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1.
J Refract Surg ; 28(9): 614-9, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22947288

RESUMO

PURPOSE: To evaluate the visual outcomes, efficacy, predictability, and short-term safety of implanting the Sulcoflex (Rayner Intraocular Lenses Ltd) intraocular lens (IOL) to correct residual pseudophakic errors. METHODS: Retrospective study of patients undergoing implantation of the Sulcoflex IOL. Uncorrected (UDVA) and corrected (CDVA) distance visual acuity and refractive outcomes were evaluated. Postoperative follow-up was at 1 week and 1, 3, 6, and 12 months. RESULTS: Fifteen eyes (13 patients) were evaluated. Mean follow-up was 20 months (range: 14 to 30 months). The Sulcoflex aspheric (653L) and toric (653T) IOLs were implanted in 3 and 12 eyes, respectively. Preoperatively, mean logMAR (Snellen) UDVA and CDVA were 0.44 (20/55) and 0.05 (20/22), respectively. At 3 months, all eyes achieved logMAR UDVA of 0.20 (20/32) or better, with 10 (67%) eyes achieving UDVA of 0 (20/20) or better. Preoperative mean spherical and astigmatic errors were 1.07±0.83 diopters (D) and -1.45±0.98 D, respectively. Preoperative mean spherical equivalent refraction was -0.54±1.11 (D). Postoperative mean sphere and astigmatism at 3 months were -0.25±0.38 D and -0.50±0.57 D, respectively. Postoperative mean spherical equivalent refraction at 3 months was -0.15±0.28 D. All patients were within 1.00 D of attempted correction, with 93% within 0.50 D. Linear regression analysis showed good correlation (R²=0.72) between attempted versus achieved spherical equivalent refractions. No significant intra- or postoperative complications occurred. CONCLUSIONS: Implantation of the Sulcoflex IOL was found to be an effective and predictable option for enhancing postoperative refractive results and reducing spectacle dependence for distance after surgery. The IOL was well tolerated in all eyes.


Assuntos
Astigmatismo/cirurgia , Implante de Lente Intraocular , Lentes Intraoculares , Miopia/cirurgia , Complicações Pós-Operatórias , Pseudofacia/cirurgia , Idoso , Idoso de 80 Anos ou mais , Astigmatismo/etiologia , Astigmatismo/fisiopatologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Miopia/etiologia , Miopia/fisiopatologia , Desenho de Prótese , Pseudofacia/fisiopatologia , Estudos Retrospectivos , Resultado do Tratamento , Acuidade Visual/fisiologia
2.
J Cataract Refract Surg ; 31(6): 1163-6, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16039491

RESUMO

PURPOSE: To determine whether the use of prophylactic intracameral cefuroxime during phacoemulsification cataract surgery is associated with increased macular thickening in the postoperative period. SETTING: Hull and East Yorkshire Eye Hospital, Hull, United Kingdom. METHODS: In this prospective randomized double-masked clinical study, the study group received 1 mg of intracameral cefuroxime and the control group received intracameral balanced salt solution only. Ocular coherence tomography was performed 5 (+/-1) weeks after surgery. RESULTS: Intracameral cefuroxime did not have a statistically significant effect on postoperative macular thickness compared with nonadministration of intracameral antibacterials. All patients in both groups achieved a postoperative best corrected visual acuity of 6/9 or better. CONCLUSION: Use of 1 mg of intracameral cefuroxime was not associated with increased macular thickness 4 weeks to 6 weeks postoperatively.


Assuntos
Antibacterianos/administração & dosagem , Cefuroxima/administração & dosagem , Facoemulsificação , Retina/efeitos dos fármacos , Acetatos/administração & dosagem , Câmara Anterior/efeitos dos fármacos , Antibacterianos/efeitos adversos , Cefuroxima/efeitos adversos , Método Duplo-Cego , Combinação de Medicamentos , Humanos , Implante de Lente Intraocular , Edema Macular/induzido quimicamente , Edema Macular/diagnóstico , Minerais/administração & dosagem , Complicações Pós-Operatórias , Estudos Prospectivos , Retina/patologia , Cloreto de Sódio/administração & dosagem , Tomografia de Coerência Óptica , Acuidade Visual/efeitos dos fármacos
3.
J Cataract Refract Surg ; 31(4): 725-34, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15899449

RESUMO

PURPOSE: To determine whether Hartmann-Shack wavefront sensing detects differences in optical performance in vivo between poly(methyl methacrylate) (PMMA) and foldable acrylic intraocular lenses (IOLs) and between clear corneal and scleral tunnel incisions and whether optical differences are manifested as differences in visual performance. SETTING: Department of Optometry, University of Bradford, West Yorkshire, United Kingdom. METHODS: This study comprised 74 subjects; 17 were phakic with no ocular pathology, 20 had implantation of a Pharmacia 722C PMMA IOL through a scleral tunnel, 21 had implantation of an Alcon AcrySof IOL through a scleral tunnel, and 16 had implantation of an AcrySof IOL through a corneal incision. Visual acuity and contrast sensitivity testing, ocular optical quality measurement using Hartmann-Shack wavefront sensing, and corneal surface measurement with a videokeratoscope were performed in all cases. RESULTS: There were significant differences between groups in the total root-mean-square (RMS) wavefront aberration over a 6.0 mm pupil (F=3.91; degrees of freedom=3,70; P<.05) mediated at the 4th-order RMS, specifically spherical and tetrafoil aberrations. The PMMA-scleral group had the least aberrations and the AcrySof-corneal group the most. For a 3.5 mm diameter pupil, the total higher-order RMS wavefront aberration was not significantly different between the groups (P>.05). There were no differences between groups in corneal shape, visual acuity, or contrast sensitivity. CONCLUSIONS: Implantation of the spherical PMMA IOL led to a slight reduction in total wavefront aberration compared to phakic eyes. AcrySof IOLs induced more aberrations, especially spherical aberration. Corneal-based incisions for IOL implantation compounded this increase. Studies of the optical performance of IOLs in vivo should use wavefront sensing as the main outcome measure rather than visual measures, which are readily confounded by multiple factors.


Assuntos
Resinas Acrílicas , Lentes Intraoculares , Facoemulsificação/métodos , Polimetil Metacrilato , Erros de Refração/etiologia , Idoso , Sensibilidades de Contraste/fisiologia , Córnea/cirurgia , Topografia da Córnea , Humanos , Implante de Lente Intraocular , Refração Ocular/fisiologia , Esclera/cirurgia , Acuidade Visual/fisiologia
5.
Cornea ; 22(4): 371-3, 2003 May.
Artigo em Inglês | MEDLINE | ID: mdl-12792483

RESUMO

PURPOSE: Deep lamellar keratoplasty (DLKP) is an intricate procedure that preserves the host's endothelium, thus eliminating the possibility of endothelial graft rejection and potentially offering great benefits over penetrating keratoplasty. DLKP may be performed by a variety of techniques including viscodelamination, in which the stroma is separated from Descemet's membrane using viscoelastic. METHODS: Here we present an operative complication of this technique, which was not initially recognized, that caused significant morbidity to our patient and eventually led to the eye requiring a full thickness regraft. We also attempt to reproduce the lesion using nonviable cadaver corneas and illustrate histologically the nature of the corneal stroma and its relationship to Descemet's membrane following viscoelastic delamination.


Assuntos
Cicatriz/cirurgia , Doenças da Córnea/cirurgia , Herpes Zoster , Ácido Hialurônico/efeitos adversos , Ceratite/virologia , Ceratoplastia Penetrante/efeitos adversos , Cicatriz/etiologia , Córnea/patologia , Doenças da Córnea/etiologia , Transplante de Córnea , Feminino , Humanos , Ceratite/complicações , Ceratoplastia Penetrante/métodos , Pessoa de Meia-Idade , Reoperação
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