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EDITORIAL
Year : 2011  |  Volume : 33  |  Issue : 2  |  Page : 103-105  

Electro-convulsive therapy: A few lingering thoughts/doubts!


Asha Hospital, Hyderabad, Andhra Pradesh, India

Date of Web Publication20-Jan-2012

Correspondence Address:
M S Reddy
Asha Hospital, Hyderabad, Andhra Pradesh
India
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DOI: 10.4103/0253-7176.92042

PMID: 22345830

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How to cite this article:
Reddy M S. Electro-convulsive therapy: A few lingering thoughts/doubts!. Indian J Psychol Med 2011;33:103-5

How to cite this URL:
Reddy M S. Electro-convulsive therapy: A few lingering thoughts/doubts!. Indian J Psychol Med [serial online] 2011 [cited 2014 Oct 1];33:103-5. Available from: http://www.ijpm.info/text.asp?2011/33/2/103/92042

Electro-convulsive therapy (ECT) was introduced in 1938 and has been in continuous use since then as a tool for therapeutic neuromodulation in the treatment of various psychiatric disorders. ECT celebrates its 74th birthday this year and is neither tired nor retired as a treatment modality. It remains an important component in the armamentarium of biological therapeutic tools in psychiatry. ECT remains invaluable, and can be termed life saving, in the management of patients with acute suicidal risk, severely retarded depression, catatonia, etc.

ECT differs from psychopharmacology in several clinically relevant aspects: action on electrical depolarization and not at receptors at synapses, independent of renal clearance, hepatic metabolism, compliance of patient, drug interactions, etc. [1] As of today there is no single unifying explanation how ECT works so well in a variety of conditions.

Since its introduction in 1938 there were several advances in the practice of ECT with introduction of modified ECT, brief pulse and ultrabrief pulse current, unilateral electrode placement, seizure threshold titration, etc. with the goal to increase efficacy and minimize the risk, special focus being on minimizing cognitive side effects. Risk of death with ECT is relatively low at 1 in 10,000 patients. At Asha hospital, Hyderabad, about 30,000 patients received ECT in the last 8 years, mostly modified, without any mortality (oral communication). Amnesia, both anterograde and retrograde, remains a significant troublesome side effect. Generally it is transient but some reports comment on many patients having incomplete recovery in retrograde amnesia. [2] The reasonable safety of unmodified ECT has been well described. [3],[4],[5],[6],[7] The safety profile of ECT remains neighbors's (other biological treatments) envy. Scalia et al.[8] reported the case of a 92-year-old woman who had received 91 ECTs in her lifetime and showed no pathological effects at postmortem examination of her brain when she died of other causes. Dwork et al.[9] reported no evidence of any significant neuro-pathological lesions in nonhuman primates after receiving multiple ECTs.

Broadly ECT can be categorized based on the phase of treatment:

  1. Acute (phase) ECT - till response/remission
  2. Continuation (phase) ECT (C - ECT) - few weeks/months after remission to prevent relapse
  3. Maintenance (phase) ECT (M - ECT) - few months or longer to prevent recurrence
ECT is used in the management of depression and every psychotic disorder in psychiatry, though depression remains the most common indication. The Consortium for esearch in ECT (CORE) reported a 75% remission in depression [10] which is supported by the UK ECT Review group. [11] Patients with psychotic subtype of depression respond much higher. [12] But there are reports that success rates in community hospital settings have been less at 30-45% as reported by Prudic et al.. [13] There was another report by Sackeim et al.[14] that documented remission rates in depression with ECT at 54%. Another interesting component of this study was that without any form of maintenance treatment 84% of patients relapsed at the end of 6-month follow-up. The CORE group also reported 46% relapse at the end of 6 months. One of their recommendations underscores the need to "treat to wellness" and not prematurely terminate the acute course of ECT. The clinical utility of continuation ECT and maintenance ECT was well discussed by Andrade et al.[15] and Kellner et al.[16]

Most guidelines recommend ECT only for resistant depression and at a much later stage in the treatment process. The National Institute for Clinical Excellence (NICE) guidelines recommend restriction of ECT only for patients with severe depression and state that ECT is not recommended as maintenance therapy. [17]

ECT is underutilized as a treatment modality by some psychiatrists, at some institutions and in some geographical locations of the world. Similarly with some psychiatrists, at some institutions and in some geographical locations, ECT is an overused, rather abused, treatment modality. Each group has its own rationalizations and justifications.

The Grand Old Lady of the biological treatments in psychiatry stood the test of time for three quarters of a century and is going strong, a standing testimonial to its therapeutic benefits.
"In all affairs it is a healthy thing now and then to hang a question mark on the things you have long taken for granted."

After having said so a few lingering thoughts/doubts cross my mind, which I thought, I will share with you all:

  1. After introduction of ECT as a treatment modality for depression whether there is any decreased risk of suicide among patients with depression! There is published data that indicate reduction in suicide rates after usage of SSRI. [18]
  2. Is there any increased risk of suicide, in the immediate period, after administration of ECT, similar to reports of increased suicidality with antidepressants? ECT is generally indicated in retarded, suicidal patients and it is the retardation component, which improves earlier.
  3. Acute (phase) ECT is given 2-3 times a week. What is the prescribed guideline for continuation/maintenance ECT? At what frequency and for how long?
  4. Is ECT used as monotherapy or only as an adjunct to pharmacotherapy in the management of Major Depressive Disorder (MDD)! Complete management of MDD includes five phases - 1. Response, 2. Remission, 3. Relapse prevention, 4. Recovery, 5. Recurrence prevention and extends for a period of about 9-12 months. The beneficial effect of ECT will be acute ECT in phases 1 and 2, continuation ECT in phases 3 and 4, and maintenance ECT in phases 4 and 5. At least in India, most likely in most other countries, C-ECT and M-ECT are administered extremely rarely, if at all. Without the component of M-ECT the modality of convulsive therapy is incomplete and can only remain an adjunct to antidepressants!
  5. NICE guidelines restrict use of ECT only for severe/resistant depression and also do not recommend M-ECT. Definition of resistant depression includes no or not satisfactory response to multiple antidepressant treatment trials either as mono/polypharmacy. After satisfactory treatment of resistant depression with ECT (acute phase) what can be the rationale in maintenance pharmacotherapy with antidepressant medication, which proved otherwise useless in the acute phase?
  6. MDD includes a very heterogeneous group of patients with depressive symptoms. Leaving aside psychotic, melancholia, and recurrent depression subgroups how effective is ECT in the management of MDD? This question becomes more relevant in the current context of:
    1. Recent controversies regarding the unsatis-factory benefit with antidepressant medication in bipolar depression (Systematic Treatment Enhancement Programme - Bipolar Disorder (STEP-BD)) and in MDD (Sequenced Treatment Alternatives to Relieve Depression (STAR-D))
    2. Reemergence of the concept; neurotic depression constituting a significant percentage of patients with MDD. [19]
  7. ECT as Mood Stabiliser (MS) in Bipolar Disorders (BD): It is an established fact that the bipolar patient spends three times more duration in depressive phase than in the manic phase. ECT is effective in acute management of depression and also in acute management of Mania. We all, practicing psychiatrists, have reasonable chunk of very difficult BD patients with significant suicidal risk, social and vocational disruptions with frequent episodes. Should maintenance ECT be given a chance to prove its worth in mood stabilization and if not what could be the valid reason? Does any guideline include M-ECT as one of the options as mood stabilizer? Many may argue that there is no evidence. Let me remind that absence of evidence is not evidence ofabsence of effect and scientific temperament demands some extrapolation of data and testing of hypothesis.
  8. What are the short- and long-term effects of ECT in children where the process of neuronal demyelination is not complete and also the effect of ECT on the neuronal circuits in the light of recent evidence on Neuroplasticity?
If an young/old scientist takes up any "doubt" as a research project, I salute him. If somebody leaves it as the ramblings of another "Doubting Thomas," I will not be unhappy with him.

Truth is the goal at which the gradual process of corrected error aims.

 
   References Top

1.Tasman A. Psychiatry, 3 rd ed. 2008  Back to cited text no. 1
    
2.Donahue AB. ECT and memory loss: A personal journey. J ECT 2000;16:133-43.  Back to cited text no. 2
[PUBMED]    
3.Tharyan P, Saju PJ, Datta S, John JK, Kuruvilla K. Physical morbidity with unmodified ECT: A decade of experience. Indian J Psychiatry 1993;35:211-4.  Back to cited text no. 3
[PUBMED]  Medknow Journal  
4.Andrade C, Agarwal AK, Reddy MV. The practice of ECT in India. 2. The practical administration of ECT. Indian J Psychiatry 1993;35:81-6.  Back to cited text no. 4
    
5.Shah N, Mahadeswar S, Bhakta S, Bhirud M, Fernandez P, Andrade C. The safety and efficacy of Benzodiazepine modified treatment as a special form of unmodified ECT. J ECT 2010;26:242.  Back to cited text no. 5
    
6.Andrade C, Shah N, Tharyan P. The dilemma of unmodified ECT. J Clin Psychiatry 2003;64:1147-52.  Back to cited text no. 6
[PUBMED]  [FULLTEXT]  
7.Tharyan P, Adams CE. ECT for Schizophrenia. Cochrane Database Syst Rev 2005;2:CD000076.  Back to cited text no. 7
[PUBMED]  [FULLTEXT]  
8.Scalia J, Lisanby SH, Dwork AJ, Johnson JE, Bernhardt ER, Arango V, et al. Neuro Pathological examination after 91 ECT treatments in a 92 year old woman with late onset depression. J ECT 2007;23:96-8.  Back to cited text no. 8
[PUBMED]  [FULLTEXT]  
9.Dwork AJ, Arango V, Underwood M, Ilievski B, Rosoklija G, Sackeim HA, et al. Absence of histological leisons in primate models of ECT and magnetic seizure therapy. Am J Psychiatry 2004;161:576-8.  Back to cited text no. 9
[PUBMED]  [FULLTEXT]  
10.Husain MM, Rush AJ, Fink M, Knapp R, Petrides G, Rummans T, et al. Speed of response and remission in MDD with Acute ECT: A Consortium for Research in ECT (CORE) report. J Clin Psychiatry 2004;65:485-91.  Back to cited text no. 10
[PUBMED]  [FULLTEXT]  
11.UK ECT Review Group. Efficacy and Safety of ECT in depressive disorders: A systematic review and meta analysis. Lancet 2003;36:799-808.  Back to cited text no. 11
    
12.Petrides G, Fink M, Husain MM, Knapp RG, Rush AJ, Mueller M, et al. ECT remission In psychotic vs nonpsychotic depressed patients. A report from CORE. J ECT 2001;17: 244-53.  Back to cited text no. 12
[PUBMED]  [FULLTEXT]  
13.Prudic J, Olfson M, Marcus SC, Fuller RB, Sackeim HA. Effectiveness of ECT in community settings. Biol Psychiatry 2004;55:301-12.  Back to cited text no. 13
[PUBMED]  [FULLTEXT]  
14.Sackeim HA, Haskett RF, Mulsant BH, Thase ME, Mann JJ, Pettinati HM, et al. Continuation pharmacotherapy in the prevention of relapse following ECT: A randomized controlled trial. J Am Med Assoc 2001;285:1299-307.  Back to cited text no. 14
    
15.Andrade C, Kurinji S. Continuation and Maintenance ECT: A Review of recent Research. J ECT 2002;18:149-58.  Back to cited text no. 15
[PUBMED]  [FULLTEXT]  
16.Kellner CH, Knapp RG, Petrides G, Rummans TA, Husain MM, Rasmussen K, et al. Continuous ECT vs Pharmacotherapy for relapse prevention in MDD. A multisite study from the Consortium for Research in ECT (CORE). Arch Gen Psychiatry 2006;63:1337-44.  Back to cited text no. 16
[PUBMED]  [FULLTEXT]  
17.National Institute for Clinical Excellence (NICE), Technology Appraisal No. 59. Guidance on the use of ECT. London.UK. 2003.  Back to cited text no. 17
    
18.Gibbons RD, Brown CH, Hur K, Marcus SM, Bhaumik DK, Mann JJ. Relationship between antidepressants and suicide attempts: An analysis of the Veterans Health Administration data sets. Am J Psychiatry 2007;164:1044-9.  Back to cited text no. 18
[PUBMED]  [FULLTEXT]  
19.Ghaemi SN. Why Antidepressants are not Antidepressants: STEP - BD and STAR*D and the return of Neurotic Depression. Bipolar Disord 2008;10:957-68.  Back to cited text no. 19
[PUBMED]  [FULLTEXT]  




 

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