Long-term response to successful acute pharmacological treatment of psychotic depression

Background bout follow-up after acute pharmacological treatment of psychotic depression are scarce. s nth open follow-up was done, preferentially with same medication as during acute treatment, of patients (n = 59) with DSM-IV-TR major depressive disorder with psychotic features, aged 18 to 65 years, who had completed as responders an acute double-blind 7 week trial with imipramine, venlafaxine or venlafaxine plus quetiapine. Main outcome measures were Hamilton Rating Scale for Depression and Clinical Global Impression Scale. s tients dropped out during the 4 month follow-up. Almost all patients (86.4%; 51/59) remained responder while remission rate increased from 59.3% (35/59) to 86.8% (46/53), independent of treatment. Relapse rate was low (3.8%; 2/53). Tolerability was good. Weight increased with all treatments. tions tions were the limited sample size and consequent limited statistical power. The treatment during follow-up was not double-blind. sions uation treatment with the same medication that was effective in the acute treatment trial, remained effective during the 4 month follow-up in many patients leading to further improvement, and was well tolerated.