Abstract
Purpose
To demonstrate the safety and efficacy of 27-gauge pars plana vitrectomy (PPV) in selected patients with vitreoretinal diseases requiring silicone oil (SO) tamponade.
Methods
Retrospective review of a consecutive interventional case series at a single center.
Results
Twenty-one eyes of 19 patients were included in the study. The indications for PPV and SO tamponade were as follows: fibrovascular tractional retinal detachment (12 eyes), rhegmatogenous retinal detachment with proliferative vitreoretinopathy (three eyes), primary rhegmatogenous retinal detachment (two eyes), macular hole (two eyes), vitreous hemorrhage (one eye), and endophthalmitis (one eye). All eyes underwent transconjunctival sutureless 27-gauge PPV with either 1000-cS (16 eyes) or 5000-cS (five eyes) SO tamponade. No intraoperative complications occurred. Mean preoperative best-corrected visual acuity (BCVA) was 20/300 (range, light perception to 20/40; median, counting fingers). Mean postoperative BCVA was 20/160 (range, no light perception to 20/25; median 20/300; p = 0.022). Follow-up was 6.4 ± 8.8 months (range, 1–38 months; median, 4 months). No complications relating to 27-gauge placement of SO were observed.
Conclusions
Results show that 27-gauge PPV with SO injection appears safe, is efficient, and may be considered for the surgical management of vitreoretinal diseases requiring SO tamponade.
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Funding
This work was supported in part by Research to Prevent Blindness, Inc., New York, NY, in the form of an unrestricted research grant to the University of Cincinnati, Department of Ophthalmology. The sponsor had no role in the design or conduct of this research.
Conflict of interest
DMM is a consultant to Synergetics USA, Inc. CDR is a consultant to Alcon Laboratories and MedOne Surgical, Inc.
OT and CWM certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; or expert testimony or patent-licensing arrangements) or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in the subject matter or materials discussed in this manuscript.
Ethical approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Informed consent
For this type of study (retrospective study), formal consent is not required. Informed consent for the surgical procedure was obtained from all individual participants.
No identifying information about participants is available in the article.
Additional information
This study was performed at the Cincinnati Eye Institute and University of Cincinnati, Department of Ophthalmology
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Toygar, O., Mi, C.W., Miller, D.M. et al. Outcomes of transconjunctival sutureless 27-gauge vitrectomy with silicone oil infusion. Graefes Arch Clin Exp Ophthalmol 254, 2111–2118 (2016). https://doi.org/10.1007/s00417-016-3355-5
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DOI: https://doi.org/10.1007/s00417-016-3355-5