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The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey
PURPOSE: This study reviews evidence and provides recommendations for the ideal setting of intravitreal injection (IVI) administration of vascular endothelial growth factor (VEGF) inhibitors. METHODS: A multi-step approach was employed, including content analysis of regulations and guidelines, a sys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587024/ https://www.ncbi.nlm.nih.gov/pubmed/37199802 http://dx.doi.org/10.1007/s00417-023-06108-y |
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author | Veritti, Daniele Sarao, Valentina Chhablani, Jay Loewenstein, Anat Lanzetta, Paolo |
author_facet | Veritti, Daniele Sarao, Valentina Chhablani, Jay Loewenstein, Anat Lanzetta, Paolo |
author_sort | Veritti, Daniele |
collection | PubMed |
description | PURPOSE: This study reviews evidence and provides recommendations for the ideal setting of intravitreal injection (IVI) administration of vascular endothelial growth factor (VEGF) inhibitors. METHODS: A multi-step approach was employed, including content analysis of regulations and guidelines, a systematic literature review, and an international survey assessing perioperative complications and endophthalmitis incidence in relation to injection settings. The literature review searched PubMed and Cochrane databases from 2006 to 2022, focusing on studies reporting correlations between complications and treatment settings. The survey utilized a web-based questionnaire distributed to clinical sites and the international ophthalmic community, with data managed using electronic capture tools. RESULTS: We reviewed regulations and guidelines from 23 countries across five continents, finding significant variation in IVI administration settings. In most countries, IVI is primarily administered in outpatient clean rooms (96%) or offices (39%), while in others, it is restricted to ambulatory surgery rooms or hospital-based operating theatres (4%). The literature review found that endophthalmitis risk after IVI is generally low (0.01% to 0.26% per procedure), with no significant difference between office-based and operating room settings. The international survey (20 centers, 96,624 anti-VEGF injections) found low overall incidences of severe perioperative systemic adverse events and endophthalmitis, independent of injection settings. CONCLUSION: No significant differences in perioperative complications were observed among various settings, including operating theatres, ambulatory surgery rooms, offices, hospitals, or extra-hospital environments. Choosing the appropriate clinical setting can optimize patient management, potentially increasing effectiveness, quality, productivity, and capacity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00417-023-06108-y. |
format | Online Article Text |
id | pubmed-10587024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-105870242023-10-21 The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey Veritti, Daniele Sarao, Valentina Chhablani, Jay Loewenstein, Anat Lanzetta, Paolo Graefes Arch Clin Exp Ophthalmol Mini Review PURPOSE: This study reviews evidence and provides recommendations for the ideal setting of intravitreal injection (IVI) administration of vascular endothelial growth factor (VEGF) inhibitors. METHODS: A multi-step approach was employed, including content analysis of regulations and guidelines, a systematic literature review, and an international survey assessing perioperative complications and endophthalmitis incidence in relation to injection settings. The literature review searched PubMed and Cochrane databases from 2006 to 2022, focusing on studies reporting correlations between complications and treatment settings. The survey utilized a web-based questionnaire distributed to clinical sites and the international ophthalmic community, with data managed using electronic capture tools. RESULTS: We reviewed regulations and guidelines from 23 countries across five continents, finding significant variation in IVI administration settings. In most countries, IVI is primarily administered in outpatient clean rooms (96%) or offices (39%), while in others, it is restricted to ambulatory surgery rooms or hospital-based operating theatres (4%). The literature review found that endophthalmitis risk after IVI is generally low (0.01% to 0.26% per procedure), with no significant difference between office-based and operating room settings. The international survey (20 centers, 96,624 anti-VEGF injections) found low overall incidences of severe perioperative systemic adverse events and endophthalmitis, independent of injection settings. CONCLUSION: No significant differences in perioperative complications were observed among various settings, including operating theatres, ambulatory surgery rooms, offices, hospitals, or extra-hospital environments. Choosing the appropriate clinical setting can optimize patient management, potentially increasing effectiveness, quality, productivity, and capacity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00417-023-06108-y. Springer Berlin Heidelberg 2023-05-18 2023 /pmc/articles/PMC10587024/ /pubmed/37199802 http://dx.doi.org/10.1007/s00417-023-06108-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) . |
spellingShingle | Mini Review Veritti, Daniele Sarao, Valentina Chhablani, Jay Loewenstein, Anat Lanzetta, Paolo The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey |
title | The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey |
title_full | The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey |
title_fullStr | The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey |
title_full_unstemmed | The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey |
title_short | The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey |
title_sort | ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? a narrative review and international survey |
topic | Mini Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587024/ https://www.ncbi.nlm.nih.gov/pubmed/37199802 http://dx.doi.org/10.1007/s00417-023-06108-y |
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