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Naslov:Leber hereditary optic neuropathy in Slovenia : quality of life and costs from patient perspective
Avtorji:ID Hawlina, Marko (Avtor)
ID Kovač, Lea (Avtor)
ID Breciková, Katarína (Avtor)
ID Žigmond, Jan (Avtor)
ID Rogalewicz, Vladimír (Avtor)
ID Tichopád, Aleš (Avtor)
ID Pfiegler, György (Avtor)
ID Šarkanová, Ivana (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (921,36 KB)
MD5: 9690386AE95F039EFB9FDCEDC4943DA7
 
URL URL - Izvorni URL, za dostop obiščite https://ojrd.biomedcentral.com/articles/10.1186/s13023-024-03329-0)
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek: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.
Ključne besede:LHON, socioeconomic burden, absenteeism, productivity loss, quality of life
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2024
Št. strani:str. 1-6
Številčenje:Vol. 19
PID:20.500.12556/DiRROS-27838 Novo okno
UDK:616.1
ISSN pri članku:1750-1172
DOI:10.1186/s13023-024-03329-0 Novo okno
COBISS.SI-ID:227326979 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 25. 5. 2025; Članek št. 318;
Datum objave v DiRROS:26.02.2026
Število ogledov:150
Število prenosov:60
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Orphanet journal of rare diseases
Založnik:BioMed Central
ISSN:1750-1172
COBISS.SI-ID:514009369 Novo okno

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Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
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