Responses to antipsychotic therapy among patients with schizophrenia or schizoaffective disorder and either predominant or prominent negative symptoms
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Stauffer, Virginia L.
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Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USAEli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Stauffer, Virginia L.
[1
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Song, Guochen
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I3 Clin Data Serv, Cary, NC 27513 USAEli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Song, Guochen
[2
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Kinon, Bruce J.
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Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USAEli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Kinon, Bruce J.
[1
]
Ascher-Svanum, Haya
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Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USAEli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Ascher-Svanum, Haya
[1
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Chen, Lei
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Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USAEli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Chen, Lei
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Feldman, Peter D.
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Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USAEli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Feldman, Peter D.
[1
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Conley, Robert R.
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Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Univ Maryland, Baltimore, MD 21201 USAEli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Conley, Robert R.
[1
,3
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[1] Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Indianapolis, IN 46285 USA
Patients with schizophrenia who have predominant negative symptoms are often considered less responsive to treatment. This analysis of patients with schizophrenia or schizoaffective disorder compares changes in symptom severity between those with predominant versus merely prominent negative symptoms. Prominent negative symptoms were defined by a baseline score of >= 4 on at least 3, or >= 5 on at least 2, of the 7 Positive and Negative Syndrome Scale (PANSS) negative subscale items. Predominant negative symptoms were defined by the foregoing plus a PANSS positive score of <19, a Barnes Akathisia score of <2, a Simpson-Angus score of <4, and a Calgary Depressive Scale score of <9. Adult patients with schizophrenia (n=227) or schizoaffective disorder (n=116) received either olanzapine (10-20 mg/day, n=169) or quetiapine (300-700 mg/day, n=174) for up to 24 weeks. Data for both medications were pooled. Of the 343 patients enrolled in the study, 34.7% met the criteria for predominant negative symptoms, the remaining 653% being characterized only by their prominent negative symptoms. Changes in the severity of negative symptoms in both patient types largely followed similar trajectories during treatment, as reflected both in Marder PANSS negative subscale scores and in the Scale for Assessment of Negative Symptoms total and domain scores. Patients with either predominant or prominent negative symptoms therefore appear to respond similarly to atypical antipsychotic treatment. This distinction, incorporating an evaluation of the presence of positive, affective, and extrapyramidal symptoms, may therefore not have prognostic implications for the responsiveness of patients' negative symptoms to treatment. (C) 2011 Elsevier B.V. All rights reserved.
机构:
Karolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, SwedenKarolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, Sweden
Reutfors, Johan
Brandt, Lena
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Karolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, SwedenKarolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, Sweden
Brandt, Lena
Stephansson, Olof
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Karolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, SwedenKarolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, Sweden
Stephansson, Olof
Kieler, Helle
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Karolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, SwedenKarolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, Sweden
Kieler, Helle
Andersen, Morten
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Karolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, SwedenKarolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, Sweden
Andersen, Morten
Boden, Robert
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Karolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, Sweden
Uppsala Univ, Dept Neurosci, Uppsala, SwedenKarolinska Inst, Ctr Pharmacoepidemiol, Dept Med Solna, SE-17176 Stockholm, Sweden
机构:
Karolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, SwedenKarolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, Sweden
Reutfors, Johan
Brandt, Lena
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Karolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, SwedenKarolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, Sweden
Brandt, Lena
Stephansson, Olof
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机构:
Karolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, SwedenKarolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, Sweden
Stephansson, Olof
Kieler, Helle
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h-index: 0
机构:
Karolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, SwedenKarolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, Sweden
Kieler, Helle
Andersen, Morten
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h-index: 0
机构:
Karolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, SwedenKarolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, Sweden
Andersen, Morten
Boden, Robert
论文数: 0引用数: 0
h-index: 0
机构:
Karolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, Sweden
Uppsala Univ, Dept Neurosci, Uppsala, SwedenKarolinska Inst, Dept Med, Ctr Pharmacoepidemiol, Stockholm, Sweden