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Corneal Changes After Laser Refractive Surgery For Myopia
Corneal changes after laser refractive surgery for myopia: comparison of Orbscan II and Pentacam findings.
Author: Hashemi H , Mehravaran S
Source: J Cataract Refract Surg, 33(5): 841-7 2007
Summary of Research:
The purpose of the study was to determine the agreement between scanning slit topography (Orbscan II, Bausch & Lomb) and Scheimpflug imaging (Pentacam, Oculus) in corneal elevation, corneal curvature, and anterior chamber depth (ACD) measurements before and after laser refractive surgery for myopia and to compare the postoperative changes seen with these devices. SETTING: Noor Vision Correction Center, Tehran, Iran.
The methods used in the research:
In a prospective observational case-series study, 23 consecutive myopic patients having laser refractive surgery were examined with the Orbscan II and Pentacam preoperatively and 6 weeks postoperatively. Readings of ACD, anterior (A-) and posterior (P-) best-fit sphere (BFS) size, central elevation (CE), maximum elevation (ME), axial power in the 3.0 mm zone
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(AX3) and 5.0 mm zone (AX5), and tangential power in these zones (TG3 and TG5, respectively) were collected and used in the analyses.
Results & Conclusion:
Statistically significant interdevice differences were found preoperatively for all parameters except P-TG3 (P = .014) and in operated eyes for ACD, anterior parameters of A-AX3 and A-AX5, and all posterior corneal parameters. In posterior corneal measurements, Orbscan II demonstrated significant postoperative changes in all parameters except P-AX5 (P = .004) and P-TG5 (P = .034), although none of the differences was statistically significant with the Pentacam. The devices measured similar postoperative changes in anterior curvature parameters and in P-AX5 and P-TG5; all other changes were significantly different.
CONCLUSIONS:
Compared to the Pentacam, the Orbscan II yielded larger posterior elevation values before and after surgery and significant postoperative changes in P-CE and P-ME. Further studies can determine which device gives more accurate images of the cornea and redefine screening criteria.
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