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Qfix™ Access 360™ Prone Breast Treatment Solution

Treating women with breast cancer in the prone position during radiation therapy may substantially cut the radiation dose that reaches their heart and lungs.

Avondale, PA – September 28, 2011 – Qfix (www.qfix.com) announces the release of the kVue Access 360 Prone Breast treatment solution to improve treatment options for women with breast cancer.  Studies suggest that using this prone breast technique during radiotherapy minimizes the risk of damage to the heart, lungs and surrounding structures.  This lowers the risk of complications, such as future heart disease, lung damage and poor cosmesis. 

The kVue Access 360features a specially designed opening which allows the ipsilateral breast and chest wall to hang down away from the thorax, while the contralateral breast remains cushioned on the foam pad on top of the device.  The unique design provides near 360 degree access to the breast and supraclavicular nodes for improved imaging and treatment.  A CT docking solution allows seamless transition from simulation to treatment. 

Qfix and Varian Medical systems have joined efforts to design the Access 360™ for prone breast care.  Varian Medical Systems Pivotal™ Treatment Solutions combines prone techniques with the innovative kVue™ Access 360™ device.  The design enables treatment of both right and left breast, including whole breast, partial breast and accelerated partial breast treatments (APBI).    

“The kVue™ Access 360™ is the latest offering in a line of unique and innovative positioning devices that we at Qfix have developed over the past decade,” commented Dan Coppens, CEO & Technical Director of Qfix.  “We are thrilled to have Varian as our partner in developing such innovative treatment solutions.  With the launch of the kVue Access 360™, we have an opportunity to make a significant difference in breast cancer treatment.” 

About kVue IGRT
The kVue™ IGRT Couchtop is a state-of-the-art radiotherapy couchtop optimized for the most recent advances in technology to guide your patient from simulation through treatment.  It is designed for superior performance when used with kilovoltage imaging, such as cone beam CT, while simultaneously reducing skin dose for treatments that pass through the couchtop.  The kVue™ IGRT Couchtop allows the ability to replace the standard indexing insert with modular immobilization devices that mount directly into the top surface of the couch.  It’s one couchtop with multiple treatment solutions. 
About Qfix
Qfix, headquartered in Avondale, PA, is a world leader in the design, manufacturing and marketing of radiation therapy patient positioning and immobilization products.  For more information about Qfix please visit www.qfix.com.
Cautionary Statement Regarding Forward-Looking Statements

This news release may contain forward-looking statements based on current assumptions made by Qfix.  These forward-looking statements are based on our beliefs, assumptions and estimates using information available to us at the time and are not intended to be guarantees of future events or performance.  Qfix undertakes no obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise.

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For additional information contact:
Chuck Hiltunen
chuck.hiltunen@qfix.com


WFR

QfixTM Announces
Distribution Agreement with Dyn’R

SpiroDynr’X (SDX) Radiotherapy Breathing Control System

Avondale, PA, July 20, 2010 – QfixTM has announced an exclusive distribution agreement with Dyn’R for the company’s SDX™ Radiation Therapy Breathing Control System, now available to healthcare providers throughout the United States.

The SDX enables reproducible positioning of the tumor from medical imaging through the final session of the treatment, thus reducing the irradiation of healthy tissues and contiguous organs. During the initial preparation phase, the patient learns to use the spirometer, and the clinical team determines the optimal breath hold level according to the patient’s respiratory capacity. The patient is then asked to voluntarily reproduce the breath holds at the same pulmonary volume level during each subsequent medical imaging and radiation therapy session.

The SDX’s ergonomics are expressly designed for passage through existing CT scanners. Coupled with intuitive software, the SDX is easy to use by the Radiation Therapy team. The voluntary breath hold method makes it possible to obtain high quality images in which the effects of respiratory movement are minimized, thus contributing to optimized dosimetry planning. During each Radiation Therapy session, the patient produces several breath holds, lasting from a few to approximately 20 seconds. The use of video goggles provides bio-feedback to the patient indicating when and for how long to produce the breath hold.

95% of patients are able to master this method, regardless of the respiratory pathology from which they suffer. The patient’s active involvement is an important motivating factor contributing to successful completion of the treatment cycle.

“We are excited about driving SDX™ availability throughout North America. The SDX breath hold system provides a unique and patented method for ensuring accurate tumor motion control and positioning. It represents a valuable complement to our extensive portfolio of patient positioning products which also includes our Stradivarius™ system for SBRT”, says Dan Coppens, Chief Executive Officer of Qfix. “Our partnership with Dyn’R provides additional proof of our determination to bring premium solutions to the radiation oncology community.

About Qfix
Qfix, headquartered in Avondale, PA, is a world leader in the design, manufacturing and marketing of radiation therapy patient positioning and immobilization products. The company’s thermoplastic, Aquaplast RT™, is the most recognized brand of radiation therapy patient immobilization thermoplastic in the world. In addition, the company’s revolutionary kVue™ IGRT couchtop is the only metal-free couchtop with moving support beams, offering an unrivaled combination of kV imaging and MV treatment. More company information is available at www.qfix.com.

About Dyn’R
Dyn’R SAS, headquartered in Aix-en-Provence, France, has specialized in the conception, development and fabrication of medical devices for Pulmonary Function Testing. All Dyn’R spirometers conform to American Thoracic Society (ATS) recommendations. In 2000, Dyn’R enlarged its range with the SDX, new device of breathing control for imaging and radiation therapy applications, using the voluntary breath hold method. SDX is now used daily in more than 60 Radiation Therapy centers in Europe (France, UK, Germany, Netherland, Belgium, Switzerland, Italy, and Spain). Dyn’R received FDA 510K approval for the SDX in the beginning of 2010. More information is available at www.dynr.com and www.sdx.fr.

Forward-Looking Statements
This news release may contain forward-looking statements based on current assumptions made by Qfix. The company assumes no liability whatsoever to update these forward-looking statements or to conform them to future events or developments.

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For additional information contact:
Chuck Hiltunen
chuck.hiltunen@qfix.com


Qfix™ AnnouncesDistribution Agreement with MEDRAD

PRO-TEKT™ Endorectal Balloon Enables Repeatable Positioning with New Design to Minimize Discomfort During Radiation Therapy

Avondale, Pa., August 19, 2010 – Qfix™ has announced an exclusive distribution agreement with MEDRAD for the company’s PRO-TEKT™ endorectal balloon device. The PRO-TEKT device immobilizes structures that surround the rectum, such as the prostate, for radiation therapy treatment. The device is now available to healthcare providers throughout the United States, Australia and Europe.

The disposable single-use device immobilizes the rectal wall and adjacent structures of the
anatomy, and enables repeatable positioning throughout the course of treatment. The design features a smooth rubberized tip, flexible shaft and gas venting that allows for easy insertion and withdrawal while minimizing discomfort to the patient. Physicians inflate the latex-free endorectal balloon with air or fluid.

”The PRO-TEKT device can help the radiation oncologist consider reducing field margins which may decrease side effects to organs that are adjacent to the tumor,” says Anthony Cinalli, Executive Director of Marketing, MEDRAD Radiology. We are enthusiastic about accelerating PRO-TEKT product availability worldwide through Qfix distribution.”

“The PRO-TEKT device strengthens our leadership position in delivering a comprehensive suite
of cutting-edge patient positioning products to the radiation therapy community worldwide,”
says Dan Coppens, Chief Executive Officer of Qfix. “We are excited to have been selected by MEDRAD as the exclusive PRO-TEKT distributor and about our partnership’s potential to further serve our customers’ needs in the fight against cancer.”

MEDRAD has developed and manufactured products designed to support prostate cancer management for more than a decade. In addition to manufacturing the PRO-TEKT endorectal balloon, MEDRAD manufactures and sells the Prostate eCoil™ MRI endorectal coil, a device that enables improved insight for early prostate cancer detection.

About Qfix
Qfix, headquartered in Avondale, PA, is a world leader in the design, manufacturing and marketing of radiation therapy patient positioning and immobilization products. The company’s thermoplastic, Aquaplast RT™, is the most recognized brand of radiation therapy patient immobilization thermoplastic in the world. In addition, the Company’s revolutionary kVue™ IGRT couchtop is the only metal-free couchtop with moving support beams, offering an unrivaled combination of kV imaging and MV treatment. More company information is available at www.qfix.com.

About MEDRAD, Inc.
MEDRAD, Inc. also develops, markets and services medical devices used to diagnose and treat disease. Its product offerings include fluid injection systems for radiology and cardiology, endovascular devices for the safe treatment of cardiovascular disease, magnetic resonance compatible accessories and equipment services. The company’s world headquarters is near Pittsburgh, Pennsylvania, in the United States. MEDRAD is a business of Bayer Medical Care. More company information is available at www.medrad.com.

Forward-Looking Statements
This news release may contain forward-looking statements based on current assumptions made by Qfix. The company assumes no liability whatsoever to update these forward-looking statements or to conform them to future events or developments.

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For additional information contact:
Chuck Hiltunen
chuck.hiltunen@qfix.com

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