Elsevier

Epilepsy & Behavior

Volume 20, Issue 3, March 2011, Pages 545-549
Epilepsy & Behavior

Long-term outcomes from the PEARLS randomized trial for the treatment of depression in patients with epilepsy

https://doi.org/10.1016/j.yebeh.2011.01.017Get rights and content

Abstract

Depression is associated with higher rates of suicide and lower quality of life in individuals with epilepsy. We previously published the 12-month outcome from our randomized clinical trial of PEARLS (Ciechanowski P, Chaytor N, Miller J, et al. Epilepsy Behav. Epub 5 July 2010). The purpose of this study was to determine the long-term effectiveness of PEARLS, a home-based collaborative care intervention consisting of problem-solving treatment, behavioral activation, and psychiatric consultation, in individuals with epilepsy. Patients were randomly assigned to PEARLS (N = 40) or usual care (N = 40), and assessed at baseline and 6, 12, and 18 months. Patients assigned to PEARLS achieved lower depression severity (P < 0.05) (Hopkins Symptoms Checklist-20), lower suicidal ideation (P < 0.02), and better emotional well being (QOLIE-31) (P < 0.02) over 18 months, compared with patients given the usual care. The PEARLS program significantly reduces depressive symptoms in adults with epilepsy, and this effect is maintained for 18 months after baseline and for more than 1 year after completion of home visits.

Research Highlights

► Long-term outcomes of depression treatment in epilepsy have not been reported. ► The PEARLS intervention resulted in reduction in depression symptoms. ► The PEARLS intervention resulted in reduction in suicidal ideation. ► The PEARLS intervention resulted in improvement in emotional well-being. ► This improvement persisted to the 18-month follow-up.

Introduction

Depression affects 30–50% of individuals with epilepsy [1], [2], [3] and contributes to functional impairment [4], [5], [6], unemployment [7], lower quality of life (QOL), and suicide rates 5–25 times higher than those in the general population [2], [4]. Epilepsy leads to unique challenges that contribute to depression, including driving restrictions [8], physical inactivity [9], social isolation, and unemployment [10]. Depression is suboptimally treated in epilepsy [4], [11], [12], and there are few clinical trials of psychotherapeutic or pharmacological depression treatment in this population. We adapted PEARLS [13] to treat adults with epilepsy through collaboration between public health, psychiatric, and epilepsy professionals. We conducted a randomized controlled trial of PEARLS for treatment of clinically significant depression in people with epilepsy. In 2010, we published the short-term findings from this study showing that PEARLS reduced depression and suicidal ideation and increased emotional well-being compared with usual care over 1 year [14]. Because depression is chronic and recurrent, it is important to explore the long-term impact of this intervention. The current study extends our previous findings to include the 18-month outcome of the PEARLS intervention (i.e., 13 months after services were withdrawn). The PEARLS intervention focuses on teaching participants problem-solving skills and encouraging more active and pleasurable lives, as well as initiation of psychotropic medication when appropriate. It was expected that these skills and behaviors would be maintained after the intervention was withdrawn and result in long-lasting benefits. Specifically, we hypothesized that the benefits of the PEARLS intervention would be maintained over 18 months despite the withdrawal of in-home treatment sessions at 5 months.

Section snippets

Methods

The PEARLS trial was conducted at the University of Washington Regional Epilepsy Center and neurology clinics in Seattle, WA, USA. This study was reviewed and approved by the University of Washington Human Subjects Division and was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki. All persons gave their informed consent prior to their inclusion in the study. The 80 study participants were recruited by neurologist referrals or identified by

Results

Of the 80 subjects enrolled in the study at baseline, 51 completed all three follow-up assessments (6, 12, and 18 months); 29 (36.3%) had at least one missing assessment. Nine (11.3%) subjects did not complete any follow-up assessment. Of the 40 subjects in each arm, 30 PEARLS subjects and 28 UC subjects completed the 18-month follow-up assessment (PEARLS: 6 were unreachable, 2 moved, 1 withdrew, and 1 died; UC: 7 were unreachable, 1 moved, 3 withdrew, and 1 died). There was no significant

Discussion

The PEARLS trial is the first published randomized controlled effectiveness trial of an intervention specifically tailored to treat depression in patients with epilepsy, to our knowledge. The PEARLS intervention resulted in improvement in depressive symptoms, suicidal ideation, and emotional well being that persisted to the 18-month follow-up despite withdrawal of in-home treatment sessions at 19 weeks and monthly phone contacts at 12 months. This persistence of treatment effect is even more

Acknowledgments

We acknowledge the generous funding of the Prevention Research Centers Program and Epilepsy Program of the Centers for Disease Control and Prevention and the University of Washington Health Promotion Research Center (No. U48DP000050) and the support of CHAMMP (Center for Healthcare Improvement for Addictions, Mental Illness and Medically Vulnerable Populations) at Harborview Medical Center, Seattle WA, USA. We also thank our PEARLS research staff: Eddie Edmondson, Emily Rosenberger, Gina

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