Endothelial cell loss 5 years after Preserflo MicroShunt implantation: About two cases

Chloé Chamard1,2, Sirine Hammoud3, Elisa Bluwol3

  • 1Department of Ophthalmology, Gui de Chauliac Hospital, Montpellier, F-34000, France.

Abstract

Insights

The Preserflo MicroShunt, a glaucoma drainage device, may cause endothelial cell loss in some patients, necessitating further long-term studies to assess risks and impact.

Area of Science:

  • Ophthalmology
  • Medical Devices

Background:

  • Preserflo MicroShunt is a minimally-invasive glaucoma drainage device.
  • It shunts aqueous humor from the anterior chamber to the subtenon space.
  • Initial safety profile considered satisfactory with minor side effects.

Observation:

  • This report details 5-year outcomes of Preserflo implantation in two primary open-angle glaucoma patients.
  • Case 1: Device-cornea touch due to backward migration.
  • Case 2: Device modification associated with inflammatory reaction.

Findings:

  • Both patients required device explantation due to complications.
  • Preserflo MicroShunt, similar to other glaucoma devices, can cause endothelial cell loss.
  • Complications included device migration and inflammatory reactions.

Implications:

  • Long-term prospective studies are needed to evaluate Preserflo MicroShunt's real-world impact.
  • Assessing pre- and post-operative endothelial cell counts is crucial.
  • Anterior segment OCT or ultrasound biomicroscopy can evaluate device positioning and identify risk factors for endothelial cell loss.

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