Bupropion sustained release for bereavement: results of an open trial

The present study was conducted to assess whether DSM-IV-defined bereavement responds to bupropion sustained release (SR). Twenty-two subjects who had lost their spouses within the previous 6 to 8 weeks and who met DSM-IV symptomatic/functional criteria for a major depressive episode were evaluated....

Full description

Saved in:
Bibliographic Details
Published inThe journal of clinical psychiatry Vol. 62; no. 4; p. 227
Main Authors Zisook, S, Shuchter, S R, Pedrelli, P, Sable, J, Deaciuc, S C
Format Journal Article
LanguageEnglish
Published United States 01.04.2001
Subjects
Online AccessGet more information

Cover

Loading…
More Information
Summary:The present study was conducted to assess whether DSM-IV-defined bereavement responds to bupropion sustained release (SR). Twenty-two subjects who had lost their spouses within the previous 6 to 8 weeks and who met DSM-IV symptomatic/functional criteria for a major depressive episode were evaluated. Subjects completed the Hamilton Rating Scale for Depression (HAM-D), the Clinical Global Impressions scale, the Texas Revised Inventory of Grief, and the Inventory of Complicated Grief at baseline and follow-up. Subjects were treated with bupropion SR, 150 to 300 mg/day, for 8 weeks. Improvement was noted in both depression and grief intensity. For the intent-to-treat group. 59% experienced a reduction of > or = 50% on HAM-D scores. The correlations between changes in the HAM-D scores and the grief scale scores were high, ranging from 0.61 (p = .006) to 0.44 (p = .054). Major depressive symptoms occurring shortly after the loss of a loved one (i.e., bereavement) appear to respond to bupropion SR. Treatment of these symptoms does not intensify grief; rather, improvement in depression is associated with decreases in grief intensity. The results of this study challenge prevailing clinical wisdom that DSM-IV-defined bereavement should not be treated. Larger, placebo-controlled studies are indicated.
ISSN:0160-6689
1555-2101
DOI:10.4088/JCP.v62n0403