Toric Implantable Collamer Lens for Moderate to High Myopic Astigmatism

Sanders, Donald R.; Schneider, David; Martin, Robert; Brown, David; Dulaney, David; Vukich, John; Slade, Stephen; Schallhorn, Steven

doi:10.1016/j.ophtha.2006.08.049

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Volume 114, Issue 1 , Pages 54-61, January 2007

Toric Implantable Collamer Lens for Moderate to High Myopic Astigmatism

Donald R. Sanders, MD, PhD
- Department of Ophthalmology, University of Illinois at Chicago College of Medicine, Chicago, Illinois.
- Drs Sanders, Slade, and Vukich are consultants to STAAR Surgical.
- Reprint requests to Darcy Smith, STAAR Surgical, 1911 Walker Avenue, Monrovia, CA 91016.
David Schneider, MD
- Midwest Eye Center, Cincinnati, Ohio.
Robert Martin, MD
- Carolina Eye Associates, Southern Pines, North Carolina.
David Brown, MD
- Eye Centers of Florida, Ft. Myers, Florida.
David Dulaney, MD
- Barnet Dulaney Perkins Eye Center, Phoenix, Arizona.
John Vukich, MD
- Department of Ophthalmology, University of Wisconsin School of Medicine, and Davis Duehr Dean Medical Center, Madison, Wisconsin.
- Drs Sanders, Slade, and Vukich are consultants to STAAR Surgical.
Stephen Slade, MD
- The Laser Center, Houston, Texas.
- Drs Sanders, Slade, and Vukich are consultants to STAAR Surgical.
Steven Schallhorn, MD
- Department of Ophthalmology, Navy Medical Center San Diego, San Diego, Califoronia.

Received 13 August 2004; accepted 30 August 2006.

Purpose

To assess the efficacy of the Toric Implantable Collamer Lens (ICL) to treat moderate to high myopic astigmatism.

Design

Prospective nonrandomized clinical trial.

Participants

Two hundred ten eyes of 124 patients with between 2.38 and 19.5 diopters (D) of myopia (spherical equivalent [SE]) and 1 to 4 D of astigmatism participating in the United States Food and Drug Administration clinical trial of the Toric ICL.

Intervention

Implantation of the Toric ICL.

Main Outcome Measures

Uncorrected visual acuity (UCVA), refraction, best spectacle-corrected visual acuity (BSCVA), adverse events, and postoperative complications.

Results

At 12 months postoperatively, the proportion of eyes with 20/20 or better UCVA (83.1%) was identical to the proportion of eyes with preoperative 20/20 or better BSCVA (83.1%); 76.5% had postoperative UCVA better than or equal to preoperative BSCVA. The mean manifest refractive cylinder dropped from 1.93 D (±0.84) at baseline to 0.51 D (±0.48) postoperatively, a 73.6% decrease in astigmatism. Although only 21.0% of eyes had 1-D refractive cylinder preoperatively (none less), 91.4% of cases had ≤1 D of cylinder postoperatively. Furthermore, 65.6% had ≤0.5 D and 40.9% had ≤0.25 D of refractive cylinder postoperatively. Mean manifest refraction SE (MRSE) improved from −9.36 D (±2.66) preoperatively to 0.05 D (±0.46) postoperatively. A total of 76.9% of eyes were predicted accurately to within ±0.5 D, 97.3% to within ±1.0 D, and 100% to within ±2.0 D of predicted MRSE. Postoperatively, 37.6% of eyes had a BSCVA of 20/12.5 or better, compared with a preoperative level of 4.8%. Furthermore, BSCVA of 20/20 or better occurred in 96.8% postoperatively, compared with 83.1% preoperatively. Mean improvement in BSCVA was 0.88 lines; there were 3 cases (1.6%) that lost ≥2 lines of BSCVA after 12 months postoperatively, whereas 18.9% of cases improved by ≥2 lines. A total of 76.4% of cases gained ≥1 lines of BSCVA, whereas only 7.5% of cases lost the equivalent amount. Three ICL removals were performed without significant loss of BSCVA, and 1 clinically significant lens opacity was observed.

Conclusion

The results support the efficacy and predictability of Toric ICL implantation to treat moderate to high myopic astigmatism. Important safety concerns were not identified.