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Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs
Retinitis Pigmentosa (RP), a group of inherited retinal dystrophies characterised by progressive vision loss, is the leading cause of visual disability and blindness in subjects less than 60 years old. Currently incurable, therapy is aimed at restricting degeneration of vision, treating complication...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232096/ https://www.ncbi.nlm.nih.gov/pubmed/35757022 http://dx.doi.org/10.2147/OPTH.S365486 |
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author | Cross, Nancy van Steen, Cécile Zegaoui, Yasmina Satherley, Andrew Angelillo, Luigi |
author_facet | Cross, Nancy van Steen, Cécile Zegaoui, Yasmina Satherley, Andrew Angelillo, Luigi |
author_sort | Cross, Nancy |
collection | PubMed |
description | Retinitis Pigmentosa (RP), a group of inherited retinal dystrophies characterised by progressive vision loss, is the leading cause of visual disability and blindness in subjects less than 60 years old. Currently incurable, therapy is aimed at restricting degeneration of vision, treating complications, and helping patients to cope with the psychosocial impact of their disease. Hence, RP is associated with a high burden of disease. This paper describes the current therapeutic landscape for RP and the disease burden for patients, caregivers, and society. A review of available data was conducted in three stages: (1) a literature search of publicly available information on all domains of RP; (2) a systematic literature review using Medline, Embase, the Cochrane Library and grey literature (GlobalData) on epidemiology and cost of RP; and (3) qualitative research with senior physicians treating RP patients in the EU4 and the UK to validate research findings from secondary sources. RP severely impacts the daily lives of over a million people worldwide. Progressive vision loss significantly affects the ability to perform basic daily tasks, to maintain employment, and maintain independence. Consequently, most patients will experience reduced quality of life, with a greater emotional and psychological impact than other conditions related to vision loss such as diabetic retinopathy or age-related macular degeneration. RP is also associated with a high level of carer burden, arising from psychological and financial stress. The therapeutic landscape for RP is limited, with few treatment options and minimal guidance for the diagnosis, treatment, and care of patients. A curative intervention, voretigene neparvovec (Luxturna(®)), only exists for 1–6% of patients. Although disease management can be successful in developing coping strategies, most patients live with this chronic, progressive condition without interventions to change the disease course. Innovative new therapies can transform the therapeutic landscape, provided appropriate clinical guidance is forthcoming. |
format | Online Article Text |
id | pubmed-9232096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-92320962022-06-25 Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs Cross, Nancy van Steen, Cécile Zegaoui, Yasmina Satherley, Andrew Angelillo, Luigi Clin Ophthalmol Perspectives Retinitis Pigmentosa (RP), a group of inherited retinal dystrophies characterised by progressive vision loss, is the leading cause of visual disability and blindness in subjects less than 60 years old. Currently incurable, therapy is aimed at restricting degeneration of vision, treating complications, and helping patients to cope with the psychosocial impact of their disease. Hence, RP is associated with a high burden of disease. This paper describes the current therapeutic landscape for RP and the disease burden for patients, caregivers, and society. A review of available data was conducted in three stages: (1) a literature search of publicly available information on all domains of RP; (2) a systematic literature review using Medline, Embase, the Cochrane Library and grey literature (GlobalData) on epidemiology and cost of RP; and (3) qualitative research with senior physicians treating RP patients in the EU4 and the UK to validate research findings from secondary sources. RP severely impacts the daily lives of over a million people worldwide. Progressive vision loss significantly affects the ability to perform basic daily tasks, to maintain employment, and maintain independence. Consequently, most patients will experience reduced quality of life, with a greater emotional and psychological impact than other conditions related to vision loss such as diabetic retinopathy or age-related macular degeneration. RP is also associated with a high level of carer burden, arising from psychological and financial stress. The therapeutic landscape for RP is limited, with few treatment options and minimal guidance for the diagnosis, treatment, and care of patients. A curative intervention, voretigene neparvovec (Luxturna(®)), only exists for 1–6% of patients. Although disease management can be successful in developing coping strategies, most patients live with this chronic, progressive condition without interventions to change the disease course. Innovative new therapies can transform the therapeutic landscape, provided appropriate clinical guidance is forthcoming. Dove 2022-06-20 /pmc/articles/PMC9232096/ /pubmed/35757022 http://dx.doi.org/10.2147/OPTH.S365486 Text en © 2022 Cross et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Perspectives Cross, Nancy van Steen, Cécile Zegaoui, Yasmina Satherley, Andrew Angelillo, Luigi Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs |
title | Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs |
title_full | Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs |
title_fullStr | Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs |
title_full_unstemmed | Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs |
title_short | Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs |
title_sort | retinitis pigmentosa: burden of disease and current unmet needs |
topic | Perspectives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232096/ https://www.ncbi.nlm.nih.gov/pubmed/35757022 http://dx.doi.org/10.2147/OPTH.S365486 |
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