Comparison between risperidone, olanzapine, and clozapine in the management of chronic schizophrenia: a naturalistic prospective 12-week observational study
Risperidone, olanzapine, and clozapine are three atypical antipsychotic medications commonly used in the management of chronic schizophrenia. While they offer advantages with regard to clinical efficacy and side‐effect profile, few studies have compared them in a naturalistic prospective observation...
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Veröffentlicht in: | Human psychopharmacology 2006-06, Vol.21 (4), p.235-243 |
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description | Risperidone, olanzapine, and clozapine are three atypical antipsychotic medications commonly used in the management of chronic schizophrenia. While they offer advantages with regard to clinical efficacy and side‐effect profile, few studies have compared them in a naturalistic prospective observational manner. This study therefore investigated their comparative efficacy over 12 weeks including illness characteristics and adverse effects. One hundred thirty‐one patients (76 M, 55 F) with DSMI‐V schizophrenia or schizoaffective disorder were treated with risperidone (n = 38), olanzapine (n = 38), or clozapine (n = 55). All patients showed a significant decrease of Positive and Negative Syndrome Scale (PANSS)‐positive scores. Decreases in tardive dyskinesia and impulsivity scores were noted with clozapine and olanzapine, respectively. No differences between the medications were noted on depression, anxiety, EPS, or overt aggression scores. Olanzapine and clozapine appeared to be more effective in females. Males showed a decreased sexual performance irrespective of the medication and those treated with risperidone and clozapine showed greater proportional reduction of overt aggression. Clozapine‐treated patients showed significant increased weight, increased glucose levels, and lowered sexual performance. Risperidone patients tended to exhibit reduced cholesterol levels. Higher creatine kinase (CK) levels were noted in risperidone‐treated patients. While cautious given the nature of the study design, results suggest differences in the response to various atypical antipsychotic medications regarding efficacy and side‐effect susceptibility. Copyright © 2006 John Wiley & Sons, Ltd. |
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While they offer advantages with regard to clinical efficacy and side‐effect profile, few studies have compared them in a naturalistic prospective observational manner. This study therefore investigated their comparative efficacy over 12 weeks including illness characteristics and adverse effects. One hundred thirty‐one patients (76 M, 55 F) with DSMI‐V schizophrenia or schizoaffective disorder were treated with risperidone (n = 38), olanzapine (n = 38), or clozapine (n = 55). All patients showed a significant decrease of Positive and Negative Syndrome Scale (PANSS)‐positive scores. Decreases in tardive dyskinesia and impulsivity scores were noted with clozapine and olanzapine, respectively. No differences between the medications were noted on depression, anxiety, EPS, or overt aggression scores. Olanzapine and clozapine appeared to be more effective in females. Males showed a decreased sexual performance irrespective of the medication and those treated with risperidone and clozapine showed greater proportional reduction of overt aggression. Clozapine‐treated patients showed significant increased weight, increased glucose levels, and lowered sexual performance. Risperidone patients tended to exhibit reduced cholesterol levels. Higher creatine kinase (CK) levels were noted in risperidone‐treated patients. While cautious given the nature of the study design, results suggest differences in the response to various atypical antipsychotic medications regarding efficacy and side‐effect susceptibility. 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Psychopharmacol. Clin. Exp</addtitle><description>Risperidone, olanzapine, and clozapine are three atypical antipsychotic medications commonly used in the management of chronic schizophrenia. While they offer advantages with regard to clinical efficacy and side‐effect profile, few studies have compared them in a naturalistic prospective observational manner. This study therefore investigated their comparative efficacy over 12 weeks including illness characteristics and adverse effects. One hundred thirty‐one patients (76 M, 55 F) with DSMI‐V schizophrenia or schizoaffective disorder were treated with risperidone (n = 38), olanzapine (n = 38), or clozapine (n = 55). All patients showed a significant decrease of Positive and Negative Syndrome Scale (PANSS)‐positive scores. Decreases in tardive dyskinesia and impulsivity scores were noted with clozapine and olanzapine, respectively. No differences between the medications were noted on depression, anxiety, EPS, or overt aggression scores. Olanzapine and clozapine appeared to be more effective in females. Males showed a decreased sexual performance irrespective of the medication and those treated with risperidone and clozapine showed greater proportional reduction of overt aggression. Clozapine‐treated patients showed significant increased weight, increased glucose levels, and lowered sexual performance. Risperidone patients tended to exhibit reduced cholesterol levels. Higher creatine kinase (CK) levels were noted in risperidone‐treated patients. While cautious given the nature of the study design, results suggest differences in the response to various atypical antipsychotic medications regarding efficacy and side‐effect susceptibility. Copyright © 2006 John Wiley & Sons, Ltd.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aggression - drug effects</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>atypical antipsychotic</subject><subject>Benzodiazepines - therapeutic use</subject><subject>Blood Glucose - analysis</subject><subject>Body Weight - drug effects</subject><subject>Cholesterol - blood</subject><subject>Chronic Disease</subject><subject>clozapine</subject><subject>Clozapine - therapeutic use</subject><subject>Creatine Kinase - blood</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>naturalistic</subject><subject>olanzapine</subject><subject>Prospective Studies</subject><subject>risperidone</subject><subject>Risperidone - therapeutic use</subject><subject>schizophrenia</subject><subject>Schizophrenia - blood</subject><subject>Schizophrenia - drug therapy</subject><subject>Sex Factors</subject><subject>Triglycerides - blood</subject><issn>0885-6222</issn><issn>1099-1077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EotuC-AfIJzhAip0P2-EGq26LVAFCBY7WxJmwpokd7KRl-1v4sXiVFZwQp5nRPHrn4yXkCWennLH81XYeT6Uo75EVZ3WdcSblfbJiSlWZyPP8iBzH-J2x1GP1Q3LEhVSF4tWK_Fr7YYRgo3e0wekW0dFUjRhs6x2-pL4Hdwej3efgWmp6v5TUOjptkQ7g4BsO6CbqO2q2wTtraDRbe-fHbUBn4TUF6mCaA_Q2Tqk7Bp9GmMneIOV5lqZeU99EDDcwWe-gp3Ga290j8qCDPuLjQzwhV5uzq_VFdvnh_N36zWVmClWWWY3CKDBClp1E0yheFkyJQhU5oFSCtSznAAYZa8pOQS2x5BKRK1l1SkFxQp4tsmmtHzPGSQ82GuzT5ejnqIWqhJSV-i-YMyVlIasEPl9Akw6NATs9BjtA2GnO9N4wnQzTybBEPj1Izs2A7V_u4FACXizAre1x9y8dffH54yKXLXT6M_78Q0O41mK_mf76_lxvai7fftp80bz4DaTosYQ</recordid><startdate>200606</startdate><enddate>200606</enddate><creator>Strous, Rael D.</creator><creator>Kupchik, Marina</creator><creator>Roitman, Suzana</creator><creator>Schwartz, Sima</creator><creator>Gonen, Noach</creator><creator>Mester, Roberto</creator><creator>Weizman, Abraham</creator><creator>Spivak, Baruch</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>200606</creationdate><title>Comparison between risperidone, olanzapine, and clozapine in the management of chronic schizophrenia: a naturalistic prospective 12-week observational study</title><author>Strous, Rael D. ; Kupchik, Marina ; Roitman, Suzana ; Schwartz, Sima ; Gonen, Noach ; Mester, Roberto ; Weizman, Abraham ; Spivak, Baruch</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3844-9e6c8ac674f7ecb81430863832ae7860d021aace00b4f8a97e417ee1875f88a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aggression - drug effects</topic><topic>Antipsychotic Agents - therapeutic use</topic><topic>atypical antipsychotic</topic><topic>Benzodiazepines - therapeutic use</topic><topic>Blood Glucose - analysis</topic><topic>Body Weight - drug effects</topic><topic>Cholesterol - blood</topic><topic>Chronic Disease</topic><topic>clozapine</topic><topic>Clozapine - therapeutic use</topic><topic>Creatine Kinase - blood</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>naturalistic</topic><topic>olanzapine</topic><topic>Prospective Studies</topic><topic>risperidone</topic><topic>Risperidone - therapeutic use</topic><topic>schizophrenia</topic><topic>Schizophrenia - blood</topic><topic>Schizophrenia - drug therapy</topic><topic>Sex Factors</topic><topic>Triglycerides - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strous, Rael D.</creatorcontrib><creatorcontrib>Kupchik, Marina</creatorcontrib><creatorcontrib>Roitman, Suzana</creatorcontrib><creatorcontrib>Schwartz, Sima</creatorcontrib><creatorcontrib>Gonen, Noach</creatorcontrib><creatorcontrib>Mester, Roberto</creatorcontrib><creatorcontrib>Weizman, Abraham</creatorcontrib><creatorcontrib>Spivak, Baruch</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strous, Rael D.</au><au>Kupchik, Marina</au><au>Roitman, Suzana</au><au>Schwartz, Sima</au><au>Gonen, Noach</au><au>Mester, Roberto</au><au>Weizman, Abraham</au><au>Spivak, Baruch</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison between risperidone, olanzapine, and clozapine in the management of chronic schizophrenia: a naturalistic prospective 12-week observational study</atitle><jtitle>Human psychopharmacology</jtitle><addtitle>Hum. Psychopharmacol. Clin. Exp</addtitle><date>2006-06</date><risdate>2006</risdate><volume>21</volume><issue>4</issue><spage>235</spage><epage>243</epage><pages>235-243</pages><issn>0885-6222</issn><eissn>1099-1077</eissn><abstract>Risperidone, olanzapine, and clozapine are three atypical antipsychotic medications commonly used in the management of chronic schizophrenia. While they offer advantages with regard to clinical efficacy and side‐effect profile, few studies have compared them in a naturalistic prospective observational manner. This study therefore investigated their comparative efficacy over 12 weeks including illness characteristics and adverse effects. One hundred thirty‐one patients (76 M, 55 F) with DSMI‐V schizophrenia or schizoaffective disorder were treated with risperidone (n = 38), olanzapine (n = 38), or clozapine (n = 55). All patients showed a significant decrease of Positive and Negative Syndrome Scale (PANSS)‐positive scores. Decreases in tardive dyskinesia and impulsivity scores were noted with clozapine and olanzapine, respectively. No differences between the medications were noted on depression, anxiety, EPS, or overt aggression scores. Olanzapine and clozapine appeared to be more effective in females. Males showed a decreased sexual performance irrespective of the medication and those treated with risperidone and clozapine showed greater proportional reduction of overt aggression. Clozapine‐treated patients showed significant increased weight, increased glucose levels, and lowered sexual performance. Risperidone patients tended to exhibit reduced cholesterol levels. Higher creatine kinase (CK) levels were noted in risperidone‐treated patients. While cautious given the nature of the study design, results suggest differences in the response to various atypical antipsychotic medications regarding efficacy and side‐effect susceptibility. Copyright © 2006 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>16783815</pmid><doi>10.1002/hup.764</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aggression - drug effects Antipsychotic Agents - therapeutic use atypical antipsychotic Benzodiazepines - therapeutic use Blood Glucose - analysis Body Weight - drug effects Cholesterol - blood Chronic Disease clozapine Clozapine - therapeutic use Creatine Kinase - blood Female Humans Male Middle Aged naturalistic olanzapine Prospective Studies risperidone Risperidone - therapeutic use schizophrenia Schizophrenia - blood Schizophrenia - drug therapy Sex Factors Triglycerides - blood |
title | Comparison between risperidone, olanzapine, and clozapine in the management of chronic schizophrenia: a naturalistic prospective 12-week observational study |
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