Focus on quetiapine

被引:39
作者
Green, B
机构
[1] Halton Hosp, Runcorn, Cheshire, England
[2] Univ Liverpool, Liverpool L69 3BX, Merseyside, England
关键词
schizophrenia; quetiapine; antipsychotics; atypical; neuroleptics; pharmacology;
D O I
10.1185/03007999909114085
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Quetiapine fumarate is a novel dibenzothiazepine antipsychotic developed by Zeneca. It is marketed under the trade name 'Seroquel'. Quetiapine is well tolerated and clinically effective in the treatment of schizophrenia. The initial hope of investigators was that quetiapine would have antipsychotic potential and that it might share some of the properties of clozapine without its toxicity to white blood cells. The effective dosage range is usually 300-450 mg/day split inta two doses. The dose is titrated upwards from 25 mg twice daily from day 1 to 300 mg/day on day 4. Elderly patients or patients with liver problems should be started on lower doses. It is both superior to placebo and comparable to haloperidol in reducing positive symptoms at doses ranging from 150 mg/day to 750 mg/day, and is an effective treatment for negative symptoms. Somnolence is the mast common adverse event. Abnormalities of the QT interval on ECG appear very infrequently and there is no need for a baseline ECG or blood pressure monitoring, as used to be the case with sertindole. There is no need for haematological monitoring as with clozapine. Quetiapine, across the full dosage range, is associated with no greater extrapyramidal symptoms than placebo. Quetiapine's general efficacy and side-effect profile suggest that, unless there are unforeseen past-marketing complications, it deserves a major place in the initial and long-term management of schizophreniform disorders.
引用
收藏
页码:145 / 151
页数:7
相关论文
共 24 条
[1]  
AIZENBERG D, 1995, J CLIN PSYCHIAT, V56, P137
[2]   Multiple fixed doses of ''Seroquel'' (quetiapine) in patients with acute exacerbation of schizophrenia: A comparison with haloperidol and placebo [J].
Arvanitis, LA ;
Miller, BG ;
Borison, RL ;
Pitts, WM ;
Sharif, ZA ;
Hamner, MB ;
Herz, MI ;
True, JE ;
Velligan, D ;
Knesevich, MA ;
Small, J ;
Steinbook, R ;
Hertzman, M ;
Keck, PE ;
Newcomer, JW ;
Grace, J ;
Rotrosen, J ;
Tandon, R ;
Dott, SG ;
Ferguson, JM ;
Addington, DEN ;
MacEwan, GW ;
Nair, VNP ;
Shriqui, CL ;
Williams, R ;
Daniel, DG ;
Shehi, GM ;
Patterson, WM ;
Merideth, CH .
BIOLOGICAL PSYCHIATRY, 1997, 42 (04) :233-246
[3]   ICI 204,636, an atypical antipsychotic: Efficacy and safety in a multicenter, placebo-controlled trial in patients with schizophrenia [J].
Borison, RL ;
Arvanitis, LA ;
Miller, BG ;
Alphs, LD ;
Carman, JS ;
Diamond, B ;
Gewirtz, G ;
Hamner, MB ;
Hirshfield, R ;
McEvoy, JP ;
Mukherjee, S ;
Nasrallah, HA ;
Oxenkrug, G ;
Ryan, W ;
Smith, N ;
Tamminga, C .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1996, 16 (02) :158-169
[4]  
Casey DE, 1996, J CLIN PSYCHIAT, V57, P40
[5]   Antipsychotic medications and fertility [J].
Currier, GW ;
Simpson, GM .
PSYCHIATRIC SERVICES, 1998, 49 (02) :175-176
[6]  
Ereshefsky L, 1996, J CLIN PSYCHIAT, V57, P12
[7]   ICI-204,636, A NOVEL, ATYPICAL ANTIPSYCHOTIC - EARLY INDICATION OF SAFETY AND EFFICACY IN PATIENTS WITH CHRONIC AND SUBCHRONIC SCHIZOPHRENIA [J].
FABRE, LF ;
ARVANITIS, L ;
PULTZ, J ;
JONES, VM ;
MALICK, JB ;
SLOTNICK, VB .
CLINICAL THERAPEUTICS, 1995, 17 (03) :366-378
[8]  
FULTON B, 1995, CNS DRUGS, V4, P66
[9]   Time course of central nervous dopamine-D2 and 5-HT2 receptor blockade and plasma drug concentrations after discontinuation of quetiapine (Seroquel®) in patients with schizophrenia [J].
Gefvert, O ;
Bergström, M ;
Långström, B ;
Lundberg, T ;
Lindström, L ;
Yates, R .
PSYCHOPHARMACOLOGY, 1998, 135 (02) :119-126
[10]  
GOLDSTEIN JM, 1998, LOW INCIDENCE REPROD