Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano

Detalhes bibliográficos
Autor(a) principal: Silva, Maria Carolina Marquezan Da [UNIFESP]
Data de Publicação: 2020
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=10074198
https://hdl.handle.net/11600/64865
Resumo: Purpose: To describe a new approach for corneal remodeling. Methods: Some pilot studies were conducted to practice handling and implanting the lenticule for corneal remodeling technique. At the final study, it was used a new biocompatible agent, collagen type 1, excimer laser shaped, measured approximately 240 micrometers (μm) and inserted intrastromal post mortem pig eyes. The biomaterial was shaped with the excimer laser on the posterior surface to create planoconcave shapes, which were divided in three different groups and inserted into a manually dissected stromal pocket, at approximately 200 micrometer (μm) depth. Group A (three eyes) 70 μm maximal ablation depth; group B (three eyes) 64 μm maximal ablation depth, and group C (three eyes) 104 μm maximal ablation depth, with a lost of total central thickness (central hole, created unscheduled). Group D (three eyes) was included as a control group with creation of a pocket but without insertion of biomaterial. Evaluation of porcine eyes was performed by optical coherence tomography (AS-OCT Visante®) and corneal tomography (Pentacam®). Results: Pentacam® showed that the average keratometry (Km) in group A decreased from 36.80 to 28.90. Reduction was observed in group B, in which Km decreased from 34.00 to 33.88, and in group C, Km decreased from 34.67 to 32.13. For control group D, Km decreased from 33.78 to 33.12. Corneal flattening was more evident in the biomaterial (A, B and C) implant groups, with a larger reduction in Km (delta 3.52) compared to the control group (delta 0.67), but this reduction was not statistically significant (p=0.405). When K1 and K2 were evaluated separately, between the groups with the intrastromal implant, there was a statistically significant reduction (p=0.021) of K1. The OCT corneas of groups A, B and C showed the implant located in the anterior stroma and with displacement of the endotelial face backward, which was not observed in the control group. The main complications occurred performing the pocket, sometimes very deep, or superficial, as well as the tearing of the implant during the intrastromal insertion, especially during the first experiments in the pilot study, as well as the liquid leakage during the sample excimer laser treatment. Conclusions: The novel planoconcave biomaterial implant was able to reshape the cornea in a post mortem model, resulting in flattening of the cornea. This approach could represent a novel treatment for refractive error in eyes not amenable to currently available technique options such as those with high myopia and corneal ectasia, as well as other refractive errors, according to the lenticule shape, as aphakia and hyperopia.
id UFSP_98b3b8ab3eb26ebccdd43ba0781df61d
oai_identifier_str oai:repositorio.unifesp.br/:11600/64865
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneanoCorneal RemodelingCorneal ImplantEximer LaserRemodelamento CorneanoImplante CorneanoEximer LaserPurpose: To describe a new approach for corneal remodeling. Methods: Some pilot studies were conducted to practice handling and implanting the lenticule for corneal remodeling technique. At the final study, it was used a new biocompatible agent, collagen type 1, excimer laser shaped, measured approximately 240 micrometers (μm) and inserted intrastromal post mortem pig eyes. The biomaterial was shaped with the excimer laser on the posterior surface to create planoconcave shapes, which were divided in three different groups and inserted into a manually dissected stromal pocket, at approximately 200 micrometer (μm) depth. Group A (three eyes) 70 μm maximal ablation depth; group B (three eyes) 64 μm maximal ablation depth, and group C (three eyes) 104 μm maximal ablation depth, with a lost of total central thickness (central hole, created unscheduled). Group D (three eyes) was included as a control group with creation of a pocket but without insertion of biomaterial. Evaluation of porcine eyes was performed by optical coherence tomography (AS-OCT Visante®) and corneal tomography (Pentacam®). Results: Pentacam® showed that the average keratometry (Km) in group A decreased from 36.80 to 28.90. Reduction was observed in group B, in which Km decreased from 34.00 to 33.88, and in group C, Km decreased from 34.67 to 32.13. For control group D, Km decreased from 33.78 to 33.12. Corneal flattening was more evident in the biomaterial (A, B and C) implant groups, with a larger reduction in Km (delta 3.52) compared to the control group (delta 0.67), but this reduction was not statistically significant (p=0.405). When K1 and K2 were evaluated separately, between the groups with the intrastromal implant, there was a statistically significant reduction (p=0.021) of K1. The OCT corneas of groups A, B and C showed the implant located in the anterior stroma and with displacement of the endotelial face backward, which was not observed in the control group. The main complications occurred performing the pocket, sometimes very deep, or superficial, as well as the tearing of the implant during the intrastromal insertion, especially during the first experiments in the pilot study, as well as the liquid leakage during the sample excimer laser treatment. Conclusions: The novel planoconcave biomaterial implant was able to reshape the cornea in a post mortem model, resulting in flattening of the cornea. This approach could represent a novel treatment for refractive error in eyes not amenable to currently available technique options such as those with high myopia and corneal ectasia, as well as other refractive errors, according to the lenticule shape, as aphakia and hyperopia.Objetivo: Descrever uma nova técnica para o remodelamento corneano. Métodos: Foram realizados experimentos-piloto para avaliar manuseio e implante da lentícula para o remodelamento corneano. No estudo final, foi usado um novo agente modelador biocompatível, de colágeno tipo 1, moldado com excimer laser, com aproximadamente 240 micrômetros (μm), o qual foi implantado no estroma corneano em olhos de porco post mortem. Esse material foi moldado em sua face posterior, com excimer laser, para criar formatos planocôncavos, os quais foram então divididos em três diferentes grupos e inseridos em um pocket (bolsão), dissecado manualmente, a 200 μm de profundidade. O grupo A (três olhos) teve a profundidade máxima de ablação de 70 μm; o grupo B (três olhos), de 64 μm; e o grupo C (três olhos), de 104 μm, com perda da espessura total central (buraco central, criado de forma não programada). O grupo D (três olhos) foi incluído como grupo controle com a criação do pocket, porém sem inserir o material. A avaliação desses olhos foi realizada por tomografia de coerência óptica (AS-OCT Visante®) e por tomografia corneana (Pentacam®). Resultados: O Pentacam® mostrou que a ceratometria média (Km) no grupo A diminuiu de 36,80 para 28,90. Foi observado redução no grupo B, no qual o Km diminuiu de 34,00 para 33,88, e no grupo C, diminuiu de 34,67 para 32,13. Para o grupo controle D, o Km diminuiu de 33,78 para 33,12. O aplanamento corneano foi mais evidente nos grupos com implante do biomaterial (A, B e C), com uma redução maior do Km (delta 3,52) em comparação com o grupo controle (delta 0,67), mas essa redução não foi estatisticamente significante (p=0,405). Quando K1 e K2 foram avaliados separadamente entre os grupos com o implante intraestromal, houve uma redução estatisticamente significante (p=0,021) do K1. O OCT das córneas dos grupos A, B e C mostrou o implante localizado no estroma anterior e com deslocamento da face endotelial posteriormente, o que não foi observado no grupo controle. As principais complicações ocorreram durante a confecção do bolsão intraestromal, ora profundo, ora muito superficial, bem como a rasgadura do implante durante a inserção intraestromal, principalmente durante os primeiros experimentos no estudo-piloto, assim como a saída de líquido durante o tratamento da lentícula com o excimer laser. Conclusões: O novo implante de biomaterial planocôncavo foi capaz de remodelar a córnea em modelo de animal post mortem, resultando no aplanamento corneano. Esse procedimento pode representar um novo tratamento para olhos não elegíveis às técnicas usuais, como em casos de alta miopia e ectasia corneana, bem como para outros erros refracionais, de acordo com o formato da lentícula, como afacia e hipermetropia.Dados abertos - Sucupira - Teses e dissertações (2020)Universidade Federal de São Paulo (UNIFESP)Freitas, Denise De [UNIFESP]Universidade Federal de São PauloSilva, Maria Carolina Marquezan Da [UNIFESP]2022-07-25T12:51:08Z2022-07-25T12:51:08Z2020-12-18info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion83 p.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=10074198MARIA CAROLINA MARQUEZAN DA SILVA.pdfhttps://hdl.handle.net/11600/64865porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-27T04:07:20Zoai:repositorio.unifesp.br/:11600/64865Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-27T04:07:20Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
title Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
spellingShingle Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
Silva, Maria Carolina Marquezan Da [UNIFESP]
Corneal Remodeling
Corneal Implant
Eximer Laser
Remodelamento Corneano
Implante Corneano
Eximer Laser
title_short Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
title_full Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
title_fullStr Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
title_full_unstemmed Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
title_sort Ceratofacia com novo biomaterial: etapas de desenvolvimento visando à remodelação corneana usando implante intracorneano
author Silva, Maria Carolina Marquezan Da [UNIFESP]
author_facet Silva, Maria Carolina Marquezan Da [UNIFESP]
author_role author
dc.contributor.none.fl_str_mv Freitas, Denise De [UNIFESP]
Universidade Federal de São Paulo
dc.contributor.author.fl_str_mv Silva, Maria Carolina Marquezan Da [UNIFESP]
dc.subject.por.fl_str_mv Corneal Remodeling
Corneal Implant
Eximer Laser
Remodelamento Corneano
Implante Corneano
Eximer Laser
topic Corneal Remodeling
Corneal Implant
Eximer Laser
Remodelamento Corneano
Implante Corneano
Eximer Laser
description Purpose: To describe a new approach for corneal remodeling. Methods: Some pilot studies were conducted to practice handling and implanting the lenticule for corneal remodeling technique. At the final study, it was used a new biocompatible agent, collagen type 1, excimer laser shaped, measured approximately 240 micrometers (μm) and inserted intrastromal post mortem pig eyes. The biomaterial was shaped with the excimer laser on the posterior surface to create planoconcave shapes, which were divided in three different groups and inserted into a manually dissected stromal pocket, at approximately 200 micrometer (μm) depth. Group A (three eyes) 70 μm maximal ablation depth; group B (three eyes) 64 μm maximal ablation depth, and group C (three eyes) 104 μm maximal ablation depth, with a lost of total central thickness (central hole, created unscheduled). Group D (three eyes) was included as a control group with creation of a pocket but without insertion of biomaterial. Evaluation of porcine eyes was performed by optical coherence tomography (AS-OCT Visante®) and corneal tomography (Pentacam®). Results: Pentacam® showed that the average keratometry (Km) in group A decreased from 36.80 to 28.90. Reduction was observed in group B, in which Km decreased from 34.00 to 33.88, and in group C, Km decreased from 34.67 to 32.13. For control group D, Km decreased from 33.78 to 33.12. Corneal flattening was more evident in the biomaterial (A, B and C) implant groups, with a larger reduction in Km (delta 3.52) compared to the control group (delta 0.67), but this reduction was not statistically significant (p=0.405). When K1 and K2 were evaluated separately, between the groups with the intrastromal implant, there was a statistically significant reduction (p=0.021) of K1. The OCT corneas of groups A, B and C showed the implant located in the anterior stroma and with displacement of the endotelial face backward, which was not observed in the control group. The main complications occurred performing the pocket, sometimes very deep, or superficial, as well as the tearing of the implant during the intrastromal insertion, especially during the first experiments in the pilot study, as well as the liquid leakage during the sample excimer laser treatment. Conclusions: The novel planoconcave biomaterial implant was able to reshape the cornea in a post mortem model, resulting in flattening of the cornea. This approach could represent a novel treatment for refractive error in eyes not amenable to currently available technique options such as those with high myopia and corneal ectasia, as well as other refractive errors, according to the lenticule shape, as aphakia and hyperopia.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-18
2022-07-25T12:51:08Z
2022-07-25T12:51:08Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=10074198
MARIA CAROLINA MARQUEZAN DA SILVA.pdf
https://hdl.handle.net/11600/64865
url https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=10074198
https://hdl.handle.net/11600/64865
identifier_str_mv MARIA CAROLINA MARQUEZAN DA SILVA.pdf
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 83 p.
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
_version_ 1814268328734097408