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比较他克莫司(0.03%)和地塞米松(0.05%)治疗腺病毒结膜炎后上皮下浸润的安全性和疗效。

Comparison of the safety and efficacy of topical Tacrolimus (0.03%) versus dexamethasone (0.05%) for subepithelial infiltrates after adenoviral conjunctivitis.

机构信息

Department of Ophthalmology, Laser Eye Clinic, Noida, UP, India.

出版信息

Indian J Ophthalmol. 2019 May;67(5):594-598. doi: 10.4103/ijo.IJO_1352_18.

Abstract

PURPOSE

To compare the safety and efficacy of tacrolimus 0.03% ointment with dexamethasone 0.05% ointment for subepithelial infiltrates (SEIs) following adenoviral keratoconjunctivitis (AK).

METHODS

A randomized, double blind trial was done. Eligibility criteria was corrected distance visual acuity of 6/9 Snellen or worse for at least 4 weeks with corneal SEIs following AK. The grading of SEIs was done on a scale of 0 to 3; 0, no infiltrates, 1 mild infiltration, 2 moderate infiltration and 3, severe infiltration. Consecutive patients with SEIs following AK were randomized to receive either topical tacrolimus 0.03% or dexamethasone 0.05% ointment twice daily for 6 months. Treatment was successful if there was reduction of SEIs and improvement in vision.

RESULTS

A total of 45 patients each were assigned to the Tacro and Dexa groups, respectively. Baseline characteristics of patients did not differ significantly (P > 0.001). There was a significant change in symptoms, vision and SEIs in both the groups. However, the magnitude was greater in tacro group. Treatment was successful in 37 (92.5%) patients in Tacro and 34 (85%) patients in dexa group. In dexa group, after a period of 1.24 ± 0.24 months, 7 (15.6%) patients developed a significant rise in intraocular pressure (IOP). Three (7.5%) eyes in tacro and 6 (15%) eyes in dexa group had recurrence of SEIs after cessation of therapy.

CONCLUSION

Tacrolimus 0.03% is an effective alternative to dexamethasone 0.05% with low recurrence rate, no significant rise in IOP but may cause burning and foreign body sensation in some patients.

摘要

目的

比较他克莫司 0.03%软膏与地塞米松 0.05%软膏治疗腺病毒角膜炎(AK)后上皮下浸润(SEI)的安全性和疗效。

方法

进行了一项随机、双盲试验。入选标准为 AK 后至少 4 周,角膜 SEI 导致矫正远视力低于 6/9 (Snellen 视力表)。SEI 分级为 0 至 3 级;0 级,无浸润;1 级,轻度浸润;2 级,中度浸润;3 级,重度浸润。连续出现 AK 后 SEI 的患者随机分为两组,分别接受每日两次他克莫司 0.03%或地塞米松 0.05%软膏治疗,疗程 6 个月。如果 SEI 减少和视力改善,则治疗成功。

结果

共有 45 例患者分别被分配至他克莫司组和地塞米松组。患者的基线特征无显著差异(P > 0.001)。两组患者的症状、视力和 SEI 均有显著变化,但他克莫司组的变化幅度更大。他克莫司组 37 例(92.5%)患者和地塞米松组 34 例(85%)患者治疗成功。地塞米松组中有 7 例(15.6%)患者在 1.24±0.24 个月后出现明显的眼压升高(IOP)。他克莫司组中有 3 例(7.5%)眼和地塞米松组中有 6 例(15%)眼在停止治疗后出现 SEI 复发。

结论

他克莫司 0.03%是地塞米松 0.05%的有效替代药物,复发率低,眼压升高不明显,但可能会引起部分患者烧灼感和异物感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d17f/6498921/907177dc88b4/IJO-67-594-g001.jpg

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