Gil-Cazorla Raquel, Teus Miguel A, Hernández-Verdejo Jose L, De Benito-Llopis Laura, García-González Monsterrat
Vissum Madrid, Madrid, Spain.
Optom Vis Sci. 2008 Sep;85(9):884-8. doi: 10.1097/OPX.0b013e31818527fd.
To evaluate two silicone hydrogel contact lens materials as continuous-wear bandage contact lenses after laser-assisted subepithelial keratomileusis (LASEK).
The inclusion criteria were myopia of -6.00 diopters (D) or less, astigmatism lower than -1.5 D, bilateral best-corrected visual acuity of 20/20 or better, and candidates for bilateral LASEK. The patients were randomized to be fitted with a Balafilcon A (PureVision) lens in one eye and Galyfilcon A (Acuvue Advance) in the fellow eye. Uncorrected visual acuity, corneal epithelial status, conjunctival and limbal hyperemia, lens movement, contact lens debris, and the responses to a subjective-comfort questionnaire were assessed postoperatively. The parameters were evaluated before and 1 and 5 days after the procedure. A paired Student's t-test and chi-square tests were used when appropriate.
We analyzed 44 eyes of 22 consecutive patients who underwent LASEK to correct low-to-moderate myopia. The mean spherical equivalent was -3.25 +/- 2.36 D. There was no difference in conjunctival or limbal hyperemia, lens movement, uncorrected visual acuity, or epithelial healing between the two lenses at any visit. A significant difference was found in lens deposition and discomfort, which were greater with the PureVision lens 5 days postoperatively (p = 0.01 for both comparisons).
PureVision and Acuvue Advance contact lenses seem to be useful as continuous wear bandage contact lenses. There is no major clinical difference between the lenses, although patients report greater comfort with Acuvue Advance.
评估两种硅水凝胶隐形眼镜材料作为激光辅助上皮下角膜磨镶术(LASEK)后连续佩戴的绷带型隐形眼镜的效果。
纳入标准为近视度数-6.00屈光度(D)及以下、散光度数低于-1.5 D、双眼最佳矫正视力为20/20或更好,且为双眼LASEK手术的候选者。患者被随机分为一只眼佩戴Balafilcon A(PureVision)镜片,另一只眼佩戴Galyfilcon A(Acuvue Advance)镜片。术后评估未矫正视力、角膜上皮状态、结膜和角膜缘充血、镜片移动、隐形眼镜碎片以及主观舒适度问卷的回答情况。在手术前、术后1天和5天对这些参数进行评估。适当情况下使用配对学生t检验和卡方检验。
我们分析了22例连续接受LASEK矫正低度至中度近视患者的44只眼。平均球镜等效度数为-3.25±2.36 D。在任何一次随访中,两种镜片在结膜或角膜缘充血、镜片移动、未矫正视力或上皮愈合方面均无差异。在镜片沉积和不适感方面发现有显著差异,术后5天PureVision镜片的这些情况更严重(两项比较p值均为0.01)。
PureVision和Acuvue Advance隐形眼镜似乎可作为连续佩戴的绷带型隐形眼镜。两种镜片之间没有重大临床差异,尽管患者报告佩戴Acuvue Advance时舒适度更高。