Efficacy and Safety of Antidepressants Added to Antipsychotics for Schizophrenia: A Systematic Review and Meta-Analysis

Objective:The authors examined the safety and efficacy of antidepressants added to antipsychotic drugs in the treatment of schizophrenia.Method:Multiple databases and previous publications were searched through June 2015 to identify all randomized controlled trials of any add-on antidepressants comp...

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Veröffentlicht in:The American journal of psychiatry 2016-09, Vol.173 (9), p.876-886
Hauptverfasser: Helfer, Bartosz, Samara, Myrto T, Huhn, Maximilian, Klupp, Elisabeth, Leucht, Claudia, Zhu, Yikang, Engel, Rolf R, Leucht, Stefan
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container_end_page 886
container_issue 9
container_start_page 876
container_title The American journal of psychiatry
container_volume 173
creator Helfer, Bartosz
Samara, Myrto T
Huhn, Maximilian
Klupp, Elisabeth
Leucht, Claudia
Zhu, Yikang
Engel, Rolf R
Leucht, Stefan
description Objective:The authors examined the safety and efficacy of antidepressants added to antipsychotic drugs in the treatment of schizophrenia.Method:Multiple databases and previous publications were searched through June 2015 to identify all randomized controlled trials of any add-on antidepressants compared with placebo or no-treatment in schizophrenia. Depressive and negative symptoms (primary outcomes), overall symptoms, positive symptoms, side effects, exacerbation of psychosis, and responder rates were examined. Subgroup, meta-regression, and sensitivity analyses were performed, as well as investigations of publication bias and risk of bias.Results:Eighty-two randomized controlled trials with a total of 3,608 participants were included. Add-on antidepressants appeared more efficacious than controls for depressive symptoms (standardized mean difference: –0.25, 95% CI=–0.38 to –0.12), negative symptoms (standardized mean difference: –0.30, 95% CI=–0.44 to –0.16), overall symptoms (standardized mean difference: –0.24, 95% CI=–0.39 to –0.09), positive symptoms (standardized mean difference: –0.17, 95% CI=–0.33 to –0.01), quality of life (standardized mean difference: –0.32, 95% CI=–0.57 to –0.06), and responder rate (risk ratio: 1.52, 95% CI=1.29 to 1.78; number-needed-to-treat-to-benefit: 5, 95% CI=4 to 7). The effects on depressive and negative symptoms appeared more pronounced when minimum thresholds of these symptoms were inclusion criteria (standardized mean difference: –0.34, 95% CI=–0.58 to –0.09 and standardized mean difference: –0.58, 95% CI=–0.94 to –0.21, respectively). There were no significant differences between antidepressants and controls in terms of exacerbation of psychosis, premature discontinuation, and the number of participants with at least one adverse event. More patients taking add-on antidepressants suffered from abdominal pain, constipation, dizziness, and dry mouth.Conclusions:Analysis of primary outcomes (depressive and negative symptoms) suggests small, beneficial effects of adjunctive antidepressants. It would appear that this augmentation can be accomplished with a low risk of exacerbation of psychosis and adverse effects. However, secondary and subgroup analyses should be interpreted cautiously and considered exploratory.
doi_str_mv 10.1176/appi.ajp.2016.15081035
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Depressive and negative symptoms (primary outcomes), overall symptoms, positive symptoms, side effects, exacerbation of psychosis, and responder rates were examined. Subgroup, meta-regression, and sensitivity analyses were performed, as well as investigations of publication bias and risk of bias.Results:Eighty-two randomized controlled trials with a total of 3,608 participants were included. Add-on antidepressants appeared more efficacious than controls for depressive symptoms (standardized mean difference: –0.25, 95% CI=–0.38 to –0.12), negative symptoms (standardized mean difference: –0.30, 95% CI=–0.44 to –0.16), overall symptoms (standardized mean difference: –0.24, 95% CI=–0.39 to –0.09), positive symptoms (standardized mean difference: –0.17, 95% CI=–0.33 to –0.01), quality of life (standardized mean difference: –0.32, 95% CI=–0.57 to –0.06), and responder rate (risk ratio: 1.52, 95% CI=1.29 to 1.78; number-needed-to-treat-to-benefit: 5, 95% CI=4 to 7). The effects on depressive and negative symptoms appeared more pronounced when minimum thresholds of these symptoms were inclusion criteria (standardized mean difference: –0.34, 95% CI=–0.58 to –0.09 and standardized mean difference: –0.58, 95% CI=–0.94 to –0.21, respectively). There were no significant differences between antidepressants and controls in terms of exacerbation of psychosis, premature discontinuation, and the number of participants with at least one adverse event. More patients taking add-on antidepressants suffered from abdominal pain, constipation, dizziness, and dry mouth.Conclusions:Analysis of primary outcomes (depressive and negative symptoms) suggests small, beneficial effects of adjunctive antidepressants. It would appear that this augmentation can be accomplished with a low risk of exacerbation of psychosis and adverse effects. However, secondary and subgroup analyses should be interpreted cautiously and considered exploratory.</description><identifier>ISSN: 0002-953X</identifier><identifier>EISSN: 1535-7228</identifier><identifier>DOI: 10.1176/appi.ajp.2016.15081035</identifier><identifier>PMID: 27282362</identifier><identifier>CODEN: AJPSAO</identifier><language>eng</language><publisher>United States: American Psychiatric Association</publisher><subject>Antidepressants ; Antidepressive Agents - adverse effects ; Antidepressive Agents - therapeutic use ; Antipsychotic Agents - adverse effects ; Antipsychotic Agents - therapeutic use ; Depressive Disorder - diagnosis ; Depressive Disorder - drug therapy ; Depressive Disorder - psychology ; Drug Therapy, Combination ; Humans ; Mental depression ; Meta-analysis ; Psychiatric Status Rating Scales - statistics &amp; numerical data ; Psychometrics ; Randomized Controlled Trials as Topic ; Schizophrenia ; Schizophrenia - diagnosis ; Schizophrenia - drug therapy ; Schizophrenic Psychology ; Systematic review ; Treatment Outcome</subject><ispartof>The American journal of psychiatry, 2016-09, Vol.173 (9), p.876-886</ispartof><rights>Copyright © 2016 by the American Psychiatric Association 2016</rights><rights>Copyright American Psychiatric Publishing, Inc. 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The effects on depressive and negative symptoms appeared more pronounced when minimum thresholds of these symptoms were inclusion criteria (standardized mean difference: –0.34, 95% CI=–0.58 to –0.09 and standardized mean difference: –0.58, 95% CI=–0.94 to –0.21, respectively). There were no significant differences between antidepressants and controls in terms of exacerbation of psychosis, premature discontinuation, and the number of participants with at least one adverse event. More patients taking add-on antidepressants suffered from abdominal pain, constipation, dizziness, and dry mouth.Conclusions:Analysis of primary outcomes (depressive and negative symptoms) suggests small, beneficial effects of adjunctive antidepressants. It would appear that this augmentation can be accomplished with a low risk of exacerbation of psychosis and adverse effects. 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Helfer, Bartosz</au><au>Samara, Myrto T</au><au>Huhn, Maximilian</au><au>Klupp, Elisabeth</au><au>Leucht, Claudia</au><au>Zhu, Yikang</au><au>Engel, Rolf R</au><au>Leucht, Stefan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and Safety of Antidepressants Added to Antipsychotics for Schizophrenia: A Systematic Review and Meta-Analysis</atitle><jtitle>The American journal of psychiatry</jtitle><addtitle>Am J Psychiatry</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>173</volume><issue>9</issue><spage>876</spage><epage>886</epage><pages>876-886</pages><issn>0002-953X</issn><eissn>1535-7228</eissn><coden>AJPSAO</coden><abstract>Objective:The authors examined the safety and efficacy of antidepressants added to antipsychotic drugs in the treatment of schizophrenia.Method:Multiple databases and previous publications were searched through June 2015 to identify all randomized controlled trials of any add-on antidepressants compared with placebo or no-treatment in schizophrenia. Depressive and negative symptoms (primary outcomes), overall symptoms, positive symptoms, side effects, exacerbation of psychosis, and responder rates were examined. Subgroup, meta-regression, and sensitivity analyses were performed, as well as investigations of publication bias and risk of bias.Results:Eighty-two randomized controlled trials with a total of 3,608 participants were included. Add-on antidepressants appeared more efficacious than controls for depressive symptoms (standardized mean difference: –0.25, 95% CI=–0.38 to –0.12), negative symptoms (standardized mean difference: –0.30, 95% CI=–0.44 to –0.16), overall symptoms (standardized mean difference: –0.24, 95% CI=–0.39 to –0.09), positive symptoms (standardized mean difference: –0.17, 95% CI=–0.33 to –0.01), quality of life (standardized mean difference: –0.32, 95% CI=–0.57 to –0.06), and responder rate (risk ratio: 1.52, 95% CI=1.29 to 1.78; number-needed-to-treat-to-benefit: 5, 95% CI=4 to 7). The effects on depressive and negative symptoms appeared more pronounced when minimum thresholds of these symptoms were inclusion criteria (standardized mean difference: –0.34, 95% CI=–0.58 to –0.09 and standardized mean difference: –0.58, 95% CI=–0.94 to –0.21, respectively). There were no significant differences between antidepressants and controls in terms of exacerbation of psychosis, premature discontinuation, and the number of participants with at least one adverse event. More patients taking add-on antidepressants suffered from abdominal pain, constipation, dizziness, and dry mouth.Conclusions:Analysis of primary outcomes (depressive and negative symptoms) suggests small, beneficial effects of adjunctive antidepressants. It would appear that this augmentation can be accomplished with a low risk of exacerbation of psychosis and adverse effects. However, secondary and subgroup analyses should be interpreted cautiously and considered exploratory.</abstract><cop>United States</cop><pub>American Psychiatric Association</pub><pmid>27282362</pmid><doi>10.1176/appi.ajp.2016.15081035</doi><tpages>11</tpages></addata></record>
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subjects Antidepressants
Antidepressive Agents - adverse effects
Antidepressive Agents - therapeutic use
Antipsychotic Agents - adverse effects
Antipsychotic Agents - therapeutic use
Depressive Disorder - diagnosis
Depressive Disorder - drug therapy
Depressive Disorder - psychology
Drug Therapy, Combination
Humans
Mental depression
Meta-analysis
Psychiatric Status Rating Scales - statistics & numerical data
Psychometrics
Randomized Controlled Trials as Topic
Schizophrenia
Schizophrenia - diagnosis
Schizophrenia - drug therapy
Schizophrenic Psychology
Systematic review
Treatment Outcome
title Efficacy and Safety of Antidepressants Added to Antipsychotics for Schizophrenia: A Systematic Review and Meta-Analysis
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