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Neurocognitive effects of clozapine, olanzapine, risperidone, and haloperidol in patients with chronic schizophrenia or schizoaffective disorder

Bilder, Robert M; Goldman, Robert S; Volavka, Jan; Czobor, Pal; Hoptman, Matthew; Sheitman, Brian; Lindenmayer, Jean-Pierre; Citrome, Leslie; McEvoy, Joseph; Kunz, Michal; Chakos, Miranda; Cooper, Thomas B; Horowitz, Terri L; Lieberman, Jeffrey A
OBJECTIVE: Newer antipsychotic drugs have shown promise in ameliorating neurocognitive deficits in patients with schizophrenia, but few studies have compared newer antipsychotic drugs with both clozapine and conventional agents, particularly in patients who have had suboptimal response to prior treatments. METHOD: The authors examined the effects of clozapine, olanzapine, risperidone, and haloperidol on 16 measures of neurocognitive functioning in a double-blind, 14-week trial involving 101 patients. A global score was computed along with scores in four neurocognitive domains: memory, attention, motor function, and general executive and perceptual organization. RESULTS: Global neurocognitive function improved with olanzapine and risperidone treatment, and these improvements were superior to those seen with haloperidol. Patients treated with olanzapine exhibited improvement in the general and attention domains but not more than that observed with other treatments. Patients treated with risperidone exhibited improvement in memory that was superior to that of both clozapine and haloperidol. Clozapine yielded improvement in motor function but not more than in other groups. Average effect sizes for change were in the small to medium range. More than half of the patients treated with olanzapine and risperidone experienced 'clinically significant' improvement (changes in score of at least one-half standard deviation relative to baseline). These findings did not appear to be mediated by changes in symptoms, side effects, or blood levels of medications. CONCLUSIONS: Patients with a history of suboptimal response to conventional treatments may show cognitive benefits from newer antipsychotic drugs, and there may be differences between atypical antipsychotic drugs in their patterns of cognitive effects
PMID: 12042192
ISSN: 0002-953x
CID: 36859

Community violence and inpatient assaults: neurobiological deficits

Krakowski M; Czobor P; Carpenter MD; Libiger J; Kunz M; Papezova H; Parker BB; Schmader L; Abad T
The goals of this study were to examine the relationship between community violence and inpatient assaults and to identify neurological and neuropsychological deficits underlying violent behavior. Thirty-three inpatients with a history of community violence were compared with 69 patients who did not have such a history. Inpatient assaults were recorded for 4 weeks; a neurological/neuropsychological battery was then administered. Patients without community violence were more likely to show transient or no violence while in the hospital. Patients with community violence performed more poorly on the Wisconsin Card Sorting Test and on psychomotor tasks, impairments that are consistent with frontal lobe dysfunction. Inpatient assaults were not associated with these neuropsychological impairments. They were related, however, to impairment on frontal motor programming tasks and a history of community violence
PMID: 9447495
ISSN: 0895-0172
CID: 60291

An open label trial of venlafaxine in adults with attention deficit disorder [Meeting Abstract]

Adler, LA; Resnick, S; Kunz, M; Devinsky, O
ISI:A1996UE89300407
ISSN: 0006-3223
CID: 52982

Violent crime in psychiatric patients: relationship to frontal lobe impairment

Krakowski M; Czobor P; Carpenter MD; Nolan K; Libiger J; Kunz M; Papezova H; Parker BB; Schmader L
ORIGINAL:0004126
ISSN: 0163-1942
CID: 18207

Serotonin in violent patients with schizophrenia

Kunz M; Sikora J; Krakowski M; Convit A; Cooper TB; Volavka J
CSF levels of 5-hydroxyindolacetic acid (5-HIAA), the serotonin metabolite, were assayed in 10 violent and 10 matched nonviolent patients with schizophrenia. Mean group levels of 5-HIAA in cerebrospinal fluid were found to be nearly identical. Possible explanations, including effects of medications, are discussed
PMID: 8771232
ISSN: 0165-1781
CID: 60301

Open-label trial of venlafaxine in adults with attention deficit disorder

Adler LA; Resnick S; Kunz M; Devinsky O
Antidepressants or stimulants are commonly used to treat attention deficit disorder (ADD). We report the results of an open-label trial of the recently marketed antidepressant venlafaxine in 16 adult patients with ADD. Patients were treated with venlafaxine (25 to 225 mg/day) for 8 weeks. Four patients discontinued treatment within the first week because of sedation, agitation, or nausea. In the remaining 12 patients, venlafaxine treatment decreased ADD ratings by almost half
PMID: 8851654
ISSN: 0048-5764
CID: 12816

Long-term high-dose neuroleptic treatment: who gets it and why?

Krakowski MI; Kunz M; Czobor P; Volavka J
OBJECTIVE: High doses of neuroleptic medication are still administered to many patients, although many studies have shown the effectiveness of low-dose strategies. The purposes of the study were to determine whether and in what ways high-dose patients differed from patients on regular dosages and whether the higher dosages were more effective. METHODS: In a case-control study at two large state hospitals, 38 high-dose patients were compared with 29 regular-dose patients. RESULTS: The high-dose patients had a persistent course of illness, with severe chronic symptoms resulting in hospitalizations of much longer duration than those of the regular-dose patients. The high-dose patients evidenced more regressed functioning and were more violent. To control these behaviors, clinicians increased neuroleptic dosages. CONCLUSIONS: The high-dose patients represented a subgroup of chronic regressed and violent patients. Clinicians prescribed high dosages and continued to use them despite a lack of clear evidence that such treatment is effective
PMID: 8102617
ISSN: 0022-1597
CID: 61038