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16 - Management commentary

Published online by Cambridge University Press:  13 August 2009

Terence A. Ketter
Affiliation:
Bipolar Disorders Clinic, Stanford, University School of Medicine, Stanford, USA
Po W. Wang
Affiliation:
Department of Psychiatry and Behavioral Sciences, Bipolar Disorders Clinic, Stanford, University School of Medicine, California, USA
Gordon Parker
Affiliation:
University of New South Wales, Sydney
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Summary

Introduction

As noted by Parker, management of Bipolar II Disorder is challenging for several reasons, including the scarcity of controlled data to inform evidence-based care. Such limited data mean that clinicians commonly extrapolate information regarding BP I and/or (unipolar) major depressive disorder, and view BP II as an intermediate category. Such an approach has strengths and limitations. One notable limitation is that it may underemphasise the heterogeneity of BP II, a condition with substantial inter-patient variability.

Thus, some patients with BP II may have an illness more like major depressive disorder: relatively infrequent recurrent pure (with minimal mixed features) depressive episodes, rare hypomanias, and – with antidepressants – they experience relief of depression without treatment-emergent affective switch (TEAS) into hypomania or accelerating episodes. Antidepressants may be considered foundational treatments for this presentation. In academic centres with specialty clinics, such patients are more likely referred to major depressive disorder clinics, where clinicians may view antidepressants as the treatment of choice for this type of BP II.

However, other patients with BP II may have an illness more akin to BP I. These patients experience relatively frequent recurrent depressive episodes that include mixed features (in some instances with concurrent depression and hypomania, i.e. dysphoric hypomania), common hypomanias and, in some instances, rapid cycling. Antidepressants give inadequate relief of their depression and can confer TEAS, and/or cycle acceleration. For these patients, mood stabilisers or atypical antipsychotics – not antidepressants – may be considered foundational treatments.

Type
Chapter
Information
Bipolar II Disorder
Modelling, Measuring and Managing
, pp. 217 - 231
Publisher: Cambridge University Press
Print publication year: 2008

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References

American Psychiatric Association (2000). Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM–IV–TR). Washington. DC: American Psychiatric Association.
Amsterdam, J. (1998). Efficacy and safety of venlafaxine in the treatment of Bipolar II major depressive episode. Journal of Clinical Psychopharmacology, 18, 414–17.CrossRefGoogle ScholarPubMed
Amsterdam, J. D. and Brunswick, D. J. (2003). Antidepressant monotherapy for Bipolar Type II major depression. Bipolar Disorders, 5, 388–95.CrossRefGoogle ScholarPubMed
Amsterdam, J. D. and Garcia-Espana, F. (2000). Venlafaxine monotherapy in women with Bipolar II and unipolar major depression. Journal of Affective Disorders, 59, 225–9.CrossRefGoogle ScholarPubMed
Amsterdam, J. D., Garcia-Espana, F., Fawcett, J.et al. (1998). Efficacy and safety of fluoxetine in treating Bipolar II major depressive episode. Journal of Clinical Psychopharmacology, 18, 435–40.CrossRefGoogle ScholarPubMed
Amsterdam, J. D., Shults, J., Brunswick, D. J. and Hundert, M. (2004). Short-term fluoxetine monotherapy for Bipolar Type II or Bipolar NOS major depression – low manic switch rate. Bipolar Disorders, 6, 75–81.CrossRefGoogle ScholarPubMed
Baron, M., Gershon, E. S., Rudy, V., Jonas, W. Z. and Buchsbaum, M. (1975). Lithium carbonate response in depression. Prediction by unipolar/bipolar illness, average-evoked response, catechol-O-methyl transferase, and family history. Archives of General Psychiatry, 32, 1107–11.CrossRefGoogle ScholarPubMed
Bowden, C. L., Grunze, H., Mullen, J.et al. (2005). A randomized, double-blind, placebo-controlled efficacy and safety study of quetiapine or lithium as monotherapy for mania in bipolar disorder. Journal of Clinical Psychiatry, 66, 111–21.CrossRefGoogle ScholarPubMed
Brown, E. B., McElroy, S. L., Keck, P. E. Jr.et al. (2006). A 7-week, randomized, double-blind trial of olanzapine/fluoxetine combination versus lamotrigine in the treatment of Bipolar I depression. Journal of Clinical Psychiatry, 67, 1025–33.CrossRefGoogle ScholarPubMed
Calabrese, J. R., Keck, P. E. Jr., Macfadden, W.et al. (2005). A randomized, double-blind, placebo-controlled trial of quetiapine in the treatment of Bipolar I or II depression. American Journal of Psychiatry, 162, 1351–60.CrossRefGoogle ScholarPubMed
Calabrese, J. R., Suppes, T., Bowden, C. L.et al. (2000). Lamictal 614 Study Group. A double-blind, placebo-controlled, prophylaxis study of lamotrigine in rapid-cycling bipolar disorder. Journal of Clinical Psychiatry, 61, 841–50.CrossRefGoogle Scholar
Colom, F., Vieta, E., Martinez-Aran, A.et al. (2003). A randomized trial on the efficacy of group psychoeducation in the prophylaxis of recurrences in bipolar patients whose disease is in remission. Archives of General Psychiatry, 60, 402–7.CrossRefGoogle ScholarPubMed
Dunner, D. L., Stallone, F. and Fieve, R. R. (1976). Lithium carbonate and affective disorders. A double-blind study of prophylaxis of depression in bipolar illness. Archives of General Psychiatry, 33, 117–20.CrossRefGoogle ScholarPubMed
Dunner, D. L., Stallone, F. and Fieve, R. R. (1982). Prophylaxis with lithium carbonate: an update. Archives of General Psychiatry, 39, 1344–5.Google ScholarPubMed
Fieve, R. R. (1997). Moodswing (2nd edn). New York: Bantam Books.Google Scholar
Fieve, R. R., Kumbaraci, T. and Dunner, D. L. (1976). Lithium prophylaxis of depression in Bipolar I, Bipolar II, and unipolar patients. American Journal of Psychiatry, 133, 925–9.Google ScholarPubMed
Frank, E., Kupfer, D. J., Thase, M. E.et al. (2005). Two-year outcomes for interpersonal and social rhythm therapy in individuals with Bipolar I Disorder. Archives of General Psychiatry, 62, 996–1004.CrossRefGoogle ScholarPubMed
Frye, M. A., Grunze, H., Suppes, T.et al. (2007). A placebo-controlled evaluation of adjunctive modafinil in the treatment of bipolar depression. American Journal of Psychiatry, 164, 1242–9.CrossRefGoogle ScholarPubMed
Ghaemi, S. N., Hsu, D. J., Soldani, F. and Goodwin, F. K. (2003). Antidepressants in bipolar disorder: the case for caution. Bipolar Disorders, 5, 421–33.CrossRefGoogle ScholarPubMed
Goldberg, J. F., Burdick, K. E. and Endick, C. J. (2004). Preliminary randomized, double-blind, placebo-controlled trial of pramipexole added to mood stabilizers for treatment-resistant bipolar depression. American Journal of Psychiatry, 161, 564–6.CrossRefGoogle ScholarPubMed
Goodwin, F. K., Murphy, D. L., Dunner, D. L. and Bunney, W. E. Jr. (1972). Lithium response in unipolar versus bipolar depression. American Journal of Psychiatry, 129, 44–7.CrossRefGoogle ScholarPubMed
Greil, W. and Kleindienst, N. (1999). Lithium versus carbamazepine in the maintenance treatment of Bipolar II Disorder and Bipolar Disorder Not Otherwise Specified. International Clinical Psychopharmacology, 14, 283–5.CrossRefGoogle Scholar
Greil, W., Ludwig-Mayerhofer, W., Erazo, N.et al. (1997). Lithium versus carbamazepine in the maintenance treatment of bipolar disorders: a randomised study. Journal of Affective Disorders, 43, 151–61.CrossRefGoogle ScholarPubMed
Greil, W., Kleindienst, N., Erazo, N. and Müller-Oerlinghausen, B. (1998). Differential response to lithium and carbamazepine in the prophylaxis of bipolar disorder. Journal of Clinical Psychopharmacology, 18, 455–60.CrossRefGoogle ScholarPubMed
Haykal, R. F. and Akiskal, H. S. (1990). Bupropion as a promising approach to rapid-cycling Bipolar II patients. Journal of Clinical Psychiatry, 51, 450–5.Google ScholarPubMed
Himmelhoch, J. M., Thase, M. E., Mallinger, A. G. and Houck, P. (1991). Tranylcypromine versus imipramine in anergic bipolar depression. American Journal of Psychiatry, 1487, 910–16.Google Scholar
Hirschfeld, R. M., Williams, J. B., Spitzer, R. L.et al. (2000). Development and validation of a screening instrument for bipolar spectrum disorder: the Mood Disorder Questionnaire. American Journal of Psychiatry, 157, 1873–5.CrossRefGoogle ScholarPubMed
Hirschfeld, R. M., Weisler, R. H., Raines, S. R. and Macfadden, W. (2006). Quetiapine in the treatment of anxiety in patients with Bipolar I or II depression: a secondary analysis from a randomized, double-blind, placebo-controlled study. Journal of Clinical Psychiatry, 67, 355–62.CrossRefGoogle ScholarPubMed
Judd, L. L., Akiskal, H. S., Schettler, P. J.et al. (2003). A prospective investigation of the natural history of the long-term weekly symptomatic status of Bipolar II Disorder. Archives of General Psychiatry, 60, 261–9.CrossRefGoogle ScholarPubMed
Kane, J. M., Quitkin, F. M., Rifkin, A.et al. (1982). Lithium carbonate and imipramine in the prophylaxis of unipolar and Bipolar II illness: a prospective, placebo-controlled comparison. Archives of General Psychiatry, 39, 1065–9.CrossRefGoogle ScholarPubMed
Keck, P. E. Jr., Calabrese, J. R., McQuade, R. D.et al. for the Aripiprazole Study Group (2006). A randomized, double-blind, placebo-controlled 26-week trial of aripiprazole in recently manic patients with Bipolar I Disorder. Journal of Clinical Psychiatry, 67, 626–37.CrossRefGoogle ScholarPubMed
Lam, D. H., Watkins, E. R., Hayward, P.et al. (2003). A randomized controlled study of cognitive therapy for relapse prevention for bipolar affective disorder: outcome of the first year. Archives of General Psychiatry, 60, 145–52.CrossRefGoogle ScholarPubMed
Lam, D. H., Hayward, P., Watkins, E. R., Wright, K. and Sham, P. (2005). Relapse prevention in patients with bipolar disorder: cognitive therapy outcome after 2 years. American Journal of Psychiatry, 162, 324–9.CrossRefGoogle ScholarPubMed
McIntyre, R. S., Brecher, M., Paulsson, B., Huizar, K. and Mullen, J. (2005). Quetiapine or haloperidol as monotherapy for bipolar mania: a 12-week, double-blind randomised, parallel-group, placebo-controlled trial. European Neuropsychopharmacology, 15, 573–85.CrossRefGoogle ScholarPubMed
Miklowitz, D. J., George, E. L., Richards, J. A., Simoneau, T. L. and Suddath, R. L. (2003). A randomized study of family-focused psychoeducation and pharmacotherapy in the outpatient management of bipolar disorder. Archives of General Psychiatry, 60, 904–12.CrossRefGoogle ScholarPubMed
Nemeroff, C. B., Evans, D. L., Gyulai, L.et al. (2001). Double-blind, placebo-controlled comparison of imipramine and paroxetine in the treatment of bipolar depression. American Journal of Psychiatry, 158, 906–12.CrossRefGoogle ScholarPubMed
Nierenberg, A. A., Fava, M., Trivedi, M. H.et al. for the STAR∗D Study Team (2006a). A comparison of lithium and T(3) augmentation following two failed medication treatments for depression: a STAR∗D report. American Journal of Psychiatry, 163, 1519–30; Quiz, 1665.CrossRefGoogle Scholar
Nierenberg, A. A., Ostacher, M. J., Calabrese, J. R.et al. and STEP-BD Investigators (2006b). Treatment-resistant bipolar depression: a STEP-BD equipoise randomized effectiveness trial of antidepressant augmentation with lamotrigine, inositol, or risperidone. American Journal of Psychiatry, 163, 210–16.CrossRefGoogle Scholar
Peet, M. (1994). Induction of mania with selective serotonin re-uptake inhibitors and tricyclic antidepressants. British Journal of Psychiatry, 164, 549–50.CrossRefGoogle ScholarPubMed
Post, R. M., Altshuler, L. L., Leverich, G. S.et al. (2006). Mood switch in bipolar depression: comparison of adjunctive venlafaxine, bupropion and sertraline. British Journal of Psychiatry, 189, 124–31.CrossRefGoogle ScholarPubMed
Prien, R. F. (1984). NIMH report. Five-center study clarifies use of lithium and imipramine for recurrent affective disorders. Hospital and Community Psychiatry, 35, 1097–8.Google ScholarPubMed
Prien, R. F., Caffey, E. M. Jr. and Klett, C. J. (1973). Prophylactic efficacy of lithium carbonate in manic-depressive illness. Report of the Veterans Administration and National Institute of Mental Health collaborative study group. Archives of General Psychiatry, 28, 337–41.CrossRefGoogle ScholarPubMed
Quitkin, F., Rifkin, A., Kane, J., Ramos-Lorenzi, J. R. and Klein, D. F. (1978). Prophylactic effect of lithium and imipramine in unipolar and Bipolar II patients: a preliminary report. American Journal of Psychiatry, 135, 570–2.Google ScholarPubMed
Quitkin, F. M., Kane, J. M., Rifkin, A.et al. (1981). Lithium and imipramine in the prophylaxis of unipolar and Bipolar II depression: a prospective, placebo-controlled comparison. Psychopharmacology Bulletin, 17, 142–4.Google ScholarPubMed
Rea, M. M., Tompson, M. C., Miklowitz, D. J.et al. (2003). Family-focused treatment versus individual treatment for bipolar disorder: results of a randomized clinical trial. Journal of Consulting and Clinical Psychology, 71, 482–92.CrossRefGoogle ScholarPubMed
Sachs, G., Altshuler, L., Ketter, T. et al. (2001). Divalproex versus placebo for the treatment of bipolar depression. 40th Annual Meeting of the American College of Neuropsychopharmacology, Waikaloa, Hawaii, December 9–13.
Scott, J., Paykel, E., Morriss, R.et al. (2006). Cognitive-behavioural therapy for severe and recurrent bipolar disorders: randomised controlled trial. British Journal of Psychiatry, 188, 313–20.CrossRefGoogle ScholarPubMed
Shelton, R. C., Williamson, D. J., Corya, S. A.et al. (2005). Olanzapine/fluoxetine combination for treatment-resistant depression: a controlled study of SSRI and nortriptyline resistance. Journal of Clinical Psychiatry, 66, 1289–97.CrossRefGoogle ScholarPubMed
Thase, M. E., Macfadden, W., Weisler, R. H. for the BOLDER II Study Group (2006). Efficacy of quetiapine monotherapy in Bipolar I and II depression: a double-blind, placebo-controlled study (the BOLDER II study). Journal of Clinical Psychopharmacology, 26, 600–9.CrossRefGoogle Scholar
Tohen, M., Vieta, E., Calabrese, J.et al. (2003). Efficacy of olanzapine and olanzapine-fluoxetine combination in the treatment of Bipolar I depression. Archives of General Psychiatry, 60, 1079–88.CrossRefGoogle ScholarPubMed
Tohen, M., Greil, W., Calabrese, J. R.et al. (2005). Olanzapine versus lithium in the maintenance treatment of bipolar disorder: a 12-month, randomized, double-blind, controlled clinical trial. American Journal of Psychiatry, 162, 1281–90.CrossRefGoogle ScholarPubMed
Tohen, M., Calabrese, J. R., Sachs, G. S.et al. (2006). Randomized, placebo-controlled trial of olanzapine as maintenance therapy in patients with Bipolar I Disorder responding to acute treatment with olanzapine. American Journal of Psychiatry, 163, 247–56.CrossRefGoogle ScholarPubMed
Tondo, L., Baldessarini, R. J., Floris, G. and Rudas, N. (1997). Effectiveness of restarting lithium treatment after its discontinuation in Bipolar I and Bipolar II disorders. American Journal of Psychiatry, 154, 548–50.Google ScholarPubMed
Tondo, L., Baldessarini, R. J., Hennen, J. and Floris, G. (1998). Lithium maintenance treatment of depression and mania in Bipolar I and Bipolar II disorders. American Journal of Psychiatry, 155, 638–45.CrossRefGoogle ScholarPubMed
Vieta, E., Martinez-Aran, A., Goikolea, J. M.et al. (2002). A randomized trial comparing paroxetine and venlafaxine in the treatment of bipolar depressed patients taking mood stabilizers. Journal of Clinical Psychiatry, 63, 508–12.CrossRefGoogle ScholarPubMed
Wehr, T. A. and Goodwin, F. K. (1979). Rapid cycling in manic-depressives induced by tricyclic antidepressants. Archives of General Psychiatry, 36, 555–9.CrossRefGoogle ScholarPubMed
Winsberg, M. E., DeGolia, S. G., Strong, C. M. and Ketter, T. A. (2001). Divalproex therapy in medication-naive and mood-stabilizer-naive Bipolar II depression. Journal of Affective Disorders, 67, 207–12.CrossRefGoogle ScholarPubMed
Zarate, C., Payne, J., Singh, J.et al. (2004). Pramipexole for Bipolar II depression: a placebo-controlled proof of concept study. Biological Psychiatry, 56, 54–60.CrossRefGoogle ScholarPubMed

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  • Management commentary
    • By Terence A. Ketter, Bipolar Disorders Clinic, Stanford, University School of Medicine, Stanford, USA, Po W. Wang, Department of Psychiatry and Behavioral Sciences, Bipolar Disorders Clinic, Stanford, University School of Medicine, California, USA
  • Edited by Gordon Parker, University of New South Wales, Sydney
  • Book: Bipolar II Disorder
  • Online publication: 13 August 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544187.018
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  • Management commentary
    • By Terence A. Ketter, Bipolar Disorders Clinic, Stanford, University School of Medicine, Stanford, USA, Po W. Wang, Department of Psychiatry and Behavioral Sciences, Bipolar Disorders Clinic, Stanford, University School of Medicine, California, USA
  • Edited by Gordon Parker, University of New South Wales, Sydney
  • Book: Bipolar II Disorder
  • Online publication: 13 August 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544187.018
Available formats
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  • Management commentary
    • By Terence A. Ketter, Bipolar Disorders Clinic, Stanford, University School of Medicine, Stanford, USA, Po W. Wang, Department of Psychiatry and Behavioral Sciences, Bipolar Disorders Clinic, Stanford, University School of Medicine, California, USA
  • Edited by Gordon Parker, University of New South Wales, Sydney
  • Book: Bipolar II Disorder
  • Online publication: 13 August 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511544187.018
Available formats
×