Literature DB >> 32047367

Complex Combination Pharmacotherapy for Bipolar Disorder: Knowing When Less Is More or More Is Better.

Joseph F Goldberg1.   

Abstract

Combination pharmacotherapy for bipolar disorder is commonplace and often reflects the severity and complexity of the illness and the comorbid conditions frequently associated with it. Across treatment settings, about one-fifth of patients with bipolar disorder appear to receive four or more psychotropic medications. Practice patterns often outpace the evidence-based literature, insofar as few systematic studies have examined the efficacy and safety of two or more medications for any given phase of illness. Most randomized trials of combination pharmacotherapy focus on the utility of pairing a mood stabilizer with a second-generation antipsychotic for prevention of either acute mania or relapse. In real-world practice, patients with bipolar disorder often take more elaborate combinations of mood stabilizers, antipsychotics, antidepressants, anxiolytics, stimulants, and other psychotropics for indefinite periods that do not necessarily arise purposefully and logically. In this article, I identify clinical factors associated with complex combination pharmacotherapy for patients with bipolar disorder; describe approaches to ensuring that each component of a treatment regimen has a defined role; discuss the elimination of unnecessary, ineffective, or redundant drugs in a regimen; and address complementary, safe, rationale-based drug combinations that target specific domains of psychopathology for which monotherapies often provide inadequate benefit.
Copyright © 2019 by the American Psychiatric Association.

Entities:  

Keywords:  Drug treatment/psychopharmacology; Mood Disorders-Bipolar

Year:  2019        PMID: 32047367      PMCID: PMC6999211          DOI: 10.1176/appi.focus.20190008

Source DB:  PubMed          Journal:  Focus (Am Psychiatr Publ)        ISSN: 1541-4094


  108 in total

1.  The mechanism of activity-dependent sodium channel inhibition by the antidepressants fluoxetine and desipramine.

Authors:  N Lenkey; R Karoly; J P Kiss; B K Szasz; E S Vizi; A Mike
Journal:  Mol Pharmacol       Date:  2006-09-19       Impact factor: 4.436

2.  The NMDA receptor/nitric oxide pathway: a target for the therapeutic and toxic effects of lithium.

Authors:  Mehdi Ghasemi; Ahmad Reza Dehpour
Journal:  Trends Pharmacol Sci       Date:  2011-04-13       Impact factor: 14.819

Review 3.  Allopurinol as add-on treatment for mania symptoms in bipolar disorder: systematic review and meta-analysis of randomised controlled trials.

Authors:  Francesco Bartoli; Cristina Crocamo; Massimo Clerici; Giuseppe Carrà
Journal:  Br J Psychiatry       Date:  2016-11-17       Impact factor: 9.319

4.  A double-blind, placebo-controlled study of quetiapine and paroxetine as monotherapy in adults with bipolar depression (EMBOLDEN II).

Authors:  Susan L McElroy; Richard H Weisler; William Chang; Bengt Olausson; Björn Paulsson; Martin Brecher; Vasavan Agambaram; Charles Merideth; Arvid Nordenhem; Allan H Young
Journal:  J Clin Psychiatry       Date:  2010-01-26       Impact factor: 4.384

5.  Depressive illness burden associated with complex polypharmacy in patients with bipolar disorder: findings from the STEP-BD.

Authors:  Joseph F Goldberg; John O Brooks; Keiko Kurita; Jennifer C Hoblyn; S Nassir Ghaemi; Roy H Perlis; David J Miklowitz; Terence A Ketter; Gary S Sachs; Michael E Thase
Journal:  J Clin Psychiatry       Date:  2009-02-10       Impact factor: 4.384

6.  Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): a randomised open-label trial.

Authors:  John R Geddes; Guy M Goodwin; Jennifer Rendell; Jean-Michel Azorin; Andrea Cipriani; Michael J Ostacher; Richard Morriss; Nicola Alder; Ed Juszczak
Journal:  Lancet       Date:  2010-01-19       Impact factor: 79.321

7.  Polypharmacy in Maintenance of Bipolar Disorder.

Authors:  Eric D Peselow; Lancer Naghdechi; Demetria Pizano; Waguih William IsHak
Journal:  Clin Neuropharmacol       Date:  2016 May-Jun       Impact factor: 1.592

8.  Lamotrigine as add-on treatment to lithium and divalproex: lessons learned from a double-blind, placebo-controlled trial in rapid-cycling bipolar disorder.

Authors:  David E Kemp; Keming Gao; Elizabeth B Fein; Philip K Chan; Carla Conroy; Sarah Obral; Stephen J Ganocy; Joseph R Calabrese
Journal:  Bipolar Disord       Date:  2012-11       Impact factor: 6.744

9.  Chronic carbamazepine administration reduces N-methyl-D-aspartate receptor-initiated signaling via arachidonic acid in rat brain.

Authors:  Mireille Basselin; Nelly E Villacreses; Mei Chen; Jane M Bell; Stanley I Rapoport
Journal:  Biol Psychiatry       Date:  2007-07-12       Impact factor: 13.382

10.  Prescribing trends in bipolar disorder: cohort study in the United Kingdom THIN primary care database 1995-2009.

Authors:  Joseph Hayes; Philip Prah; Irwin Nazareth; Michael King; Kate Walters; Irene Petersen; David Osborn
Journal:  PLoS One       Date:  2011-12-07       Impact factor: 3.240

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  2 in total

Review 1.  Efficacy and safety of adjunctive therapy to lamotrigine, lithium, or valproate monotherapy in bipolar depression: a systematic review and meta-analysis of randomized controlled trials.

Authors:  Taku Maruki; Tomohiro Utsumi; Masahiro Takeshima; Yu Fujiwara; Marie Matsui; Yumi Aoki; Hiroyuki Toda; Norio Watanabe; Koichiro Watanabe; Yoshikazu Takaesu
Journal:  Int J Bipolar Disord       Date:  2022-10-21

Review 2.  Real-World Patterns of Utilization and Costs Associated with Second-Generation Oral Antipsychotic Medication for the Treatment of Bipolar Disorder: A Literature Review.

Authors:  Michael J Doane; Kristine Ogden; Leona Bessonova; Amy K O'Sullivan; Mauricio Tohen
Journal:  Neuropsychiatr Dis Treat       Date:  2021-02-16       Impact factor: 2.570

  2 in total

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