Societal costs and quality of life associated with arginase 1 deficiency in a European setting – a multinational, cross-sectional survey
Open Access
- 7 September 2024
- journal article
- research article
- Published by Taylor & Francis in Journal of Medical Economics
- Vol. 27 (1) , 1146-1156
Abstract
Arginase 1 deficiency (ARG1-D) is a ultrarare disease with manifestations that cause mobility and cognitive impairment that progress over time and may lead to early mortality. Diseases such as ARG1-D have a major impact also outside of the health care sector and the aim of this study was to estimate the current burden of disease associated with ARG1-D from a societal perspective. The study was performed as a web-based survey of patients with ARG1-D and their caregivers in four European countries (France, Portugal, Spain, United Kingdom). The survey was distributed at participating clinics and included questions on e.g., symptoms (including the Gross Motor Function Classification System, GMFCS, and cognitive impairment), health care use, medication, ability to work, caregiving, and impact on health-related quality-of-life (HRQoL) using the EQ-5D-5L. The estimated total mean societal cost per patient and year was £63,775 (SD: £49,944). The cost varied significantly with both mobility impairment (from £49,809 for GMFCS level 1 to £103,639 for GMFCS levels 3-5) and cognitive impairment (from £43,860 for mild level to £99,162 for severe level). The mean utility score on the EQ-5D-5L for patients was 0.498 (SD: 0.352). The utility score also varied significantly with both mobility impairment (from 0.783 for GMFCS level 1 to 0.153 for GMFCS level 3-5) and cognitive impairment (from 0.738 for mild level to 0.364 for severe level). Similar to other studies of rare diseases, the study is based on a limited number of observations. However, the sample appear to be reasonably representative when comparing to previous studies of ARG1-D. This study shows that ARG1-D is associated with a high societal cost and significant impact on HRQoL. Earlier diagnosis and better treatment options that can postpone or withhold progression may therefore have a potential for improved HRQoL and savings for the patient, caregiver, and society.Keywords
Funding Information
- Immedica Pharma AB
This publication has 27 references indexed in Scilit:
- Efficacy and safety of pegzilarginase in arginase 1 deficiency (PEACE): a phase 3, randomized, double-blind, placebo-controlled, multi-centre trialeClinicalMedicine, 2024
- Natural history of arginase 1 deficiency and the unmet needs of patients: A systematic review of case reportsJIMD Reports, 2022
- Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiencyJIMD Reports, 2021
- Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiencyJournal of Inherited Metabolic Disease, 2020
- Health-related quality of life in adults with cerebral palsy living in Sweden and relation to demographic and disability-specific factorsDisability and Health Journal, 2019
- Suggested guidelines for the diagnosis and management of urea cycle disorders: First revisionJournal of Inherited Metabolic Disease, 2019
- Valuing health-related quality of life: An EQ-5D-5L value set for EnglandHealth Economics, 2017
- The Health and Quality of Life Outcomes Among Youth and Young Adults With Cerebral PalsyArchives of Physical Medicine and Rehabilitation, 2010
- Arginine metabolism and nutrition in growth, health and diseaseAmino Acids, 2008
- Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiencyAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2006