The ideal intravitreal injection setting: office, ambulatory surgery room or operating theatre? A narrative review and international survey

Author:

Veritti DanieleORCID,Sarao ValentinaORCID,Chhablani JayORCID,Loewenstein AnatORCID,Lanzetta PaoloORCID,Bandello Francesco,Midena Edoardo,Nicolò Massimo,Parravano Mariacristina,Pilotto Elisabetta,Ricci Federico,Staurenghi Giovanni,Virgili Gianni,Arnold Jennifer J.,Augustin Albert J.,Creuzot-Garcher Catherine,Adrian Monica Lövestam,Mekjavić Polona Jaki,Patel Praveen J.,Rodriguez Francisco J.,Schumann Ricarda,Sharma Ashish,Silva Rufino,Zarranz-Ventura Javier, ,

Abstract

Abstract 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.

Funder

Università degli Studi di Udine

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

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