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

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

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242 B. Birmaher <strong>and</strong> D. Axelsonet al., 1985; Bowring <strong>and</strong> Kovacs, 1992; Carlson <strong>and</strong> Weintraub, 1993;Carlson, 1995; Geller et al., 1995, 1998a, b; 2000a, b; 2002a, b; Lewinsohnet al., 1995, 2000; Weller et al., 1995;Wozniaket al., 1995;Axelsonet al., 1998).(3) Most children <strong>and</strong> adolescents with BP disorder have comorbidity withADHD <strong>and</strong> behavior-disruptive disorders (Bowring <strong>and</strong> Kovacs, 1992;Carlson, 1995; Geller et al., 1995, 1998a, b, 2002a; Kovacs <strong>and</strong> Pollock, 1995;Lewinsohn et al., 1995, 2000; Weller et al., 1995; Wozniak et al., 1995; Axelsonet al., 1998; Biederman, 1998). These comorbid conditions usually confoundthe diagnosis of BP disorder in youth.(4) It appears that early-onset BP disorder conveys a worse course <strong>and</strong> outcomethan BP disorder that started during adulthood (Geller et al., 2002a, b).(5) The child’s emotional, cognitive, <strong>and</strong> behavioral developmental stages need tobe taken into consideration when assessing symptoms of BP disorder (e.g.,fantasies versus gr<strong>and</strong>iosity; Bowring <strong>and</strong> Kovacs, 1992; Carlson, 1995).(6) Environmental factors (e.g., family conflicts, parental psychopathology, negativelife events) may affect the clinical presentation <strong>and</strong> course of illness(Geller et al., 2002b).(7) Overdiagnosis of BP disorder in children <strong>and</strong> adolescents also has seriousconsequences, as youth with other psychiatric conditions are unnecessarilyexposed to medications with significant risk for side-effects <strong>and</strong> do not receivepotentially therapeutic treatments for their actual disorder.Longitudinal courseLewinsohn et al. (1995) evaluated 1709 high-schoolers (ages 16.6 1.2 years old,54% females, 91% Caucasian) with the K-SADS Present <strong>and</strong> Epidemiological versions<strong>and</strong> found 1% (18) with BP disorder (mainly BP-II <strong>and</strong> cyclothymia) <strong>and</strong> 5.7%(97) with subsyndromal BP symptoms. These patients were reinterviewed 14 monthsafter intake <strong>and</strong> compared with 316 subjects with MDD <strong>and</strong> 845 normal controls.The BP patients had the worse course, with a median duration for their index episodeof illness of 80 weeks. Also they had more functional impairment, psychosis, suicidality,comorbid anxiety <strong>and</strong> disruptive disorders, <strong>and</strong> mental health utilization thanthe other two groups (Fig. 10.3). The subjects with subsyndromal BP symptoms hadlevels of impairment <strong>and</strong> comorbidity that were comparable to the BP group.Strober et al. (1995) reported results from a 5-year naturalistic, prospectivefollow-up of a small sample (n ¼ 54) of inpatient adolescents with BP-I disorderutilizing semiannual assessments. Although the absolute likelihood of recovery( 8 weeks with < 2 symptoms) was high in the sample as a whole, 20% of thesample had suicide attempts requiring medical attention <strong>and</strong> time to recovery

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