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1.
Knee ; 45: 128-136, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37925803

ABSTRACT

BACKGROUND: Early studies have found Oxidised Zirconium (OxZr-Nb) total knee arthroplasties to have a low incidence of failure in young, high demand patients. Theoretically this is because they are low friction and hard wearing. However, there are a paucity of studies reporting on the outcome of these implants beyond ten years. The purpose of our study was to present an in-depth 15-year survival analysis of a cemented OxZr-Nb knee arthroplasty. METHODS: Data was collected prospectively and survival analysis undertaken with multiple strict end-points. Complication rates and patient reported outcomes were measured post-operatively. RESULTS: Six hundred and seventeen knee arthroplasties were analysed. Forty-nine patients required a reoperation for various reasons. Aseptic tibial loosening was the most common cause of failure (32.7%), occurring, on average, 2.8 years after the primary procedure. There was only one oxidised zirconium femoral failure recorded. Cumulative survivorship for reoperation for any reason was 91.52% at 15-years. On average, WOMAC (Western Ontario and McMaster University) score improved by 21.2 points at one-year post-surgery, which is beyond the considered minimum clinically important difference. CONCLUSION: This study presents a 15-year survival analysis of a cemented oxidised zirconium knee arthroplasty showing good survivorship over a range of analyses.


Subject(s)
Arthroplasty, Replacement, Knee , Knee Prosthesis , Humans , Arthroplasty, Replacement, Knee/adverse effects , Arthroplasty, Replacement, Knee/methods , Knee Prosthesis/adverse effects , Zirconium , Prosthesis Failure , Prosthesis Design , Survival Analysis , Reoperation , Treatment Outcome
2.
J Orthop Surg (Hong Kong) ; 31(1): 10225536231169572, 2023.
Article in English | MEDLINE | ID: mdl-37088733

ABSTRACT

AIM OF THE STUDY: To compare the outcomes of three knee arthroplasty design philosophies and surface tribology.• A zirconium-surfaced, bicruciate-stabilised implant designed to mimic kinematic movement and improve flexion and outcomes;• A cobalt-chrome surfaced, multi-radius design with built-in femoral external rotation to aid balancing and patella tracking through a deeper trochlea groove;• A zirconium-surfaced, single-radius implant designed on surface conformity, particularly within the patello-femoral joint. METHODS: 313 knee replacements - 103 Journey II, 103 Genesis II and 107 Profix - were statistically assessed at a minimum of 2 years using WOMAC, Oxford and SF-12 scores, and range of movement. RESULTS: There was no difference between the actual or unit change in WOMAC scores (p = 0.140 and p = 0.287), SF-12 physical (p = 0.088) or mental scores (p = 0.975) between the three implants; or between the actual or unit change in Oxford score (p = 0.912 and p = 0.874) for the Journey II or Genesis II. The Journey II produced more flexion and range of movement than the Genesis II (p < 0.001 and p = 0.018) and Profix (p < 0.001 and <0.001) with no difference between the latter two (p = 0.402 and 0.568); with no difference in extension between the three implants (p = 0.086). There was no difference between those with or without a resurfaced patella. CONCLUSION: The three design philosophies and surfaces yielded no difference in outcome scores at 2 years post-operatively. The Journey II demonstrated better post-operative flexion. Resurfacing the patella did not alter the outcome scores or flexion.


Subject(s)
Arthroplasty, Replacement, Knee , Knee Prosthesis , Osteoarthritis, Knee , Humans , Knee Joint/surgery , Zirconium , Femur/surgery , Patella/surgery , Prosthesis Design , Range of Motion, Articular , Osteoarthritis, Knee/surgery , Biomechanical Phenomena
3.
J Knee Surg ; 35(7): 767-775, 2022 Jun.
Article in English | MEDLINE | ID: mdl-33111275

ABSTRACT

The Journey-I total knee replacement was designed to improve knee kinematics but had several complications including early dislocation. The Journey-II modification was introduced to reduce these while maintaining high function. To assess whether the modified Journey-II prosthesis has succeeded in its designers aims, we undertook an observational study of prospectively recorded data to analyze and compare the two knees. A total of 217 Journey-I and 129 Journey-II knees were identified from the department's prospectively collated registry and were assessed at 1 year by a comparative statistical analysis using numerous factors including pain, functional activity, physical assessment, Short Form-12 (SF-12), Western Ontario and McMaster Universities Arthritis Index (WOMAC), and Oxford scores. The statistical tests included Chi-square, Wilcoxon's rank and Mann-Whitney U-tests with the level of significance set at p < 0.05. There was a variation in primary patella resurfacing between the two groups with 14.3% in the Journey-I cohort and 66.7% in the Journey-II cohort. Both replacements demonstrated excellent postoperative function, but the Journey II performed significantly better than Journey I with fewer complications (37 vs. 10) and better improvement in almost all clinical scores including pain (p < 0.01), mobility outcomes (p = 0.018), Oxford (p = 0.004), and WOMAC (p = 0.039) scores but not with flexion improvement and SF-12 score. There was significant improvement in patellofemoral pain postoperatively in both the Journey I (p = 0.011) and Journey II (p = 0.042) arthroplasty; however the primarily resurfaced patella in a Journey-II implant had better postoperative scores. The main complication of dislocation in the Journey I was not seen in the modified Journey-II implant with stiffness requiring intervention reduced in Journey II. These results suggest that the Journey II has improved short-term clinical outcomes compared with Journey I with reduction of dislocation and other complications.


Subject(s)
Arthroplasty, Replacement, Knee , Joint Dislocations , Knee Prosthesis , Osteoarthritis, Knee , Arthroplasty, Replacement, Knee/adverse effects , Arthroplasty, Replacement, Knee/methods , Humans , Joint Dislocations/surgery , Knee Joint/surgery , Osteoarthritis, Knee/surgery , Pain , Patella/surgery , Treatment Outcome
4.
J Arthroplasty ; 35(10): 2837-2842, 2020 10.
Article in English | MEDLINE | ID: mdl-32498968

ABSTRACT

BACKGROUND: Total knee arthroplasty is a successful elective orthopedic procedure with an increasing number being undertaken. Original knee arthroplasties used an all-polyethylene tibia; however, with concerns over tibial loosening, the trend moved toward the metal-backed variety. Modern designs providing more conformity and changes in manufacturing of the polyethylene make it an equivalent but cheaper option. METHODS: We analyzed the medium-term outcome in 1092 patients with an all-polyethylene tibial component in their total knee arthroplasty. RESULTS: Twenty-six patients had further surgery on their knee for a variety of reasons. Assessing reoperation for any reason, the 7-year survival rate was 96.96% with an overall infection rate of 0.37%. Seven-year survival analysis using aseptic loosening as a criteria was 99.28%. Both the Short Form 12 physical score and Western Ontario and McMaster Universities Osteoarthritis Index score significantly improved and was sustained at 7 years. Body mass did not correlate to either outcomes or complications. CONCLUSION: An all-polyethylene tibia in a total knee arthroplasty has good outcome data and high patient satisfaction with good survivorship in the medium term, coupled with potential cost-saving benefits.


Subject(s)
Knee Prosthesis , Tibia , Humans , Knee Prosthesis/adverse effects , Polyethylene , Prosthesis Design , Prosthesis Failure , Reoperation , Survival Analysis , Tibia/surgery , Treatment Outcome
6.
Knee ; 25(4): 617-622, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29703630

ABSTRACT

BACKGROUND: Oxidised zirconium has the wear properties of ceramic with the breakage resistance of metal. This results in less wear and is of benefit to younger, higher demand patients. We report the short- to mid-term survival of 103 Profix zirconium total knee replacements performed in patients under 50years of age at time of surgery. METHODS: Data was collected prospectively and survival analysis undertaken with strict end points used. SF (Short Form) 12 and WOMAC (Western Ontario and McMaster University) scores were recorded at pre-operatively and at twelve months, one, three, five, seven and ten years. RESULTS: The average age at operation was 43.21years (range 20-50years) with a mean follow-up of 8.56years (range five to 15years). No patients died with one patient lost to follow-up after seven year review. The mean WOMAC score improved from 53 to 29, and the mean SF12 physical component improved from 29 to 36. The five year survivorship for implant related complications was 99.03% (95% CI 94.64-100.0) due to tibial component aseptic loosening at year one. Reoperation for any cause at five years including stiffness was 94.09% (95% CI 88.69-98.11). Forty-four patients were at least ten years post-operative at the time of analysis, with no aseptic loosening of either component giving 10year femoral component survival of 100% and all cause revision of 95.4%. The only zirconium femoral failure was at 12years. CONCLUSIONS: Our data shows excellent mid-term survivorship of oxidised zirconium total knee replacements in younger, higher demand patients.


Subject(s)
Arthroplasty, Replacement, Knee/instrumentation , Joint Diseases/surgery , Knee Prosthesis , Postoperative Complications/epidemiology , Prosthesis Failure , Zirconium , Adult , Age Factors , Female , Femur , Follow-Up Studies , Humans , Male , Middle Aged , Ontario , Range of Motion, Articular , Reoperation , Survival Analysis , Young Adult
7.
Mayo Clin Proc ; 91(8): 1074-83, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27113199

ABSTRACT

UNLABELLED: The objective of this study was to empirically demonstrate the use of a new framework for describing the strategies used to implement quality improvement interventions and provide an example that others may follow. Implementation strategies are the specific approaches, methods, structures, and resources used to introduce and encourage uptake of a given intervention's components. Such strategies have not been regularly reported in descriptions of interventions' effectiveness, or in assessments of how proven interventions are implemented in new settings. This lack of reporting may hinder efforts to successfully translate effective interventions into "real-world" practice. A recently published framework was designed to standardize reporting on implementation strategies in the implementation science literature. We applied this framework to describe the strategies used to implement a single intervention in its original commercial care setting, and when implemented in community health centers from September 2010 through May 2015. Per this framework, the target (clinic staff) and outcome (prescribing rates) remained the same across settings; the actor, action, temporality, and dose were adapted to fit local context. The framework proved helpful in articulating which of the implementation strategies were kept constant and which were tailored to fit diverse settings, and simplified our reporting of their effects. Researchers should consider consistently reporting this information, which could be crucial to the success or failure of implementing proven interventions effectively across diverse care settings. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT02299791.


Subject(s)
Cardiotonic Agents/administration & dosage , Cardiovascular Diseases/prevention & control , Diabetes Complications/prevention & control , Quality Improvement/organization & administration , Angiotensin-Converting Enzyme Inhibitors/administration & dosage , Angiotensin-Converting Enzyme Inhibitors/standards , Aspirin/administration & dosage , Aspirin/standards , Cardiotonic Agents/standards , Cardiovascular Diseases/drug therapy , Cardiovascular Diseases/etiology , Diabetes Complications/drug therapy , Guideline Adherence/statistics & numerical data , Health Maintenance Organizations/organization & administration , Health Maintenance Organizations/standards , Health Plan Implementation/methods , Health Plan Implementation/organization & administration , Health Plan Implementation/standards , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage , Hydroxymethylglutaryl-CoA Reductase Inhibitors/standards , Practice Guidelines as Topic , Quality Improvement/standards
8.
Am J Health Syst Pharm ; 72(2): 133-42, 2015 Jan 15.
Article in English | MEDLINE | ID: mdl-25550137

ABSTRACT

PURPOSE: Pharmacists' satisfaction with a computerized prescriber order-entry (CPOE) system and the impact of CPOE on pharmacy workflows and order verification were investigated. SUMMARY: A mixed-method study was conducted to evaluate the implementation of a CPOE system in three hospitals of a large Michigan-based health system and early user experience with the system. Surveys of pharmacists before (n = 54) and after (n = 42) CPOE implementation indicated that they held generally positive expectations about CPOE prior to and during system implementation and continued to hold positive views about CPOE after several months of system use. In interviews and focus group discussions, pharmacists reported a number of important CPOE benefits, but they also cited challenges related to CPOE provider alerts, uncertainty about medication timing, and the need to support providers by serving as informal CPOE system trainers. Direct observation of pharmacists before and after CPOE implementation indicated decreases in both the rate of order clarification events (from 0.89 to 0.35 per hour, p < 0.001) and the average time spent per hour clarifying orders (from 4.75 to 2.11 minutes, p = 0.008). CONCLUSION: Several months after CPOE implementation, pharmacists indicated that several aspects of their workload had improved, including the process of medication order clarification, their ability to prioritize work, and their ability to move around within the hospital to respond to demand. However, pharmacists also noted that order ambiguity still existed and that the system needed to be optimized to gain efficiencies and increase clarity.


Subject(s)
Community Health Planning/trends , Medical Order Entry Systems/trends , Medication Systems, Hospital/trends , Pharmacists/trends , Pharmacy/trends , Clinical Pharmacy Information Systems/trends , Community Health Planning/methods , Data Collection/methods , Data Collection/trends , Humans , Michigan , Pharmacy/methods
9.
Knee ; 20(6): 384-7, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23159720

ABSTRACT

BACKGROUND: Zirconium total knee arthroplasties theoretically have a low incidence of failure as they are low friction, hard wearing and hypoallergenic. We report the five year survival of 213 Profix zirconium total knee arthroplasties with a conforming all polyethylene tibial component. METHODS: Data was collected prospectively and multiple strict end points were used. SF12 and WOMAC scores were recorded pre-operatively, at three months, at twelve months, at 3 years and at 5 years. RESULTS: Eight patients died and six were "lost to follow-up". The remaining 199 knees were followed up for five years. The mean WOMAC score improved from 56 to 35 and the mean SF12 physical component score improved from 28 to 34. The five year survival for failure due to implant related reasons was 99.5% (95% CI 97.4-100). This was due to one tibial component becoming loose aseptically in year zero. CONCLUSIONS: Our results demonstrate that the Profix zirconium total knee arthroplasty has a low medium term failure rate comparable to the best implants. Further research is needed to establish if the beneficial properties of zirconium improve long term implant survival.


Subject(s)
Arthroplasty, Replacement, Knee/methods , Compressive Strength , Knee Prosthesis , Materials Testing , Prosthesis Failure/trends , Zirconium , Aged , Arthroplasty, Replacement, Knee/adverse effects , Databases, Factual , Female , Humans , Middle Aged , Polyethylene , Prognosis , Prospective Studies , Prosthesis Design , Range of Motion, Articular/physiology , Risk Assessment , Time Factors , Treatment Outcome
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