Vitreous Retina, Macula Consultants of New York, New York, New York, USA.
Heidelberg Engineering GmbH, Heidelberg, Germany.
Transl Vis Sci Technol. 2022 Jan 3;11(1):28. doi: 10.1167/tvst.11.1.28.
The lateral resolution of an optical coherence tomography (OCT) instrument was considered to be equal to the illumination spot size on the retina. To evaluate the potential lateral resolution of the Spectralis OCT, an instrument calculated to have a 14 µm resolution.
The lateral point spread function (PSF) was evaluated using diamond abrasive powder 0 to 1 µm in diameter in silicone elastomer and a validated target with 800 nm FeO particles in urethane. The amplitude transfer function was calculated from human OCT images. Finally, resolution was measured using the 1951 USAF target.
Measurement of the lateral PSF from 1215 diamond particle images yielded a full-width half maximum (FWHM) to be 5.11 µm and for 732 FeO particles, 4.9 µm. From the amplitude transfer function, the FWHM of the diffraction limited PSF was calculated to be 5.0 µm. The USAF target imaging showed a lateral resolution of 4.6 µm.
Although a calculation of the spot size of the illumination beam was reported in the past as the lateral resolution of the OCT instrument, the actual lateral resolution is better by a factor of at least 2.5 times. The clinically used A-scan spacing was derived from the calculated, and not the true resolution, and results in under sampling. This set of findings likely apply to all commercial clinical instruments.
The scan density parameters of past and present commercial OCT instruments were based on earlier translational concepts, which now appear to have been incorrect.
光学相干断层扫描(OCT)仪器的横向分辨率被认为等于视网膜上的照明光斑大小。为了评估 Spectralis OCT 的潜在横向分辨率,该仪器的分辨率预计为 14 µm。
使用直径为 0 至 1 µm 的金刚石磨料粉末在硅酮弹性体和带有验证的 800nmFeO 颗粒的聚氨脂验证目标中评估横向点扩展函数(PSF)。从人体 OCT 图像计算振幅传递函数。最后,使用 1951 年美国空军靶标测量分辨率。
从 1215 个金刚石颗粒图像测量横向 PSF 得到半峰全宽(FWHM)为 5.11 µm,对于 732 个 FeO 颗粒为 4.9 µm。从振幅传递函数中,计算出衍射受限 PSF 的 FWHM 为 5.0 µm。美国空军靶标成像显示横向分辨率为 4.6 µm。
尽管过去曾报道过光束照射光斑的计算尺寸作为 OCT 仪器的横向分辨率,但实际的横向分辨率要好 2.5 倍以上。临床上使用的 A 扫描间距是从计算中得出的,而不是真实分辨率,导致欠采样。这一系列发现可能适用于所有商业临床仪器。
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