García-Porta Nery, Rico-Del-Viejo Laura, Martin-Gil Alba, Carracedo Gonzalo, Pintor Jesus, González-Méijome José Manuel
Clinical & Experimental Optometry Research Lab (CEORLab), Center of Physics (Optometry), School of Sciences, University of Minho, Gualtar, 4710-057 Braga, Portugal; Ocular Surface and Contact Lenses Research Group, University of Santiago de Compostela, Santiago de Compostela, 15782 A Coruña, Spain.
Clinical & Experimental Optometry Research Lab (CEORLab), Center of Physics (Optometry), School of Sciences, University of Minho, Gualtar, 4710-057 Braga, Portugal.
Biomed Res Int. 2016;2016:1242845. doi: 10.1155/2016/1242845. Epub 2016 Aug 31.
. To compare the ocular surface symptoms and signs in an adult population of silicone-hydrogel (Si-Hy) contact lens (CL) wearers with another modality of CL wear, overnight orthokeratology (OK). . This was a prospective and comparative study in which 31 myopic subjects were fitted with the same Si-Hy CL and 23 underwent OK treatment for 3 months. Dry eye questionnaire (DEQ) was filled in at the beginning of the study and then after 15 days, 1 month, and 3 months using each CL modality. The tear quality was evaluated with noninvasive tear break-up time. Tear production was measured with Schirmer test. Tear samples were collected with Schirmer strips being frozen to analyze the dinucleotide diadenosine tetraphosphate (ApA) concentration with High-Performance Liquid Chromatography (HPLC). . After refitting with ortho-k, a reduction in discomfort and dryness symptoms at the end of the day ( < 0.05, ) was observed. No significant changes were observed in ApA concentration in any group. Bulbar redness, limbal redness, and conjunctival staining increased significantly in the Si-Hy group ( < 0.05, Kruskal-Wallis test). . Discomfort and dryness symptoms at the end of the day are lower in the OK CL group than in the Si-Hy CL group.
比较成年硅水凝胶(Si-Hy)隐形眼镜佩戴者与另一种隐形眼镜佩戴方式——夜间角膜塑形术(OK)的眼表症状和体征。这是一项前瞻性比较研究,31名近视受试者佩戴相同的Si-Hy隐形眼镜,23名接受OK治疗3个月。在研究开始时以及使用每种隐形眼镜方式15天、1个月和3个月后填写干眼问卷(DEQ)。使用无创泪膜破裂时间评估泪液质量。用Schirmer试验测量泪液分泌量。用Schirmer试纸收集泪液样本并冷冻,用高效液相色谱法(HPLC)分析二磷酸腺苷四磷酸(ApA)浓度。重新佩戴角膜塑形镜后,观察到一天结束时不适和干眼症状减轻(<0.05,)。任何组的ApA浓度均未观察到显著变化。Si-Hy组的球结膜充血、角膜缘充血和结膜染色显著增加(<0.05,Kruskal-Wallis检验)。OK隐形眼镜组一天结束时的不适和干眼症状低于Si-Hy隐形眼镜组。