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DOI: 10.1055/s-2005-922242
© Georg Thieme Verlag Stuttgart · New York
CATIE: Die Auswahl von Antipsychotika bei Schizophrenie
CATIE: choice of antipsychotics in schizophreniaPublication History
Publication Date:
22 November 2005 (online)
Zusammenfassung
Das Projekt CATIE des NIMH hat nur für das atypische Neuroleptikum Olanzapin, nicht aber für Risperidon, Quetiapin und Ziprasidon, begrenzte Überlegenheit gegenüber dem typischen Neuroleptikum Perphenazin gezeigt. Hauptzielvariable waren die Abbruchraten. Ziel der Therapie sind aber symptomatische Besserung, einschließlich kognitiver Störungen und Lebensqualität, die CATIE nicht erfasst hat, bei Vermeiden motorischer Nebenwirkungen, insbesondere von Spätdyskinesien, die unter atypischen Neuroleptika seltener sind. Das kann CATIE wegen eines methodischen Mangels nicht widerlegen. Entscheidend ist individualisierte Therapieanpassung.
Summary
The CATIE project of the NIMH has revealed moderately superior effectiveness of atypical neuroleptics only for olanzapine, but not risperidone, quetiapine and ziprasidone, compared to the typical perphenazine. Primary outcome measure was the discontinuation for any cause. The aim of routine treatment, however, is symptomatic improvement including cognitive functioning and quality of life which were not assessed in CATIE, and the avoidance of motor side effects, especially tardive dyskinesia which occurs less frequently under atypical neuroleptics. Due to a methodological flaw CATIE cannot disprove this. Individualized adaption of treatment is decisive.
Key words
CATIE - atypical neuroleptics - schizophrenia
Literatur:
- 1 Adams CE, Fenton MKP, Quraishi S, David AS. Systematic meta-review of depot antipsychotic drugs for people with schizophrenia. Br J Psychiatry. 2001; 179 290-299
- 2 Awad AG, Voruganti LNP. New Antipsychotics, Compliance, Quality of Life, and Subjective Tolerability - Are Patients Better Off?. Can J Psychiatry. 2004; 49 297-302
- 3 Barnes TR, McPhillips MA. Novel antipsychotics, extrapyramidal side effects and tardive dyskinesia. Int Clin Psychopharmacol. 1998; 13 3; 49-57
- 4 Fritze J. Psychopharmaka-Verordnungen: Ergebnisse und Kommentare zum Arzneiverordnungsreport 2004. Psychoneuro. 2005; 31 46-52
- 5 Jeste DV. Tardive dyskinesia rates with atypical antipsychotics in older adults. J Clin Psychiatry. 2004; 65 21-24
- 6 Kane JM. Tardive dyskinesia rates with atypical antipsychotics in adults: prevalence and incidence. J Clin Psychiatry. 2004; 65 16-20
- 7 Keefe RS, Silva SG, Perkins DO, Lieberman JA. The effects of atypical antipsychotic drugs on neurocognitive impairment in schizophrenia: a review and meta-analysis. Schizophr Bull. 1999; 25 201-222
- 8 Lambert M, Naber D. Current issues in schizophrenia: overview of patient acceptability, functioning capacity and quality of life. CNS Drugs. 2004; 18 5-17
- 9 Lieberman JA, Stroup TS, McEvoy JP, Swartz MS, Rosenheck RA, Perkins DO, Keefe RSE, Davis SM, Davis CE, Lebowitz BD, Severe J, Hsiao JK. Effectiveness of Antipsychotic Drugs in Patients with Chronic Schizophrenia. New England Journal of Medicine. 2005; 353 1209-1223
- 10 Miyamoto S, Duncan GE, Marx CE, Lieberman JA. Treatments for schizophrenia: a critical review of pharmacology and mechanisms of action of antipsychotic drugs. Molecular Psychiatry. 2005; 10 79-104
- 11 Pekkala E, Merinder L. Psychoeducation for schizophrenia. Cochrane Database Syst Rev 2002
- 12 Stroup TS, McEvoy JP, Swartz MS, Byerly MJ, Glick ID, Canive JM, McGee MF, Simpson GM, Stevens MC, Lieberman JA. The National Institute of Mental Health Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) project: schizophrenia trial design and protocol development. Schizophr Bull. 2003; 29 15-31
- 13 Weiden PJ, Olfson M. Cost of relapse in schizophrenia. Schizophr Bull. 1995; 21 419-429
Korrespondenzadresse:
Prof. Dr. med. Jürgen Fritze
Gesundheitspolitischer Sprecher
Deutsche Gesellschaft für Psychiatrie, Psychotherapie & Nervenheilkunde (DGPPN)
Asternweg 65
50259 Pulheim