Introduction
Electroconvulsive therapy is one of the brain stimulation therapies where we use electric current to induce neurobiological and biochemical changes in the brain [1]. The current induces widespread electrical discharges (seizure) in the brain which is responsible for the therapeutic effect of ECT as well as some of its side-effects [2]. About 13.4 to 14.3% patients in India receive ECT, which is far more than in developed countries [3]. ECT is the most effective and rapid treatment available for patients with resistant depression, bipolar disorder and acute psychosis. For patients who suffer from intractable catatonia and neuroleptic malignant syndrome, ECT can be life saving [4].
Since the exact mechanisms underlying ECT remain unknown, the postulated hypothesis relates to its role in alteration of various neurotransmitters and peptides in the brain. ECT works by producing generalised seizure, thereby modulating the various monoamines in the brain circuitry which also result in various side effects of the procedure [5]. Despite being so effective in treating various psychiatric disorders, the use of ECT remains restricted to few conditions due to lack of knowledge and negative attitude towards the procedure even among medical professionals [6]. There are very less studies showing the effectiveness of ECT in patients having mental retardation although some studies have shown it to be effective in severe or refractory psychotic symptoms in such patients [7]. Administering ECT early, in the course of illness leads to quick recovery as compared to pharmacotherapy. It also improves the quality of life and activities of daily living [8]. We therefore, studied the effectiveness of ECT in various psychiatric disorders.
Materials and Methods
The study was carried out at a tertiary care hospital in Kashmir which caters to the psychiatric needs of whole of Jammu and Kashmir state including Ladakh. The study was carried over a period of one year from July 2016 to June 2017. It was a longitudinal study where a patients receiving ECT were enrolled. A total of 40 patients were included in present study. Patients’ ≥12 years of age who were resistant to pharmacotherapy or who had life-threatening conditions like catatonia, refusal to feed or suicidality were included in present study. Only those patients who gave consent for the procedure were included. In patients aged less than 18 years, consent was taken from the caregivers who in most cases were parents of the patient. Patients having contraindications to general anaesthesia or having history of recent intracranial haemorrhage, cardiac arrhythmias, myocardial infarction or pheochromocytoma were excluded from present study. Patients with features of raised intracranial tension were also excluded.
General information including age, sex, residence, occupation, socioeconomic status was recorded. The variables analysed in the study included sociodemographic information, clinical profile (diagnosis, previous psychiatric hospitalisations, family history of mental disorders, presence of clinical comorbidities), and ECT data, i.e., number of sessions, complications during and immediately after the procedure (within 72 hours), late complications (more than 72 hours after the procedure) and treatment response.
Sample size was calculated using parametric statistics to calculate the Chi-square value which has been applied in the data collected. Since our study was a longitudinal follow-up study, we could not get more than the collected number of cases.
ECT Parameters
ECT was administered by a junior resident in psychiatry under the supervision of senior resident and a consultant. The procedure was carried out under general anaesthesia given by an anaesthetist. Propofol or thiopentone was used as an inducing agent and succinylcholine as muscle relaxant. An indigenously manufactured brief-pulse, constant energy machine (Medicaid Systems, Chandigarh, India) was used where duration of current, frequency and pulse width was adjusted as per the dose needed to induce an effective seizure. Motor seizure was monitored by the cuff method. Motor seizure lasting more than 15 seconds was taken as adequate seizure.
Scales Used
Montgomery Asberg Depression Rating Scale (MADRS): It is a 10 item scale with each item having a maximum score of 6, thus total score of the scale is 60. It helps to measure the severity of depression [9].
Yale-Brown Obsessive Compulsive Scale (YBOCS): It is a 10 item balanced scale designed to rate both the severity and type of symptoms in patients with Obsessive Compulsive Disorder (OCD) [10].
Young’s Mania Rating Scale (YMRS): It is an 11 item scale used to assess disease severity in patients with mania [11].
Bush Francis Catatonia Rating Scale (BFCRS): It is a 23 item scale used to assess the severity of catatonia [12].
Becks Suicide Intent Scale (BSIS): It includes 20 items to assess the severity of suicidal attempt. It also gives us the risk of repeated attempts by the severity level [13].
Clinical Global Impressions Scale (Severity index) CGI-S: It measures illness severity and is one among the three domains of CGI scale which includes CGI Improvement Index (CGII) and Efficacy Index (EI). CGIS helps us to measure the response at various intervals by comparing the scores [14]. The improvement was graded as more than 50% or less than 50% as assessed by various scales.
Statistical Analysis
Data were filled into Microsoft Excel. Continuous variables were analysed in the form of mean and standard deviation. Categorical variables were summed up as frequency and percentages. Chi-square test was applied to analyse the relationship between categorical variables. Fisher’s-exact test was used wherever chi-square test did not meet Cochrane criteria. Difference between two means were analysed using unpaired t-test.
Results
Majority of the patients 15 (37.5%) were in the age-group of 38-47 years followed by 9 (22.5%) in 28-37 years. Only 2 (5%) of patients were aged >60 years. Males were slightly higher in number as compared to females (21:19). Majority of our patients 25 (62.5%) were married. which could be due to the fact that affective disorders, forming the major lot of our patients receiving ECT, have a relatively late age of onset. With regards to the dwelling, the patients were from rural background mostly which is a reflection of the fact that majority of our population hails from a rural background. About 75% of the patients were having affective disorders with the rest having OCD (10%), schizophrenia (10%) and mental retardation in 5%. About 36 (90%) of our patients received a mean of 8 ECT sessions while only 4 (10%) received more than 9 sessions of ECT [Table/Fig-1].
Sociodemographic and baseline characteristics of cases.
Age (years) | Number of patients | Percentage |
---|
18-27 | 8 | 20 |
28-37 | 9 | 22.5 |
38-47 | 15 | 37.5 |
48-57 | 6 | 15 |
58-67 | 2 | 5 |
Sex |
Male | 21 | 52.5 |
Female | 19 | 47.5 |
Marital status |
Married | 25 | 62.5 |
Unmarried | 15 | 37.5 |
Occupation |
Unemployed | 22 | 55 |
Employed | 18 | 45 |
Residence |
Rural | 22 | 55 |
Urban | 18 | 45 |
Clinical Diagnosis |
Unipolar depression | 16 | 40 |
BPAD-I | 10 | 25 |
BPAD-II | 4 | 10 |
OCD | 4 | 10 |
MR | 2 | 5 |
Schizophrenia | 4 | 10 |
Number of ECTs received |
6-9 sessions | 36 | 90 |
10-14 sessions | 4 | 10 |
BPAD= Bipolar affective disorder; OCD=Obsessive compulsive disorder; MR=Mental retardation; ECT=Electroconvulsive therapy.
Applying chi-square test, p-value was calculated to be >0.05 and was not statistically significant.
Among patients presenting with unipolar depression, about 69% showed ≥50% improvement after ECT as assessed by MADRS with the remaining showing ≥50% response. It could be because majority of patients with unipolar depression were having resistant depression where the response rates are a bit lower as compared to bipolar depression or other forms of depression. In patients of mania, 90% showed ≥50% improvement in symptoms as assessed by YMRS. Among patients of mania, we had a pregnant female not responding to mood stabilizers who was given ECT in her second trimester and showed good response. In patients suffering from schizophrenia, ECT was administered for catatonia (2 patients), affective symptoms (1 patient) and agitation (1 patient). ECT has been regarded as the treatment of choice for catatonia. There was more than 50% improvement in all patients of schizophrenia who received ECT. In patients suffering from OCD, ECT was administered for severe depression seen in 3 patients and suicidality in 1 patient. We had two patients of mental retardation; one had affective symptoms (mania) and the other agitation. Both the patients did not respond to pharmacotherapy, but their response to ECT was very good (≤ 50% improvement on CGI-I) [Table/Fig-2,3].
Improvement in various psychiatric disorders after ECT.
Patients with unipolar depression (n=16) |
---|
| Number of patients | Pre-ECT score | Post-ECT score | p-value |
---|
Indication for ECT |
Suicidality | 5 | Mean BSIS=84.5 | Mean BSIS=40 | <0.05 |
Resistant depression | 11 | Mean MADRS=45.14 | Mean MADRS=20 | <0.05 |
Patients with BPAD-I |
Mania(resistant) | 10 | Mean YMRS=31.37 | Mean YMRS=10.87 | <0.05 |
Patients with BPAD-II |
Depression(resistant) | 4 | Mean MADRS=46 | Mean MADRS=19 | <0.05 |
Patients with schizophrenia |
Catatonia | 2 | Mean BFCRS=22 | Mean BFCRS=7 | <0.05 |
Affective symptoms | 1 | YMRS=22 | YMRS=11 | <0.05 |
Agitation | 1 | CGI (S)=6 | CGI (S)=4 | <0.05 |
Patients with OCD |
Suicidality | 1 | YBOCS=24 BSIS=21 | YBOCS=16 BSIS=13 | <0.05 |
MDE | 3 | Mean YBOCS=23 Mean MADRS=24.3 | Mean YBOCS=14 Mean MADRS=14.3 | <0.05 |
Patients with mental retardation |
BPAD (mania) | 1 | YMRS=38 | YMRS=16 | <0.05 |
Agitation | 1 | CGI (S)=6 | CGI (S)=4 | <0.05 |
Applying chi-square test, p-value was calculated to be <0.05 and was statistically significant. ECT=Electroconvulsive therapy; BSIS=Becks suicide intent scale; MADRS=Montgomery asberg depression rating scale; YMRS=Young’s mania rating scale; BFCRS=Bush francis catatonia rating scale; CGIS=Clinical global improvement (severity index); YBOCS=Yale brown obsessive compulsive scale, MDE=Major depressive episode, BPAD=Bipolar affective disorder.
Response to electroconvulsive therapy in various psychiatric disorders.
Psychiatric disorder | Total patients | Number of patients improved (>50% response) |
---|
Unipolar depression | 16 (100%) | 11 (68.75%) |
Bipolar depression | 04 (100%) | 03 (75%) |
Mania | 10 (100%) | 09 (90%) |
Schizophrenia | 04 (100%) | 03 (75%) |
OCD | 04 (100%) | 02 (50%) |
Mental retardation | 2 (100%) | 2 (100%) |
OCD: Obsessive compulsive disorder
Regarding the relation of seizure duration and the response to ECT shown by patients, no significant association was found. While analysing the cumulative seizure duration in various cases, it was found that about 21 patients had cumulative seizure duration < 200 seconds and 19 patients had >200 seconds. The two groups did not differ significantly in the remission rates. It may be due to the varied clinical conditions for which ECT was given and also, due to the heterogeneity of medications our patients were taking [Table/Fig-4].
Relation of seizure duration and response.
Cumulative seizure duration | Number of patients | Response to treatment |
---|
<200 seconds | 21 | Remission in 18 patients (85.7%) 50% response in 3 patients (14.3%) |
>200 seconds | 19 | Remission in 15 patients (78.9%) 50% response in 4 patients (21.05%) |
Applying chi-square test, p-value calculated was 0.57 (not significant).
In present study, the side-effects noted immediately after the procedure were confusion seen in 20 (50%) patients. It was self-limiting and resolved after 10-15 minutes. Delirium after the procedure was present in two patients only and both patients were taking lithium. Low doses of midazolam were used to manage delirium. Late complications after ECT included body aches reported by 10 (25%) patients, headache by 8 (20%) and forgetfulness by 16 (40%) patients. In patients complaining of body aches and headache, paracetamol was given which relieved the symptoms. Most of the patients had retrograde amnesia which improved within a few months but, patients needed reassurance regarding the temporary nature of their memory impairment.
Discussion
Electroconvulsive therapy is widely used to treat psychiatric disorders and has stood the test of time for proving effective in various conditions especially in some life-threatening ones like Suicidality, catatonia, refusal to feed [15].
In present study, majority of patients were in fourth decade of their life which is about one decade earlier age as compared to that of western nations [16,17], but is similar to the results seen in Indian studies [18]. Also, similar results have been found in a study done in Thailand [19]. Among our patients, sex ratio was about 1:1 which is also seen in other studies done on ECT [20,21]. Majority of our patients were married which may be due to late age of onset of unipolar depression which forms the major indication for ECT [22].
In present study, majority of patients were receiving ECT for treatment of affective disorders which formed about 75% of total patients receiving ECT. Similar pattern has been seen in a study done in USA where they found that about 72-92% of patients receiving ECT were having affective disorders [23,24]. Affective disorders have been the main diagnosis in Australia and New-Zealand [25,26]. An Indian analysis on the practice of ECT revealed that following schizophrenia, major depression (both bipolar and unipolar) and mania are the main indications for performing ECT [27].
The less number of schizophrenics receiving ECT in present study could be due to various reasons like newly launched long-acting antipsychotics which help in keeping such patients stable, poor patient preference for the procedure, bias of including more patients with affective disorders due to their good response to ECT.
Among patients with unipolar depression, about 72% patients showed more than 50% response as assessed by MADRS which is in concordance with the results shown in other studies [28,29]. Randomised controlled trials have revealed that up to 70% of patients with depression who do not respond to antidepressants may respond favorably to ECT [30]. Resistant depression is one of the few conditions approved as per (NICE) guidelines as an indication for administering ECT. However, among patients of resistant depression, only 60-70% of patients show remission even after administering ECT [31]. Among patients suffering from depressive phase of bipolar illness, about 75% patients showed >50% response as assessed by MADRS with the remaining showing 25-50% response to ECT. This shows the effectiveness of ECT in treating such severe cases which is also supported by a study done by Kho KH et al., [32]. In patients suffering from manic phase of bipolar affective disorder, almost 90% showed >50% response as assessed by YMRS which is similar to the rates seen in other studies done on bipolar patients [33,34].
In a study done in 2012 from Northern part of India, it was found that 90% patients of mania showed >50% response to ECT [35]. Similar results were found by Alexander RC and Strömgren IS who found good results with ECT in bipolar patients in manic phase not responding to drugs [36,37]. A rapid response was seen in catatonic symptoms in schizophrenia even after administering 2 sessions of modified ECT, although 4-6 sessions were given for complete remission in above patients. Schizophrenia has been one of the first indications for administering ECT [38].
It has been seen that in acute phase of schizophrenia, ECT given in combination with antipsychotics brings faster recovery as compared to drugs alone [39,40]. Among schizophrenics, those with affective symptoms respond equally to ECT and antipsychotics [41]. In present study, catatonia resolved completely with few (2-3) sessions of ECT, while higher number of ECT sessions were needed in affective symptoms and agitation in which >50% response was seen.
A review of literature regarding OCD treatment shows that use of ECT in treatment resistant OCD is quite sparse. To the best of the knowledge of the authors, only isolated case reports showing efficacy of ECT in OCD have been reported. The primary indications in all case reports for ECT use would be OCD with severe depression [42,43]. In present study, patients with OCD had comorbid depression (3 patients) and suicidality (1 patient) which improved but the core symptoms of OCD did not improve much, although mild improvement in symptoms of OCD was seen in our patients.
Regarding the number of ECT sessions received by our patients, majority of patients received around 6-9 sessions with few needing more number of sessions. Same has been studied in other studies done in Asia [44]. The number of sessions described above was in reference to the acute phase of ECT while maintenance phase was not included. It was due to the fact that we wanted to study the response of various psychiatric illnesses to ECT which was achieved at the end of acute phase. Also, maintenance phase would require longer follow-up which was difficult.
Seizure Duration and Response to ECT
Majority of our patients received a mean of 8 ECT treatments during the acute phase. Maintenance phase ECT sessions were not included in present study since our primary aim was to see the response of various psychiatric disorders to ECT in the acute phase. It has been seen that motor seizure of <15 seconds are not effective for inducing remission [45]. No significant relation was seen between cumulative seizure duration and the response to ECT. A number of studies show positive correlation between seizure duration and response [46] however, some others do not find any relationship between seizure duration and response rate [47]. The data regarding relationship between seizure duration and response to ECT has been conflicting due to many factors like concurrent medications, underlying conditions for which ECT is administered and other comorbidities present in patients seen in clinical settings for ECT.
Limitation
The study did not include maintenance ECT sessions which could have an impact on course of illness and give us an idea about the relapse rates in different psychiatric disorders on maintenance ECT. Also, we did not take into account the medications our patients were taking which can influence the response to ECT in various disorders. Another limitation was the small sample size; higher number of patients would give us better insight into effectiveness of ECT in various disorders.
Conclusion
The present study substantiates the role of ECT in treating psychiatric disorders especially affective disorders where remission is achieved in the majority of patients. Also, ECT is life saving in some conditions like catatonia, suicidality and severe depression with refusal to take orals. In OCD, the core symptoms did not improve much, however the comorbid depression responded to ECT.
BPAD= Bipolar affective disorder; OCD=Obsessive compulsive disorder; MR=Mental retardation; ECT=Electroconvulsive therapy.Applying chi-square test, p-value was calculated to be >0.05 and was not statistically significant.Applying chi-square test, p-value was calculated to be <0.05 and was statistically significant. ECT=Electroconvulsive therapy; BSIS=Becks suicide intent scale; MADRS=Montgomery asberg depression rating scale; YMRS=Young’s mania rating scale; BFCRS=Bush francis catatonia rating scale; CGIS=Clinical global improvement (severity index); YBOCS=Yale brown obsessive compulsive scale, MDE=Major depressive episode, BPAD=Bipolar affective disorder.OCD: Obsessive compulsive disorderApplying chi-square test, p-value calculated was 0.57 (not significant).
[1]. Skapanalis P, Gerasi E, ECT (Electro-Convulsive Therapy)Available from http://web4health.info/en/answers/bipolar-treat-ect.htm./200810.1016/j.cnr.2004.06.013 [Google Scholar] [CrossRef]
[2]. Sackeim HA, Convulsant and anticonvulsant properties of electroconvulsive therapy: towards a focal form of brain stimulation Clinical Neuroscience Research 2004 4(1-2):39-57. [Google Scholar]
[3]. Agrawal AK, Andrade C, Reddy MV, The practice of ECT in India: issues related to administration of ECT Indian J Psychiatr 1992 34(4):285-97. [Google Scholar]
[4]. Kerner N, Prudic J, Current electroconvulsive therapy, practice and research in the geriatric population Neuropsychiatry (London) 2014 4(1):33-54.10.2217/npy.14.324778709 [Google Scholar] [CrossRef] [PubMed]
[5]. Shah AJ, Wadoo O, Latoo J, Electroconvulsive Therapy (ECT): important parameters which influence its effectiveness BJMP 2013 6(4):a634 [Google Scholar]
[6]. Downman J, Patel A, Rajput K, Electroconvulsive therapy: attitude and misconceptions J ECT 2005 21(1)(1):84-87.10.1097/01.yct.0000161043.00911.4515905748 [Google Scholar] [CrossRef] [PubMed]
[7]. Aziz M, Maixner DF, DeQuardo J, Aldridge A, Tandon R, ECT and mental retardation; a review and case reports J ECT 2001 17(2):149-52.10.1097/00124509-200106000-0001211417928 [Google Scholar] [CrossRef] [PubMed]
[8]. Mccall WV, Dunn A, Rosenquist PB, Quality of life and function after electroconvulsive therapy Br J Psychiatry 2004 185:405-09.10.1192/bjp.185.5.40515516549 [Google Scholar] [CrossRef] [PubMed]
[9]. Montgomery SA, Asberg M, A new depression scale designed to be sensitive to change British Journal of Psychiatry 1979 134(4):382-89.10.1192/bjp.134.4.382444788 [Google Scholar] [CrossRef] [PubMed]
[10]. Goodman WK, Price LH, Rasmussen SA, Mazure C, Fleischmann RL, Hill CL, The Yale-Brown Obsessive-Compulsive Scale. I. Development, use, and reliability 1989 Gen Psychiatry 2003 46:1006-11.10.1001/archpsyc.1989.018101100480072684084 [Google Scholar] [CrossRef] [PubMed]
[11]. Young RC, Biggs JT, Ziegler VE, Meyer DA, A rating scale for mania: reliability, validity and sensitivity Br J Psychiatry 1978 133:429-35.10.1192/bjp.133.5.429728692 [Google Scholar] [CrossRef] [PubMed]
[12]. Bush G, Fink M, Petrides G, Dowling F, Francis A, Catatonia I: rating scale and standardized examination Acta Psychiatr Scand 1996 93:129-36.10.1111/j.1600-0447.1996.tb09814.x8686483 [Google Scholar] [CrossRef] [PubMed]
[13]. Beck A, Schuyler D, Herman J, Development of suicidal intent scales. In The Prediction of Suicide (Eds A. Beck, H Resnik, DJ. Lettieri) 1974 :45-56.10.1037/t15303-000 [Google Scholar] [CrossRef]
[14]. Guy W, CGI, ECDEU Assessment Manual for Psychopharmacology. DHEW Publication revised no (ADM) 1976 76:33810.1037/e591322011-001 [Google Scholar] [CrossRef]
[15]. Reddy MS, Electro-convulsive therapy: a few lingering thoughts/doubts! Indian J Psychol Med 2011 33(2):103-05.10.4103/0253-7176.9204222345830 [Google Scholar] [CrossRef] [PubMed]
[16]. Prudic J, Olfson M, Sackeim HA, Electro-convulsive therapy practices in the community Psychol Med 2001 31:929-34.10.1017/S003329170100375011459391 [Google Scholar] [CrossRef] [PubMed]
[17]. Baghai TC, Marcuse A, Mğller HJ, Rupprecht R, Electroconvulsive therapy at the Department of Psychiatry and Psychotherapy, University of Munich. Development during the years 1995-2002 Nervenarzt 2005 76:597-612.10.1007/s00115-004-1813-510.1007/s00115-004-1813-515448918 [Google Scholar] [CrossRef] [PubMed] [PubMed]
[18]. Dar MA, Wani RA, Rather YH, Wani ZA, Hussain A, Shah AS, Sharma MS, An audit of clinical and sociodemographic profile of electroconvulsive therapy in Kashmir J Psychiatry 2014 17:410.4172/Psychiatry.1000129 [Google Scholar] [CrossRef]
[19]. Chanpattana W, Kramer BA, Electroconvulsive therapy practice in Thailand J ECT. 2004 20:94-98.10.1097/00124509-200406000-0000415167425 [Google Scholar] [CrossRef] [PubMed]
[20]. Chanpattana W, Kunigiri G, Kramer BA, Gangadhar BN, Survey of the practice of electroconvulsive therapy in teaching hospitals in India J ECT 2005 21:100-04.10.1097/01.yct.0000166634.73555.e615905751 [Google Scholar] [CrossRef] [PubMed]
[21]. Teh SP, Xiao AJ, Helmes E, Drake DG, Electroconvulsive therapy practice in Western Australia J ECT 2005 21:145-50.10.1097/01.yct.0000171611.86728.7016127302 [Google Scholar] [CrossRef] [PubMed]
[22]. Bharadwaj V, Grover S, Chakrabarti S, Avasthi A, Kate N, Electroconvulsive therapy: a study from north India Indian J Psychiatr 2012 54(1):41-47.10.4103/0019-5545.9464422556436 [Google Scholar] [CrossRef] [PubMed]
[23]. Rosenbach ML, Hermann RC, Dorwart RA, Use of electroconvulsive therapy in the Medicare population between 1987 and 1992 Psychiatr Serv 1997 48:1537-42.10.1176/ps.48.12.15379406260 [Google Scholar] [CrossRef] [PubMed]
[24]. Scarano VR, Felthous AR, Early TS, The state of electroconvulsive therapy in Texas. Part I: reported data on 41,660 ECT treatments in 5971 patients J Forensic Sci 2000 45:1197-202.10.1520/JFS14867J11110170 [Google Scholar] [CrossRef] [PubMed]
[25]. Wood DA, Burgess PM, Epidemiological analysis of electroconvulsive therapy in Victoria, Australia Aust N Z J Psychiatry 2003 37:307-11.10.1046/j.1440-1614.2003.01182.x12780469 [Google Scholar] [CrossRef] [PubMed]
[26]. O’Dea JF, Mitchell PB, Hickie IB, Unilateral or bilateral electroconvulsive therapy for depression? A survey of practice and attitudes in Australia and New Zealand Med J Aust 1991 155:09-11.10.5694/j.1326-5377.1991.tb116367.x [Google Scholar] [CrossRef]
[27]. Bharadwaj V, Grover S, Chakrabarti S, Avasthi A, Natasha Kate, Electroconvulsive therapy: a study from north India Indian J Psychiatr 2012 54(1):41-47.10.4103/0019-5545.9464422556436 [Google Scholar] [CrossRef] [PubMed]
[28]. Khalid N, Atkins M, Tredget J, Giles M, Champney-Smith K, Kirov G, The effectiveness of electroconvulsive therapy in treatment-resistant depression: a naturalistic study J ECT 2008 24(2):141-45.10.1097/YCT.0b013e318157ac5818580559 [Google Scholar] [CrossRef] [PubMed]
[29]. Eranti S, Mogg A, Pluck G, Landau S, Purvis R, Brown RG, A randomized, controlled trial with 6-month follow-up of repetitive transcranial magnetic stimulation and electroconvulsive therapy for severe depression Am J Psychiatry 2007 164(1):73-81.10.1176/ajp.2007.164.1.7317202547 [Google Scholar] [CrossRef] [PubMed]
[30]. Coffey CE, Cummings JL, Textbook of Geriatric Neuropsychiatry 2000 2nd EditionWashington DCAmerican Psychiatric Press, Inc.:829-85. [Google Scholar]
[31]. Khalid N, Atkins M, Tredget J, Giles M, Champney-Smith K, Kirov G, The effectiveness of ECT in treatment resistant depression: a naturalistic study J ECT 2008 24(2):141-45.10.1097/YCT.0b013e318157ac5818580559 [Google Scholar] [CrossRef] [PubMed]
[32]. Kho KH, Zwinderman AH, Blansjaar BA, Predictors for the efficacy of electroconvulsive therapy: chart review of a naturalistic study J Clin Psychiatry 2005 66:894-99.10.4088/JCP.v66n071216013905 [Google Scholar] [CrossRef] [PubMed]
[33]. Mukherjee S, Sackeim HA, Schnur DB, Electroconvulsive therapy of acute manic episodes: a review of 50 years experience Am J Psychiatry 1994 151:169-76.10.1176/ajp.151.2.1698296883 [Google Scholar] [CrossRef] [PubMed]
[34]. Hiremani RM, Thirthalli J, Tharayil BS, Gangadhar BN, Double-blind randomized controlled study comparing short-term efficacy of bifrontal and bitemporal electroconvulsive therapy in acute mania Bipolar Disorder 2008 10:701-07.10.1111/j.1399-5618.2008.00608.x18837864 [Google Scholar] [CrossRef] [PubMed]
[35]. Bharadwaj V, Grover S, Chakrabarti S, Avasthi A, Kate N, Clinical profile and outcome of bipolar disorder patients receiving electroconvulsive therapy: a study from north India Indian J Psychiatry 2012 54(1):41-47.10.4103/0019-5545.9464422556436 [Google Scholar] [CrossRef] [PubMed]
[36]. Alexander RC, Salomon M, Pioggia I, Cole JO, Convulsive therapy in the treatment of mania: McLean Hospital 1973-1986 Convulsive Ther 1988 4:115-25. [Google Scholar]
[37]. Stromgren IS, Electroconvulsive therapy in Aarhus, Denmark, in 1984: its application in non depressive disorders Convulsive Ther 1988 4:306-13. [Google Scholar]
[38]. Abraham K, Kulhara P, The efficacy of ECT in the treatment of schizophrenia British Journal of Psychiatry 1987 15:152-55.10.1192/bjp.151.2.1523318990 [Google Scholar] [CrossRef] [PubMed]
[39]. Smith K, ECT/chlorpromazine and chlorpromazine compared in the treatment of schizophrenia J Nerv Ment Dis 1967 144:284-90.10.1097/00005053-196704000-00006 [Google Scholar] [CrossRef]
[40]. Janakiramaiah N, Channabasavanna SM, Murthy NS, ECT/chlorpromazine combination versus chlorpromazine alone in acutely schizophrenic patients Acta Psychiatr Scand. 1982 66:464-70.10.1111/j.1600-0447.1982.tb04504.x7180565 [Google Scholar] [CrossRef] [PubMed]
[41]. Pankratz WJ, Electroconvulsive therapy: the position of the Canadian Psychiatric Association Can J Psychiatry 1980 25(6):509-14.10.1177/0706743780025006097417928 [Google Scholar] [CrossRef] [PubMed]
[42]. Husted DS, Shapira NA, A review of the treatment for refractory obsessivecompulsive disorder: from medicine to deep brain stimulation CNS Spectr 2004 9:833-47.10.1017/S109285290000225X15520607 [Google Scholar] [CrossRef] [PubMed]
[43]. Rosenthal DL, Leibu E, Aloysi SA, Kopell BH, Goodman WK, Kellner CH, Safety and efficacy of electroconvulsive therapy for depression in the presence of deep brain stimulation in obsessive-compulsive disorder J Clin Psychiatry 2016 77(5):689-90.10.4088/JCP.15lr1042027249078 [Google Scholar] [CrossRef] [PubMed]
[44]. Leiknes KA, Jarosh-von SL, Hoie B, Contemporary use and practice of electroconvulsive therapy worldwide Brain Behav 2012 2:283-344.10.1002/brb3.3722741102 [Google Scholar] [CrossRef] [PubMed]
[45]. Scott AIF, Lock T, Monitoring seizure activity. In The ECT Handbook 1995 1st Edition C. P. FreemanLondonRoyal College of Psychiatrists:62-66. [Google Scholar]
[46]. Maletzky BM, Seizure duration and clinical effect in electro convulsive therapy Comprehensive Psychiatry 1978 19:541-50.10.1016/0010-440X(78)90086-X [Google Scholar] [CrossRef]
[47]. Sackeim HA, Devanand DP, Prudic J, Stimulus intensity, seizure threshold, and seizure duration: impact on the efficacy and safety of electro convulsive therapy Psychiatric Clinics of North America 1991 14:803-43.10.1016/S0193-953X(18)30271-5 [Google Scholar] [CrossRef]