Purpose: To evaluate the repeatability of measurements obtained with a new spectral-domain optical coherence tomography-based biometer (Colombo IOL II, Moptim) and assess their agreement with those provided by the IOLMaster 700 (Zeiss).
Setting: I.R.C.C.S. Bietti Foundation, Rome, Italy.
Design: Prospective evaluation of diagnostic test.
Methods: Patients underwent 3 consecutive scans with the Colombo IOL II and 1 with the IOLMaster 700. Two groups were analyzed: Group A included a series of consecutive patients undergoing phacoemulsification and Group B a series of subjects with a clear lens. Axial length (AL), keratometry, keratometric astigmatism, anterior chamber depth (ACD), lens thickness (LT), corneal diameter (CD), central corneal thickness (CCT) and retinal thickness (RT) were analyzed. The within-subject standard deviation (Sw), intrasession test variability, coefficient of variation (CoV) and intraclass correlation coefficient (ICC) were calculated for repeatability analysis. 95% limits of agreement were calculated to assess agreement with the IOLMaster 700.
Results: Ninety-six unoperated eyes of 96 patients were enrolled (Group A: 45 Group B: 51). The CoV was low for most parameters, as it ranged between 0.04% (AL) to 4.47% (RT) in Group A and from 0.03% (AL) to 2.23% (LT) in Group B. Keratometric astigmatism measurements were less repeatable. Good agreement with the IOLMaster 700 was found for K, LT and AL, whereas the mean ACD was higher by 0.07±0.11 mm with the Colombo IOL II (p <0.0001).
Conclusion: Measurements by the Colombo IOL II showed high repeatability and good agreement with those provided by the IOLMaster 700.
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http://dx.doi.org/10.1097/j.jcrs.0000000000001650 | DOI Listing |
J Cataract Refract Surg
March 2025
IRCCS Bietti Foundation, Rome, Italy.
Purpose: To evaluate the repeatability of measurements obtained with a new spectral-domain optical coherence tomography-based biometer (Colombo IOL II, Moptim) and assess their agreement with those provided by the IOLMaster 700 (Zeiss).
Setting: I.R.
Eye Vis (Lond)
February 2025
Eye Institute and Department of Ophthalmology and Vision Science, Eye & ENT Hospital, Fudan University, Shanghai, 200031, China.
Background: To assess the repeatability and reproducibility of the Colombo IOL biometer (Moptim, China), which utilizes spectral-domain optical coherence tomography (SD-OCT), in measuring ocular parameters of normal subjects and to compare its agreement with the swept-source optical coherence tomography (SS-OCT)-based IOLMaster 700 biometer (Carl Zeiss Meditec AG, Germany).
Methods: This prospective study included 91 eyes from 91 normal subjects. The evaluated parameters were axial length (AL), central corneal thickness (CCT), aqueous depth (AQD), anterior chamber depth (ACD), lens thickness (LT), flattest and steepest meridian keratometry (Kf and Ks), mean keratometry (Km), astigmatism (AST) magnitude, white-to-white (WTW) distance, and pupil diameter (PD).
Sci Rep
October 2024
Shenzhen Eye Hospital, Shenzhen Eye Institute, Jinan University, Shenzhen, China.
With the advancements in ocular biometric technology, there have been significant improvements in accurately and efficiently measuring ocular parameters. The aim of this study is to compare the reliability of biometric parameters obtained using a new frequency-domain optical coherence tomography (SD-OCT) biometer with the measurements obtained from swept-source OCT (SS-OCT) and optical low coherence reflectometry (OLCR) biometers. This study employed an observational cross-sectional design.
View Article and Find Full Text PDFBMC Ophthalmol
July 2024
Eye Institute and Department of Ophthalmology, Eye and ENT Hospital, Fudan University, No. 19 Baoqing Road, Shanghai, 200031, China.
BJOG
August 2024
Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, Victoria, Australia.
Background: Induction of labour (IOL) is common practice and different methods carry different effectiveness and safety profiles.
Objectives: To compare the effectiveness, and maternal and perinatal safety outcomes of IOL with vaginal misoprostol versus vaginal dinoprostone using individual participant data from randomised clinical trials.
Search Strategy: The following databases were searched from inception to March 2023: CINAHL Plus, ClinicalTrials.
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