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Bipolar Disorders: Mixed States, Rapid-Cycling, and Atypical Forms

Bipolar Disorders: Mixed States, Rapid-Cycling, and Atypical Forms

Bipolar Disorders: Mixed States, Rapid-Cycling, and Atypical Forms

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77 <strong>Rapid</strong>-cycling bipolar disorderDespite the generally positive outcomes of the previously cited studies on theuse of lamotrigine in the treatment of rapid-cycling bipolar disorder, more controlledstudies with longer courses are needed to clarify the role of this promisingagent.LithiumDespite being the oldest among the pharmacological armamentarium in thetreatment of bipolar disorder, lithium continues to draw attention to its utilityas an effective agent in the treatment of different aspects <strong>and</strong> phases of thisdisorder, <strong>and</strong> especially in the rapid-cycling course. While some researchers continueto demonstrate <strong>and</strong> advocate for lithium efficacy in the treatment of rapidcyclingbipolar disorder (Baldessarini et al., 2000, 2002; Swann et al., 2000; Vigueraet al., 2001; Tondo et al., 2001), others have argued that lithium has a poor efficacyin treating rapid-cycling bipolar disorder, even when supplemented by antidepressants<strong>and</strong> neuroleptics (Post et al., 2000; Bowden, 2001).Baldessarini et al.(2000) concluded, in a study evaluating the factors associatedwith rapid-cycling status, that this subtype of bipolar disorder was stronglyassociated with type II diagnosis, higher average pre-lithium episode frequency<strong>and</strong> percentage time ill, <strong>and</strong> weakly with female sex, but not with greater overallmorbidity during treatment. In 360 DSM-IV BP-I (n ¼ 218), <strong>and</strong> BP-II (n ¼ 142)disorder subjects (64% women) followed over an average of 13.3 years, researchersevaluated factors associated with rapid-cycling status with bivariate <strong>and</strong> multivariatetechniques, <strong>and</strong> response to lithium maintenance treatment (recurrencerates, time ill, survival analysis of time to recurrence on lithium). Their resultsindicated that the rapid-cycling risk (15.6% of cases) was 5.1 times greater in BP-IIversus BP-I subjects (30.3% versus 6.0%), in minor excess in women versus men(17.9% versus 11.5%), <strong>and</strong> associated with premorbid cyclothymia, depressive firstepisodes, older onset age, <strong>and</strong> being employed or married. Before lithium, rapidcyclingversus non-rapid-cycling cases had more mean total (3.9 / 1.2), manic, <strong>and</strong>depressive episodes/year, <strong>and</strong> greater percent time ill (60% versus 38%). Duringtreatment, prior rapid-cycling status was unrelated to time to first recurrence <strong>and</strong>other measures of morbidity <strong>and</strong> improvement, including percent time ill, althoughdepressive episodes were 2.7 times more frequent, <strong>and</strong> there was 13.7% less chanceof full protection from all recurrences in rapid-cycling cases. Limitations of the studyincluded that it was naturalistic, without r<strong>and</strong>om assignment or blind assessment.However, its length <strong>and</strong> the number of subjects studied make its conclusionsnoteworthy.On the other h<strong>and</strong>, Swann et al. (2000) reported that at least four previousdepressive or 12 previous manic episodes are associated with reduced antimanic

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