Evaluation of a self-imaging SD-OCT system designed for remote home monitoring

被引:32
作者
Kim, Judy E. [1 ]
Tomkins-Netzer, Oren [2 ]
Elman, Michael J. [3 ]
Lally, David R. [4 ]
Goldstein, Michaella [5 ]
Goldenberg, Dafna [6 ]
Shulman, Shiri [6 ]
Benyamini, Gidi [7 ]
Loewenstein, Anat [5 ]
机构
[1] Med Coll Wisconsin, Eye Inst, 925 N 87th St, Milwaukee, WI 53226 USA
[2] Technion, Ruth & Bruce Rappaport Fac Med, Lady Davis Carmel Med Ctr, Dept Ophthalmol, Haifa, Israel
[3] Elman Retina Grp PA, Baltimore, MD USA
[4] New England Retina Consultants, Retina Res Inst, Springfield, MA USA
[5] Tel Aviv Med Ctr & Sch Med, Tel Aviv, Israel
[6] Assuta Med Ctr, Tel Aviv, Israel
[7] Notal Vis, Tel Aviv, Israel
关键词
Age-related macular degeneration; HOME OCT; Home monitoring; TREAT-AND-EXTEND; MACULAR DEGENERATION; RETINAL FLUID;
D O I
10.1186/s12886-022-02458-z
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose To compare identification rates of retinal fluid of the Notal Vision Home Optical Coherence Tomography (OCT) device (NVHO) when used by people with age-related macular degeneration (AMD) to those captured by a commercial OCT. Methods Prospective, cross-sectional study where patients underwent commercial OCT imaging followed by self-imaging with either the NVHO 2.5 or the NVHO 3 in clinic setting. Outcomes included patients' ability to acquire analyzable OCT images with the NVHO and to compare those with commercial images. Results Successful images were acquired with the NVHO 2.5 in 469/531 eyes (88%) in 264/290 subjects (91%) with the mean (SD) age of 78.8 (8.8); 153 (58%) were female with median visual acuity (VA) of 20/40. In the NVHO 3 cohort, 69 eyes of 45 subjects (93%) completed the self-imaging. Higher rates of successful imaging were found in eyes with VA >= 20/320. Positive percent agreement/negative percent agreement for detecting the presence of subretinal and/or intraretinal fluid when reviewing for fluid in three repeated volume scans were 97%/95%, respectively for the NVHO v3. Conclusion Self-testing with the NVHO can produce high quality images suitable for fluid identification by human graders, suggesting the device may be able to complement standard-of-care clinical assessments and treatments.
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