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Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography

PURPOSE: To determine microvascular changes in children with a history of retinopathy of prematurity (ROP) and in a control group of full‐term children. METHODS: In a cross‐sectional study, 30 eyes of 15 children aged 6–8 years with a history of ROP were evaluated with swept‐source optical coherence...

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Autores principales: Rezar‐Dreindl, Sandra, Eibenberger, Katharina, Told, Reinhard, Neumayer, Thomas, Steiner, Irene, Sacu, Stefan, Schmidt‐Erfurth, Ursula, Stifter, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984179/
https://www.ncbi.nlm.nih.gov/pubmed/32749763
http://dx.doi.org/10.1111/aos.14557
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author Rezar‐Dreindl, Sandra
Eibenberger, Katharina
Told, Reinhard
Neumayer, Thomas
Steiner, Irene
Sacu, Stefan
Schmidt‐Erfurth, Ursula
Stifter, Eva
author_facet Rezar‐Dreindl, Sandra
Eibenberger, Katharina
Told, Reinhard
Neumayer, Thomas
Steiner, Irene
Sacu, Stefan
Schmidt‐Erfurth, Ursula
Stifter, Eva
author_sort Rezar‐Dreindl, Sandra
collection PubMed
description PURPOSE: To determine microvascular changes in children with a history of retinopathy of prematurity (ROP) and in a control group of full‐term children. METHODS: In a cross‐sectional study, 30 eyes of 15 children aged 6–8 years with a history of ROP were evaluated with swept‐source optical coherence tomography angiography (SS‐OCTA). Twenty‐eight eyes of 22 age‐matched full‐term children served as a healthy control group. The foveal avascular zone (FAZ), vessel density (VD) and choroidal vascular flow area (VFA) were evaluated on OCTA and correlated with central retinal thickness (CRT), visual acuity (VA), birth weight (BW), gestational age (GA) and ROP stages. RESULTS: Twenty‐two eyes of 14 children with a history of ROP (stage 1–3) and 25 eyes of 19 full‐term children were available for evaluation. In the ROP group, the gestational age was 27 ± 2 weeks and birth weight was 781 ± 164 g. In the ROP group, CRT was higher in the central ETDRS segment (mean difference [95% CI]: 32.8 µm [18.7; 47.0], p = 0.0002) compared to the controls. Smaller mean FAZ area (−0.12 [−0.19; −0.04], p = 0.004) and perimeter (−662 [−1228; −96], p = 0.03) was found in comparison to the control group. An oval shape of the FAZ was observed among patients with a history of ROP. The mean central VD of the superficial plexus was 28 ± 8/23 ± 8% and of the deep plexus 7 ± 7/3 ± 5% (ROP group/control group; p > 0.05). No statistically significant difference was found regarding the choroidal VFA. Only weak correlation of FAZ and VD with function was observed. CONCLUSIONS: Swept‐source optical coherence tomography angiography imaging revealed significant microvascular anomalies in children with a history of ROP indicating disturbance of early morphological development of the central retina.
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spelling pubmed-79841792021-03-24 Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography Rezar‐Dreindl, Sandra Eibenberger, Katharina Told, Reinhard Neumayer, Thomas Steiner, Irene Sacu, Stefan Schmidt‐Erfurth, Ursula Stifter, Eva Acta Ophthalmol Original Articles PURPOSE: To determine microvascular changes in children with a history of retinopathy of prematurity (ROP) and in a control group of full‐term children. METHODS: In a cross‐sectional study, 30 eyes of 15 children aged 6–8 years with a history of ROP were evaluated with swept‐source optical coherence tomography angiography (SS‐OCTA). Twenty‐eight eyes of 22 age‐matched full‐term children served as a healthy control group. The foveal avascular zone (FAZ), vessel density (VD) and choroidal vascular flow area (VFA) were evaluated on OCTA and correlated with central retinal thickness (CRT), visual acuity (VA), birth weight (BW), gestational age (GA) and ROP stages. RESULTS: Twenty‐two eyes of 14 children with a history of ROP (stage 1–3) and 25 eyes of 19 full‐term children were available for evaluation. In the ROP group, the gestational age was 27 ± 2 weeks and birth weight was 781 ± 164 g. In the ROP group, CRT was higher in the central ETDRS segment (mean difference [95% CI]: 32.8 µm [18.7; 47.0], p = 0.0002) compared to the controls. Smaller mean FAZ area (−0.12 [−0.19; −0.04], p = 0.004) and perimeter (−662 [−1228; −96], p = 0.03) was found in comparison to the control group. An oval shape of the FAZ was observed among patients with a history of ROP. The mean central VD of the superficial plexus was 28 ± 8/23 ± 8% and of the deep plexus 7 ± 7/3 ± 5% (ROP group/control group; p > 0.05). No statistically significant difference was found regarding the choroidal VFA. Only weak correlation of FAZ and VD with function was observed. CONCLUSIONS: Swept‐source optical coherence tomography angiography imaging revealed significant microvascular anomalies in children with a history of ROP indicating disturbance of early morphological development of the central retina. John Wiley and Sons Inc. 2020-08-04 2021-03 /pmc/articles/PMC7984179/ /pubmed/32749763 http://dx.doi.org/10.1111/aos.14557 Text en © 2020 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rezar‐Dreindl, Sandra
Eibenberger, Katharina
Told, Reinhard
Neumayer, Thomas
Steiner, Irene
Sacu, Stefan
Schmidt‐Erfurth, Ursula
Stifter, Eva
Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography
title Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography
title_full Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography
title_fullStr Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography
title_full_unstemmed Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography
title_short Retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography
title_sort retinal vessel architecture in retinopathy of prematurity and healthy controls using swept‐source optical coherence tomography angiography
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984179/
https://www.ncbi.nlm.nih.gov/pubmed/32749763
http://dx.doi.org/10.1111/aos.14557
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