Clinical Experiences of Hydroxyapatite Implant
Journal of the Korean Ophthalmological Society
;
: 411-417, 1996.
Artigo
em Coreano
| WPRIM
| ID: wpr-184953
ABSTRACT
The hydroxyapatite has been used as an orbital implant for reconstruction after enucleation or evisceration. It has been known to be a biocompatible and nontoxic implant with good fibrovascular ingrowth, few postoperative complications, excellent prosthesis motility, and good cosmesis. We performed 36 cases of hydroxyapatite implantation with enucleation or evisceration from July 1992 to August 1994. The mean follow-up period was 7.4 months(range, 4 to 13 months). There were nine cases of implant exposure. three cases of peg extrusion, three cases of superficial conjunctival wound dehiscence, and one case of granulation tissue overgrowth. There was no infection of implant. Improving the postoperative results and reducing the postoperative complications, it requires proper surgical techniques including the selection of adequate implant size and good doctor-patient relationship.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Complicações Pós-Operatórias
/
Próteses e Implantes
/
Ferimentos e Lesões
/
Seguimentos
/
Durapatita
/
Implantes Orbitários
/
Tecido de Granulação
Tipo de estudo:
Estudo observacional
/
Estudo prognóstico
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1996
Tipo de documento:
Artigo
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