Duke-National University of Singapore Graduate Medical School, Singapore, Singapore.
Singapore Eye Research Institute, Singapore, Singapore.
Ophthalmol Ther. 2014 Dec;3(1-2):37-48. doi: 10.1007/s40123-014-0025-8. Epub 2014 Aug 26.
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.
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.
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.
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.
睑板腺功能障碍(MGD)是干眼症的主要原因,其主要治疗方法是眼睑热敷。治疗失败的主要原因是依从性差。这导致了安全、有效和方便的眼睑加热设备的发展。为了获得强有力的证据证明其疗效,作者进行了一项 3 臂随机临床试验。
作者对来自新加坡国家眼科中心的至少有 8 种干眼症症状中的 1 种“经常”或“一直”的患者进行了为期 3 个月的评估者盲、随机、对照试验。不包括佩戴隐形眼镜、有活动性感染或已知甲状腺功能减退和类风湿关节炎诊断的患者。MGD 参与者被随机分配到热毛巾(n=25)、EyeGiene(®)(Eyedetec Medical Inc.,Danville,CA,USA)(n=25)和 Blephasteam(®)(Spectrum Thea Pharmaceuticals LTD,Macclesfield,UK)(n=25)治疗组。主要疗效和安全性结局分别包括症状改善的参与者比例和最佳矫正视力(BCVA)的变化。其他结果包括泪膜破裂时间(TBUT)、泪液分泌试验、角膜荧光素染色和可见阻塞的睑板腺(MG)开口数量。
研究人群的年龄为 53.5±11.1 岁,主要为中国人。治疗 3 个月后,78.3%的 Blephasteam(®)患者报告症状改善,而热毛巾组为 45.5%(p=0.023)。相应的改善症状频率比例分别为 82.6%和 50.0%(p=0.020)。EyeGiene(®)患者症状改善的比例与热毛巾干预组无显著差异。治疗 1 个月时,与对照组相比,Blephasteam(®)改善刺激严重程度的粗比值比为 3.0(95%置信区间 0.88-10.18)。然而,经年龄调整后的比值比为 5.67(1.30-24.66)。研究期间,眼睑加热治疗均未显著改变 TBUT、泪液分泌试验结果或可见阻塞的 MG 数量。所有治疗方法在 3 个月后均未使 BCVA 恶化。
与热毛巾相比,Blephasteam(®)治疗 MGD 更有效,热毛巾和 EyeGiene(®)的疗效相当。年龄较大可能预示着治疗效果更好。所有研究的治疗方法在 3 个月的治疗期间对视力(VA)都是安全的。