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Long-acting injectable antipsychotics for the prevention of relapse in patients with recent-onset psychotic disorders: A systematic review and meta-analysis of randomized controlled trials
Abstract This meta-analysis of randomized controlled trials (RCTs) investigated the advantages of long-acting injectable antipsychotics (LAI-APs) over oral antipsychotics (OAPs) with regard to efficacy and safety for patients with recent-onset psychotic disorders. Effect sizes and 95% confidence int...
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Published in: | Psychiatry research 2016-12, Vol.246, p.750-755 |
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description | Abstract This meta-analysis of randomized controlled trials (RCTs) investigated the advantages of long-acting injectable antipsychotics (LAI-APs) over oral antipsychotics (OAPs) with regard to efficacy and safety for patients with recent-onset psychotic disorders. Effect sizes and 95% confidence intervals (95%CIs) were calculated. We identified five RCTs (1022 patients, mean study duration=18±7.59 months) that compared LAI-APs (paliperidone or risperidone) with OAPs. Pooled LAI-APs did not outperform OAPs in terms of the preventing of relapse (N=3, n=875). However, there was significant heterogeneity (I2 =76%), with one study showing no superiority of LAI-APs over OAPs [Malla 2013: risk ratio (RR)=1.83, 95%CI=0.70–4.77, n=77] and the other two studies showing LAI-APs to be superior [Schreiner 2015: [RR=0.71, 95%CI=0.51–0.97, number needed to treat (NNT)=−17, n=715, Subotnik 2015: RR=0.15, 95%CI=0.04–0.63, NNT=−4, n=83]. Pooling the studies, there were no significant differences between LAI-APs and OAPs in the improvement of Positive and Negative Syndrome Scale scores or in discontinuation due to all-cause, adverse events (AEs), and death, but LAI-APs outperformed OAPs in terms of discontinuation due to inefficacy (RR=0.34, NNT=−50) and nonadherence (RR=0.30, NNT=−33). However, the LAI-APs were associated with a higher incidence of at least one AE (RR=1.13) and tremor (RR=2.38) compared with OAPs. |
doi_str_mv | 10.1016/j.psychres.2016.10.053 |
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Effect sizes and 95% confidence intervals (95%CIs) were calculated. We identified five RCTs (1022 patients, mean study duration=18±7.59 months) that compared LAI-APs (paliperidone or risperidone) with OAPs. Pooled LAI-APs did not outperform OAPs in terms of the preventing of relapse (N=3, n=875). However, there was significant heterogeneity (I2 =76%), with one study showing no superiority of LAI-APs over OAPs [Malla 2013: risk ratio (RR)=1.83, 95%CI=0.70–4.77, n=77] and the other two studies showing LAI-APs to be superior [Schreiner 2015: [RR=0.71, 95%CI=0.51–0.97, number needed to treat (NNT)=−17, n=715, Subotnik 2015: RR=0.15, 95%CI=0.04–0.63, NNT=−4, n=83]. Pooling the studies, there were no significant differences between LAI-APs and OAPs in the improvement of Positive and Negative Syndrome Scale scores or in discontinuation due to all-cause, adverse events (AEs), and death, but LAI-APs outperformed OAPs in terms of discontinuation due to inefficacy (RR=0.34, NNT=−50) and nonadherence (RR=0.30, NNT=−33). However, the LAI-APs were associated with a higher incidence of at least one AE (RR=1.13) and tremor (RR=2.38) compared with OAPs.</description><identifier>ISSN: 0165-1781</identifier><identifier>EISSN: 1872-7123</identifier><identifier>DOI: 10.1016/j.psychres.2016.10.053</identifier><identifier>PMID: 27863801</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Antipsychotic Agents - administration & dosage ; Antipsychotic Agents - pharmacology ; Delayed-Action Preparations - administration & dosage ; Delayed-Action Preparations - pharmacology ; Humans ; Long-acting injectable antipsychotics ; Meta-analysis ; Psychiatry ; Psychotic Disorders - drug therapy ; Randomized Controlled Trials as Topic - statistics & numerical data ; Recent-onset psychotic disorders ; Relapse rate ; Schizophrenia - drug therapy ; Secondary Prevention ; Systematic review</subject><ispartof>Psychiatry research, 2016-12, Vol.246, p.750-755</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-ce3661856200ecff1a62d69d00c2757a4818472bb336d6d869b6625387872a473</citedby><cites>FETCH-LOGICAL-c423t-ce3661856200ecff1a62d69d00c2757a4818472bb336d6d869b6625387872a473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27863801$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kishi, Taro</creatorcontrib><creatorcontrib>Oya, Kazuto</creatorcontrib><creatorcontrib>Iwata, Nakao</creatorcontrib><title>Long-acting injectable antipsychotics for the prevention of relapse in patients with recent-onset psychotic disorders: A systematic review and meta-analysis of randomized controlled trials</title><title>Psychiatry research</title><addtitle>Psychiatry Res</addtitle><description>Abstract This meta-analysis of randomized controlled trials (RCTs) investigated the advantages of long-acting injectable antipsychotics (LAI-APs) over oral antipsychotics (OAPs) with regard to efficacy and safety for patients with recent-onset psychotic disorders. Effect sizes and 95% confidence intervals (95%CIs) were calculated. We identified five RCTs (1022 patients, mean study duration=18±7.59 months) that compared LAI-APs (paliperidone or risperidone) with OAPs. Pooled LAI-APs did not outperform OAPs in terms of the preventing of relapse (N=3, n=875). However, there was significant heterogeneity (I2 =76%), with one study showing no superiority of LAI-APs over OAPs [Malla 2013: risk ratio (RR)=1.83, 95%CI=0.70–4.77, n=77] and the other two studies showing LAI-APs to be superior [Schreiner 2015: [RR=0.71, 95%CI=0.51–0.97, number needed to treat (NNT)=−17, n=715, Subotnik 2015: RR=0.15, 95%CI=0.04–0.63, NNT=−4, n=83]. Pooling the studies, there were no significant differences between LAI-APs and OAPs in the improvement of Positive and Negative Syndrome Scale scores or in discontinuation due to all-cause, adverse events (AEs), and death, but LAI-APs outperformed OAPs in terms of discontinuation due to inefficacy (RR=0.34, NNT=−50) and nonadherence (RR=0.30, NNT=−33). However, the LAI-APs were associated with a higher incidence of at least one AE (RR=1.13) and tremor (RR=2.38) compared with OAPs.</description><subject>Antipsychotic Agents - administration & dosage</subject><subject>Antipsychotic Agents - pharmacology</subject><subject>Delayed-Action Preparations - administration & dosage</subject><subject>Delayed-Action Preparations - pharmacology</subject><subject>Humans</subject><subject>Long-acting injectable antipsychotics</subject><subject>Meta-analysis</subject><subject>Psychiatry</subject><subject>Psychotic Disorders - drug therapy</subject><subject>Randomized Controlled Trials as Topic - statistics & numerical data</subject><subject>Recent-onset psychotic disorders</subject><subject>Relapse rate</subject><subject>Schizophrenia - drug therapy</subject><subject>Secondary Prevention</subject><subject>Systematic review</subject><issn>0165-1781</issn><issn>1872-7123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFUk1v1DAQjRCILoW_UPnIJYs_EjvhgKgqvqSVOABny-tMul6SOHi8rZbfxo9j0m174MJp7Pl4T_PeFMWF4GvBhX6zX8949LsEuJb0p-Sa1-pJsRKNkaURUj0tVlSoS2EacVa8QNxzzqVo2-fFmTSNVg0Xq-LPJk7XpfM5TNcsTHvw2W0HYG7K4Y4h5uCR9TGxvAM2J7gBKsWJxZ4lGNyMQHNsdjlQAdltyDsqePqUcULI7BGGdQFj6iDhW3bJ8IgZRrfkCTTALXF2bITsSje54YgB7zgoG8fwGzrm45RTHAZ65hTcgC-LZz0FeHUfz4sfHz98v_pcbr5--nJ1uSl9JVUuPSitRVNryTn4vhdOy063Hedemtq4qhFNZeR2q5TudNfodqu1rFVjSEtXGXVevD7hzin-OgBmOwb0MAxugnhAS-PCtJWqNbXqU6tPETFBb-cURpeOVnC7OGf39sE5uzi35Mk5Gry45zhsR-gexx6soob3pwagTUmvZNGT5B66QHJn28Xwf453_0D4IUzBu-EnHAH38ZBIedrHorTcflvuZzkfoRVvK2PUXyP7x38</recordid><startdate>20161230</startdate><enddate>20161230</enddate><creator>Kishi, Taro</creator><creator>Oya, Kazuto</creator><creator>Iwata, Nakao</creator><general>Elsevier B.V</general><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>20161230</creationdate><title>Long-acting injectable antipsychotics for the prevention of relapse in patients with recent-onset psychotic disorders: A systematic review and meta-analysis of randomized controlled trials</title><author>Kishi, Taro ; Oya, Kazuto ; Iwata, Nakao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-ce3661856200ecff1a62d69d00c2757a4818472bb336d6d869b6625387872a473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antipsychotic Agents - administration & dosage</topic><topic>Antipsychotic Agents - pharmacology</topic><topic>Delayed-Action Preparations - administration & dosage</topic><topic>Delayed-Action Preparations - pharmacology</topic><topic>Humans</topic><topic>Long-acting injectable antipsychotics</topic><topic>Meta-analysis</topic><topic>Psychiatry</topic><topic>Psychotic Disorders - drug therapy</topic><topic>Randomized Controlled Trials as Topic - statistics & numerical data</topic><topic>Recent-onset psychotic disorders</topic><topic>Relapse rate</topic><topic>Schizophrenia - drug therapy</topic><topic>Secondary Prevention</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kishi, Taro</creatorcontrib><creatorcontrib>Oya, Kazuto</creatorcontrib><creatorcontrib>Iwata, Nakao</creatorcontrib><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>Psychiatry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kishi, Taro</au><au>Oya, Kazuto</au><au>Iwata, Nakao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-acting injectable antipsychotics for the prevention of relapse in patients with recent-onset psychotic disorders: A systematic review and meta-analysis of randomized controlled trials</atitle><jtitle>Psychiatry research</jtitle><addtitle>Psychiatry Res</addtitle><date>2016-12-30</date><risdate>2016</risdate><volume>246</volume><spage>750</spage><epage>755</epage><pages>750-755</pages><issn>0165-1781</issn><eissn>1872-7123</eissn><abstract>Abstract This meta-analysis of randomized controlled trials (RCTs) investigated the advantages of long-acting injectable antipsychotics (LAI-APs) over oral antipsychotics (OAPs) with regard to efficacy and safety for patients with recent-onset psychotic disorders. Effect sizes and 95% confidence intervals (95%CIs) were calculated. We identified five RCTs (1022 patients, mean study duration=18±7.59 months) that compared LAI-APs (paliperidone or risperidone) with OAPs. Pooled LAI-APs did not outperform OAPs in terms of the preventing of relapse (N=3, n=875). However, there was significant heterogeneity (I2 =76%), with one study showing no superiority of LAI-APs over OAPs [Malla 2013: risk ratio (RR)=1.83, 95%CI=0.70–4.77, n=77] and the other two studies showing LAI-APs to be superior [Schreiner 2015: [RR=0.71, 95%CI=0.51–0.97, number needed to treat (NNT)=−17, n=715, Subotnik 2015: RR=0.15, 95%CI=0.04–0.63, NNT=−4, n=83]. Pooling the studies, there were no significant differences between LAI-APs and OAPs in the improvement of Positive and Negative Syndrome Scale scores or in discontinuation due to all-cause, adverse events (AEs), and death, but LAI-APs outperformed OAPs in terms of discontinuation due to inefficacy (RR=0.34, NNT=−50) and nonadherence (RR=0.30, NNT=−33). However, the LAI-APs were associated with a higher incidence of at least one AE (RR=1.13) and tremor (RR=2.38) compared with OAPs.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>27863801</pmid><doi>10.1016/j.psychres.2016.10.053</doi><tpages>6</tpages></addata></record> |
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subjects | Antipsychotic Agents - administration & dosage Antipsychotic Agents - pharmacology Delayed-Action Preparations - administration & dosage Delayed-Action Preparations - pharmacology Humans Long-acting injectable antipsychotics Meta-analysis Psychiatry Psychotic Disorders - drug therapy Randomized Controlled Trials as Topic - statistics & numerical data Recent-onset psychotic disorders Relapse rate Schizophrenia - drug therapy Secondary Prevention Systematic review |
title | Long-acting injectable antipsychotics for the prevention of relapse in patients with recent-onset psychotic disorders: A systematic review and meta-analysis of randomized controlled trials |
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