Feasibility Of Implementing A Multimedia Patient Education And Informed Consent Tool For Cataract Surgery
Published 2025 - 43rd Congress of the ESCRS
Reference: PP18.11 | Type: Poster | DOI: 10.82333/qjt0-7v78
Authors: Lucia Schartner* 1 , Sophia A Reifeltshammer 2 , Leon Pomberger 2 , Matthias Bolz 2 , Nino Hirnschall 2
1Karl Landsteiner University of Health Sciences,Krems,Austria, 2Department of Ophthalmology and Optometry,Kepler University Hospital,Linz,Austria
Purpose
To develop and evaluate an informed consent multimedia tool for cataract surgery in order to enhance patient satisfaction, engagement, in-person counseling time, and understanding.
Setting
Department of Ophthalmology and Optometry, Kepler University Hospital and Johannes Kepler University, Linz, Austria
Methods
In this monocentric pilot study, a multimedia-informed consent tool was developed incorporating visual aids, interactive checkpoints, simplified medical explanations and a voiceover. Focus groups, including patients and clinicians, were conducted to refine content based on feedback regarding clarity and effectiveness using a questionnaire.
Results
In the focus groups, the tool was improved using understandable language to allow patients of different educational backgrounds and different native languages enhanced patient education. Additionally, based on PubMed research, more visual aids and animations were added to visually underline the key points.
Conclusions
The development of a multimedia-informed consent tool for cataract surgery demonstrated potential in enhancing patient education and satisfaction. By integrating visual aids, animations, interactive checkpoints and simplified medical explanations, the tool ensures a clearer understanding of the procedure. This approach not only improves the informed consent process but also reduces in-person counseling time while maintaining high-quality communication. Ultimately, enhancing patient comprehension may contribute to better decision-making and improved patient outcomes of cataract surgery. A future randomized controlled trial should evaluate its efficacy compared to traditional verbal patient informed consent discussions.