Retinitis Pigmentosa: Burden of Disease and Current Unmet Needs

医学 色素性视网膜炎 社会心理的 黄斑变性 疾病 生活质量(医疗保健) 科克伦图书馆 梅德林 视力障碍 糖尿病性视网膜病变 家庭医学 老年学 精神科 替代医学 眼科 病理 护理部 视网膜 政治学 法学 糖尿病 内分泌学
作者
Nancy E. Cross,Cécile van Steen,Yasmina Zegaoui,Andrew Satherley,Luigi Angelillo
出处
期刊:Clinical Ophthalmology 卷期号:Volume 16: 1993-2010 被引量:15
标识
DOI:10.2147/opth.s365486
摘要

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.
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