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Bypass Micros tent 2017 Coding and Billing Guide Bypass Micros tent Description and Indication The Bypass Micros tent received FDA approval on July 29, 2016. The Bypass System is indicated for use
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How to fill out cypass micro-stent

01
Wash your hands thoroughly before starting the procedure.
02
Open the packaging of the Cypass micro-stent and prepare all the necessary equipment.
03
Ensure the patient is in a comfortable position and administer local anesthesia.
04
Make a small incision near the patient's eye and create a scleral tunnel.
05
Insert the Cypass micro-stent through the incision into the anterior chamber of the eye.
06
Position the micro-stent correctly to ensure proper drainage of fluid.
07
Secure the micro-stent in place and close the incision.
08
Monitor the patient's condition and provide post-operative care as instructed by the healthcare professional.

Who needs cypass micro-stent?

01
Individuals diagnosed with primary open-angle glaucoma (POAG) may benefit from a Cypass micro-stent.
02
Patients who have not responded well to medications or other treatments for reducing intraocular pressure (IOP) may be candidates for a Cypass micro-stent.
03
Those who require a minimally invasive surgical option for controlling glaucoma may be suitable for the Cypass micro-stent.
04
Consult with an ophthalmologist or glaucoma specialist for a thorough evaluation and to determine if the Cypass micro-stent is appropriate for your condition.
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Cypass micro-stent is a device used to lower intraocular pressure in patients with mild to moderate primary open-angle glaucoma.
Ophthalmologists or eye surgeons who perform the implantation of the cypass micro-stent are required to file the necessary documentation.
The filing process involves submitting the patient's information, details of the procedure, and any complications or follow-up care required after the implantation.
The purpose of the cypass micro-stent is to help improve the drainage of fluid in the eye, thereby reducing intraocular pressure and managing glaucoma.
The information reported must include patient demographics, procedure details, device information, and any adverse events or complications.
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