Accurate Intraocular Lens Position Determination in Pseudophakic Eyes

Detalhes bibliográficos
Autor(a) principal: Ribeiro, Filomena
Data de Publicação: 2018
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.48560/rspo.10193
Resumo: OBJECTIVES  This work seeks to validate postoperative Anterior Chamber Depth (ACDpost) mesurement devices based in optical low-coherence reflectometry (Lenstar LS 900, (Haag-Streit AG, Köniz, Switzerland) and optical coherence tomography (Visante OCT, Carl Zeiss Meditec Inc., Dublin, California, USA). MATERIAL AND METHODS  A pseudophakic eye phantom was built to check the calibration of both devices. A clinical study involving 40 pseudophakic eyes was conducted and 3 months after surgery ACDpost was measured with both devices and compared. RESULTS Zeiss Visante calibrations had a R.M.S error smaller than the device’s 18 μm resolution in all the measurement sets. No span shift nor zero shift errors were found. Lenstar calibrations had a larger R.M.S error in the order of the device’s 20 μm resolution. In the clinical study, Lenstar failed to measure ACDpost 11% of the times. Additionally Lenstar measured an average IOL thickness of 0.74μm with σ = 0.08mm and a 16% failure rate. Bland-Altman (BA) analysis was performed and a mean difference of 74μm between the measurements was found. The dioptric shift induced by the difference between measurements was calculated in a worst case scenario and a 0.18D difference was found. This is clinically insignificant and the measurements can be considered to be interchangeable. CONCLUSIONS Both devices performed accurate measurements of ACDpost. Results from the clinical trial proved the interchangeability of the measurements in vivo. This will certainly contribute to the improvement of ACDpost estimation methodologies and ultimately contribute to the improvement of IOL power calculation methodologies.
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spelling Accurate Intraocular Lens Position Determination in Pseudophakic EyesArtigos OriginaisOBJECTIVES  This work seeks to validate postoperative Anterior Chamber Depth (ACDpost) mesurement devices based in optical low-coherence reflectometry (Lenstar LS 900, (Haag-Streit AG, Köniz, Switzerland) and optical coherence tomography (Visante OCT, Carl Zeiss Meditec Inc., Dublin, California, USA). MATERIAL AND METHODS  A pseudophakic eye phantom was built to check the calibration of both devices. A clinical study involving 40 pseudophakic eyes was conducted and 3 months after surgery ACDpost was measured with both devices and compared. RESULTS Zeiss Visante calibrations had a R.M.S error smaller than the device’s 18 μm resolution in all the measurement sets. No span shift nor zero shift errors were found. Lenstar calibrations had a larger R.M.S error in the order of the device’s 20 μm resolution. In the clinical study, Lenstar failed to measure ACDpost 11% of the times. Additionally Lenstar measured an average IOL thickness of 0.74μm with σ = 0.08mm and a 16% failure rate. Bland-Altman (BA) analysis was performed and a mean difference of 74μm between the measurements was found. The dioptric shift induced by the difference between measurements was calculated in a worst case scenario and a 0.18D difference was found. This is clinically insignificant and the measurements can be considered to be interchangeable. CONCLUSIONS Both devices performed accurate measurements of ACDpost. Results from the clinical trial proved the interchangeability of the measurements in vivo. This will certainly contribute to the improvement of ACDpost estimation methodologies and ultimately contribute to the improvement of IOL power calculation methodologies.Ajnet2018-03-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.48560/rspo.10193eng1646-69501646-6950Ribeiro, Filomenainfo: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:RCAAP2022-09-22T17:06:02Zoai:ojs.revistas.rcaap.pt:article/10193Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:01:39.302718Repositório 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 Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
title Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
spellingShingle Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
Ribeiro, Filomena
Artigos Originais
title_short Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
title_full Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
title_fullStr Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
title_full_unstemmed Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
title_sort Accurate Intraocular Lens Position Determination in Pseudophakic Eyes
author Ribeiro, Filomena
author_facet Ribeiro, Filomena
author_role author
dc.contributor.author.fl_str_mv Ribeiro, Filomena
dc.subject.por.fl_str_mv Artigos Originais
topic Artigos Originais
description OBJECTIVES  This work seeks to validate postoperative Anterior Chamber Depth (ACDpost) mesurement devices based in optical low-coherence reflectometry (Lenstar LS 900, (Haag-Streit AG, Köniz, Switzerland) and optical coherence tomography (Visante OCT, Carl Zeiss Meditec Inc., Dublin, California, USA). MATERIAL AND METHODS  A pseudophakic eye phantom was built to check the calibration of both devices. A clinical study involving 40 pseudophakic eyes was conducted and 3 months after surgery ACDpost was measured with both devices and compared. RESULTS Zeiss Visante calibrations had a R.M.S error smaller than the device’s 18 μm resolution in all the measurement sets. No span shift nor zero shift errors were found. Lenstar calibrations had a larger R.M.S error in the order of the device’s 20 μm resolution. In the clinical study, Lenstar failed to measure ACDpost 11% of the times. Additionally Lenstar measured an average IOL thickness of 0.74μm with σ = 0.08mm and a 16% failure rate. Bland-Altman (BA) analysis was performed and a mean difference of 74μm between the measurements was found. The dioptric shift induced by the difference between measurements was calculated in a worst case scenario and a 0.18D difference was found. This is clinically insignificant and the measurements can be considered to be interchangeable. CONCLUSIONS Both devices performed accurate measurements of ACDpost. Results from the clinical trial proved the interchangeability of the measurements in vivo. This will certainly contribute to the improvement of ACDpost estimation methodologies and ultimately contribute to the improvement of IOL power calculation methodologies.
publishDate 2018
dc.date.none.fl_str_mv 2018-03-01T00:00:00Z
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