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Eye Contact Lens ; 29(1 Suppl): S153-6; discussion S166, S192-4, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12772755

RESUMO

PURPOSE: This analysis reports on risk factors for corneal infiltrative events from a 1-year, randomized clinical trial of lotrafilcon A lenses. METHODS: Six hundred fifty-eight subjects randomized to lotrafilcon A lenses were observed in a 1-year clinical trial in the United States. Risk factors gathered at baseline were analyzed to determine their association with corneal infiltrative events. RESULTS: Factors examined but not found to be associated with events were male sex, history of extended or daily lens wear, refractive error, neovascularization, or assessment of lens fit. Significant factors included subject age 18 to 29 years, smoking, smoking and young age combined, history of corneal scar, contact lens acute red eye (CLARE), and corneal infiltrates. CONCLUSION: Risk factors for corneal infiltrative events with silicone hydrogel lenses worn for 30 nights of continuous wear have been identified. Wearers with a history of inflammatory events such as contact lens peripheral ulcer or CLARE should consider 30-night continuous wear with these lenses. Careful counseling of wearers who smoke is advised.


Assuntos
Materiais Biocompatíveis/efeitos adversos , Lentes de Contato de Uso Prolongado/efeitos adversos , Úlcera da Córnea/epidemiologia , Infecções Oculares Bacterianas/epidemiologia , Infecções Relacionadas à Prótese/epidemiologia , Elastômeros de Silicone/efeitos adversos , Adulto , Úlcera da Córnea/microbiologia , Infecções Oculares Bacterianas/etiologia , Feminino , Humanos , Masculino , Infecções Relacionadas à Prótese/etiologia , Fatores de Risco
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