Results of phase III excimer laser photorefractive keratectomy for myopia. The Summit PRK Study Group

Ophthalmology. 1997 Oct;104(10):1535-53. doi: 10.1016/s0161-6420(97)30073-6.


Objective: The purpose of the study is to determine safety and efficacy outcomes of excimer laser photorefractive keratectomy (PRK) for the treatment of mild-to-moderate myopia.

Design: A prospective, multicenter, phase III clinical trial.

Participants: A total of 701 eyes of 701 patients were entered in the study; 612 eyes were examined at 2 years after surgery.

Intervention: Intervention was photorefractive keratectomy using the Summit ExciMed UV200LA excimer laser (Summit Technology, Inc., Waltham, MA). The treatment zone diameter used was 4.5 mm in 251 eyes (35.8%) and 5 mm in 450 eyes (64.2%). Attempted corrections ranged from 1.50 to 6.00 diopters (D).

Main outcome measures: Predictability and stability of refraction, uncorrected and spectacle-corrected visual acuity, refractive and keratometric astigmatism, corneal haze, contrast sensitivity, subjective reported problems of glare and halo, and patient satisfaction were the parameters measured.

Results: At 2 years, 407 (66.5%) eyes achieved 20/20 or better uncorrected visual acuity and 564 (92.5%) eyes achieved 20/40 or better visual acuity. Three hundred thirty-six (54.9%) eyes were within 0.5 D and 476 (77.8%) eyes were within 1.0 D of attempted correction. Stability of refraction improved with time; 86.8% of eyes were stable within 1.0 D from 6 to 12 months, 94% were stable from 12 to 18 months, and 96.3% were stable from 18 to 24 months. There was no evidence of progressive or late myopic or hyperopic refractive shifts. One hundred fourteen (18.6%) eyes gained 2 or more lines of spectacle-corrected visual acuity, whereas 42 (6.9%) eyes lost 2 or more lines; however, of the latter, 32 (76.2%) had spectacle-corrected visual acuity of 20/25 or better and 39 (92.9%) eyes had 20/40 or better. Four hundred forty-two (72.2%) corneas were clear, 138 (22.5%) showed trace haze, 20 (3.3%) mild haze, 9 (1.5%) moderate haze, and 3 (0.5%) marked haze. On patient questionnaires, 87 (29.7%) patients reported worsening of glare from preoperative baseline; 133 (50.1%) reported worsening of halo symptoms from baseline.

Conclusions: Photorefractive keratectomy appears effective for myopic corrections of -1.50 to -6.00 D. Uncorrected visual acuity is maximized in most eyes by 3 months, although some patients require between 6 months and 1 year to attain their best postoperative uncorrected visual acuity and some may require from 1 to 2 years for stabilization of refraction. Refraction stabilizes progressively without evidence of late myopic or hyperopic refractive shifts. Optical sequelae of glare and halo occur in some patients treated with a 4.5- or 5-mm treatment zone.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase III
  • Controlled Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Astigmatism / physiopathology
  • Contrast Sensitivity / physiology
  • Cornea / physiopathology
  • Cornea / surgery*
  • Corneal Opacity / physiopathology
  • Female
  • Glare
  • Humans
  • Intraocular Pressure / physiology
  • Lasers, Excimer
  • Male
  • Middle Aged
  • Myopia / physiopathology
  • Myopia / surgery*
  • Pain, Postoperative / physiopathology
  • Patient Satisfaction
  • Photorefractive Keratectomy*
  • Prospective Studies
  • Safety
  • Treatment Outcome
  • Visual Acuity / physiology