoking behavior
and cognition in patients with schizophrenia and non-psychiatric controls. Schizophr Res.
2018;197:441–3.
54. Vercammen A, Knegtering H, Bruggeman R, Westenbroek HM, Jenner JA, Slooff CJ,
Wunderink L, Aleman A.Effects of bilateral repetitive transcranial magnetic stimulation on
treatment resistant auditory-verbal hallucinations in schizophrenia: a randomized controlled
trial. Schizophr Res. 2009;114:172–9.
55. Cauleld KA, Fleischmann HH, George MS, McTeague LM.A transdiagnostic review of
safety, efcacy, and parameter space in accelerated transcranial magnetic stimulation. J
Psychiatr Res. 2022;152:384–96.
56. Brunelin J, Poulet E, Bediou B, Kallel L, Dalery J, D’amato T, Saoud M.Low frequency
repetitive transcranial magnetic stimulation improves source monitoring decit in hallucinating patients with schizophrenia. Schizophr Res. 2006;81:41–5.
57. Sverak T, Mayerova M, Obdrzalkova M, Ustohal L.Accelerated repetitive transcranial magnetic stimulation in the treatment of negative symptoms of schizophrenia: an open-label
study. J ECT. 2022;38:e24–5.
135

136
58. Chauhan P, Garg S, Tikka SK, Khattri S.Efcacy of intensive cerebellar intermittent theta
burst stimulation (iCiTBS) in treatment-resistant schizophrenia: a randomized placebo-controlled study. Cerebellum (Lond Engl). 2021;20:116–23.
59. Rachid F.Accelerated transcranial magnetic stimulation for the treatment of patients with
depression: a review. Asian J Psychiatry. 2019;40:71–5.
60. Desbeaumes Jodoin V, Miron J-P, Lespérance P.Safety and efcacy of accelerated repetitive
transcranial magnetic stimulation protocol in elderly depressed unipolar and bipolar patients.
Am J Geriatr Psychiatry. 2019;27:548–58.
61. Bersani FS, Minichino A, Enticott PG, etal. Deep transcranial magnetic stimulation as a
treatment for psychiatric disorders: a comprehensive review. Eur Psychiatry. 2013;28:30–9.
62. Di Passa A-M, Prokop-Millar S, Yaya H, Dabir M, McIntyre-Wood C, Fein A, MacKillop E,
MacKillop J, Duarte D.Clinical efcacy of deep transcranial magnetic stimulation (dTMS) in
psychiatric and cognitive disorders: a systematic review. J Psychiatr Res. 2024;175:287–315.
63. Lu M, Ueno S.Comparison of the induced elds using different coil congurations during
deep transcranial magnetic stimulation. PLoS One. 2017;12:e0178422.
64. Moeller SJ, Gil R, Weinstein JJ, etal. Deep rTMS of the insula and prefrontal cortex in smokers with schizophrenia: proof-of-concept study. Schizophrenia. 2022;8:6.
65. Rosenberg O, Gersner R, Klein LD, Kotler M, Zangen A, Dannon P.Deep transcranial magnetic stimulation add-on for the treatment of auditory hallucinations: a double-blind study.
Ann General Psychiatry. 2012;11:13.
66. Cole JC, Green Bernacki C, Helmer A, Pinninti N, O’Reardon JP.Efcacy of transcranial
magnetic stimulation (TMS) in the treatment of schizophrenia: a review of the literature to
date. Innov Clin Neurosci. 2015;12:12–9.
67. Soltani E, Bateni H, Shad MU.Different modalities of transcranial magnetic stimulation to
manage schizophrenia. Prim Care Companion CNS Disord. 2022;24:21r03144.
68. Birdi A, Kumar PK, Nebhinani N, Gupta T, Tomo S, Purohit P, Banerjee M, Mitra P, Sharma
P, Yadav D.Association of circulatory Klotho levels and its expression with miRNA-339in
patients with schizophrenia. Behav Brain Res. 2023;445:114359.
69. Rosenberg O, Roth Y, Kotler M, Zangen A, Dannon P.Deep transcranial magnetic stimulation for the treatment of auditory hallucinations: a preliminary open-label study. Ann General
Psychiatry. 2011;10:3.
70. Iyer MB, Schleper N, Wassermann EM. Priming stimulation enhances the depressant effect of low-frequency repetitive transcranial magnetic stimulation. J Neurosci.
2003;23:10867–72.
71. Slotema CW, Blom JD, Hoek HW, Sommer IEC.Should we expand the toolbox of psychiatric
treatment methods to include repetitive transcranial magnetic stimulation (rTMS)? A metaanalysis of the efcacy of rTMS in psychiatric disorders. J Clin Psychiatry. 2010;71:873–84.
72. Hasan A, Strube W, Palm U, Wobrock T.Repetitive noninvasive brain stimulation to modulate cognitive functions in schizophrenia: a systematic review of primary and secondary outcomes. Schizophr Bull. 2016;42:S95–109.
73. Marzouk T, Winkelbeiner S, Azizi H, Malhotra AK, Homan P.Transcranial magnetic stimulation for positive symptoms in schizophrenia: a systematic review. Neuropsychobiology.
2020;79:384–96.
74. Di Hou M, Santoro V, Biondi A, Shergill SS, Premoli I.A systematic review of TMS and
neurophysiological biometrics in patients with schizophrenia. J Psychiatry Neurosci.
2021;46:E675–701.
75. Barr MS, Farzan F, Arenovich T, Chen R, Fitzgerald PB, Daskalakis ZJ.The effect of repetitive transcranial magnetic stimulation on gamma oscillatory activity in schizophrenia. PLoS
One. 2011;6:e22627.
76. Farzan F, Barr MS, Levinson AJ, Chen R, Wong W, Fitzgerald PB, Daskalakis ZJ.Evidence
for gamma inhibition decits in the dorsolateral prefrontal cortex of patients with schizophrenia. Brain J Neurol. 2010;133:1505–14.
H. Deng et al.

5 Schizophrenia
77. Ferrarelli F, Massimini M, Peterson MJ, etal. Reduced evoked gamma oscillations in the frontal cortex in schizophrenia patients: a TMS/EEG study. Am J Psychiatry. 2008;165:996–1005.
78. Barr MS, Farzan F, Rusjan PM, Chen R, Fitzgerald PB, Daskalakis ZJ.Potentiation of gamma
oscillatory activity through repetitive transcranial magnetic stimulation of the dorsolateral
prefrontal cortex. Neuropsychopharmacology. 2009;34:2359–67.
79. Farzan F, Barr MS, Sun Y, Fitzgerald PB, Daskalakis ZJ.Transcranial magnetic stimulation on
the modulation of gamma oscillations in schizophrenia. Ann N Y Acad Sci. 2012;1265:25–35.
80. Levit-Binnun N, Handzy NZ, Moses E, Modai I, Peled A.Transcranial magnetic stimulation
at M1 disrupts cognitive networks in schizophrenia. Schizophr Res. 2007;93:334–44.
81. Mehta UM, Naik SS, Thanki MV, Thirthalli J.Investigational and therapeutic applications of
transcranial magnetic stimulation in schizophrenia. Curr Psychiatry Rep. 2019;21:89.
82. Ferrarelli F, Phillips ML.Examining and modulating neural circuits in psychiatric disorders
with transcranial magnetic stimulation and electroencephalography: present practices and
future developments. Am J Psychiatry. 2021;178:400–13.
83. Guo Q, Li C, Wang J.Updated review on the clinical use of repetitive transcranial magnetic
stimulation in psychiatric disorders. Neurosci Bull. 2017;33:747–56.
84. Santoro V, Hou MD, Premoli I, et al. Investigating cortical excitability and inhibition in
patients with schizophrenia: a TMS-EEG study. Brain Res Bull. 2024;212:110972.
85. Chung SW, Hill AT, Rogasch NC, Hoy KE, Fitzgerald PB.Use of theta-burst stimulation
in changing excitability of motor cortex: a systematic review and meta-analysis. Neurosci
Biobehav Rev. 2016;63:43–64.
86. Li Y-T, Chen S-C, Yang L-Y, Hsieh T-H, Peng C-W.Designing and implementing a novel
transcranial electrostimulation system for neuroplastic applications: a preliminary study.
IEEE Trans Neural Syst Rehabil Eng. 2019;27:805–13.
87. Huang Y-Z, Edwards MJ, Rounis E, Bhatia KP, Rothwell JC.Theta burst stimulation of the
human motor cortex. Neuron. 2005;45:201–6.
88. Gamboa OL, Antal A, Moliadze V, Paulus W.Simply longer is not better: reversal of theta
burst after-effect with prolonged stimulation. Exp Brain Res. 2010;204:181–7.
89. Goldsworthy MR, Pitcher JB, Ridding MC. The application of spaced theta burst protocols induces long-lasting neuroplastic changes in the human motor cortex. Eur J Neurosci.
2012;35:125–34.
90. Goldsworthy MR, Pitcher JB, Ridding MC.A comparison of two different continuous theta
burst stimulation paradigms applied to the human primary motor cortex. Clin Neurophysiol.
2012;123:2256–63.
91. Daskalakis ZJ, Fitzgerald PB, Christensen BK.The role of cortical inhibition in the pathophysiology and treatment of schizophrenia. Brain Res Rev. 2007;56:427–42.
92. Poulet E, Haesebaert F, Saoud M, Suaud-Chagny MF, Brunelin J.Treatment of shizophrenic
patients and rTMS.Psychiatr Danub. 2010;22(Suppl 1):S143–6.
93. Rossini PM, Burke D, Chen R, etal. Non-invasive electrical and magnetic stimulation of
the brain, spinal cord, roots and peripheral nerves: basic principles and procedures for routine clinical and research application. An updated report from an I.F.C.N.Committee. Clin
Neurophysiol. 2015;126:1071–107.
94. Voineskos D, Daskalakis ZJ.A primer on the treatment of schizophrenia through repetitive
transcranial magnetic stimulation. Expert Rev Neurother. 2013;13:1079–82.
95. Poorganji M, Goeke K, Zomorrodi R, Voineskos D, Rajji TK, Daskalakis ZJ, Blumberger
DM.The use of theta burst stimulation in patients with schizophrenia—a systematic review.
Schizophr Res. 2023;261:245–55.
96. Kishi T, Ikuta T, Sakuma K, Hamanaka S, Nishii Y, Hatano M, Kito S, Iwata N.Theta burst
stimulation protocols for schizophrenia. JAMA Netw Open. 2024;7:e2441159.
97. Chu C-S, Li C-T, Brunoni AR, etal. Cognitive effects and acceptability of non-invasive brain
stimulation on Alzheimer’s disease and mild cognitive impairment: a component network
meta-analysis. J Neurol Neurosurg Psychiatry. 2021;92:195–203.
137

138
98. Di Lazzaro V, Dileone M, Pilato F, etal. Modulation of motor cortex neuronal networks by
rTMS: comparison of local and remote effects of six different protocols of stimulation. J
Neurophysiol. 2011;105:2150–6. https://doi.org/10.1152/jn.00781.2010.
99. Blumberger DM, Vila-Rodriguez F, Thorpe KE, etal. Effectiveness of theta burst versus
high-frequency repetitive transcranial magnetic stimulation in patients with depression
(THREE-D): a randomised non-inferiority trial. Lancet. 2018;391:1683–92.
100. Jin Y, Tong J, Huang Y, Shi D, Zhu N, Zhu M, Liu M, Liu H, Sun X. Effectiveness of
accelerated intermittent theta burst stimulation for social cognition and negative symptoms among individuals with schizophrenia: a randomized controlled trial. Psychiatry Res.
2023;320:115033.
101. Zhang X, Yang X, Shi Z, Xu R, Tan J, Yang J, Huang X, Huang X, Zheng W.A systematic
review of intermittent theta burst stimulation for neurocognitive dysfunction in older adults
with schizophrenia. J Pers Med. 2023;13:485.
102. Lisman JE, Idiart MA. Storage of 7 +/− 2 short-term memories in oscillatory subcycles.
Science. 1995;267:1512–5.
103. Di Lazzaro V, Pilato F, Saturno E, et al. Theta-burst repetitive transcranial magnetic
stimulation suppresses specic excitatory circuits in the human motor cortex. J Physiol.
2005;565:945–50.
104. Di Lazzaro V, Pilato F, Dileone M, etal. The physiological basis of the effects of intermittent
theta burst stimulation of the human motor cortex. J Physiol. 2008;586:3871–9.
105. Wischnewski M, Schutter DJLG.Efcacy and time course of theta burst stimulation in
healthy humans. Brain Stimul. 2015;8:685–92.
106. Nguyen V-T, Wu C-W, Chen C-A, Lo C-C, Chen F-Y, Wu C-I, Sung P-S, Lin C-C, Chen
J-J.Modulation of interhemispheric synchronization and cortical activity in healthy subjects
by high-denition theta-burst electrical stimulation. Neural Plast. 2022;2022:3593262.
107. Hong YH, Wu SW, Pedapati EV, Horn PS, Huddleston DA, Laue CS, Gilbert DL.Safety and
tolerability of theta burst stimulation vs. single and paired pulse transcranial magnetic stimulation: a comparative study of 165 pediatric subjects. Front Hum Neurosci. 2015; https://doi.
org/10.3389/fnhum.2015.00029.
108. Purushotham A, Sinha VK, Goyal N, Tikka SK.Intermittent theta burst stimulation induced
seizure in a child with schizophrenia: a case report. Brain Stimul Basic Transl Clin Res
Neuromodul. 2018;11:1415–6.
109. Sha MM. Seizures with TMS: much ado about (almost) nothing? Clin Neurophysiol.
2019;130:1397–8.
110. Merabet LB, Pascual-Leone A.Transcranial magnetic stimulation. In: Squire LR, editor.
Encyclopedia of neuroscience. Oxford: Academic; 2009. p.1055–62.
111. Rossi S, Hallett M, Rossini PM, Pascual-Leone A.Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and
research. Clin Neurophysiol. 2009;120:2008–39.
112. Demirtas-Tatlidede A, Freitas C, Cromer JR, Safar L, Ongur D, Stone WS, Seidman LJ,
Schmahmann JD, Pascual-Leone A.Safety and proof of principle study of cerebellar vermal
theta burst stimulation in refractory schizophrenia. Schizophr Res. 2010;124:91–100.
113. Elmaghraby R, Sun Q, Ozger C, Shekunov J, Romanowicz M, Croarkin PE.A systematic
review of the safety and tolerability of theta burst stimulation in children and adolescents.
Neuromodulation. 2022;25:494–503.
114. Bation R, Magnin C, Poulet E, Mondino M, Brunelin J.Intermittent theta burst stimulation
for negative symptoms of schizophrenia—a double-blind, sham-controlled pilot study. NPJ
Schizophr. 2021;7:1–7.
115. Zhu L, Zhang W, Zhu Y, Mu X, Zhang Q, Wang Y, Cai J, Xie B.Cerebellar theta burst stimulation for the treatment of negative symptoms of schizophrenia: a multicenter, double-blind,
randomized controlled trial. Psychiatry Res. 2021;305:114204.
116. Wang L, Chen X, Wu Y, He K, Xu F, Xiao G, Hu P, Qiu B, Ji G-J, Wang K.Intermittent
theta burst stimulation (iTBS) adjustment effects of schizophrenia: results from an
H. Deng et al.

5 Schizophrenia
exploratory outcome of a randomized double-blind controlled study. Schizophr Res.
2020;216:550–3.
117. Wang L, Li Q, Wu Y, etal. Intermittent theta burst stimulation improved visual-spatial working
memory in treatment-resistant schizophrenia: a pilot study. J Psychiatr Res. 2022;149:44–53.
118. Duprat R, Desmyter S, Rudi DR, etal. Accelerated intermittent theta burst stimulation treatment in medication-resistant major depression: a fast road to remission? J Affect Disord.
2016;200:6–14.
119. Chung SW, Hoy KE, Fitzgerald PB.Theta-burst stimulation: a new form of TMS treatment
for depression? Depress Anxiety. 2015;32:182–92.
120. Duprat R, Wu G-R, De Raedt R, Baeken C.Accelerated iTBS treatment in depressed patients
differentially modulates reward system activity based on anhedonia. World J Biol Psychiatry.
2018;19:497–508.
121. Chithra U, Samantaray S, Kumar V, etal. Add-on accelerated continuous theta burst stimulation (a-cTBS) over the left temporoparietal junction for the management of persistent
auditory hallucinations in schizophrenia: a case series. Brain Stimul Basic Transl Clin Res
Neuromodul. 2022;15:1511–2.
122. Chen L, Klooster DCW, Tik M, Thomas EHX, Downar J, Fitzgerald PB, Williams NR,
Baeken C.Accelerated repetitive transcranial magnetic stimulation to treat major depression:
the past, present, and future. Harv Rev Psychiatry. 2023;31:142–61.
123. Kishi T, Ikuta T, Sakuma K, etal. Theta burst stimulation for depression: a systematic review
and network and pairwise meta-analysis. Mol Psychiatry. 2024; https://doi.org/10.1038/
s41380- 024- 02630- 5.
124. Steele VR, Maxwell AM, Ross TJ, Stein EA, Salmeron BJ.Accelerated intermittent thetaburst stimulation as a treatment for cocaine use disorder: a proof-of-concept study. Front
Neurosci. 2019;13:1147.
125. Williams NR, Sudheimer KD, Bentzley BS, etal. High-dose spaced theta-burst TMS as a
rapid-acting antidepressant in highly refractory depression. Brain. 2018;141:e18.
126. Kumar N, Vishnubhatla S, Wadhawan AN, Minhas S, Gupta P.A randomized, double blind,
sham-controlled trial of repetitive transcranial magnetic stimulation (rTMS) in the treatment
of negative symptoms in schizophrenia. Brain Stimul Basic Transl Clin Res Neuromodul.
2020;13:840–9.
127. Cole EJ, Phillips AL, Bentzley BS, etal. Stanford neuromodulation therapy (SNT): a doubleblind randomized controlled trial. Am J Psychiatry. 2022;179:132–41.
128. Noda Y, Fujii K, Tokura F, Nakajima S, Kitahata R.A case series of continuous theta burst
stimulation treatment for the supplementary motor area twice a day in patients with obsessivecompulsive disorder: a real world TMS registry study in Japan. J Pers Med. 2023;13:875.
129. Sharbafshaaer M, Gigi I, Lavorgna L, Esposito S, Bonavita S, Tedeschi G, Esposito F, Trojsi
F.Repetitive transcranial magnetic stimulation (rTMS) in mild cognitive impairment: effects
on cognitive functions—a systematic review. J Clin Med. 2023;12:6190.
130. Schraven SP, Plontke SK, Rahne T, Wasserka B, Plewnia C. Hearing safety of long-term
treatment with theta burst stimulation. Brain Stimul. 2013;6:563–8.
131. Chistyakov AV, Rubicsek O, Kaplan B, Zaaroor M, Klein E.Safety, tolerability and preliminary evidence for antidepressant efcacy of theta-burst transcranial magnetic stimulation in
patients with major depression. Int J Neuropsychopharmacol. 2010;13:387–93.
132. Gao X, Ni Y, Hu W, Wang G, He X.Comparative study about the therapeutic effect of cTBS
and rTMS in the treatment of auditory verbal hallucinations in schizophrenia. Postgrad Med
J. 2024;101:qgae119.
133. Nyffeler T, Wurtz P, Lüscher H-R, Hess CW, Senn W, Pugshaupt T, von Wartburg R, Lüthi
M, Müri RM.Extending lifetime of plastic changes in the human brain. Eur J Neurosci.
2006;24:2961–6.
134. Ye S-Y, Chen C-N, Wei B, Zhan J-Q, Li Y-H, Zhang C, Huang J-J, Yang Y-J.The efcacy
and safety of continuous theta burst stimulation for auditory hallucinations: a systematic
139

140
review and meta-analysis of randomized controlled trials. Front Psych. 2024; https://doi.
org/10.3389/fpsyt.2024.1446849.
135. Kang D, Song C, Peng X, Yu G, Yang Y, Chen C, Long Y, Shao P, Wu R.The effect of continuous theta burst stimulation on antipsychotic-induced weight gain in rst-episode drug-naive
individuals with schizophrenia: a double-blind, randomized, sham-controlled feasibility trial.
Transl Psychiatry. 2024;14:1–8.
136. Zöllner R, Hübener A-F, Dannlowski U, Kircher T, Sommer J, Zavorotnyy M.Theta-burst
stimulation for auditory-verbal hallucination in very-late-onset schizophrenia-like psychosis—a functional magnetic resonance imaging case study. Front Psych. 2020; https://doi.
org/10.3389/fpsyt.2020.00294.
137. Rachid F, Vianin P, Besse C. Safety and efcacy of continuous theta burst stimulation at
30Hz in a patient with chronic auditory hallucinations: a case study in a private practice setting. Brain Stimul Basic Transl Clin Res Neuromodul. 2013;6:707–8.
138. Purushotham A, Goyal N, Sinha VK, Tikka SK, Garg S, Desarkar P. Motor cortical plasticity in adolescents with early onset schizophrenia: a TMS-EMG study assessing the perturbation effect of intermittent and continuous theta burst stimulation. Int J Dev Neurosci.
2022;82:576–83.
139. Eberle M-C, Wildgruber D, Wasserka B, Fallgatter AJ, Plewnia C.Relief from chronic
intractable auditory hallucinations after Long-term bilateral theta burst stimulation. Am J
Psychiatry. 2010;167:1410.
140. Poulet E, Brunelin J, Makhlouf WB, D’Amato T, Saoud M.A case report of cTBS for the
treatment of auditory hallucinations in a patient with schizophrenia. Brain Stimul Basic
Transl Clin Res Neuromodul. 2009;2:118–9.
141. Sidhoumi D, Braha S, Bouaziz N, Brunelin J, Benadhira R, Januel D. Evaluation of the
therapeutic effect of theta burst stimulation on drug-resistant auditory hallucinations in a
schizophrenic patient and its impact on cognitive function and neuronal excitability: a case
study. Clin Neurophysiol. 2010;121:802.
142. Kindler J, Homan P, Flury R, Strik W, Dierks T, Hubl D.Theta burst transcranial magnetic
stimulation for the treatment of auditory verbal hallucinations: results of a randomized controlled study. Psychiatry Res. 2013;209:114–7.
143. Homan P, Kindler J, Hauf M, Hubl D, Dierks T. Cerebral blood ow identies responders to transcranial magnetic stimulation in auditory verbal hallucinations. Transl Psychiatry.
2012;2:e189.
144. Plewnia C, Zwissler B, Wasserka B, Fallgatter AJ, Klingberg S.Treatment of auditory hallucinations with bilateral theta burst stimulation: a randomized controlled pilot trial. Brain
Stimul Basic Transl Clin Res Neuromodul. 2014;7:340–1.
145. Koops S, van Dellen E, Schutte MJL, Nieuwdorp W, Neggers SFW, Sommer IEC.Theta burst
transcranial magnetic stimulation for auditory verbal hallucinations: negative ndings from a
double-blind-randomized trial. Schizophr Bull. 2016;42:250–7.
146. Jandl M, Steyer J, Weber M, Linden DEJ, Rothmeier J, Maurer K, Kaschka WP.Treating
auditory hallucinations by transcranial magnetic stimulation: a randomized controlled crossover trial. Neuropsychobiology. 2006;53:63–9.
147. Lee S-H, Kim W, Chung Y-C, Jung K-H, Bahk W-M, Jun T-Y, Kim K-S, George MS, Chae
J-H.A double blind study showing that two weeks of daily repetitive TMS over the left or
right temporoparietal cortex reduces symptoms in patients with schizophrenia who are having treatment-refractory auditory hallucinations. Neurosci Lett. 2005;376:177–81.
148. Plewnia C, Brendel B, Schwippel T, Martus P, Cordes J, Hasan A, Fallgatter AJ.Treatment of
auditory hallucinations with bilateral theta burst stimulation (cTBS): protocol of a randomized, double-blind, placebo-controlled, multicenter trial. Eur Arch Psychiatry Clin Neurosci.
2018;268:663–73.
149. Guelke E, Horn MA, Cafer J, Pinnschmidt H, Hamel W, Moll CKE, Gulberti A, PoetterNerger M.Comparison of subthalamic unilateral and bilateral theta burst deep brain stimulation in Parkinson’s disease. Front Hum Neurosci. 2023;17:1233565.
H. Deng et al.
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