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Comparison of central corneal thickness with four different optical devices
Authors:Kuddusi Teberik  Mehmet Tahir Eski  Murat Kaya  Handan Ankaralı
Affiliation:1.Department of Ophthalmology,Düzce University Medical School,Düzce,Turkey;2.Department of Biostatistics and Medical Informatics,Düzce University Medical School,Düzce,Turkey
Abstract:

Background

To compare the consistency between the average scores of the contact central corneal thickness measurements from ultrasound pachymetry devices still gold standard, such as iPac® and Echoscan US-500, and noncontact measurements via Pentacam HR and Sirius topography.

Methods

This prospective study, subsequently admitted to the ophthalmology department, 76 healthy individuals were performed. The measurements were repeated three times for each eye, and average scores were statistically analyzed on the same day and almost at the same time. While measuring the eyes, Pentacam HR, Sirius topography, iPac®, and Echoscan US-500 were used, respectively. The inter-rater agreement of measurements from the devices was assessed with intraclass correlation coefficient, and 95% Confidence Interval and p values demonstrating statistically significance were also presented. In the graphical assessment of the agreement, the Bland–Altman graph was used.

Results

Among 76 study participants, 43 (56.6%) were composed of women, and age level was 38.6 ± 12.5 years, ranging between 18 and 69. It was observed that the highest agreement was between the measurements obtained from Echoscan US-500 and iPac® devices, but the agreement between the measurements of different devices was higher than 0.90. Bland–Altman graphics were also investigated; the results of four different devices were seen to be consistent with one another.

Conclusions

Therefore, the devices we compared in the study can be used as alternatives to one another due to the higher consistency between CCT measurements provided with through UP devices of Echoscan US-500 and iPac®, and Pentacam HR and Sirius topography devices.Clinical Trial Registration number: 2016/112
Keywords:
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