# Efficacy of Ophthalmic Viscosurgical Device–Assisted Vitrectomy for Membrane Removal in Patients With Complex Proliferative Diabetic Retinopathy

**Authors:** Su Zhang, Hui-Ying Zhang, Lushu Chen, Qin Jiang, Jin Yao

PMC · DOI: 10.1155/joph/5436368 · Journal of Ophthalmology · 2026-03-01

## TL;DR

This study shows that using a special device during eye surgery helps remove membranes in diabetic retinopathy patients more safely and efficiently.

## Contribution

A new application of ophthalmic viscosurgical devices during vitrectomy for complex diabetic retinopathy is demonstrated.

## Key findings

- OVD-assisted vitrectomy reduced the need for electrocoagulation and shortened surgery time.
- Both groups showed improved vision post-surgery, with no significant difference in visual outcomes.
- OVD facilitated membrane removal and maintained a clear surgical field without causing retinal damage.

## Abstract

To assess the application of an ophthalmic viscosurgical device (OVD) for stripping proliferative membranes during vitrectomy in patients with complex proliferative diabetic retinopathy (PDR).

This was a prospective cohort study that enrolled 28 patients (30 eyes) diagnosed with complex PDR at the Affiliated Eye Hospital of Nanjing Medical University. The patients were randomly divided into two groups based on different surgical procedures: The patients who received vitrectomy combined with OVD‐assisted internal limiting membrane peeling were assigned to Group A (15 eyes of 13 patients), while Group B patients (15 eyes of 15 patients) underwent vitrectomy without OVD‐assisted internal limiting membrane peeling. The primary outcomes measured included intraoperative bleeding, operation duration, electrocoagulation for hemostasis, occurrence of iatrogenic retinal holes, postoperative best‐corrected visual acuity (BCVA), and complications such as recurrent retinal detachment and vitreous hemorrhage.

Compared with the mean preoperative BCVA, the mean postoperative BCVA at the last follow‐up improved significantly in both groups (all p < 0.05), but no significant difference in mean BCVA improvement was found between the two groups (p > 0.05). Regarding intraoperative complications, no iatrogenic retinal tears or retinal detachments occurred in any group. Intraoperative observations revealed that the preretinal injection of OVD facilitated the rapid separation of fibrous vascular membranes from the retina, while also serving a hemostatic function, thus maintaining a clear visual field. In Group A, photocoagulation was utilized for hemostasis in two eyes, whereas in Group B, it was employed in 9 cases, with a statistically significant difference between the groups (p < 0.05). The average surgical duration was 37.47 ± 4.69 min for Group A and 52 ± 6.26 min for Group B, with a statistically significant difference noted (p < 0.05). No iatrogenic retinal holes, recurrent vitreous hemorrhages, retinal detachments, choroidal hemorrhages, or endophthalmitis were observed in both groups.

Our study demonstrates a new application of OVD in proliferative membrane removal during vitrectomy, particularly in patients with PDR characterized by strong adhesions and complex structures. This method offers a potentially safer and more effective option for treating patients with PDR.

## Linked entities

- **Diseases:** diabetic retinopathy (MONDO:0005266), retinal detachment (MONDO:0008375)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** iris or angle neovascularization (MESH:D007499), vitreous hemorrhage (MESH:D014823), glaucoma (MESH:D005901), uveitis (MESH:D014605), Bleeding (MESH:D006470), cataract (MESH:D002386), rhegmatogenous retinal detachment (MESH:C563710), macular hole (MESH:D012167), blindness (MESH:D001766), choroidal hemorrhage (MESH:D002832), OVD (MESH:D009471), necrosis (MESH:D009336), Fibrous hyperplasia (MESH:D006965), retinal detachment (MESH:D012163), ischemia (MESH:D007511), epiretinal (MESH:D019773), PVD (MESH:D020255), fibrosis (MESH:D005355), retinal neovascularization (MESH:D015861), ocular trauma (MESH:D014947), edema (MESH:D004487), vascular damage (MESH:D057772), endophthalmitis (MESH:D009877), Postoperative Complications (MESH:D011183), ocular tumor (MESH:D009369), DR (MESH:D003930), retinal compromise (MESH:D012173), diabetes (MESH:D003920), PDR (OMIM:603933)
- **Chemicals:** silicone oil (MESH:D012827), hyaluronic acid (MESH:D006820), glucose (MESH:D005947), OVD (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12950999/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12950999/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950999/full.md

---
Source: https://tomesphere.com/paper/PMC12950999