10.07.2015 Views

Cornea - ARVO

Cornea - ARVO

Cornea - ARVO

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

<strong>ARVO</strong> 2013 Annual Meeting Abstracts by Scientific Section/Group - <strong>Cornea</strong>Commercial Relationships: Brien C. David, Bausch + Lomb (E);Denise Callahan, Bausch and Lomb, Inc. (E); Julie Bair, Bausch &Lomb, Inc. (E); Susan E. Norton, Bausch and Lomb, Inc. (E)Program Number: 523 Poster Board Number: B0160Presentation Time: 10:30 AM - 12:15 PMEfficacy Of Contact Lens Solutions Against Achromobacterxylosoxidans Biofilms Using Confocal MicroscopyDavid J. McCanna, Jaclyn M. Chang, Lakshman N. Subbaraman,Lyndon W. Jones. Centre for Contact Lens Research, School ofOptometry and Vision Science, Waterloo, ON, Canada.Purpose: Biofilms of Achromobacter xylosoxidans (Ax) can developin contact lens cases. These microorganisms can attach to the contactlens and cause microbial keratitis. This study evaluated theantimicrobial efficacy of contact lens solutions against Ax biofilmsby measuring the damage to cell membranes of Ax using confocalmicroscopy.Methods: Ax biofilms were formed by incubating the bacteriaovernight on glass coverslips. The biofilms were then exposed tocontact lens solutions for four hours. Commercial contact lenssolutions evaluated contained the antimicrobials polyhexamethylenebiguanide (PHMB), polyquaternium-1 (PQ1) and alexidine (ALX),and PQ1 and Aldox (AD). After exposure, the bacteria were stainedwith SYTO 9 and propidium iodide (PI). Using a confocalmicroscope with a 488nm laser and the appropriate emission filtersthe number of cells with damaged cell membranes was determined.In addition to evaluating contact lens solutions, four concentrations ofbenzalkonium chloride (BAK) 0.05%, 0.01%, 0.005% and 0.001% inphosphate buffer saline were also evaluated to demonstrate doserelated effects at exposure times as short as 5 minutes.Results: The contact lens solution that caused the greatest damage tothe Ax cell membranes was the formulation based on PQ1-ALX. Theother formulations tested based on PHMB and PQ1 with AD causedsome of the bacteria to lose membrane integrity but did not cause asmuch damage to the bacteria cell membranes (p < 0.05) as the PQ-ALX formulation. Dose effects of the preservative BAK could beseen at 5 minutes of exposure time. BAK at 0.005% and 0.01%caused an increase in the number of cells that were permeable to PIcompared to the phosphate buffered control (48% and 62%respectively, p < 0.05). All of the Ax bacteria were permeable to PIafter exposure to 0.05% BAK.Conclusions: One of the five lens care systems tested caused asubstantial number of Ax bacteria to lose membrane integrity. Also,this method was able to detect the effect different concentrations ofBAK have on the membrane integrity of the Ax biofilm bacteria.Understanding the ability of antimicrobials to damage bacteria cellmembranes could help in the development of lens care solutions thatcan reduce and/or eliminate Ax biofilms from lens cases.Commercial Relationships: David J. McCanna, None; Jaclyn M.Chang, None; Lakshman N. Subbaraman, None; Lyndon W.Jones, Alcon (F), Alcon (R), Allergan (F), Abbott Medical Optics(R), Bausch & Lomb (R), Ciba Vision (F), Ciba Vision (R),CooperVision (F), Johnson & Johnson (F), Johnson & Johnson (R)Body mass index, peripheral corneal thickness and anteriorchamber depth in young European adults - A pilot studySven Jonuscheit 1, 2 , Michael J. Doughty 1 , Raul Martin 3 , Ana del RioSan Cristóbal 3 , Lisa J. Mackintosh 1 , David MacTaggart 1 , MichaelHiscock 1 . 1 Vision Sciences, Dept. of Life Sciences, GlasgowCaledonian University, Glasgow, United Kingdom; 2 DiabetesResearch Group, Institute for Applied Health Research, GlasgowCaledonian University, Glasgow, United Kingdom; 3 OptometryResearch Group, Instituto Universitario de Oftalmobiología Aplicada(IOBA), Universidad de Valladolid, Valladolid, Spain.Purpose: To assess the relationship of body mass index (BMI) andthe corneal thickness profile in normal white European individuals.Methods: For this pilot study, 63 eyes of 63 healthy subjects wereassessed. Following completion of an ocular and general healthquestionnaire body height and weight were measured and the BMIcalculated. Ocular assessments included habitual visual acuity, slitlampbiomicroscopy, and optical coherence tomography. Non-contactspecular microscopy was performed to rule out cornealendotheliopathy. Scheimpflug photography (Pentacam) was used toassess central, mid-peripheral and peripheral corneal thickness aswell as anterior chamber depth (ACD) at eleven locations nominally1 mm apart along the horizontal meridian. Two consecutiveScheimpflug scans were performed and the mean value used foranalyses. Descriptive statistics were generated. The associationbetween BMI, corneal thickness and ACD at central as well as offcenterlocations was assessed using univariate regression analyses.The coefficient of correlation (r) was calculated.Results: The mean [SD] age was 27 [7] years. Mean body height andbody weight were 1.69 [0.08] meters and 64.6 [11.4] kilogramsrespectively, the mean BMI was 22.7 [3.1]. Mean central cornealthickness was 558 [33] micrometers (µm). <strong>Cornea</strong>l thicknessincreased progressively and asymmetrically from the corneal centerto the periphery with a significantly greater thickness at all nasallocations as compared to the respective temporal sites (P0.05).Conclusions: For this cohort of young, healthy white Europeanadults with normal-weight average BMI, peripheral corneal thicknesswas inversely related to BMI. The findings suggest the possibility ofa different corneal thickness profile in individuals with aboveaverageBMI. Further studies on the relationship between BMI,obesity and corneal parameters are indicated.Commercial Relationships: Sven Jonuscheit, Santander UK plc(F); Michael J. Doughty, None; Raul Martin, None; Ana del RioSan Cristóbal, None; Lisa J. Mackintosh, Santander UK plc (F);David MacTaggart, Santander UK PLC (F); Michael Hiscock,NoneSupport: Santander UK plc Grant127 <strong>Cornea</strong>l Epithelium and Imaging ISunday, May 05, 2013 10:30 AM-12:15 PMExhibit Hall Poster SessionProgram #/Board # Range: 524-567/B0161-B0204Organizing Section: <strong>Cornea</strong>Program Number: 524 Poster Board Number: B0161Presentation Time: 10:30 AM - 12:15 PMProgram Number: 525 Poster Board Number: B0162Presentation Time: 10:30 AM - 12:15 PMObjective Estimation for Uncertainty of Restoring <strong>Cornea</strong>lTopography SurfaceAnatoly Fabrikant. R&D, Abbott Medical Optics, Fremont, CA.Purpose: <strong>Cornea</strong>l topography (CT) field can be restored frommeasurements data by decomposing available data into Zernikepolynomials and mapping the CT field in the desired area. Theaccuracy of such restoration depends on the measurement noise and©2013, Copyright by the Association for Research in Vision and Ophthalmology, Inc., all rights reserved. Go to iovs.org to access the version of record. For permissionto reproduce any abstract, contact the <strong>ARVO</strong> Office at arvo@arvo.org.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!