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首页> 外文期刊>Ophthalmology and therapy. >A Randomized, Controlled Treatment Trial of Eyelid-Warming Therapies in Meibomian Gland Dysfunction
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A Randomized, Controlled Treatment Trial of Eyelid-Warming Therapies in Meibomian Gland Dysfunction

机译:睑板腺功能异常的眼睑温暖疗法的随机对照治疗试验

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Aim The main treatment for meibomian gland dysfunction (MGD), a major cause of dry eye, is eyelid warming. Lack of compliance is the main reason for treatment failure. This has led to the development of eyelid-warming devices that are safe, effective and convenient. To obtain robust evidence demonstrating their efficacy, the authors conducted a 3-arm randomized clinical study. Methods The authors conducted a 3-month assessor-blinded, randomized, controlled trial of patients from the Singapore National Eye Centre experiencing at least one of eight dry eye symptoms ‘often’ or ‘all the time’. Patients who wore contact lenses, had an active infection or known diagnosis of thyroid dysfunction and rheumatoid arthritis were excluded from the study. MGD participants were randomly assigned to warm towel ( n =?25), EyeGiene? (Eyedetec Medical Inc., Danville, CA, USA) ( n =?25) and Blephasteam? (Spectrum Thea Pharmaceuticals LTD, Macclesfield, UK) ( n =?25) treatments. The primary efficacy and safety outcomes included the proportions of participants with improved symptoms and changes in best corrected visual acuity (BCVA), respectively. Other outcomes included tear break up time (TBUT), Schirmer test, corneal fluorescein dye staining and number of visibly occluded meibomian gland (MG) orifices. Results The study population was 53.5?±?11.1?years old and predominantly Chinese. For severity of symptom after 3?months of treatment, 78.3% Blephasteam? participants reported improvement compared to 45.5% warm towel participants ( p =?0.023). The corresponding proportions for improvement in the frequency of symptoms were 82.6% and 50.0%, respectively ( p =?0.020). The proportions of improvement of symptoms in EyeGiene? patients were not significantly different from warm towel intervention. At 1?month of treatment, the crude odds ratio of improvement of severity of irritation for Blephasteam? compared to control was 3.0 (95% CI 0.88–10.18). However, the odds ratio adjusted by age was 5.67 (1.30–24.66). The lid-warming treatments did not significantly change the TBUT, Schirmer test results or number of visibly occluded MGs in the study period. All treatment modalities did not worsen BCVA after 3?months. Conclusion Blephasteam? is more effective than warm towel for MGD treatment, with warm towel and EyeGiene? being comparable effective. Older age might predict for treatment efficacy. All studied therapies were safe for visual acuity (VA) for 3?months of treatment.
机译:目的睑板腺功能障碍(MGD)(干眼症的主要原因)的主要治疗方法是眼睑变暖。缺乏依从性是治疗失败的主要原因。这导致安全,有效和方便的眼睑加热装置的发展。为了获得有力的证据证明其功效,作者进行了3组随机临床研究。方法作者对来自新加坡国家眼科中心的“经常”或“一直”出现八种干眼症状中的至少一种进行了为期3个月的评估者盲目的随机对照试验。该研究排除了戴隐形眼镜,活动性感染或已知甲状腺功能低下和类风湿关节炎的患者。 MGD参与者随机分配到暖毛巾(n =?25),EyeGiene ?(Eyedetec Medical Inc.,Danville,CA,USA)(n =?25)和Blephasteam ? sup>(Spectrum Thea Pharmaceuticals LTD,英国Macclesfield)(n =?25)治疗。主要疗效和安全性结果分别包括症状改善和最佳矫正视力(BCVA)改变的参与者比例。其他结果包括撕裂时间(TBUT),Schirmer测试,角膜荧光素染料染色和明显闭塞的睑板腺(MG)孔口数量。结果研究人群年龄为53.5?±?11.1?岁,以华人为主。就治疗3个月后的症状严重程度而言,Blephasteam ?参与者报告的症状有所改善,而暖毛巾参与者为45.5%(p =?0.023)。改善症状频率的相应比例分别为82.6%和50.0%(p =?0.020)。 EyeGiene ?患者症状改善的比例与温暖毛巾干预无显着差异。在治疗的1个月时,与对照组相比,Blephasteam ?刺激严重程度改善的总体比值比为3.0(95%CI 0.88-10.18)。但是,按年龄调整的优势比为5.67(1.30-24.66)。在研究期间,盖热疗法并没有显着改变TBUT,Schirmer测试结果或明显闭塞的MG数量。 3个月后,所有治疗方式均未使BCVA恶化。结论Blephasteam ?在MGD治疗中比保暖毛巾更有效,保暖毛巾和EyeGiene ?的效果相当。年龄较大可能预示治疗效果。所有研究的疗法在3个月的治疗中对视力(VA)都是安全的。

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