Purpose: To determine whether intraocular lens (IOL) power calculations for cataract surgery as measured by postoperative refractive error using partial coherence interferometry (PCI) are more accurate in improving postoperative outcomes than applanation ultrasound biometry (AUS).
Methods: A double-blind randomized controlled trial consisting of 205 patients was undertaken by the Southern Health Ophthalmology Unit, Victoria, Australia. Mean absolute postoperative refractive error (MAE) represented the dependent variable; the biometric technique (PCI; AUS) used to determine the IOL power to be implanted in the surgical eye represented the independent variable. An intention-to-treat analysis was used to prevent loss of randomization caused by the effects of crossover and drop-out.
Results: The MAE in patients with implanted PCI-calculated IOLs was 0.40 +/- 0.37 D (SD; 95% confidence interval [CI], 0.32-0.48 D) compared with 0.45 +/- 0.41 D (SD; 95% CI, 0.36-0.54 D) for patients with implanted AUS-calculated IOLs. There was no statistically significant difference between MAE in patients with implanted PCI-calculated IOLs and that in patients with AUS-calculated IOLs in analysis of best possible outcomes (t(167) = 1.0, P = 0.315).
Conclusions: The results of this trial demonstrated that the calculation of IOL power based on ocular axial length measurement with PCI technology provided no clinical advantage over conventional applanation ultrasound, as measured by postoperative refractive outcome (anzctr.org.au number, ACTRN12608000077369).
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http://dx.doi.org/10.1167/iovs.08-3087 | DOI Listing |
BMC Ophthalmol
January 2025
Department of Ophthalmology, Eye & ENT Hospital, Fudan University, 83 Fenyang Road, Xuhui District, Shanghai, 200031, China.
Background: To investigate the impact of central corneal astigmatism on postoperative visual outcomes in patients with trifocal intraocular lens (IOL) implantation.
Methods: This retrospective study included 278 eyes of 278 patients who underwent uneventful cataract surgery with implantation of the trifocal IOL (AT LISA tri 839MP). Patients were divided into two groups according to the total corneal refractive power (TCRP) in 3 mm zone centered on the corneal apex: low astigmatism group, TCRP ≤ 0.
Klin Monbl Augenheilkd
January 2025
Department of Ophthalmology, Pallas Kliniken, Olten/Bern/Zürich/Dübendorf, Switzerland.
Background: Extended monovision is a novel mix-and-match approach that has been recently introduced. It involves implanting an aspherical monofocal intraocular lens (IOL) for distance vision in the dominant eye, and a bifocal extended depth-of-focus (EDOF) IOL in the nondominant eye. The target refraction for the nondominant eye is - 1.
View Article and Find Full Text PDFBackground: To determine whether accounting for posterior corneal surgically induced astigmatism (SIA) would improve toric intraocular lens power calculation prediction error.
Methods: A total of 189 eyes of 148 patients undergoing routine cataract surgery were included in the study. Standard and posterior keratometry were measured pre- and postoperatively.
PLoS One
January 2025
Department of Ophthalmology, Pennsylvania State University, Hershey, PA, United States of America.
Purpose: To investigate different measures for corneal astigmatism in the context of reconstructed corneal astigmatism (recCP) as required to correct the pseudophakic eye, and to derive prediction models to map measured corneal astigmatism to recCP.
Methods: Retrospective single centre study of 509 eyes of 509 cataract patients with monofocal (MX60P) IOL. Corneal power measured with the IOLMaster 700 keratometry (IOLMK), and Galilei G4 keratometry (GK), total corneal power (TCP2), and Alpin's integrated front (CorT) and total corneal power (CorTTP).
Diagnostics (Basel)
December 2024
Department of Ophthalmology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Republic of Korea.
Objectives: This study compared the visual outcomes and optical quality of two monofocal, aspheric intraocular lenses (IOLs; CT LUCIA 621P, Carl Zeiss Meditec; Eyhance ICB00, Johnson & Johnson Vision) by evaluating visual acuity, contrast sensitivity, and higher-order aberrations 1 month post-cataract surgery.
Methods: In this retrospective, comparative study, 120 eyes (72 patients) that underwent cataract surgery with either CT LUCIA 621P (Lucia group) or Eyhance ICB00 (Eyhance group) implantation (60 eyes/group) were retrospectively investigated. Visual acuity at various distances and defocus curves were measured 1 month postoperatively.
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