Journal List > J Korean Ophthalmol Soc > v.55(11) > 1009833

Lim, Lee, and Kim: Comparison of Ocular Biometry Measured Using Four Applanation Ultrasonographic Biometry Devices

Abstract

Purpose

To compare ocular biometry measured using 4 applanation ultrasonographic biometry devices and evaluate the accuracies of the refractive outcomes after cataract surgery.

Methods

A total of 60 eyes in 60 patients who received cataract surgery were included in the present study. The axial length was measured using applanation ultrasonographic biometry devices (Aviso®, Hi-Scan®, UD-6000®, P37-II®). Additionally, keratometry was measured using an autokeratometer (Topcon KR 8000) and the SRK/T formula was used to calculate intraocular lens (IOL) power. Two months after cataract surgery, the refractive outcome was determined, and results from the 4 different applanation ultrasonographic biometry devices were compared.

Results

Axial lengths were 23.52 ± 1.45 mm, 23.51 ± 1.04 mm, 23.54 ± 1.58 mm, and 23.52 ± 1.38 mm measured using Aviso®, Hi-Scan®, UD-6000®, and P37-II®, respectively with no statistically significant differences observed (p = 0.92). The mean absolute error (MAE) of the Aviso®, Hi-Scan®, UD-6000®, and P37-II® was 0.41 ± 0.32 diopter (D), 0.40 ± 0.30 D, 0.36 ± 0.26 D, and 0.39 ± 0.26 D, respectively. The mean numerical error (MNE) was 0.39 ± 0.37 D, 0.36 ± 0.32 D, 0.26 ± 0.29 D, and 0.38 ± 0.32 D, respectively. The differences between the 4 different applanation ultrasonographic biometry devices were not statistically significant (p = 0.90, p = 0.81).

Conclusions

The ocular biometric measurements and prediction of postoperative refraction using Aviso®, Hi-Scan®, UD-6000®, P37-II® showed no significant differences.

References

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Table 1.
The differences between target refraction and refraction after cataract operation
Aviso® Hi-scan® UD-6000® P37-II® p-value
MAE 0.90
 Mean ± SD 0.41 ± 0.32 0.40 ± 0.30 0.36 ± 0.26 0.39 ± 0.26
 Range 0.02-1.22 0.03-1.34 0.00-1.15 0.00-1.30
MNE 0.81
 Mean ± SD 0.39 ± 0.37 0.36 ± 0.32 0.26 ± 0.29 0.38 ± 0.32
 Range −0.56-1.32 −0.62-1.39 −0.57-1.33 −0.59-1.30

MAE = mean absolute error; MNE = mean numerical error.

Kruskal-Wallis test.

Table 2.
Percentage of cases predicted to within ±0.50 D, ±1.00 D, and ±1.50 D of each groups
Device Eye within
0.50 D 1.00 D 1.50 D 2.00 D
Aviso® (%) 79 96 100 100
Hi-scan® (%) 79 97.5 100 100
UD-6000® (%) 75 97 100 100
P37-II® (%) 73.5 98 100 100

D = diopter.

Percentage of eyes within 0.50 D, 1.00 D, 1.50 D, and 2.00 D from intended refraction.

Table 3.
Technical information of Aviso®, Hi-Scan®, UD-6000®, P37-II®
Variable Aviso® Hi-Scan® UD-6000® P37-II®
Frequency (MHz) 11 10 10 10
Gain (dB) 110 115 80 98
Diameter of tip (mm) 6 5.3
Resolution (mm) 0.04 0.015 0.01 0.01
Measuring mode Contact, immersion Contact, immersion Contact, immersion Contact, immersion
Biometry accuracy (mm) ±0.04 Adjustable ±0.1 ±0.06
Measuring range (mm) 10-45 1-60 15-40 15-39
IOL formulas SRK-T, SRK II, HOLLADAY, BINKHORST-II, HOFFER-Q, HAIGIS SRK-T, SRK II, HOLLADAY, HOFFER-Q, HAIGIS, Post-refractive (Camellin-Calossi) SRK-T, SRK II, HOLLADAY, HOFFER-Q, HAIGIS, Showa SRK-T, SRK II, HOLLADAY, BINKHORST-II, HOFFER-Q, HAIGIS
Velocity Adjustable for each segment Preset for each segment or modified by user
Number of measurement 10 5 10 8-10

IOL = intraocular lens.

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