A prospective comparative study of risperidone long-acting injectable for treatment-resistant schizophrenia with dopamine supersensitivity psychosis

Abstract Objective Dopamine supersensitivity psychosis (DSP) is considered to be one cause of treatment-resistant schizophrenia (TRS). The authors investigated the efficacy of risperidone long-acting injections (RLAI) in patients with TRS and DSP. Method This is a multicenter, prospective, 12-month...

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Veröffentlicht in:Schizophrenia research 2014-05, Vol.155 (1), p.52-58
Hauptverfasser: Kimura, Hiroshi, Kanahara, Nobuhisa, Komatsu, Naoya, Ishige, Minoru, Muneoka, Katsumasa, Yoshimura, Masayuki, Yamanaka, Hiroshi, Suzuki, Tomotaka, Komatsu, Hideki, Sasaki, Tsuyoshi, Hashimoto, Tasuku, Hasegawa, Tadashi, Shiina, Akihiro, Ishikawa, Masatomo, Sekine, Yoshimoto, Shiraishi, Tetsuya, Watanabe, Hiroyuki, Shimizu, Eiji, Hashimoto, Kenji, Iyo, Masaomi
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container_end_page 58
container_issue 1
container_start_page 52
container_title Schizophrenia research
container_volume 155
creator Kimura, Hiroshi
Kanahara, Nobuhisa
Komatsu, Naoya
Ishige, Minoru
Muneoka, Katsumasa
Yoshimura, Masayuki
Yamanaka, Hiroshi
Suzuki, Tomotaka
Komatsu, Hideki
Sasaki, Tsuyoshi
Hashimoto, Tasuku
Hasegawa, Tadashi
Shiina, Akihiro
Ishikawa, Masatomo
Sekine, Yoshimoto
Shiraishi, Tetsuya
Watanabe, Hiroyuki
Shimizu, Eiji
Hashimoto, Kenji
Iyo, Masaomi
description Abstract Objective Dopamine supersensitivity psychosis (DSP) is considered to be one cause of treatment-resistant schizophrenia (TRS). The authors investigated the efficacy of risperidone long-acting injections (RLAI) in patients with TRS and DSP. Method This is a multicenter, prospective, 12-month follow-up, observational study that included unstable and severe TRS patients with and without DSP. 115 patients with TRS were recruited and divided into two groups according to the presence or absence of DSP which was judged on the basis of the clinical courses and neurological examinations. RLAI was administered adjunctively once every 2 weeks along with oral antipsychotics. We observed changes in scores for the Brief Psychiatric Rating Scales (BPRS), Clinical Global Impression—Severity of Illness (CGI-S), Global Assessment of Functioning Scale (GAF), and Extrapyramidal Symptom Rating Scale (ESRS) during the study. Of the assessed 94 patients, 61 and 33 were categorized into the DSP and NonDSP groups, respectively. Results While baseline BPRS total scores, CGI-S scores and GAF scores did not differ, the ESRS score was significantly higher in the DSP group compared with the NonDSP group. Treatment significantly reduced BPRS total scores and CGI-S scores, and increased GAF scores in both groups, but the magnitudes of change were significantly greater in the DSP group relative to the NonDSP group. ESRS scores were also reduced in the DSP group. Responder rates (≥ 20% reduction in BPRS total score) were 62.3% in the DSP group and 21.2% in the NonDSP group. Conclusions It is suggested that DSP contributes to the etiology of TRS. Atypical antipsychotic drugs in long-acting forms, such as RLAI, can provide beneficial effects for patients with DSP. Clinical trials registration : UMIN (UMIN000008487).
doi_str_mv 10.1016/j.schres.2014.02.022
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The authors investigated the efficacy of risperidone long-acting injections (RLAI) in patients with TRS and DSP. Method This is a multicenter, prospective, 12-month follow-up, observational study that included unstable and severe TRS patients with and without DSP. 115 patients with TRS were recruited and divided into two groups according to the presence or absence of DSP which was judged on the basis of the clinical courses and neurological examinations. RLAI was administered adjunctively once every 2 weeks along with oral antipsychotics. We observed changes in scores for the Brief Psychiatric Rating Scales (BPRS), Clinical Global Impression—Severity of Illness (CGI-S), Global Assessment of Functioning Scale (GAF), and Extrapyramidal Symptom Rating Scale (ESRS) during the study. Of the assessed 94 patients, 61 and 33 were categorized into the DSP and NonDSP groups, respectively. Results While baseline BPRS total scores, CGI-S scores and GAF scores did not differ, the ESRS score was significantly higher in the DSP group compared with the NonDSP group. Treatment significantly reduced BPRS total scores and CGI-S scores, and increased GAF scores in both groups, but the magnitudes of change were significantly greater in the DSP group relative to the NonDSP group. ESRS scores were also reduced in the DSP group. Responder rates (≥ 20% reduction in BPRS total score) were 62.3% in the DSP group and 21.2% in the NonDSP group. Conclusions It is suggested that DSP contributes to the etiology of TRS. Atypical antipsychotic drugs in long-acting forms, such as RLAI, can provide beneficial effects for patients with DSP. Clinical trials registration : UMIN (UMIN000008487).</description><identifier>ISSN: 0920-9964</identifier><identifier>EISSN: 1573-2509</identifier><identifier>DOI: 10.1016/j.schres.2014.02.022</identifier><identifier>PMID: 24667073</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Administration, Oral ; Adolescent ; Adult ; Adult and adolescent clinical studies ; Aged ; Antipsychotic Agents - administration &amp; dosage ; Antipsychotics ; Biological and medical sciences ; Dopamine - adverse effects ; Dopamine D2 receptor ; Drug Administration Routes ; Drug Delivery Systems ; Female ; Follow-Up Studies ; Humans ; Male ; Medical sciences ; Middle Aged ; Neuropharmacology ; Occupancy rate ; Pharmacology. Drug treatments ; Prospective Studies ; Psychiatric Status Rating Scales ; Psychiatry ; Psycholeptics: tranquillizer, neuroleptic ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychopharmacology ; Psychoses ; Psychotic Disorders - complications ; Psychotic Disorders - drug therapy ; Risperidone - administration &amp; dosage ; Schizophrenia ; Schizophrenia - complications ; Schizophrenia - drug therapy ; Tolerance ; Treatment Outcome ; Young Adult</subject><ispartof>Schizophrenia research, 2014-05, Vol.155 (1), p.52-58</ispartof><rights>The Authors</rights><rights>2014 The Authors</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 The Authors. Published by Elsevier B.V. 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The authors investigated the efficacy of risperidone long-acting injections (RLAI) in patients with TRS and DSP. Method This is a multicenter, prospective, 12-month follow-up, observational study that included unstable and severe TRS patients with and without DSP. 115 patients with TRS were recruited and divided into two groups according to the presence or absence of DSP which was judged on the basis of the clinical courses and neurological examinations. RLAI was administered adjunctively once every 2 weeks along with oral antipsychotics. We observed changes in scores for the Brief Psychiatric Rating Scales (BPRS), Clinical Global Impression—Severity of Illness (CGI-S), Global Assessment of Functioning Scale (GAF), and Extrapyramidal Symptom Rating Scale (ESRS) during the study. Of the assessed 94 patients, 61 and 33 were categorized into the DSP and NonDSP groups, respectively. Results While baseline BPRS total scores, CGI-S scores and GAF scores did not differ, the ESRS score was significantly higher in the DSP group compared with the NonDSP group. Treatment significantly reduced BPRS total scores and CGI-S scores, and increased GAF scores in both groups, but the magnitudes of change were significantly greater in the DSP group relative to the NonDSP group. ESRS scores were also reduced in the DSP group. Responder rates (≥ 20% reduction in BPRS total score) were 62.3% in the DSP group and 21.2% in the NonDSP group. Conclusions It is suggested that DSP contributes to the etiology of TRS. Atypical antipsychotic drugs in long-acting forms, such as RLAI, can provide beneficial effects for patients with DSP. 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Psychiatry</subject><subject>Psychopharmacology</subject><subject>Psychoses</subject><subject>Psychotic Disorders - complications</subject><subject>Psychotic Disorders - drug therapy</subject><subject>Risperidone - administration &amp; dosage</subject><subject>Schizophrenia</subject><subject>Schizophrenia - complications</subject><subject>Schizophrenia - drug therapy</subject><subject>Tolerance</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>0920-9964</issn><issn>1573-2509</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUsuKFTEUDKI419E_EMlGcNPXvPq1EYbBFwy4UNchnT6Zm7Y7aZPukfY7_GDP9V4V3AiBBFJ1qqg6hDzlbM8Zr14O-2wPCfJeMK72TOAR98iOl7UsRMna-2THWsGKtq3UBXmU88AY4yWrH5ILoaqqZrXckR9XdE4xz2AXfwfUxmk2yfx652XtNxodTR7_k-9jADrGcFsYBIdb6sOANNONQF1MdElglgnCUqArnxcTFooW_fc4o8_gDf3mlwPt42wmj6PyilMzhOxRzi8bnfNmDxGpj8kDZ8YMT873Jfn85vWn63fFzYe376-vbgqrWCMKJ6zgsmwYKCFrrsC4pgduueq5BWmqvrSdlFZyVnetK1nZYgJd2TnGRedaeUlenOZiBF9XyIuefLYwjiZAXLPmJW8bVddcIlSdoBbTygmcnpOfTNo0Z_rYhx70qQ997EMzgUcg7dlZYe0m6P-QfheAgOdngMnWjC6ZYH3-i2tUySulEPfqhAPM485DQjUPwULvE5ag--j_5-TfAXb0waPmF9ggD3FNAbPWXGck6I_H3TmuDleYGasq-RP8YsRz</recordid><startdate>201405</startdate><enddate>201405</enddate><creator>Kimura, Hiroshi</creator><creator>Kanahara, Nobuhisa</creator><creator>Komatsu, Naoya</creator><creator>Ishige, Minoru</creator><creator>Muneoka, Katsumasa</creator><creator>Yoshimura, Masayuki</creator><creator>Yamanaka, Hiroshi</creator><creator>Suzuki, Tomotaka</creator><creator>Komatsu, Hideki</creator><creator>Sasaki, Tsuyoshi</creator><creator>Hashimoto, Tasuku</creator><creator>Hasegawa, Tadashi</creator><creator>Shiina, Akihiro</creator><creator>Ishikawa, Masatomo</creator><creator>Sekine, Yoshimoto</creator><creator>Shiraishi, Tetsuya</creator><creator>Watanabe, Hiroyuki</creator><creator>Shimizu, Eiji</creator><creator>Hashimoto, Kenji</creator><creator>Iyo, Masaomi</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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>7X8</scope></search><sort><creationdate>201405</creationdate><title>A prospective comparative study of risperidone long-acting injectable for treatment-resistant schizophrenia with dopamine supersensitivity psychosis</title><author>Kimura, Hiroshi ; Kanahara, Nobuhisa ; Komatsu, Naoya ; Ishige, Minoru ; Muneoka, Katsumasa ; Yoshimura, Masayuki ; Yamanaka, Hiroshi ; Suzuki, Tomotaka ; Komatsu, Hideki ; Sasaki, Tsuyoshi ; Hashimoto, Tasuku ; Hasegawa, Tadashi ; Shiina, Akihiro ; Ishikawa, Masatomo ; Sekine, Yoshimoto ; Shiraishi, Tetsuya ; Watanabe, Hiroyuki ; Shimizu, Eiji ; Hashimoto, Kenji ; Iyo, Masaomi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4082-f2c213580e423714eaf8de1c14d1ce3a6d5cb33c3107b9f5059001b5bf012bf93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Administration, Oral</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Aged</topic><topic>Antipsychotic Agents - administration &amp; dosage</topic><topic>Antipsychotics</topic><topic>Biological and medical sciences</topic><topic>Dopamine - adverse effects</topic><topic>Dopamine D2 receptor</topic><topic>Drug Administration Routes</topic><topic>Drug Delivery Systems</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neuropharmacology</topic><topic>Occupancy rate</topic><topic>Pharmacology. 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Psychiatry</topic><topic>Psychopharmacology</topic><topic>Psychoses</topic><topic>Psychotic Disorders - complications</topic><topic>Psychotic Disorders - drug therapy</topic><topic>Risperidone - administration &amp; dosage</topic><topic>Schizophrenia</topic><topic>Schizophrenia - complications</topic><topic>Schizophrenia - drug therapy</topic><topic>Tolerance</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimura, Hiroshi</creatorcontrib><creatorcontrib>Kanahara, Nobuhisa</creatorcontrib><creatorcontrib>Komatsu, Naoya</creatorcontrib><creatorcontrib>Ishige, Minoru</creatorcontrib><creatorcontrib>Muneoka, Katsumasa</creatorcontrib><creatorcontrib>Yoshimura, Masayuki</creatorcontrib><creatorcontrib>Yamanaka, Hiroshi</creatorcontrib><creatorcontrib>Suzuki, Tomotaka</creatorcontrib><creatorcontrib>Komatsu, Hideki</creatorcontrib><creatorcontrib>Sasaki, Tsuyoshi</creatorcontrib><creatorcontrib>Hashimoto, Tasuku</creatorcontrib><creatorcontrib>Hasegawa, Tadashi</creatorcontrib><creatorcontrib>Shiina, Akihiro</creatorcontrib><creatorcontrib>Ishikawa, Masatomo</creatorcontrib><creatorcontrib>Sekine, Yoshimoto</creatorcontrib><creatorcontrib>Shiraishi, Tetsuya</creatorcontrib><creatorcontrib>Watanabe, Hiroyuki</creatorcontrib><creatorcontrib>Shimizu, Eiji</creatorcontrib><creatorcontrib>Hashimoto, Kenji</creatorcontrib><creatorcontrib>Iyo, Masaomi</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Schizophrenia research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimura, Hiroshi</au><au>Kanahara, Nobuhisa</au><au>Komatsu, Naoya</au><au>Ishige, Minoru</au><au>Muneoka, Katsumasa</au><au>Yoshimura, Masayuki</au><au>Yamanaka, Hiroshi</au><au>Suzuki, Tomotaka</au><au>Komatsu, Hideki</au><au>Sasaki, Tsuyoshi</au><au>Hashimoto, Tasuku</au><au>Hasegawa, Tadashi</au><au>Shiina, Akihiro</au><au>Ishikawa, Masatomo</au><au>Sekine, Yoshimoto</au><au>Shiraishi, Tetsuya</au><au>Watanabe, Hiroyuki</au><au>Shimizu, Eiji</au><au>Hashimoto, Kenji</au><au>Iyo, Masaomi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A prospective comparative study of risperidone long-acting injectable for treatment-resistant schizophrenia with dopamine supersensitivity psychosis</atitle><jtitle>Schizophrenia research</jtitle><addtitle>Schizophr Res</addtitle><date>2014-05</date><risdate>2014</risdate><volume>155</volume><issue>1</issue><spage>52</spage><epage>58</epage><pages>52-58</pages><issn>0920-9964</issn><eissn>1573-2509</eissn><abstract>Abstract Objective Dopamine supersensitivity psychosis (DSP) is considered to be one cause of treatment-resistant schizophrenia (TRS). The authors investigated the efficacy of risperidone long-acting injections (RLAI) in patients with TRS and DSP. Method This is a multicenter, prospective, 12-month follow-up, observational study that included unstable and severe TRS patients with and without DSP. 115 patients with TRS were recruited and divided into two groups according to the presence or absence of DSP which was judged on the basis of the clinical courses and neurological examinations. RLAI was administered adjunctively once every 2 weeks along with oral antipsychotics. We observed changes in scores for the Brief Psychiatric Rating Scales (BPRS), Clinical Global Impression—Severity of Illness (CGI-S), Global Assessment of Functioning Scale (GAF), and Extrapyramidal Symptom Rating Scale (ESRS) during the study. Of the assessed 94 patients, 61 and 33 were categorized into the DSP and NonDSP groups, respectively. Results While baseline BPRS total scores, CGI-S scores and GAF scores did not differ, the ESRS score was significantly higher in the DSP group compared with the NonDSP group. Treatment significantly reduced BPRS total scores and CGI-S scores, and increased GAF scores in both groups, but the magnitudes of change were significantly greater in the DSP group relative to the NonDSP group. ESRS scores were also reduced in the DSP group. Responder rates (≥ 20% reduction in BPRS total score) were 62.3% in the DSP group and 21.2% in the NonDSP group. Conclusions It is suggested that DSP contributes to the etiology of TRS. Atypical antipsychotic drugs in long-acting forms, such as RLAI, can provide beneficial effects for patients with DSP. Clinical trials registration : UMIN (UMIN000008487).</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>24667073</pmid><doi>10.1016/j.schres.2014.02.022</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Administration, Oral
Adolescent
Adult
Adult and adolescent clinical studies
Aged
Antipsychotic Agents - administration & dosage
Antipsychotics
Biological and medical sciences
Dopamine - adverse effects
Dopamine D2 receptor
Drug Administration Routes
Drug Delivery Systems
Female
Follow-Up Studies
Humans
Male
Medical sciences
Middle Aged
Neuropharmacology
Occupancy rate
Pharmacology. Drug treatments
Prospective Studies
Psychiatric Status Rating Scales
Psychiatry
Psycholeptics: tranquillizer, neuroleptic
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychopharmacology
Psychoses
Psychotic Disorders - complications
Psychotic Disorders - drug therapy
Risperidone - administration & dosage
Schizophrenia
Schizophrenia - complications
Schizophrenia - drug therapy
Tolerance
Treatment Outcome
Young Adult
title A prospective comparative study of risperidone long-acting injectable for treatment-resistant schizophrenia with dopamine supersensitivity psychosis
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