Journal List > J Korean Ophthalmol Soc > v.50(5) > 1008555

Lee, Lee, and Joo: Measurements of Dynamic Contour Tonometry After Penetrating Keratoplasty and Epi-LASIK

Abstract

Purpose

To analyze the clinical results of Goldmann applanation tonometry (GAT) and Pascal dynamic contour tonometry (PDCT) and the influences of central corneal thickness and keratometric power in eyes that underwent Epi-LASIK or penetrating keratoplasty.

Methods

Measurements of intraocular pressure by GAT and PDCT as well as keratometric power and central corneal thickness were measured in 45 eyes that underwent penetrating keratopasty and 63 eyes that underwent Epi-LASIK. These parameters were also measured in healthy eyes with no specific disorders to create a control group.

Results

In the keratoplasty group, the PDCT results were significantly higher than the GAT results by 1.22±2.84 mmHg (p=0.006), but neither method showed a significant correlation with CCT or keratometric power. In the Epi-LASIK group, PDCT was higher as 3.45±2.35 mmHg than GAT, and the corrected results of GAT were not different from the results of PDCT. In the control group, GAT was affected by central corneal thickness and keratometric power, but PDCT showed no significant relationship with these two factors.

Conclusions

After Epi-LASIK or penetrating keratoplasty, both of which change CCT and keratometric power, IOP cannot be accurately measured by GAT. In these patients, PDCT may play an important clinical role since it is less affected by corneal properties.

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Figure 1.
Schematic diagram of Non-applanating contour-matched tip of the Pascal tonometer. When the match is achieved, the sensor tip embeddd in tip measures38
jkos-50-749f1.tif
Figure 2.
Difference between PDCT and GAT IOP measurements, plotted against the mean of the two measurements. The measurements obtained by these two techniques were found to be within ±5.61 mm Hg of each other in 95% of cases (PPKP group).
jkos-50-749f2.tif
Figure 3.
Effect of CCT on PDCT and GAT in Epi-LASIK group Cross and dotted line represents PDCT result and its estimated regression line according to CCT. PDCT does not correlate with CCT in contrast to GAT. Dotted line (PDCT); IOP=0.005× CCT+13.725 (R2=0.009, p-value=2.479), Solid line (GAT); IOP= 0.029× CCT–0.597 (R2=0.266, p-value=0.000).
jkos-50-749f3.tif
Figure 4.
Difference between PDCT and GAT IOP measurements, plotted against the mean of the two measurements. The measurements obtained by these two techniques were found to be within ±4.62 mmHg of each other in 95% of cases (EpiLasik group).
jkos-50-749f4.tif
Table 1.
Subject characteristics
Number of case s Sex (M:F) Age CCT (μm) K Keratometric power (D)
PPKP group 45 21:24 41.55±18.14 514.80±46.13 44.20±2.04
Epi-LASIK group 63 21:42 29.82±7.26 449.14±44.15 40.00±1.77
Control group 38 17:21 42.26±16.40 545.10±29.24 43.85±1.22
Table 2.
Methods of IOP measurements in PPKP group
Method GAT PDCT Corrected GAT 5 mmHg/70 μm Corrected GAT 0.027 mmHg/1 μm Corrected GAT Equation
Mean (mm Hg) 15.99±3.59 17.22±3.73 16.36±4.89 16.13±3.81 16.65±3.56
t-test with GAT (p-value) 0.006* 0.117 0.010* 0.177

* p –value<0.05

Equation; IOP (real)=IOP (measured by GAT)+(540-CCT)/71+(43-Kvalue)/2.7+0.75 mmHg.

Table 3.
Correlation of methods and Keratometry or CCT (Pearson correlation)
GAT coefficient (p-value) PDCT coefficient (p-value)
Keratometry (p-value)
PPKP 0.260 (0.084) 0.201 (0.186)
Epi-Lasik 0.488 (0.000)* 0.158 (0.216)
Control −0.026 (0.875) −0.100 (0.550)
CCT(p-value)
PPKP −0.008 (0.958) −0.249 (0.098)
Epi-Lasik 0.515 (0.000)* 0.093 (0.469)
Control 0.376 (0.020) 0.185 (0.265)

* p-value<0.05.

Table 4.
Mean of IOP measurements in Epi-Lasik group
Method GAT PDCT Corrected GAT 5 mmHg/70 μm Corrected GAT 0.027 mmHg/1 μm Corrected GAT CA equation
Mean (mmHg) 12.60±2.51 16.06±2.47 17.64±2.84 14.50±2.15 15.72±2.08
t-test with GAT (p-value) 0.000* 0.000* 0.000* 0.216

* p-value<0.05.

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