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To describe the surgical outcomes and implant complications in 1,800 patients undergoing evisceration with primary implant An Electronic Medical Record-driven analysis of 1,800 patients undergoing evisceration with primary implant between 2013 and 2019. Implant sizing was performed intra-operatively to place the largest implant without tension on the wound closure. Outcome measures included implant complications, prosthesis measurements, and incidence of a good aesthetic outcome. Good outcome was defined as &lt;2 mm enophthalmos and grade 1 or less superior sulcus deformity with a custom ocular prosthesis. Eighteen hundred eyes of 1800 patients were included. The mean age at surgery was 36 ± 21 years (median 32 years). Implants used were poly(methyl methacrylate) (PMMA) in 1737 (97%) and porous polyethylene in 63 (3%) patients. Two-petal sclerotomy was performed in 1512 (88%) and four-petal sclerotomy in 165 (10%) patients. The mean diameter of the implant used was 19.35 ± 1.18 mm (median 20, range 10–22 mm). The implant extrusion rate was 3% (56) and implant displacement was seen in none. The mean prosthesis volume and thickness were 2.22 ± 0.67 ml (median 2, range 1–6.5 ml) and 6 ± 1 mm (median 6, range 2–9 mm). The mean difference in prosthesis projection on Hertel’s exophthalmometer was 0.28 ± 1 mm (median 0, range 0–1 mm). Good outcome was observed in 93%. The mean follow-up period was 351 ± 386 days (median 194). Evisceration with empirically selected primary orbital implant placement is associated with minimal implant complications and gives a good aesthetic outcome in 93% of the patients.

Outcomes and complications of evisceration with primary implant: an electronic medical record driven analytics of 1800 cases