Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
DOI: | 10.48560/rspo.25976 |
Texto Completo: | https://doi.org/10.48560/rspo.25976 |
Resumo: | INTRODUCTION: Keratoconus (KC) is a corneal ectatic disorder characterized by pro- gressive corneal thinning and steepening. Corneal collagen cross-linking (CXL) uses riboflavin and ultraviolet-A radiation to induce cross-links in the stromal collagen, increasing its biomechanical rigidity and halting the progression of KC. Different protocols of CXL have been proposed throughout the years to improve clinical results and patient comfort. However, management of pediatric cases remains particularly challenging because younger patients tend to exhibit a more rapid progression of the disease. In this study we aim to evaluate the efficacy of CXL in a population of pediatric patients aged 18 years or less with progressive KC. MATERIAL AND METHODS: Multi-center, retrospective, cross-sectional study. Patients with progressive KC, aged ≤ 18, who underwent CXL between 2010 and 2021 were reviewed. Different modalities of CXL were used: Standard CXL, Accelerated CXL, Combined CXL and partial topography-guided PRK (photorefractive keratectomy), and Customized CXL. Evaluation included best spectacle corrected visual acuity (BSCVA), manifest refraction, and Scheimpflugtomography evaluation. Baseline and follow-up values were compared. RESULTS AND DISCUSSION: The study included 44 eyes of 33 patients, 26 (78.8%) male and 7 (21.2%) female. Mean age at time of CXL was 15.2±3.1 years [range 10-18]. Convention- al CXL was performed in 9 eyes, and accelerated CXL in 14 eyes. Seven eyes performed combined CXL and simultaneous topography guided PRK. Fourteen eyes performed customized irradiation CXL. Epithelium was removed before CXL in all patients. Mean follow-up was 21.9±16.6 months [range 4-66]. At the last follow-up, mean BSCVA was improved from 0.43±0.26 to 0.38±0.25 Log- MAR (p=0.067). Preoperative mean spherical equivalent increased from -1.97±2.44 to -2.41±3.60 D (p=0.509) and cylinder decreased from 2.85±1.92 to 2.34±1.77 D (p=0.045). The flat keratometric values (K1) remained stable, from 48.04±4.87 to 48.74±5.12 D (p=0.358), as well as the steep keratometric values (K2), from 53.63±6.60 to 53.98±6.09 D (p=0.721), and maximum keratometry values (K max), from 62.45±10.38 to 62.20±10.01 D (p=0.764). Thinnest corneal thickness decreased from 452.03±39.63 to 423.59±43.17 μm (p<0.001). Mean spherical equivalent increased in conventional CXL eyes, and had a greater decrease in those having undergone combined CXL and PRK (p=0.042). Thinnest corneal thickness decreased more significantly in the combined CXL and PRK eyes (p<0.001). No other differences between different CXL protocols were significant. Success rate at the last follow-up was 90.9%, with 4 eyes (9.1%) showing progression after CXL: 2 following accelerated CXL and 2 following customized irradiation CXL. CONCLUSION: CXL seems to halt the progression of KC in pediatric patients and result in stabilization of visual acuity and topographic parameters. Our results are in line with the published international series for pediatric KC, showing overall good results but more risk of progression than adult patients. Alternative protocols seem to be equally effective as standard-CXL in pediatric KC. |
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Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year ExperienceCross-Linking Corneano em Idade Pediátrica: Dez Anos de ExperiênciaArtigos OriginaisINTRODUCTION: Keratoconus (KC) is a corneal ectatic disorder characterized by pro- gressive corneal thinning and steepening. Corneal collagen cross-linking (CXL) uses riboflavin and ultraviolet-A radiation to induce cross-links in the stromal collagen, increasing its biomechanical rigidity and halting the progression of KC. Different protocols of CXL have been proposed throughout the years to improve clinical results and patient comfort. However, management of pediatric cases remains particularly challenging because younger patients tend to exhibit a more rapid progression of the disease. In this study we aim to evaluate the efficacy of CXL in a population of pediatric patients aged 18 years or less with progressive KC. MATERIAL AND METHODS: Multi-center, retrospective, cross-sectional study. Patients with progressive KC, aged ≤ 18, who underwent CXL between 2010 and 2021 were reviewed. Different modalities of CXL were used: Standard CXL, Accelerated CXL, Combined CXL and partial topography-guided PRK (photorefractive keratectomy), and Customized CXL. Evaluation included best spectacle corrected visual acuity (BSCVA), manifest refraction, and Scheimpflugtomography evaluation. Baseline and follow-up values were compared. RESULTS AND DISCUSSION: The study included 44 eyes of 33 patients, 26 (78.8%) male and 7 (21.2%) female. Mean age at time of CXL was 15.2±3.1 years [range 10-18]. Convention- al CXL was performed in 9 eyes, and accelerated CXL in 14 eyes. Seven eyes performed combined CXL and simultaneous topography guided PRK. Fourteen eyes performed customized irradiation CXL. Epithelium was removed before CXL in all patients. Mean follow-up was 21.9±16.6 months [range 4-66]. At the last follow-up, mean BSCVA was improved from 0.43±0.26 to 0.38±0.25 Log- MAR (p=0.067). Preoperative mean spherical equivalent increased from -1.97±2.44 to -2.41±3.60 D (p=0.509) and cylinder decreased from 2.85±1.92 to 2.34±1.77 D (p=0.045). The flat keratometric values (K1) remained stable, from 48.04±4.87 to 48.74±5.12 D (p=0.358), as well as the steep keratometric values (K2), from 53.63±6.60 to 53.98±6.09 D (p=0.721), and maximum keratometry values (K max), from 62.45±10.38 to 62.20±10.01 D (p=0.764). Thinnest corneal thickness decreased from 452.03±39.63 to 423.59±43.17 μm (p<0.001). Mean spherical equivalent increased in conventional CXL eyes, and had a greater decrease in those having undergone combined CXL and PRK (p=0.042). Thinnest corneal thickness decreased more significantly in the combined CXL and PRK eyes (p<0.001). No other differences between different CXL protocols were significant. Success rate at the last follow-up was 90.9%, with 4 eyes (9.1%) showing progression after CXL: 2 following accelerated CXL and 2 following customized irradiation CXL. CONCLUSION: CXL seems to halt the progression of KC in pediatric patients and result in stabilization of visual acuity and topographic parameters. Our results are in line with the published international series for pediatric KC, showing overall good results but more risk of progression than adult patients. Alternative protocols seem to be equally effective as standard-CXL in pediatric KC.INTRODUÇÃO: O queratocone (QC) é uma doença ectásica corneana que se caracteriza por um adelgaçamento e encurvamento corneanos progressivos. O cross-linking corneano (CXL) utiliza riboflavina e radiação ultravioleta-A para induzir ligações cruzadas no colagénio estromal, aumentando a sua rigidez biomecânica e impedindo a progressão do QC. Ao longo dos anos, diferentes protocolos de CXL foram propostos para melhorar resultados clínicos e o conforto dos doentes. Contudo, a orientação de casos pediátricos permanece particularmente desafiante, uma vez que doentes mais novos tendem a demonstrar progressão mais rápida da doença. Neste estudo pretendemos avaliar a eficácia do CXL numa população de doentes pediátricos com 18 anos ou menos, com QC em progressão. MATERIAL E MÉTODOS: Estudo multicêntrico, retrospetivo, cross-sectional. Os processos dos doentes com QC em progressão, com idade ≤ 18 anos, que foram submetidos a CXL entre 2010 e 2021 foram revistos. Diferentes modalidades de CXL foram utilizadas: CXL standard, CXL acelerado, CXL combinado com PRK (photorefractive keratectomy) parcialmente topoguiado, e CXL customizado. A avaliação incluiu melhor acuidade visual corrigida (BSCVA), refração subjetiva e tomografia Scheimpflug. Os valores base e no follow-up foram comparados. RESULTADOS E DISCUSSÃO: O estudo incluiu 44 olhos de 33 doentes, 26 do sexo masculino (78,8%) e 7 (21,2%) do sexo feminino. A idade média à data do CXL foi 15,2±3,1 anos [entre 10-18]. CXL convencional foi feito em 9 olhos, e CXL acelerado em 14 olhos. Sete olhos foram submetidos a CXL combinado com PRK, e 14 olhos a CXL com irradiação customizada. O epitélio foi removido previamente ao CXL em todos os doentes. O follow-up médio foi de 21,9±16,6 meses [entre 4-66]. À data do último follow-up, a BSCVA média melhorou de 0,43±0,26 para 0,38±0,25 LogMAR (p=0,067). O equivalente esférico médio pré-operatório aumentou de -1,97±2,44 para -2,41±3,60 D (p=0,509) e o cilindro diminuiu de 2,85±1,92 para 2,34±1,77 D (p=0,045). Os valores do meridiano mais plano (K1) mantiveram-se estáveis, de 48,04±4,87 para 48,74±5,12 D (p=0,358), bem como os do meridiano mais curvo (K2), de 53,63±6,60 para 53,98±6,09 D (p=0,721), e os valores do ponto de curvatura máxima (K max.), de 62,45±10,38 para 62,20±10,01 D (p=0,764). A espessura corneana no ponto mais fino diminuiu de 452,03±39,63 para 423,59±43,17 μm (p<0,001). O equivalente esférico médio aumentou nos olhos com CXL convencional, e teve uma maior diminuição naqueles submetidos a CXL e PRK combinados (p=0,042). A espessura de córnea mais fina diminuiu mais significativamente nos olhos com CXL combinado com PRK (p<0,001). Não houve outras diferenças significativas entre os diferentes protocolos de CXL. A taxa de sucesso no último follow-up foi de 90,9%, com 4 olhos (9,1%) a demonstrar progressão após o CXL: 2 após CXL acelerado e 2 após CXL com irradiação customizada. CONCLUSÃO: O CXL parece parar a progressão do QC em doentes pediátricos e resultar na estabilização da acuidade visual e parâmetros topográficos. Os nossos resultados encontram-se em linha com as séries internacionais publicadas para QC pediátrico, mostrando globalmente bons resultados mas com maior risco de progressão do que em doentes adultos. Os protocolos alternativos parecem ser igualmente eficazes ao CXL standard no QC pediátrico.Ajnet2022-09-30T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.48560/rspo.25976eng1646-69501646-6950Félix, RaquelGonçalves, GuilhermeGil, JoãoCosta, EsmeraldaRosa, AndreiaTavares, CristinaQuadrado, Maria JoãoMurta, Joaquiminfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-10-13T20:30:16Zoai:ojs.revistas.rcaap.pt:article/25976Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:11:23.129707Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience Cross-Linking Corneano em Idade Pediátrica: Dez Anos de Experiência |
title |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience |
spellingShingle |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience Félix, Raquel Artigos Originais Félix, Raquel Artigos Originais |
title_short |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience |
title_full |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience |
title_fullStr |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience |
title_full_unstemmed |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience |
title_sort |
Corneal Collagen Cross-Linking in Pediatric Patients: Ten Year Experience |
author |
Félix, Raquel |
author_facet |
Félix, Raquel Félix, Raquel Gonçalves, Guilherme Gil, João Costa, Esmeralda Rosa, Andreia Tavares, Cristina Quadrado, Maria João Murta, Joaquim Gonçalves, Guilherme Gil, João Costa, Esmeralda Rosa, Andreia Tavares, Cristina Quadrado, Maria João Murta, Joaquim |
author_role |
author |
author2 |
Gonçalves, Guilherme Gil, João Costa, Esmeralda Rosa, Andreia Tavares, Cristina Quadrado, Maria João Murta, Joaquim |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Félix, Raquel Gonçalves, Guilherme Gil, João Costa, Esmeralda Rosa, Andreia Tavares, Cristina Quadrado, Maria João Murta, Joaquim |
dc.subject.por.fl_str_mv |
Artigos Originais |
topic |
Artigos Originais |
description |
INTRODUCTION: Keratoconus (KC) is a corneal ectatic disorder characterized by pro- gressive corneal thinning and steepening. Corneal collagen cross-linking (CXL) uses riboflavin and ultraviolet-A radiation to induce cross-links in the stromal collagen, increasing its biomechanical rigidity and halting the progression of KC. Different protocols of CXL have been proposed throughout the years to improve clinical results and patient comfort. However, management of pediatric cases remains particularly challenging because younger patients tend to exhibit a more rapid progression of the disease. In this study we aim to evaluate the efficacy of CXL in a population of pediatric patients aged 18 years or less with progressive KC. MATERIAL AND METHODS: Multi-center, retrospective, cross-sectional study. Patients with progressive KC, aged ≤ 18, who underwent CXL between 2010 and 2021 were reviewed. Different modalities of CXL were used: Standard CXL, Accelerated CXL, Combined CXL and partial topography-guided PRK (photorefractive keratectomy), and Customized CXL. Evaluation included best spectacle corrected visual acuity (BSCVA), manifest refraction, and Scheimpflugtomography evaluation. Baseline and follow-up values were compared. RESULTS AND DISCUSSION: The study included 44 eyes of 33 patients, 26 (78.8%) male and 7 (21.2%) female. Mean age at time of CXL was 15.2±3.1 years [range 10-18]. Convention- al CXL was performed in 9 eyes, and accelerated CXL in 14 eyes. Seven eyes performed combined CXL and simultaneous topography guided PRK. Fourteen eyes performed customized irradiation CXL. Epithelium was removed before CXL in all patients. Mean follow-up was 21.9±16.6 months [range 4-66]. At the last follow-up, mean BSCVA was improved from 0.43±0.26 to 0.38±0.25 Log- MAR (p=0.067). Preoperative mean spherical equivalent increased from -1.97±2.44 to -2.41±3.60 D (p=0.509) and cylinder decreased from 2.85±1.92 to 2.34±1.77 D (p=0.045). The flat keratometric values (K1) remained stable, from 48.04±4.87 to 48.74±5.12 D (p=0.358), as well as the steep keratometric values (K2), from 53.63±6.60 to 53.98±6.09 D (p=0.721), and maximum keratometry values (K max), from 62.45±10.38 to 62.20±10.01 D (p=0.764). Thinnest corneal thickness decreased from 452.03±39.63 to 423.59±43.17 μm (p<0.001). Mean spherical equivalent increased in conventional CXL eyes, and had a greater decrease in those having undergone combined CXL and PRK (p=0.042). Thinnest corneal thickness decreased more significantly in the combined CXL and PRK eyes (p<0.001). No other differences between different CXL protocols were significant. Success rate at the last follow-up was 90.9%, with 4 eyes (9.1%) showing progression after CXL: 2 following accelerated CXL and 2 following customized irradiation CXL. CONCLUSION: CXL seems to halt the progression of KC in pediatric patients and result in stabilization of visual acuity and topographic parameters. Our results are in line with the published international series for pediatric KC, showing overall good results but more risk of progression than adult patients. Alternative protocols seem to be equally effective as standard-CXL in pediatric KC. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09-30T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.48560/rspo.25976 |
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https://doi.org/10.48560/rspo.25976 |
dc.language.iso.fl_str_mv |
eng |
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eng |
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1646-6950 1646-6950 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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Ajnet |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1822183306365501440 |
dc.identifier.doi.none.fl_str_mv |
10.48560/rspo.25976 |