DEXAMETHASONE SUPPRESSION TEST AND ONSET OF POSTSTROKE DEPRESSION IN PATIENTS WITH ISCHEMIC INFARCTION

Citation
Jh. Harney et al., DEXAMETHASONE SUPPRESSION TEST AND ONSET OF POSTSTROKE DEPRESSION IN PATIENTS WITH ISCHEMIC INFARCTION, The Journal of clinical psychiatry, 54(9), 1993, pp. 343-348
Citations number
38
Categorie Soggetti
Psycology, Clinical",Psychiatry,Psychiatry
ISSN journal
01606689
Volume
54
Issue
9
Year of publication
1993
Pages
343 - 348
Database
ISI
SICI code
0160-6689(1993)54:9<343:DSTAOO>2.0.ZU;2-P
Abstract
Background: Studies documenting abnormal results in the 1.0-mg dexamet hasone suppression test (DST) and the prevalence of depression in stro ke patients are usually accomplished between 1 and 6 months poststroke . One study, however, reported that 27% of patients met DSM-III criter ia for major depression and 20% for minor depression 1 to 3 weeks post stroke even though previous research has indicated that the prevalence of poststroke depression was greatest at approximately 6 months. Ther efore, we decided to assess DST abnormalities and depression within th e first month of stroke. Method. Twelve patients with single, computed tomography (CT)-verified, ischemic infarctions were administered the DST at 1 and 3 weeks poststroke. Each patient also received a complete psychiatric evaluation, including a special clinical interview and th e 17-item Hamilton Rating Scale for Depression (HAM-D), 3 to 4 weeks p oststroke. Results: DST results were abnormal in 75% of the patients a t 1 week poststroke and 50% of the patients at 3 weeks poststroke. Tho se patients whose HAM-D scores revealed more depressive symptoms at 3 to 4 weeks were more likely to evidence abnormal DST results (cortisol nonsuppression). None of the patients, however, met either DSM-III or modified criteria for clinical depression at 3 to 4 weeks. Conclusion : Poststroke depression appears to have a delayed clinical onset. Abno rmal DST results at 3 weeks poststroke may serve as a potential marker for those patients at risk for developing poststroke depression.