Logean E, Schmetterer L F, Geiser M H, Riva C E
Institut de Recherche en Ophtalmologie (IRO), Sion, Suisse.
Klin Monbl Augenheilkd. 2000 May;216(5):313-5. doi: 10.1055/s-2000-10992.
To report on a novel approach to measure the velocity of red blood cells (RBCs) at different retinal vessel depths.
The technique is an extension of conventional laser Doppler velocimetry using light sources of various coherence lengths (CL). Light scattered by the moving RBCs interferes with that reflected from the anterior vessel wall only if the optical path difference is shorter than CL. Therefore, using low coherence light sources, localized measurements of RBCs velocity can be performed.
Measurements of RBCs velocity at different depths in a main retinal vein (diameter: 152 microns) of a volunteer has been performed using 4 different light sources with CLs of 14 microns, 21 microns, 32 microns and > m. Measured values are in good agreement with theoretically predicted values.
This new approach permits to measure RBCs velocity at different depths of retinal vessels in the human retina.
报告一种测量不同视网膜血管深度处红细胞(RBC)速度的新方法。
该技术是对传统激光多普勒测速技术的扩展,使用了具有不同相干长度(CL)的光源。只有当光程差短于CL时,移动的红细胞散射的光才会与从前血管壁反射的光发生干涉。因此,使用低相干光源,可以对红细胞速度进行局部测量。
使用4种不同的光源,其CL分别为14微米、21微米、32微米和>m,对一名志愿者视网膜主静脉(直径:152微米)不同深度处的红细胞速度进行了测量。测量值与理论预测值高度吻合。
这种新方法能够测量人视网膜中不同深度视网膜血管处的红细胞速度。