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June 28, 2017 OrthoSpineNews

Paxeon Reconstruction, a manufacturer of best-in-class orthopedic products including derivative and emerging products, announces that Dr. Christian Christensen has completed a retrospective study that included 579 patients during a one-and-a-half-year period with at least three months follow-up on each patient.

Postoperative peri-prosthetic fractures are a common complication of direct anterior total hip arthroplasty. These femoral fractures generally require complex femoral revision. Dr. Christensen of Lexington, Kentucky has compared surgical outcomes of the anterior approach with two different implants. His results suggest that femoral implant design affects peri-prosthetic fracture rate following direct anterior total hip arthroplasty. These results were recently presented at the 9th Annual Emily Berend Adult Reconstruction Symposium at Duke University in Durham, NC in March 2016.

From February 2015 through June 2016, Dr. Christensen performed a total of 381 direct anterior total hip replacements using the flat tapered wedged femoral implant. In June of 2016, Dr. Christensen began utilizing the Origin by Paxeon Reconstruction. Origin is a dual taper, hydroxyapatite coated implant that was used in a total of 198 consecutive, anterior hips.

Each patient was monitored for three months after surgery to identify the frequency of peri-prosthetic femur fractures in each group. In the first cohort, 5 out of 381 patients (1.3%) sustained femur fractures at an average of 19.6 days after surgery. All five of these patients had a Vancouver type B2 fracture and required femoral revision. However, in the second cohort, when using the Origin, no patients sustained femoral fractures. These results suggest that using the Origin stem when doing the anterior approach will result in a lower postoperative fracture rate.

The Origin by Paxeon Reconstruction showed a reduced fracture rate than a plasma sprayed, flat-taper, wedged design. Dr. Christensen’s group continues to accumulate data and plans to submit the findings to the Journal of Arthroplasty this fall when the data reaches a clinically significant value.

Kyle Sineath, President of Paxeon Reconstruction said: “We are thankful to Dr. Christensen for bringing to light the fact that our implants can reduce or eliminate postoperative peri-prosthetic fractures as a complication of direct anterior total hip arthroplasty.”

______

About Paxeon Reconstruction

Paxeon Reconstruction builds best-in-class orthopaedic products, including derivative and emerging products. We collaborate with hospitals, health systems and physicians to create alignment and utilization of value-based solutions combined with efficiency models for today’s changing healthcare environment. Paxeon Reconstruction offer the world’s most comprehensive portfolio of orthopaedic products and services for joint reconstruction. Paxeon Reconstruction has a celebrated clinical history, and has evolved to meet the needs of the changing orthopaedics marketplace. The history that weaves the fabric of the Paxeon Reconstruction is one that is rich with innovation and demonstrates sustained leadership in an ever-changing landscape of patient and professional needs.


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June 28, 2017 OrthoSpineNews

WARSAW, Ind., June 28, 2017 /PRNewswire/ — Zimmer Biomet Holdings, Inc. (NYSE and SIX: ZBH), a global leader in musculoskeletal healthcare, today introduced its X-ray-based Patient Specific Instrument, X-PSI Knee System, which is the world’s first CE Marked surgical planning system that allows for patient specific implant positioning solely utilizing X-ray technology. X-PSI Knee System, for use with Zimmer Biomet’s flagship total knee brands, allows surgeons to use X-ray images to generate three-dimensional anatomic models. Zimmer Biomet’s Patient Specific Instruments Planner is then used to view the patient’s anatomy and develop a 3D customized surgical plan. That plan is used to manufacture patient-specific guides and bone models intended to improve implant fit and placement accuracy. This new generation of Zimmer Biomet Patient Specific Instruments can now leverage standard of care preoperative X-ray imaging instead of Magnetic Resonance Imaging (MRI) and Computerized Tomography (CT) scans.

“The use of innovative preoperative planning to enable patient-specific customization has the potential to become the gold standard in joint replacement care; however, its widespread clinical utility has been limited by its reliance on MRI and CT imaging, which are less accessible and not typically used for preoperative evaluation,” said Dan Williamson, Zimmer Biomet’s Group President, Joint Reconstruction. “Conversely, virtually every candidate for joint replacement surgery undergoes X-ray imaging, so we are thrilled to debut the first CE Marked, X-ray-based Patient Specific Instrument System, and extend the benefits of customized surgical planning to joint replacement patients across the European Union. This new offering was conceptualized and developed in collaboration with Dr. Mohamed Mahfouz, Professor of Biomedical Engineering at the University of Tennessee, who pioneered the original concept.”

X-PSI Knee System, the company’s fourth patient specific guide offering in its Personalized Solutions franchise, will be initially launched in five countries across the European Union.

“The growing use of MRI and CT-based planning software to customize implant placement has meaningfully improved patient outcomes in joint replacement surgery1-5,” said Raju S. Ghate, M.D., lead investigator of the X-PSI Knee System Investigational Device Exemption study, and a practicing orthopaedic surgeon at NorthShore University HealthSystem in Evanston, Ill. “Our study6 found that X-PSI Knee System, which uses X-ray imaging with Zimmer Biomet’s Patient Specific Instruments Planner, yields comparably high implant placement accuracy as MRI and CT-based systems, while significantly improving accessibility and clinical utility to a broader patient population.”

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.

References

  1. Kassab, S., Pietrzak, W. Intraoperative Benefits of Signature Personalized Patient Care in Total Knee Arthroplasty. White Paper. 2012.
  2. Lombardi, A., Berend, K., Adams, J. Patient-Specific Approach in Total Knee Arthroplasty. Orthopedics, 31(9), 927-930. 2008. doi:10.3928/01477447-20080901-21
  3. Schotanus, M., Boonen, B., Kort, N. Patient specific guides for total knee arthroplasty are ready for primetime; World J Orthop 2016 January 18; 7(1): 61-68 ISSN 2218-5836
  4. Silva, A., Sampaio, R., Pinto, E. Patient-specific instrumentation improves tibial component rotation in TKA. Knee Surgery, Sports Traumatology, Arthroscopy, 22(3), 636-642. 2013. doi:10.1007/s00167-013-2639-0
  5. Ng, V., et al. Comparison of custom to standard TKA instrumentation with computed tomography. Knee Surgery, Sports Traumatology, Arthroscopy. 2013. DOI 10.100/s00167-01302632-7
  6. Data on File at Zimmer Biomet. Protocol No. CSU2015-12K.

Disclaimer

X-Patient Specific Instrument, X-PSI Knee System, is not available in the U.S.

For complete prescription information, please contact Zimmer Biomet. Check for country product clearances and reference product specific instructions for use.  Not for distribution in France.

Cautionary Statement Regarding Forward-Looking Statements
This news 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 and uncertainties 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.  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, except as may be set forth in its periodic reports.  Accordingly, such forward-looking statements speak only as of the date made.  Readers of this news release are cautioned not to place undue reliance on these forward-looking statements, since, while management believes the assumptions on which the forward-looking statements are based are reasonable, 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 news release.

ZBH-Corp

SOURCE Zimmer Biomet Holdings, Inc.

Related Links

http://www.zimmerbiomet.com


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June 27, 2017 OrthoSpineNews

June 27, 2017

CASTEL SAN PIETRO, Switzerland–(BUSINESS WIRE)–Hirslanden Clinique La Colline, an internationally renowned clinic in Geneva and part of the first Swiss private clinic group Hirslanden, has optimized instrument management and implant stock for its total knee replacement (TKR) procedures by introducing Medacta’s Efficiency KneePack as the new standard in its practice. This advanced solution has helped Clinique La Colline to improve its supply chain and TKR procedure workflow, reducing the resources needed to manage procedures and enabling an even stronger focus on surgeons’ needs and patients’ well being.

“I was already using Medacta’s MyKnee Patient-Specific cutting blocks, which have helped me achieve higher dependability with greater ease and comfort of use in every case,” said Dr. med. Jean-Philippe Corsat.

“The Single Use Instruments, delivered brand new and unworn every time, have been a great addition,” added Dr. med. Marc Saudan. “I didn’t have to change my technique at all; after a few cases, I was completely used to them.”

Delivered sterile and ready for use, the Efficiency KneePack is the ultimate solution to implant Medacta’s GMK® Primary or GMK®Sphere in a TKR procedure. The Efficiency KneePack includes femur and tibia implants, MyKnee® Patient-Matched cutting blocks and GMK® Efficiency single use instruments.

“Thanks to Medacta’s Efficiency KneePack, we have drastically streamlined our logistic workflow,” said André Joyeusaz, a Hirslanden Clinique La Colline logistics department representative. “Instrumentation sets and implants are delivered just a few days before surgery, limiting the stock here at the surgical unit. Everything we need is packaged together, minimizing any source of error and helping us more swiftly to manage the logistics. This is very important on busy days. Any problem related to lost or worn out instruments has been eliminated, including paperwork.”

“The first thing that I noticed was that these instruments are much lighter than the metal ones,” said Veronique Guerraz, a perioperative nurse at the clinic. “They are also very intuitive to assemble and require less thought process to set them up. I can quickly find the instruments needed at each surgical step thanks to their different colors and the organized layout. The packaged sets arrive already sterile and organized, so we do not have to check them before surgery; we can just open the blisters and start using the instruments.”

In order to facilitate the best possible outcomes, Medacta utilizes pre-operative computer-based surgical planning software to deliver exactly what is needed for the surgical procedure, including the Efficiency Instruments and implants. This minimizes inventory constraints and provides the necessary inventory to complete the specific surgical procedure.

“It is Medacta’s mission to address surgeon and hospital needs with advanced technologies that encourage patient wellbeing and healthcare system sustainability,” said Francesco Siccardi, Executive Vice President of Medacta International. “The Efficiency KneePack embodies this as it addresses pain points at every level. We believe it will become the gold standard for clinics and ambulatory surgical centers looking to optimize their resources.”

Clinique La Colline is the first center to use Medacta’s Efficiency KneePack, and other centers are now following suit.

About Medacta® International

Medacta® International is a world leading manufacturer of orthopedic implants, neurosurgical systems, and instrumentation. Medacta’s revolutionary approach and responsible innovation have resulted in standard of care breakthroughs in hip replacement with the AMIS®system and total knee replacement with MyKnee® patient matched technology. Over the last 10 years, Medacta has grown dramatically by taking a holistic approach and placing value on all aspects of the care experience from design to training to sustainability. Medacta is headquartered in Castel San Pietro, Switzerland, and operates in over 30 countries.

To learn more about Medacta International, please visit: https://www.medacta.com.

Contacts

for Medacta International
Jill Bongiorni, 516-729-2250
Jill@torchcomllc.com


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June 23, 2017 OrthoSpineNews

June 22, 2017

GAINESVILLE, Fla.–(BUSINESS WIRE)–Exactech, Inc. (Nasdaq: EXAC), a developer and producer of bone and joint restoration products and biologic solutions for extremities, knee and hip, announced today that the company marked the first clinical use of recently approved shoulder, knee and hip replacement systems in Japan this quarter. These surgeries coincide with the series of new product introductions the company has reported in the U.S.

Exactech has gained regulatory approval to introduce additional products from each of its three major product segments to the Japanese market. The first Optetrak Logic® CR knee system was implanted on April 6 at Taketa Medical Association Hospital in Oita. The Novation® Crown Cup acetabular component debuted on April 26 in Ukubo City. The first Exactech total hip replacement surgery in Japan took place on May 16 at the Taketa Medical Association Hospital when a surgeon implanted the Alteon Tapered Wedge Stem along with the Crown Cup. The first Equinoxe Reverse Shoulder system was implanted June 5 at Sano Memorial Hospital.

“Exactech has maintained direct distribution in Japan since 2008 with consistent growth. These new product introductions are important milestones for Exactech in one of our key global markets,” said Exactech Vice President of International Sales and Market Development Daniel Berdat. “We are pleased to expand our offerings with these important innovations to better serve surgeons and patients.”

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.

A current investment profile on Exactech (Nasdaq: EXAC) is available online at http://www.hawkassociates.com/profile/exac.cfm. To receive future releases in e-mail alerts, sign up at http://www.hawkassociates.com/about/alert.

This release contains various forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, which represent the company’s expectations or beliefs concerning future events of the company’s financial performance. These forward-looking statements are further qualified by important factors that could cause actual results to differ materially from those in the forward-looking statements. These factors include the effect of competitive pricing, the company’s dependence on the ability of third party manufacturers to produce components on a basis which is cost-effective to the company, market acceptance of the company’s products and the effects of government regulation. Results actually achieved may differ materially from expected results included in these statements.

Contacts

Exactech, Inc.
Investor contacts
Jody Phillips, 352-377-1140
Executive Vice President of Finance & Chief Financial Officer
or
Hawk Associates
Julie Marshall or Frank Hawkins, 305-451-1888
EXAC@hawkassociates.com
or
Exactech
Media contacts
Priscilla Bennett, 352-377-1140
Vice President, Corporate & Marketing Communication


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June 20, 2017 OrthoSpineNews

American College of Rheumatology – For Immediate Release, June 16, 2017

ATLANTA – According to a new guideline released by the American College of Rheumatology (ACR) and American Association of Hip and Knee Surgeons (AAHKS), the risk of joint infection resulting from total hip and knee replacements can be reduced with careful management of anti-rheumatic medications during the perioperative process. The guideline represents the first time rheumatologists and orthopaedic surgeons have collaborated to develop recommendations.

“Periprosthetic joint infection remains one of the most common reasons for failure of hip and knee replacement,” said Bryan D. Springer, MD, an orthopedic surgeon at the OrthoCarolina Hip and Knee Center in Charlotte, N.C., and AAHKS Education Council Chair, who served as a co-principal investigator for the guideline project. “Because periprosthetic joint infections are associated with such high morbidity and mortality, we felt there was a dire need for perioperative management recommendations that could be subscribed to by both disciplines in order to provide arthritis patients with better outcomes.”

The guideline includes eight recommendations regarding when to continue, withhold and re-start medications commonly used to treat inflammatory rheumatic diseases (e.g., rheumatoid arthritis, spondyloarthritis and systemic lupus erythematosus), as well as the optimal perioperative dosing of glucocorticoids. Key recommendations for reducing the risk of infection include:

  • Discontinuing biologic therapy prior to surgery in patients with inflammatory arthritis.
  • Withholding tofacitinib for at least seven days prior to surgery in rheumatoid arthritis, spondyloarthritis and juvenile idiopathic arthritis patients.
  • Withholding rituximab and belimumab prior to surgery in all systemic lupus erythematosus patients undergoing arthroplasty.

In addition to rheumatology and orthopedic experts, a patient panel was incorporated to ensure the guidelines adequately represented patients’ concerns and preferences.

 

READ THE REST HERE


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June 20, 2017 OrthoSpineNews

BILLERICA, Mass., June 20, 2017 (GLOBE NEWSWIRE) — ConforMIS, Inc. (NASDAQ:CFMS), a medical technology company that offers knee replacement implants customized to fit each patient’s unique anatomy, today announced it has received FDA 510(k) clearance of the Company’s primary iTotal Hip replacement system.

“Having treated over 50,000 patients with customized knee replacement implants, ConforMIS brings over a decade of experience in patient-specific technology to the hip replacement market,” said Mark Augusti, Chief Executive Officer and President of ConforMIS.  “FDA clearance of iTotal Hip demonstrates the ability to apply our proprietary iFit® image-to-implant technology to other joints.  There has been a trend towards personalized healthcare and we believe patients expect and deserve personalized treatment.”

The ConforMIS iTotal Hip system features proprietary iFit technology similar to that used to design, manufacture and deliver customized knee implants.  The system utilizes ConforMIS’s patient-specific technology, single-use 3D printed instruments and just-in-time delivery model to create a system that requires limited reusable instruments.

“Standard hip replacement surgery can be challenging, presenting risks of dislocation, discrepancies in leg length and limited reproducibility,” said Scott Ball, MD, Department of Orthopaedic Surgery, University of California, San Diego and a member of the iTotal Hip design team.  “With the ability to achieve a better match to a patient’s own anatomy, the iTotal Hip system aims to address these shortcomings and improve patient outcomes.”

“We expect to leverage synergies with sales representatives, surgeons and hospitals upon limited launch, which is anticipated for 2019,” added Augusti.  “We are excited about the opportunity iTotal Hip represents in expanding our product portfolio to address a broader orthopedic market with our proprietary technology.”

In the United States, approximately 400,000 hip replacements were performed in 2016.  The global hip joint reconstruction market is projected at over $6B.

 

A photo accompanying this announcement is available at:

http://www.globenewswire.com/NewsRoom/AttachmentNg/a2f06ce1-6e8f-4f5e-b521-0a2f9b95aef4


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June 16, 2017 OrthoSpineNews

WARSAW, IN – June 15, 2017 – When it comes to evaluating a knee replacement’s long-term performance, registry data is extremely important, but not the only tool. Another well-established, but less universally-known, technique is Radiostereometric Analysis (RSA), an imaging technique that precisely measures implant migration and can help predict implant survivorship.1-3

Given the increasing utilization of, and demand for, RSA evidence in many countries, DePuy Synthes*, part of the Johnson & Johnson Family of Companies, made the decision in 2013 to incorporate RSA into its ATTUNE® Knee Evidence Generation Program strategy, and today announced results of the first and recently-completed two-year investigator-initiated study that evaluated the implant fixation of the ATTUNE Knee tibial base using RSA.4

In this study, conducted by the Canadian RSA Network, tiny beads of less than 1 mm were inserted into the bone surrounding the ATTUNE Knee implant at the time of surgery. These beads, made of tantalum, a metal that is well tolerated by the body, served as markers by which X-rays were used to detect 3D changes in the position of the tibial base relative to the bone over time (implant fixation). This particular study included 30 patients, which is a statistically appropriate sample size in RSA research.

Results of this study, presented at the Canadian Orthopaedic Association Annual Meeting (June 15-18, 2017, Ottawa, CA)4, showed that the ATTUNE Knee tibial base migrated an average of 0.02 mm in the superior-inferior (up and down) direction over 24 months, with an average maximum total point motion of 0.21 mm. Applying published criteria which helps interpret how RSA data can help predict future revision rates1,3, this study’s 2-year RSA results showed that the ATTUNE Knee tibial base achieved stable fixation by demonstrating average micromotion of 0.17 mm between one and two years. This is consistent with implants that have acceptable revision rates due to aseptic loosening.1

“These results are another component of the breadth of data that continue to be generated around the ATTUNE Knee,” said Kim Dwyer, Ph.D., Clinical Research Director, Knees, DePuy Synthes Joint Reconstruction. “The importance of RSA is that it can help predict an implant’s long-term performance while larger and longer survivorship studies are underway.”

Dwyer added that the importance of RSA continues to move from its well-established roots in the Nordic countries of Europe to other parts of the world, including North America. RSA Networks like the Canadian RSA Network can play a pivotal role in enhancing evidence-generation timelines, standardizing methodologies, increasing diversity by including more patients at different sites, and meeting the needs of stakeholders who value fixation evidence.


About DePuy Synthes
DePuy Synthes, part of the Johnson & Johnson Family of Companies, provides one of the most comprehensive portfolios of orthopaedic solutions in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, neurological, 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.

©DePuy Synthes 2017. All rights reserved.
DSUS/JRC/0617/2182
June 2017

  1. Ryd L, Albrektsson BE, Carlssson L, Dansgård FHerberts P, Lindstrand A, Dansgård, Regner L, toksvig-Larsen S, Roentgen stereophotogrammetric analysis as a predictor of mechanical loosening of knee prostheses. J Bone Joint Surg Br 1995;77:377-83.
  2. Kärrholm, J, Gill, RHS, and Valstar, ER, The History and Future of Radiostereometric Analysis. Clin Orthop Rel Res, 2006: 448, 10-21.
  3. Pijls BG, Valstar ER, Nouta KA, Plevier JW, Fiocco M, Middeldorp S, Nelissen RG, Early migration of tibial components is associated with late revision: a systematic review and meta-analysis of 21,000 knee arthroplasties. Acta Orthop 2012;83:614-24.
  4. Richardson, G, Turgeon, T, Gascoyne, T, Laende, E, Bohm, E, Dunbar, M. Stability assessment of a new knee replacement product using radiostereometric analysis. Poster Presentation at the Canadian Orthopaedic Association Meeting, Ottawa, Ontario, 15-18 June 2017.

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June 15, 2017 OrthoSpineNews

NEWPORT BEACH, CA–(Marketwired – Jun 14, 2017) – ORHub, Inc. (OTC: ORHB), a cloud-based medical software company established as the Operating Room Hub for data and analytics, today announces that it is launching its new service module for hip and knee surgical procedures, July 2017. With over 100 million surgeries performed in the U.S. every year and growing, this new service line significantly expands the addressable market for the Company’s dynamic analytics capabilities and Surgical Resource Management platform.

“The launch of this new module follows the successful launch of our spine module, which for the past eight months has been in continuous use in two nationally recognized hospitals, achieving overwhelming success. Our hips and knees module is the second of many on our technical road map that will allow us to exponentially grow our addressable market and take advantage of the resulting opportunities,” says ORHub CEO Colt Melby.

According to the Agency for Healthcare Research and Quality, more than 300,000 total hip replacements and 600,000 knee replacements are performed each year in the United States, a figure expected to grow by 13.19 % per year for the next five years. ORHub’s hip and knee service module presents to this growing market unprecedented procedure data and advanced analytics.

ORHub’s Surgical Resource Management software transforms the OR into a highly efficient information center that provides the ability to track and monitor surgical implants, compare material costs, and identify physician and financial impacts in the operating room at the point of surgery. The software also tackles the data chaining needed for cost, usage and eventual outcome correlation in all surgeries without heavy IT investments in infrastructure.

The Company’s spine service line is currently being used for all spine cases in the operating room of two major hospitals in Southern California, where the company recently announced it has successfully collected data from more than 500 surgeries (http://nnw.fm/DTkw3), a number that continues to grow on a daily basis. The data collected provides the hospitals valuable insight that helps identify user needs and make near real-time data driven decisions to improve profitability and the quality of patient care.

“We look forward to updating shareholders on our progress as we continue to build new service modules at a rapid pace conducive to increased corporate value,” says Melby.

ORHub, Transforming the Business of Surgery
The ease of deployment is weeks instead of years, and the power to provide process data for illumination of costs and improvement, gives OR directors and hospital administrators powerful new capabilities to transform the business of surgery. ORHub is capable of agile, low-cost integration with a hospital’s system of choice to complement existing capabilities and provide analytics that are currently not available in the OR suite as a comprehensive view of each episode of care. This puts decision making power at the fingertips of directors and administrators as well as physicians and vendors.

Its case-based subscription model also transforms the business of surgery by moving the infrastructure costs from a CAPEX budget cycle into the operational budget of the OR director. A hospital’s time to insight is transformed from months or weeks to minutes, and the revenue cycle is compressed so time to money is quicker for substantial cash flow improvement.

About ORHub, Inc.
ORHub is a cloud-based software company focused on delivering performance-based medicine at the speed of surgery. The system is in full operation and in daily use at two major hospitals in Southern California.

ORHub enables all parties involved in surgical care to work together to organize, deliver, measure and reimburse in a single uniform process. ORHub’s cloud capabilities also provide a bridge for hospitals in their hybrid cloud strategies, integrating with EHRs and other systems as requested. ORHub is an agile answer for hospitals looking to unlock the power of the OR. Its case-based subscription revenue model also transforms the economics of hospital software from a CAPEX to an OPEX budgeting process.

The need for ORHub is clear. Health care comprises more than 17% of US GDP at over $3 trillion per year. With costs rising every year due to an aging population and more expensive treatments, providers are under severe pressure to become more efficient and reduce costs from payers who are aggressively reducing reimbursements and moving away from fee-for-service and toward performance-based reimbursement. ORHub enables providers to thrive in this new environment by addressing the single largest segment of health care, which is surgical care. ORHub replaces numerous legacy systems with a 360-degree system that is focused on tracking cost from diagnosis to discharge. ORHub has offices in Phoenix, Arizona; Newport Beach, California; and Bellevue, Washington.

Forward-Looking Statements
This news release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Although the Company believes the expectations reflected in any forward-looking statements are based on reasonable assumptions, it can give no assurances that its expectations will be attained. Such statements are inherently uncertain, and actual results and activities may differ materially from those estimated or projected. Certain factors that can affect the Company’s ability to achieve its anticipated results include, among others, uncertainties inherent in the development of a new software product business.

CONTACT INFORMATION


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June 14, 2017 OrthoSpineNews

OrthAlign, Inc., a privately held U.S.-based medical device and technology company providing orthopedic surgeons with advanced precision technologies, announced today the first set of KneeAlign® cases completed for total knee arthroplasty (TKA) in Greece. These cases were completed by Athens-based orthopaedic surgeon Spyridon Armpis, MD, MSc and continue to reflect the rapid adoption of OrthAlign’s handheld precision alignment and positioning technologies, by surgeons throughout the world.

OrthAlign provides highly accurate, computer-assisted, handheld technologies for surgeons to receive real-time, actionable data for precise alignment and positioning of components in total knee, unicondylar knee, and total hip (both posterior and anterior) arthroplasty surgeries. Over 15 peer-reviewed clinical studies have been published to date, validating OrthAlign’s accuracy, simplicity of use, and benefits in recovery for the patient.

“The accuracy and simplicity of KneeAlign surprised me,” said Dr. Armpis. “The technology not only gives me confidence in my cuts, but allows me to elevate my standard of care for patients. I no longer have to invade the intramedullary canal, I don’t have to make multiple cuts, and it makes me, my OR staff, and the recovery process for my patients more efficient. Going forward, KneeAlign will be a key part of my practice and my patient-tailored recovery program, as I am convinced it will give my patients the best possible outcomes.”

In a published TKA clinical study by Denis Nam, M.D. (Rush University Medical Center, Chicago, IL), significant differences favoring the use of KneeAlign vs. conventional Computer Assisted Surgery were found with regard to the accuracy of femoral component alignment, with 94.9% of patients in the KneeAlign cohort having an alignment within 2° of neutral vs. 92.5% in the CAS cohort. There was also a significant difference in overall mean mechanical alignment of the limb, with 92.5% of patients within 3° of neutral mechanical axis in the KneeAlign cohort vs. 86.3% in the CAS cohort.

In another study by Dr. Nam (conducted as a randomized controlled trial, consisting of five different surgeons), it was found that KneeAlign decreases the incidence of outliers for tibial component alignment in both the coronal and sagittal planes, and improves the surgeon’s ability to achieve a specific, intraoperative goal, compared to conventional, tibial extramedullary (EM) alignment guides in TKA. In the KneeAlign cohort, 95.7% of tibial components were within 2° of perpendicular to the tibial mechanical axis and 95% of tibial components were within 2° of a 3° posterior slope (compared to 68.1% and 72.1% in the EM cohort, respectively).

“OrthAlign is delighted to have successfully completed its first KneeAlign cases in Athens,” said James Young Kim, OrthAlign’s Vice President and General Manager of International. “As Greece comprises of 25,000 TKAs annually, it is seeking a cost-effective solution that helps surgeons achieve quicker, more precise results for their patients. Dr. Armpis approached us with this strong desire and was the first surgeon in Greece to experience the power of KneeAlign. As OrthAlign continues to focus on expanding customer reach and portfolio expansion, we welcome the country of Greece to the OrthAlign family and look forward to further introducing it in the Greek orthopaedic market.”

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 http://www.orthalign.com.

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


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June 13, 2017 OrthoSpineNews

BILLERICA, Mass., June 13, 2017 (GLOBE NEWSWIRE) — ConforMIS, Inc. (NASDAQ:CFMS), a medical technology company that offers joint replacement implants customized to fit each patient’s unique anatomy, today announced the publication of a retrospective study comparing adverse events rates and cost of care for total knee arthroplasty (TKA) patients treated with either customized individually made (CIM) implants or standard off-the-shelf (OTS) implants.  Results were published in the peer-reviewed journal Arthroplasty Today on June 8, 2017.

According to the study results, a smaller percentage of TKA patients treated with customized implants experienced adverse events at both discharge (3.3% vs OTS 14.1%; P = .003) and 90 days after discharge (8.1% vs OTS 18.2%; P = .023).  A greater proportion of patients who received customized implants were discharged in less than 3 days (42.1% vs OTS 30.3%; P = .037).  In addition, a smaller percentage of patients treated with customized implants (4.8% vs OTS 16.4%; P = .003) were discharged to a rehabilitation center or other post-acute care facility.  Further, fewer patients treated with customized implants (2.4% vs OTS 11.6%; P = .005) required blood a transfusion.

Furthermore, the total average real hospital costs between the CIM and OTS groups were nearly identical (customized implant $16,192 vs OTS $16,240; P = .913), suggesting that patients with customized implants received improved hospital outcomes at no additional cost to the hospital.  However, risk-adjusted per patient total cost of care showed a net savings of $913.87 (P = .240) per patient for the customized implant group for bundle of care, including the preoperative computed tomography scan, TKA hospitalization, and discharge disposition.  Follow-up care costs demonstrated a savings of $1,313 (customized implant $5,048 vs OTS $6,361; P = .007).

“Our results in this single-site population of patients illustrate that treatment with a customized implant led to significantly lower transfusion rates, fewer adverse events and reduced need for discharge to a rehabilitation facility or post-acute care facility,” said Steven Culler, PhD, a healthcare economist at Emory University.  “We also found that improved outcomes among patients treated with customized implants were achieved without increasing overall costs and that post-discharge costs were significantly lower among patients treated with customized implants.”

In this study, which was financially supported by ConforMIS, researchers completed a retrospective review of outcomes and costs for 248 consecutive TKA patients treated at a single institution and by the same surgeon.  All surgeries occurred between April 1, 2010, and November 11, 2013 based on consistent intraoperative protocols.  Patients received either a customized knee implant (designed and developed based on their unique anatomy (n=126)) or an OTS implant selected from a range of pre-manufactured sizes (n=122). Study data were collected from patients’ medical record or the hospital’s administrative billing record.

When controlling for gender, age, body mass index (BMI) and selected comorbid conditions, patients in the OTS arm were 5.5 times more likely to be discharged to a rehab or post-acute care facility. Patients treated with OTS implants were also 4.6 times more likely to require blood transfusion and 4.4 times more likely to experience an adverse event.

“This study provides compelling data indicating that patients treated with customized total knee implants achieve better outcomes on several important measures without increasing real hospital costs and while reducing the average total cost of the episode of care and the average cost of follow-up care,” said Mark Augusti, Chief Executive Officer and President of ConforMIS. “These findings further demonstrate the benefits of customized total knee implants technology to patients, surgeons, hospitals and payers.  Additionally, they are part of an important and changing conversation about the role of total knee implants in the delivery of better outcomes at lower costs – a conversation that we are committed to pursuing.”

About ConforMIS, Inc.

ConforMIS is a medical technology company that uses its proprietary iFit Image-to-Implant technology platform to develop, manufacture and sell joint replacement implants that are individually sized and shaped, or customized, to fit each patient’s unique anatomy. ConforMIS offers a broad line of customized knee implants and pre-sterilized, single-use instruments delivered in a single package to the hospital. In clinical studies, ConforMIS iTotal CR demonstrated superior clinical outcomes, including better function and greater patient satisfaction, compared to traditional, off-the-shelf implants. ConforMIS owns or exclusively in-licenses approximately 450 issued patents and pending patent applications that cover customized implants and patient-specific instrumentation for all major joints.

For more information, visit www.conformis.com. To receive future releases in e-mail alerts, sign up at http://ir.conformis.com/.

Cautionary Statement Regarding Forward-Looking Statements

Any statements in this press release about future expectations, plans and prospects for ConforMIS, including statements about ConforMIS’ clinical strategy, the potential clinical, economic or other impacts and advantages of using customized implants, the changing view of CIM v. OTS implants, as well as other statements containing the words “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” or “would” and similar expressions, constitute forward-looking statements within the meaning of the safe harbor provisions of The Private Securities Litigation Reform Act of 1995. We may not actually achieve the plans, intentions or expectations disclosed in our forward-looking statements, and you should not place undue reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements we make as a result of a variety of risks and uncertainties, including risks related to our clinical studies and the other risks and uncertainties described in the “Risk Factors” sections of our public filings with the Securities and Exchange Commission. In addition, the forward-looking statements included in this press release represent ConforMIS’s views as of the date hereof. ConforMIS anticipates that subsequent events and developments may cause ConforMIS’s views to change. However, while ConforMIS may elect to update these forward-looking statements at some point in the future, ConforMIS specifically disclaims any obligation to do so. These forward-looking statements should not be relied upon as representing ConforMIS’s views as of any date subsequent to the date hereof.

CONTACT:

Media contacts:
Bill Berry
Berry & Company Public Relations
Bberry@berrypr.com
(212) 253-8881

Lynn Granito
Berry & Company Public Relations
Lgranito@berrypr.com
(212) 253-8881

Investor contact
Oksana Bradley
ir@conformis.com
(781) 374-5598