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准分子激光原位角膜磨镶术作为高度远视的一种解决方案。

Lasik as a Solution for High Hypermetropia.

作者信息

Biscevic Alma, Pidro Ajla, Pjano Melisa Ahmedbegovic, Grisevic Senad, Ziga Nina, Bohac Maja

机构信息

Eye Clinic "Svjetlost Sarajevo", Sarajevo, Bosnia and Herzegovina.

University Eye Clinic "Svjetlost" Zagreb, Zagreb, Croatia.

出版信息

Med Arch. 2019 Jun;73(3):191-194. doi: 10.5455/medarh.2019.73.191-194.

DOI:10.5455/medarh.2019.73.191-194
PMID:31402804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6643362/
Abstract

AIM

To evaluate safety and efficacy of Laser in situ Keratomileusis (LASIK) procedure for the correction of high hypermetropia.

METHODS

Retrospective study of 160 patients (266 eyes) who underwent LASIK procedure for the correction of hypermetropia between +3.00 and +7.00 diopters(D) and cylinder up to 2.00D from January 2013 and August 2015. All ablations were performed with Wavelight Allegretto Eye-Q400Hzexcimer laser (Alcon, Forth Worth, TX, USA) with aberration free module and were centered on a corneal vertex. All flaps were made with Moria M2 (Moria, Antony, France) mechanical microkeratome (90μm head). Preoperative and postoperative uncorrected and corrected distant visual acuity (UDVA, CDVA), spherical equivalent (SE) and a berrometry for 5mm pupil were measured. Measurements were taken at 1 week, 1,3,6 and 12 months after the surgery. Wilcoxon Signed Ranks Test was used for statistical analysis.

RESULTS

Postoperative UDVA was lower than preoperative CDVA at 1 week(=0.001), at 1 month there was no difference (=0.099), and at 3,6 and 12 months UDVA was better (<0.0001). Preoperative SE was 4.69±1.20D (+3.75 to +7.50D). At 1 week SE was 0.03±0.67D (-0.50 to +0.63D), while at 1 year regressed to 0.58±0.56D (+0.25 to +0.88D). Sphere shifted from negative values targeted in treatment planning to compensate for regression to positive values. There was significant difference in SE at every time point (<0.0005). There was a significant increase in coma (<0.0001), trefoil (<0.0001, =0.0006) and spherical aberration (=0.022, =0.0052) at 1 week and 1 month postoperatively, without change throughout the rest of follow up.

CONCLUSION

LASIK for high hypermetropia showed satisfactory results in postoperative refraction with reasonable regression without significant loss of lines of visual acuity. However, more test are necessary to asses optical quality.

摘要

目的

评估准分子原位角膜磨镶术(LASIK)矫正高度远视的安全性和有效性。

方法

回顾性研究2013年1月至2015年8月期间接受LASIK手术矫正3.00至7.00屈光度(D)远视且散光达2.00D的160例患者(266只眼)。所有切削均使用具有无像差模块的威视 Allegretto Eye-Q400Hz准分子激光(美国德克萨斯州沃思堡爱尔康公司),并以角膜顶点为中心。所有角膜瓣均由 Moria M2(法国安东尼市 Moria公司)机械微型角膜刀(90μm刀头)制作。测量术前及术后未矫正和矫正的远视力(UDVA、CDVA)、等效球镜度(SE)以及5mm瞳孔的像差测量值。在术后1周、1个月、3个月、6个月和12个月进行测量。采用Wilcoxon符号秩和检验进行统计分析。

结果

术后1周时UDVA低于术前CDVA(P = 0.001),1个月时无差异(P = 0.099),3个月、6个月和12个月时UDVA改善(P < 0.0001)。术前SE为4.69±1.20D(+3.75至 +7.50D)。1周时SE为0.03±0.67D(-0.50至 +0.63D),而1年时回退至0.58±0.56D(+0.25至 +0.88D)。球镜度从治疗计划中设定的负值转变为正值以补偿回退。各时间点的SE均有显著差异(P < 0.0005)。术后1周和1个月时彗差(P < 0.0001)、三叶草像差(P < 0.0001,P = 0.0006)和球差(P = 0.022,P = 0.0052)显著增加,随访其余时间无变化。

结论

LASIK矫正高度远视术后屈光效果满意,回退合理,视力无明显下降。然而,需要更多测试来评估光学质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/6643362/79cfa2bba007/medarch-73-191-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/6643362/038cef4400f0/medarch-73-191-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/6643362/05e2c67855de/medarch-73-191-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/6643362/79cfa2bba007/medarch-73-191-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/6643362/038cef4400f0/medarch-73-191-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/6643362/05e2c67855de/medarch-73-191-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef6/6643362/79cfa2bba007/medarch-73-191-g003.jpg

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