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 inThe American journal of psychiatry Vol. 162; no. 5; pp. 947 - 953
Main Authors Schooler, Nina, Rabinowitz, Jonathan, Davidson, Michael, Emsley, Robin, Harvey, Philip D., Kopala, Lili, McGorry, Patrick D., Van Hove, Ilse, Eerdekens, Marielle, Swyzen, Wim, De Smedt, Goedele
Format Journal Article
LanguageEnglish
Published Washington, DC American Psychiatric Publishing 01.05.2005
American Psychiatric Association
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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.
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
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  surname: Schooler
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  surname: Davidson
  fullname: Davidson, Michael
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  surname: Emsley
  fullname: Emsley, Robin
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  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
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  fullname: Swyzen, Wim
– sequence: 11
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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
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Psychosis
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Schizophreniform disorder
Risperidone
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Snippet OBJECTIVE: The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept...
The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further,...
Following the first episode of psychosis, treatment with antipsychotic medication is associated with rapid improvement in a majority of individuals. Schooler...
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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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