Barriers to progress - the impact of tolerability problems

被引:20
作者
Casey, DE [1 ]
机构
[1] Vet Affairs Med Ctr, Mental Hlth Div P3 MHDC, Psychiat Res & Psychopharmacol, Portland, OR USA
关键词
antipsychotics; tolerability; side-effects; compliance;
D O I
10.1097/00004850-200101001-00004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Side-effects of antipsychotic treatment are important factors in patients' compliance with treatment regimens. Of particular relevance to compliance are extrapyramidal symptoms (EPS), sedation, weight gain and sexual dysfunction, The new atypical antipsychotics offer several tolerability benefits over conventional neuroleptics, particularly with respect to EPS. However, differences in their receptor binding characteristics result in different side-effect profiles, All novel antipsychotics have a high 5-MT2 to D-2 receptor binding ratio, which is postulated to be important for a low liability for EPS, Ziprasidone, a new antipsychotic in the late stages of clinical development, has a low affinity for some receptor types, activation of which has been linked with adverse events such as sedation, postural hypotension, weight gain and cognitive impairment; for example, ziprasidone has minimal activity at muscarinic (M-1), histaminergic (H-1) and alpha (1)-adrenergic receptors. In short- and long-term clinical trials. ziprasidone had a low Liability for side-effects typically associated with poor compliance, such as EPS, weight gain and sexual dysfunction, The tolerability profiles of the new antipsychotics represent a major improvement over the older neuroleptics. The more favourable the benefit/risk ratios of these new drugs throughout all phases of treatment, the greater the likelihood that patients will have better outcomes. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:S15 / S19
页数:5
相关论文
共 22 条
[11]   An exploratory haloperidol-controlled dose-finding study of ziprasidone in hospitalized patients with schizophrenia or schizoaffective disorder [J].
Goff, DC ;
Posever, T ;
Herz, L ;
Simmons, J ;
Kletti, N ;
Lapierre, K ;
Wilner, KD ;
Law, CG ;
Ko, GN .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1998, 18 (04) :296-304
[12]  
GOLDSTEIN JM, 1996, SCHIZOPHRENIA BREAKI, P177
[13]  
KANE JM, 1999, J CLIN PSYCH S12, V60, pS13
[14]   Ziprasidone 40 and 120 mg/day in the acute exacerbation of schizophrenia and schizoaffective disorder: a 4-week placebo controlled trial [J].
Keck, P ;
Buffenstein, A ;
Ferguson, J ;
Feighner, J ;
Jaffe, W ;
Harrigan, EP ;
Morrissey, MR .
PSYCHOPHARMACOLOGY, 1998, 140 (02) :173-184
[15]  
LEYSEN JE, 1998, INT J PSYCHIAT CLIN, V2, pS3
[17]   Predictors of relapse following response from a first episode of schizophrenia or schizoaffective disorder [J].
Robinson, D ;
Woerner, MG ;
Alvir, JMJ ;
Bilder, R ;
Goldman, R ;
Geisler, S ;
Koreen, A ;
Sheitman, B ;
Chakos, M ;
Mayerhoff, D ;
Lieberman, JA .
ARCHIVES OF GENERAL PSYCHIATRY, 1999, 56 (03) :241-247
[18]   PREVALENCE OF OBESITY IN PATIENTS RECEIVING DEPOT ANTIPSYCHOTICS [J].
SILVERSTONE, T ;
SMITH, G ;
GOODALL, E .
BRITISH JOURNAL OF PSYCHIATRY, 1988, 153 :214-217
[19]   Double-blind comparison of olanzapine versus risperidone in the treatment of schizophrenia and other psychotic disorders [J].
Tran, PV ;
Hamilton, SH ;
Kuntz, AJ ;
Potvin, JH ;
Andersen, SW ;
Beasley, C ;
Tollefson, GD .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1997, 17 (05) :407-418
[20]  
VANPUTTEN T, 1974, ARCH GEN PSYCHIAT, V31, P67