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Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder
BACKGROUND: Duloxetine and venlafaxine extended release (venlafaxine XR) are SNRIs indicated for the treatment of MDD. This study addresses whether duloxetine and venlafaxine XR are interchangeable in their patterns of use with patients who are depressed or are used more selectively based on treatme...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044657/ https://www.ncbi.nlm.nih.gov/pubmed/21281479 http://dx.doi.org/10.1186/1471-244X-11-19 |
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author | Ye, Wenyu Zhao, Yang Robinson, Rebecca L Swindle, Ralph W |
author_facet | Ye, Wenyu Zhao, Yang Robinson, Rebecca L Swindle, Ralph W |
author_sort | Ye, Wenyu |
collection | PubMed |
description | BACKGROUND: Duloxetine and venlafaxine extended release (venlafaxine XR) are SNRIs indicated for the treatment of MDD. This study addresses whether duloxetine and venlafaxine XR are interchangeable in their patterns of use with patients who are depressed or are used more selectively based on treatment history, background characteristics, and presenting symptoms. METHODS: This was a retrospective analysis of an administrative insurance claims database. We studied patients in managed care with major depressive disorder (MDD) treated with duloxetine or venlafaxine XR. Predictors of treatment and cost were assessed using Chi-square and logistic regression analyses of demographics and past-year medication use and comorbidities. RESULTS: Patients with MDD treated with duloxetine (n = 9,641) versus venlafaxine XR (n = 8,514) tended to be older, slightly more likely to be female, and treated by a psychiatrist (P < 0.0001). In the prior year, more duloxetine patients (vs. venlafaxine XR) received ≥3 unique antidepressants (20.8% vs. 16.6%), ≥3 unique pain medications (25.5% vs. 15.6%), and had ≥8 unique diagnosed comorbid medical and psychiatric conditions (38.6% vs. 29.1%). The prior 6-month total health care costs were $1,731 higher for duloxetine than for venlafaxine XR and declined for both medications in the 6 months after treatment began. Logistic regression analysis revealed that 61% of duloxetine patients and 61% of venlafaxine XR patients were predictable from prior patient and treatment factors. CONCLUSIONS: Patients with MDD treated with duloxetine tended to have a more complex and costly antecedent clinical presentation compared with venlafaxine XR patients, suggesting that physicians do not use the medications interchangeably. |
format | Text |
id | pubmed-3044657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30446572011-02-25 Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder Ye, Wenyu Zhao, Yang Robinson, Rebecca L Swindle, Ralph W BMC Psychiatry Research Article BACKGROUND: Duloxetine and venlafaxine extended release (venlafaxine XR) are SNRIs indicated for the treatment of MDD. This study addresses whether duloxetine and venlafaxine XR are interchangeable in their patterns of use with patients who are depressed or are used more selectively based on treatment history, background characteristics, and presenting symptoms. METHODS: This was a retrospective analysis of an administrative insurance claims database. We studied patients in managed care with major depressive disorder (MDD) treated with duloxetine or venlafaxine XR. Predictors of treatment and cost were assessed using Chi-square and logistic regression analyses of demographics and past-year medication use and comorbidities. RESULTS: Patients with MDD treated with duloxetine (n = 9,641) versus venlafaxine XR (n = 8,514) tended to be older, slightly more likely to be female, and treated by a psychiatrist (P < 0.0001). In the prior year, more duloxetine patients (vs. venlafaxine XR) received ≥3 unique antidepressants (20.8% vs. 16.6%), ≥3 unique pain medications (25.5% vs. 15.6%), and had ≥8 unique diagnosed comorbid medical and psychiatric conditions (38.6% vs. 29.1%). The prior 6-month total health care costs were $1,731 higher for duloxetine than for venlafaxine XR and declined for both medications in the 6 months after treatment began. Logistic regression analysis revealed that 61% of duloxetine patients and 61% of venlafaxine XR patients were predictable from prior patient and treatment factors. CONCLUSIONS: Patients with MDD treated with duloxetine tended to have a more complex and costly antecedent clinical presentation compared with venlafaxine XR patients, suggesting that physicians do not use the medications interchangeably. BioMed Central 2011-01-31 /pmc/articles/PMC3044657/ /pubmed/21281479 http://dx.doi.org/10.1186/1471-244X-11-19 Text en Copyright ©2011 Ye et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ye, Wenyu Zhao, Yang Robinson, Rebecca L Swindle, Ralph W Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder |
title | Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder |
title_full | Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder |
title_fullStr | Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder |
title_full_unstemmed | Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder |
title_short | Treatment patterns associated with Duloxetine and Venlafaxine use for Major Depressive Disorder |
title_sort | treatment patterns associated with duloxetine and venlafaxine use for major depressive disorder |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044657/ https://www.ncbi.nlm.nih.gov/pubmed/21281479 http://dx.doi.org/10.1186/1471-244X-11-19 |
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