• Users Online: 82
  • Print this page
  • Email this page


 
 
Table of Contents
LETTER TO THE EDITOR
Year : 2020  |  Volume : 34  |  Issue : 2  |  Page : 94-95

Add-on subanesthetic ketamine in electroconvulsive therapy: A case report of a patient with bipolar depression


1 Department of Psychiatry, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan
2 Department of Anesthesiology, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan

Date of Submission21-Nov-2019
Date of Decision22-Jan-2020
Date of Acceptance19-Feb-2020
Date of Web Publication26-Jun-2020

Correspondence Address:
Chen- Hsiu Chen
Department of Anesthesiology, Kaohsiung Veterans General Hospital, Kaohsiung
Taiwan
Cheng- Ho Chang
No. 386, Ta-Chung First Road, Tzuo-Yin District, Kaohsiung City 81362
Taiwan
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/TPSY.TPSY_16_20

Rights and Permissions

How to cite this article:
Hsu TW, Pan CC, Chen CH, Chang CH. Add-on subanesthetic ketamine in electroconvulsive therapy: A case report of a patient with bipolar depression. Taiwan J Psychiatry 2020;34:94-5

How to cite this URL:
Hsu TW, Pan CC, Chen CH, Chang CH. Add-on subanesthetic ketamine in electroconvulsive therapy: A case report of a patient with bipolar depression. Taiwan J Psychiatry [serial online] 2020 [cited 2020 Jul 13];34:94-5. Available from: http://www.e-tjp.org/text.asp?2020/34/2/94/288007



The evidence showed that add-on ketamine anesthesia in electroconvulsive therapy (ECT) enhances the treatment effect, but this is a rare practice in clinical settings because of some safety concerns [1],[2]. We are presenting a case of a male patient with a recurrent difficult-to-treat major depressive episode, who received a course of ECT with ketamine as the anesthetic agent.


  Case Report Top


A 57-year-old successful businessman patient experienced his first major depressive episode at the age of 42 years. During the age of 43–45 years, he had an elevated mood, during which he had had a buying spree having spent about 100 million New Taiwan dollars in three years. He retained occupational function during that time, and the hypomanic condition was remitted spontaneously. After that, he remained in a persistent dysphoric state for 10 years, and he retired from his job at 50 years of age. He had his second major depressive episode when he was 55 years old, and he attempted suicide with a drug overdose. His third major depressive episode began at the end of 2018. The symptoms and signs included all-day depressive mood, loss of interest, intense anxiety, poor appetite with bodyweight loss, insomnia, low motivation with poor energy, psychomotor retardation, and attempted suicide with another drug overdose again in June 2019. He was then admitted to our psychiatric inpatient ward.

Tracing back to his medication record, the patient had received psychotropic treatment since the first episode. He had received many kinds of antidepressants, mood stabilizers, and several types of antipsychotic drugs. The regimen of daily venlafaxine (225 mg) combined with mirtazapine (30 mg) and olanzapine (10 mg) as augmentation was effective before but was ineffective for the third major depressive episode.

Under the impression of treatment-resistant bipolar depression, we decided to treat him with bitemporal ECT plus intravenous ketamine as added on anesthetic after his giving written informed consent. During the admission, we maintained his main daily medication as venlafaxine (225 mg), agomelatine (25 mg), and olanzapine (10 mg). We arranged six sessions of ECT with two-seizure episodes in one session. We did ECT twice per week with an anesthesiologist's assistance in every session. Every week, we rated him with the Hamilton Depression Rating 17 (HAMD-17) score before and after the treatment to assess the therapeutic effect.

The patient was treated with a seizure threshold of 120 millicoulombs (mC) in the first session of ECT. For evaluation of response to anesthesia, we used only propofol (80 mg, 1 mg/kg) and succinylcholine (20 mg, 0.25 mg/kg) in the first ECT session (the first and the second seizures). From the second to the sixth session, we added on ketamine (40 mg) with the same dose of propofol and succinylcholine in every session. After using ketamine, we noted that he showed elevated blood pressure (around 180–220 mmHg of systolic blood pressure) and tachycardia (about 120 beat/minute) after ECT, and this condition sometimes persisted for 20–30 min. We considered to give nicardipine (0.5 mg). His blood pressure and heart rate would have declined to normal ranges. Despite hypertension and tachycardia, he only complained about impaired memory without other discomforts. The weekly HAMD-17 score was declined from 30 points to 25, 21, and finally, 10 points after the treatment course of the ECT. The HAMD-17 score was decreased from the suicidal ideation domain first, and then, it was declined globally. After 12 seizures of ECT, he was discharged from our ward without complications.


  Comment Top


ECT is a promised treatment for severe or treatment-resistant major depression or bipolar depression [3]. Treatment-resistant depression still remains an operational definition, and several different definitions have been suggested [4]. We defined treatment-resistant depression here as “failure of three or more adequate antidepressant or psychotherapy trials from different classes (either in combination or succession) in the current episode [5].”

In the challenging cases, the use of ECT has generally shown a response rate of 60%–80% and a remission rate of 50%–60% [3]. Ketamine, an anesthetic agent with N-methyl-D-aspartic acid receptor antagonist and opioid receptor agonist properties, can rapidly and transiently improve treatment-resistant depression, including suicide ideation [6]. The optimal method and dose of giving ketamine and for those treatment-resistant depressions have not been established [7],[8]. But the dosage of 0.5 mg/kg with an intravenous method has been used in the majority of studies, and one study revealed that doses below 0.5 mg/kg are not efficacious [8],[9]. Clear evidence existed to confirm that the efficacy of a single infusion of ketamine can have a remarkable antidepressant effect [8],[10]. A few studies suggested that repeated giving ketamine can improve and maintain the antidepressant effect [11],[12].

Some evidence suggested that ketamine can hasten the response of depressive symptoms to ECT [1]. The antidepressant effect of add-on ketamine anesthesia in ECT is remarkably higher than that of other anesthetics in both the short term (1–2 weeks) and long term (3–4 weeks) [2]. Compared to other anesthetics, those given with ketamine group have a higher risk of hallucinations, confusion, hypertension, tachycardia, and a longer recovery time from anesthetic agent [2].

In our patient, the average seizure duration according to an electroencephalogram was 26.5 s, which has been considered long enough in previous studies [13]. Although the combined anesthetic of propofol has remarkable seizure threshold-elevating properties [14], another anesthetic containing ketamine has the effect of lowering the seizure threshold in contrast [1]. The effect of lowering the seizure threshold is related to seizure quality [1]. This patient had a positive response to our treatment protocol with the HAM-D 17 score declining more than 50% (30 to 10), and the suicidal ideation was declined immediately after two sessions of ECT. We did identify hypertension and tachycardia after ECT treatment and needed hypertensive drugs for those side effects, but we did not observe hallucinations or confusion. Generally speaking, those side effects in this patient were manageable and acceptable. Under the consideration of those side effects, the prescription of add-on ketamine anesthesia in ECT should be carefully given and monitored by anesthesiologists, especially in elderly patients and those with heart failure or other physical problems.

Our case report here is limited to be only one patient. To our best knowledge, we have not found any other published reports. But we have experienced a successful case of a patient treated with add-on ketamine combined with bitemporal ECT. We cannot attribute the antidepressant effect to ECT, intravenous ketamine, or a combination of these methods. (The institutional review board at Kaohsiung Veterans General Hospital approved the publication of this case report (protocol number = VGHKS19-CT12-11 and date of approval = December 5, 2019) with the waiver to obtain written consent from the patient.)


  Financial Support and Sponsorship Top


None.


  Conflicts of Interest Top


All authors declare no potential conflicts of interest in writing this case report.



 
  References Top

1.
Ritter P, Findeis H, Bauer M: Ketamine in the treatment of depressive episodes. Pharmacopsychiatry 2020; 53: 45-50.  Back to cited text no. 1
    
2.
Li DJ, Wang FC, Chu CS, et al.: Significant treatment effect of add-on ketamine anesthesia in electroconvulsive therapy in depressive patients: a meta-analysis. Eur Neuropsychopharmacol 2017; 27: 29-41.  Back to cited text no. 2
    
3.
Weiner RD, Reti IM: Key updates in the clinical application of electroconvulsive therapy. Int Rev Psychiatry 2017; 29: 54-62.  Back to cited text no. 3
    
4.
Fava M: Diagnosis and definition of treatment-resistant depression. Biol Psychiatry 2003; 53: 649-59.  Back to cited text no. 4
    
5.
Conway CR, George MS, Sackeim HA: Toward an evidence-based, operational definition of treatment-resistant depression: when enough is enough. JAMA Psychiatry 2017; 74: 9-10.  Back to cited text no. 5
    
6.
Nemeroff CB: Ketamine: quo vadis? Am J Psychiatry 2018; 175: 297-9.  Back to cited text no. 6
    
7.
Loo C: Can we confidently use ketamine as a clinical treatment for depression? Lancet Psychiatry 2018; 5: 11-2.  Back to cited text no. 7
    
8.
Fond G, Loundou A, Rabu C, et al.: Ketamine administration in depressive disorders: a systematic review and meta-analysis. Psychopharmacology (Berl) 2014; 231: 3663-76.  Back to cited text no. 8
    
9.
Fava M, Freeman MP, Flynn M, et al.: Double-blind, placebo-controlled, dose-ranging trial of intravenous ketamine as adjunctive therapy in treatment-resistant depression (TRD). Mol Psychiatry 2018; Advance online publication.  Back to cited text no. 9
    
10.
Romeo B, Choucha W, Fossati P, et al.: Meta-analysis of short- and mid-term efficacy of ketamine in unipolar and bipolar depression. Psychiatry Res 2015; 230: 682-8.  Back to cited text no. 10
    
11.
Thomas RK, Baker G, Lind J, et al.: Rapid effectiveness of intravenous ketamine for ultraresistant depression in a clinical setting and evidence for baseline anhedonia and bipolarity as clinical predictors of effectiveness. J Psychopharmacol 2018; 32: 1110-7.  Back to cited text no. 11
    
12.
Singh JB, Fedgchin M, Daly EJ, et al.: A double-blind, randomized, placebo-controlled, dose-frequency study of intravenous ketamine in patients with treatment-resistant depression. Am J Psychiatry 2016; 173: 816-26.  Back to cited text no. 12
    
13.
Lee WG, Chang SS: Monitoring the seizure efficacy during electroconvulsive therapy. Taiwan J Psychiatry (Taipei) 2009; 23: 4-13.  Back to cited text no. 13
    
14.
Fava M, Freeman MP, Flynn M, et al.: Double-blind, proof-of-concept (POC) trial of Low-Field Magnetic Stimulation (LFMS) augmentation of antidepressant therapy in treatment-resistant depression (TRD). Brain Stimul 2018; 11: 75-84.  Back to cited text no. 14
    




 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
  Case Report
  Comment
   Financial Suppor...
   Conflicts of Int...
   References

 Article Access Statistics
    Viewed39    
    Printed0    
    Emailed0    
    PDF Downloaded7    
    Comments [Add]    

Recommend this journal