CONTROLLED COMPARISON OF PAROXETINE AND FLUVOXAMINE IN MAJOR DEPRESSION

被引:18
作者
ANSSEAU, M
GABRIELS, A
LOYENS, J
BARTHOLOME, F
EVRARD, JL
DENAYER, A
LINHART, R
WIRTZ, J
BRUYNOOGHE, F
SURINX, K
CLARYSSE, H
MARGANNE, R
PAPART, P
机构
[1] ONZE LIEVE VROUW HOSP,B-9300 AALST,BELGIUM
[2] ST JOSEFS HOSP,B-8400 OOSTENDE,BELGIUM
[3] HOP ST JOSEPH,B-4000 LIEGE,BELGIUM
[4] CLIN ST THERESE,B-6080 MONTIGNIES SAMBRE,BELGIUM
[5] ST JOSEFS HOSP,B-2300 TURNHOUT,BELGIUM
[6] HOP NEUROPSYCHIAT ETAT,L-9012 ETTELBRUCK,LUXEMBOURG
[7] ST LUCASZIEKENHUIS,B-8200 BRUGGE,BELGIUM
[8] STEDELIJK ZIEKENHUIS VIRGA JESSE,B-3500 HASSELT,BELGIUM
[9] KLIN HEILIGE HART,B-8800 ROESELARE,BELGIUM
[10] CTR MED SERBIE,B-4000 LIEGE,BELGIUM
关键词
PAROXETINE; FLUVOXAMINE; SELECTIVE SEROTONIN REUPTAKE INHIBITORS; ANTIDEPRESSANT; MAJOR DEPRESSION;
D O I
10.1002/hup.470090502
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A multicentre study compared the antidepressant efficacy and the tolerance of two selective serotonin reuptake inhibitors, paroxetine (20-30 mg/d) and fluvoxamine (50-200 mg/d) in two parallel groups of respectively 56 and 64 patients with major depression, as defined by DSM-III-R criteria. The duration of the study was six weeks, with assessments at baseline and at the end of weeks 1, 2, 4, and 6. For efficacy the Hamilton depression, the Hamilton anxiety scales and the clinical global impressions were used; adverse events were assessed by means of a non-leading question. Results showed a similar improvement in both groups on all rating instruments. The total number of patients reporting adverse events did not significantly differ between paroxetine (52 per cent) and fluvoxamine (64 per cent); severe adverse events were however significantly less frequently reported with paroxetine than with fluvoxamine (13 per cent versus 28 per cent), and resulted less frequently in the discontinuation of treatment (5 per cent versus 17 per cent).
引用
收藏
页码:329 / 336
页数:8
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