Alcon features new technology upgrades for the ORA System® and the VERION™ Image Guided System at ASCRS
Apr 14, 2015
The ORA System® with the new VerifEye+™ Technology and VERION™ 2.6 software introduced at the American Society of Cataract and Refractive Surgery.
Product enhancements provide improved functionality, usability and connectivity to help surgeons more easily identify and address potential sources of measurement error.
San Diego, California, April 14, 2015 – Alcon, the global leader in eye care, will introduce enhancements to both the ORA System® and the VERION™ Image Guided System, providing improved capabilities and efficiency during both preoperative planning and intraoperative guidance during the cataract surgery procedure. The new VerifEye+™ Technology and VERION 2.6 software update will be on display at the Alcon booth (#1127) and demonstrated during a Live Surgery event at the American Society of Cataract and Refractive Surgery (ASCRS) in San Diego, California.
The VerifEye+ Technology in the ORA System offers the following enhancements to the previous version:
Provides on demand information to assist in intraoperative decision making and delivers this information to the surgeon via a dynamic reticle visible through the right ocular
This leads to a more efficient workflow and surgeon usability in the operating room
The 2.6 software in the VERION Image Guided System offers the following enhancements to the previous version:
Improved functionality and usability in the clinic, at the LenSx® Laser and at the microscope in the operating room
Compatibility with existing local area network (LAN) based networks configured to connect the VERION components and replace the USB as the primary data transfer process
Remote accessibility to the VERION Reference Unit planner database
Upgraded LenStar import and integration with compatible electronic medical record systems (EMRs)
VERION Quick Snap image capture at the measurement module for surgeons using VERION image-based guidance on astigmatism axis with imported LenStar or manually entered K values
Optical enhancement of the microscope-integrated display (MID) for surgeons in need of improved low light registration and tracking
"The VERION Image Guided System and the ORA System with VerifEye+ Technology are complementary devices that make cataract surgery even more precise," said Dr. John Davidson, MD., Miramar Eye Specialists Medical Group. "I find the cyclotorsional compensation aspect of the VERION combined with the ORA System’s guidance is particularly important in achieving consistent correction of astigmatism with the use of arcuate incisions and/or toric IOLs. The new software upgrades for these devices provide surgeons with the tools they need to more efficiently and systematically address variables affecting refractive outcomes."
Learn more about Dr. Davidson’s and other world-renowned eye care professionals’ experiences with the upgraded platforms during the booth talk "Innovative Technologies Designed to Improve Outcomes" on Sunday, April 19, 2015, 12:00 –1:00 pm.
The new VERION 2.6 software will be released for new customers’ installation and current customers’ upgrades following the ASCRS conference. The new VerifEye+ Technology will launch later this quarter. Demonstrations of both the VerifEye+ Technology and the VERION 2.6 software enhancements can be seen during ASCRS Live surgery and at the Alcon Cataract Refractive Suite in the Alcon booth. Those interested in learning more may also visit www.MyAlcon.com.
About the ORA System with VerifEye+ Technology
The ORA System with VerifEye+™ Technology allows surgeons to evaluate refractive findings, refine IOL power, cylinder power, and IOL alignment in real time to provide optimal refractive outcomes in cataract surgery. For additional information about the ORA System with VerifEye+ Technology, please refer to the important product information on the following page.
About the VERION Image Guided System
The VERION Image Guided System is a suite of integrated surgical planning and digital guidance technologies designed to help eye surgeons consistently achieve their refractive targets for patients undergoing cataract surgery. It consists of multiple proprietary technologies, including the VERION Reference Unit and the VERION Digital Markers, each designed to help eye surgeons add greater accuracy and efficiency during the planning and executing of refractive cataract surgery. For additional information about the VERION Image Guided System, please refer to the important product information on the following pages.
Alcon, the global leader in eye care, provides innovative products that enhance quality of life by helping people worldwide see better. Alcon’s three businesses, Surgical, Pharmaceutical and Vision Care, offer the widest spectrum of eye care products in the world. Alcon is the second largest division of the Novartis Group, with pro-forma sales of USD 10.8 billion in 2014.
Headquartered in Fort Worth, Texas, USA, Alcon has more than 25,000 employees worldwide, operations in 75 countries and products available in 180 markets.
Elizabeth Harness Murphy Alcon Global Communications 817.551.8696 (office) 585.435.7379 (mobile) [email protected]
Donna Lorenson US Head of Communications 817.615.5092 (office) 410.258.8571 (mobile) [email protected]
IMPORTANT PRODUCT INFORMATION ABOUT THE ORA SYSTEM
CAUTION: Federal (USA) law restricts this device to sale by, or on the order of, a physician.
INTENDED USE: The ORA System uses wavefront aberrometry data in the measurement and analysis of the refractive power of the eye (i.e. sphere, cylinder, and axis measurements) to support cataract surgical procedures.
CONTRAINDICATIONS: The ORA System is contraindicated for patients: • who have progressive retinal pathology such as diabetic retinopathy, macular degeneration, or any other pathology that the physician deems would interfere with patient fixation; • who have corneal pathology such as Fuchs’, EBMD, keratoconus, advanced pterygium impairing the cornea, or any other pathology that the physician deems would interfere with the measurement process; • whose preoperative regimen includes residual viscous substances left on the corneal surface such as lidocaine gel or viscoelastics; • with visually significant media opacity (such as prominent floaters or asteroid hyalosis) what will either limit or prohibit the measurement process; or • who have received retro or peribulbar block or any other treatment that impairs their ability to visualize the fixation light. In addition, utilization of iris hooks during an ORA System image capture is contraindicated, because the use of iris hooks will yield inaccurate measurements.
WARNINGS AND PRECAUTIONS: • Significant central corneal irregularities resulting in higher order aberrations might yield inaccurate refractive measurements. • Post refractive keratectomy eyes might yield inaccurate refractive measurement. • The safety and effectiveness of using the data from the ORA System have not been established for determining treatments involving higher order aberrations of the eye such as coma and spherical aberrations. • The ORA System is intended for use by qualified health personnel only. • Improper use of this device may result in exposure to dangerous voltage or hazardous laser-like radiation exposure. • Do not operate the ORA System in the presence of flammable anesthetics or volatile solvents such as alcohol or benzene, or in locations that present an explosion hazard.
ATTENTION: Refer to the ORA System Operator’s Manual for a complete description of proper use and maintenance of the ORA System, as well as a complete list of contraindications, warnings and precautions.
IMPORTANT PRODUCT INFORMATION ABOUT VERION REFERENCE UNIT and VERION DIGITAL MARKER
CAUTION: Federal (USA) law restricts this device to sale by, or on the order of, a physician.
INTENDED USES: The VERION Reference Unit is a preoperative measurement device that captures and utilizes a high-resolution reference image of a patient's eye. In addition, the VERION Reference Unit provides pre-operative surgical planning functions to assist the surgeon with planning cataract surgical procedures. The VERION Reference Unit also supports the export of the reference image, preoperative measurement data, and surgical plans for use with the VERION Digital Marker and other compatible devices through the use of a USB memory stick. The VERION Digital Marker links to compatible surgical microscopes to display concurrently the reference and microscope images, allowing the surgeon to account for lateral and rotational eye movements. In addition, details from the VERION Reference Unit surgical plan can be overlaid on a computer screen or the physician's microscope view.
CONTRAINDICATIONS: The following conditions may affect the accuracy of surgical plans prepared with the VERION Reference Unit: a pseudophakic eye, eye fixation problems, a non-intact cornea, or an irregular cornea. In addition, patients should refrain from wearing contact lenses during the reference measurement as this may interfere with the accuracy of the measurements. The following conditions may affect the proper functioning of the VERION Digital Marker: changes in a patient's eye between pre-operative measurement and surgery, an irregular elliptic limbus (e.g., due to eye fixation during surgery, and bleeding or bloated conjunctiva due to anesthesia). In addition, the use of eye drops that constrict sclera vessels before or during surgery should be avoided.
WARNINGS: Only properly trained personnel should operate the VERION Reference Unit and VERION Digital Marker. Use only the provided medical power supplies and data communication cable. Power supplies for the VERION Reference Unit and the VERION Digital Marker must be uninterruptible. Do not use these devices in combination with an extension cord. Do not cover any of the component devices while turned on. The VERION Reference Unit uses infrared light. Unless necessary, medical personnel and patients should avoid direct eye exposure to the emitted or reflected beam.
PRECAUTIONS: To ensure the accuracy of VERION Reference Unit measurements, device calibration and the reference measurement should be conducted in dimmed ambient light conditions. Only use the VERION Digital Marker in conjunction with compatible surgical microscopes.
ATTENTION: Refer to the user manuals for the VERION Reference Unit and the VERION Digital Marker for a complete description of proper use and maintenance of these devices, as well as a complete list of contraindications, warnings and precautions.