Purpose
To compare objective and subjective metrics from regular and high resolution Scheimpflug devices (Pentacam, Oculus, Inc.) to determine their equivalence and interchangeability for refractive surgery screening.
Setting
Emory Vision at Emory University, Atlanta, GA, USA
Design
Retrospective comparative case series.
Methods
One hundred eyes from 50 consecutive screened refractive surgery patients evaluated with both high resolution (HR) and regular (REG) devices were evaluated. Objective parameters evaluated included keratometry (K), central corneal thickness (CCT), and device-generated keratoconus screening indices (KI). Evaluations by masked expert reviewers subjectively graded images as normal, suspicious, or abnormal.
Results
Keratometry values were not significantly different (Anterior K (HR) 1.21 ± 1.13 vs. (REG) 1.15 ± 1.16, P = 0.73, Posterior K (HR) 0.34 ± 0.23 vs. (REG) 0.35 ± 0.23, P = 0.67). CCT was significantly thinner in the HR group (514.7 ± 26.6 vs. 527.6 ± 27.6, p<0.0001) with limits of agreement of −12.9 to +17.5 microns. Most KI were more suspicious for HR than REG except index of height asymmetry (IHA) and index of height deviation (IHD). Subjectively, 60% of cases received the same score, HR was more suspicious in 30%, and REG was more suspicious in 12% of cases, with only slight subjective agreement (kappa = 0.26 to 0.31) between technologies.
Conclusions
Regular and high resolution Scheimpflug imaging devices generated different objective values and significantly different subjective interpretations with poor inter-reviewer agreement. The high resolution device provided a more conservative overall output. For refractive surgical screening the two devices are not interchangeable.