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dc.contributor.authorAndreescu, Carmen
dc.contributor.authorMulsant, Benoit H.
dc.contributor.authorPeasley-Miklus, Catherine
dc.contributor.authorRothschild, Anthony J.
dc.contributor.authorFlint, Alastair J.
dc.contributor.authorHeo, Moonseong
dc.contributor.authorCaswell, Melynda
dc.contributor.authorWhyte, Ellen M.
dc.contributor.authorMeyers, Barnett S.
dc.date2022-08-11T08:10:29.000
dc.date.accessioned2022-08-23T17:10:44Z
dc.date.available2022-08-23T17:10:44Z
dc.date.issued2007-03-06
dc.date.submitted2010-05-05
dc.identifier.citationJ Clin Psychiatry. 2007 Feb;68(2):194-200.
dc.identifier.issn0160-6689 (Linking)
dc.identifier.pmid17335316
dc.identifier.urihttp://hdl.handle.net/20.500.14038/46112
dc.description.abstractOBJECTIVE: Practice guidelines recommend the use of a combination of an antidepressant and an antipsychotic for the pharmacologic treatment of major depressive disorder with psychotic features (MD-Psy). We assessed the extent to which the pharmacotherapy received by patients with MD-Psy under usual care conforms to these recommendations. METHOD: We assessed the pharmacotherapy received under usual care conditions by 100 patients with MD-Psy prior to enrollment in STOP-PD (Study of the Pharmacotherapy of Psychotic Depression), a 12-week randomized, controlled trial comparing olanzapine plus sertraline to olanzapine plus placebo. Our assessment took place from January 2003 to May 2004. The strength of antidepressant trials was rated using the Antidepressant Treatment History Form (ATHF). The strength of antipsychotic trials or combinations of antidepressants and antipsychotics was rated using a modified version of the ATHF. We also determined whether the strength of antipsychotic or combination trials was associated with age, the duration of the current depressive episode, medical burden, cognitive status, or the severity of depressive or psychotic symptoms. RESULTS: Most patients with MD-Psy were treated with antidepressants (N = 82, 82%) or antipsychotics (N = 65, 65%). About half of the patients (N = 48, 48%) received therapeutic doses of an antidepressant; 10% (N = 10) received an intermediate dose of an antipsychotic, and 6% (N = 6) received a high dose. Overall, only 5% (N = 5) received a combination of an adequate dose of an antidepressant and a high dose of an antipsychotic. The strength of both antipsychotic trials (p = .021) and combination trials (p = .039) was significantly associated only with a longer duration of the current depressive episode. CONCLUSIONS: These findings show a persisting low use of antipsychotics in the treatment of MD-Psy. Given the high morbidity rates associated with MD-Psy, it is important to continue to educate clinicians regarding its identification and treatment. CLINICAL TRIALS REGISTRATION: ClinicalTrials.gov identifier NCT00056472.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=17335316&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.psychiatrist.com/privatepdf/2007/v68n02/v68n0203.pdf
dc.subjectAdult
dc.subjectAged
dc.subjectAntidepressive Agents
dc.subjectAntipsychotic Agents
dc.subjectClinical Trials as Topic
dc.subjectDepressive Disorder, Major
dc.subjectFemale
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectPhysician's Practice Patterns
dc.subjectPrognosis
dc.subjectPsychotic Disorders
dc.subjectTreatment Outcome
dc.subjectPsychiatry
dc.titlePersisting low use of antipsychotics in the treatment of major depressive disorder with psychotic features
dc.typeJournal Article
dc.source.journaltitleThe Journal of clinical psychiatry
dc.source.volume68
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/psych_pp/65
dc.identifier.contextkey1299412
html.description.abstract<p>OBJECTIVE: Practice guidelines recommend the use of a combination of an antidepressant and an antipsychotic for the pharmacologic treatment of major depressive disorder with psychotic features (MD-Psy). We assessed the extent to which the pharmacotherapy received by patients with MD-Psy under usual care conforms to these recommendations.</p> <p>METHOD: We assessed the pharmacotherapy received under usual care conditions by 100 patients with MD-Psy prior to enrollment in STOP-PD (Study of the Pharmacotherapy of Psychotic Depression), a 12-week randomized, controlled trial comparing olanzapine plus sertraline to olanzapine plus placebo. Our assessment took place from January 2003 to May 2004. The strength of antidepressant trials was rated using the Antidepressant Treatment History Form (ATHF). The strength of antipsychotic trials or combinations of antidepressants and antipsychotics was rated using a modified version of the ATHF. We also determined whether the strength of antipsychotic or combination trials was associated with age, the duration of the current depressive episode, medical burden, cognitive status, or the severity of depressive or psychotic symptoms.</p> <p>RESULTS: Most patients with MD-Psy were treated with antidepressants (N = 82, 82%) or antipsychotics (N = 65, 65%). About half of the patients (N = 48, 48%) received therapeutic doses of an antidepressant; 10% (N = 10) received an intermediate dose of an antipsychotic, and 6% (N = 6) received a high dose. Overall, only 5% (N = 5) received a combination of an adequate dose of an antidepressant and a high dose of an antipsychotic. The strength of both antipsychotic trials (p = .021) and combination trials (p = .039) was significantly associated only with a longer duration of the current depressive episode.</p> <p>CONCLUSIONS: These findings show a persisting low use of antipsychotics in the treatment of MD-Psy. Given the high morbidity rates associated with MD-Psy, it is important to continue to educate clinicians regarding its identification and treatment.</p> <p>CLINICAL TRIALS REGISTRATION: ClinicalTrials.gov identifier NCT00056472.</p>
dc.identifier.submissionpathpsych_pp/65
dc.contributor.departmentDepartment of Psychiatry
dc.source.pages194-200


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