Long-term results of preconditioning treatment with bevacizumab in high-risk patients
Session Details
Session Title: Cornea Surgical: Keratoplasties
Session Date/Time: Monday 16/09/2019 | 16:30-18:00
Paper Time: 17:18
Venue: Free Paper Forum: Podium 1
First Author: : R.Fasciani ITALY
Co Author(s): : A. Caristia L. Mosca A. Caporossi
Abstract Details
Purpose:
The aim of this study is to evaluate the effect of subconjunctival and/or intrastromal Bevacizumab injections on corneal graft survival rate in high-risk patients.
Main outcomes were the number of immune rejection and the graft survival at the end of follow up.
Setting:
Ophthalmology Institute Agostino Gemelli University Policlinic Fondation - IRCCS.
Methods:
In this prospective interventional case-control series were included thirty seven eyes of 37 high-risk patients (case group: 24 patients / control group: 13 eyes). Case group eyes received a cycle of three subconjunctival and/or intrastromal injection of 5 mg/0.2 ml Bevacizumab. Control group did not receive any Bevacizumab injection and directly underwent keratoplasty. All patients were sistematically evaluated by slit-lamp examination and corneal digital photography.
Mean follow-up was 61.2 months ± 24 DS for case group and 26.1 months ±5.7 DS (range 16-36 months) for control group.
Results:
In the case group 33.3% haven’t had keratoplasy because regression of vessels guaranteed good visual acuity.
Patients who received Bevacizumab injections showed less ocular inflammation and activity of vessels. One corneal graft rejection (4%) was seen during the follow-up after 24 months. At the end of follow-up 20.8% had graft failure. Graft survival occurred in 79.1% of patients. No side effects were detected after the injection procedure. In the control group we observed 46.1%graft rejection 3.8 months ± 1.4 SD after keratoplasty. Graft survival occurred in 53.8% of patients.
Conclusions:
The inflammation reduction and the immunomodulation obtained with the administration of Bevacizumab seems to be a safe and valid possibility to reduce the incidence of graft rejection and to improve the corneal graft survival rate in high risk patients.
Financial Disclosure:
None