The Economic and societal burden of multiple sclerosis on lebanese society: a cost-of-illness and quality of life study protocol
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Taylor and Francis Ltd.
Abstract
This protocol describes the estimation of the societal costs and quality-of-life (QOL) burden of multiple sclerosis (MS) in Lebanon. This cross-sectional, prevalence-based burden-of-illness study was carried out in a premier MS center in Lebanon. We enrolled Lebanese patients aged 18 years and older who had been diagnosed with MS more than 6 months. The study uses a bottom-up approach to estimate the cost-of-illness (COI) and QOL using a retrospective face-to-face interview questionnaire. This resource utilization questionnaire was adapted to the Lebanese context by clinical and health economics experts. The methodologies used to estimate the consumption of healthcare resources, informal care, and productivity losses are well-defined and aligned with the Lebanese healthcare system. Costs are presented overall and by MS severity levels. QOL is measured using the EuroQOL (EQ-5D-5 L) and Multiple Sclerosis International Quality of Life (MusiQoL) instrument. This protocol pioneers in informing the design of future COI and QOL studies in low–and middle-income countries (LMICs), as the methods used could be applied in similar LMICs. Furthermore, we provide recommendations and discuss the challenges of conducting a high-quality burden-of-illness study in LMICs and the steps taken to meet them, using the case of Lebanon. © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
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Keywords
Cost-of-illness, Economic burden, Lebanon, Multiple sclerosis, Study protocol, Utilities, Caregivers, Cost of illness, Cross-sectional studies, Health care costs, Humans, Quality of life, Retrospective studies, Adult, Article, Cross-sectional study, Disease burden, Disease duration, Economic aspect, European quality of life 5 dimensions questionnaire, Expanded disability status scale, Health care cost, Health care system, Health economics, Health status, Human, Multiple sclerosis international quality of life instrument, Practice guideline, Prevalence, Productivity, Quality of life assessment, Retrospective study, Social aspect, Caregiver