Brissette Ashley R, Mednick Zale D, Schweitzer Kelly D, Bona Mark D, Baxter Stephanie A
Department of Ophthalmology, Queen's University and Hotel Dieu Hospital, Kingston, Ontario, Canada.
Department of Ophthalmology, Queen's University and Hotel Dieu Hospital, Kingston, Ontario, Canada.
Am J Ophthalmol. 2015 Aug;160(2):238-242.e1. doi: 10.1016/j.ajo.2015.05.013. Epub 2015 May 18.
To compare retention rates of Super Flex (Eagle Vision, Memphis, Tennessee, USA; Softplug-Oasis Medical Inc, Glendora, California, USA) vs Parasol (Odyssey Medical, Memphis, Tennessee, USA; Beaver Visitec International, Waltham, Massachusetts, USA) punctal plugs.
Randomized, double-masked, interventional controlled clinical trial.
Institutional study at Hotel Dieu Hospital (Queen's University) of 50 eyes, from patients with moderate to severe dry eye. Each eye from eligible patients was separately randomized to receive Super Flex or Parasol punctal plugs. The main outcome measure was plug retention at 6 months. Secondary outcome measures included objective tests of Schirmer I (mm), tear meniscus height (mm), tear break-up time (s), inferior fluorescein corneal staining (National Eye Institute [NEI] scale), and average lissamine green conjunctival staining (NEI scale).
Punctal plug retention was significantly different at 6 months (P = .011). Sixty-eight percent of Parasol plugs were retained compared to 32% of Super Flex plugs. Parasol plugs required less frequent artificial tear use at 6 months (P = .024). There was a statistically significant improvement in all secondary outcome measures (Schirmer, tear meniscus height, tear break-up time, fluorescein corneal staining) at 6 months within plug groups except conjunctival staining. There were no additional significant differences between groups and no plug complications reported.
Punctal plugs improve symptoms of moderate to severe dry eye; however, retention rates differ significantly. These data will allow us to guide patient decision making for the safe and effective treatment of punctal plugs for moderate to severe dry eye.
比较Super Flex(美国田纳西州孟菲斯市鹰视公司;美国加利福尼亚州格伦多拉市Softplug - Oasis医疗公司)与Parasol(美国田纳西州孟菲斯市奥德赛医疗公司;美国马萨诸塞州沃尔瑟姆市比弗视科国际公司)泪小点栓子的留存率。
随机、双盲、干预性对照临床试验。
在迪厄医院(女王大学)对50例中重度干眼症患者的50只眼进行机构研究。符合条件患者的每只眼分别随机接受Super Flex或Parasol泪小点栓子。主要观察指标为6个月时栓子的留存情况。次要观察指标包括Schirmer I试验(毫米)、泪河高度(毫米)、泪膜破裂时间(秒)、下方荧光素角膜染色(美国国立眼科研究所[NEI]分级)以及平均丽丝胺绿结膜染色(NEI分级)。
6个月时泪小点栓子的留存情况有显著差异(P = 0.011)。Parasol栓子的留存率为68%,而Super Flex栓子的留存率为32%。6个月时,Parasol栓子所需人工泪液使用频率更低(P = 0.024)。除结膜染色外,6个月时各栓子组内所有次要观察指标(Schirmer试验、泪河高度、泪膜破裂时间、荧光素角膜染色)均有统计学意义上的显著改善。组间无其他显著差异,且未报告栓子相关并发症。
泪小点栓子可改善中重度干眼症症状;然而,留存率有显著差异。这些数据将有助于我们指导患者在中重度干眼症泪小点栓子安全有效治疗方面的决策。