Journal of the American Academy of Child & Adolescent Psychiatry
Volume 46, Issue 7 , Pages 831-839, July 2007

Adherence to Pharmacological Treatment for Juvenile Bipolar Disorder

Accepted 22 February 2007.

ABSTRACT 

Objective

The objective of this study was to describe the prevalence and correlates of adherence to divalproex sodium (DVPX) and lithium carbonate (Li) combination treatment during the initial stabilization treatment phase.

Method

Adherence to Li/DVPX combination therapy was measured by the presence or absence of minimum serum concentrations of DVPX (50 μg/mL) or Li (0.6 mmol/L). Secondary measures included pill count, patient/parent report, and clinical judgment. Correlates of adherence, including patient characteristics, medication side effects, and family variables, were evaluated.

Results

One hundred seven patients (70 males and 37 females) were studied. The proportion of serum concentrations in the therapeutic range across the study period was 0.84 for DVPX and 0.66 for Li. Maternal (r = −0.31; p<.01) and paternal (r = −0.44; p < .01) hospitalization for a psychiatric disorder and less adaptive family functioning (r=−0.26; p < .05) related to treatment nonadherence for DVPX. Better treatment adherence to DVPX (r = 0.21; p < .05) and Li (r = 0.23; p < .05) was associated with a greater number of side effects, whereas male sex was associated with worse adherence to both DVPX (r= −0.24; p < .05) and Li (r = −0.22; p < .05) pharmacotherapy. Clinical response to treatment correlated with adherence to DVPX treatment (r = 0.33; p < .01).

Conclusions

Nonadherence may limit the statistical power of treatment efficacy studies and the effectiveness of pharmacotherapy treatment for juvenile BPD and necessitate strategies to evaluate and enhance levels of treatment adherence.

Key Words:  treatment adherence , bipolar disease , pharmacotherapy

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 The Stanley Medical Research Institute primarily supported this study. It was also supported in part by an NIMH Developing Centers for Interventions and Services Research Grant ( P20 MH-66054 ), NIHT32 HD041923-05 , NIHT32 HD041923-05 . Medications for the clinical trial were provided in part by Abbott Laboratories. The work of Susan Wood in processing this manuscript is gratefully acknowledged.Disclosure: Dr. Calabrese has received pharmaceutical income, research grant support, honoraria, and compensation for consultation from Abbott, AstraZeneca, France Foundation, GlaxoSmithKline, Janssen, Johnson & Johnson Pharmaceutical Research & Development, Solvay/Wyeth, Bristol-Myers Squibb, and Eli Lilly. Dr. Findling receives or has received research support from, acted as a consultant to, and/or served on the speakers' bureaus of Abbott, AstraZeneca, Bristol-Myers Squibb, Celltech-Medeva, Forest, GlaxoSmithKline, Johnson & Johnson, Eli Lilly, New River, Novartis, Otsuka, Pfizer, Sanofi-Aventis, Shire, Solvay, and Wyeth. The other authors have no financial relationships to disclose.

PII: S0890-8567(09)62171-7

doi:10.1097/chi.0b013e31805c7421

Journal of the American Academy of Child & Adolescent Psychiatry
Volume 46, Issue 7 , Pages 831-839, July 2007