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Citing URL: http://www.in-cites.com/research/2006/december_25_2006-3.html

SCI-BYTES What's New in Research:
December 25, 2006
             

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Hot Paper in Medicine

"Effectiveness of antipsychotic drugs in patients with chronic schizophrenia," by J.A. Lieberman and 11 others (the CATIE Investigators), New England Journal of Medicine, 353(12): 1209-23, 22 September 2005.

[Authors' affiliations: Columbia University, New York, NY; University of North Carolina, Chapel Hill; John Umstead Hospital, Butner, NC; Duke University Medical Center, Durham, NC; Yale University, New Haven, CT; NIMH, Bethesda, MD]

Abstract: "BACKGROUND The relative effectiveness of second-generation (atypical) antipsychotic drugs as compared with that of older agents has been incompletely addressed, though newer agents are currently used far more commonly. We compared a first-generation antipsychotic, perphenazine, with several newer drugs in a double-blind study. METHODS A total of 1493 patients with schizophrenia were recruited at 57 U.S. sites and randomly assigned to receive olanzapine (7.5 to 30 mg per day), perphenazine (8 to 32 mg per day), quetiapine (200 to 800 mg per day), or risperidone (1.5 to 6.0 mg per day) for up to 18 months. Ziprasidone (40 to 160 mg per day) was included after its approval by the Food and Drug Administration. The primary aim was to delineate differences in the overall effectiveness of these five treatments. RESULTS Overall, 74 percent of patients discontinued the study medication before 18 months (1061 of the 1432 patients who received at least one dose): 64 percent of those assigned to olanzapine, 75 percent of those assigned to perphenazine, 82 percent of those assigned to quetiapine, 74 percent of those assigned to risperidone, and 79 percent of those assigned to ziprasidone. The time to the discontinuation of treatment for any cause was significantly longer in the olanzapine group than in the quetiapine (P<0.001) or risperidone (P=0.002) group, but not in the perphenazine (P=0.021) or ziprasidone (P=0.028) group. The times to discontinuation because of intolerable side effects were similar among
the groups, but the rates differed (P=0.04); olanzapine was associated with more discontinuation for weight gain or metabolic effects, and perphenazine was associated with more discontinuation for extrapyramidal effects. CONCLUSIONS The majority of patients in each group discontinued their assigned treatment owing to inefficacy or intolerable side effects or for other reasons. Olanzapine was the most effective in terms of the rates of discontinuation, and the efficacy of the conventional antipsychotic agent perphenazine appeared similar to that of quetiapine, risperidone, and ziprasidone. Olanzapine was associated with greater weight gain and increases in measures of glucose and lipid metabolism."

This 2005 report from the New England Journal of Medicine was cited 50 times in current journal articles
indexed by Thomson Scientific during September-October 2006. Only one other medicine paper published in
the last two years (aside from reviews) garnered a greater number of citations during that two-month period. Prior
to the most recent bimonthly count, citations to the paper have accrued as follows:

July-August 2006: 32 citations
May-June 2006: 30
March-April 2006: 24
January-February 2006: 15
November-December 2005: 4
September-October 2005: 3

Total citations to date: 158

SOURCE: Hot Papers Database (Included with a subscription to the print newsletter Science Watch®, available from the Research Services Group. Packaged on a CD that is mailed with each Science Watch issue, the Hot Papers Database contains data on hundreds of highly cited papers published during the last two years. User interface permits searching by author, organization, journal, field, and more. Total citations, as well as citations accrued during successive bimonthly periods, can be assessed and graphed. An updated CD containing the most recent bimonthly data is mailed with every new issue of Science Watch, six times a year. The CD also includes an electronic version of the Science Watch issue in HTML format, for personal desktop access


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