Validation and Repeatability of Differential Light Sensitivity Measurements with the Novel MAIA Microperimetry Device

IF 4.6 Q1 OPHTHALMOLOGY
Georg Ansari MD , Nina L. Giudici MD , Giuseppe Cancian MD , Petra Rossouw , Chiara Rui PhD , Alberto Rosso PhD , Silvia Gazzina PhD , Nicolas Feltgen MD , Kristina Pfau MD , Maximilian Pfau MD
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引用次数: 0

Abstract

Objective

Microperimetry is critical for the evaluation of macular light sensitivity, enabling disease monitoring in patients with either center-involving scotoma or initial sparing of the center. The purpose of this study was to investigate the validity and repeatability of light sensitivity measurements with the novel Macular Integrity Assessment (MAIA3) microperimeter compared with the established gold standard MAIA 2013 edition device (MAIA2).

Design

A prospective, cross-sectional, premarket clinical investigation on a medical device in a tertiary referral center (ClinicalTrials.gov ID: NCT06071546).

Participants

Thirty-four healthy volunteers (median age: 28 years, interquartile range [IQR]: [26–32] years) and 34 patients with retinal pathologies (66 years, IQR: [50.5–74.5] years) were enrolled. All participants underwent comprehensive ophthalmic evaluation, including best-corrected visual acuity testing and OCT imaging. The diagnosis of retinal disease in patients was confirmed through fundoscopy and imaging.

Main Outcome Measures

Agreement between MAIA3 and MAIA2 measurements with mean sensitivity (MS) and at the pointwise sensitivity (PWS) level and test–retest (TRT) repeatability of MAIA3 and MAIA2 devices (using Bland–Altman statistics).

Results

The bias for the agreement between MAIA3 and MAIA2 measurements was below the established International Organization for Standardization standard of <1 decibel (dB). Healthy participants showed a bias of 0.39 dB for both MS and PWS, 95% confidence interval (CI): 0.11−0.67 dB for MS, 0.30−0.48 dB for PWS. The bias in retinal patients was 0.76 dB (CI: 0.40−1.12 for MS, 0.59−0.93 dB for PWS). The overall bias was 0.57 dB (CI: 0.35−0.80 dB for MS and 0.48−0.67 dB for PWS). Overall TRT repeatability was similar between MAIA3 and MAIA2 devices for MS (Bland–Altman 95% limits of repeatability: −1.16 to 1.53 dB for MAIA3 and −1.49 to 2.06 dB for MAIA2). The examination duration with the MAIA3 device was shorter by 43 seconds compared with the MAIA2 device (median duration: 482.5 seconds [IQR: 451.8–537.5 seconds] for MAIA3 vs. 525.5 seconds [IQR: 500.8–562.3 seconds] for MAIA2).

Conclusions

The MAIA3 microperimetry enables valid and reliable measurements of macular light sensitivity compared with the established device (MAIA2).

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
新型MAIA显微测量装置差分光敏度测量的验证和可重复性
目的显微镜检查对于评估黄斑光敏性至关重要,可用于黄斑中心暗斑累及或中心初始保留患者的疾病监测。本研究的目的是研究新型黄斑完整性评估(MAIA3)微周光敏测量的有效性和可重复性,并与已建立的金标准MAIA 2013版设备(MAIA2)进行比较。设计一个三级转诊中心医疗器械的前瞻性、横断面、上市前临床研究(ClinicalTrials.gov ID: NCT06071546)。参与者纳入34名健康志愿者(中位年龄:28岁,四分位间距[IQR]:[26-32]岁)和34名视网膜病变患者(66岁,IQR:[50.5-74.5]岁)。所有参与者都进行了全面的眼科评估,包括最佳矫正视力测试和OCT成像。通过眼底镜检查和影像学检查确认视网膜疾病的诊断。MAIA3和MAIA2测量结果的平均灵敏度(MS)和点向灵敏度(PWS)水平以及MAIA3和MAIA2设备的重测(TRT)可重复性之间的一致性(使用Bland-Altman统计)。结果MAIA3和MAIA2测量结果的一致性偏差低于国际标准化组织(International Organization for Standardization,简称iso)制定的1分贝(dB)标准。健康受试者对MS和PWS的偏倚均为0.39 dB, 95%置信区间(CI): MS为0.11 ~ 0.67 dB, PWS为0.30 ~ 0.48 dB。视网膜患者的偏倚为0.76 dB (MS组CI: 0.40 - 1.12, PWS组CI: 0.59 - 0.93 dB)。总体偏倚为0.57 dB (CI: MS为0.35 ~ 0.80 dB, PWS为0.48 ~ 0.67 dB)。总的TRT重复性在MAIA3和MAIA2设备之间相似(Bland-Altman 95%重复性限:MAIA3为- 1.16至1.53 dB, MAIA2为- 1.49至2.06 dB)。与MAIA2相比,使用MAIA3设备的检查时间缩短了43秒(MAIA3的中位持续时间:482.5秒[IQR: 451.8-537.5秒],MAIA2的中位持续时间为525.5秒[IQR: 500.8-562.3秒])。结论与现有仪器(MAIA2)相比,MAIA3显微镜能有效、可靠地测量黄斑光敏度。财务披露专有或商业披露可在本文末尾的脚注和披露中找到。
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
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
自引率
0.00%
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审稿时长
89 days
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