Morgan William H, Hazelton Martin L, Betz-Stablein Brigid D, Yu Dao-Yi, Lind Christopher R P, Ravichandran Vignesh, House Philip H
Lions Eye Institute, University of Western Australia, Nedlands, Western Australia, Australia.
Statistics and Bioinformatics Group, Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
Invest Ophthalmol Vis Sci. 2014 Sep 2;55(9):5998-6006. doi: 10.1167/iovs.14-15104.
Retinal vein pulsation properties are altered by glaucoma, intracranial pressure (ICP) changes, and retinal venous occlusion, but measurements are limited to threshold measures or manual observation from video frames. We developed an objective retinal vessel pulsation measurement technique, assessed its repeatability, and used it to determine the phase relations between retinal arteries and veins.
Twenty-three eyes of 20 glaucoma patients had video photograph recordings from their optic nerve and peripapillary retina. A modified photoplethysmographic system using video recordings taken through an ophthalmodynamometer and timed to the cardiac cycle was used. Aligned video frames of vessel segments were analyzed for blood column light absorbance, and waveform analysis was applied. Coefficient of variation (COV) was calculated from data series using recordings taken within ±1 unit ophthalmodynamometric force of each other. The time in cardiac cycles and seconds of the peak (dilation) and trough (constriction) points of the retinal arterial and vein pulse waveforms were measured.
Mean vein peak time COV was 3.4%, and arterial peak time COV was 4.4%. Lower vein peak occurred at 0.044 cardiac cycles (0.040 seconds) after the arterial peak (P = 0.0001), with upper vein peak an insignificant 0.019 cardiac cycles later. No difference in COV for any parameter was found between upper or lower hemiveins. Mean vein amplitude COV was 12.6%, and mean downslope COV was 17.7%.
This technique demonstrates a small retinal venous phase lag behind arterial pulse. It is objective and applicable to any eye with clear ocular media and has moderate to high reproducibility. ( http://www.anzctr.org.au number, ACTRN12608000274370.).
青光眼、颅内压(ICP)变化和视网膜静脉阻塞会改变视网膜静脉搏动特性,但测量仅限于阈值测量或从视频帧进行手动观察。我们开发了一种客观的视网膜血管搏动测量技术,评估了其重复性,并使用它来确定视网膜动脉和静脉之间的相位关系。
对20例青光眼患者的23只眼睛进行了视神经和视乳头周围视网膜的视频拍摄记录。使用了一种改良的光电容积描记系统,该系统通过眼底动脉压计拍摄视频记录,并与心动周期同步。对血管段的对齐视频帧进行血柱光吸收分析,并应用波形分析。变异系数(COV)由彼此在±1个单位眼底动脉压计力范围内拍摄的记录数据系列计算得出。测量视网膜动脉和静脉脉搏波形的峰值(扩张)和谷值(收缩)点在心动周期中的时间和秒数。
静脉峰值时间的平均COV为3.4%,动脉峰值时间的COV为4.4%。静脉峰值较低出现在动脉峰值后0.044个心动周期(0.040秒)(P = 0.0001),静脉峰值较高则在0.019个心动周期后,差异不显著。上半侧或下半侧视网膜静脉之间在任何参数的COV上均未发现差异。静脉平均振幅COV为12.6%,平均下降斜率COV为17.7%。
该技术表明视网膜静脉相位滞后于动脉搏动。它是客观的,适用于任何眼内介质清晰的眼睛,具有中度至高重复性。(澳大利亚新西兰临床试验注册中心编号,ACTRN12608000274370.)