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Bone & Joint Open
Vol. 4, Issue 10 | Pages 782 - 790
18 Oct 2023
Hamilton DF Gaston P Macpherson GJ Simpson P Clement ND

Aims

The primary aim of this study is to assess the survival of the uncemented hydroxyapatite (HA) coated Trident II acetabular component as part of a hybrid total hip arthroplasty (THA) using a cemented Exeter stem. The secondary aims are to assess the complications, joint-specific function, health-related quality of life, and radiological signs of loosening of the acetabular component.

Methods

A single-centre, prospective cohort study of 125 implants will be undertaken. Patients undergoing hybrid THA at the study centre will be recruited. Inclusion criteria are patients suitable for the use of the uncemented acetabular component, aged 18 to 75 years, willing and able to comply with the study protocol, and provide informed consent. Exclusion criteria includes patients not meeting study inclusion criteria, inadequate bone stock to support fixation of the prosthesis, a BMI > 40 kg/m2, or THA performed for pain relief in those with severely restricted mobility.


Bone & Joint Open
Vol. 4, Issue 7 | Pages 490 - 495
4 Jul 2023
Robinson PG Creighton AP Cheng J Dines JS Su EP Gulotta LV Padgett D Demetracopoulos C Hawkes R Prather H Press JM Clement ND

Aims

The primary aim of this prospective, multicentre study is to describe the rates of returning to golf following hip, knee, ankle, and shoulder arthroplasty in an active golfing population. Secondary aims will include determining the timing of return to golf, changes in ability, handicap, and mobility, and assessing joint-specific and health-related outcomes following surgery.

Methods

This is a multicentre, prospective, longitudinal study between the Hospital for Special Surgery, (New York City, New York, USA) and Edinburgh Orthopaedics, Royal Infirmary of Edinburgh, (Edinburgh, UK). Both centres are high-volume arthroplasty centres, specializing in upper and lower limb arthroplasty. Patients undergoing hip, knee, ankle, or shoulder arthroplasty at either centre, and who report being golfers prior to arthroplasty, will be included. Patient-reported outcome measures will be obtained at six weeks, three months, six months, and 12 months. A two-year period of recruitment will be undertaken of arthroplasty patients at both sites.


Bone & Joint Open
Vol. 3, Issue 10 | Pages 753 - 758
4 Oct 2022
Farrow L Clement ND Smith D Meek DRM Ryan M Gillies K Anderson L Ashcroft GP

Aims

The extended wait that most patients are now experiencing for hip and knee arthroplasty has raised questions about whether reliance on waiting time as the primary driver for prioritization is ethical, and if other additional factors should be included in determining surgical priority. Our Prioritization of THose aWaiting hip and knee ArthroplastY (PATHWAY) project will explore which perioperative factors are important to consider when prioritizing those on the waiting list for hip and knee arthroplasty, and how these factors should be weighted. The final product will include a weighted benefit score that can be used to aid in surgical prioritization for those awaiting elective primary hip and knee arthroplasty.

Methods

There will be two linked work packages focusing on opinion from key stakeholders (patients and surgeons). First, an online modified Delphi process to determine a consensus set of factors that should be involved in patient prioritization. This will be performed using standard Delphi methodology consisting of multiple rounds where following initial individual rating there is feedback, discussion, and further recommendations undertaken towards eventual consensus. The second stage will then consist of a Discrete Choice Experiment (DCE) to allow for priority setting of the factors derived from the Delphi through elicitation of weighted benefit scores. The DCE consists of several choice tasks designed to elicit stakeholder preference regarding included attributes (factors).


Orthopaedic Proceedings
Vol. 101-B, Issue SUPP_6 | Pages 23 - 23
1 May 2019
Tsang B Clarke A Dobson P Thomas P Jameson S Baker P
Full Access

Background. There is significant variation and inconsistencies in the current advice and information delivered to patients undergoing total hip replacement (THR). The aim of this study was to assess a locally developed web-based electronic resource system for patients undergoing total hip replacement (THR) surgery to see if this improves and standardises the content, structure, and delivery of information delivered to patients prior to and after surgery. Patients/Materials and Methods. Prospective study with patients recruited in clinic when listed for THR surgery. Patients are emailed login details for the web based electronic resource system (GoWellHealth). The platform delivers content in a time-lined fashion and is individualised to the patient. Data gathered includes the number of patients registering to use this system, their engagement and use of the resources, and results from forms and questionnaires administered. Results. Over a period of 11 months, 228 patients of the 302 activated their accounts (75%). The average age of patients was 64 years (range 33–94 years). A total of 107 patients have had surgery where 76% (n=81) activated their account and of these 81% had been actively using the system. Patients spent on average 2 hours and 2 minutes on the system. Overall 1448 separate ‘hits’ were recorded with each person viewing an average of 31 pieces of content (Range 1 to 90). Computers (45%) were the most commonly used device to access the platform. Discussion. Age did not seem to be a factor and the mean of the most enthusiastic users was greater than the mean of the entre cohort. This system allows data collection and PROMs measurement and supports the consent process. Conclusion. We have shown that patients will engage with an online system and believe it as a useful method of delivering information to our patients; thus, improving their overall surgical care


The Journal of Bone & Joint Surgery British Volume
Vol. 94-B, Issue 4 | Pages 454 - 458
1 Apr 2012
Goldberg AJ MacGregor A Spencer SA

With the established success of the National Joint Registry and the emergence of a range of new national initiatives for the capture of electronic data in the National Health Service, orthopaedic surgery in the United Kingdom has found itself thrust to the forefront of an information revolution. In this review we consider the benefits and threats that this revolution poses, and how orthopaedic surgeons should marshal their resources to ensure that this is a force for good.


Orthopaedic Proceedings
Vol. 92-B, Issue SUPP_I | Pages 169 - 169
1 Mar 2010
Bauer DA
Full Access

Computers arrived late in orthopaedic surgery. While the rest of the world already happily integrated computers into daily life, business and production, orthopaedic surgeons remained sceptical and denied any need for help from modern technology. It was in the mid-eighties though, that a young veterinary surgeon from California, specializing in total hip replacement in dogs, was contemplating the problems that he encountered during surgery. This veterinary surgeon, the late Hap Paul, was one of the founding members of the custom – implant society, from which evolved ISTA. He struggled with wrong positioning of implants and broken bones, and wondered why implants that were manufactured with highest technology finally were placed into the bone with crude instruments reminiscent of those found in a carpenters workshop. With the help of IBM and engineers from the University of California he created a system which he called ROBODOC. ®. , and it became the first computer based system helping the surgeon during an orthopaedic procedure. The technological effort was huge, as many parts of the system and of the procedure using advance robotic tools had to be invented from scratch. There was nothing there they could copy, and the system they invented – an active robot performing a critical part of surgery – represented a very ambitious step forward. Some compare the development of ROBODOC. ®. with the technological history of the Concorde: very sophisticated technology, very early and very advanced, somewhat expensive and with an aura of vision and adventure. Of course this was not the only and ultimate solution of bringing computers into surgery. Other researchers took a step backwards: they invented systems that helped the surgeon to navigate hand held instruments and implants within the surgical field, so-called navigation systems. These were initially used by neurosurgeons to navigate probes within the brain. As neurosurgeons were closely related to and depending on CT-scan, the logic step was to use the CT- datasets, match them with real world (the process of registration) and create a virtual 3D space that is congruent to the real 3D space. Using CT provided orthopaedic surgeons increase visibility with less required exposure. With the help of optical systems (other options are mechanical or magnetic systems) instruments can be tracked outside and inside the surgical object and allow precise navigation within the surgical field. However, preparation of tissue and/or placement of implants were still done with manual tools. Very early application of this navigation technology was spine surgery in the mid-nineties, where utmost precision was needed during the placement of pedicle screws. Further applications were knee replacement, hip replacement and numerous applications in trauma surgery. Also the source of data was further developed: from the very precise but costly CT-scan to simple radiographs taken during surgery to so-called image free surgery, where data are retrieved directly from the surgical object and approximations are created to direct the placement of implants. Navigation systems, in contrast to the original robotic system, presented two major advantages: they were much cheaper, and they allowed the surgeon to use his standard instruments and, most important, to play a more active part in the surgery, “to stay in the loop” (Tony DiGioia). Today there are thousands of navigations systems in routine use all over the world. Published results show benefits, but also limits. Surgery using navagation has become more precise and results more reproducible, yet there are still outliers which mainly stem from technical problems, but which are hard to detect and cause significant inaccuracy. Therefore the era of the robots is not over: robotic technology is currently revisited by numerous groups, and technically more advanced robots are developed and currently under testing. Robotic technology has continued to make inroads into the market with demonstrated capacity to assist the surgeon to reduce intraoperative complications, eliminate outliers, and achieve improved surgical outcomes consistently. Different types of robots (active, semi active and passive robots, such as systems which provide for constrained motion in the surgical field) are successfully moving into the operating theatre. ROBODOC. ®. , the forefather of all computer-assisted orthopaedic systems, is still around and actively applied during surgery, with published good results and high reliability. The history of ROBODOC. ®. is a master piece of technological history. After initial successful human surgeries, embedded in the feasibility study required by the FDA, the next step was more difficult: the randomized study for FDA approval to prove the efficacy almost killed the company and with it the technology. In early optimistic statements the inventors foresaw major benefits, but overlooked the difficulties to prove these in the postoperative outcome. Disadvantages of the system, like longer OR times and higher blood loss, at least prevalent in the in the early trials of the FDA study, were obvious while the “clear” benefits in outcome were not so obvious. Thus marketing abroad became a major option, and Europe became the prime target. The attempt was successful, and rapidly 30 systems were busy all over Europe. This development was brought to a halt by a couple of unsubstantiated lawsuits in Germany and unprecedented negative press campaign accompanying this effort. The lawsuits were sponsored by the illusion to finally sue an American company and gain millions from that lawsuit. This process started in the early days of this century, and so far, in spite of numerous sentences proclaimed, not one court has condemned the technology or found any wrong doing in applying it. In parallel with the declining European market, the Asian market was developed, and surgeons there benefited from the experiences in Europe and the consecutive improvements of the system. Currently TKR and THR are routinely performed using the ROBODOC. ®. system in Japan, Korea and India. This process let to recovery of the company, which tells us that technological progress also in medicine is inherently coupled to economic success. Although the first system applied in CAOS, Robodoc still is the most advanced system in technological terms. This is finally also accepted by the very critical USFDA, which had problems with the approval for such a long time because the system represents an autonomous robotic system working on patients. Initial problems like bulkiness, software bugs and invasiveness have been overcome. Work is underway even now to make the system more flexible covering a wider range of surgical procedures like uni and multi compartmental knee, hip resurfacing and acetabular cup in THR and further expanding the functionality of the system supporting not just orthopedic procedures but Neurosurgical procedures as well. Many of these developments are in the final stages of testing. In the meantime the CAOS community, i.e. the surgeons and engineers primarily working in application and development of the existing systems, more and more become convinced that computer assisted surgery undoubtedly is heading towards the integration of robotic systems into surgery: this is where ROBODOC. ®. came from


The Journal of Bone & Joint Surgery British Volume
Vol. 84-B, Issue 4 | Pages 481 - 485
1 May 2002
Clough JFM Oliver CW