TY - JOUR
T1 - Citalopram versus desipramine in treatment resistant depression
T2 - Effect of continuation or switching strategies. A randomized open study
AU - Souery, Daniel
AU - Serretti, Alessandro
AU - Calati, Raffaella
AU - Oswald, Pierre
AU - Massat, Isabelle
AU - Konstantinidis, Anastasios
AU - Linotte, Sylvie
AU - Kasper, Siegfried
AU - Montgomery, Stuart
AU - Zohar, Joseph
AU - Mendlewicz, Julien
N1 - Funding Information:
The study was sponsored by Lundbeck A/S and the Belgian National Fund for Scientific Research (FNRS; 3.4.530.07 F) by means of an unrestricted grant for the Group for the Study of Resistant Depression (GSRD). The sponsors had no role in the study design, analysis and writing of the paper. All authors were actively involved in the analytical method of the study, selection and review of all scientific content and had full editorial control during writing of the manuscript.
PY - 2011/8
Y1 - 2011/8
N2 - 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), MontgomeryAsberg 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 ≤≠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.
AB - 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), MontgomeryAsberg 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 ≤≠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.
KW - Antidepressants
KW - Major depressive disorder
KW - Pharmacotherapy
KW - Resistant depression
KW - Switch
UR - http://www.scopus.com/inward/record.url?scp=79960779425&partnerID=8YFLogxK
U2 - 10.3109/15622975.2011.590225
DO - 10.3109/15622975.2011.590225
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AN - SCOPUS:79960779425
VL - 12
SP - 364
EP - 375
JO - World Journal of Biological Psychiatry
JF - World Journal of Biological Psychiatry
SN - 1562-2975
IS - 5
ER -