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首页> 外文期刊>Medicine. >The protective efficacy and safety of bandage contact lenses in children aged 5 to 11 after frontalis muscle flap suspension for congenital blepharoptosis: A single-center randomized controlled trial
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The protective efficacy and safety of bandage contact lenses in children aged 5 to 11 after frontalis muscle flap suspension for congenital blepharoptosis: A single-center randomized controlled trial

机译:额叶肌皮瓣悬吊术对先天性眼睑下垂术后5至11岁儿童的绷带隐形眼镜的保护功效和安全性:单中心随机对照试验

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Background: Postoperative complications, lagophthalmos and exposure keratopathy sometimes occur after surgery for congenital blepharoptosis. Bandage contact lenses (BCL) can help prevent some ocular surface disorders. The study aims to evaluate the efficacy and safety of BCL for protection of the ocular surface in children aged 5 to 11 years after frontalis muscle flap suspension for congenital blepharoptosis. Methods: We conducted a prospective randomized clinical study of 30 eyes of 30 patients with congenital blepharoptosis consecutively enrolled at the Ophthalmology Ward of the Children's Hospital of Chongqing Medical University, China from September 1, 2016, to February 30, 2017. After frontalis muscle flap suspension surgery, patients were randomly assigned to undergo BCL application (BCL group, 15 eyes) or no BCL application (control group, 15 eyes). All patients were treated with bramycin 0.3% and polyvinyl alcohol drops after surgery. The primary outcomes were dry eye assessed by tear film break time (TFBUT), fluoresce in corneal staining (FCS) on slit-lamp on days 1, 3, and 15 postoperatively, and lower tear meniscus height (LTMH) on optical coherence tomography on days 1 and 15 postoperatively. Secondary outcomes were pairwise correlation of TFBUT, FCS and LTMH. Results: In the BCL group, abnormal TFBUT and FCS were only found in 2 patients (13.33%) on postoperative day 15. In the control group, the incidence of dry eye assessed by TFBUT was 67.00% (10/15 eyes) on day 1, 73.33% (11/15 eyes) on day 3, and 53.33% (8/15 eyes) on day 15 ( P < .001). LTMH were significantly higher in the BCL group than the control group postoperatively ( P < .001). Significant positive correlations were found between LTMH and TFBUT pre-operation and on days 1 and 15 post-operation. For LTMH and FCSS ( R = ?0.815, P < .001), and TFBUT and FCS ( R = ?0.837, P < .001), the Pearson coefficient was negative on postoperative day 1, but not correlated on day 15. Conclusions: Silicone hydrogel BCL were safe and efficacious for protective use in children after frontalis muscle flap suspension for congenital blepharoptosis.
机译:背景:先天性睑缘下垂手术后有时会发生术后并发症,眼睑结石和暴露性角膜病变。绷带隐形眼镜(BCL)可以帮助预防某些眼表疾病。这项研究旨在评估BCL在额叶肌皮瓣悬吊治疗先天性眼睑下垂病后5至11岁儿童中保护眼表的有效性和安全性。方法:我们于2016年9月1日至2017年2月30日在中国重庆医科大学附属儿童医院眼科病房连续入组30例先天性眼睑下垂病患者的30只眼,进行了一项前瞻性随机临床研究。悬吊手术后,患者被随机分配接受BCL应用(BCL组,15眼)或不进行BCL应用(对照组,15眼)。术后所有患者均接受0.3%的霉素缓释剂和聚乙烯醇滴剂治疗。主要结果是在术后第1、3和15天通过泪膜破裂时间(TFBUT)评估干眼,在裂隙灯上角膜染色发荧光(FCS),在光学相干断层扫描术中通过泪液弯液面高度降低(LTMH)。术后第1天和第15天。次要结果是TFBUT,FCS和LTMH的成对相关。结果:BCL组在术后第15天仅发现2例患者的TFBUT和FCS异常(13.33%)。在对照组中,当日通过TFBUT评估的干眼症发生率为67.00%(10/15眼)。 1,第3天占73.33%(11/15眼),第15天占53.33%(8/15眼)(P <.001)。术后BLT组LTMH明显高于对照组(P <.001)。 LTMH和TFBUT术前以及术后1和15天发现显着正相关。对于LTMH和FCSS(R =?0.815,P <.001),以及TFBUT和FCS(R =?0.837,P <.001),皮尔逊系数在术后第1天为负,但在第15天无相关性。 :有机硅水凝胶BCL安全有效地用于额叶肌皮瓣悬吊治疗先天性眼睑下垂病的儿童。

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