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Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema

PURPOSE: Intravitreal anti-vascular endothelial growth factor (VEGF) agents are effective in the treatment of central involving diabetic macular oedema (DMO). Vitreoretinal interface abnormalities (VRIA) are common in patients with DMO, and the effect of these on the response to anti-VEGF treatment...

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Autores principales: Wong, Yun, Steel, David H. W., Habib, Maged S., Stubbing-Moore, Alex, Bajwa, Dalvir, Avery, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364245/
https://www.ncbi.nlm.nih.gov/pubmed/27957600
http://dx.doi.org/10.1007/s00417-016-3562-0
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author Wong, Yun
Steel, David H. W.
Habib, Maged S.
Stubbing-Moore, Alex
Bajwa, Dalvir
Avery, Peter J.
author_facet Wong, Yun
Steel, David H. W.
Habib, Maged S.
Stubbing-Moore, Alex
Bajwa, Dalvir
Avery, Peter J.
author_sort Wong, Yun
collection PubMed
description PURPOSE: Intravitreal anti-vascular endothelial growth factor (VEGF) agents are effective in the treatment of central involving diabetic macular oedema (DMO). Vitreoretinal interface abnormalities (VRIA) are common in patients with DMO, and the effect of these on the response to anti-VEGF treatment is unclear. Furthermore the effect of anti-VEGF agents on the VRIA itself is uncertain. METHOD: Prospective study of consecutive patients treated with ranibizumab (RZB) for DMO as part of routine clinical care in one eye unit over a 1-year period. Visual acuity (Va), central retinal thickness (CRT) and injection frequency data was recorded on an electronic database. Treatment was initiated with four monthly RZB injections and then a monthly PRN regime. All patients underwent high-density spectral-domain optical coherence tomography (SDOCT) at baseline and 12 months. The SDOCTs were graded by two observers masked to the outcome. RESULTS: One hundred and four eyes (77 patients) were included in the analysis. The mean age was 62 years, and 62% were male. The mean presenting vision was 62 letters and CRT 472 μm. Eighty eyes retained stable Va, and 17 had an improvement in Va. At baseline, 39 eyes had associated focal vitreomacular adhesion (VMA) and by 12 months this reduced to 30 (p = 0.04), with 12 releasing VMA and three developing it. Patients with VMA had significantly better final Va than those without VMA. Improvement in CRT was greatest in those where VMA released during the study. Forty-five eyes had some degree of foveal involving epiretinal membrane (ERM) at baseline, and 28 were considered to have clinically significant ERM. There was no clinically relevant change in ERM during the study. Patients with significant ERM at baseline had a lower final vision. Multivariate analysis showed that ERM and more severe retinopathy at baseline were predictive of less visual improvement (p < 0.01). Shorter intraretinal cyst length, ERM and the absence of VMA at baseline were predictive of a worsened anatomical response (p < 0.001). CONCLUSION: VRIA are related to outcome in patients treated with RZB. ERM was associated with a worsened visual and anatomic response, and VMA with an improved anatomical response particularly when spontaneous VMA release occurred during treatment. The presence and severity of ERM was not affected by RZB treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00417-016-3562-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-53642452017-04-07 Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema Wong, Yun Steel, David H. W. Habib, Maged S. Stubbing-Moore, Alex Bajwa, Dalvir Avery, Peter J. Graefes Arch Clin Exp Ophthalmol Retinal Disorders PURPOSE: Intravitreal anti-vascular endothelial growth factor (VEGF) agents are effective in the treatment of central involving diabetic macular oedema (DMO). Vitreoretinal interface abnormalities (VRIA) are common in patients with DMO, and the effect of these on the response to anti-VEGF treatment is unclear. Furthermore the effect of anti-VEGF agents on the VRIA itself is uncertain. METHOD: Prospective study of consecutive patients treated with ranibizumab (RZB) for DMO as part of routine clinical care in one eye unit over a 1-year period. Visual acuity (Va), central retinal thickness (CRT) and injection frequency data was recorded on an electronic database. Treatment was initiated with four monthly RZB injections and then a monthly PRN regime. All patients underwent high-density spectral-domain optical coherence tomography (SDOCT) at baseline and 12 months. The SDOCTs were graded by two observers masked to the outcome. RESULTS: One hundred and four eyes (77 patients) were included in the analysis. The mean age was 62 years, and 62% were male. The mean presenting vision was 62 letters and CRT 472 μm. Eighty eyes retained stable Va, and 17 had an improvement in Va. At baseline, 39 eyes had associated focal vitreomacular adhesion (VMA) and by 12 months this reduced to 30 (p = 0.04), with 12 releasing VMA and three developing it. Patients with VMA had significantly better final Va than those without VMA. Improvement in CRT was greatest in those where VMA released during the study. Forty-five eyes had some degree of foveal involving epiretinal membrane (ERM) at baseline, and 28 were considered to have clinically significant ERM. There was no clinically relevant change in ERM during the study. Patients with significant ERM at baseline had a lower final vision. Multivariate analysis showed that ERM and more severe retinopathy at baseline were predictive of less visual improvement (p < 0.01). Shorter intraretinal cyst length, ERM and the absence of VMA at baseline were predictive of a worsened anatomical response (p < 0.001). CONCLUSION: VRIA are related to outcome in patients treated with RZB. ERM was associated with a worsened visual and anatomic response, and VMA with an improved anatomical response particularly when spontaneous VMA release occurred during treatment. The presence and severity of ERM was not affected by RZB treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00417-016-3562-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-12-12 2017 /pmc/articles/PMC5364245/ /pubmed/27957600 http://dx.doi.org/10.1007/s00417-016-3562-0 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Retinal Disorders
Wong, Yun
Steel, David H. W.
Habib, Maged S.
Stubbing-Moore, Alex
Bajwa, Dalvir
Avery, Peter J.
Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema
title Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema
title_full Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema
title_fullStr Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema
title_full_unstemmed Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema
title_short Vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema
title_sort vitreoretinal interface abnormalities in patients treatedwith ranibizumab for diabetic macular oedema
topic Retinal Disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364245/
https://www.ncbi.nlm.nih.gov/pubmed/27957600
http://dx.doi.org/10.1007/s00417-016-3562-0
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