18 - References
References
346 The Maudsley® Prescribing Guidelines in Psychiatry CHAPTER 3 in treatment (British Association for Psychopharmacology guidelines suggest 4 weeks).3 If there is some improvement at this time, continue and assess for a further 2–3 weeks (see section on general overview of antidepressants in this chapter). ■ ■Our algorithm conveniently dichotomises outcome as response or non-response (effective, not effective). Real-life outcomes include partial response – a positive change that falls short of recovery or remission. In those circumstances there is little evidence to guide practice, but the aim should be to achieve remission by means of dose increase and, if unsuccessful, by changing the antidepressant. ■ ■Adjunctive treatments shown to be effective after the failure of only one antidepressant (early-stage treatment resistance) include (es)ketamine, risperidone, lithium and aripiprazole.36 Dextromethorphan may improve initial outcomes if added to SSRI treatment.37 References
- Leuchter AF, et al. Role of pill-taking, expectation and therapeutic alliance in the placebo response in clinical trials for major depression. Br J Psychiatry 2014; 205:443–449.
- American Psychiatric Association. Practice Guideline for the Treatment of Patients with Major Depressive Disorder, 3rd edn. Washington, DC: American Psychiatric Association; 2010.
- Anderson IM, 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.
- Crismon ML, et al. The Texas Medication Algorithm Project: report of the Texas Consensus Conference Panel on Medication Treatment of Major Depressive Disorder. J Clin Psychiatry 1999; 60:142–156.
- Kocsis JH, et al. Maintenance therapy for chronic depression: a controlled clinical trial of desipramine. Arch Gen Psychiatry 1996; 53:769–774.
- Dekker J, et al. The use of antidepressants after recovery from depression. Eur J Psychiatry 2000; 14:207–212.
- Nelson JC. Treatment of antidepressant nonresponders: augmentation or switch? J Clin Psychiatry 1998; 59 Suppl 15:35–41.
- Joffe RT. Substitution therapy in patients with major depression. CNS Drugs 1999; 11:175–180.
- National Institute for Health and Care Excellence. Depression in adults: treatment and management. NICE guideline [NG222]. 2022 (last reviewed September 2024, last checked November 2024); https://www.nice.org.uk/guidance/ng222.
- Montgomery SA, et al. A randomised, double-blind study in adults with major depressive disorder with an inadequate response to a single course of selective serotonin reuptake inhibitor or serotonin-noradrenaline reuptake inhibitor treatment switched to vortioxetine or agomelatine. Human Psychopharmacol 2014; 29:470–482.
- Sparshatt A, et al. A naturalistic evaluation and audit database of agomelatine: clinical outcome at 12 weeks. Acta Psychiatr Scand 2013; 128:203–211.
- Montgomery SA, et al. A new depression scale designed to be sensitive to change. Br J Psychiatry 1979; 134:382–389.
- Hamilton M. Development of a rating scale for primary depressive illness. Br J Soc Clin Psychol 1967; 6:278–296.
- Kroenke K, et al. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med 2001; 16:606–613.
- Cipriani A, et al. Comparative efficacy and acceptability of 21 antidepressant drugs for the acute treatment of adults with major depressive disorder: a systematic review and network meta-analysis. Lancet 2018; 391:1357–1366.
- Wagner G, et al. Efficacy and safety of levomilnacipran, vilazodone and vortioxetine compared with other second-generation antidepressants for major depressive disorder in adults: a systematic review and network meta-analysis. J Affect Disord 2018; 228:1–12.
- de Vries YA, et al. Predicting antidepressant response by monitoring early improvement of individual symptoms of depression: individual patient data meta-analysis. Br J Psychiatry 2019; 214:4–10.
- Köhler-Forsberg O, et al. Efficacy of anti-inflammatory treatment on major depressive disorder or depressive symptoms: meta-analysis of clinical trials. Acta Psychiatr Scand 2019; 139:404–419.
- Thase ME, et al. Citalopram treatment of fluoxetine nonresponders. J Clin Psychiatry 2001; 62:683–687.
- Rush AJ, et al. Bupropion-SR, sertraline, or venlafaxine-XR after failure of SSRIs for depression. N Engl J Med 2006; 354:1231–1242.
- Ruhe HG, et al. Switching antidepressants after a first selective serotonin reuptake inhibitor in major depressive disorder: a systematic review. J Clin Psychiatry 2006; 67:1836–1855.
- Brent D, et al. Switching to another SSRI or to venlafaxine with or without cognitive behavioral therapy for adolescents with SSRI-resistant depression: the TORDIA randomized controlled trial. JAMA 2008; 299:901–913.
- Papakostas GI, et al. Treatment of SSRI-resistant depression: a meta-analysis comparing within- versus across-class switches. Biol Psychiatry 2008; 63:699–704.
- Bschor T, et al. Switching the antidepressant after nonresponse in adults with major depression: a systematic literature search and meta- analysis. J Clin Psychiatry 2018; 79:16r10749.
Depression and anxiety disorders CHAPTER 3 25. Henssler J, et al. Combining antidepressants vs antidepressant monotherapy for treatment of patients with acute depression: a systematic review and meta-analysis. JAMA Psychiatry 2022; 79:300–312. 26. Adli M, et al. 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. 27. Hieronymus F, et al. A mega-analysis of fixed-dose trials reveals dose-dependency and a rapid onset of action for the antidepressant effect of three selective serotonin reuptake inhibitors. Transl Psychiatry 2016; 6:e834. 28. Zhou S, et al. Efficacy and dose-response relationships of antidepressants in the acute treatment of major depressive disorders: a systematic review and network meta-analysis. Chin Med J (Engl) 2024: doi: 10.1097/CM9.0000000000003138. 29. Furukawa TA, et al. Optimal dose of selective serotonin reuptake inhibitors, venlafaxine, and mirtazapine in major depression: a systematic review and dose–response meta-analysis. Lancet Psychiatry 2019; 6:601–609. 30. Papakostas GI, et al. A meta-analysis of early sustained response rates between antidepressants and placebo for the treatment of major depressive disorder. J Clin Psychopharmacol 2006; 26:56–60. 31. Taylor MJ, et al. Early onset of selective serotonin reuptake inhibitor antidepressant action: systematic review and meta-analysis. Arch Gen Psychiatry 2006; 63:1217–1223. 32. Posternak MA, et al. Is there a delay in the antidepressant effect? A meta-analysis. J Clin Psychiatry 2005; 66:148–158. 33. Szegedi A, et al. Early improvement in the first 2 weeks as a predictor of treatment outcome in patients with major depressive disorder: a meta-analysis including 6562 patients. J Clin Psychiatry 2009; 70:344–353. 34. Baldwin DS, et al. How long should a trial of escitalopram treatment be in patients with major depressive disorder, generalised anxiety disorder or social anxiety disorder? An exploration of the randomised controlled trial database. Hum Psychopharmacol 2009; 24:269–275. 35. Nierenberg AA, et al. Early nonresponse to fluoxetine as a predictor of poor 8-week outcome. Am J Psychiatry 1995; 152:1500–1503. 36. Scott F, et al. Systematic review and meta-analysis of augmentation and combination treatments for early-stage treatment-resistant depression. J Psychopharmacol 2023; 37:268–278. 37. Maji S, et al. Early augmentation therapy with dextromethorphan in mild to moderate major depressive disorder: a group sequential, response adaptive randomized controlled trial. Psychiatry Res 2024; 342:116257.
No comments to display
No comments to display