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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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 & 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</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. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4082-f2c213580e423714eaf8de1c14d1ce3a6d5cb33c3107b9f5059001b5bf012bf93</citedby><cites>FETCH-LOGICAL-c4082-f2c213580e423714eaf8de1c14d1ce3a6d5cb33c3107b9f5059001b5bf012bf93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0920996414001066$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28451644$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24667073$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>A prospective comparative study of risperidone long-acting injectable for treatment-resistant schizophrenia with dopamine supersensitivity psychosis</title><title>Schizophrenia research</title><addtitle>Schizophr Res</addtitle><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).</description><subject>Administration, Oral</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Aged</subject><subject>Antipsychotic Agents - administration & dosage</subject><subject>Antipsychotics</subject><subject>Biological and medical sciences</subject><subject>Dopamine - adverse effects</subject><subject>Dopamine D2 receptor</subject><subject>Drug Administration Routes</subject><subject>Drug Delivery Systems</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neuropharmacology</subject><subject>Occupancy rate</subject><subject>Pharmacology. Drug treatments</subject><subject>Prospective Studies</subject><subject>Psychiatric Status Rating Scales</subject><subject>Psychiatry</subject><subject>Psycholeptics: tranquillizer, neuroleptic</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychopharmacology</subject><subject>Psychoses</subject><subject>Psychotic Disorders - complications</subject><subject>Psychotic Disorders - drug therapy</subject><subject>Risperidone - administration & 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 & 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. Drug treatments</topic><topic>Prospective Studies</topic><topic>Psychiatric Status Rating Scales</topic><topic>Psychiatry</topic><topic>Psycholeptics: tranquillizer, neuroleptic</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Psychoses</topic><topic>Psychotic Disorders - complications</topic><topic>Psychotic Disorders - drug therapy</topic><topic>Risperidone - administration & 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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