Official ESCRS | European Society of Cataract & Refractive Surgeons
London 2014 Registration Visa Letters Programme Satellite Meetings Glaucoma Day 2014 Exhibition Hotel Booking Virtual Exhibition Star Alliance
london escrs

Course handouts are now available
Click here


Come to London

video-icon

WATCH to find out why


Site updates:

Programme Updates. Programme Overview and - Video Symposium on Challenging Cases now available.


Optimizing fluence settings and riboflavin composition for PACK-CXL in antimicrobial efficiency against P aeruginosa and S aureus

Search Abstracts by author or title
(results will display both Free Papers & Poster)

Session Details

Session Title: Cornea Medical

Session Date/Time: Tuesday 16/09/2014 | 14:00-16:00

Paper Time: 15:06

Venue: Capital Hall A

First Author: : O.Richoz SWITZERLAND

Co Author(s): :    F. Hafezi              

Abstract Details

Purpose:

When treating bacterial keratitis, determination of the correct pathogen is often clinically challenging. The benefits of using PACK (Photoactivated chromophore for infectious keratitis)-CXL to treat corneal infections is that the treatment is not pathogen-specific. In an attempt to optimize the treatment parameters, we analyzed the effect of high intensity PACK-CXL on the bacterial killing rate in an in vitro model using Pseudomonas aeruginosa.

Setting:

Geneva university hospital, ophthalmology department.

Methods:

The killing rate of a known concentration of bacterias (Pseudomonas aeruginosa and Staphylococcus aureus) was analyzed for the following conditions: 1) preservative-free riboflavin, with UV-A irradiation @ 18 mW/cm2 for 5 minutes  2) preservative-free riboflavin, with UV-A irradiation @ 36 mW/cm2 for 2.5 minutes  3) riboflavin with preservatives, with UV-A irradiation @ 18 mW/cm2  for 5 minutes  4) riboflavin with preservatives, with UV-A irradiation @ 36 mW/cm2 for 2.5 minutes  5) riboflavin only, no UVA  6) riboflavin with preservatives, no UVA. We used 0.1% riboflavin in all experiments.

Results:

The groups with preservative-free riboflavin showed a pathogen reduction (killing rate) of 2 log units with 18 mW/cm2 and of one log unit with 36 mW/cm2. The groups with riboflavine with preservatives showed a killing rate of 2 log units (98 %) at both irradiation levels.

Conclusions:

The P. aeruginosa and S. aureus killing rate is intensity-dependent when using conventional riboflavin and intensity-independent when preservatives are added to the riboflavin solution. These findings will allow the generation of optimized riboflavin solutions for the treatment of bacterial keratitis.

Financial Interest:

One or more of the authors... has significant investment interest in a company producing, developing or supplying product or procedure presented

Back to previous