2020-10-06

Purpose: Various materials are used in orbital blowout fracture repair. We describe a series of patients with orbital blowout fractures that were repaired using porous polyethylene (Medpor) sheets. Methods: A non-comparative interventional case series is described of 30 blowout fractures of 30 patients aged 7-60 years (median 29 years) who underwent orbital blowout fracture repair with Medpor sheets.

Effekten av COVID-19. PCA Infusion System Noris Medical Zygomatic Dental Implant System Stryker MEDPOR TITAN 3D Orbital Floor Implant Terumo Circuit Utförs om patienten vägrar implantation, i närvaro av intra-orbital infektion, omöjligt med korrekt ögonvård efter operation. Om materialet tillåter suturering (brosk, medpor, teflonimplantat Schiff eller Chelyabinsk, Pobedy Ave., 287, 9th floor. We designed our exclusive MEDPOR TITAN 3D orbital floor implant to enhance the effectiveness and efficiency of orbital reconstruction. We use CT-scan data to design the titantium implants to approximate the anatomy of the orbital floor and medial wall.

Pre-operatively, severe orbital floor and medial wall fractures can be seen obliterating the right ethmoid sinus. This causes extreme scarring and recession of the right eyeball into the orbit. The procedure begins with a transconjunctival incision and placement of a Medpor implant into the orbital floor. 2010-09-23 MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma.

Medpor porous polyethylene and Case of a malpositioned Medpor Titan implant.

New MEDPOR Orbital Floor Implan Implants and Prosthesis For Sale - DOTmed Listing #799031: Medpor Surgical Implant by Porex Surgical Products Group. This is Medpor Surgical Implant Cat:8305 DIM

Zygoma fracture elevation and fixation would be performed through an intraoral approach to avoid external scar formation. The cost for a single 4 × 4-cm SupraFOIL implant is $9.13, which is inexpensive compared with a 0.85-mm-thick Medpor implant (Porex Surgical Inc, Newnan, Ga), the orbital floor implant of choice at our institution, which costs $345, roughly 38 times the cost of SupraFOIL. MEDPOR TITAN 3D Orbital Floor Implant falls within the scope of the broader Indications for Use statement of the reference device. The difference in the Indications statement for the proposed device in comparison to the reference device does not constitute a new intended use.

The present study is to compare the effectiveness of iliac crest graft and medpor implant, for repairing traumatic orbital floor defects. A total of 20 patients were included in the study.

Stryker MEDPOR TITAN® 3D Orbital Floor Implant Indications for Use (Describe) The MEDPOR TITAN® 3D Orbital Floor Implant is indicated for the reconstructive treatment of orbital floor and/or medial wall trauma or bone excision in patients 15 years of age and older. Type of Use (Select one or both, as applicable) floor implants. J Oral Maxillofac Surg 1993;1:1217–1220. In conclusion, porous polyethylene sheets are safe and efficacious in the repair of orbital wall fractures. The implants are biocompatible, stable, and easy to handle.

We describe a series of patients with orbital blowout fractures that were repaired using porous polyethylene (Medpor) sheets.

We describe a series of patients with orbital blowout fractures that were repaired using porous polyethylene (Medpor) sheets.Methods A non-comparative interventional case series is described of 30 blowout fractures of 30 patients aged 7-60 years (median 29 years) who underwent orbital blowout fracture repair with Medpor sheets.
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tive differences were statistically significant. Complications of orbital blowout fractures should be treated early via surgery. A titanium mesh (MEDPOR®TITANTM) implant is an excellent material for reconstruction of the orbital wall. Keywords: Orbital blow-out fracture, titanium mesh (MEDPOR®TITANTM), implantation Introduction

. Patients who had diplopia or limited extraocular motion floor implants.