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Orthopedic Coordinated Registry Network (Ortho-CRN): advanced infrastructure for real-world evidence generation
  1. Laura Elisabeth Gressler1,
  2. Vincent Devlin2,
  3. Mary Jung2,
  4. Danica Marinac-Dabic2,
  5. Art Sedrakyan3,
  6. Elizabeth W Paxton4,
  7. Patricia Franklin5,
  8. Ronald Navarro4,
  9. Said Ibrahim3,
  10. Jonathan Forsberg6,7,
  11. Paul E Voorhorst8,
  12. Robbert Zusterzeel9,
  13. Michael Vitale10,
  14. Michelle C Marks11,
  15. Peter O Newton12 and
  16. Raquel Peat2
  1. 1Department of Pharmaceutical Evaluation and Policy, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA
  2. 2Center for Devices and Radiological Health, United States Food and Drug Administration, Silver Spring, Maryland, USA
  3. 3Healthcare Policy and Research, Weill Cornell Medical College, New York, New York, USA
  4. 4Southern California Permanente Medical Group, Kaiser Permanente, Harbor City, California, USA
  5. 5Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA
  6. 6Department of Defense Osseointegration, Murtha Cancer Center, Bethesda, MD, USA
  7. 7Orthopaedic Oncology, Sibley Memorial Hospital, Johns Hopkins University, Washington, DC, USA
  8. 8DePuySynthes Companies, Warsaw, Indiana, USA
  9. 9Center for Drug Evaluation and Research, United States Food and Drug Administration, Silver Spring, Maryland, USA
  10. 10Pediatric Spine and Scoliosis Service, Morgan Stanley Children's Hospital, New York, New York, USA
  11. 11Setting Scoliosis Straight Foundation, San Diego, California, USA
  12. 12Orthopedics & Scoliosis, Rady Children's Hospital, San Diego, California, USA
  1. Correspondence to Dr Art Sedrakyan; ars2013{at}

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Key messages

  • There is a need to advance the medical device ecosystem and build a national infrastructure for faster, better and less costly evidence generation for orthopedic technologies.

  • The Orthopedic Coordinated Registry Network (Ortho-CRN) attempts to address gaps in clinical evidence to reliably capture real-world data for a range of orthopedic devices by promoting the development of systematic collaboration among existing national orthopedic registries, claims databases and other data sources.

  • Continuously addressing stakeholder needs, expanding the scope of the Ortho-CRN, amalgamating data sources and developing objective performance criteria is crucial for the generation of high-quality real-world evidence needed for the assessment of orthopedic devices.


Musculoskeletal conditions affect nearly three out of four persons aged 65 and older, one out of every two persons aged 18 and above and are responsible for up to one-third of pediatric medical problems.1 2 The aging of the baby boomer generation, the increased demand for orthopedic procedures, and higher rates of osteoarthritis diagnoses have led to an exponential growth in orthopedic device-based procedures.3–8 Total joint arthroplasty (TJA), one of the fastest-growing and most commonly performed surgeries, has a projected growth rate of 284% for total hip arthroplasty and 401% for total knee arthroplasty by 2040.9–11

The burden of treating musculoskeletal diseases has increased and accelerated medical product development. Each innovation shares a common goal, to repair, reconstruct, and replace musculoskeletal structures compromised by joint diseases, trauma, deformities, tumors, infections and painful orthopedic conditions in order to improve patients’ physical function, self-image and ability to work. To meet the growing demand for the treatment of musculoskeletal conditions and ensure that orthopedic patients have access to high-quality, safe and effective medical devices, a different approach to support regulatory decision making is required. This article aims to summarize the role and next steps of the Orthopedic Coordinated Registry Network (Ortho-CRN) in the generation of real-world evidence (RWE) for the assessment and regulation of orthopedic devices.

The role of real-world data and device regulation

For manufacturers to receive regulatory approval or clearance for a medical device, available evidence on the safety and effectiveness of orthopedic devices is assessed and based on non-clinical and clinical studies. However, clinical studies are often hindered by small sample sizes, limited follow-up and potential conflicts of interest among various stakeholders. In this complex environment, there is an increased need to advance the medical device ecosystem and build a national infrastructure to address the performance of orthopedic devices.12 In some cases, real-world data (RWD) derived from sources outside of typical clinical trial settings, including electronic health records (EHRs), claims data, medical device and disease registries, patient-generated health data and data gathered through personal devices and health applications, may be of sufficient quality to evaluate the safety and effectiveness of devices. RWD provides insight into the use and performance of the device in clinical practice, can capture a broader variety of patients, and can capture longer follow-up times if found to be fit-for-purpose. RWD can generate RWE to inform and support regulatory decisions, associated core research and surveillance infrastructure.13 The evaluation of the performance of orthopedic devices using RWE can help make healthcare systems more efficient, aid in quality improvement and provide important evidence for decision-makers.14

CRNs play a pivotal role in developing high-quality evidence due to their ability to creatively organize real-world data collection systems, such as registries, that are relevant to the evaluation of medical devices, establish and grow the capacity of existing data sources, and leverage data sources that are created for other purposes such as documentation and billing for care.15–17 The efficient capture of needed evidence makes CRNs a strong source of real-world data needed to evaluate the use of medical devices during clinical care.18

Development of the Ortho-CRN

In September 2017, the Medical Device Epidemiology Network (MDEpiNet) launched the Ortho-CRN to build on the successes of the previously established International Consortium of Orthopedic Registries and promote the development of novel test methods, infrastructure and partnerships within the USA.19 This collaboration of data partners and orthopedic community led to the creation of a CRN tasked with addressing the gaps related to orthopedic device evaluation across their total product life cycle. With the help of the MDEpiNet coordinating center, this organization leads the establishment of a broad infrastructure, through the systematic collaboration among existing national orthopedic registries, claims databases, and EHR data. The overarching objective of the Ortho-CRN is to promote the sharing of knowledge regarding best practices for data collection, linkages with other data systems, analytics, the dissemination of findings, and the development of innovative approaches for robust, relevant and reliable clinical evidence generation throughout the medical device total product lifecycle.19

These collaborations allow existing orthopedic registries to expand and further serve as high-quality data sources for comparative effectiveness research, aid in the generation of useful reports to health systems, conduct signal detection as well as implant tracking, and enhance the overall regulatory process through active surveillance. The Ortho-CRN is made possible by successful collaborations and partnerships among registries, regulatory agencies, and academic institutions.20–24 ,25 All included registries (summarized in online supplemental appendix B) capture a variety of orthopedic procedures and include over 2 million patients and up to 17 years of follow-up data.

Aligning stakeholder motivations to leverage current orthopedic registries

To maximize the capabilities and applications of the Ortho-CRN, the needs and challenges faced by patient groups, clinicians, registry leaders, medical device manufacturers, medical device regulators and other stakeholders must be assessed and accounted for. From a patient’s perspective, registries incorporated within the CRN provide an opportunity to capture outcomes that are meaningful to patients, including patient preference data and can be leveraged to support patients in numerous ways. This includes supporting patient engagement and education, aiding in the understanding of patient perspectives, in the identification of preferred areas for research prioritization, and assisting in shared decision making between patients and clinicians.26 Within the clinical community, the focus is primarily on the value of registries in relation to quality performance measurement and reporting, as well as documentation of the efficiency of care. The ability of registries to provide actionable feedback to clinicians regarding quality-of-care metrics, performance benchmarks and patient outcomes is crucial. Challenges identified by clinicians, researchers, and registry leaders are primarily related to data collection and curation, including preservation of patient privacy, the associated time, cost, personnel, and accuracy issues associated with data collection.27

Medical device industry representatives identified the potential benefits and cost saving of a single source of data available to all companies, as this avoids the need for dual data entry by leveraging an existing network of data sources.28 These data could be used for postmarket device surveillance when postmarket data collection is required by Food and Drug Administration (FDA) or other regulatory authorities. Registries can also supplement an existing company’s claims data to increase long-term follow-up, capture additional outcomes including radiographic imaging, support clinical trial designs and mitigate shortcomings and biases inherent in retrospective data collection. The economic benefits of leveraging existing registries rather than creating new registries or conducting clinical trials were acknowledged. Registries are also a potential source for additional evidence required for the expansion of indications and can become a source of controls for new device trials. From a regulatory viewpoint, major goals related to the Ortho-CRN include the development of a framework to allow US orthopedic device registries to conduct signal detection and confirmatory studies using existing US registry data; to collaborate with international registries to investigate device signals and conduct comparative effectiveness research; to provide a platform for collaborative post-market surveillance of implants in the USA; and to facilitate tracking of implants and optimize premarket regulatory processes.29 30

Moving forward: areas of expansion

The registries currently included within the Ortho-CRN primarily capture data related to hip and knee arthroplasty procedures. Stakeholders recognize that additional opportunities exist across multiple orthopedic device areas for the detection of safety events and evaluation of clinical effectiveness for currently marketed medical devices. Specific subspecialty areas that could benefit from the expansion of the Ortho-CRN include pediatric and adult spinal disorders, shoulder disorders, foot and ankle disorders, trauma and osseointegrated prostheses. Registries are an ideal method for postmarket evaluation among these aforementioned clinical spaces given that patients are treated with a relatively new class of orthopedic implants used with increasing frequency, are implanted in small heterogeneous populations, require long-term follow-up during critical phases of growth and development, experience concomitant use of combination products including biologics, and experience adverse events and outcomes that may be device and clinical are specific such as local infections and osseous union.

Moving forward: methodological advancements to strengthen the generated RWE

Identified methodological advancements that promote the objective of the Ortho-CRN for the development of innovative approaches for robust, relevant and reliable clinical evidence generation throughout the medical device total product lifecycle include data linkages and the generation of objective performance criteria (OPC).

Data linkages are especially crucial for postapproval safety evaluations of orthopedic devices, where important outcomes often do not occur until many years following implantation. Data linkage between registries and claims data may present a potentially cost-effective option for the evaluation of a device’s total product life cycle and overcome the limitations of the respective data sources. Registries are limited in their capture of long-term follow-up data and capture of events or diagnoses that are not directly reported to the registry or occur outside the registry’s health system. Meanwhile, claims data capture care received in various settings and provide more long-term information regarding experienced outcomes.17 The MDEpiNet’s coordinating center has initiated the data linkage process that allows for a more comprehensive assessment of orthopedic devices. More specifically, the center has previously successfully linked registry participants within the American Joint Replacement Registry to New York State claims data captured by the Statewide Planning and Research Cooperative System.31

OPC refer to a numerical target value derived from historical data.13 32 Technologies, such as orthopedic devices that undergo incremental but important changes, may greatly benefit from OPC creation. The creation of OPCs may allow for comparison of important outcomes, such as revision rates, at specific time points to a defined standard or equivalent standards, which can be used as a comparison for devices seeking approval.33 From a regulatory premarket standpoint, leveraging OPCs may reduce the sample size requirements for studies, be cost-effective, and may promote the use of RWE if appropriately developed, applied, and disseminated. For postmarket surveillance, OPCs allow for the examination of the impact of incremental innovations in implant characteristics. There are some legacy benchmarks developed for certain orthopedic device types, however, there is still a need to advance the methodology for the creation of OPC.34–37

Research needs: disparities in orthopedic procedural outcomes

Sex differences in the prevalence of common indications for orthopedic devices exist.38 39 A higher proportion of women undergo TJA and experience unfavorable outcomes following TJA.38 39 Furthermore, it is known that sex is associated with varying effectiveness and safety profiles among medical devices.40 For these reasons, the FDA released specific guidance regarding the investigation of sex differences among patients receiving medical devices, and the FDA Center for Devices and Radiological Health (CDRH) initiated efforts to increase women’s access to safe medical devices through the CDRH Health of Women Strategic Plan.41 Racial disparities have also been identified within orthopedic procedures and outcomes.42 Racial and ethnic disparities for joint arthroplasty outcomes in the USA have been well documented in literature and may, at times, also result in conflicting evidence.43–46 Additionally, strong and growing evidence demonstrates that social determinants of health (SDoH), defined as the structural determinants and conditions in which people are born, raised, reside, work and age, often predict healthcare access, health status, utilization of healthcare, and health outcomes.47 48

Further investigation into sex, gender, racial disparities, and SDoH will help clinicians and regulators gain an understanding of the effects of utilization and can serve as a decision aid in selecting treatment.


The Ortho-CRN and its overarching objectives are crucial to ensure advancements related to infrastructure building, regulatory investigations, and quality improvement across a range of orthopedic device areas. Continuously growing the capacity of the Ortho-CRN may contribute to the enhancement the data, advancement of methodologies, and aid in the goal of near-real-time access to RWD that can be used for active safety surveillance. As a member of the CRN Collaborative Learning Communities, Ortho-CRN is well positioned to continue to build a strong foundation and promote the efforts of the National Evaluation System for health Technology in the registry-based domain.


Ethics statements

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The authors would like to acknowledge the speakers and presenters of the 2018 and 2019 Orthopedic Coordinated Registry Network Annual Meeting listed in online supplemental appendix A.



  • Twitter @Artsytwits

  • Contributors The manuscript was drafted by LG. Critical edits were performed by VD, MJ, DM-D, AS, EWP, PF, RN, SI, CAPT JF, PEV, RZ, MV, MCM, PON and RP.

  • Funding This work was supported by the Office of the Secretary Patient-Centered Outcomes Research Trust Fund under Interagency Agreement #750119PE060048.

  • Competing interests PF reports grants from DePuy, grants from NIAMS, grants from PCORI, outside the submitted work. JF reports personal fees from The Solsidan Group, grants from Zimmer-Biomet, outside the submitted work; and as a minority shareholder of Prognostix AB. PON reports grants and other from Setting Scoliosis Straight Foundation, other from Rady Children’s Specialists of San Diego, grants, personal fees and non-financial support from DePuy Synthes Spine, grants and other from Scoliosis Research Society, grants from EOS imaging, personal fees from Thieme Publishing, grants from NuVasive, other from Electrocore, other from International Pediatric Orthopedic Think Tank, grants, non-financial support and other from Orthopediatrics, grants, personal fees and non-financial support from Stryker K2M, grants and non-financial support from Alphatech, grants from Mazor Robotics, personal fees from Pacira, personal fees from Globus Medical, personal fees from Medtronic, outside the submitted work; In addition, PON has a patent Anchoring systems and methods for correcting spinal deformities (8540754) with royalties paid to DePuy Synthes Spine, a patent Low profile spinal tethering systems (8123749) licensed to DePuy Spine, a patent Posterior spinal fixation licensed to Stryker/K2M, and a patent Posterior cervical fixation with royalties paid to Stryker/K2M.

    Danica Marinac-Dabic is an Editorial Board Member.

  • Provenance and peer review Commissioned; externally peer reviewed.