To assess the interaction of air puff deformation on tear film dynamics, 20 healthy volunteers were recruited. The study was approved by Institutional Review Board (IRB) of The Ohio State University. Informed consent was obtained from the subjects after explanation of the nature and possible consequences of the study. The exclusion criteria were clinical history of dry eye or tear film instability. Testing was conducted in the right eyes only.
The robust study design was intentional using two different NCTs, video analyzers were masked meaning that the analyzers were not aware of the lubricant, and to compare these two NCTs with the contact tonometers. To compare tear film dynamics in response to contact and NCTs, subjects were tested with four tonometers.
Two NCT devices were used: Ocular Response Analyzer (ORA; Reichart Ophthalmic Instruments, Buffalo, NY, USA) and Corvis ST (Oculus, Wetzlar, Germany). The two contact tonometers used in this study included a rebound tonometer, iCare (Tiolat Oy, Helsinki, Finland) and an applanation tonometer, Tono-Pen (Reichart Ophthalmic Instruments).
To evaluate the effect of tear load from an eye drop administration on droplet formation, NCT tests were repeated with administration of one drop of lubricant immediately after the initial standard examination with NCT devices. A preservative free lubricant eye drop with a viscosity close to that of the tears was used for these tests which contained 0.1% dextran 70 and 0.3% hypomellose (GenTeal Tears; KC Pharmaceuticals Inc., Pomona, CA, USA). Each eye drop was administered by slightly tilting the subject's head back and pulling the lower eyelid downward, away from the cornea. The eye drop vial would then be held over the eyelid pocket and one drop would be gently administered. The testing order was as follows: (1) the first NCT device, (2) the first NCT device after one drop of lubricant was administered, (3) the second NCT device, (4) the second NCT device after one lubricant eye drop was administered, (5) iCare testing, and followed by (6) administration of topical anesthetic containing 0.5% proparacaine hydrochloride ophthalmic solution (Akorn, Inc., Lake Forest, IL, USA) and Tono-Pen testing. Note that several minutes elapsed between tests two and three to allow for movement of the NCTs and camera setup. Further, to account for the potential effect of order of testing, 10 subjects received ORA testing first, followed by CorVis ST, whereas the other 10 subjects received CorVis ST measurement first, followed by ORA. To evenly distribute the order between the two NCT devices, ORA and Corvis ST were selected as the first device for every other subject.
A high-speed video camera (Phantom VEO 340S; Vision Research, Inc., Wayne, NJ, USA) coupled with a 100 mm f/2.8 macro lens was used to capture corneal deformation, eye lid motion, tear film dynamics, and droplet formation at a spatial resolution of 20 microns/px and a frame rate of 2400 fps. Continuous and consistent lighting was produced by a 10-inch bi-color, on-camera, LED ring light (Smith-Victor, Bartlett, IL, USA). The camera was placed perpendicular to the direction of the air puff to capture the temporal view of the right eye (
Fig. 1).