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PublicationStudy  typePatient  characteristicaInterventionComparisonEfficacy  measurementResult/Outcome1:  Ray  S.  et  al

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A  P  P  E  N  D  I  X    1

Publication Study  type Patient  characteristica Intervention Comparison Efficacy  measurement Result/Outcome

1:  Ray  S.  et  al   randomized 45  right  handed  moderate  to  severe   HF-­‐rTMS  (10  Hz)  at  90%  of  MT sham Structured  Interview  Guide  for  the  Hamilton  Depression  Rating  Scale  (SIGH-­‐D) High-­‐frequency  left  prefrontal  rTMS  was  well  tolerated  and  found 2011  [41]   sham-­‐controlled depression  patients  according  to 20  trains,  6  s  train  duration,  1200  pulses/day,  10  days Brief  Psychiatric  Rating  Scale  (BPRS) to  be  effective  as  add-­‐on  to  standard  pharmacotherapy  in  

single-­‐blind ICD-­‐10  DCR  criteria right  DLPFC nonpsychotic  as  well  as  psychotic  depression.  

2:  Huang  ML.  et  al   randomized 60  first-­‐episode  young  major   citalopram  in  combination  with  2  weeks  of  active  rTMS  treatment citalopram  in  combination 17-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐17) rTMS  accelerated  the  rapidity  of  the  antidepressant  response   2012  [88]   sham-­‐controlled depressive  patients HF-­‐rTMS  (10Hz)  at  90%  MT,  20  trains,  800  pulses/day with  sham  rTMS  treatment Montgomery-­‐Asberg  depression  rating  scale  (MADRS) in  first-­‐episode  young  depressive  patients.  rTMS  can  be  considered  a  safe

double-­‐blind 4  s  train  duration,  26  s  intertrain  interval augmentative  treatment  to  SSRI.

left  DLPFC

3:  Blumberger  DM.  et  al randomized 74 subjects with TRD HF-­‐rTMS  to  left  DLFPC  (10Hz)  and  sequential  LF-­‐rTMS sham 17-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐17) The  remission  rate  was  significantly  higher  in  the  bilateral  group 2012  [43]   sham-­‐controlled 17-item Hamilton Depression to  right  DLPFC  (1Hz)  at  100%  MT  (120%  MT  for  patients  over  60  years) than  the  sham  group.  The  remission  rate  in  the  unilateral

double-­‐blind Rating  Scale  greater  than  21 unilateral  and  bilateral  intervention group  did  not  differ  from  either  group.

4:  Fitzgerald  PB.  et  al   randomized 67  patients  with  TRD sequential  bilateral  rTMS  and  standard  HF-­‐rTMS  to  left  DLPFC sham 17-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐17) Greater  antidepressant  response  to  unilateral  left  sided  rTMS

2012  [89]   sham-­‐controlled bilateral  stimulation  was  applied  with  1Hz  on  right  DLPFC  followed  by compared  with  sham  or  bilateral  rTMS.

double-­‐blind HF-­‐rTMS  (10Hz)  on  left  DLPFC  at  120%  MT.

5:  George  MS.  et  al   randomized 199  antidepressant  drug-­‐free  patients   HF-­‐rTMS  (10Hz)  at  120%  MT sham Montgomery-­‐Asberg  depression  rating  scale  (MADRS) The  odds  of  attaining  remission  were  4.2  times  greater  with 2010  [4]   sham-­‐controlled with  unipolar  nonpsychotic  major 4  s  train  duration,  26  s  intertrain  interval 17-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐17) active  rTMS  than  with  sham  (95%  confidence  interval,  1.32-­‐13.24).

double-­‐blind depressive  disorder 3000  stimuli  per  session Clinical  Global  Impression  Severity  of  Illness  Scale

left  DLPFC

6:  Janicak  PG.  et  al   randomized 301  patients  with  unipolar,   HF-­‐rTMS  (10Hz)  at  120%  of  MT sham Montgomery-­‐Asberg  depression  rating  scale  (MADRS) Initial  data  suggest  that  the  therapeutic  effects  of  TMS  are   2010  [40]   sham-­‐controlled nonpsychotic  major  depressive  disorder 4  s  train  duration,  26  s  intertrain  interval,   17-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐17) durable  and  that  TMS  may  be  successfully  used  as  an  intermittent

double-­‐blind 3000  stimuli  per  session 24-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐24) rescue  strategy  to  preclude  impending  relapse.

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A  P  P  E  N  D  I  X    2

Publication Study  design Patient  characteristica Intervention Comparison Efficacy  measurement Result/Outcome

7:  Nongpiur  A.  et  al   randomized 40  patients  with  moderate-­‐to-­‐severe   active-­‐priming  HF-­‐rTMS  (4-­‐8Hz)  at  90%  of  MT,  400  stimuli,  followed   sham-­‐priming Montgomery-­‐Asberg  depression  rating  scale  (MADRS) Pre-­‐stimulation  with  frequency-­‐modulated  priming  stimulation  in   2011  [90]   sham-­‐controlled depression  (ICD-­‐10  DCR) by  LF-­‐rTMS  (1  Hz)  at  110%  of  MT,  900  stimuli Structured  Interview  Guide  for  the  Hamilton  Depression  Rating  Scale  (SIGH-­‐D) the  theta  range  has  greater  antidepressant  effect  than  low-­‐frequency

right  DLPFC Brief  Psychiatric  Rating  Scale  (BPRS) stimulation  alone.  There  was  significant  improvement  in  the  active  

Clinical  Global  Impression-­‐Severity  of  Illness  (CGI-­‐S) group  over  time  (SIGH-­‐D  scores).

8:  Plewnia  C.  et  al   randomized 32  patients  with  a  DSM-­‐IV  diagnosis  of  MD cTBS  and  iTBS  intensity  was  standardized  at  80%  of  MT bilateral  sham Montgomery-­‐Asberg  depression  rating  scale  (MADRS) A  significant  therapeutic  effect  of  sequential  left  excitatory  and 2014  [91]   sham-­‐controlled 50  Hz  theta  burst  protocol,  2  trains  of  600  stimuli Hamilton  depression  rating  scale  (HAMD) right  inhibitory  theta  burst  stimulation  was  found.

single-­‐blind bilateral  intervention Beck  Depression  Inventory  (BDI)

9:  Speer  AM.  et  al randomized 24  acutely  depressed  patients HF-­‐rTMS  (20Hz)  or  LF-­‐rTMS  (1Hz)  at  110%  of  MT sham 28-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐28  expanded  version) Patients  on  both  frequencies  showed  greater  improvement  than  on  sham.

2014  [92]   sham-­‐controlled 1600  stimuli/session During  7  week  continuation  of  active  treatment,  additional  improvement

double-­‐blind left  DLPFC  was  observed.

10:  Baeken,  C.  et  al randomized 20  unipolar  anti-­‐depressant  free   HF-­‐rTMS  (20  Hz)  at  110%  of  MT sham 17-­‐item  Hamilton  depression  rating  scale  (HAMD-­‐17) Intensive  HF-­‐rTMS  protocol  was  found  to  be  safe  and  well  tolerated. 2013  [93]   sham-­‐controlled TRD  patients  (stage  III  treatment  resistant) 40  trains  of  1.9  s  duration,  1560  stimuli/session and  resulted  in  fast  clinical  responses  in  those  TRD  III  patients  with

single-­‐blind 5  sessions/day  for  4  days,  15-­‐20min  delay  inbetween  sessions a  relatively  shorter  duration  of  their  current  depressive  episode.

crossover left  DLPFC Patients  with  unsuccessful  ECT  prior  to  HF-­‐rTMS  did  not  respond.

11:  Diefenbach,  GJ.  et  al CER 32  patients  with  treatment  resistant  anxious   HF-­‐rTMS  (20  Hz)  treatment  begun  at  80%  of  MT,  adjusted  up  to   non-­‐anxious  depression  (MDD) Structured  Interview  Guide  for  the  Hamilton  Depression  Rating  Scale  (SIGH-­‐D) Study  suggests  that  rTMS  may  also  be  effective  for  treating  anxiety   2013  [94]   depression  (MDD) 130%  of  MT.  4  s  train  duration,  20-­‐26  s  intertrain  interval symptoms  in  MDD  patients.  3/4  of  the  patients  in  the  anxious  depression  

left  DLPFC group  no  longer  met  criteria  for  anxious  depression  at  posttreatment.  

12:  Richieri,  R.  et  al naturalistic   59  patients  with  TRD  who  have  responded  to 20  weeks  of  maintenance  rTMS no  additional  rTMS  treatment 21-­‐item  Beck  Depression  Inventory  (BDI)   Maintenance  TMS  was  associated  with  a  significantly  lower  relapse  rate 2013  [95]   observational acute  rTMS  treatment HF-­‐rTMS  (10  Hz)  to  left  DLPFC  at  120%  of  MT State  Trait  Anxiety  Inventory  (STAI-­‐State)   in  patients  with  pharmacoresistant  depression.

5  s  train  duration,  25  s  intertrain  interval,  2000  stimuli/session

13:  Ulrich,  H.  et  al randomized 43  severely  depressed  patients UHF-­‐rTMS  (30  Hz)  as  an  add-­‐on  therapy  to  stable  antidepressant sham Hamilton  depression  rating  scale  (HAMD) A  30-­‐Hz  left  prefrontal  rTMS  in  severely  depressed  patients  was  safe,  

2012  [96]   sham-­‐controlled medication.   no  adverse  effects  occured.  Improvement  of  processing  speed

double-­‐blind performance  in  the  UHF  group  was  demonstrated,  which  covaried  

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