In vivo cellular-resolution retinal imaging in infants and children using an ultracompact handheld probe

被引:46
作者
LaRocca, Francesco [1 ,2 ]
Nankivil, Derek [1 ,2 ,4 ]
DuBose, Theodore [1 ,2 ]
Toth, Cynthia A. [1 ,2 ,3 ]
Farsiu, Sina [1 ,2 ,3 ]
Izatt, Joseph A. [1 ,2 ,3 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[2] Duke Univ, Fitzpatrick Inst Photon, Durham, NC 27708 USA
[3] Duke Univ, Med Ctr, Dept Ophthalmol, Durham, NC 27710 USA
[4] Johnson & Johnson Vis Care Inc, Jacksonville, FL 32256 USA
基金
美国国家卫生研究院;
关键词
OPTICAL COHERENCE TOMOGRAPHY; SCANNING LASER OPHTHALMOSCOPY; ADAPTIVE OPTICS; HUMAN FOVEA; SWEPT SOURCE; AXIAL SCANS; HIGH-SPEED; EYE; 2ND;
D O I
10.1038/nphoton.2016.141
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Enabled by adaptive optics, retinal photoreceptor cell imaging is changing our understanding of retinal structure(1,'2) and function(3,4), as well as the pathogenesis of numerous ocular disease(5). To date, use of this technology has been limited to cooperative adult subjects due to the size, weight and inconvenience of the equipment, thus excluding study of retinal maturation during human development. Here, we report the design and operation of a handheld probe that can perform both scanning laser ophthalmoscopy and optical coherence tomography of the parafoveal photoreceptor structure in infants and children without the need for adaptive optics. The probe, featuring a compact optical design weighing only 94 g, was able to quantify packing densities of parafoveal cone photoreceptors and visualize cross-sectional photoreceptor substructure in children with ages ranging from 14 months to 12 years. The probe will benefit paediatric research by improving the understanding of retinal development, maldevelopment and early onset of disease during human growth.
引用
收藏
页码:580 / 584
页数:5
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