Aqueous Release to Treat IOP Spikes Post-cataract Surgery
Post-Op Complication, Raised Ocular Pressure
About this trial
This is an interventional treatment trial for Post-Op Complication
Eligibility Criteria
Inclusion Criteria:
- Patient whose post-operative IOP was regarded to be too high for visual safety, or higher than 30mmHg, on the same day or within 1 week of the surgery
Exclusion Criteria:
- Patients with IOP less than 30 mmHg or IOP deemed by clinician not too high to treat
- Patients unable to cooperate
- Patients who have undergone complicated cataract surgery
Sites / Locations
Arms of the Study
Arm 1
Experimental
Aqueous release (Burping) of the wound
Following uneventful cataract surgery, wound "burping" will be performed in all eligible patients who gave their informed consent. The procedure will be offered whenever the intraocular pressure (IOP) is either higher than 30 mmHg or deemed inappropriate in view of the ocular condition (e.g. glaucoma). After 'burping' the wound, patients will have their IOP measured using Goldmann application tonometry (GAT) immediately and at 2 hours. The 'burping' procedure will be repeated until satisfactory pressure is achieved and care will be taken to avoid shallowing of the anterior chamber while fluid is released. We will assess for the presence of leaks from the wound with a Seidel test with fluorescein 5% once the IOP is satisfactory. To prevent any infection after each procedure, we will prescribe post-op drops including chloramphenicol 0.5% four times a day for 2 weeks or minimum of 3 days and these will continue as per routine. All other complications will be recorded at follow-up.