Key result
The combination of tranylcypromine and mirtazapine resulted in much or very much clinical improvement in 100% (3 of 3) of patients with electroconvulsive therapy-resistant depression.
Why the study?
Tranylcypromine is effective in treatment-refractory depression, but many antidepressants are contraindicated due to serotonin syndrome risk, and no clinical data exist on its combination with mirtazapine.
Does the combination of tranylcypromine and mirtazapine improve disease severity in patients with electroconvulsive therapy-resistant depression?
Case Report (n=3)
Does the combination of tranylcypromine and mirtazapine improve disease severity in patients with electroconvulsive therapy-resistant depression?
The combination of tranylcypromine and mirtazapine may be a viable option for severe, treatment-resistant depression when other alternatives are exhausted, though careful monitoring for serotonin syndrome is required.
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: 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: 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: 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.
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Kavakbasi et al. (2021) conducted a case report in Difficult-to-treat depression (n=3). Tranylcypromine and mirtazapine combination was evaluated on Treatment response assessed with the Clinical Global Impression-Improvement Scale. The combination of tranylcypromine and mirtazapine resulted in much or very much clinical improvement in 100% (3 of 3) of patients with electroconvulsive therapy-resistant depression.
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