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Postoperative dry eye symptoms and secondary healthcare utilization in patients prior to, during, and after the COVID 19 pandemic

Quoi:
Paper Presentation | Présentation d'article
Quand:
10:50 AM, Dimanche 18 Juin 2023 (3 minutes)
Où:
Centre des congrès de Québec - Room 307 AB | Salle 307 AB
Comment:

Author Block: Milena Cioana 1, Sohel Somani1, Eric S. Tam1, Francesca Lee2, Saffire H. Krance3, Amin Hatamnejad4, Hannah H. Chiu11Temerty Faculty of Medicine, University of Toronto, 2Faculty of Medicine and Health Sciences, McGill University, 3Schulich School of Medicine and Dentistry, Western University, 4Michael G. DeGroote School of Medicine, McMaster University.

Author Disclosure Block: M. Cioana:  None.  S. Somani:  None.  E.S. Tam:  None.  F. Lee:  None.  S.H. Krance:  None.  A. Hatamnejad:  None.  H.H. Chiu:  None., Milena Cioana: Not Current  Sohel Somani: Not Current  Eric Tam: Not Current  Francesca Lee: Not Current  Saffire Krance: Not Current  Amin Hatamnejad: Not Current  Hannah Chiu: Not Current

 

Abstract Title: Postoperative dry eye symptoms and secondary healthcare utilization in patients prior to, during, and after the COVID-19 pandemic

Abstract Body: Purpose:  Dry eye symptoms (DES) continue to be a significant side effect of cataract surgery affecting quality of life and satisfaction of patients postoperatively. The primary objective of this study is to compare DES in patients following uncomplicated cataract surgery prior to, during, and after the COVID-19 pandemic. Our secondary objective was to identify risk factors associated with postoperative dry eye symptoms.  Study Design:  Retrospective chart review.  Methods:  Data from consecutive patients who underwent uncomplicated cataract surgery in November 2019, 2020, and 2021 in a surgical centre in Ontario, Canada was extracted. Patients included were 18 years or older with preoperative Dry Eye Questionnaire 5 (DEQ5) scores (range: 0-2=none, 3-8=mild, 9-15=moderate, 16-22=severe DES). Sample size calculation based on previous studies was done, and 131 patients were included in each group. Preoperative DEQ5, prophylactic treatment, and presence of DES risk factors (ocular comorbidities, systemic diseases, use of glaucoma medications, intravitreal anti-VEGF injections, OPD mires suggestive of dry eye, previous corneal treatments) were recorded. Number of postoperative visits due to DES concerns were calculated. Odds ratios (OR) of risk of postoperative DES based on preoperative DEQ5 or prophylactic treatment were determined. DES risk factors were analyzed using multivariate regression.  Results:  Preoperative DES prevalence and DEQ5 scores pre, during and post-COVID-19 decreased (mean±SD: 6.2±5.5, 3.4±4.4, 2.3±3.4, respectively, p<0.01). While the number of total follow-ups has decreased during and post-COVID-19, the percentage of follow-ups attributed to DES has increased (26%, 50%, 40%, respectively). Percentage of patients receiving prophylactic treatment preoperatively did not differ significantly between the groups (41.9%, 37.4%, 35.9%, respectively). In the during and post-COVID-19 groups there was a higher risk of postoperative DES with increasing preoperative DEQ5 score (OR=1.13, 95%CI 1.03-1.24 and OR=1.18, 95%CI 1.03-1.35, respectively). No other risk factors predicted DES, and there was no DES risk reduction in patients receiving preoperative treatment, regardless of DEQ5 score or group.  Conclusions:  There has been an increase in postoperative DES during and after the COVID-19 pandemic despite a decrease in DES preoperatively. Preoperative DES treatment does not seem to reduce the burden of postoperative DES. More research is needed on DES treatment adherence to determine protective measures.

Présentateur.rice
University of Toronto
Medical Student (2024)
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