Purpose: To assess etiologies and visual outcomes after pars plana vitrectomy for vitreous hemorrhage
in non-diabetic patients.
Materials and Methods: This is a descriptive cross-sectional study which was conducted at the IIEI&H,
Dhaka, Bangladesh for 12 months period following approval of this protocol. Total 30 patients were
included in the study who had non-diabetic vitreous hemorrhage. Risk and benefits were discussed to all
patients and informed consent was obtained. PPV were performed in all patients with dense or non-
resolving vitreous hemorrhage. Patients had follow-up on 1st post operative day (POD), then on 7th
POD, then on 1st month, then on 3rd month and finally on 6th month. Visual acuity (VA), intraocular
pressure (IOP) and complications were recorded during follow-up