Combination of Tranylcypromine and Mirtazapine in Difficult-to-Treat Depression.


Journal

Journal of clinical psychopharmacology
ISSN: 1533-712X
Titre abrégé: J Clin Psychopharmacol
Pays: United States
ID NLM: 8109496

Informations de publication

Date de publication:
Historique:
pubmed: 10 8 2021
medline: 16 12 2021
entrez: 9 8 2021
Statut: ppublish

Résumé

About one third of depression patients do not respond to the first antidepressant trial. Difficult-to-treat depression was suggested to characterize the often chronic and severe course of disease. Previous data indicate that tranylcypromine is effective in case of treatment-refractory depression. Many antidepressants are contraindicated in combination with tranylcypromine and other monoamine-oxidase inhibitors because of the risk of serotonin syndrome. The combination of tranylcypromine and amitriptyline was reported to be efficacious and safe in patients with electroconvulsive therapy-resistant major depression. In this retrospective chart review, we report a series of 3 cases, in which patients with electroconvulsive therapy-resistant depression were treated with the combination of tranylcypromine and mirtazapine. There are no published clinical data on this combination yet. Disease severity and treatment response were retrospectively assessed with the Clinical Global Impression-Severity and Improvement Scales. All 3 patients had severe difficult-to-treat depression with chronic course of disease and several times of inpatient treatment without achieving remission. The combination treatment was tolerated well, although the patients had somatic comorbidities. One patient developed mild and self-limiting neuroleptic malignant syndrome in the long-term course after dose increase of concomitant aripiprazole. All 3 patients showed either much or very much improvement. Under tight clinical controls in inpatient setting and after exhausting of alternatives, the combination of tranylcypromine and mirtazapine could be considered in patients, who do not achieve adequate improvement through common treatment options recommended in the guidelines. The combination has to be ceased, if symptoms of possible serotonin syndrome occur.

Sections du résumé

BACKGROUND BACKGROUND
About one third of depression patients do not respond to the first antidepressant trial. Difficult-to-treat depression was suggested to characterize the often chronic and severe course of disease. Previous data indicate that tranylcypromine is effective in case of treatment-refractory depression. Many antidepressants are contraindicated in combination with tranylcypromine and other monoamine-oxidase inhibitors because of the risk of serotonin syndrome. The combination of tranylcypromine and amitriptyline was reported to be efficacious and safe in patients with electroconvulsive therapy-resistant major depression.
METHODS METHODS
In this retrospective chart review, we report a series of 3 cases, in which patients with electroconvulsive therapy-resistant depression were treated with the combination of tranylcypromine and mirtazapine. There are no published clinical data on this combination yet. Disease severity and treatment response were retrospectively assessed with the Clinical Global Impression-Severity and Improvement Scales.
RESULTS RESULTS
All 3 patients had severe difficult-to-treat depression with chronic course of disease and several times of inpatient treatment without achieving remission. The combination treatment was tolerated well, although the patients had somatic comorbidities. One patient developed mild and self-limiting neuroleptic malignant syndrome in the long-term course after dose increase of concomitant aripiprazole. All 3 patients showed either much or very much improvement.
CONCLUSIONS CONCLUSIONS
Under tight clinical controls in inpatient setting and after exhausting of alternatives, the combination of tranylcypromine and mirtazapine could be considered in patients, who do not achieve adequate improvement through common treatment options recommended in the guidelines. The combination has to be ceased, if symptoms of possible serotonin syndrome occur.

Identifiants

pubmed: 34369903
doi: 10.1097/JCP.0000000000001452
pii: 00004714-900000000-98264
doi:

Substances chimiques

Antidepressive Agents 0
Tranylcypromine 3E3V44J4Z9
Mirtazapine A051Q2099Q

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

585-588

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Références

Adli M, Wiethoff K, Baghai TC, et al. How effective is algorithm-guided treatment for depressed inpatients? Results from the randomized controlled multicenter German algorithm project 3 trial. Int J Neuropsychopharmacol. 2017;20:721–730. doi:10.1093/ijnp/pyx043.
doi: 10.1093/ijnp/pyx043
Rush AJ, Trivedi MH, Wisniewski SR, et al. Acute and longer-term outcomes in depressed outpatients requiring one or several treatment steps: a STAR*D report. Am J Psychiatry. 2006;163:1905–1917. doi:10.1176/ajp.2006.163.11.1905.
doi: 10.1176/ajp.2006.163.11.1905
Zisook S, Johnson GR, Hicks P, et al. Continuation phase treatment outcomes for switching, combining, or augmenting strategies for treatment-resistant major depressive disorder: a VAST-D report. Depress Anxiety. 2020;38:185–195. doi:10.1002/da.23114.
doi: 10.1002/da.23114
Rush AJ, Aaronson ST, Demyttenaere K. Difficult-to-treat depression: a clinical and research roadmap for when remission is elusive. Aust N Z J Psychiatry. 2019;53:109–118. doi:10.1177/0004867418808585.
doi: 10.1177/0004867418808585
Kennedy SH, Lam RW, McIntyre RS, et al. Canadian Network for Mood and Anxiety Treatments (CANMAT) 2016 clinical guidelines for the management of adults with major depressive disorder: section 3. Pharmacological Treatments. Can J Psychiatry. 2016;61:540–560. doi:10.1177/0706743716659417.
doi: 10.1177/0706743716659417
Himmelhoch JM, Thase ME, Mallinger AG, et al. Tranylcypromine versus imipramine in anergic bipolar depression. Am J Psychiatry. 1991;148:910–916. doi:10.1176/ajp.148.7.910.
doi: 10.1176/ajp.148.7.910
Fawcett J. Why aren't MAOIs used more often?J Clin Psychiatry. 2009;70:139–140. doi:10.4088/JCP.08ac04892.
doi: 10.4088/JCP.08ac04892
Fiedorowicz JG, Swartz KL. The role of monoamine oxidase inhibitors in current psychiatric practice. J Psychiatr Pract. 2004;10:239–248. doi:10.1097/00131746-200407000-00005.
doi: 10.1097/00131746-200407000-00005
Gillman PK. A review of serotonin toxicity data: implications for the mechanisms of antidepressant drug action. Biol Psychiatry. 2006;59:1046–1051. doi:10.1016/j.biopsych.2005.11.016.
doi: 10.1016/j.biopsych.2005.11.016
Ulrich S, Ricken R, Adli M. Tranylcypromine in mind (part I): review of pharmacology. Eur Neuropsychopharmacol. 2017;27:697–713. doi:10.1016/j.euroneuro.2017.05.007.
doi: 10.1016/j.euroneuro.2017.05.007
Shioda K, Nisijima K, Yoshino T, et al. Mirtazapine abolishes hyperthermia in an animal model of serotonin syndrome. Neurosci Lett. 2010;482:216–219. doi:10.1016/j.neulet.2010.07.039.
doi: 10.1016/j.neulet.2010.07.039
Busner J, Targum SD. The clinical global impressions scale: applying a research tool in clinical practice. Psychiatry (Edgmont). 2007;4:28–37. Available at: http://www.ncbi.nlm.nih.gov/pubmed/20526405. Accessed April 5, 2021.
Agrawal A, Bajaj D, Bajaj S, et al. Aripiprazole induced late neuroleptic malignant syndrome. Am J Ther. 2018;26:e772–e773. doi:10.1097/MJT.0000000000000944.
doi: 10.1097/MJT.0000000000000944
Tibrewal P, Bastiampillai T, Kannampuzha C, et al. Aripiprazole-induced neuroleptic malignant syndrome. Asian J Psychiatr. 2017;27:5–6. doi:10.1016/j.ajp.2017.02.002.
doi: 10.1016/j.ajp.2017.02.002
Odagaki Y. Atypical neuroleptic malignant syndrome or serotonin toxicity associated with atypical antipsychotics?Curr Drug Saf. 2009;4:84–93. doi:10.2174/157488609787354387.
doi: 10.2174/157488609787354387
Boyer EW, Shannon M. Current concepts: the serotonin syndrome. N Engl J Med. 2005;352:1112–1120. doi:10.1056/NEJMra041867.
doi: 10.1056/NEJMra041867
Thomas SJ, Shin M, McInnis MG, et al. Combination therapy with monoamine oxidase inhibitors and other antidepressants or stimulants: strategies for the management of treatment-resistant depression. Pharmacotherapy. 2015;35:433–449. doi:10.1002/phar.1576.
doi: 10.1002/phar.1576
Feighner JP, Herbstein J, Damlouji N. Combined MAOI, TCA, and direct stimulant therapy of treatment-resistant depression. J Clin Psychiatry. 1985;46:206–209.
Ferreira-Garcia R, Da Rocha Freire RC, Appolinário JC, et al. Tranylcypromine plus amitriptyline for electroconvulsive therapy-resistant depression. J Clin Psychopharmacol. 2018;38:502–504. doi:10.1097/JCP.0000000000000945.
doi: 10.1097/JCP.0000000000000945
Bartova L, Vogl SE, Stamenkovic M, et al. Combination of intravenous S-ketamine and oral tranylcypromine in treatment-resistant depression: a report of two cases. Eur Neuropsychopharmacol. 2015;25:2183–2184. doi:10.1016/j.euroneuro.2015.07.021.
doi: 10.1016/j.euroneuro.2015.07.021

Auteurs

Erhan Kavakbasi (E)

From the Department of Psychiatry, University Hospital Münster, University of Münster, Münster, Germany.

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