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A proteção endotelial na facectomia: avaliação de nova substância visco-elástica sintética

Endothelial protection in the facectomy: evaluation of a new sinthetic viscoelastic material

RESUMO

Objetivo:

Avaliar a segurança clínica e eficiência de nova solução visco-elástica sintética - MEDILON (poliacrilamida).

Métodos:

60 pacientes foram aleatoriamente divididos em 3 grupos de 20 pacientes e submetidos à facectomia extra-capsular. Como proteção endotelial foram utilizados os seguintes: Grupo 1 - AR, Grupo 2 - HEALON (hialuronato de sódio), e Grupo 3 - MEDILON (poliacrilamida). Exames pré e pós-operatórios (1 dia e 3 meses) avaliaram comparativamente a contagem de células endoteliais, variação da pressão intra-ocular, paquimetria corneana, tipo de incisão, complicações pós-operatórias e impressões subjetivas dos cirurgiões.

Resultados:

A perda de células endoteliais foi equivalente entre os Grupos 2 (Healon) e Grupo 3 (Medilon), e maior no Grupo 1 (ar). Em todos outros aspectos clínicos estudados não houve diferenças estatisticamente significativas entre o Grupo 2 e o Grupo 3. Quanto à impressão subjetiva dos cirurgiões verificou-se uma discreta preferência pela poliacrilamida sobre o hialuronato de sódio.

Conclusões:

Os resultados sugerem que a poliacrilamida é comparável ao hialuronato de sódio quanto à segurança clínica e eficiência como solução visco-elástica para uso intra-ocular.

Palavras-chave:
Proteção encdotelial; Poliacrilamida; Hialuronato de sódio; Visco-elásticos

SUMMARY

Purpose:

To evaluate the clinical safety and effectiveness of the novel synthetic viscoelastic solution MEDILON (polyacrylamide).

Methods:

60 cataract patients were randomly divided into 3 groups of 20 patients. Upon extracapsular cataract extraction Group 1 received injected air in the anterior chamber for endothelium protection, Group 2 received HEALON ( sodium hyaluronate) and Group 3 received MEDILON (polyacrylamide). Preoperative and postoperative ( 1 day and 3 months) examinations were conducted as well as a comparative study between groups evaluating endothelial cell count, intraocular pressure variation, corneal thickness, incision type, postoperative complications and surgeons' subjective impressions.

Results:

Endothelial cell loss was similar in Group 2 (Healon) and Group 3 (Medilon), and higher in Group 1 (Air). Regarding all other clinical aspects there were no statistically significant differences between Groups 2 and 3. As to the surgeons subjective impressions there was a discreet preference for polyacrylamide over sodium hyaluronate.

Conclusions:

Our results suggest that the clinical safety and effectiveness of polyacrylamide as a viscoelastic substance for intraocular use is comparable to sodium hyaluronate.

Keywords:
Endothelial protection; Polyacrilamide; Sodium hyaluronate; Viscoelastics

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Datas de Publicação

  • Publicação nesta coleção
    Fev 1999
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