Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-25T22:48:51.934Z Has data issue: false hasContentIssue false

Unmet Needs in the Management of Major Depressive Disorder

Published online by Cambridge University Press:  07 November 2014

Extract

For most patients with major depressive disorder (MDD) the first-line treatment is one of the selective serotonin reuptake inhibitors (SSRIs). However, some practitioners prefer to utilize a serotonin norepinephrine reuptake inhibitor (SNRI) or the norepinephrine-dopamine reuptake inhibitor bupropion as their first-line antidepressant treatments (Slide 1). Differences of opinion regarding first, second, or third choice of antidepressant often stem from regional practices or individual training.

A basic standard of practice in MDD treatment is to initiate monotherapy trials with several first-line choices of antidepressants before moving on to alternate strategies. This basic strategy was evaluated in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study. Only approximately one third of the patients remitted after being treated with the study's first-line treatment, a 12-week trial of citalopram in doses up to 60 mg/day. As in other contemporary treatment studies, remission was defined as virtually complete relief of depressive symptoms. This is defined as a Hamilton Rating Scale for Depression score of ≤7 or a score of ≤5 on the self-report version of the Quick Inventory of Depressive Symptomatology.

For those who did not obtain an adequate response to the initial course of citalopram therapy, the STAR*D study compared several alternate treatments, including switching to another antidepressant, adjunctive therapy with another type of medication (ie, a medication that is not an antidepressant), or combination treatment (ie, adding another antidepressant). At the end of four sequential treatment trials, only approximately two thirds of the patients remitted. Of those, 40% to 70% relapsed within the next year despite continued therapy.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Kennedy, SH, Lam, RW, Cohen, NL, Ravindran, AV; CANMAT Depression Work Group. Clinical guidelines for the treatment of depressive disorders. IV. Medications and other biological treatments. Can J Psychiatry. 2001;46(Suppl 1):38S58S.Google Scholar
2.Bauer, M, Bschor, T, Pfennig, A, et al.World Federation of Societies of Biological Psychiatry (WFSBP) Guidelines for Biological Treatment of Unipolar Depressive Disorders in Primary Care. World J Biol Psychiatry. 2007;8(2):67104.CrossRefGoogle ScholarPubMed
3.Fava, M, Rush, AJ, Trivedi, MH, et al.Background and rationale for the sequenced treatment alternatives to relieve depression (STAR*D) study. Psychiatr Clin North Am. 2003;26(2):457494.CrossRefGoogle ScholarPubMed
4.Fleck, MP, Horwath, E. Pharmacologic management of difficult-to-treat depression in clinical practice. Psychiatr Serv. 2005;56(8):10051011.CrossRefGoogle ScholarPubMed
5.Dodd, S, Horgan, D, Malhi, GS, Berk, M. To combine or not to combine? A literature review of antidepressant combination therapy. J Affect Disord. 2005;89(1–3):111.CrossRefGoogle ScholarPubMed
6.Rush, AJ, Trivedi, MH, Wisniewski, SR, et al.Bupropion-SR, sertraline, or venlafaxine-XR after failure of SSRIs for depression. N Engl J Med. 2006;354(12):12311242.CrossRefGoogle ScholarPubMed
7.Trivedi, MH, Rush, AJ, Wisniewski, SR, et al.Evaluation of outcomes with citalopram for depression using measurement-based care in STAR*D: implications for clinical practice. Am J Psychiatry. 2006;163(1):2840.CrossRefGoogle ScholarPubMed
8.Papakostas, GI, Fava, M, Thase, ME. Treatment of SSRI-resistant depression: a meta-analysis comparing within-versus across-class switches. Biol Psychiatry. 2008;63(7):699704.CrossRefGoogle ScholarPubMed
9.Thase, ME, Rush, AJ, Howland, RH, et al.Double-blind switch study of imipramine or sertraline treatment of antidepressant-resistant chronic depression. Arch Gen Psychiatry. 2002;59(3):233239.CrossRefGoogle ScholarPubMed
10.Thase, ME, Shelton, RC, Khan, A. Treatment with venlafaxine extended release after SSRI nonresponse or intolerance: a randomized comparison of standard- and higher-dosing strategies. J Clin Psychopharmacol. 2006;26(3):250258.CrossRefGoogle ScholarPubMed
11.Trivedi, MH, Fava, M, Wisniewski, SR, et al.Medication augmentation after the failure of SSRIs for depression. N Engl J Med. 2006;354(12):12431252.CrossRefGoogle ScholarPubMed
12.Mojtabai, R, Olfson, M. National trends in psychotherapy by office-based psychiatrists. Arch Gen Psychiatry. 2008;65(8):962970.CrossRefGoogle ScholarPubMed
13.Olfson, M, Marcus, SC. National patterns in antidepressant medication treatment. Arch Gen Psychiatry. 2009;66(8):848856.CrossRefGoogle ScholarPubMed
14.Crisp, AH, Gelder, MG, Rix, S, et al.Stigmatization of people with mental illnesses. Br J Psychiatry. 2000;177:47.CrossRefGoogle ScholarPubMed
15.Seligman, MEP. The effectiveness of psychotherapy. The Consumer Reports study. American Psychologist. 1995;50:965974.CrossRefGoogle ScholarPubMed
16.Thase, ME, Friedman, ES, Biggs, MM, et al.Cognitive therapy versus medication in augmentation and switch strategies as second-step treatments: a STAR*D report. Am J Psychiatry. 2007;164(5):739752.CrossRefGoogle ScholarPubMed
17.De Jonghe, F, Kool, S, van Aalst, G, Dekker, J, Peen, J. Combining psychotherapy and antidepressants in the treatment of depression. J Affect Disord. 2001;64(2–3):217229.CrossRefGoogle ScholarPubMed
18.Keller, MB, McCullough, JP, Klein, DN, et al.A comparison of nefazodone, the cognitive behavioral-analysis system of psychotherapy, and their combination for the treatment of chronic depression. New Eng J Med. 2000;342(20):14621470.CrossRefGoogle ScholarPubMed