Objectives. Evidence in favour of switching between selective serotonin reuptake inhibitor (SSRI) and tricyclic (TCA) antidepressants in treatment resistant depression has been tested in a few studies only, consequently a prospective study was undertaken to evaluate the impact of switching strategies. Methods. One hundred eighty-nine patients who failed to respond to a previous antidepressant were randomised to four arms: firstly they received citalopram or desipramine for a 4-week period; secondly, those who failed to respond were treated for a further 4-week period with the same antidepressant (citalopram-citalopram and desipramine-desipramine arms) or switched to the alternate one (citalopram-desipramine and desipramine-citalopram arms). Results. There was no difference in the first 4-week phase between patients receiving citalopram versus desipramine in Hamilton Rating Scale for Depression (HRSD), Montgomery--Asberg Depression Rating Scale (MADRS), and Clinical Global Impression (CGI) scores. In the second 4-week phase remitter rates were higher among non-switched patients (P == 0.04). Moreover, considering HRSD and MADRS, switched patients reported significantly higher scores (P < a parts per thousand currency sign 0.02 for both scales at each time-point). Conclusions. This study supports the thesis that switching from an SSRI to a TCA (and vice versa) in non-responders to a 4-week trial of an SSRI/TCA is not associated with improved response. The result goes in the opposite direction to that predicted by current guidelines.

Souery, D., Serretti, A., Calati, R., Oswald, P., Massat, I., Konstantinidis, A., et al. (2011). Citalopram versus desipramine in treatment resistant depression: Effect of continuation or switching strategies. A randomized open study. THE WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 12(5), 364-375 [10.3109/15622975.2011.590225].

Citalopram versus desipramine in treatment resistant depression: Effect of continuation or switching strategies. A randomized open study

Calati R;
2011

Abstract

Objectives. Evidence in favour of switching between selective serotonin reuptake inhibitor (SSRI) and tricyclic (TCA) antidepressants in treatment resistant depression has been tested in a few studies only, consequently a prospective study was undertaken to evaluate the impact of switching strategies. Methods. One hundred eighty-nine patients who failed to respond to a previous antidepressant were randomised to four arms: firstly they received citalopram or desipramine for a 4-week period; secondly, those who failed to respond were treated for a further 4-week period with the same antidepressant (citalopram-citalopram and desipramine-desipramine arms) or switched to the alternate one (citalopram-desipramine and desipramine-citalopram arms). Results. There was no difference in the first 4-week phase between patients receiving citalopram versus desipramine in Hamilton Rating Scale for Depression (HRSD), Montgomery--Asberg Depression Rating Scale (MADRS), and Clinical Global Impression (CGI) scores. In the second 4-week phase remitter rates were higher among non-switched patients (P == 0.04). Moreover, considering HRSD and MADRS, switched patients reported significantly higher scores (P < a parts per thousand currency sign 0.02 for both scales at each time-point). Conclusions. This study supports the thesis that switching from an SSRI to a TCA (and vice versa) in non-responders to a 4-week trial of an SSRI/TCA is not associated with improved response. The result goes in the opposite direction to that predicted by current guidelines.
Articolo in rivista - Articolo scientifico
Major depressive disorder, antidepressants, pharmacotherapy, resistant depression, switch
English
2011
12
5
364
375
none
Souery, D., Serretti, A., Calati, R., Oswald, P., Massat, I., Konstantinidis, A., et al. (2011). Citalopram versus desipramine in treatment resistant depression: Effect of continuation or switching strategies. A randomized open study. THE WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 12(5), 364-375 [10.3109/15622975.2011.590225].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/249228
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