Self-tonometry with the Ocuton S versus Goldmann tonometry

Citation
I. Theofylaktopoulos et al., Self-tonometry with the Ocuton S versus Goldmann tonometry, GR ARCH CL, 237(9), 1999, pp. 720-724
Citations number
12
Categorie Soggetti
Optalmology
Journal title
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
ISSN journal
0721832X → ACNP
Volume
237
Issue
9
Year of publication
1999
Pages
720 - 724
Database
ISI
SICI code
0721-832X(199909)237:9<720:SWTOSV>2.0.ZU;2-A
Abstract
Background: The purpose of the study was to evaluate the acceptance and rep roducibility of a new self-tonometer (Ocuton S) and to compare it with the Goldmann applanation tonometer. Methods: The Ocuton S was studied in 20 healthy volunteers and 100 patients . After detailed explanation to each individual and a number of test measur ements, we studied the reproducibility and accuracy of the Ocuton S in 20 h ealthy volunteers with and without topical anaesthesia. Acceptance was grad ed by means of visual analogue scales. Each volunteer had to measure his/he r own IOP in three consecutive measurements. The data were compared with Go ldmann tonometry at random times. One hundred patients were introduced to t he Ocuton S. Either three consecutive self-measurements of IOP were perform ed and then compared with three consecutive measurements by Goldmann tonome try, or vice versa. This was done randomly. Results: Forty-one of 100 patie nts were unable to perform three consecutive measurements with the Ocuton S after at least 15 min introduction time to the device (non-success). Fifty -nine of 100 patients were able to measure their IOP with the Ocuton S. The mean pressure value with the Ocuton S was 23.2+/-8.2 mmHg, compared with G oldmann 18.4+/-5.7 mmHg. The difference of 5+/-5.7 mmHg was statistically s ignificant (paired t-test p<0.01). The visual analogue scale scores of heal thy volunteers (100 mm = maximal comfort, 0 mm = not acceptable), was 72+/- 31 in anaesthetised eyes and 39+/-41 mm without anaesthesia. Conclusion: The Ocuton S seems to be an acceptable means for the majority o f patients of measuring their IOP at home. Refinement of the accuracy of th e device seems necessary.