Feasibility of in-home monitoring for people with glaucoma: the I-TRAC mixed-methods study.

IF 3.5 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Carrie Stewart, Hangjian Wu, Uma Alagappan, Augusto Azuara-Blanco, Anthony J King, Andrew J Tatham, Rodolfo Hernández, Bruce Lowe, Darian Shotton, Nana Appiah, Taylor Coffey, Thenmalar Vadiveloo, Graeme MacLennan, Katie Gillies
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引用次数: 0

Abstract

Background: Glaucoma is a chronic disease of the optic nerve and a leading cause of severe visual loss in the UK. Once patients have been diagnosed, they need regular monitoring at hospital eye services. Recent advances in technology mean patients with glaucoma can now monitor their disease at home. This could be more convenient for patients and potentially reduce costs and increase capacity for the NHS. However, it is uncertain whether self-monitoring would be acceptable or possible for patients with glaucoma.

Objectives: The objectives were to: identify which patients are most appropriate for home monitoring; understand views of key stakeholders (patients, clinicians, researchers) on whether home glaucoma monitoring is feasible and acceptable; develop a conceptual framework for the economic evaluation of home glaucoma monitoring; and explore the need for and provide evidence on the design of a future study to evaluate the clinical and cost-effectiveness of digital technologies for home monitoring of glaucoma.

Design: In-home Tracking of glaucoma: Reliability, Acceptability, and Cost (I-TRAC) was a multiphase mixed-methods feasibility study with key components informed by theoretical and conceptual frameworks.

Setting: Expert glaucoma specialists in the UK recruited through professional glaucoma societies; study site staff and patient participants recruited through three UK hospital eye services (England, Scotland, Northern Ireland); and UK research teams recruited though existing networks.

Intervention: Home tonometer that measures intraocular pressure and a tablet computer with a visual function application. Patients were asked to use the technology weekly for 12 weeks.

Results: Forty-two patients were recruited. Retention and completion of follow-up procedures was successful, with 95% (n = 40) completing the 3-month follow-up clinic visits. Adherence to the interventions was generally high [adherence to both devices (i.e. ≥ 80% adherence) was 55%]. Overall, patients and healthcare professionals were cautiously optimistic about the acceptability of digital technologies for home monitoring of patients with glaucoma. While most clinicians were supportive of the potential advantages glaucoma home monitoring could offer, concerns about the technologies (e.g. reliability and potential to miss disease progression) and how they would fit into routine care need to be addressed. Additionally, clarity is required on defining the ideal population for this intervention. Plans for how to evaluate value for money in a future study were also identified. However, the study also highlighted several unknowns relating to core components of a future evaluative study that require addressing before progression to a definitive effectiveness trial.

Limitations: The main limitation relates to our sample and its generalisability, for example, the over-representation of educated persons of white ethnicity who were generally experienced with technology and research motivated.

Conclusions: The In-home Tracking of glaucoma: Reliability, Acceptability, and Cost study has demonstrated 'cautious optimism' when considering patients' and healthcare professionals' views on the acceptability of digital technologies for home monitoring of patients with glaucoma. However, the study also highlighted several unknowns relating to the research question and design of a future evaluative study that require addressing before progression to a randomised controlled trial.

Future work: Further research is required to determine the appropriate population (i.e. low vs. high risk of progression) and further refine the intervention components and delivery for planning of future evaluation studies.

Study registration: This study is registered as Research Registry #6213.

Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (NIHR award ref: NIHR129248) and is published in full in Health Technology Assessment; Vol. 28, No. 44. See the NIHR Funding and Awards website for further award information.

对青光眼患者进行居家监测的可行性:I-TRAC 混合方法研究。
背景:青光眼是一种视神经慢性疾病,也是导致英国人视力严重下降的主要原因。患者一旦确诊,就需要在医院眼科接受定期监测。最近技术的进步意味着青光眼患者现在可以在家监测病情。这可以为患者提供更多便利,并有可能为国家医疗服务体系降低成本和提高服务能力。然而,目前还不确定青光眼患者是否可以接受或可能进行自我监测:目标:确定哪些患者最适合进行家庭监测;了解主要利益相关者(患者、临床医生、研究人员)对家庭青光眼监测是否可行和可接受的看法;为家庭青光眼监测的经济评估制定概念框架;探讨未来研究设计的必要性并提供证据,以评估数字技术用于家庭青光眼监测的临床和成本效益:设计:青光眼居家跟踪:设计:"居家青光眼跟踪:可靠性、可接受性和成本"(I-TRAC)是一项多阶段混合方法可行性研究,其主要组成部分以理论和概念框架为依据:环境:通过专业青光眼协会招募英国青光眼专家;通过英国三家医院眼科服务机构(英格兰、苏格兰、北爱尔兰)招募研究机构工作人员和患者参与者;通过现有网络招募英国研究团队:干预措施:测量眼压的家用眼压计和带有视觉功能应用程序的平板电脑。要求患者每周使用该技术12周:结果:招募了 42 名患者。成功留住并完成了随访程序,95%(n = 40)的患者完成了为期 3 个月的随访。对干预措施的依从性普遍较高[对两种设备的依从性(即依从性≥80%)为55%]。总体而言,患者和医护人员对数字技术用于青光眼患者家庭监测的可接受性持谨慎乐观态度。虽然大多数临床医生对青光眼家庭监测可能带来的潜在优势表示支持,但仍需解决对这些技术的担忧(如可靠性和错过疾病进展的可能性),以及如何将其融入常规护理中。此外,还需要明确界定这一干预措施的理想人群。此外,还确定了在未来研究中如何评估资金价值的计划。不过,该研究也强调了与未来评估研究的核心组成部分有关的几个未知因素,这些因素需要在进入最终有效性试验之前加以解决:局限性:主要局限性与我们的样本及其普遍性有关,例如,受过教育的白种人比例过高,而这些人一般都具有丰富的技术经验和研究动机:青光眼居家跟踪:结论:"青光眼的居家跟踪:可靠性、可接受性和成本 "研究在考虑患者和医护人员对数字技术用于青光眼患者居家监测的可接受性时,表现出了 "谨慎的乐观"。不过,该研究也强调了与研究问题和未来评估研究设计有关的几个未知因素,需要在进行随机对照试验之前加以解决:今后的工作:需要进一步研究,以确定合适的人群(即进展风险低的人群与进展风险高的人群),并进一步完善干预内容和实施方式,以规划未来的评估研究:研究注册:本研究已注册为研究注册 #6213:本奖项由美国国家健康与护理研究所(NIHR)健康技术评估项目资助(NIHR奖项编号:NIHR129248),全文发表于《健康技术评估》第28卷第44期。更多奖项信息请参阅 NIHR Funding and Awards 网站。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Health technology assessment
Health technology assessment 医学-卫生保健
CiteScore
6.90
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: Health Technology Assessment (HTA) publishes research information on the effectiveness, costs and broader impact of health technologies for those who use, manage and provide care in the NHS.
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