Evidence map›Paper›PMID 41034918›Full record

ArticleBMC psychiatry2025

Successful treatment of five cases of catatonia treated with guanfacine without ECT: a case series from a psychiatric hospital in Japan.

Hiroki Saito, Mikael Tiger, Ryosuke Arakawa, Amane Tateno

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Article in BMC psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hiroki SaitoOnda-Daini Hospital, Matsudo-Shi, Chiba, Japan. h-moriya@nms.ac.jp.
Mikael TigerCentre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet & Stockholm Health Care Services, Stockholm County Council, Stockholm, Sweden.
Ryosuke ArakawaDepartment of Pharmacology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Amane TatenoDepartment of Neuropsychiatry, Graduate School of Medicine, Nippon Medical School, Sendagi 1-1-5, Bunkyo-Ku, Tokyo, 113-8602, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCatatonia, including malignant catatonia, is a severe neuropsychiatric condition historically associated with schizophrenia or schizoaffective disorder. However, recent diagnostic frameworks, such as the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) and the International Classification of Diseases, 11th Revision (ICD-11), offer a broader understanding. These systems classify catatonia not as a standalone diagnosis but as a specifier that may occur alongside various psychiatric disorders, including schizophrenia spectrum disorders, mood disorders, neurodevelopmental disorders, or medical conditions. Although electroconvulsive therapy (ECT) and benzodiazepines are considered gold standard treatments for catatonia, many healthcare settings lack access to ECT, and certain physical conditions make ECT relatively contraindicated or a high-risk option. Guanfacine, a central adrenergic α2A receptor agonist, has a similar mechanism of action as the sedative dexmedetomidine, which has shown efficacy in treating catatonia. However, the effectiveness of guanfacine in this context has not been tested. CASE PRESENTATION: We report five cases of catatonia (including malignant catatonia) associated with schizophrenia or schizoaffective disorder. These cases were treated either in a psychiatric hospital or an outpatient clinic, both of which lacked access to ECT. Extended-release formulation of guanfacine was administered alongside temporary benzodiazepine use, and treatment outcomes were observed. All five patients were in syndromal remission from catatonia following treatment that included guanfacine in combination with other pharmacological interventions. Mild to moderate side effects were observed. These included dizziness and fatigue in one patient, and hypotension and bradycardia in two others. All adverse effects resolved with dose reduction. Complications of catatonia included impaired oral intake requiring nutritional support in two patients and urinary catheterization due to immobility in two patients.

conclusionsThese findings suggest that guanfacine may serve as a safe and effective alternative to ECT for catatonia in settings where ECT is unavailable or relatively contraindicated. The clinical courses also suggest that dysfunction of the central noradrenergic system may contribute to the pathophysiology of catatonia, and that guanfacine's selective α2A adrenoceptor modulation may play a role in symptom improvement. Further research is needed to validate these findings and clarify the underlying mechanisms.

Indexed as

Adrenergic alpha-2 Receptor AgonistsCatatoniaGuanfacineElectroconvulsive TherapyHospitals, PsychiatricHumansJapanPsychotic DisordersSchizophreniaTreatment OutcomeAdrenergic alpha-2 Receptor AgonistsGuanfacineCatatoniaGuanfacineSchizoaffective disorderSchizophrenia

Identifiers

PMID41034918
PMCPMC12486612

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