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12 year results of a prospective trial comparing poly(methyl methacrylate) and poly(hydroxyethyl methacrylate) intraocular lenses

Identifieur interne : 001561 ( Istex/Corpus ); précédent : 001560; suivant : 001562

12 year results of a prospective trial comparing poly(methyl methacrylate) and poly(hydroxyethyl methacrylate) intraocular lenses

Auteurs : A. Jabbar Khan ; S. Piers B. Percival

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RBID : ISTEX:DB23752781D15C9F3ABC899D78B90BDD91A604F3

Abstract

Purpose To compare long-term biocompatibility of single-piece poly(methyl methacrylate) (PMMA) and poly(hydroxyethyl methacrylate) (P-HEMA) intraocular lenses (IOLs).Setting District General Hospital, United Kingdom.Methods In a prospective trial of 250 eyes that had uncomplicated extracapsular cataract extraction, 2 groups of 125 eyes each were matched for age and sex. One group received single-piece looped PMMA IOLs and the other, single-piece solid-hapticP-HEMA IOLs. In all eyes, the IOLs were implanted in the capsular bag at the time of surgery using the envelope technique.Results Twelve years after surgery, 75 eyes were available for examination. In the PMMA group (40 eyes), 50% had a visual acuity of 20/20 and 50% had intact capsules, many of them with a degree of fibrosis. In the P-HEMA group (35 eyes), 71% had an acuity of 20/20 and 80% had intact capsules (P = .0085).Conclusion In the long term, biocompatibility was better in the P-HEMA group than in the PMMA group.

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DOI: 10.1016/S0886-3350(99)00199-6

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ISTEX:DB23752781D15C9F3ABC899D78B90BDD91A604F3

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