Risperidone and Haloperidol in First-Episode Psychosis: A Long-Term Randomized Trial
OBJECTIVE: The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further, relapse prevention is a treatment cornerstone during the first years of illness because active psychotic illness may affect lifet...
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Published in | The American journal of psychiatry Vol. 162; no. 5; pp. 947 - 953 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Psychiatric Publishing
01.05.2005
American Psychiatric Association |
Subjects | |
Online Access | Get full text |
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Abstract | OBJECTIVE: The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further, relapse prevention is a treatment cornerstone during the first years of illness because active psychotic illness may affect lifetime outcomes. Thus, initial treatment of active symptoms and subsequent relapse prevention are central goals of pharmacotherapy. This study compared long-term effectiveness of risperidone versus haloperidol in first-episode psychosis patients. METHOD: First-episode psychosis patients (N=555, mean age=25.4 years) participated in a double-blind, randomized, controlled flexible-dose trial that compared risperidone (mean modal dose=3.3 mg) and haloperidol (mean modal dose=2.9 mg). The median treatment length was 206 days (maximum=1,514). RESULTS: Positive and Negative Syndrome Scale scores and Clinical Global Impression ratings improved significantly relative to baseline, with no significant differences between groups. Three-quarters of the patients achieved initial clinical improvement, defined as >20% reduction in total Positive and Negative Syndrome Scale score. However, among those who achieved clinical improvement, 42% of the risperidone group experienced a relapse compared with 55% of the haloperidol group. The median time to relapse was 466 days for risperidone-treated subjects and 205 days for those given haloperidol. These differences were statistically significant based on Kaplan-Meier survival analysis. Adverse effects distinguished the treatments: there were significantly more extrapyramidal signs and symptoms and adjunctive medication use in the haloperidol group and greater prolactin elevation in the risperidone group. There was less weight gain with haloperidol initially but no significant differences between groups at endpoint. CONCLUSIONS: Relatively low doses of antipsychotic drugs lead to significant symptom amelioration in the majority of first-episode psychosis patients. In the long term, risperidone prevents relapse in more patients and for a longer time and also induces less abnormal movements than haloperidol. |
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AbstractList | The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further, relapse prevention is a treatment cornerstone during the first years of illness because active psychotic illness may affect lifetime outcomes. Thus, initial treatment of active symptoms and subsequent relapse prevention are central goals of pharmacotherapy. This study compared long-term effectiveness of risperidone versus haloperidol in first-episode psychosis patients.OBJECTIVEThe first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further, relapse prevention is a treatment cornerstone during the first years of illness because active psychotic illness may affect lifetime outcomes. Thus, initial treatment of active symptoms and subsequent relapse prevention are central goals of pharmacotherapy. This study compared long-term effectiveness of risperidone versus haloperidol in first-episode psychosis patients.First-episode psychosis patients (N=555, mean age=25.4 years) participated in a double-blind, randomized, controlled flexible-dose trial that compared risperidone (mean modal dose=3.3 mg) and haloperidol (mean modal dose=2.9 mg). The median treatment length was 206 days (maximum=1,514).METHODFirst-episode psychosis patients (N=555, mean age=25.4 years) participated in a double-blind, randomized, controlled flexible-dose trial that compared risperidone (mean modal dose=3.3 mg) and haloperidol (mean modal dose=2.9 mg). The median treatment length was 206 days (maximum=1,514).Positive and Negative Syndrome Scale scores and Clinical Global Impression ratings improved significantly relative to baseline, with no significant differences between groups. Three-quarters of the patients achieved initial clinical improvement, defined as >20% reduction in total Positive and Negative Syndrome Scale score. However, among those who achieved clinical improvement, 42% of the risperidone group experienced a relapse compared with 55% of the haloperidol group. The median time to relapse was 466 days for risperidone-treated subjects and 205 days for those given haloperidol. These differences were statistically significant based on Kaplan-Meier survival analysis. Adverse effects distinguished the treatments: there were significantly more extrapyramidal signs and symptoms and adjunctive medication use in the haloperidol group and greater prolactin elevation in the risperidone group. There was less weight gain with haloperidol initially but no significant differences between groups at endpoint.RESULTSPositive and Negative Syndrome Scale scores and Clinical Global Impression ratings improved significantly relative to baseline, with no significant differences between groups. Three-quarters of the patients achieved initial clinical improvement, defined as >20% reduction in total Positive and Negative Syndrome Scale score. However, among those who achieved clinical improvement, 42% of the risperidone group experienced a relapse compared with 55% of the haloperidol group. The median time to relapse was 466 days for risperidone-treated subjects and 205 days for those given haloperidol. These differences were statistically significant based on Kaplan-Meier survival analysis. Adverse effects distinguished the treatments: there were significantly more extrapyramidal signs and symptoms and adjunctive medication use in the haloperidol group and greater prolactin elevation in the risperidone group. There was less weight gain with haloperidol initially but no significant differences between groups at endpoint.Relatively low doses of antipsychotic drugs lead to significant symptom amelioration in the majority of first-episode psychosis patients. In the long term, risperidone prevents relapse in more patients and for a longer time and also induces less abnormal movements than haloperidol.CONCLUSIONSRelatively low doses of antipsychotic drugs lead to significant symptom amelioration in the majority of first-episode psychosis patients. In the long term, risperidone prevents relapse in more patients and for a longer time and also induces less abnormal movements than haloperidol. OBJECTIVE: The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further, relapse prevention is a treatment cornerstone during the first years of illness because active psychotic illness may affect lifetime outcomes. Thus, initial treatment of active symptoms and subsequent relapse prevention are central goals of pharmacotherapy. This study compared long-term effectiveness of risperidone versus haloperidol in first-episode psychosis patients. METHOD: First-episode psychosis patients (N=555, mean age=25.4 years) participated in a double-blind, randomized, controlled flexible-dose trial that compared risperidone (mean modal dose=3.3 mg) and haloperidol (mean modal dose=2.9 mg). The median treatment length was 206 days (maximum=1,514). RESULTS: Positive and Negative Syndrome Scale scores and Clinical Global Impression ratings improved significantly relative to baseline, with no significant differences between groups. Three-quarters of the patients achieved initial clinical improvement, defined as >20% reduction in total Positive and Negative Syndrome Scale score. However, among those who achieved clinical improvement, 42% of the risperidone group experienced a relapse compared with 55% of the haloperidol group. The median time to relapse was 466 days for risperidone-treated subjects and 205 days for those given haloperidol. These differences were statistically significant based on Kaplan-Meier survival analysis. Adverse effects distinguished the treatments: there were significantly more extrapyramidal signs and symptoms and adjunctive medication use in the haloperidol group and greater prolactin elevation in the risperidone group. There was less weight gain with haloperidol initially but no significant differences between groups at endpoint. CONCLUSIONS: Relatively low doses of antipsychotic drugs lead to significant symptom amelioration in the majority of first-episode psychosis patients. In the long term, risperidone prevents relapse in more patients and for a longer time and also induces less abnormal movements than haloperidol. Following the first episode of psychosis, treatment with antipsychotic medication is associated with rapid improvement in a majority of individuals. Schooler et al compare long-term effectiveness versus haloperidol in first-episode psychosis treatment. The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further, relapse prevention is a treatment cornerstone during the first years of illness because active psychotic illness may affect lifetime outcomes. Thus, initial treatment of active symptoms and subsequent relapse prevention are central goals of pharmacotherapy. This study compared long-term effectiveness of risperidone versus haloperidol in first-episode psychosis patients. First-episode psychosis patients (N=555, mean age=25.4 years) participated in a double-blind, randomized, controlled flexible-dose trial that compared risperidone (mean modal dose=3.3 mg) and haloperidol (mean modal dose=2.9 mg). The median treatment length was 206 days (maximum=1,514). Positive and Negative Syndrome Scale scores and Clinical Global Impression ratings improved significantly relative to baseline, with no significant differences between groups. Three-quarters of the patients achieved initial clinical improvement, defined as >20% reduction in total Positive and Negative Syndrome Scale score. However, among those who achieved clinical improvement, 42% of the risperidone group experienced a relapse compared with 55% of the haloperidol group. The median time to relapse was 466 days for risperidone-treated subjects and 205 days for those given haloperidol. These differences were statistically significant based on Kaplan-Meier survival analysis. Adverse effects distinguished the treatments: there were significantly more extrapyramidal signs and symptoms and adjunctive medication use in the haloperidol group and greater prolactin elevation in the risperidone group. There was less weight gain with haloperidol initially but no significant differences between groups at endpoint. Relatively low doses of antipsychotic drugs lead to significant symptom amelioration in the majority of first-episode psychosis patients. In the long term, risperidone prevents relapse in more patients and for a longer time and also induces less abnormal movements than haloperidol. |
Author | Harvey, Philip D. Kopala, Lili Eerdekens, Marielle Schooler, Nina Rabinowitz, Jonathan McGorry, Patrick D. Van Hove, Ilse Davidson, Michael Swyzen, Wim De Smedt, Goedele Emsley, Robin |
Author_xml | – sequence: 1 givenname: Nina surname: Schooler fullname: Schooler, Nina – sequence: 2 givenname: Jonathan surname: Rabinowitz fullname: Rabinowitz, Jonathan – sequence: 3 givenname: Michael surname: Davidson fullname: Davidson, Michael – sequence: 4 givenname: Robin surname: Emsley fullname: Emsley, Robin – sequence: 5 givenname: Philip D. surname: Harvey fullname: Harvey, Philip D. – sequence: 6 givenname: Lili surname: Kopala fullname: Kopala, Lili – sequence: 7 givenname: Patrick D. surname: McGorry fullname: McGorry, Patrick D. – sequence: 8 givenname: Ilse surname: Van Hove fullname: Van Hove, Ilse – sequence: 9 givenname: Marielle surname: Eerdekens fullname: Eerdekens, Marielle – sequence: 10 givenname: Wim surname: Swyzen fullname: Swyzen, Wim – sequence: 11 givenname: Goedele surname: De Smedt fullname: De Smedt, Goedele |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16738504$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/15863797$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1001/archpsyc.56.3.241 10.1001/archpsyc.1982.04290040080014 10.1093/oxfordjournals.schbul.a033413 10.1176/appi.ajp.158.11.1835 10.1001/archpsyc.1981.01780320056006 10.1001/archpsyc.60.6.553 10.1176/appi.ajp.160.8.1396 10.1001/archpsyc.60.1.82 10.1016/S0920-9964(98)00105-4 10.1176/ajp.156.11.1686 10.2337/diacare.27.2.596 10.1001/archpsyc.1991.01810320063009 10.1176/ajp.152.12.1724 10.1093/schbul/13.2.261 10.1056/NEJMoa002028 10.1176/ajp.156.4.544 10.1093/schbul/23.4.653 10.1176/appi.ajp.160.7.1209 10.1136/bmj.321.7273.1371 10.1097/00002826-199518003-00001 10.1176/ajp.156.1.79 10.1016/S0920-9964(02)00322-5 |
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Keywords | Human Schizoaffective psychosis Relapse Atypical antipsychotic Psychotropic Neuroleptic Dopamine antagonist Serotonin antagonist Treatment efficiency Schizophrenia Butyrophenone derivatives Serotonine receptor Haloperidol Long term Prevention Psychosis Chemotherapy D2 Dopamine receptor Treatment First episode Schizophreniform disorder Risperidone |
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SubjectTerms | Adult Antipsychotic Agents - adverse effects Antipsychotic Agents - therapeutic use Biological and medical sciences Clinical trials Double-Blind Method Drug Administration Schedule Drug therapy Dyskinesia, Drug-Induced - epidemiology Female Haloperidol - adverse effects Haloperidol - therapeutic use Humans Hyperprolactinemia - chemically induced Longitudinal Studies Male Medical sciences Mental disorders Neuropharmacology Obesity - chemically induced Pharmacology. Drug treatments Preventive medicine Psychiatric Status Rating Scales Psycholeptics: tranquillizer, neuroleptic Psychology. Psychoanalysis. Psychiatry Psychopharmacology Psychosis Psychotic Disorders - diagnosis Psychotic Disorders - drug therapy Psychotic Disorders - psychology Risperidone - adverse effects Risperidone - therapeutic use Schizophrenia Schizophrenia - diagnosis Schizophrenia - drug therapy Schizophrenic Psychology Secondary Prevention Treatment Outcome Weight Gain - drug effects |
Title | Risperidone and Haloperidol in First-Episode Psychosis: A Long-Term Randomized Trial |
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