HALOPERIDOL VS PHENELZINE IN CONTINUATION THERAPY OF BORDERLINE DISORDER

Citation
Jr. Cornelius et al., HALOPERIDOL VS PHENELZINE IN CONTINUATION THERAPY OF BORDERLINE DISORDER, Psychopharmacology bulletin, 29(2), 1993, pp. 333-337
Citations number
25
Categorie Soggetti
Psychiatry,Neurosciences,"Pharmacology & Pharmacy
Journal title
ISSN journal
00485764
Volume
29
Issue
2
Year of publication
1993
Pages
333 - 337
Database
ISI
SICI code
0048-5764(1993)29:2<333:HVPICT>2.0.ZU;2-Y
Abstract
We report the first double-blind, placebo-controlled continuation stud y comparison of a neuroleptic (haloperidol less-than-or-equal-to 6 mg) , monoamine oxidase inhibitor (MAOI) antidepressant (phenelzine less-t han-or-equal-to 90 mg), and placebo in 54 patients with borderline per sonality disorder. Continuation medication trials of 16 weeks followed 5 weeks of acute therapy. Haloperidol continued to be effective beyon d the acute phase only for the treatment of irritability. Higher level s of depression, hypersomnia, and leaden paralysis were noted in the h aloperidol group than in the phenelzine and placebo groups. The dropou t rate during the first half (8 weeks) of the continuation study was s ignificantly higher for the haloperidol group (64%) than for the place bo group (28%) (p < .05). Phenelzine demonstrated very modest efficacy beyond that noted in the acute phase for the treatment of depression and irritability. Phenelzine was shown to have an activating effect on measures of excitement and reactivity.