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    Antidepressant Augmentation versus Switch in Treatment-Resistant Geriatric Depression

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    Author
    Lenze, E.J.
    Mulsant, B.H.
    Roose, S.P.
    Lavretsky, H.
    Reynolds, C.F.
    Blumberger, D.M.
    Brown, P.J.
    Cristancho, P.
    Flint, A.J.
    Gebara, M.A.
    Gettinger, T.R.
    Lenard, E.
    Miller, J.P.
    Nicol, G.E.
    Oughli, H.A.
    Pham, V.T.
    Rollman, B.L.
    Yang, L.
    Karp, J.F.
    Show allShow less
    Affiliation
    Department of Psychiatry, College of Medicine, University of Arizona
    Issue Date
    2023-03-03
    Keywords
    Clinical Medicine
    Clinical Medicine General
    Depression
    Geriatrics/Aging
    Geriatrics/Aging General
    Neurology/Neurosurgery
    Neurology/Neurosurgery General
    Psychiatry
    
    Metadata
    Show full item record
    Publisher
    Massachussetts Medical Society
    Citation
    Lenze, E. J., Mulsant, B. H., Roose, S. P., Lavretsky, H., Reynolds III, C. F., Blumberger, D. M., ... & Karp, J. F. (2023). Antidepressant augmentation versus switch in treatment-resistant geriatric depression. New England Journal of Medicine, 388(12), 1067-1079.
    Journal
    New England Journal of Medicine
    Rights
    © 2023 Massachusetts Medical Society. All rights reserved.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Background: The benefits and risks of augmenting or switching antidepressants in older adults with treatment-resistant depression have not been extensively studied. Methods: We conducted a two-step, open-label trial involving adults 60 years of age or older with treatment-resistant depression. In step 1, patients were randomly assigned in a 1:1:1 ratio to augmentation of existing antidepressant medication with aripiprazole, augmentation with bupropion, or a switch from existing antidepressant medication to bupropion. Patients who did not benefit from or were ineligible for step 1 were randomly assigned in step 2 in a 1:1 ratio to augmentation with lithium or a switch to nortriptyline. Each step lasted approximately 10 weeks. The primary outcome was the change from baseline in psychological well-being, assessed with the National Institutes of Health Toolbox Positive Affect and General Life Satisfaction subscales (population mean, 50; higher scores indicate greater well-being). A secondary outcome was remission of depression. Results: In step 1, a total of 619 patients were enrolled; 211 were assigned to aripiprazole augmentation, 206 to bupropion augmentation, and 202 to a switch to bupropion. Well-being scores improved by 4.83 points, 4.33 points, and 2.04 points, respectively. The difference between the aripiprazole-augmentation group and the switch-to-bupropion group was 2.79 points (95% CI, 0.56 to 5.02; P=0.014, with a prespecified threshold P value of 0.017); the between-group differences were not significant for aripiprazole augmentation versus bupropion augmentation or for bupropion augmentation versus a switch to bupropion. Remission occurred in 28.9% of patients in the aripiprazole-augmentation group, 28.2% in the bupropion-augmentation group, and 19.3% in the switch-to-bupropion group. The rate of falls was highest with bupropion augmentation. In step 2, a total of 248 patients were enrolled; 127 were assigned to lithium augmentation and 121 to a switch to nortriptyline. Well-being scores improved by 3.17 points and 2.18 points, respectively (difference, 0.99; 95% CI, -1.92 to 3.91). Remission occurred in 18.9% of patients in the lithium-augmentation group and 21.5% in the switch-to-nortriptyline group; rates of falling were similar in the two groups. Conclusions: In older adults with treatment-resistant depression, augmentation of existing antidepressants with aripiprazole improved well-being significantly more over 10 weeks than a switch to bupropion and was associated with a numerically higher incidence of remission. Among patients in whom augmentation or a switch to bupropion failed, changes in well-being and the occurrence of remission with lithium augmentation or a switch to nortriptyline were similar. © 2023 Massachusetts Medical Society.
    Note
    6 month embargo; first published 03 March 2023
    ISSN
    0028-4793
    PubMed ID
    36867173
    DOI
    10.1056/NEJMoa2204462
    Version
    Final Published Version
    ae974a485f413a2113503eed53cd6c53
    10.1056/NEJMoa2204462
    Scopus Count
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    UA Faculty Publications

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