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Two-Year Outcome of Psychotic Depression in Late Life
OBJECTIVE: The purpose of this study was to determine whether elderly patients with psychotic depression differed in long-term outcome from patients with nonpsychotic depression. METHOD: The study group consisted of 19 patients with psychotic major depression who had responded to ECT (N=15), nortrip...
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Published in: | The American journal of psychiatry 1998-02, Vol.155 (2), p.178-183 |
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description | OBJECTIVE: The purpose of this study was to determine whether elderly patients with psychotic depression differed in long-term outcome from patients with nonpsychotic depression. METHOD: The study group consisted of 19 patients with psychotic major depression who had responded to ECT (N=15), nortriptyline and perphenazine (N=2), or nortriptyline, perphenazine, and adjunctive lithium (N=2) and 68 nonpsychotic depressed patients who had responded to either nortriptyline alone (N=61) or nortriptyline and lithium (N=7). All patients were maintained on regimens of full-dose nortriptyline. When prescribed for the index episode, adjunctive lithium was also maintained, but perphenazine was withdrawn 16 weeks after response. Patients were followed on a monthly basis for 2 years or until relapse or recurrence, whichever occurred first. RESULTS: Patients with psychotic depression had a substantially higher frequency of relapse or recurrence of depression and a shorter time to these events than nonpsychotic depressed patients. At index assessment, patients with psychosis were more severely depressed and had had more prior episodes of depression, but these factors did not account for the difference in outcome between the two groups. Furthermore, before entering the study, none of the psychotic patients had received adequate treatment for the index episode of depression, and so their poor outcome could not be attributed to prior treatment resistance. CONCLUSIONS: Even when they achieved remission and were maintained on a regimen of full-dose antidepressant medication, older patients with psychotic depression were at greater risk of relapse or recurrence than were their nonpsychotic counterparts. In particular, continuation/maintenance treatment with tricyclic monotherapy following response to ECT had limited efficacy in this group of patients. These findings raise important questions about the optimal treatment of psychotic depression in late life. (Am J Psychiatry 1998; 155:178-183) |
doi_str_mv | 10.1176/ajp.155.2.178 |
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METHOD: The study group consisted of 19 patients with psychotic major depression who had responded to ECT (N=15), nortriptyline and perphenazine (N=2), or nortriptyline, perphenazine, and adjunctive lithium (N=2) and 68 nonpsychotic depressed patients who had responded to either nortriptyline alone (N=61) or nortriptyline and lithium (N=7). All patients were maintained on regimens of full-dose nortriptyline. When prescribed for the index episode, adjunctive lithium was also maintained, but perphenazine was withdrawn 16 weeks after response. Patients were followed on a monthly basis for 2 years or until relapse or recurrence, whichever occurred first. RESULTS: Patients with psychotic depression had a substantially higher frequency of relapse or recurrence of depression and a shorter time to these events than nonpsychotic depressed patients. At index assessment, patients with psychosis were more severely depressed and had had more prior episodes of depression, but these factors did not account for the difference in outcome between the two groups. Furthermore, before entering the study, none of the psychotic patients had received adequate treatment for the index episode of depression, and so their poor outcome could not be attributed to prior treatment resistance. CONCLUSIONS: Even when they achieved remission and were maintained on a regimen of full-dose antidepressant medication, older patients with psychotic depression were at greater risk of relapse or recurrence than were their nonpsychotic counterparts. In particular, continuation/maintenance treatment with tricyclic monotherapy following response to ECT had limited efficacy in this group of patients. These findings raise important questions about the optimal treatment of psychotic depression in late life. (Am J Psychiatry 1998; 155:178-183)</description><identifier>ISSN: 0002-953X</identifier><identifier>EISSN: 1535-7228</identifier><identifier>DOI: 10.1176/ajp.155.2.178</identifier><identifier>PMID: 9464195</identifier><identifier>CODEN: AJPSAO</identifier><language>eng</language><publisher>Washington, DC: American Psychiatric Publishing</publisher><subject>Age Factors ; Aged ; Antidepressive Agents - therapeutic use ; Antidepressive Agents, Tricyclic - therapeutic use ; Biological and medical sciences ; Combined Modality Therapy ; Delusions - diagnosis ; Delusions - therapy ; Depressive Disorder - diagnosis ; Depressive Disorder - drug therapy ; Depressive Disorder - therapy ; Drug Therapy, Combination ; Electroconvulsive Therapy ; Female ; Follow-Up Studies ; Geriatric Assessment ; Geriatrics ; Hallucinations - diagnosis ; Hallucinations - therapy ; Humans ; Lithium - therapeutic use ; Male ; Medical sciences ; Mental depression ; Middle Aged ; Older people ; Outcomes ; Psychiatric Status Rating Scales - statistics & numerical data ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychotic mood disorders ; Recurrence ; Severity of Illness Index ; Survival Analysis ; Time Factors ; Treatment ; Treatment Outcome</subject><ispartof>The American journal of psychiatry, 1998-02, Vol.155 (2), p.178-183</ispartof><rights>1998 INIST-CNRS</rights><rights>Copyright American Psychiatric Association Feb 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a438t-57127bdf6e81eb810a230df4ec564d2984cc6ad88c568dd3f143e123b65d1ece3</citedby><cites>FETCH-LOGICAL-a438t-57127bdf6e81eb810a230df4ec564d2984cc6ad88c568dd3f143e123b65d1ece3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://psychiatryonline.org/doi/epdf/10.1176/ajp.155.2.178$$EPDF$$P50$$Gappi$$H</linktopdf><linktohtml>$$Uhttps://psychiatryonline.org/doi/full/10.1176/ajp.155.2.178$$EHTML$$P50$$Gappi$$H</linktohtml><link.rule.ids>314,780,784,2855,21626,21627,21628,27924,27925,31000,77794,77799</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2160526$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9464195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Flint, Alastair J.</creatorcontrib><creatorcontrib>Rifat, Sandra L.</creatorcontrib><title>Two-Year Outcome of Psychotic Depression in Late Life</title><title>The American journal of psychiatry</title><addtitle>Am J Psychiatry</addtitle><description>OBJECTIVE: The purpose of this study was to determine whether elderly patients with psychotic depression differed in long-term outcome from patients with nonpsychotic depression. METHOD: The study group consisted of 19 patients with psychotic major depression who had responded to ECT (N=15), nortriptyline and perphenazine (N=2), or nortriptyline, perphenazine, and adjunctive lithium (N=2) and 68 nonpsychotic depressed patients who had responded to either nortriptyline alone (N=61) or nortriptyline and lithium (N=7). All patients were maintained on regimens of full-dose nortriptyline. When prescribed for the index episode, adjunctive lithium was also maintained, but perphenazine was withdrawn 16 weeks after response. Patients were followed on a monthly basis for 2 years or until relapse or recurrence, whichever occurred first. RESULTS: Patients with psychotic depression had a substantially higher frequency of relapse or recurrence of depression and a shorter time to these events than nonpsychotic depressed patients. At index assessment, patients with psychosis were more severely depressed and had had more prior episodes of depression, but these factors did not account for the difference in outcome between the two groups. Furthermore, before entering the study, none of the psychotic patients had received adequate treatment for the index episode of depression, and so their poor outcome could not be attributed to prior treatment resistance. CONCLUSIONS: Even when they achieved remission and were maintained on a regimen of full-dose antidepressant medication, older patients with psychotic depression were at greater risk of relapse or recurrence than were their nonpsychotic counterparts. In particular, continuation/maintenance treatment with tricyclic monotherapy following response to ECT had limited efficacy in this group of patients. These findings raise important questions about the optimal treatment of psychotic depression in late life. (Am J Psychiatry 1998; 155:178-183)</description><subject>Age Factors</subject><subject>Aged</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Antidepressive Agents, Tricyclic - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Combined Modality Therapy</subject><subject>Delusions - diagnosis</subject><subject>Delusions - therapy</subject><subject>Depressive Disorder - diagnosis</subject><subject>Depressive Disorder - drug therapy</subject><subject>Depressive Disorder - therapy</subject><subject>Drug Therapy, Combination</subject><subject>Electroconvulsive Therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Geriatric Assessment</subject><subject>Geriatrics</subject><subject>Hallucinations - diagnosis</subject><subject>Hallucinations - therapy</subject><subject>Humans</subject><subject>Lithium - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mental depression</subject><subject>Middle Aged</subject><subject>Older people</subject><subject>Outcomes</subject><subject>Psychiatric Status Rating Scales - statistics & numerical data</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychotic mood disorders</subject><subject>Recurrence</subject><subject>Severity of Illness Index</subject><subject>Survival Analysis</subject><subject>Time Factors</subject><subject>Treatment</subject><subject>Treatment Outcome</subject><issn>0002-953X</issn><issn>1535-7228</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><recordid>eNqF0c9LHDEUB_Agiq7Wo8fCoNKDMNu8_J6jrG0tLNjDFtpTyGbe0Fl2J2Myg_jfm7LLIqXiKTzeJy8_voRcAJ0CaPXZrfopSDllU9DmgExAcllqxswhmVBKWVlJ_uuEnKa0yiXlmh2T40ooAZWcELl4CuVvdLF4GAcfNliEpviRnv2fMLS-uMM-Ykpt6Iq2K-ZuwGLeNviBHDVunfB8t56Rn1-_LGb35fzh2_fZ7bx0gpuhlBqYXtaNQgO4NEAd47RuBHqpRM0qI7xXrjYm16aueQOCIzC-VLIG9MjPyKft3D6GxxHTYDdt8rheuw7DmKyulOHK0Heh1EIbI0SGl__AVRhjlx9hGaNCU0Z5RldvIZBguMkfr7Mqt8rHkFLExvax3bj4bIHav9HYHE3eIC2zOZrsP-6mjssN1nu9yyL3r3d9l7xbN9F1vk17xkBRyVRmN1vm-r59dbH_nvkCGw6gzg</recordid><startdate>19980201</startdate><enddate>19980201</enddate><creator>Flint, Alastair J.</creator><creator>Rifat, Sandra L.</creator><general>American Psychiatric Publishing</general><general>American Psychiatric Association</general><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>HAWNG</scope><scope>HBMBR</scope><scope>IBDFT</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7QJ</scope><scope>7X8</scope></search><sort><creationdate>19980201</creationdate><title>Two-Year Outcome of Psychotic Depression in Late Life</title><author>Flint, Alastair J. ; Rifat, Sandra L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a438t-57127bdf6e81eb810a230df4ec564d2984cc6ad88c568dd3f143e123b65d1ece3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Age Factors</topic><topic>Aged</topic><topic>Antidepressive Agents - therapeutic use</topic><topic>Antidepressive Agents, Tricyclic - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Combined Modality Therapy</topic><topic>Delusions - diagnosis</topic><topic>Delusions - therapy</topic><topic>Depressive Disorder - diagnosis</topic><topic>Depressive Disorder - drug therapy</topic><topic>Depressive Disorder - therapy</topic><topic>Drug Therapy, Combination</topic><topic>Electroconvulsive Therapy</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Geriatric Assessment</topic><topic>Geriatrics</topic><topic>Hallucinations - diagnosis</topic><topic>Hallucinations - therapy</topic><topic>Humans</topic><topic>Lithium - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mental depression</topic><topic>Middle Aged</topic><topic>Older people</topic><topic>Outcomes</topic><topic>Psychiatric Status Rating Scales - statistics & numerical data</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychotic mood disorders</topic><topic>Recurrence</topic><topic>Severity of Illness Index</topic><topic>Survival Analysis</topic><topic>Time Factors</topic><topic>Treatment</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Flint, Alastair J.</creatorcontrib><creatorcontrib>Rifat, Sandra L.</creatorcontrib><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>Periodicals Index Online Segment 13</collection><collection>Periodicals Index Online Segment 14</collection><collection>Periodicals Index Online Segment 27</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</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>Flint, Alastair J.</au><au>Rifat, Sandra L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two-Year Outcome of Psychotic Depression in Late Life</atitle><jtitle>The American journal of psychiatry</jtitle><addtitle>Am J Psychiatry</addtitle><date>1998-02-01</date><risdate>1998</risdate><volume>155</volume><issue>2</issue><spage>178</spage><epage>183</epage><pages>178-183</pages><issn>0002-953X</issn><eissn>1535-7228</eissn><coden>AJPSAO</coden><abstract>OBJECTIVE: The purpose of this study was to determine whether elderly patients with psychotic depression differed in long-term outcome from patients with nonpsychotic depression. METHOD: The study group consisted of 19 patients with psychotic major depression who had responded to ECT (N=15), nortriptyline and perphenazine (N=2), or nortriptyline, perphenazine, and adjunctive lithium (N=2) and 68 nonpsychotic depressed patients who had responded to either nortriptyline alone (N=61) or nortriptyline and lithium (N=7). All patients were maintained on regimens of full-dose nortriptyline. When prescribed for the index episode, adjunctive lithium was also maintained, but perphenazine was withdrawn 16 weeks after response. Patients were followed on a monthly basis for 2 years or until relapse or recurrence, whichever occurred first. RESULTS: Patients with psychotic depression had a substantially higher frequency of relapse or recurrence of depression and a shorter time to these events than nonpsychotic depressed patients. At index assessment, patients with psychosis were more severely depressed and had had more prior episodes of depression, but these factors did not account for the difference in outcome between the two groups. Furthermore, before entering the study, none of the psychotic patients had received adequate treatment for the index episode of depression, and so their poor outcome could not be attributed to prior treatment resistance. CONCLUSIONS: Even when they achieved remission and were maintained on a regimen of full-dose antidepressant medication, older patients with psychotic depression were at greater risk of relapse or recurrence than were their nonpsychotic counterparts. In particular, continuation/maintenance treatment with tricyclic monotherapy following response to ECT had limited efficacy in this group of patients. These findings raise important questions about the optimal treatment of psychotic depression in late life. (Am J Psychiatry 1998; 155:178-183)</abstract><cop>Washington, DC</cop><pub>American Psychiatric Publishing</pub><pmid>9464195</pmid><doi>10.1176/ajp.155.2.178</doi><tpages>6</tpages></addata></record> |
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subjects | Age Factors Aged Antidepressive Agents - therapeutic use Antidepressive Agents, Tricyclic - therapeutic use Biological and medical sciences Combined Modality Therapy Delusions - diagnosis Delusions - therapy Depressive Disorder - diagnosis Depressive Disorder - drug therapy Depressive Disorder - therapy Drug Therapy, Combination Electroconvulsive Therapy Female Follow-Up Studies Geriatric Assessment Geriatrics Hallucinations - diagnosis Hallucinations - therapy Humans Lithium - therapeutic use Male Medical sciences Mental depression Middle Aged Older people Outcomes Psychiatric Status Rating Scales - statistics & numerical data Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychotic mood disorders Recurrence Severity of Illness Index Survival Analysis Time Factors Treatment Treatment Outcome |
title | Two-Year Outcome of Psychotic Depression in Late Life |
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