Efficacy and safety of Diquas in patients after LASIK surgery
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Abstract
Objective: To evaluate the efficacy and safety of Diquas in patients after LASIK surgery. Subject and method: Prospective non comparative trial. Fifty eyes of 25 patients after LASIK. Assessed TBUT, schirmer I, fluorescein, rose bengal staining score and the subjective symptoms (foreign body sensation, eye pain, dry feeling, feeling of burning, fatigue of the eyes, blurred vision, lacrimation) before and after treatment with diquas 1 month, 2 months and 3 months. Recorded the symptoms of adverse reactions (red eye, swelling of the conjunctiva or eyelid, pain eye, blurred vision, headache…). Result: At the 1 month, 2 months and 3 months after treatment with Diquas: TBUT, schirmer I increased significantly in eyes after LASIK, fluorescein and rose bengal staining score decreased significantly with p<0.01. The subjective symptoms (foreign body sensation, eye pain, dry feeling, feeling of burning, fatigue of the eyes, blurred vision) were improved as well (p<0.01). Six eyes after LASIK were red and pain itching after treatment 1 week. Conclusion: Diquas has the efficacy and safety in patients after LASIK surgery.
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References
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