BIPOLAR DISORDER RESULTS IN SIGNIFICANT BURDEN ON CAREGIVERS- ANALYSIS OF DATA FROM A LARGE MULTINATIONAL LONGITUDINAL STUDY (WAVE-BD)

Author(s)

Vieta E1, Figueira ML2, Bellivier F3, Souery D4, Blasco-Colmenares E5, Langosch JM6, Medina E71Bipolar Disorders Programme, Hospital Clínic, University of Barcelona, IDIBAPS, CIBERSAM, Barcelona, Spain, 2Hospital Santa Maria, Faculty of Medicine, Universi

OBJECTIVES: WAVE-bd (Wide AmbispectiVE study of the clinical management and burden of bipolar disorder [BD]) is ongoing to address limitations of longitudinal BD studies to-date, few of which investigate caregiver burden. Objectives are to provide reliable, real-world data, including assessment of burden among caregivers (usually unpaid relatives or friends), an important consideration in BD patient management. METHODS: Multinational, multicentre, non-interventional, longitudinal study of patients diagnosed with BD with ≥1 mood event in the preceding 12 months (retrospective data collection from index mood event to enrollment, followed by a minimum 9 months’ prospective follow-up). Patient selection provided a representative sample of BD populations in daily practice. Caregiver burden was assessed using the Burden Assessment Scale (BAS), where scores range 19–76, with higher scores indicating greater burden. Assessment was carried out once during any part of the prospective follow-up for one caregiver only per patient. RESULTS: To-date, 583/2880 patients (BD-I: 21.8%; BD-II: 16.8%) have attended their baseline appointment with their primary caregiver (caregiver mean age 50.2 years; 57% female). The majority of caregivers were patients’ partners or parents (44.1% and 33.5%, respectively), with >10 years of education. The professional status of caregivers was: employed (47.4%), retired (22.7%), homemaker (16.6%), unemployed (5.8%) and other (7.4%). BAS scores were collected from 574 caregivers, and total caregiver burden was 47.6 ± 13.7 (n=424) for BD-I and 42.4 ± 12.6 (n=150) for BD-II (p=0.0003). Burden was recorded among caregivers of patients with (at inclusion) euthymia (43.8 ± 13.1; n=329), mania (47.7 ± 13.6; n=41), hypomania (51.6 ± 12.7; n=44), depression (49.9 ± 14.4; n=137), or mixed disease status (50.2 ± 9.5; n=20). CONCLUSIONS: This ongoing study provides multinational perspectives on the high burden experienced by caregivers of individuals with BD-I and BD-II in everyday clinical practice settings. Study funded by AstraZeneca; Clinical Trials Registry: NCT01062607.

Conference/Value in Health Info

2011-05, ISPOR 2011, Baltimore, MD, USA

Value in Health, Vol. 14, No. 3 (May 2011)

Code

PMH60

Topic

Health Service Delivery & Process of Care

Topic Subcategory

Treatment Patterns and Guidelines

Disease

Mental Health

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