Retinal Prosthesis System for Advanced Retinitis Pigmentosa: A Health Technology Assessment.

Q1 Medicine
Ontario Health Technology Assessment Series Pub Date : 2016-06-01 eCollection Date: 2016-01-01
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引用次数: 0

Abstract

Background: Retinitis pigmentosa is a group of genetic disorders that involves the breakdown and loss of photoreceptors in the retina, resulting in progressive retinal degeneration and eventual blindness. The Argus II Retinal Prosthesis System is the only currently available surgical implantable device approved by Health Canada. It has been shown to improve visual function in patients with severe visual loss from advanced retinitis pigmentosa. The objective of this analysis was to examine the clinical effectiveness, cost-effectiveness, budget impact, and safety of the Argus II system in improving visual function, as well as exploring patient experiences with the system.

Methods: We performed a systematic search of the literature for studies examining the effects of the Argus II retinal prosthesis system in patients with advanced retinitis pigmentosa, and appraised the evidence according to the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) Working Group criteria, focusing on visual function, functional outcomes, quality of life, and adverse events. We developed a Markov decision-analytic model to assess the cost-effectiveness of the Argus II system compared with standard care over a 10-year time horizon. We also conducted a 5-year budget impact analysis. We used a qualitative design and an interview methodology to examine patients' lived experience, and we used a modified grounded theory methodology to analyze information from interviews. Transcripts were coded, and themes were compared against one another.

Results: One multicentre international study and one single-centre study were included in the clinical review. In both studies, patients showed improved visual function with the Argus II system. However, the sight-threatening surgical complication rate was substantial. In the base-case analysis, the Argus II system was cost-effective compared with standard care only if willingness-to-pay was more than $207,616 per quality-adjusted life-year. The 5-year budget impact of funding the Argus II system ranged from $800,404 to $837,596. Retinitis pigmentosa significantly affects people's ability to navigate physical and virtual environments. Argus II was described as enabling the fundamental elements of sight. As such, it had a positive impact on quality of life for people with retinitis pigmentosa.

Conclusions: Based on evidence of moderate quality, patients with advanced retinitis pigmentosa who were implanted with the Argus II retinal prosthesis system showed significant improvement in visual function, real-life functional outcomes, and quality of life, but there were complications associated with the surgery that could be managed through standard ophthalmologic treatments. The costs for the technology are high.

Abstract Image

视网膜假体系统治疗晚期色素性视网膜炎:一项健康技术评估。
背景:色素性视网膜炎是一组遗传性疾病,涉及视网膜光感受器的破坏和丧失,导致进行性视网膜变性和最终失明。Argus II视网膜假体系统是目前唯一获得加拿大卫生部批准的外科植入式设备。它已被证明可以改善晚期色素性视网膜炎严重视力丧失患者的视觉功能。本分析的目的是检查Argus II系统在改善视觉功能方面的临床有效性、成本效益、预算影响和安全性,以及探索患者使用该系统的体验。方法:我们系统地检索了Argus II视网膜假体系统对晚期视网膜色素变性患者影响的研究文献,并根据推荐评估、发展和评估(GRADE)工作组标准对证据进行评价,重点关注视觉功能、功能结局、生活质量和不良事件。我们开发了一个马尔可夫决策分析模型来评估Argus II系统在10年时间内与标准护理相比的成本效益。我们还进行了5年预算影响分析。我们使用定性设计和访谈方法来检查患者的生活经验,并使用改进的扎根理论方法来分析访谈信息。记录被编码,主题被相互比较。结果:临床综述纳入了一项多中心国际研究和一项单中心研究。在这两项研究中,使用Argus II系统的患者的视觉功能都得到了改善。然而,威胁视力的手术并发症发生率很高。在基本情况分析中,Argus II系统只有在每个质量调整生命年的支付意愿超过207,616美元时才与标准护理相比具有成本效益。为Argus II系统提供资金的5年预算影响从800 404美元到837 596美元不等。色素性视网膜炎严重影响人们在物理和虚拟环境中导航的能力。Argus II被描述为赋予视力的基本要素。因此,它对色素性视网膜炎患者的生活质量有积极的影响。结论:基于中等质量的证据,植入Argus II视网膜假体系统的晚期视网膜色素变性患者在视觉功能、实际功能结局和生活质量方面均有显著改善,但存在与手术相关的并发症,可通过标准眼科治疗进行管理。这项技术的成本很高。
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来源期刊
Ontario Health Technology Assessment Series
Ontario Health Technology Assessment Series Medicine-Medicine (miscellaneous)
CiteScore
4.60
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