HSS Hip and Knee Surgeon Bradford Waddell, MD, Named Chair of Young Arthroplasty Group

NEW YORKJune 14, 2018 /PRNewswire-USNewswire/ — Bradford Waddell, MD, hip and knee surgeon at Hospital for Special Surgery (HSS), has been named chair of the Young Arthroplasty Group (YAG) Committee in the American Association of Hip and Knee Surgeons (AAHKS).

Founded in 1991, the mission of AAHKS is to advance hip and knee patient care through education and advocacy.

“About two years ago, my colleague Dr. Jeff Lange and I sought to connect recently graduated hip and knee fellows for research and collaboration,” said Dr. Waddell. “We began with 10 to 12 surgeons, creating this new informal group and then brought the idea to AAHKS, where it has now grown into a larger group and committee.”

The mission of YAG is to connect young arthroplasty surgeons (with under 5 years of practice) in order to promote collaboration and young surgeon activity within AAHKS, with a particular focus on research, leadership and advocacy.

At the inaugural YAG meeting at AAHKS’ Annual meeting in 2017, over 100 surgeons were in attendance.

Dr. Waddell has been a member of AAHKS since 2014 and began his term as chair on June 1, 2018.  Previously, as a Health Policy Fellow for AAHKS, he was charged with finding new ways to bring younger surgeons into the organization. “Bringing our informal group to AAHKS was the perfect way to fulfill this duty,” says Dr. Waddell, who also practices in CT at HSS Stamford.

The YAG Committee’s co-founder, Jeffrey Lange, MD, orthopedic surgeon at Brigham and Women’s Hospital, serves as vice-chair, with 5 liaisons to different AAHKS committees comprising the rest of the committee.

“This group recruits young arthroplasty surgeons and works to encourage and empower them to take advantage of the full benefits of the organization whether it is in research, advocacy or leadership,” added Dr. Waddell. “I’m happy to say we’ve had 250 surgeons sign up for the group to date!”

Dr. Waddell joined HSS in October 2017; however he was no stranger to the organization as he completed his fellowship at HSS. He specializes in reconstruction of the hip and knee, specifically primary and revision hip and knee replacement. Devoted to getting his patients back to an active lifestyle, Dr. Waddell currently researches patient safety, new technologies and value-based care.

About HSS | Hospital for Special Surgery
HSS is the world’s leading academic medical center focused on musculoskeletal health. At its core is Hospital for Special Surgery, nationally ranked No. 1 in orthopedics (for the eighth consecutive year) and No. 3 in rheumatology by U.S. News & World Report (2017-2018). Founded in 1863, the Hospital has one of the lowest infection rates in the country and was the first in New York State to receive Magnet Recognition for Excellence in Nursing Service from the American Nurses Credentialing Center four consecutive times. The global standard total knee replacement was developed at HSS in 1969. An affiliate of Weill Cornell Medical College, HSS has a main campus in New York City and facilities in New JerseyConnecticut and in the Long Island and Westchester County regions of New York State. In 2017 HSS provided care to 135,000 patients and performed more than 32,000 surgical procedures.  People from all 50 U.S. states and 80 countries travelled to receive care at HSS. In addition to patient care, HSS leads the field in research, innovation and education. The HSS Research Institute comprises 20 laboratories and 300 staff members focused on leading the advancement of musculoskeletal health through prevention of degeneration, tissue repair and tissue regeneration. The HSS Global Innovation Institute was formed in 2016 to realize the potential of new drugs, therapeutics and devices. The culture of innovation is accelerating at HSS as 130 new idea submissions were made to the Global Innovation Institute in 2017 (almost 3x the submissions in 2015). The HSS Education Institute is the world’s leading provider of education on the topic on musculoskeletal health, with its online learning platform offering more than 600 courses to more than 21,000 medical professional members worldwide. Through HSS Global Ventures, the institution is collaborating with medical centers and other organizations to advance the quality and value of musculoskeletal care and to make world-class HSS care more widely accessible nationally and internationally.

SOURCE Hospital for Special Surgery

Related Links

http://www.hss.edu

DePuy Synthes Launches Innovative Nailing System Aimed at Improving Treatment of Femoral Shaft Fractures in the U.S.

WEST CHESTER, Pa.June 7, 2018 /PRNewswire/ — DePuy Synthes*, part of the Johnson & Johnson Medical Devices Companies**, today announces the U.S. launch of its Femoral Recon Nail System, a nailing system that provides new options for the surgical treatment of a wide variety of long thigh bone fractures. This new system builds on the company’s comprehensive trauma portfolio of innovative solutions designed to improve outcomes for patients with hip and femur fractures.

The overall annual number of femoral shaft fractures in the U.S. is estimated at approximately 90,000.1 The DePuy Synthes Femoral Recon Nail System is a fixation system that utilizes an intramedullary nail to repair femoral shaft fractures. The system provides a surgeon with a state of the art nailing system that is designed to provide stability and allow patients to move soon after surgery while optimizing patient outcomes.

The Femoral Recon Nail System offers surgical entry point and locking options to accommodate varying preferences, and enables surgeons to treat a broad range of complex fractures. The system also features radiolucent insertion handles that aim to reduce surgical complexity, facilitate intraoperative and X-ray visualization, and assist with guide wire placement.

“I believe the DePuy Synthes Femoral Recon Nail System offers the most streamlined insertion instruments on the market,” said Pete Nowotarski M.D., Professor Orthopaedic Surgery, University of Tennessee College of Medicine, Chattanooga & Orthopaedic Trauma Director, Erlanger Health Systems***. “This system, coupled with the most advanced design features in both the piriformis fossa and greater trochanter entry points, offers greater versatility in treating complex femur fractures.”

In addition, the DePuy Synthes system is also designed to address a potential operative complication called distal cortical impingement, which is often the result of the curve of the patient’s femoral anatomy being greater than the curve of the nail.2 The Femoral Recon Nail System addresses this issue as it is specifically designed to enhance anatomical fit3 by reducing the rate of nail curvature to more closely match the patient’s anatomy that may also further improve the patient’s experience.

“DePuy Synthes has a long history of innovation in the hip and femur fracture repair market with a comprehensive portfolio of implants that address a variety of patient needs,” said I.V. Hall, Global Platform Leader, DePuy Synthes Trauma. “This launch allows DePuy Synthes to offer the most comprehensive, best-in-class portfolio for hip and femur fractures as we continue to advance the standard of care for patients and improve the surgeon experience.”

About the Johnson & Johnson Medical Devices Companies
The Johnson & Johnson Medical Devices Companies’ purpose is to reach more patients and restore more lives. Having advanced patient care for more than a century, these companies represent an unparalleled breadth of products, services, programs and research and development capabilities in surgical technology, orthopaedics, and interventional solutions with an offering directed at delivering clinical and economic value to health care systems worldwide.

About DePuy Synthes
DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopaedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit www.depuysynthes.com.

*DePuy Synthes represents the products and services of DePuy Synthes, Inc. and its affiliates.
**The Johnson & Johnson Medical Devices Companies comprise the surgery, orthopaedics, and interventional solutions businesses within the Johnson & Johnson’s Medical Devices segment.
***Consultant to DePuy Synthes Trauma

Cautions Concerning Forward-Looking Statements

This press release contains “forward-looking statements” as defined in the Private Securities Litigation Reform Act of 1995 regarding the Femoral Recon Nail System. The reader is cautioned not to rely on these forward-looking statements. These statements are based on current expectations of future events. If underlying assumptions prove inaccurate or known or unknown risks or uncertainties materialize, actual results could vary materially from the expectations and projections of DePuy Synthes, any of the other Johnson & Johnson Medical Devices Companies and/or Johnson & Johnson.  Risks and uncertainties include, but are not limited to: uncertainty of commercial success; challenges to patents; competition, including technological advances, new products and patents attained by competitors; manufacturing difficulties and delays; product efficacy or safety concerns resulting in product recalls or regulatory action; changes to applicable laws and regulations, including global health care reforms; changes in behavior and spending patterns of purchasers of health care products and services; and trends toward health care cost containment. A further list and descriptions of these risks, uncertainties and other factors can be found in Johnson & Johnson’s Annual Report on Form 10-K for the fiscal year ended December 31, 2017, including in the sections captioned “Cautionary Note Regarding Forward-Looking Statements” and “Item 1A. Risk Factors,” and in the company’s subsequent Quarterly Reports on Form 10-Q and other filings with the Securities and Exchange Commission. Copies of these filings are available online at www.sec.govwww.jnj.com or on request from Johnson & Johnson. Neither the Johnson & Johnson Medical Devices Companies nor Johnson & Johnson undertakes to update any forward-looking statement as a result of new information or future events or developments.

1 Ng AC, Drake MT, Clarke BL, Sems SA, Atkinson EJ, Achenbach SJ, Melton LJ 3rd. Trends in subtrochanteric, diaphyseal, and distal femur fractures, 1984-2007. Osteoporos Int. 2012;23(6):1721-6.

2 Roberts JW, Libet LA, Wolinsky PR. Who is in danger? Impingement and penetration of the anterior cortex of the distal femur during intramedullary nailing of proximal femur fractures: preoperatively measurable risk factors. J Trauma Acute Care Surg. 2012;73(1): 249-254.

3 DePuy Synthes Trauma. Data on file. Analysis – Anatomical Study. #0000271671, 2017

092772-180607
© DePuy Synthes 2018. All rights reserved.

SOURCE DePuy Synthes

Related Links

http://www.depuysynthes.com

OrthAlign, Inc. Announces Clinical Milestone: 2,000 Cases with HipAlign®, Handheld Navigation for Direct Anterior Total Hip Replacement

Aliso Viejo, CA, June 05, 2018 (GLOBE NEWSWIRE) — OrthAlign, Inc., a privately held U.S. based medical device and technology company providing orthopedic surgeons with advanced precision technologies, announced another milestone achievement in its 2,000th HipAlign case. HipAlign was commercially launched in early 2018 for direct anterior total hip replacement.

HipAlign acts as a GPS for surgeons, using micro-electromechanical sensors like accelerometers and gyroscopes to guide hip replacement surgery, ensuring accuracy and alignment in cup placement and in tracking changes in leg-length. All of this happens in a phone-like device that sits in the surgeon’s hands and on their surgical instruments.

“We are excited to reach this milestone after a diligent limited-market release throughout 2017 and a full-launch following the AAOS annual meeting earlier this year,” said Eric B. Timko, Chief Executive Officer and Chairman of OrthAlign. “HipAlign’s rapid adoption proves there is high demand for a cost effective, minimally disruptive technology that provides increased accuracy and consistency in total hip replacements. With HipAlign, we’re able to expand our orthopedic offering and continue to provide surgeons and healthcare facilities clinically beneficial and economically friendly technologies.”

“After performing over 3,000 navigated total hip arthroplasties using a variety of different navigation devices and techniques, HipAlign has fit my workflow and made my accuracy the best by far,” said Dr. Matthew Heinrich, Orthopedic Surgeon at the Texas Institute for Hip and Knee Surgery. “I said goodbye to lead aprons due to a minimal x-ray need for my anterior total hips. My clinical results have been excellent. I have found the lower cost technique is easily portable, and have used it at five different facilities, including two surgery centers where I perform outpatient total hips.  My patients also appreciate that I utilize technology to help make sure that my accuracy is second to none!”

With no pre-operative CT-scan required, HipAlign delivers results without disruption. Patients receive the benefits of computer-guided surgery without additional time spent for pre-operative imaging procedures. With HipAlign, anatomic data is collected by the surgeon during the procedure, providing information not previously available using traditional hip surgery approaches.

About OrthAlign, Inc.

OrthAlign is a privately held medical device and technology company, developing advanced technologies that deliver healthier and more pain-free lifestyles to joint replacement patients, globally. We provide healthcare professionals with cutting edge, computer-assisted surgical tools that seamlessly and cost-effectively deliver vital data and clinical results to optimize outcomes for our patients. For more information regarding OrthAlign, please visit www.orthalign.com.

“ORTHALIGN®, ORTHALIGN PLUS®, KNEEALIGN®, KNEEALIGN® 2, HIPALIGN® and UNIALIGN™ are registered trademarks of OrthAlign, Inc.

Adam Simone
OrthAlign
asimone@orthalign.com

Local Surgeon First in Region to Use Groundbreaking Technology for Shoulder Replacement Surgeries

BETHESDA, Md.–(BUSINESS WIRE)–Orthopaedic surgeon Craig Miller, M.D., is now using a new technology to offer patients guided personalized surgery for their total shoulder replacements.

ExactechGPS® is the latest advancement in technology that provides surgeons with real-time visual guidance and alignment data in total shoulder surgery.

Similar to a navigation device in your car, this advanced platform provides a visual map of the patient’s joint on a screen, allowing surgeons to combine preoperative planning with intraoperative computer-assisted technology, to perform implant alignment specific to the patient’s needs.

“This cutting-edge technology allows me to virtually perform the patient’s surgery before going into the operating room,” said Dr. Craig Miller.

The technology’s preoperative planning tool allows surgeons to plan their cases in advance of the surgery through a virtual simulation. Surgeons can then execute their plan in real time during the surgery based on a 3-D anatomical model of the patient’s shoulder, making adjustments as needed.

ExactechGPS combines surgeon expertise with an advanced computer system to perform the patient’s shoulder surgery with a goal of improved accuracy and precision. Personalized for a patient’s unique bone structure and anatomy, ExactechGPS is designed to allow surgeons to decide where to remove bone and place the shoulder implant in the optimal position.

“Every patient’s anatomy is unique, and arthritis or injury can distort the anatomy even more, making an already challenging surgery even more difficult,” Miller said. “With ExactechGPS, I can now plan and execute shoulder replacement surgeries with more accuracy and reproducibility than ever before.”

Combined with the Equinoxe® Shoulder System which has demonstrated excellent biomechanics and outcomes in its more than 10 years of use1, surgeons are able to have the best of both worlds – a proven implant foundation1 with today’s most modern surgical technologies.

For more information about ExactechGPS or to schedule an appointment with Dr. Miller, call (301) 530-1010 or visit www.sportsdocmiller.com.

Additional information about the technology can be found at www.ExactechGPS.com.

Dr. Miller completed advanced fellowship training in sports medicine at the Kerlan Jobe Orthopaedic Clinic in Los Angeles, CA where he cared for all major sports teams. His areas of expertise include sports medicine, arthroscopic surgery of the shoulder and shoulder replacement surgery. Dr. Miller adds his ability to perform the first ExactechGPS guided total shoulder replacements in the Washington D.C. area, to numerous first time cutting edge and complex shoulder surgeries in the area. A graduate of Tufts University and George Washington Medical School, Dr. Miller completed his orthopaedic surgery residency at the Hospital for Joint Diseases Orthopaedic Institute / New York University in New York. From 2008-2016, Dr. Miller was an assistant team physician for the Washington Nationals.

References:

1. Data on file at Exactech, Inc.

Contacts

Exactech, Inc.
Allison Downey, APR, CPRC, 352-377-1140
Marketing Communications Manager
allison.downey@exac.com

LimaCorporate Celebrating 20 Years of Hip Revision Surgery

SAN DANIELE DEL FRIULI, ItalyMay 30, 2018 /PRNewswire/ —

LimaCorporate is proud to announce that the Revision Stem has achieved 20 years of clinical heritage in the Orthopaedic market. This anniversary consolidates LimaCorporate’s strong position in the Revision hip replacement market, also thanks to the combination with the Delta-One TT and Delta-Revision TT, the first 3D Printed Revision cups featuring LimaCorporate’s proprietary Trabecular Titanium technology. The only technology that boosts over 10 years of clinical heritage in Orthopaedics.

The Revision Stem allows Orthopaedic surgeons to separate the fixation aspect from biomechanics to provide an ideal stem option for a complex Revision situation. The conical stem design with longitudinal fins is designed to achieve a stable stem fixation, followed by the proper placement of the head with the different proximal body options, enhancing a real intraoperative flexibility. The Delta-One TT and Delta-Revision TT acetabular cups apply the same philosophy even to the acetabular side, thanks to the versatility in reconstructing the biomechanics offered by the spacer system, combined with the Trabecular Titanium proven reliability for the implant primary and secondary fixation.

“I started using the Revision Stem due to its simplicity in use and design inspired by the Wagner philosophy, in which a stable implant fixation is achieved through the conical stem profile with finned section. The Revision Stem combines this design with the advantages of the modularity and the wide availability of proximal bodies offered with different heights; its simplicity arises from the combination of different heights of the bodies of the neck with the stem offered with two lengths, allowing to solve the majority of Revision cases, in combination with Delta-One TT and Delta-Revision TT cups”, said Prof. Francesco Benazzo, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

The Revision Stem was fully introduced into the market in 1998, and its design is based on the experience gained by LimaCorporate with the LCR stem, released in 1982.  Available in more than 40 countries, the Revision Stem, during these 20 years, continues to represent a valid and solid option for many surgeons dealing with complex Revision surgeries who look for a reliable Revision Stem, supported by several papers published with long term follow-up. The Revision Stem has been used in more than 25,000 surgeries to date.

Most recently, LimaCorporate introduced the Revision Stem odd sizes, enlarging applicability criteria, and improved the Instrument Set layout reflecting the company’s ongoing commitment to deliver innovative, powerful, and robust solutions to Orthopaedic surgeons.

“The excellence of the Italian innovation and technology, combined with the great contribution coming from Orthopaedic surgeons are summarized in our Hip Revision portfolio. LimaCorporate is reconfirming its role in the Orthopaedic market with a special passion for complex cases, becoming the preferred choice for the experts in this field as our 3D Printed technology allows surgeons to address their patients’ needs with a new outlook, including that of custom devices from our ProMade division,” said Luigi Ferrari, CEO of LimaCorporate.

About LimaCorporate

LimaCorporate is a global medical device company providing reconstructive and custom-made Orthopaedic solutions to surgeons who face the challenges of improving the quality of life of their patients. Based in Italy, LimaCorporate is committed to the development of innovative products and procedures to enable surgeons to select ideal solution for every individual patient. LimaCorporate’s product range includes large joint revision and primary implants and complete extremities solutions including fixation.

For additional information on the Company, please visit: https://limacorporate.com/ .

SOURCE Limacorporate S.p.A.

CASE STUDY: One hospital’s quest to drive down the pricing of total joints

Getting the price right: Hospitals target variation in joint replacement (by Maria Castellucci for ModernHealth)

When HonorHealth leaders were looking for ways last year to decrease spending, the joint-replacement service line stuck out as a big opportunity.

The procedures are one of the Scottsdale, Ariz.-based system’s most popular—and lucrative—service lines and make up a significant percentage of supply chain costs, which account for nearly 40% of its $1.7 billion in revenue, according to 2016 financial data from Ernst & Young. But HonorHealth was paying more for parts than its competitors.

“If you haven’t been focused on the cost of your implants and the cost of your supplies, you get a natural creep up—we were simply paying too much. The prices we were paying exceeded what we believe is the market price,” said Alice Pope, chief financial officer at HonorHealth, which operates five hospitals in Phoenix and Scottsdale.

The system worked with Premier, the large group purchasing organization and consultancy, to figure out how its approximately 15 implant vendors compared to each other in costs. They found a lot of variability.

Costs were “anywhere from 10% to 20% higher than we should’ve been at price point,” said Timothy Miller, vice president of procurement and supply chain at HonorHealth. He added that eight of the vendors accounted for 80% of total implant costs, which are about $20 million.

Over several months, HonorHealth leaders worked with surgeons and vendors to negotiate better prices on implants. That effort was successful, to the tune of $1.5 million in annual savings.

HonorHealth is typical of providers nationwide that see joint-replacement surgery—usually a secure money-making machine for hospitals—as a prime opportunity to generate savings, especially as they face shrinking margins with declining reimbursement and patient volumes.

Tackling the wide variability in costs for joint-replacement surgery is a way to get ahead financially.

More than 1 million joint replacements are performed every year in the U.S., and by 2030 that number is expected to increase to more than 4 million as the number of senior citizens grows.

“Hospitals are looking for where they can trim. Supply costs are the largest costs, except labor, for a health system. People would much rather cut supply than cut someone’s job, period,” said Rob Austin, a director at Navigant.

And the largest portion of costs for joint-replacement procedures are supplies, specifically implants, according to a recent analysis from Premier. There is also significant variation in the cost of those expensive implants.

Premier found that among 350 hospitals, the average cost of primary knee implants was $4,464. Yet 50% of the hospitals paid between $4,066 and $5,609 on the devices.

The same group of hospitals paid an average of $5,252 for primary hip implants, with 50% paying between $4,759 and $6,463.

joint replacement surgeries

According to Premier, the 350 hospitals could save $23.7 million on knee implants and $19.1 million on hip implants if they paid the same amount as the top 25th percentile of hospitals. The cost data came from Premier’s database of 1,100 hospitals.

But convincing surgeons to switch the vendors and devices they are used to isn’t always an easy sell.

 

READ THE REST HERE

 

see HonorHealth Orthopedics Website here

OrthoAtlanta Surgeons Participate in Atlanta-Based Orthopedic Medical Mission to Honduras Providing Total Knee Replacements

ATLANTAMay 25, 2018 /PRNewswire/ — OrthoAtlanta orthopedic surgeons Michael J. Behr, M.D., and Peter J. Symbas, M.D., are two sports medicine physicians who have dedicated their careers to serving others, treating Atlanta-area patients with the most complex sports injuries, including those in need of total joint repair and joint replacement surgeries. These dedicated medical professionals are also known for generous donation of their time and talents to those in need in some of the most impoverished parts of the world. Dr. Behr and Dr. Symbas recently returned from a week-long medical mission trip in Honduras where their total joint replacement expertise contributed to a first-of-its-kind orthopedic surgical effort at Holy Family Surgery Center in May 2018.

As part of a brigade of 37 volunteer medical professionals specially trained in orthopedic surgery and surgical support, the Georgia-based team, including five orthopedic surgeons, surgical nurses and medical specialists, completed thirty-seven (37) total knee replacement surgeries in three days. This number was nearly one-third the total number of knee replacements performed the previous year throughout the entire country.

The remarkable Atlanta-based team traveled to Honduras as part of One World Surgery, a non-profit organization that founded and runs Holy Family Surgery Center in Honduras. Approximately one hour northeast of Tegucigalpa, the capital of Honduras, the surgery center is located on the property of Nuestros Pequeños Hermanos (NPH), a 2,000-acre ranch that serves as a loving home for some 500 orphaned, abandoned and disadvantaged children in Honduras. Providing educational and technical training for the youth, it’s a testament to the organization’s mission of sustainability and giving back that nearly half of the surgery center staff were NPH residents at one time. Surgeries at the center are needs-based and provided to pre-qualified patients of all ages.

Supplementing the services of this surgery center, One World Surgery coordinates brigades of volunteer medical experts for week-long service. Prior brigades have included heart surgery, OB/GYN and ophthalmology. Although orthopedic specialists have served the organization in the past, the Atlanta-based team, who have coined the name OneJoint, enabled the first-ever focused effort on total knee replacement specifically.

Preparation for the Georgia-based orthopedics team endeavor was many months in the planning. Crosslink Orthopedics, a local medical equipment supply company based in Norcross, Georgia, donated all the medical hardware for the joint replacements. Thomas Fleetwood from Crosslink reached out to orthopedic surgeons from several of Georgia’s leading orthopedic and sports medicine practices, including Dr. Symbas and Dr. Behr of OrthoAtlanta. Additional team members included skilled OR and post-operative nurses and medical technicians bringing the entire operating brigade to 37 people. The trip was entirely self-funded, from initial registration fees and flights to extra baggage fees needed for some 20 crates of equipment and supplies.

A practicing orthopedic surgeon with OrthoAtlanta for over 25 years, Michael J. Behr, M.D., has served on other medical mission trips in the past, including an Atlanta-based orthopedic group serving the country of Haiti. Dr. Behr’s first trip to Haiti was in 2010, the year of the deadly earthquake that killed thousands of people and left so much of the island in ruins. Inspired by the people of Haiti and the medical needs that continue today, Dr. Behr recently completed his ninth trip to Haiti in February 2018.

Dr. Behr, who today serves as the OrthoAtlanta medical director, shared insights into his draw to Haiti, and now Honduras. Dr. Behr said, “Impoverishment in Latin America, Central and South America is real and there is an ongoing need for quality medical care. The ability to return an individual in Honduras to a highly functional level with a ‘new knee’ does more than improve one individual’s quality of life – it affects the whole family and often an entire community.”

Peter J. Symbas, M.D., an OrthoAtlanta orthopedic surgeon with subspecialty certification in sports medicine, has also served on other medical mission trips, including a trip to Haiti in 2017. When asked why he goes on mission trips, Dr. Symbas commented, “I get so much more out of these trips than even the many people whose lives we touch. Nothing is more rewarding than the smiles we receive in return.” Dr. Symbas, who sees patients at OrthoAtlanta offices including Piedmont West, Kennesaw and Marietta, also serves as the chief medical officer for Atlanta United FC, Atlanta’sprofessional soccer team and is the chief of orthopedics for the Piedmont Clinic for Piedmont Healthcare.

The Atlanta-based team of orthopedics professionals who recently returned from a week’s accomplishments in Honduras is committed to returning to the country in 2019 as part of a sustained, long-term effort to provide orthopedic service to the Honduran people. Watch for future information about their upcoming commitment to service.

About OrthoAtlanta
OrthoAtlanta is one of the largest physician-owned orthopedic and sports medicine practices in the greater Atlanta, Georgia, area providing an integrated approach to delivering musculoskeletal care. With 38 physicians serving in 14 offices, the practice provides the highest level of patient care for injury or deformity of muscles, joints, bones and spine. OrthoAtlanta offers convenient accessibility to a full range of musculoskeletal surgeons, specialists and patient services including on-site physical therapy, pain management care, seven MRI imaging centers and workers’ compensation coordination. OrthoAtlanta Surgery Centers in Austell and Fayetteville provide cost-effective, same-day surgical procedures in an accredited outpatient center. Comprehensive operative and non-operative musculoskeletal care and expertise includes sports medicine, arthroscopic surgery, hip replacement, knee replacement, neck and spine surgery, elbow and shoulder surgery, hand and wrist surgery, foot and ankle surgery, physical medicine and rehabilitation, arthritis treatment, general orthopedics, work-related injuries and acute orthopedic urgent care.

Learn more at www.OrthoAtlanta.com.

For additional information, please contact Pat Prosser, Public Relations Manager, at OrthoAtlanta, 678-996-7254, or via email pprosser@OrthoAtlanta.com.

New GLOBAL UNITE Reverse Fracture Shoulder Implant from DePuy Synthes Addresses Unmet Needs in Complex Shoulder Fractures

WARSAW, Ind.May 22, 2018 /PRNewswire/ — DePuy Synthes*, part of the Johnson & Johnson Medical Devices Companies**, today announces the U.S. launch of the GLOBAL UNITE Reverse Fracture Shoulder, an innovative implant solution for shoulder reconstruction following complex fractures in patients with a grossly deficient rotator cuff. The new system is designed to provide increased flexibility for securely reattaching the bone to the implant, which is important for healing and function, and allowing biological fixation to the stem of the implant with a porous coating to help deliver a consistent surgical outcome. This new offering adds to DePuy Synthes’ commitment to innovative shoulder solutions that address the full continuum of shoulder disorders.

Shoulder fractures are the second most common fracture of the upper extremity, representing 10 percent of all fractures in those older than 65 years and are increasing in frequency as the elderly population grows.When patients with grossly deficient rotator cuffs suffer 3- or 4-part fractures in the upper arm bone (proximal humerus), it is often challenging to provide consistent treatment that helps healing and restores motion. Increasingly, surgeons are shifting to a reverse shoulder implant for more consistent and predictable outcomes for these patients.2

“I find that especially in my older patients whose bone quality doesn’t allow me to use the plates and screws typically used in a shoulder fracture procedure, fixation is an issue often due to weak rotator cuffs,” said Dr. Carl Basamania***, Orthopaedic Surgeon. “In my experience with the GLOBAL UNITE Reverse Fracture Shoulder System I get strong fixation and I feel a lot more confident about moving patients early so they get better motion and a quicker return to function.”

In a reverse total shoulder replacement, the ball and socket anatomy is reversed. A metal ball is fixed to the shoulder socket and a cup is fixed to the upper end of the humerus. Instead of using the rotator cuff to power the shoulder, the implant uses the deltoid muscle, which is the muscle at the top of the arm and shoulder.

The GLOBAL UNITE Reverse Fracture Shoulder provides:

  • Numerous suture holes, designed in the collar on top of the implant, and suture pockets around the backside of the implant to enhance bone fixation around the implant.
  • POROCOAT Porous Coating, a proprietary technology that consists of microscopic titanium beads. The porous structure supports biological fixation at the bone-implant interface.3
  • Backside pockets specially designed for bone graft, which may help promote bone growth and healing.
  • A streamlined instrumentation kit that is designed to improve cross compatibility across DePuy Synthes’ shoulder offerings.

“DePuy Synthes’ broad portfolio of shoulder solutions helps surgeons address a wide range of conditions from traumatic shoulder fractures to rotator cuff tears and instability,” said Stephanie Chamberlain, Global Platform Leader Mitek Sports Medicine and Shoulder. “We offer solutions for minimally invasive surgery and complete shoulder reconstruction, all designed to restore mobility for patients.”

The GLOBAL UNITE Reverse Fracture Shoulder is the latest implant offering under our GLOBAL UNITE Platform Shoulder System and builds on the company’s long history in innovative shoulder reconstruction. This includes the DELTA XTEND Reverse Shoulder System and most recently the launch of TRUMATCH Personalized Solutions Shoulder System pre-surgical planning software for shoulder reconstruction, which can be used in both reverse and anatomic total shoulder arthroplasty to optimize implant positioning and placement.

The GLOBAL UNITE Reverse Fracture Shoulder will launch in the U.S. beginning in the 2018 second quarter. For more information click here.

About the Johnson & Johnson Medical Devices Companies

The Johnson & Johnson Medical Devices Companies’ purpose is to reach more patients and restore more lives. Having advanced patient care for more than a century, these companies represent an unparalleled breadth of products, services, programs and research and development capabilities in surgical technology, orthopaedics, interventional solutions and specialty surgery with an offering directed at delivering clinical and economic value to health care systems worldwide.

About DePuy Synthes

DePuy Synthes, part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopaedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit www.depuysynthes.com.

*DePuy Synthes represents the products and services of DePuy Synthes, Inc. and DePuy Orthopaedics, Inc.

**The Johnson & Johnson Medical Devices Companies comprise the surgery, orthopaedics, and interventional solutions businesses within Johnson & Johnson’s Medical Devices segment.

***Dr. Carl Basamania is a consultant to DePuy Synthes Joint Reconstruction.

Cautions Concerning Forward-Looking Statements

This press release contains “forward-looking statements,” as defined in the Private Securities Litigation Reform Act of 1995, regarding the roll out of the GLOBAL UNITE™ Reverse Fracture Epiphysis (FX) Shoulder System. The reader is cautioned not to rely on these forward-looking statements. These statements are based on current expectations of future events. If underlying assumptions prove inaccurate or known or unknown risks or uncertainties materialize, actual results could vary materially from the expectations and projections of DePuy Synthes, Inc., any of the other Johnson & Johnson Medical Devices Companies and/or Johnson & Johnson.  Risks and uncertainties include, but are not limited to: uncertainty of commercial success; competition, including technological advances, new products and patents attained by competitors; challenges to patents; product efficacy or safety concerns resulting in product recalls or regulatory action; manufacturing difficulties and delays; changes to applicable laws and regulations, including global health care reforms; changes in behavior and spending patterns of purchasers of health care products and services; and trends toward health care cost containment. A further list and descriptions of these risks, uncertainties and other factors can be found in Johnson & Johnson’s Annual Report on Form 10-K for the fiscal year ended December 31, 2017, including in the sections captioned “Cautionary Note Regarding Forward-Looking Statements” and “Item 1A. Risk Factors,” and in the company’s subsequent filings with the Securities and Exchange Commission. Copies of these filings are available online at www.sec.govwww.jnj.com or on request from Johnson & Johnson. Neither the Johnson & Johnson Medical Devices Companies nor Johnson & Johnson undertakes to update any forward-looking statement as a result of new information or future events or developments.

Stanbury, SJ, Voloshin, I. Reverse Shoulder Arthroplasty for Acute Proximal Humeral Fractures in the Geriatric Patient Geriatr Orthop Surg Rehabil. 2011 Sep-Nov; 2(5-6): 181–186.

Gallinet D, et al. Improvement in shoulder rotation in complex shoulder fractures treated by reverse shoulder arthroplasty. J Shoulder Elbow Surg (2013) 22, 38-44.

Karageorgiou V, et al. Porosity of 3D biomaterial scaffolds and osteogenesis. Biomaterials 2005;26:5474-91.

© DePuy Synthes 2018. All rights reserved.

SOURCE DePuy Synthes

Related Links

http://www.depuysynthes.com

Exactech Provides Powerful Combination of Computer Technology and Award-Winning Instrumentation for Revision Knee Surgery

May 22, 2018

GAINESVILLE, Fla.–(BUSINESS WIRE)–Exactech, a developer and producer of bone and joint restoration products and biologic solutions for extremities, knee and hip, announced today that two of its leading technologies were used in combination for the first time to support a revision total knee surgery. Bernard Stulberg, MD, at the St. Vincent Charity Medical Center in Cleveland, Ohio, performed the first case using the new ExactechGPS® revision knee software application (RTKA), along with the company’s award-winning Truliant® Knee System instrumentation.

ExactechGPS is a surgeon-controlled, computer-assisted surgical technology that provides real-time, intraoperative data during total joint arthroplasty. The RTKA application helps orthopaedic surgeons address complex primary and challenging revision cases by providing insights into the diseased joint, feedback of anatomical and mechanical alignment, component sizing and resection validation.

According to Dr. Stulberg, a revision knee specialist, “I had the opportunity to experience firsthand the powerful potential of the Truliant instrumentation combined with ExactechGPS. The RTKA application revealed the existing abnormalities that caused my patient’s disability, and helped guide the sizing and positioning of the implants. The result was restoration of alignment and stability of a previously unstable total knee arthroplasty.”

ExactechGPS has a proven ability to achieve high accuracy and precision in resection alignment1 and is the only computer-assisted surgical technology to offer surgeons advanced ligament balancing options for RTKA. Fully integrated with the ExactechGPS technology, Exactech provides a comprehensive array of revision implant options, including metaphyseal cones, stems, augments and offset couplers.

“Exactech’s revision system leaves no doubt it can simplify procedures, while providing the framework to consistently deliver successful results for the wide range of complications in RTKA,” Stulberg said. “I am fully confident this will result in significant and meaningful benefits for both the surgeon and the patient.”

The Truliant Revision instrumentation has full U.S. market availability. The ExactechGPS RTKA application is currently in pilot launch with full availability expected in the second half of the year. For more information, visit www.TruliantKnee.com.

1. Dai Y et al. Total Knee Arthroplasty Using a Contemporary Computer Assisted Surgical System: A Review of Resection Alignment on 8,000 Clinical Cases. ORS Best Implant Poster Award. 2018.

About Exactech

Based in Gainesville, Fla., Exactech develops and markets orthopaedic implant devices, related surgical instruments and biologic materials and services to hospitals and physicians. The company manufactures many of its orthopaedic devices at its Gainesville facility. Exactech’s orthopaedic products are used in the restoration of bones and joints that have deteriorated as a result of injury or diseases such as arthritis. Exactech markets its products in the United States, in addition to more than 30 markets in Europe, Latin America, Asia and the Pacific. Additional information about Exactech can be found at http://www.exac.com.

Contacts

Exactech
Media Contact:
Priscilla Bennett, APR, 352-377-1140
VP of Corporate and Marketing Communications

Zimmer Biomet Announces Call for Applications for the 2018 Connected Health Innovation Award

WARSAW, Ind.May 21, 2018 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, today announced a call for applications for its second Connected Health Innovation Award. The Company is accepting applications from individuals, groups and organizations — including academia and industry — from all countries within Europe, the Middle East and Africa (EMEA) region. The award honors digital innovations that help solve unmet needs in the treatment of musculoskeletal and orthopaedic conditions. The winner will receive a €25,000 prize, an opportunity to pilot the technology in one of Zimmer Biomet’s partner hospitals in Europe and to promote the product in Zimmer Biomet’s Connected Health Innovation Lounge in Switzerland for one year.

“The Connected Health Innovation Award has been created to accelerate innovation in the digital health space focused on improving patient outcomes and efficiency in musculoskeletal healthcare,” said Marc Vogels, Zimmer Biomet’s Vice President of Marketing for EMEA Reconstructive and Zimmer Biomet Signature Solutions. “We are excited to acknowledge talented entrepreneurs and provide start-ups the opportunity to impact the way we are going to provide patient care in the future.”

Application Process
Applications for the second Zimmer Biomet Connected Health Innovation Award must be submitted online at www.connectedhealthaward.com/apply by June 15, 2018. Applicants must have a market-ready product, have obtained any necessary regulatory approvals, have first users willing to act as a reference and be able to demonstrate the value and core functionality of the product beyond concepts, papers, sketches, mockups, designs, formula and patents.

Applications will be reviewed by a jury composed of chief executive officers from Europe’s leading orthopaedic and musculoskeletal healthcare facilities. The jury will select five finalists. Finalists will be announced by June 30, 2018, and invited to the Zimmer Biomet EMEA headquarters in Switzerland to present their innovations and compete for the Award on July 10, 2018. Applications and additional information are available at http://www.connectedhealthaward.com.

About Zimmer Biomet
Founded in 1927 and headquartered in Warsaw, Indiana, Zimmer Biomet is a global leader in musculoskeletal healthcare. We design, manufacture and market orthopaedic reconstructive products; sports medicine, biologics, extremities and trauma products; office based technologies; spine, craniomaxillofacial and thoracic products; dental implants; and related surgical products.

We collaborate with healthcare professionals around the globe to advance the pace of innovation. Our products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Together with healthcare professionals, we help millions of people live better lives.

We have operations in more than 25 countries around the world and sell products in more than 100 countries. For more information, visit www.zimmerbiomet.com or follow Zimmer Biomet on Twitter at www.twitter.com/zimmerbiomet.

Cautionary Statement Regarding Forward-Looking Statements
This release contains forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.  Forward-looking statements include, but are not limited to, statements concerning Zimmer Biomet’s expectations, plans, prospects, and product and service offerings, including new product launches and potential clinical successes.  Such statements are based upon the current beliefs and expectations of management and are subject to significant risks, uncertainties and changes in circumstances that could cause actual outcomes and results to differ materially.  For a list and description of some of such risks and uncertainties, see Zimmer Biomet’s periodic reports filed with the U.S. Securities and Exchange Commission (SEC).  These factors should not be construed as exhaustive and should be read in conjunction with the other cautionary statements that are included in Zimmer Biomet’s filings with the SEC.  Forward-looking statements speak only as of the date they are made, and Zimmer Biomet disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.  Readers of this release are cautioned not to rely on these forward-looking statements, since there can be no assurance that these forward-looking statements will prove to be accurate.  This cautionary statement is applicable to all forward-looking statements contained in this release.

ZBH-Corp

SOURCE Zimmer Biomet Holdings, Inc.

Related Links

http://www.zimmer.com