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准分子原位角膜磨镶术治疗完全性或部分性屈光性调节性内斜视。

Laser in situ keratomileusis for treatment of fully or partially refractive accommodative esotropia.

作者信息

Polat Sibel, Can Cigdem, Ilhan Bayazit, Mutluay Ayse H, Zilelioğlu Orhan

机构信息

Ministry of Health Ulucanlar Eye Education and Research Hospital, Ankara - Turkey.

出版信息

Eur J Ophthalmol. 2009 Sep-Oct;19(5):733-7. doi: 10.1177/112067210901900508.

DOI:10.1177/112067210901900508
PMID:19787590
Abstract

PURPOSE

To evaluate the efficacy and safety of laser in situ keratomileusis (LASIK) in partially refractive accommodative esotropia (pRAE) and fully refractive accommodative esotropia (fRAE).

METHODS

Forty-two eyes of 21 patients who had LASIK for correcting hyperopic refractive error were evaluated. Refractive errors, uncorrected visual acuity (UCVA) and best-corrected visual acuity (BCVA), ocular alignment, and stereopsis were recorded before and after LASIK.

RESULTS

Sixteen patients with fRAE and 5 with pRAE were evaluated. Mean age at the time of surgery was 19.00+/-3.79 years. Mean follow-up time was 12.19+/-4.51 months. For the fRAE group, the mean preoperative angle of deviation without spectacle correction was +19.13+/-5.87 prism diopters (PD); all were orthophoric with spectacles. Postoperatively, all these patients achieved less than 10 PD of deviation without spectacles. For the pRAE group, the mean preoperative angle of deviation was +32.60+/-9.81 PD and +14.60+/-6.14 PD without and with spectacles, respectively. Postoperatively, the mean angle of deviation was +13.60+/-5.72 PD and +12.80+/-5.40 PD without and with spectacles, respectively. For all 21 patients, the preoperative mean spherical equivalent (SE) with cycloplegia was +4.94+/-1.43 diopters (D); it was +1.49D+/-0.70 D postoperatively. Three eyes lost 1 line of BCVA and 3 eyes gained 1 line. No intraoperative complication was recorded.

CONCLUSIONS

LASIK is a safe and effective method for treating refractive error and creating orthophoria in fRAE. In pRAE, it eliminates the refractive component of deviation safely and effectively.

摘要

目的

评估准分子原位角膜磨镶术(LASIK)治疗部分屈光性调节性内斜视(pRAE)和完全屈光性调节性内斜视(fRAE)的疗效和安全性。

方法

对21例行LASIK矫正远视性屈光不正的患者的42只眼进行评估。记录LASIK术前和术后的屈光不正、未矫正视力(UCVA)和最佳矫正视力(BCVA)、眼位及立体视。

结果

评估了16例fRAE患者和5例pRAE患者。手术时的平均年龄为19.00±3.79岁。平均随访时间为12.19±4.51个月。fRAE组术前无眼镜矫正时的平均斜视度为+19.13±5.87棱镜度(PD);戴眼镜时均为正位。术后,所有这些患者无眼镜时的斜视度均小于10 PD。pRAE组术前斜视度分别为无眼镜时+32.60±9.81 PD和戴眼镜时+14.60±6.14 PD。术后,无眼镜和戴眼镜时的平均斜视度分别为+13.60±5.72 PD和+12.80±5.40 PD。对所有21例患者,术前睫状肌麻痹下的平均等效球镜度(SE)为+4.94±1.43屈光度(D);术后为+1.49 D±0.70 D。3只眼最佳矫正视力下降1行,3只眼最佳矫正视力提高1行。未记录到术中并发症。

结论

LASIK是治疗fRAE屈光不正并使其眼位正位的一种安全有效的方法。在pRAE中,它能安全有效地消除斜视度的屈光成分。

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