Risk of extrapyramidal syndrome in schizophrenic patients treated with antipsychotics: A population-based study

被引:39
作者
Yang, S-Y
Yang, Y-H Kao [1 ]
Chong, M-Y
Yang, Y-H [1 ]
Chang, W-H
Lai, C-S
机构
[1] Natl Cheng Kung Univ, Inst Clin Pharm, Tainan 70101, Taiwan
[2] Kaohsiung Med Univ, Coll Med, Grad Inst Med, Kaohsiung, Taiwan
[3] Tsyr Huey Mental Hosp, Dept Pharm, Kaohsiung, Taiwan
[4] Kaohsiung Chang Gung Mem Hosp, Dept Psychiat, Kaohsiung, Taiwan
[5] Chang Gung Univ, Taipei, Taiwan
[6] Kaohsiung Med Univ, Stat Anal Lab, Dept Clin Res, Kaohsiung, Taiwan
[7] Tzu Chi Univ, Dept Psychiat, Hualien, Taiwan
关键词
D O I
10.1038/sj.clpt.6100069
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To compare the prevalence of extrapyramidal syndrome (EPS) between the first-generation antipsychotics (FGAs) and second-generation antipsychotics (SGAs), the co-prescribing rate of anti-Parkinson drugs (APDs) of each antipsychotic drug was analyzed using population database. Fourteen antipsychotics had been prescribed during the 5-year study period. Among the SGAs, quetiapine had the lowest crude co-prescribing rate of APDs (27.09%), whereas risperidone had the highest rate (66.50%). Among the FGAs, thioridazine and loxapine had the lowest (60.99%) and highest rates (96.35%), respectively. The rankings of the co-prescribing rate of APDs among antipsychotics, in increasing order, were quetiapine, clozapine, olanzapine, thioridazine, zotepine, chlorpromazine, risperidone, sulpiride, clotiapine, flupentixol, haloperidol, zuclopentixol, trifluoperazine, and loxapine. The results indicate that the risk of EPS appears to be lower in SGAs than in FGAs; however, the considerably high rate of EPS in some of the newer generation of antipsychotics warrants clinical attention.
引用
收藏
页码:586 / 594
页数:9
相关论文
共 59 条
[1]  
[Anonymous], PSYCHIAT B
[2]  
[Anonymous], 2000, Atlas of psychiatric pharmacotherapy
[3]   NEUROLEPTIC DRUG EXPOSURE AND TREATMENT OF PARKINSONISM IN THE ELDERLY - A CASE-CONTROL STUDY [J].
AVORN, J ;
BOHN, RL ;
MOGUN, H ;
GURWITZ, J ;
MONANE, M ;
EVERITT, D ;
WALKER, A .
AMERICAN JOURNAL OF MEDICINE, 1995, 99 (01) :48-54
[4]   Medications and verbal memory impairment in schizophrenia:: the role of anticholinergic drugs [J].
Brébion, G ;
Bressan, RA ;
Amador, X ;
Malaspina, D ;
Gorman, JM .
PSYCHOLOGICAL MEDICINE, 2004, 34 (02) :369-374
[5]   Selective prescribing of atypical antipsychotics [J].
Breekveldt-Postma, NS ;
Schillevoort, I ;
Nolen, WA ;
Veraart, CPWM ;
Herings, RMC .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2005, 14 (01) :25-30
[6]   The use of antiparkinsonian agents in the management of drug-induced extrapyramidal symptoms [J].
Burgyone, K ;
Aduri, K ;
Ananth, J ;
Parameswaran, S .
CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (18) :2239-2248
[7]   Olanzapine - Pharmacokinetic and pharmacodynamic profile [J].
Callaghan, JT ;
Bergstrom, RF ;
Ptak, LR ;
Beasley, CM .
CLINICAL PHARMACOKINETICS, 1999, 37 (03) :177-193
[8]  
Caroff SN, 2002, J CLIN PSYCHIAT, V63, P12
[9]  
Casey DE, 2004, J CLIN PSYCHIAT, V65, P25
[10]   Baseline use of concomitant psychotropic medications to treat schizophrenia in the CATIE trial [J].
Chakos, Miranda H. ;
Glick, Ira D. ;
Miller, Alexander L. ;
Hamner, Mark B. ;
Miller, Del D. ;
Patel, Jayendra K. ;
Tapp, Andre ;
Keefe, Richard S. E. ;
Rosenheck, Robert A. .
PSYCHIATRIC SERVICES, 2006, 57 (08) :1094-1101