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Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes

BACKGROUND: This study was to evaluate the efficacy and safety of the implantation of foldable capsular vitreous body (FCVB) in severe retinal detachment eyes. METHODS: A retrospective study in retinal detachment eyes was performed at Shandong Provincial Hospital Affiliated to Shandong First Medical...

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Autores principales: Ma, Shengnan, Zhao, Suzhen, Zhang, Chunxiao, Tang, Xia, Zhou, Weiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756693/
https://www.ncbi.nlm.nih.gov/pubmed/36522622
http://dx.doi.org/10.1186/s12886-022-02729-9
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author Ma, Shengnan
Zhao, Suzhen
Zhang, Chunxiao
Tang, Xia
Zhou, Weiyan
author_facet Ma, Shengnan
Zhao, Suzhen
Zhang, Chunxiao
Tang, Xia
Zhou, Weiyan
author_sort Ma, Shengnan
collection PubMed
description BACKGROUND: This study was to evaluate the efficacy and safety of the implantation of foldable capsular vitreous body (FCVB) in severe retinal detachment eyes. METHODS: A retrospective study in retinal detachment eyes was performed at Shandong Provincial Hospital Affiliated to Shandong First Medical University. A standard three-port pars plana vitrectomy was performed, and the FCVB was triple folded and implanted into the vitreous cavity. The silicone oil (SO) was then injected into the capsule of the FCVB to support the retina and eye. During the follow-up period, The treated eyes were examined by ophthalmoscopy, fundus photography, and tonometry. B-scan ultrasonography, optical coherence tomography (OCT), and computed tomography (CT), were also performed. RESULTS: From May 2020 to November 2021, 31 cases with severe retinal detachment were enrolled in the study. The postoperative follow-up time gradient ranged from 1 to 72 weeks, At various observation time points during the 72 weeks after surgery, The postoperative IOP was maintained at around 10 mmhg at various time points, with a slight decrease compared to the preoperative IOP (14.2 ± 4.6 mmHg n = 18), and was statistically significant. 9 of 31 patients had clear refractive media, both fundus and OCT showed retinal reattachment, OCT showed the 200 μm thick FCVB capsule support retina. The remaining 22 patients with unclear refractive media, B-scan showed arcuate hyperechoes in front of the retina. There was also no significant difference in visual acuity compared to preoperative. The FCVB was well positioned in the vitreous cavity, and no serious complications such as endophthalmitis, glaucoma, silicone oil emulsification, product exposure, or sympathetic uveitis were found. CONCLUSIONS: FCVB has retinal support with certain ability to maintain IOP and eye morphology and avoid eye removal in patients with severe retinal detachment during the 72-week observation period. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-022-02729-9.
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spelling pubmed-97566932022-12-17 Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes Ma, Shengnan Zhao, Suzhen Zhang, Chunxiao Tang, Xia Zhou, Weiyan BMC Ophthalmol Research BACKGROUND: This study was to evaluate the efficacy and safety of the implantation of foldable capsular vitreous body (FCVB) in severe retinal detachment eyes. METHODS: A retrospective study in retinal detachment eyes was performed at Shandong Provincial Hospital Affiliated to Shandong First Medical University. A standard three-port pars plana vitrectomy was performed, and the FCVB was triple folded and implanted into the vitreous cavity. The silicone oil (SO) was then injected into the capsule of the FCVB to support the retina and eye. During the follow-up period, The treated eyes were examined by ophthalmoscopy, fundus photography, and tonometry. B-scan ultrasonography, optical coherence tomography (OCT), and computed tomography (CT), were also performed. RESULTS: From May 2020 to November 2021, 31 cases with severe retinal detachment were enrolled in the study. The postoperative follow-up time gradient ranged from 1 to 72 weeks, At various observation time points during the 72 weeks after surgery, The postoperative IOP was maintained at around 10 mmhg at various time points, with a slight decrease compared to the preoperative IOP (14.2 ± 4.6 mmHg n = 18), and was statistically significant. 9 of 31 patients had clear refractive media, both fundus and OCT showed retinal reattachment, OCT showed the 200 μm thick FCVB capsule support retina. The remaining 22 patients with unclear refractive media, B-scan showed arcuate hyperechoes in front of the retina. There was also no significant difference in visual acuity compared to preoperative. The FCVB was well positioned in the vitreous cavity, and no serious complications such as endophthalmitis, glaucoma, silicone oil emulsification, product exposure, or sympathetic uveitis were found. CONCLUSIONS: FCVB has retinal support with certain ability to maintain IOP and eye morphology and avoid eye removal in patients with severe retinal detachment during the 72-week observation period. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12886-022-02729-9. BioMed Central 2022-12-15 /pmc/articles/PMC9756693/ /pubmed/36522622 http://dx.doi.org/10.1186/s12886-022-02729-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ma, Shengnan
Zhao, Suzhen
Zhang, Chunxiao
Tang, Xia
Zhou, Weiyan
Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes
title Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes
title_full Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes
title_fullStr Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes
title_full_unstemmed Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes
title_short Study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes
title_sort study on the efficacy and safety of foldable capsular vitreous body in the severe retinal detachment eyes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756693/
https://www.ncbi.nlm.nih.gov/pubmed/36522622
http://dx.doi.org/10.1186/s12886-022-02729-9
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