SALUS-a non-inferiority trial to compare self-tonometry in glaucoma patients with regular inpatient intraocular pressure controls: study design and set-up.

Kristina Oldiges, Maren Steinmann, Juliane Andrea Duevel, Sebastian Gruhn, Raphael Diener, Martin Dominik Leclaire, Sami Al-Nawaiseh, Nicole Eter
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引用次数: 1

Abstract

Purpose: The SALUS study aims to improve the healthcare situation for glaucoma patients in Germany. In order to detect diurnal intraocular pressure (IOP) fluctuations, inpatient monitoring of IOP in an eye hospital for a minimum of 24 h is the current standard. SALUS assesses the benefits of a new form of outpatient care, where IOP can be measured by the patients themselves at home using a self-tonometer. This approach should promote the patient's health competence and empowerment within the healthcare system while reducing treatment costs.

Methods: The SALUS study is a randomized controlled, open non-inferiority trial, alongside an economic analysis, determining whether outpatient monitoring of IOP with self-tonometry is at least as effective as current standard care and would reduce treatment costs. Participants (n = 1980) will be recruited by local ophthalmologists in the area of Westphalia-Lippe, Germany, and randomized to receive 7-day outpatient or 24-h inpatient monitoring. Participants in both study arms will also receive 24-h blood pressure monitoring. Furthermore, patient data from both study groups will be collected in an electronic case file (ECF), accessible to practitioners, hospitals, and the study participants. The primary endpoint is the percentage of patients with IOP peaks, defined as levels 30% above the patient-specific target pressure. Data will also be collected during initial and final examinations, and at 3, 6, and 9 months after the initial examination.

Results: The study implementation and trial management are represented below.

Conclusion: SALUS is a pioneering prospective clinical trial focused on the care of glaucoma patients in Germany. If SALUS is successful, it could improve the healthcare situation and health literacy of the patients through the introduction of various telemedical components. Furthermore, the approach would almost certainly reduce the treatment costs of glaucoma care.

Trial registration: ClinicalTrials.gov ID: NCT04698876, registration date: 11/25/2020.

Drks-id: DRKS00023676, registration date: 11/26/2020.

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salus -一项比较青光眼患者自我眼压测量与常规住院患者眼压控制的非效性试验:研究设计和设置。
目的:SALUS研究旨在改善德国青光眼患者的医疗状况。为了检测眼内压(IOP)的昼夜波动,目前的标准是在眼科医院住院监测眼压至少24小时。SALUS评估了一种新的门诊治疗形式的益处,在这种情况下,IOP可以由患者自己在家使用自测眼压仪测量。这种方法应促进病人的健康能力和授权内的医疗保健系统,同时降低治疗费用。方法:SALUS研究是一项随机对照、开放的非效性试验,同时进行了经济分析,以确定门诊用自测眼压法监测IOP是否至少与目前的标准治疗一样有效,并能降低治疗成本。参与者(n = 1980)将由德国威斯特伐利亚-利佩地区的当地眼科医生招募,并随机接受7天门诊或24小时住院监测。两个研究组的参与者还将接受24小时血压监测。此外,来自两个研究组的患者数据将收集在电子病例档案(ECF)中,供医生、医院和研究参与者访问。主要终点是IOP峰值患者的百分比,定义为高于患者特定目标压的30%。在初次检查和期末检查期间以及初次检查后3、6和9个月收集数据。结果:研究实施和试验管理如下。结论:SALUS是一项开创性的前瞻性临床试验,专注于德国青光眼患者的护理。如果SALUS取得成功,它可以通过引入各种远程医疗组成部分来改善医疗状况和患者的健康素养。此外,这种方法几乎肯定会降低青光眼护理的治疗费用。试验注册:ClinicalTrials.gov ID: NCT04698876,注册日期:11/25/2020。Drks-id: DRKS00023676,注册日期:11/26/2020。
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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