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Title:Leber hereditary optic neuropathy in Slovenia : quality of life and costs from patient perspective
Authors:ID Hawlina, Marko (Author)
ID Kovač, Lea (Author)
ID Breciková, Katarína (Author)
ID Žigmond, Jan (Author)
ID Rogalewicz, Vladimír (Author)
ID Tichopád, Aleš (Author)
ID Pfiegler, György (Author)
ID Šarkanová, Ivana (Author)
Files:.pdf PDF - Presentation file, download (921,36 KB)
MD5: 9690386AE95F039EFB9FDCEDC4943DA7
 
URL URL - Source URL, visit https://ojrd.biomedcentral.com/articles/10.1186/s13023-024-03329-0)
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Introduction Leber hereditary optic neuropathy (LHON) is the most commonly diagnosed mitochondrial disorder, resulting in colour vision abnormalities and rapid but painless deterioration of central vision. While numerous studies have assessed the impact of LHON on the quality of life (QoL) of LHON patients, the financial impact of the disease remains unexplored. This study attempts to calculate both the direct non-medical costs and the indirect costs associated with productivity losses experienced by people with LHON and their unpaid caregivers in Slovenia, in addition to assessing their QoL. Due to the rarity of the disease, the study involved a small sample size, which is important to note for interpreting the results. Methods The analysis was conducted on nine adult participants diagnosed with LHON, representing one-third of the total number of known Slovenian patients with this condition. To thoroughly assess the economic and social impact of LHON, tailored questionnaires were designed to collect information on demographics, socioeconomic status, LHON severity, and associated non-medical and indirect costs. Results The mean age of the study participants was 48.8 years (SD 13.3; n=9). The annual productivity loss attributable to LHON, taking both absenteeism and relative presenteeism into account, was calculated to be EUR 11,608 per person affected. The mean VFQ-25 score, a measure of vision-related quality of life, for adult LHON patients was 30.4 (SD 12.9). Conclusion The findings highlight the significant economic and social burden of LHON on patients and their families. Ensuring prompt, accurate diagnosis, access to treatment, financial support, and psychological counselling and services are critical to helping individuals cope with and mitigate the profound challenges of vision loss and living with LHON.
Keywords:LHON, socioeconomic burden, absenteeism, productivity loss, quality of life
Publication status:Published
Publication version:Version of Record
Year of publishing:2024
Number of pages:str. 1-6
Numbering:Vol. 19
PID:20.500.12556/DiRROS-27838 New window
UDC:616.1
ISSN on article:1750-1172
DOI:10.1186/s13023-024-03329-0 New window
COBISS.SI-ID:227326979 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 25. 5. 2025; Članek št. 318;
Publication date in DiRROS:26.02.2026
Views:153
Downloads:60
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Record is a part of a journal

Title:Orphanet journal of rare diseases
Publisher:BioMed Central
ISSN:1750-1172
COBISS.SI-ID:514009369 New window

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License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

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