Risperidone dose and blood level variability: Accumulation effects and interindividual and intraindividual variability in the nonresponder patient in the clinical practice setting

被引:43
作者
Darby, JK
Pasta, DJ
Elfand, L
Dabiri, L
Clark, L
Herbert, J
机构
[1] SAN MATEO CTY MENTAL HLTH SERV,DEPT PSYCHIAT,SAN MATEO,CA
[2] UNIV OKLAHOMA,SCH MED,DEPT PSYCHIAT & BEHAV SCI,OKLAHOMA CITY,OK
[3] UNIV UTAH,SCH MED,DEPT PSYCHIAT,SALT LAKE CITY,UT
[4] UNIV UTAH,SCH MED,DEPT PSYCHOPHARMACOL,SALT LAKE CITY,UT
关键词
D O I
10.1097/00004714-199712000-00007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Risperidone blood levels mere measured every 2 weeks after initiation of therapy in 24 refractory chronic schizophrenic patients referred to a locked, skilled nursing facility for long-term treatment. Blood levels were assessed on 285 occasions over a 1- to 16-month treatment program. Drug plasma level increases peaked by 2 months for risperidone at 334% and by 6 months for 9-hydroxy-risperidone at 104% over the baseline levels. Total blood levels (risperidone plus 9-hydroxy-risperidone) peaked at 111% increase at 6 months and then declined 8% per month to 12 months, stabilizing at a value 31% higher than the initial value. Significant dose to blood level interindividual variation was noted. Considerable blood level variation was evident in single blood level sample determinations. The results suggest the value of risperidone blood levels, consideration of reduction of initial recommended starting dosages, and a need to optimize risperidone dosage approaches individually to patients.
引用
收藏
页码:478 / 484
页数:7
相关论文
共 20 条
[1]  
ABDELRAZZAK Z, 1993, MOL PHARMACOL, V44, P707
[2]  
ANDERSON CB, 1993, ANN M AM PSYCH ASS S, P113
[3]   DETERMINATION OF RISPERIDONE IN PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH ELECTROCHEMICAL DETECTION - APPLICATION TO THERAPEUTIC DRUG-MONITORING IN SCHIZOPHRENIC-PATIENTS [J].
ARAVAGIRI, M ;
MARDER, SR ;
VANPUTTEN, T ;
MIDHA, KK .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1993, 82 (05) :447-449
[4]  
Borison RL, 1994, J CLIN PSYCHIAT, V12, P46
[5]   REGULATION OF CYTOCHROME-P450 2C11 (CYP2C11) GENE-EXPRESSION BY INTERLEUKIN-1, SPHINGOMYELIN HYDROLYSIS, AND CERAMIDES IN RAT HEPATOCYTES [J].
CHEN, JQ ;
NIKOLOVAKARAKASHIAN, M ;
MERRILL, AH ;
MORGAN, ET .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :25233-25238
[6]  
CHOUINARD G, 1993, J CLIN PSYCHOPHARM, V13, P25
[7]   INVOLVEMENT OF CYP2D6, CYP3A4, AND OTHER CYTOCHROME-P-450 ISOZYMES IN N-DEALKYLATION REACTIONS [J].
COUTTS, RT ;
SU, P ;
BAKER, GB .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 1994, 31 (04) :177-186
[8]   PLASMA-LEVEL MONITORING OF ANTIPSYCHOTIC-DRUGS CLINICAL UTILITY [J].
DAHL, SG .
CLINICAL PHARMACOKINETICS, 1986, 11 (01) :36-61
[9]   HALOPERIDOL DOSE AND BLOOD LEVEL VARIABILITY - TOXICITY AND INTERINDIVIDUAL AND INTRAINDIVIDUAL VARIABILITY IN THE NONRESPONDER PATIENT IN THE CLINICAL-PRACTICE SETTING [J].
DARBY, JK ;
PASTA, DJ ;
DABIRI, L ;
CLARK, L ;
MOSBACHER, D .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1995, 15 (05) :334-340
[10]   RISPERIDONE IN PARKINSONS-DISEASE [J].
FORD, B ;
LYNCH, T ;
GREENE, P .
LANCET, 1994, 344 (8923) :681-681