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Published on: May 31, 2024
Randomised controlled single-blind study of conventional versus depot mydriatic drug delivery prior to cataract
Vincent Dubois1, Nadia Wittles, Meon Lamont
1Eye Unit, Royal United Hospital, Combe Park, Bath, B&NES, BA1 3NG, UK. vincent_dubois@doctors.org.uk
Background:
A prerequisite for safe cataract surgery is an adequately dilated pupil. The authors conducted a trial to assess the efficacy (in terms of pupil diameter) of a depot method of pre-operative pupil dilatation, as compared with repeated instillations of drops (which is time-consuming for the nursing staff and uncomfortable for the patient).
Methods:
A prospective randomised masked trial was conducted comprising 130 patients with no significant ocular history undergoing elective clear corneal phacoemulsification. 65 patients had mydriatic drops (Tropicamide 1%, Phenylephrine 2.5%, Diclofenac sodium 0.1%) instilled prior to surgery, 65 had a wick soaked in the same drop mixture placed in the inferior fornix. Horizontal pupil diameters were recorded on a millimetre scale immediately prior to surgery.
Results:
There was no significant difference in pupil size between the two groups (p = 0.255, Student's t-test).
Conclusion:
There was no significant difference between the mydriasis obtained with the depot system compared with conventional drop application. Use of a depot mydriatic delivery system appears to be a safe and efficient method of drug delivery.
Trial Registration:
International Standard Randomised Controlled Trial Number Register ISRCTN78047760.
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