J Korean Neuropsychiatr Assoc.  2013 Sep;52(5):386-401.

Evidence-Based Korean Pharmacological Treatment Guideline for Depression, Revised Edition (III) : Dose Increment, Switching, Combination, and Augmentation Strategy in Antidepressant Therapy

Affiliations
  • 1Department of Psychiatry, College of Medicine, Korea University, Seoul, Korea. leeminso@korea.ac.kr
  • 2Department of Psychiatry, Yong-In Mental Hospital, Yongin, Korea.
  • 3Department of Psychiatry, College of Medicine, Soonchunhyang University, Cheonan, Korea.
  • 4Department of Cancer Management, Gachon University Gil Medical Center, Incheon, Korea.
  • 5Department of Psychiatry, School of Medicine, KyungHee University, Seoul, Korea.
  • 6Department of Psychiatry, School of Medicine, Sungkyunkwan University, Seoul, Korea.
  • 7Department of Psychiatry, College of Medicine, Inje University, Busan, Korea.
  • 8Department of Psychiatry, College of Medicine, Hanyang University, Seoul, Korea.

Abstract


OBJECTIVES
The aim of this study was to demonstrate the recommendations for antidepressant treatment strategy of dose increment, switching, combination, and augmentation therapy derived from Evidence-Based Korean Pharmacological Treatment Guideline for Depression, Revised Edition.
METHODS
The guideline was developed through adaptation of 12 domestic and foreign clinical guidelines for depression, with key questions concerning pharmacotherapy of depression, and drawing of recommendations.
RESULTS
The guideline strongly recommended dose increment, switching, and combination and augmentation therapy of antidepressant when patients with depression showed inadequate treatment outcomes from initial antidepressant treatment. The dose increment was strongly recommended when the patients had insufficient response from treatment with tricyclic antidepressants (TCAs), monoamine oxidase inhibitors, selective serotonin reuptake inhibitors (SSRIs), and serotonin and norepinephrine reuptake inhibitors (SNRIs). Switching from SSRI to non-SSRI was also strongly recommended. The combination of initial medication and other classes of antidepressants could benefit from treatment with TCAs, SSRIs, SNRIs, and noradrenergic and specific serotonergic antidepressants. Combination with norepinephrine and dopamine reuptake inhibitors or serotonin-2 antagonist/reuptake inhibitors was weakly recommended. The guideline strongly recommended use of the augmentation strategy of adding lithium or benzodiazepine to initial antidepressants. Augmentation of lamotrigine, T3, methylphenidate, and modafinil was weakly recommended.
CONCLUSION
If the initial outcomes of antidepressant therapy are unsatisfactory to the patients the next-step strategies of dose increment, switching, combination and augmentation of antidepressants should be considered after rechecking the patients' drug compliance, dose, and diagnosis.

Keyword

Major depressive disorder; Guideline; Antidepressant; Switching; Combination; Augmentation

MeSH Terms

Antidepressive Agents
Antidepressive Agents, Tricyclic
Benzhydryl Compounds
Benzodiazepines
Compliance
Depression*
Depressive Disorder, Major
Dopamine Uptake Inhibitors
Drug Therapy
Humans
Lithium
Methylphenidate
Monoamine Oxidase Inhibitors
Norepinephrine
Serotonin
Serotonin Uptake Inhibitors
Triazines
Antidepressive Agents
Antidepressive Agents, Tricyclic
Benzhydryl Compounds
Benzodiazepines
Dopamine Uptake Inhibitors
Lithium
Methylphenidate
Monoamine Oxidase Inhibitors
Norepinephrine
Serotonin
Serotonin Uptake Inhibitors
Triazines

Reference

1. Dupuy JM, Ostacher MJ, Huffman J, Perlis RH, Nierenberg AA. A critical review of pharmacotherapy for major depressive disorder. Int J Neuropsychopharmacol. 2011; 14:1417–1431.
Article
2. Cipriani A, Furukawa TA, Salanti G, Geddes JR, Higgins JP, Churchill R, et al. Comparative efficacy and acceptability of 12 new-generation antidepressants: a multiple-treatments meta-analysis. Lancet. 2009; 373:746–758.
Article
3. Gaynes BN, Warden D, Trivedi MH, Wisniewski SR, Fava M, Rush AJ. What did STAR*D teach us? Results from a large-scale, practical, clinical trial for patients with depression. Psychiatr Serv. 2009; 60:1439–1445.
Article
4. 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.
Article
5. Gelenberg AJ. A review of the current guidelines for depression treatment. J Clin Psychiatry. 2010; 71:e15.
6. Preskorn SH. Treatment options for the patient who does not respond well to initial antidepressant therapy. J Psychiatr Pract. 2009; 15:202–210.
Article
7. Lee MS, Lim SW, Cha JH, Chung SK, Kim KS, Kasper S. The Executive Committee for the Korean Medication Algorithm Project for Major Depressive Disorder. The development of the Korean medication algorithm for major depressive disorder. Psychiatry Investig. 2005; 2:60–69.
8. Clinical Research Center for Depression. Evidence-based Korean pharmacological treatment guideline for depression. Seoul: ML Communication;2008.
9. Clinical Research Center for Depression. Evidence-based Korean non-pharmacological treatment guideline for depression. Seoul: ML Communication;2009.
10. Huang X, Lin J, Demner-Fushman D. Evaluation of PICO as a knowledge representation for clinical questions. AMIA Annu Symp Proc. 2006; 359–363.
11. Kim SY KN, Shin SS, Kim DW, Ji SM, Lee SJ. ADAPTE: Manual for guildeline adaptation version 1.0. Seoul: National Clinical Research Coordination Center;2009.
12. Steering Committee for Clinical Practice Guideline. Korean Appraisal of Guidelines for Research & Evaluation II. Seoul: Ministry of Health & Welfare and Korean Academy of Medical Science;2009.
13. New Zealand Guidelines Group. Identification of Common Mental Disorders and Management of Depression in Primary Care. New Zealand: Ministry of Health;2008.
14. National Institute for Health and Clinical Excellence (NICE). Depression: the treatment and management of depression in adults (National Clinical Practice Guideline 90). National Institute for Health and Clinical Experience;2009.
15. American Psychiatric Association (APA). Practice Guideline for the treatment of Patients with major depressive disorder. Arlington: American Psychiatric Association (APA);2010.
16. Anderson IM, Ferrier IN, Baldwin RC, Cowen PJ, Howard L, Lewis G, et al. Evidence-based guidelines for treating depressive disorders with antidepressants: a revision of the 2000 British Association for Psychopharmacology guidelines. J Psychopharmacol. 2008; 22:343–396.
Article
17. Bauer M, Bschor T, Pfennig A, Whybrow PC, Angst J, Versiani M, 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; 8:67–104.
Article
18. Lam RW, Kennedy SH, Grigoriadis S, McIntyre RS, Milev R, Ramasubbu R, et al. Canadian Network for Mood and Anxiety Treatments (CANMAT) clinical guidelines for the management of major depressive disorder in adults. III. Pharmacotherapy. J Affect Disord. 2009; 117:Suppl 1. S26–S43.
19. Texas Department of Mental Health and Mental Retardation (TDMHMR) in collaboration with Texa universities. Texas Medication Algorithm Project Procedural Manual-Major Depressive Disorder Algorithms. 2008.
20. Korean Medication Algorithm Project for Depressive Disorder. Korean Medication Algorithm for Depressive Disorder 2008. Korean Society for Depressive and Bipolar Disorders and Korean College of Neuropsychopharmacology. 2008.
21. Professional Development & Quality Assurance prepared by a group of family physicians. Guideline on Management of Depression in Primary Care Hong Kong. 2009.
22. Malhi GS, Adams D, Porter R, Wignall A, Lampe L, O'Connor N, et al. Clinical practice recommendations for depression. Acta Psychiatr Scand Suppl. 2009; 8–26.
Article
23. 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; 89:1–11.
Article
24. Furukawa TA, McGuire H, Barbui C. Meta-analysis of effects and side effects of low dosage tricyclic antidepressants in depression: systematic review. BMJ. 2002; 325:991.
Article
25. Bollini P, Pampallona S, Tibaldi G, Kupelnick B, Munizza C. Effectiveness of antidepressants. Meta-analysis of dose-effect relationships in randomised clinical trials. Br J Psychiatry. 1999; 174:297–303.
26. Ramana R, Paykel ES, Surtees PG, Melzer D, Mehta MA. Medication received by patients with depression following the acute episode: adequacy and relation to outcome. Br J Psychiatry. 1999; 174:128–134.
Article
27. Adli M, Baethge C, Heinz A, Langlitz N, Bauer M. Is dose escalation of antidepressants a rational strategy after a medium-dose treatment has failed? A systematic review. Eur Arch Psychiatry Clin Neurosci. 2005; 255:387–400.
Article
28. Amsterdam JD, Berwish NJ. High dose tranylcypromine therapy for refractory depression. Pharmacopsychiatry. 1989; 22:21–25.
Article
29. Schatzberg AF. Dosing strategies for antidepressant agents. J Clin Psychiatry. 1991; 52:Suppl. 14–20.
30. Tyrer P, Gardner M, Lambourn J, Whitford M. Clinical and pharmacokinetic factors affecting response to phenelzine. Br J Psychiatry. 1980; 136:359–365.
Article
31. Angst J, Amrein R, Stabl M. Moclobemide and tricyclic antidepressants in severe depression: meta-analysis and prospective studies. J Clin Psychopharmacol. 1995; 15:4 Suppl 2. 16S–23S.
32. Fritze J, Laux G, Sofic E, Koronakis P, Schoerlin MP, Riederer P, et al. Plasma moclobemide and metabolites: lack of correlation with clinical response and biogenic amines. Psychopharmacology (Berl). 1989; 99:252–256.
Article
33. Gagiano CA, Müller FG, Berk M, Joubert PM, Brown RG, Schall R. Moclobemide twice daily in the treatment of major depressive episode: a double-blind, multicenter comparison with different three times daily dosage schedules. J Clin Psychopharmacol. 1995; 15:4 Suppl 2. 4S–9S.
34. Radat F, Berlin I, Spreux-Varoquaux O, Elatki S, Ferreri M, Puech AJ. Initial monoamine oxidase-A inhibition by moclobemide does not predict the therapeutic response in patients with major depression. A double blind, randomized study. Psychopharmacology (Berl). 1996; 127:370–376.
Article
35. Bech P, Tanghøj P, Andersen HF, Overø K. Citalopram dose-response revisited using an alternative psychometric approach to evaluate clinical effects of four fixed citalopram doses compared to placebo in patients with major depression. Psychopharmacology (Berl). 2002; 163:20–25.
Article
36. Burke WJ, Gergel I, Bose A. Fixed-dose trial of the single isomer SSRI escitalopram in depressed outpatients. J Clin Psychiatry. 2002; 63:331–336.
Article
37. Schweizer E, Rickels K, Amsterdam JD, Fox I, Puzzuoli G, Weise C. What constitutes an adequate antidepressant trial for fluoxetine? J Clin Psychiatry. 1990; 51:8–11.
38. Licht RW, Qvitzau S. Treatment strategies in patients with major depression not responding to first-line sertraline treatment. A randomised study of extended duration of treatment, dose increase or mianserin augmentation. Psychopharmacology (Berl). 2002; 161:143–151.
Article
39. Benkert O, Szegedi A, Wetzel H, Staab HJ, Meister W, Philipp M. Dose escalation vs. continued doses of paroxetine and maprotiline: a prospective study in depressed out-patients with inadequate treatment response. Acta Psychiatr Scand. 1997; 95:288–296.
Article
40. Rudolph RL, Fabre LF, Feighner JP, Rickels K, Entsuah R, Derivan AT. A randomized, placebo-controlled, dose-response trial of venlafaxine hydrochloride in the treatment of major depression. J Clin Psychiatry. 1998; 59:116–122.
Article
41. Schweizer E, Weise C, Clary C, Fox I, Rickels K. Placebo-controlled trial of venlafaxine for the treatment of major depression. J Clin Psychopharmacol. 1991; 11:233–236.
Article
42. Rush AJ, Trivedi MH, Wisniewski SR, Stewart JW, Nierenberg AA, Thase ME, et al. Bupropion-SR, sertraline, or venlafaxine-XR after failure of SSRIs for depression. N Engl J Med. 2006; 354:1231–1242.
Article
43. Ruhé HG, Huyser J, Swinkels JA, Schene AH. Switching antidepressants after a first selective serotonin reuptake inhibitor in major depressive disorder: a systematic review. J Clin Psychiatry. 2006; 67:1836–1855.
Article
44. Tanghe A, Steeman J. Moclobemide and amitriptyline, alone or in combination, in therapy resistant depression, Letter to the Editor. Human Psychopharmacology. 1997.
45. Nelson JC, Mazure CM, Jatlow PI, Bowers MB Jr, Price LH. Combining norepinephrine and serotonin reuptake inhibition mechanisms for treatment of depression: a double-blind, randomized study. Biol Psychiatry. 2004; 55:296–300.
Article
46. Lader M. Combined use of tricyclic antidepressants and monoamine oxidase inhibitors. J Clin Psychiatry. 1983; 44(9 Pt 2):20–24.
47. Carpenter LL, Yasmin S, Price LH. A double-blind, placebo-controlled study of antidepressant augmentation with mirtazapine. Biol Psychiatry. 2002; 51:183–188.
Article
48. McGrath PJ, Stewart JW, Fava M, Trivedi MH, Wisniewski SR, Nierenberg AA, et al. Tranylcypromine versus venlafaxine plus mirtazapine following three failed antidepressant medication trials for depression: a STAR*D report. Am J Psychiatry. 2006; 163:1531–1541. quiz 1666.
Article
49. Medhus A, Heskestad S, Tjemsland L. Mianserin added to tricyclic antidepressants in depressed patients not responding to a tricyclic antidepressant alone: a randomized, placebo-controlled, double-blind study. Nord J Psychiatry. 1994; 48:335–358.
Article
50. Ferreri M, Lavergne F, Berlin I, Payan C, Puech AJ. Benefits from mianserin augmentation of fluoxetine in patients with major depression non-responders to fluoxetine alone. Acta Psychiatr Scand. 2001; 103:66–72.
Article
51. Maes M, Libbrecht I, van Hunsel F, Campens D, Meltzer HY. Pindolol and mianserin augment the antidepressant activity of fluoxetine in hospitalized major depressed patients, including those with treatment resistance. J Clin Psychopharmacol. 1999; 19:177–182.
Article
52. Trivedi MH, Fava M, Wisniewski SR, Thase ME, Quitkin F, Warden D, et al. Medication augmentation after the failure of SSRIs for depression. N Engl J Med. 2006; 354:1243–1252.
Article
53. Lam RW, Hossie H, Solomons K, Yatham LN. Citalopram and bupropion-SR: combining versus switching in patients with treatment-resistant depression. J Clin Psychiatry. 2004; 65:337–340.
54. Maes M, Vandoolaeghe E, Desnyder R. Efficacy of treatment with trazodone in combination with pindolol or fluoxetine in major depression. J Affect Disord. 1996; 41:201–210.
Article
55. Crossley NA, Bauer M. Acceleration and augmentation of antidepressants with lithium for depressive disorders: two meta-analyses of randomized, placebo-controlled trials. J Clin Psychiatry. 2007; 68:935–940.
Article
56. Bauer M, Bschor T, Kunz D, Berghöfer A, Ströhle A, Müller-Oerlinghausen B. Double-blind, placebo-controlled trial of the use of lithium to augment antidepressant medication in continuation treatment of unipolar major depression. Am J Psychiatry. 2000; 157:1429–1435.
Article
57. Birkenhäger TK, van den Broek WW, Moleman P, Bruijn JA. Outcome of a 4-step treatment algorithm for depressed inpatients. J Clin Psychiatry. 2006; 67:1266–1271.
Article
58. Schindler F, Anghelescu IG. Lithium versus lamotrigine augmentation in treatment resistant unipolar depression: a randomized, open-label study. Int Clin Psychopharmacol. 2007; 22:179–182.
Article
59. Joffe RT, Singer W, Levitt AJ, MacDonald C. A placebo-controlled comparison of lithium and triiodothyronine augmentation of tricyclic antidepressants in unipolar refractory depression. Arch Gen Psychiatry. 1993; 50:387–393.
Article
60. Altshuler LL, Bauer M, Frye MA, Gitlin MJ, Mintz J, Szuba MP, et al. Does thyroid supplementation accelerate tricyclic antidepressant response? A review and meta-analysis of the literature. Am J Psychiatry. 2001; 158:1617–1622.
Article
61. Nierenberg AA, Fava M, Trivedi MH, Wisniewski SR, Thase ME, McGrath PJ, et al. A comparison of lithium and T(3) augmentation following two failed medication treatments for depression: a STAR*D report. Am J Psychiatry. 2006; 163:1519–1530. quiz 1665.
Article
62. Aronson R, Offman HJ, Joffe RT, Naylor CD. Triiodothyronine augmentation in the treatment of refractory depression. A meta-analysis. Arch Gen Psychiatry. 1996; 53:842–848.
Article
63. Guaiana G, Barbui C, Hotopf M. Amitriptyline versus other types of pharmacotherapy for depression. Cochrane Database Syst Rev. 2003; CD004186.
Article
64. Furukawa TA, Streiner DL, Young LT. Antidepressant and benzodiazepine for major depression. Cochrane Database Syst Rev. 2002; CD001026.
65. Lavretsky H, Park S, Siddarth P, Kumar A, Reynolds CF 3rd. Methylphenidate-enhanced antidepressant response to citalopram in the elderly: a double-blind, placebo-controlled pilot trial. Am J Geriatr Psychiatry. 2006; 14:181–185.
Article
66. Fava M, Thase ME, DeBattista C, Doghramji K, Arora S, Hughes RJ. Modafinil augmentation of selective serotonin reuptake inhibitor therapy in MDD partial responders with persistent fatigue and sleepiness. Ann Clin Psychiatry. 2007; 19:153–159.
Article
67. DeBattista C, Doghramji K, Menza MA, Rosenthal MH, Fieve RR. Modafinil in Depression Study Group. Adjunct modafinil for the short-term treatment of fatigue and sleepiness in patients with major depressive disorder: a preliminary double-blind, placebo-controlled study. J Clin Psychiatry. 2003; 64:1057–1064.
Article
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