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Posterior capsule opacification: Silicone plate-haptic versus AcrySof intraocular lenses

Identifieur interne : 007463 ( Main/Merge ); précédent : 007462; suivant : 007464

Posterior capsule opacification: Silicone plate-haptic versus AcrySof intraocular lenses

Auteurs : Kiran A. Abhilakh Missier [Pays-Bas] ; Rudy M. M. A. Nuijts [Pays-Bas] ; Khiun F. Tjia [Pays-Bas]

Source :

RBID : Pascal:03-0435723

Descripteurs français

English descriptors

Abstract

Purpose: To evaluate posterior capsule opacification (PCO) in fellow eyes, 1 receiving a silicone intraocular lens (IOL) and the other, an acrylate IOL. Setting: Department of Ophthalmology, Isala Clinics, Zwolle, The Netherlands. Methods: This retrospective study comprised 107 patients (214 eyes). In each patient, 1 eye was randomly selected to have implantation of an acrylate IOL (AcrySof® MA30BA or MA60BM, Alcon) and the other eye, a plate-haptic silicone IOL (AA4203VF, Staar). Outcome measures were the total PCO index, percentage of neodymium:YAG (Nd:YAG) capsulotomies performed, and logMAR best corrected visual acuity (BCVA). The follow-up was 3 years. Results: The total PCO index was significantly lower in the AcrySof group than in the plate-haptic silicone group (P<.0001). There was no significant difference in logMAR BCVA between groups (P>.05). The percentage of Nd:YAG laser treatments was significantly lower in the AcrySof group (2.8%) than in the plate-haptic silicone group (23.1 %) (P<.05). Conclusions: There was significantly less PCO and a lower Nd:YAG laser capsulotomy rate after AcrySof IOL implantation than after plate-haptic silicone IOL implantation. These results did not seem to affect the logMAR BCVA as there were no significant differences between groups in this parameter.

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Pascal:03-0435723

Le document en format XML

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<term>Implantation</term>
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<term>Postérieur</term>
<term>Capsule</term>
<term>Gélule</term>
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<div type="abstract" xml:lang="en">Purpose: To evaluate posterior capsule opacification (PCO) in fellow eyes, 1 receiving a silicone intraocular lens (IOL) and the other, an acrylate IOL. Setting: Department of Ophthalmology, Isala Clinics, Zwolle, The Netherlands. Methods: This retrospective study comprised 107 patients (214 eyes). In each patient, 1 eye was randomly selected to have implantation of an acrylate IOL (AcrySof® MA30BA or MA60BM, Alcon) and the other eye, a plate-haptic silicone IOL (AA4203VF, Staar). Outcome measures were the total PCO index, percentage of neodymium:YAG (Nd:YAG) capsulotomies performed, and logMAR best corrected visual acuity (BCVA). The follow-up was 3 years. Results: The total PCO index was significantly lower in the AcrySof group than in the plate-haptic silicone group (P<.0001). There was no significant difference in logMAR BCVA between groups (P>.05). The percentage of Nd:YAG laser treatments was significantly lower in the AcrySof group (2.8%) than in the plate-haptic silicone group (23.1 %) (P<.05). Conclusions: There was significantly less PCO and a lower Nd:YAG laser capsulotomy rate after AcrySof IOL implantation than after plate-haptic silicone IOL implantation. These results did not seem to affect the logMAR BCVA as there were no significant differences between groups in this parameter.</div>
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