Are we treating schizophrenia effectively? Understanding the primary outcomes of the catie study

CNS Spectrums

Volumn 11, Issue SUPPL. 10, 2006, Pages 1-11

  Glazer, William M ^a   Conley, Robert R ^b,c,d   Citrome, Leslie ^e,f  

^a Glazer Medical Solutions   (United States)

^b UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

^c MARYLAND PSYCHIATRIC RESEARCH CENTER   (United States)

^d NATIONAL INSTITUTE ON DRUG ABUSE   (United States)

^e NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f NATHAN S KLINE INSTITUTE FOR PSYCHIATRIC RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATYPICAL ANTIPSYCHOTIC AGENT; NEUROLEPTIC AGENT; OLANZAPINE; PERPHENAZINE; QUETIAPINE; RISPERIDONE; ZIPRASIDONE;

CLINICAL PRACTICE; CLINICAL TRIAL; DECISION MAKING; DOCTOR PATIENT RELATION; DRUG CHOICE; DRUG EFFECT; DRUG EFFICACY; DRUG SAFETY; DRUG TOLERABILITY; EVALUATION; HUMAN; OUTCOME ASSESSMENT; PATIENT PARTICIPATION; PRIORITY JOURNAL; REVIEW; SCHIZOPHRENIA; SEDATION; SIDE EFFECT; SYMPTOM; TREATMENT DURATION; WEIGHT GAIN;

EID: 33748929105     PISSN: 10928529     EISSN: None     Source Type: Journal    
DOI: 10.1017/s1092852900025748     Document Type: Review

References (13)

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3. McEvoy JP, Lieberman JA, Stroup TS, et al. Effectiveness of clozapine versus olanzapine, quetiapine, and risperidone in patients with chronic schizophrenia who did not respond to prior atypical antipsychotic treatment. Am J Psychiatry. 2006;16(4):600-610.
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7. Stroup TS (2004) Antipsychotic drug treatment of schizophrenia: update on the CATIE trial. In: NCDEU Abstracts from the 44th Annual Meeting, June 1-4, 2004, Phoenix, Arizona. Department of Health and Human Services, National Institutes of Health, National Institute of Mental Health, Bethesda, MD.
8. McEvoy JP, Meyer JM, Goff DC, et al. Prevalence of the metabolic syndrome in patients with schizophrenia: baseline results from the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) schizophrenia trial and comparison with national estimates from NHANES III. Schizophr Res. 2005;80(1):19-32. Epub 2005 Aug 30.
9. Nasrallah HA, Meyer JM, Goff DC, et al. Low rates of treatment for hypertension, dyslipidemia and diabetes in schizophrenia: Data from the CATIE schizophrenia trial sample at baseline. Schizophr Res. 2006 Jul 31; [Epub ahead of print].
10. Lehman AF, Lieberman JA, Dixon LB, et al. Practice guideline for the treatment of patients with schizophrenia, second edition. Am J Psychiatry. 2004;161(2 Suppl):1-56.
11. Swartz MS, Perkins DO, Stroup TS, McEvoy JP, Nieri JM, Haak DC. Assessing clinical and functional outcomes in the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) schizophrenia trial. Schizophr Bull. 2003;29(1):33-43.
12. Citrome L, Stroup TS: Schizophrenia, Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) and number needed to treat: how can CATIE inform clinicians? Int J Clin Pract. 2006;60(8):933-940.
13. Moore A, McQuay HJ. What is an NNT? www.evidence-based-medicine.co.uk. 2001;1(1):2. Available at: www.jr2.ox.ac.uk/bandolier/painres/download/whatis/ NNT.pdf. Accessed: June 8, 2006.