Evaluation of the Ultrastructural and In Vitro Flow Properties of the PRESERFLO MicroShunt

• DOI: 10.1167/tvst.10.13.26
• Publication Date: 2021-11-18T17:32:22Z
• Authors: Marta Ibarz Barberá; Jose Luis Hernánd...; Jean Bragard; Javier Burguete; Laura Morales Fer...; Pedro Tañá Rivero; Rosario Gómez de ...; Miguel A. Teus
• Keywords: 617.7-007.681-089; Hagen-Poiseuille; Article; Aqueous Humor; Glaucoma surgery; Tonometry, Ocular; 03 medical and health sciences; 0302 clinical medicine; Cirugía; Aqueous flow; 3201.09 Oftalmología; Oftalmología; PRESERFLO; Materiales ópticos; Pressure drop; Glaucoma Drainage Implants; 617.749; 612.842.6; Óptica y optometría; Intraocular Pressure; 3213 Cirugía

To measure the in vitro flow properties of the PRESERFLO implant for comparison with the theoretical resistance to flow.The PRESERFLO was designed to control the flow of aqueous humor according to the Hagen-Poiseuille (HP) equation. Scanning electron microscopy (SEM) was performed to analyze the ultrastructure, and flow measurements were carried out using a gravity-flow setup.SEM images of the PRESERFLO showed luminal diameters of 67.73 × 65.95 µm and 63.66 × 70.54 µm. The total diameter was 337.2 µm, and the wall was 154 µm wide. The theoretical calculation of the resistance to flow (R) for an aqueous humor (AH) viscosity of 0.7185 centipoises (cP) was 1.3 mm Hg/(µL/min). Hence, assuming a constant AH flow of 2 µL/min, the pressure differential across the device (ΔP) was estimated to be 2.6 mm Hg. The gravity-flow experiment allowed us to measure the experimental resistance to flow, which was RE = 1.301 mm Hg/(µL/min), in agreement with the theoretical resistance to flow R given by the HP equation.The experimental and theoretical flow testing showed that the pressure drop across this device would not be large enough to avoid hypotony unless the resistance to outflow of the sub-Tenon space was sufficient to control the intraocular pressure in the early postoperative period.The fluid properties of glaucoma subconjunctival drainage devices determine their specific bleb-forming capacity and ability to avoid hypotony and therefore their safety and efficacy profile.