利伯遗传性视神经病变:公用事业和照顾者负担从英国和爱尔兰参与者。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Claire Lawrence, Emma Williams, Andrew Mumford, Steve Bojakowski, Julio Benedicto, Andrew Lloyd
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引用次数: 0

摘要

背景:Leber遗传性视神经病变(LHON)是一种罕见的母系遗传性线粒体疾病,导致突发性进行性中央视力丧失。这种情况影响日常生活、功能和整体健康相关生活质量(HRQL)的许多方面,这可能会波及到护理人员。方法:两项研究旨在评估LHON患者与不同视力相关的效用(研究1),并探讨护理人员负担(研究2)。在研究1中,8名LHON健康状态小受试者(轻度视力丧失[LogMAR])结果:研究1表明视力功能较差的人效用较低。结论:研究结果表明,与EQ-5D和TTO方法相比,HUI-3可能对视力丧失对HRQL的影响更敏感。这些数据表明一种有效治疗LHON的潜在价值。定性研究结果描述了LHON对护理人员的影响。然而,定性数据中描述的负担与定量测量不一致,特别是EQ-5D-5L。这表明进行混合方法研究的价值和选择能够捕捉到与人口有关的概念的措施的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leber hereditary optic neuropathy: utilities and carer burden from British and Irish participants.

Background: Leber hereditary optic neuropathy (LHON) is a rare, maternally inherited, mitochondrial disease resulting in sudden, progressive central vision loss. The condition affects numerous aspects of daily life, functioning and overall health-related quality of life (HRQL), which may spillover to carers.

Methods: Two studies were designed to estimate patient utilities associated with varying visual acuity in LHON (study 1) and to explore carer burden (study 2). In study 1, eight LHON health state vignettes (mild vision loss [LogMAR < 0.3] through to light perception [LogMAR ≥ 4]) were valued by the UK and Republic of Ireland (ROI) general pubic using the Health Utilities Index- 3 (HUI-3) and EQ-5D in an online survey (N = 360) and in time trade-off interviews (TTO; n = 120). In study 2, nine carers completed in-depth interviews exploring carer burden, the Care-related Quality of Life instrument (CarerQol), EQ-5D-5L and the Work Productivity and Activity Impairment Questionnaire (WPAI).

Results: Study 1 demonstrated lower utilities for people with worse visual function. Mild vision loss (LogMAR < 0.3) was rated as 0.84 (HUI-3), 0.79 (EQ-5D) and 0.88 (TTO). Light perception (LogMAR ≥ 4), the most severe health state, was rated as 0.18 (HUI-3), 0.34 (EQ-5D), and 0.36 (TTO). In study 2, qualitative findings revealed substantial burden for many carers and family members. The most prominent impacts were emotional (e.g., guilt, devastation), especially related to the maternal inheritance of LHON. Impacts to carers' daily life, social life and relationships, work, and finances were also described. Standardised measures identified little impact on HRQL (EQ-5D-5L = 0.89), but some carer related burden (CarerQol-7D = 78.4). The WPAI revealed an overall work impairment of 15% and activity impairment of 37%.

Conclusions: Findings suggest the HUI-3 may be more sensitive to the HRQL impact of vision loss compared to the EQ-5D and TTO method. The data indicate the potential value of an effective treatment for LHON. Qualitative findings describe the impact of LHON on carers. However, the burden described in the qualitative data was incongruent with quantitative measures, particularly the EQ-5D-5L. This demonstrates the value of conducting mixed-methods research and the importance of selecting measures which capture population-relevant concepts.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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