Abstract
Objective
To explore the demographic and clinical features of severe catatonic patients, comparing responders and non-responders to ECT in order to detect possible predictors of non-response.
Methods
This naturalistic study included 59 catatonic inpatients with a diagnosis of mood disorder according to DSM-IV-TR criteria. All patients were treated with bilateral ECT and evaluated before and after ECT course. The response to ECT was defined as a Clinical Global Impression (Improvement subscale) rating 1 ‘very much improved’ or 2 ‘much improved’. Clinical variables were compared between responders and non-responders; logistic regression was used to predict the probability of non-response, with regard to the symptoms presented by the patients.
Results
The response rate was 83.1%. Non-responders (n = 10) to ECT showed neurological comorbidities, treatments with dopamine agonists and anticholinergic drugs, waxy flexibility, and echophenomena more frequently than respondents (n = 49). Echophenomena resulted a significant predictor of non-response in the multivariate analysis.
Conclusion
In line with previous reports, ECT resulted effective in the vast majority of severe catatonic patients. The association between ECT resistant catatonia and neurological comorbidity, use of dopamine-agonist and anticholinergic medications is consistent with the hypothesis that ECT is more effective in ‘top-down’ than in ‘bottom-up’ variant of catatonia.
Catatonic symptoms are frequently associated with severe and psychotic mood disorders.
Electroconvulsive therapy is effective in treating most forms of severe catatonia.
Neurological comorbidity and the presence of ‘echopraxia/echolalia’ could represent predictors of non-response to ECT.
Key points
Acknowledgements
The authors thank Dr. Federica Luchini who, under the supervision of Prof. Perugi, conducted a study on catatonic patients for her specialization thesis in psychiatry, on which we relied to conduct the present study.
Disclosure statement
Prof. Perugi acted as consultant to Lundbeck, Angelini, FB-Health. He received a scholarship/research support from Lundbeck and Angelini. He is a member of the speaker/advisory board of Sanofi-Aventis, Lundbeck, FB-Health, Angelini. Other authors have no affiliation or financial interest in any organisation that may constitute a conflict of interest.
Data availability statement
The data that support the findings of this study are available from the corresponding author, upon reasonable request.