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中华眼科医学杂志(电子版) ›› 2025, Vol. 15 ›› Issue (02) : 87 -92. doi: 10.3877/cma.j.issn.2095-2007.2025.02.004

论著

射频技术用于睑板腺功能障碍相关干眼治疗安全性与有效性的临床研究
文皓男1, 闻雅2, 吴彬阁1, 吴倩如2, 刘晶1, 接英2, 田磊1,2,   
  1. 1. 014000 内蒙古科技大学包头医学院第二附属医院眼科
    2. 100730 首都医科大学附属北京同仁医院 北京同仁眼科中心 北京市眼科研究所眼科学与视觉科学北京市重点实验室
  • 收稿日期:2025-03-02 出版日期:2025-04-28
  • 通信作者: 田磊
  • 基金资助:
    首都卫生发展科研专项(2024-2-1082)

Safety and efficacy of radio frequency technology in the treatment of meibomian gland dysfunction associated with dry eye

Haonan Wen1, Ya Wen2, Binge Wu1, Qianru Wu2, Jing Liu1, Ying Jie2, Lei Tian1,2,   

  1. 1. Department of Ophthalmology,The Second Affiliated Hospital of Baotou Medical College,Inner Mongolia University of Science and Technology,Baotou 014000,China
    2. Beijing Tongren Eye Center,Beijing Tongren Hospital,Beijing Ophthalmology and Visual Science Key Lab,Beijing Institute of Ophthalmology,Capital Medical University,Beijing 100730,China
  • Received:2025-03-02 Published:2025-04-28
  • Corresponding author: Lei Tian
引用本文:

文皓男, 闻雅, 吴彬阁, 吴倩如, 刘晶, 接英, 田磊. 射频技术用于睑板腺功能障碍相关干眼治疗安全性与有效性的临床研究[J/OL]. 中华眼科医学杂志(电子版), 2025, 15(02): 87-92.

Haonan Wen, Ya Wen, Binge Wu, Qianru Wu, Jing Liu, Ying Jie, Lei Tian. Safety and efficacy of radio frequency technology in the treatment of meibomian gland dysfunction associated with dry eye[J/OL]. Chinese Journal of Ophthalmologic Medicine(Electronic Edition), 2025, 15(02): 87-92.

目的

探讨射频技术治疗睑板腺功能障碍(MGD)相关干眼的安全性与有效性。

方法

选取2024年4月至2024年6月于首都医科大学附属北京同仁医院眼科中心就诊的MGD相关干眼患者共21例(42只眼)作为研究对象。其中,男性7例(14只眼),女性14例(28只眼);年龄23~73岁,平均年龄为(47.3±17.2)岁。所有患者均接受双眼睑射频治疗,每周1次,每次20 min,共4次。治疗前后的非接触眼压、眼表疾病指数问卷(OSDI)评分、症状视觉模拟量表(VAS)评分、睑板腺分泌能力评级、睑酯质量评分、荧光素染色泪膜破裂时间、角膜荧光素染色评分、SchirmerⅠ试验、最佳矫正视力、泪河高度(TMH)、泪膜脂质层厚度及非侵入性泪膜破裂时间符合正态分布,以±s描述,不同时间的比较采用单因素重复测量方差分析,治疗前与末次随访时各指标的比较采用配对t检验。

结果

MGD相关干眼患者治疗前、治疗后1周、治疗后2周、治疗后3周及治疗后4周OSDI评分分别为(55.86±20.80)分、(46.56±20.06)分、(33.30±18.75)分、(35.60±17.48)分及(25.99±11.15)分;烧灼或刺痛感、瘙痒感、异物感、眼干涩、畏光、眼疼痛及眼不适VAS评分分别为(47.71±22.71)分、(42.90±23.28)分、(35.57±19.82)分、(31.86±19.49)分、(28.67±17.83)分、(46.95±20.12)分、(45.95±21.89)分、(34.05±16.02)分、(31.14±21.90)分、(22.95±15.57)分、(53.57±25.48)分、(48.48±22.22)分、(36.43±19.23)分、(35.76±21.89)分、(22.48±12.71)分、(65.67±27.58)分、(55.90±23.22)分、(43.76±22.99)分、(37.86±18.79)分、(28.90±14.22)分、(53.71±21.57)分、(45.57±23.25)分、(36.38±23.47)分、(29.05±18.28)分、(21.10±12.66)分、(53.86±20.82)分、(44.55±19.23)分、(31.71±17.87)分、(33.50±16.98)分、(24.71±10.87)分、(70.67±17.84)分、(51.90±20.77)分、(39.52±21.52)分、(34.10±18.23)分及(24.81±12.86)分;不同时间OSDI评分和不适VAS评分的比较,差异均有统计学意义(F=9.103,2.958,5.870,7.211,9.334,8.457,9.103,19.340;P<0.05)。治疗后第4周与治疗前OSDI评分和不适VAS评分比较,差异有统计学意义(t=-5.22,-8.43,-6.91,-7.85,-8.98,-9.32,-9.16,-13.85;P<0.05)。患者治疗前、治疗后1周、治疗后2周、治疗后3周及治疗后4周,上睑睑板腺分泌能力评分分别为(5.10±1.87)分、(3.90±1.30)分、(3.29±1.55)分、(3.38±1.66)分及(3.14±1.31)分;下睑评分分别为(4.57±1.99)分、(3.33±1.28)分、(2.90±1.51)分、(3.05±1.36)分及(2.38±1.07)分;上睑睑酯质量评分分别为(5.86±1.82)分、(4.76±1.41)分、(4.29±1.79)分、(3.81±1.36)分及(3.57±1.66)分;下睑评分分别为(5.19±2.14)分、(3.90±1.22)分、(3.43±1.47)分、(3.57±1.40)分及(3.38±1.43)分;荧光素泪膜破裂时间分别为(3.21±1.00)s、(3.73±0.82)s、(4.06±0.98)s、(4.62±1.38)s及(4.48±0.98)s;角膜荧光素染色评分分别为(4.76±2.72)分、(3.24±1.58)分、(2.90±1.70)分、(2.67±1.49)分及(2.33±1.53)分;不同时间上下睑睑板腺分泌能力、上下睑睑酯质量、荧光素泪膜破裂时间及角膜荧光素染色的比较,差异均有统计学意义(F=5.552,6.440,6.559,4.867,6.239,5.393;P<0.05)。治疗后第4周与治疗前上下睑睑板腺分泌能力、上下睑睑酯质量、荧光素泪膜破裂时间及角膜荧光素染色评分比较,差异有统计学意义(t=-5.68,-6.42,-6.91,-4.67,6.02,-5.17;P<0.05)。治疗后第4周与治疗前非接触泪膜破裂时间比较,差异有统计学意义(t=2.12,P<0.05)。治疗前、治疗后1周、治疗后2周、治疗后3周及治疗后4周非接触眼压分别为(13.19±2.79)mmHg(1 mmHg=0.133 kPa)、(13.80±3.29)mmHg、(14.36±2.49)mmHg、(13.31±2.17)mmHg及(13.51±3.34)mmHg。眼前节和彩色眼底照相检查均未见明显变化及异常,患者眶周皮肤及毛发未见明显变化及异常且无特殊不适。

结论

使用射频技术治疗MGD相关干眼可改善患者的睑板腺分泌功能和泪膜稳定性,能有效地减轻患者的症状并改善相关体征,未发现不良反应。

Objective

The aim of this study is to investigate the safety and efficacy of radio frequency technique in the treatment of meibomian gland dysfunction(MGD)associated with dry eye.

Methods

A total of 21 patients(42 eyes)with MGD-related dry eye who visited the Ophthalmology Center of Beijing Tongren Hospital,Capital Medical University,from April 2024 and June 2024 were enrolled.Among them,7 were male(14 eyes)and 14 were female(28 eyes),with a mean age of(47.3±17.2)years(ranging from 23 to 73 years).Each patient received bilateral eyelid radiofrequency treatment once per week for 20 minutes per session,for a total of four sessions.Non-contact intraocular pressure,anterior segment imaging,ocular surface disease index(OSDI)scores,symptom visual analog scale(VAS)scores,meibomian gland secretion grading,meibum quality scores,fluorescein tear film break-up time(FBUT),corneal fluorescein staining scores,and SchirmerⅠtest,best-corrected visual acuity,tear meniscus height(TMH),lipid layer thickness(LLT),and non-invasive tear break-up time(NITBUT)were assessed before treatment and post-treatment conformed normal distribution and presented as±s,and compared by ANOVA for intergroup,and compared by paired t-tests for changes in each parameter from baseline to the final follow-up.

Results

The OSDI scores for patients with MGD-related dry eye before treatment and at 1,2,3,and 4 weeks after treatment were(55.86±20.80)scores,(46.56±20.06)scores,(33.30±18.75)scores,(35.60±17.48)scores,and(25.99±11.15)scores,respectively.VAS scores for symptoms including burning or stinging,itching,foreign body sensation,dryness,photophobia,eye pain,and ocular discomfort were as follows:(47.71±22.71)scores,(42.90±23.28)scores,(35.57±19.82)scores,(31.86±19.49)scores,(28.67±17.83)scores,(46.95±20.12)scores,(45.95±21.89)scores,(34.05±16.02)scores,(31.14±21.90)scores,(22.95±15.57)scores,(53.57±25.48)scores,(48.48±22.22)scores,(36.43±19.23)scores,(35.76±21.89)scores,(22.48±12.71)scores,(65.67±27.58)scores,(55.90±23.22)scores,(43.76±22.99)scores,(37.86±18.79)scores,(28.90±14.22)scores,(53.71±21.57)scores,(45.57±23.25)scores,(36.38±23.47)scores,(29.05±18.28)scores,(21.10±12.66)scores,(53.86±20.82)scores,(44.55±19.23)scores,(31.71±17.87)scores,(33.50±16.98)scores,(24.71±10.87)scores,(70.67±17.84)scores,(51.90±20.77)scores,(39.52±21.52)scores,(34.10±18.23)scores,and(24.81±12.86)scores.The differences in OSDI and VASscores across time points were statistically significant(F=9.103,2.958,5.870,7.211,9.334,8.457,9.103,19.340;P<0.05).By the 4th week post-treatment,compared with baseline,the changes in OSDI and VAS scores for burning/stinging,itching,foreign body sensation,dryness,photophobia,eye pain,and discomfort had statistically significant(t=-5.22,-8.43,-6.91,-7.85,-8.98,-9.32,-9.16,-13.85;P<0.05).The meibomian gland secretion scores(upper lid)at baseline and at 1,2,3,and 4 weeks posttreatment were(5.10±1.87)scores,(3.90±1.30)scores,(3.29±1.55)scores,(3.38±1.66)scores,and(3.14±1.31)scores;lower lid scores were(4.57±1.99)scores,(3.33±1.28)scores,(2.90±1.51)scores,(3.05±1.36)scores,and(2.38±1.07)scores.Meibum quality scores(upper lid)were(5.86±1.82)scores,(4.76±1.41)scores,(4.29±1.79)scores,(3.81±1.36)scores,and(3.57±1.66)scores;lower lid scores were(5.19±2.14)scores,(3.90±1.22)scores,(3.43±1.47)scores,(3.57±1.40)scores,and(3.38±1.43)scores.Fluorescein tear break-up times were(3.21±1.00)scores,(3.73±0.82)scores,(4.06±0.98)scores,(4.62±1.38)scores,and(4.48±0.98)seconds;corneal fluorescein staining scores were(4.76±2.72)scores,(3.24±1.58)scores,(2.90±1.70)scores,(2.67±1.49)scores,and(2.33±1.53)scores.These indicators showed significant differences over time(F=5.552,6.440,6.559,4.867,6.239,5.393;P<0.05).By the 4th week,compared to baseline,upper lid secretion,lower lid,upper lid meibum quality,lower lid,tear breakup time,and corneal staining had statistically significant the changes(t=-5.68,-6.42,-6.91,-4.67,6.02,-5.17;P<0.05).There was a significant increase between before and after treatment in non-invasive tear break-up time(t=2.12,P<0.05).Non-contact intraocular pressure at baseline,1,2,3,and 4 weeks post-treatment were(13.19±2.79)mmHg(1 mmHg=0.133 kPa),(13.80±3.29)mmHg,(14.36±2.49)mmHg,(13.31±2.17)mmHg,and(13.51±3.34)mmHg,respectively.It has showed no notable abnormalities or changes in periocular skin or eyelashes,and no patients reported any specific discomfort.

Conclusions

The radio frequency technology had a capacity of improving the secretion function of meibomian gland and tear film stability,effectively alleviate the symptoms and improve the relevant signs of patients with dry eye associated with MGD,and non-adverse reactions.

表1 睑板腺功能障碍相关干眼患者治疗前及每次随访症状评分和重要体征的变化(±s)
时间 眼数(只眼) OSDI评分(分) 烧灼或刺痛感VAS(分) 瘙痒感VAS(分) 异物感VAS(分) 眼干涩VAS(分) 畏光VAS(分) 眼疼痛VAS(分)
治疗前 42 55.86±20.80 47.71±22.71 46.95±20.12 53.57±25.48 65.67±27.58 53.71±21.57 53.86±20.82
治疗后1周 42 46.56±20.06 42.90±23.28 45.95±21.89 48.48±22.22 55.90±23.22 45.57±23.25 44.55±19.23
治疗后2周 42 33.30±18.75 35.57±19.82 34.05±16.02 36.43±19.23 43.76±22.99 36.38±23.47 31.71±17.87
治疗后3周 42 35.60±17.48 31.86±19.49 31.14±21.90 35.76±21.89 37.86±18.79 29.05±18.28 33.50±16.98
治疗后4周 42 25.99±11.15* 28.67±17.83* 22.95±15.57* 22.48±12.71* 28.90±14.22* 21.10±12.66* 24.71±10.87*
F 9.103 2.958 5.870 7.211 9.334 8.457 9.103
P <0.05 <0.05 <0.05 <0.05 <0.05 <0.05 <0.05
时间 眼数(只眼) 眼不适VAS(分) 上睑睑板腺分泌能力(分) 下睑睑板腺分泌能力(分) 上睑睑酯质量(分) 下睑睑酯质量(分) 荧光素泪膜破裂时间(s) 角膜荧光素染色(分)
治疗前 42 70.67±17.84 5.10±1.87 4.57±1.99 5.86±1.82 5.19±2.14 3.21±1.00 4.76±2.72
治疗后1周 42 51.90±20.77 3.90±1.30 3.33±1.28 4.76±1.41 3.90±1.22 3.73±0.82 3.24±1.58
治疗后2周 42 39.52±21.52 3.29±1.55 2.90±1.51 4.29±1.79 3.43±1.47 4.06±0.98 2.90±1.70
治疗后3周 42 34.10±18.23 3.38±1.66 3.05±1.36 3.81±1.36 3.57±1.40 4.62±1.38 2.67±1.49
治疗后4周 42 24.81±12.86* 3.14±1.31* 2.38±1.07* 3.57±1.66* 3.38±1.43* 4.48±0.98* 2.33±1.53*
F 19.340 5.552 6.440 6.559 4.867 6.239 5.393
P <0.05 <0.05 <0.05 <0.05 <0.05 <0.05 <0.05
表2 睑板腺功能障碍相关干眼患者射频治疗前后次要指标的变化情况(±s)
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