Experienced Urologists to Present Latest Findings and Host Multiple Educational Sessions
WAYNE, Pa., April 24, 2025 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE:TFX), a leading global provider of medical technologies, today announced the presentation of several clinical studies at the 2025 American Urological Association Annual Meeting, which is being held in Las Vegas from April 26 - 29, 2025. These studies contribute to the expanding body of clinical and real-world evidence supporting innovations in benign prostatic hyperplasia (BPH) treatment and rectal spacing to protect tissue during radiation treatment for prostate cancer.
“Understanding how leading treatment options perform—both in rigorous clinical trials and in everyday practice—is essential to empowering the future of healthcare for patients,” said Travis Gay, president and general manager of Teleflex Interventional Urology. “At Teleflex, we are deeply committed to advancing evidence-based innovation. Through ongoing real-world clinical trial research, we continue to support the safe and effective use of the UroLift™ System and Barrigel™ rectal spacer, helping physicians enhance outcomes and quality of life for patients.”
Clinical Study Presentations:
Teleflex and AUA are also hosting multiple educational events:
“Semi-Live Barrigel Case Review and Discussion” on Saturday, April 26, 2:35 – 3:05 pm in the Venetian Ballroom. In this AUA event, Dr. Varun Sundaram*, a urologist with Urology Austin, in Tex., will present insights from a recent Barrigel™ rectal spacer case, offering commentary and technical guidance on spacing procedures. This is an AUA event for which Teleflex provided funding.
The second annual advanced practice provider (APP) educational breakfast, “Engaging the APP in an Efficient Urology Practice” on Sunday, April 27, 6:45 – 8:00 am in Palazzo Ballroom B. Dr. Gregg Eure* with University of Virginia Health, Culpeper, Va.; Janelle Bunce*, PA-C with Advanced Urology Institute in Naples, Fla.; and Jamie Giovanelli*, PA-C with Urology of Virginia in Suffolk, Va. will discuss how to empower APPs to support the patient care pathway for patients with BPH and lower urinary tract symptoms. The discussion will center on the role of the APP in minimally invasive surgical therapies, including ultrasound gland sizing, if within scope of practice; in-office post procedure observations; and return post-op visits.
Prostate Health Symposium, “Transforming Quality of Life Through Personalized Prostate Care” on Sunday, April 27, 5:15 – 8:00 pm at Allegiant Stadium. In this first-ever combined UroLift™ System and Barrigel™ rectal spacer forum, a panel of experienced physicians—Dr. Zachary Klaassen*, urologic oncologist with Augusta University Medical Center/Georgia Cancer Center; Dr. Olubayo Tojuola*, urologist with Memorial Hermann Hospital at Houston, Tex.; and Dr. Ned Ruhotina*, a urologist with Associated Medical Professionals in Syracuse, N.Y.—will share real-world techniques for optimizing prostate radiation therapy with Barrigel™ rectal spacer and enhancing BPH outcomes with the UroLift™ System.
In addition to these events, presentations will take place daily at Teleflex booth 1401 as follows:
Presentations focused on Barrigel™ rectal spacer:
Zachary Klaassen, MD, MSC* – Getting Started with Barrigel Rectal Spacer
Saturday, April 26, 3:00 pm
Anne Hong, MD* – RWIs & Reversibility
Sunday, April 27, 11:00 am
Presentations focused on UroLift™ System:
David Sussman, DO, FACOS* – The Importance of Implant Density & Updates Regarding Recent Publications
Saturday, April 26, 1:30 pm
Silvia Secco, MD* – UroLift System: Surgical Experience & Competitive Advantages
Sunday, April 27, 1:30 pm
For more information about the UroLift System, visit www.UroLift.com, and for more information about Barrigel Rectal Spacer, visit www.Barrigel.com.
About the UroLift™ System
The UroLift™ System is a minimally invasive treatment for lower urinary tract symptoms due to benign prostatic hyperplasia (BPH). It is indicated for the treatment of symptoms of an enlarged prostate up to 100cc in men 45 years or older (50 years outside U.S.). The UroLift™ System permanent implants, which can be delivered during an outpatient procedure,5 relieve prostate obstruction without heating, cutting, destruction of, or removing prostate tissue. The UroLift™ System can be used to treat a broad spectrum of anatomies, including obstructive median lobe.6 It is the only leading BPH procedure shown to not cause new onset, sustained erectile or ejaculatory dysfunction.**7-8 A study conducted over 5 years showed a low retreatment rate of about 2-3% per year, or a total of 13.6% over the course of the study, demonstrating UroLift™ System durability.9 Most common side effects are temporary and can include hematuria, dysuria, micturition urgency, pelvic pain, and urge incontinence.10 Rare side effects, including bleeding and infection, may lead to a serious outcome and may require intervention. Individual results may vary. The prostatic urethral lift procedure (using the UroLift™ System) is recommended for the treatment of BPH in both the 2021 American Urological Association and 2022 European Association of Urology clinical guidelines. 500,000 men have been treated with the UroLift™ System in select markets worldwide.11 Learn more at www.UroLift.com.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
About Barrigel™ Rectal Spacer
Barrigel™ rectal spacer is the first and only hyaluronic acid rectal spacer that separates the prostate from the rectum to protect the rectum during radiation therapy treatment for prostate cancer.12 Barrigel™ rectal spacer is made from Non-Animal Stabilized Hyaluronic Acid (NASHA).13
Hyaluronic acid is a substance naturally present in the human body and is highly biocompatible and fully absorbable. NASHA has a proven history of safety and efficacy in a wide variety of medical applications in men, women and children worldwide.14-15
Barrigel™ rectal spacer has been proven to significantly reduce unwanted side effects from prostate cancer radiation therapy12 and is cleared for rectal spacing in the United States, Australia, and Europe.16 Barrigel™ rectal spacer is indicated for prostate cancer patients with T1-T3b disease. For more information about Barrigel™ rectal spacer, please visit https://barrigel.com/hcp/barrigel-control-matters.
Barrigel™ Rectal Spacer Important Safety Information
Barrigel™ rectal spacer is intended to temporarily position the anterior rectal wall away from the prostate during radiotherapy for prostate cancer and, in creating this space, it is the intent of Barrigel™ rectal spacer to reduce the radiation dose delivered to the anterior rectum. Barrigel™ rectal spacer is composed of biodegradable material and maintains space for the entire course of prostate radiotherapy treatment and is intended to be absorbed by the patient’s body over time.
Barrigel™ rectal spacer should only be administered by qualified and properly trained physicians with experience in ultrasound guidance and injection techniques in the urogenital/pelvic area.
As with any medical treatment, there are some risks involved with the use of Barrigel™ rectal spacer. Potential complications associated with the use of Barrigel™ rectal spacer include, but are not limited to: pain associated with Barrigel™ rectal spacer injection; needle penetration of the bladder, prostate, rectal wall, rectum, or urethra; injection of Barrigel™ rectal spacer into the bladder, prostate, rectal wall, rectum, urethra, or intravascularly; local inflammatory reactions; infection; urinary retention; rectal mucosal damage, ulcers, necrosis; bleeding; constipation; and rectal urgency. More information on indications, contraindications, warnings and instructions for use can be found in the Instructions For Use at www.barrigel.com. Individual results may vary.
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Forward-Looking Statements
Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements. Any forward-looking statements contained herein are based on our management’s current beliefs and expectations, but are subject to a number of risks, uncertainties and changes in circumstances, which may cause actual results or company actions to differ materially from what is expressed or implied by these statements. These risks and uncertainties are identified and described in more detail in our filings with the Securities and Exchange Commission, including our Annual Report on Form 10-K.
Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rüsch, UroLift, and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. All other trademarks are the property of their respective owners.
© 2025 Teleflex Incorporated. All rights reserved.
References
*Paid consultants of Teleflex.
**No instances of new, sustained erectile or ejaculatory dysfunction in the L.I.F.T. pivotal study
†Studies sponsored by Teleflex.
Contacts:
Teleflex
Lawrence Keusch
Vice President, Investor Relations and Strategy Development
investor.relations@teleflex.com
610-948-2836
Media Contact:
Glenn Silver
Partner National Media Relations Specialist
glenn.silver@finnpartners.com
646-871-8485
MAC03077-01 Rev A
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