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Trends in Managed Behavioral Healthcare: A Focus on Improving Depression Outcomes
Volume 13
Issue 4 Suppl

Depression: The Benefits of Early and Appropriate Treatment

Author(s):

Depression has a profound impact on patient health, individual and family quality of life, activities of daily living, and daily functioning, as well as on healthcare providers, payers, and employers. Persons with depression tend to have multiple comorbidities that compound the negative effects and increase costs. The economic burden of the disease is significant, with direct medical costs estimated at $3.5 million per 1000 plan members with depression. Depression is significantly underdiagnosed and undertreated, particularly in primary care where the majority of patients with depression seek care. Effective strategies to achieve remission have been identified and have proven effective in clinical trials. Early detection, intervention, and appropriate treatment can promote remission, prevent relapse, and reduce the emotional and financial burden of the disease.

(Am J Manag Care. 2007;13:S92-S97)

Burden of Depression

Usual care for depression typically consists of a prescribed antidepressant, psychotherapy, or both. However, mental health specialists encourage earlier and more aggressive therapy to help increase the likelihood of achieving remission and therefore lead to a lower overall cost of care. Accepted clinical practice guidelines state that patients with depression should progress through 3 phases of antidepressant medication treatment (ie, acute, continuation, maintenance), culminating in remission characterized

depressive symptoms through medication or psychotherapy, eventually culminating in remission or absence of all residual symptoms. The recommended acute phase of treatment generally lasts a minimum of 6 to 12 weeks.20 It is important to note that if symptoms improve during this period but do not return to normal functional levels, the course of therapy should be modified toward aggressive measures (ie, maximum dosing of the primary agent) in an attempt to achieve remission.19 Patients with residual symptoms at the end of the acute phase have a 76% relapse rate compared with a 25% relapse rate for patients who reach remission.21

After remission has been achieved and physical and emotional functions have been restored, the continuation phase of treatment begins. At this point in the treatment process, the main goal is to prevent relapse, defined as a regression of the patient's condition to less than optimal physical and psychological status, or, more simply, a return of depressive symptoms. Relapse may occur before remission is achieved; however, the continuation phase does not begin until remission has been achieved.20 The minimum recommended duration of treatment in the continuation phase is 4 to 9 months.20

The maintenance phase of treatment is essentially long-term management of the depressive disorder. In this phase, treatment is continued with the desired goal of preventing recurrence of a depressive episode.19 Recurrence, like relapse, is characterized by a regression of the patient's condition or a return of depressive symptoms. Recurrence, however, is only considered to have occurred after recovery has been achieved. The maintenance phase of treatment may continue indefinitely, depending on an individual's risk of recurrence, but for the first episode of depression, it is usually recommended to continue for 12 months.

Considering the long-term and progressive nature of depression, achieving remission is crucial for predicting future outcomes in the severity of the disease or in the emergence of new depressive episodes. Current data predict a greater than 50% probability that an individual who has had 1 episode of depression will experience a second episode within 5 years. After a second episode of depression, the likelihood of recurrence increases to roughly 70%. The risk of recurrence is greater than 90% after a patient has a third episode of depression.22-24 Unfortunately, less than one third of adults with depression obtain appropriate professional treatment, 12 and a majority are not treated sufficiently to achieve remission.25 Patients who do not achieve remission are at greater risk for relapse and recurrence, more long-term depressive episodes, and a shorter duration between depressive episodes.

Presence of residual symptoms after treatment is a predictor of poor outcomes. Results of the National Institute of Mental Health's Collaborative Depression Study demonstrated that patients with residual symptoms during recovery had significantly more severe and long-term future courses of disease than those with no residual symptoms.26 Likewise, those with residual symptoms experienced a relapse more than 3 times faster and had more recurrences, and fewer symptom-free weeks during follow-up than asymptomatic patients.26

Individuals who fail to achieve remission also tend to use more healthcare resources as suggested by a report that employees with a history of treatment- resistant depression (TRD) used more than twice as many medical services as those without TRD.27 In the TRD patients, the average annual medical cost was $14 490 per employee versus $6665 for employees who were depressed, but not considered treatment-resistant.27 Similar results were found by a second study that demonstrated that patients with persistent depression had nearly twice the annual healthcare costs of those who had achieved remission.28

Choice of Antidepressant TherapyThe choice of an antidepressant should be based mainly on the unique medical-historical profile of the individual patient. Drug safety, side effect profile, tolerability, and the potential for drug interactions should be considered because these variables can affect adherence to treatment. Several different classes of medications are currently used to treat depression. First-line medications typically used in the treatment of depression include the selective serotonin reuptake inhibitors (SSRIs), which have reasonable efficacy and a relatively low rate of adverse events. There are a number of agents in this class available as generics. Although effective, older agents, such as monoamine oxidase inhibitors (MAOIs) and tricyclic antidepressants (TCAs), are associated with cardiac, anticholinergic, and hypotensive side effects, as well as the potential for severe toxicity. Consequently, these agents are more frequently used as secondary or adjunctive therapies. Several different combination and augmentation strategies are also employed in an effort to improve outcomes.

Despite the existence of multiple classes of pharmacotherapies, many patients experience an inadequate response to initial antidepressant treatment. One study reported that two thirds of patients treated with fluoxetine, paroxetine, or sertraline were nonresponders (ie, failed to exhibit a clinically significant symptom reduction) to initial SSRI therapy (Figure 2).29 These patients who failed to achieve an adequate response on initial therapy often continued to cycle through several other antidepressants without reaching the treatment goal of remission. This inadequate response often results because of insufficient dosing for an inadequate duration and/or drug intolerance. The positive dose-response relationship observed with antidepressant therapy dictates that the dose should be pushed to the highest tolerable levels to achieve remission and prevent relapse. If a patient does not demonstrate adequate response with a particular antidepressant after 4 to 6 weeks of therapy at the initial dose or after 2 to 4 additional weeks at the maximum dose, therapy should be adjusted by either treatment substitution using another antidepressant, adding another antidepressant to the current therapy, or augmenting therapy with another agent.30,31

SummaryDepression is a long-term and progressive condition that when not treated adequately can lead to severe morbidity and mortality and increased costs for payers, employers, and patients. Despite the significant burden of depression, the majority of patients do not receive treatment adequate enough to achieve remission. While remission is the primary goal of treatment, it is sometimes the most difficult to achieve. Effective strategies to achieve remission include an increase in dose, augmentation of medication, combination of psychotherapy and antidepressant treatments, or using medications with more than 1 mechanism of action. These strategies may be most easily applied through the use of a treatment algorithm. Patients who do not achieve remission, including those cycling on ineffective therapies, are at greater risk for relapse and recurrence, more long-term depressive episodes, and a shorter duration between depressive episodes. SSRIs are widely used first-line agents for the treatment of depression because of their efficacy, tolerability, and generic status, but when treatment fails, another class of antidepressants, such as an SNRI, should be attempted. Clinical trials provide good evidence to show that achieving and sustaining the fully remitted state is an attainable goal in the management of patients with depression.

Address correspondence to: Aron Halfin, MD, 3350 Peachtree Rd NE, Mail Stop G005-0001, Atlanta, GA 30326. E-mail: Aron.Halfin@wellpoint.com.

1. National Institute of Mental Health. Pathways to Health: Charting the Science of Brain, Mind, Behavior. A Research Strategic Plan for the National Institute ofMental Health Fiscal Year 2000–2001. Bethesda, MD: National Institute of Mental Health, National Institutes of Health, US Department of Health and Human Services. Available at: http://www.nimh.nih.gov/about/strategic-planning-reports/pathways-to-health-chartingthe-science-of-brain-mind-and-behavior.pdf. Accessed October 7, 2007.

3. Pratt LA, Ford DE, Crum RM, Armenian HK, Gallo JJ, Eaton WW. Depression, psychotropic medication, and risk of myocardial infarction. Prospective data from the Baltimore ECA follow-up. Circulation. 1996;94:3123-3129.

5. Rice DP, Miller LS. Health economics and cost implications of anxiety and other mental disorders in the United States. Br J Psychiatry Suppl. 1998:4-9.

7. Henk HJ, Katzelnick DJ, Kobak KA, Greist JH, Jefferson JW. Medical costs attributed to depression among patients with a history of high medical expenses in a health maintenance organization. Arch Gen Psychiatry. 1996;53:899-904.

9. Stewart WF, Ricci JA, Chee E, Hahn SR, Morganstein D. Cost of lost productive work time among US workers with depression. JAMA. 2003;289:3135-3144.

11. Greden JF. The burden of recurrent depression: causes, consequences, and future prospects. J Clin Psychiatry. 2001;62(suppl 22):5-9.

13. Katon W, Schulberg H. Epidemiology of depression in primary care. Gen Hosp Psychiatry. 1992;14:237-247.

15. Callahan EJ, Bertakis KD, Azari R, Robbins J, Helms LJ, Miller J. The influence of depression on physicianpatient interaction in primary care. Fam Med. 1996;28:346-351.

17. Coulehan JL, Schulberg HC, Block MR, Madonia MJ, Rodriguez E.Treating depressed primary care patients improves their physical, mental, and social functioning. Arch Intern Med. 1997;157:1113-1120.

19. American Psychiatric Association. Practice guideline for the treatment of patients with major depressive disorder (revision). Am J Psychiatry. 2000;157:1-45.

21. Paykel ES, Ramana R, Cooper Z, Hayhurst H, Kerr J, Barocka A. Residual symptoms after partial remission: an important outcome in depression. Psychol Med. 1995;25:1171-1180.

23. Judd LL, Paulus MJ, Schettler PJ, Akiskal HS, Endicott J, Leon AC. Does incomplete recovery from first lifetime major depressive episode herald a chronic course of illness? Am J Psychiatry. 2000;157:1501-1504.

25. Dunn JD, Tierney JG. A step therapy algorithm for the treatment and management of chronic depression. Am J Manag Care. 2006;12(suppl 12):S335-S343.

27. Greenberg P, Corey-Lisle PK, Birnbaum H, Marynchenko M, Claxton A. Economic implications of treatmentresistant depression among employees. Pharmacoeconomics. 2004;22:363-373.

29. Corey-Lisle PK, Nash R, Stang P, Swindle R. Response, partial response, and nonresponse in primary care treatment of depression. Arch Intern Med. 2004;164:

30. Nelson JC. Managing treatment-resistant major depression. J Clin Psychiatry. 2003;64(suppl 1):5-12.

32. 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;163:28-40.

34. Kruzikas D, Khandker RK, McLaughlin T, Tedeschi M. Patterns of antidepressant use and cost implications of product switching. Presented at: the Academy of Managed Care Pharmacy Educational Meeting. Nashville, TN, October 5-8, 2005.

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