Long-Term Visual Quality after Microincision Cataract Surgery

Huang, Qing; Li, Ruili; Feng, Liwen; Miao, Na; Fan, Wei

doi:10.1155/2020/9318436

Cited by 2 publications

(3 citation statements)

References 24 publications

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“…The mean CDVA of all eyes in our study improved from 0.43 ± 0.43 logMAR pre-operatively, to 0.05 ± 0.11 logMAR post-operatively ( p < 0.05). Again, this result is comparable to those in recent studies involving similar IOLs [ 12 – 15 ]. A marginally superior post-operative mean CDVA result has been reported in the EUREQUO 2018 annual report for Cataract and Refractive Surgery [ 16 ].…”

Section: Discussionsupporting

confidence: 91%

Clinical safety and efficacy of a preloaded monofocal hydrophobic acrylic intraocular lens in a real-world population

et al. 2021

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Background This study was designed to evaluate visual, refractive and safety outcomes in eyes after they underwent phacoemulsification and implantation of a preloaded monofocal hydrophobic acrylic intraocular lens. Methods This was a single center observational study conducted at Ashford and St Peter’s Hospitals NHS Foundation Trust, United Kingdom. Patients were included if they had cataract extraction with in-the-bag implantation of the EyeCee® One preloaded intraocular lens from August to October 2019. Pre-operative, surgery-related and 2 weeks and 3 months post-operative data was collected. Surgeons at this trust were then asked to complete a feedback form to evaluate their experience of implanting the EyeCee® One. Results One hundred fifty-two eyes were included in the study. Ninety-four (62%) of these eyes had cataract but no concomitant ocular pathology that could potentially affect visual acuity. Three months post-operatively, 98.7% of all eyes had monocular CDVA ≤0.3 logMAR. 100% of the eyes without concomitant ocular pathology achieved this target. The mean CDVA of all eyes in this study improved from 0.43 ± 0.43 logMAR pre-operatively, to 0.05 ± 0.11 logMAR post-operatively (p < 0.05). The mean sphere and spherical equivalent values showed significant improvements (p < 0.05) and (p < 0.05). There were no intraoperative complications and 1.3% of patients reported complications 2 weeks post-operatively. All of the participating surgeons said they would use the EyeCee® One again with 64% providing an overall rating of ‘excellent’ for their experience of implanting this intraocular lens. Conclusions This study indicates excellent post-operative visual acuity and refractive outcomes in eyes after EyeCee® One implantation. This is accompanied with very little risk of intraoperative and post-operative complications.

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Section: Discussionsupporting

confidence: 91%

Clinical safety and efficacy of a preloaded monofocal hydrophobic acrylic intraocular lens in a real-world population

et al. 2021

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“…The mean CDVA of all eyes in our study improved from 0.43 ± 0.43 logMAR pre-operatively, to 0.05 ± 0.11 logMAR post-operatively (p < 0.05). Again, this result is comparable to those in recent studies involving similar IOLs [11][12][13][14] . A marginally superior post-operative mean CDVA result has been reported in the EUREQUO 2018 annual report for Cataract and Refractive Surgery 15 .…”

Section: Discussionsupporting

confidence: 91%

“…Again, this result is comparable to those in recent studies involving similar IOLs[11][12][13][14] . A marginally superior post-operative mean CDVA result has been reported in the EUREQUO 2018 annual report for Cataract and Refractive Surgery 15 .However, the smaller percentage of eyes with concomitant ocular pathologies included in this report is a noteworthy factor.…”

supporting

confidence: 91%

Clinical Safety and Efficacy of a Preloaded Monofocal Hydrophobic Acrylic Intraocular Lens in a Real-world Population

Latham

Carr

Ali

et al. 2021

Preprint

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Background: This study was designed to evaluate visual, refractive and safety outcomes in eyes after they underwent phacoemulsification and implantation of a preloaded monofocal hydrophobic acrylic intraocular lens.Methods: This was a single center prospective study conducted at Ashford and St Peter’s Hospitals NHS Foundation Trust, United Kingdom. Patients were included if they had cataract extraction with in-the-bag implantation of the EyeCee® One preloaded intraocular lens from August to October 2019. Pre-operative, surgery-related and 2 weeks and 3 months post-operative data was collected. Surgeons at this trust were then asked to complete a feedback form to evaluate their experience of implanting the EyeCee® One. Results: 152 eyes were included in the study. 94 (62%) of these eyes had cataract but no concomitant ocular pathology that could potentially affect visual acuity. Three months post-operatively, 98.7% of all eyes had monocular CDVA ≤ 0.3 logMAR. 100% of the eyes without concomitant ocular pathology achieved this target. The mean CDVA of all eyes in this study improved from 0.43 ± 0.43 logMAR pre-operatively, to 0.05 ± 0.11 logMAR post-operatively (p < 0.05). The mean sphere and spherical equivalent values showed significant improvements (p <0.05) and (p < 0.05). There were no intraoperative complications and 1.3% of patients reported complications 2 weeks post-operatively. All of the participating surgeons said they would use the EyeCee® One again with 64% providing an overall rating of ‘excellent’ for their experience of implanting this intraocular lens. Conclusions: This study indicates excellent post-operative visual acuity and refractive outcomes in eyes after EyeCee® One implantation. This is accompanied with very little risk of intraoperative and post-operative complications.

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Long-Term Visual Quality after Microincision Cataract Surgery

Cited by 2 publications

References 24 publications

Clinical safety and efficacy of a preloaded monofocal hydrophobic acrylic intraocular lens in a real-world population

Clinical safety and efficacy of a preloaded monofocal hydrophobic acrylic intraocular lens in a real-world population

Clinical Safety and Efficacy of a Preloaded Monofocal Hydrophobic Acrylic Intraocular Lens in a Real-world Population

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