Advertisement for orthosearch.org.uk
Results 1 - 20 of 461
Results per page:
Orthopaedic Proceedings
Vol. 104-B, Issue SUPP_12 | Pages 27 - 27
1 Dec 2022
Falsetto A Bohm E Wood G
Full Access

Recent registry data from around the world has strongly suggested that using cemented hip hemiarthroplasty has lower revision rates compared to cementless hip hemiarthroplasty for acute femoral neck hip fractures. The adoption of using cemented hemiarthroplasty for hip fracture has been slow as many surgeons continue to use uncemented stems. One of the reasons is that surgeons feel more comfortable with uncemented hemiarthroplasty as they have used it routinely. The purpose of this study is to compare the difference in revision rates of cemented and cementless hemiarthroplasty and stratify the risk by surgeon experience. By using a surgeons annual volume of Total Hip Replacements performed as an indicator for surgeon experience. The Canadian Joint Replacement Registry Database was used to collect and compare the outcomes to report on the revision rates based on surgeon volume. This is a large Canadian Registry Study where 68447 patients were identified for having a hip hemiarthroplasty from 2012-2020. This is a retrospective cohort study, identifying patients that had cementless or cemented hip hemiarthroplasty. The surgeons who performed the procedures were linked to the procedure Total Hip Replacement. Individuals were categorized as experienced hip surgeons or not based on whether they performed 50 hip replacements a year. Identifying high volume surgeon (>50 cases/year) and low volume (<50 cases/year) surgeons. Hazard ratios adjusted for age and sex were performed for risk of revision over this 8-year span. A p-value <0.05 was deemed significant. For high volume surgeons, cementless fixation had a higher revision risk than cemented fixation, HR 1.29 (1.05-1.56), p=0.017. This pattern was similar for low volume surgeons, with cementless fixation having a higher revision risk than cemented fixation, HR 1.37 (1.11-1.70) p=0.004 We could not detect a difference in revision risk for cemented fixation between low volume and high volume surgeons; at 0-1.5 years the HR was 0.96 (0.72-1.28) p=0.786, and at 1.5+ years the HR was 1.61 (0.83-3.11) p=0.159. Similarly, we could not detect a difference in revision risk for cementless fixation between low volume and high volume surgeons, HR 1.11 (0.96-1.29) p=0.161. Using large registry data, cemented hip hemiarthroplasty has a significant lower revision rate than the use of cementless stems even when surgeons are stratified to high and low volume. Low volume surgeons who use uncemented prostheses have the highest rate of revision. The low volume hip surgeon who cements has a lower revision rate than the high volume cementless surgeon. The results of this study should help to guide surgeons that no matter the level of experience, using a cemented hip hemiarthroplasty for acute femoral neck fracture is the safest option. That high volume surgeons who perform cementless hemiarthroplasty are not immune to having revisions due to their technique. Increased training and education should be offered to surgeons to improve comfort when using this technique


Orthopaedic Proceedings
Vol. 104-B, Issue SUPP_12 | Pages 1 - 1
1 Dec 2022
Falsetto A Bohm E Wood G
Full Access

Recent registry data from around the world has strongly suggested that using cemented hip hemiarthroplasty has lower revision rates compared to cementless hip hemiarthroplasty for acute femoral neck hip fractures. The adoption of using cemented hemiarthroplasty for hip fracture has been slow as many surgeons continue to use uncemented stems. One of the reasons is that surgeons feel more comfortable with uncemented hemiarthroplasty as they have used it routinely. The purpose of this study is to compare the difference in revision rates of cemented and cementless hemiarthroplasty and stratify the risk by surgeon experience. By using a surgeons annual volume of Total Hip Replacements performed as an indicator for surgeon experience. The Canadian Joint Replacement Registry Database was used to collect and compare the outcomes to report on the revision rates based on surgeon volume. This is a large Canadian Registry Study where 68447 patients were identified for having a hip hemiarthroplasty from 2012-2020. This is a retrospective cohort study, identifying patients that had cementless or cemented hip hemiarthroplasty. The surgeons who performed the procedures were linked to the procedure Total Hip Replacement. Individuals were categorized as experienced hip surgeons or not based on whether they performed 50 hip replacements a year. Identifying high volume surgeon (>50 cases/year) and low volume (<50 cases/year) surgeons. Hazard ratios adjusted for age and sex were performed for risk of revision over this 8-year span. A p-value <0.05 was deemed significant. For high volume surgeons, cementless fixation had a higher revision risk than cemented fixation, HR 1.29 (1.05-1.56), p=0.017. This pattern was similar for low volume surgeons, with cementless fixation having a higher revision risk than cemented fixation, HR 1.37 (1.11-1.70) p=0.004 We could not detect a difference in revision risk for cemented fixation between low volume and high volume surgeons; at 0-1.5 years the HR was 0.96 (0.72-1.28) p=0.786, and at 1.5+ years the HR was 1.61 (0.83-3.11) p=0.159. Similarly, we could not detect a difference in revision risk for cementless fixation between low volume and high volume surgeons, HR 1.11 (0.96-1.29) p=0.161. Using large registry data, cemented hip hemiarthroplasty has a significant lower revision rate than the use of cementless stems even when surgeons are stratified to high and low volume. Low volume surgeons who use uncemented prostheses have the highest rate of revision. The low volume hip surgeon who cements has a lower revision rate than the high volume cementless surgeon. The results of this study should help to guide surgeons that no matter the level of experience, using a cemented hip hemiarthroplasty for acute femoral neck fracture is the safest option. That high volume surgeons who perform cementless hemiarthroplasty are not immune to having revisions due to their technique. Increased training and education should be offered to surgeons to improve comfort when using this technique


Orthopaedic Proceedings
Vol. 103-B, Issue SUPP_3 | Pages 47 - 47
1 Mar 2021
Martin K Persson A Moatshe G Fenstad A Engebretsen L Visnes H
Full Access

Surgery performed in low-volume centres has been associated with longer operating time, longer hospital stays, lower functional outcomes, and higher rates of revision surgery, complications, and mortality. This has been reported consistently in the arthroplasty literature, but there is a paucity of data regarding the relationship between surgical volume and outcome following anterior cruciate ligament (ACL) reconstruction. The purpose of this study was to compare the ACL reconstruction failure rate between hospitals performing different annual surgical volumes. The hypothesis was that ACL reconstructions performed at low-volume hospitals would be associated with higher failure rates than those performed at high-volume centres. This level-II cohort study included all patients from the Norwegian Knee Ligament Registry that underwent isolated primary autograft ACL reconstruction between 2004 and 2016. Hospital volume was divided into quintiles based on the number of ACL reconstructions performed annually, defined arbitrarily as: 1–12 (V1), 13–24 (V2), 25–49 (V3), 50–99 (V4), and ≥100 (V5) annual procedures. Kaplan-Meier estimated survival curves and survival percentages were calculated with revision ACL reconstruction as the end point. Mean change in Knee Injury and Osteoarthritis Outcome Score (KOOS) Quality of Life and Sport subsections from pre-operative to two-year follow-up were compared using t-test. 19,204 patients met the inclusion criteria and 1,103 (5.7%) underwent subsequent revision ACL reconstruction over the study period. Patients in the lower volume categories (V1-3) were more often male (58–59% vs. 54–55% p=<0.001) and older (27 years vs. 24–25 years, p=<0.001) compared to the higher volume hospitals (V4-5). Concomitant meniscal injuries (52% vs. 40%) and participation in pivoting sports (63% vs. 56%) were most common in V5 compared with V1 (p=<0.001). Median operative time decreased as hospital volume increased, ranging from 90 minutes at V1 hospitals to 56 minutes at V5 hospitals (p=<0.005). Complications occurred at a rate of 3.8% at low-volume (V1) hospitals versus 1.9% at high-volume (V5) hospitals (p=<0.001). Unadjusted 10-year survival with 95% confidence intervals for each hospital volume category were: V1 – 95.1% (93.7–96.5%), V2 – 94.1% (93.1–95.1%), V3 – 94.2% (93.6–94.8%), V4 – 92.6% (91.8–93.4%), and V5 – 91.9% (90.9–92.9%). There was no difference in improvement between pre-operative and two-year follow-up KOOS scores between hospital volume categories. Patients having ACL reconstruction at lower volume hospitals did not have inferior clinical or patient reported outcomes, and actually demonstrated a lower revision rate. Complications occurred more frequently however, and operative duration was longer. The decreased revision rate is an interesting finding that may be partly explained by the fact that patients being treated in these small, often rural hospitals, may be of lower demand as suggested by the increased age and decreased participation in pivoting sports. In addition, patients with more complicated pathology such as meniscal tears were more commonly treated in the larger volume hospitals. The most significant limitation of this study is that provider volume was not assessed, and the number of surgeons dividing up the surgical volume at each hospital is not known


Orthopaedic Proceedings
Vol. 105-B, Issue SUPP_2 | Pages 56 - 56
10 Feb 2023
Vaotuua D O'Connor P Belford M Lewis P Hatton A McAuliffe M
Full Access

Deep infection is a devastating complication of total knee arthroplasty (TKA). This study aimed to determine if there was a relationship between surgeon volume and the incidence of revision for infection after primary TKA. Data from the Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR) from 1 September 1999 to 31 December 2020 for primary TKA for osteoarthritis that were revised for infection. Surgeon volume was defined by the number of primary TKA procedures performed by the surgeon in the year the primary TKA was performed and grouped as <25, 25-49, 50-74, 75-99, >100 primary TKA procedures per year. Kaplan Meir estimates for cumulative percent revision (CPR) and Cox Proportional Hazard Ratios were performed to compare rates of revision for infection by surgeon volume, with sub-analyses for patella and polyethylene use, age <65 years and male gender. 5295 of 602,919 primary TKA for osteoarthritis were revised for infection. High volume surgeons (>100 TKA/year) had a significantly lower rate of revision for infection with a CPR at 1 and 17 years of 0.4% (95% CI 0.3, 0.4) and 1.5% (95% CI 1.2, 2.0), respectively, compared with 0.6% (95% CI 0.5, 0.7) and 2.1% (95% CI 1.8, 2.3), respectively, for low volume surgeons (<25 TKR/year). Differences between the high-volume group and the remaining groups remained when sub-analysis for age, gender, ASA, BMI, patella resurfacing and the use of cross-linked polyethylene (XLPE). High volume surgeons have lower rates of revision for infection in primary TKA


Strategy regarding patella resurfacing in total knee replacement (TKR) remains controversial. TKR revision rates are reportedly influenced by surgeon procedure volume. The study aim was to compare revision outcomes of TKR with and without patella resurfacing in different surgeon volume groups using data from the AOANJRR. The study population included 571,149 primary TKRs for osteoarthritis. Surgeons were classified as low, medium, or high-volume based on the quartiles of mean primary TKR volume between 2011 and 2020. Cumulative percent revision (CPR) using Kaplan-Meier estimates of survivorship were calculated for the three surgeon volume groups with and without patella resurfacing. Cox proportional hazards models, adjusted for age and sex, were used to compare revision risks. High-volume surgeons who did not resurface the patella had the highest all-cause CPR (20-year CPR 10.9%, 95% CI [10.0%, 12.0%]). When the patella was resurfaced, high-volume surgeons had the lowest revision rate (7.3%, 95% CI [6.4%, 8.4%]). When the high-volume groups were compared there was a higher rate of revision for the non-resurfaced group after 6 months. When the medium-volume surgeon groups were compared, not resurfacing the patella also was associated with a higher rate of revision after 3 months. The low-volume comparisons showed an initial higher rate of revision with patella resurfacing, but there was no difference after 3 months. When only patella revisions were considered, there were higher rates of revision in all three volume groups where the patella was not resurfaced. TKR performed by high and medium-volume surgeons without patella resurfacing had higher revision rates compared to when the patella was resurfaced. Resurfacing the patella in the primary procedure protected against revision for patella reasons in all surgeon volume groups. Level of evidence: III (National registry analysis)


Orthopaedic Proceedings
Vol. 103-B, Issue SUPP_3 | Pages 71 - 71
1 Mar 2021
Ibe I Perera J Aoude A Griffin A Wunder J Ferguson P Tsoi K
Full Access

Ewing Sarcoma is the second most common primary bone sarcoma in young patients, however, there remains geographical variation in the treatment of these tumours. All patients receive neoadjuvant chemotherapy and, in most cases, the soft tissue mass diminishes significantly in volume. Controversy surrounds whether to then treat the pre- or post-chemotherapy tumour volume. Many centres advocate either (1) resection of the pre-chemotherapy volume or (2) treatment of the pre-chemotherapy volume with radiation followed by resection of the post-chemotherapy volume. These approaches increase both the short and long-term morbidity for this young patient population. In this study, we retrospectively reviewed our experience resecting only the post-chemotherapy volume without the use of (neo)adjuvant radiotherapy. A retrospective analysis of all patients with Ewing Sarcoma treated at a tertiary orthopaedic oncology centre was conducted. All patients were treated as per the consensus opinion of the multidisciplinary tumour board. Demographic and oncological variables were collected from our institutional database. Presentation and re-staging MRI scans were reviewed to evaluate pre- and post-chemotherapy tumour volumes. Operative and pathology reports were utilized to determine the extent of the surgical resection. Outcome variables included local recurrence free-, metastasis free- and overall survival. Sixty-five patients were identified in our institutional database of which 56 did not receive (neo)adjuvant radiotherapy. Median age at diagnosis was 24 years (range 13–64), 60% of patients were male and 67.6% of tumours were located in the appendicular skeleton. All 56 patients not treated with radiotherapy had resection of the post-chemotherapy tumour volume. There were 3 local recurrences in this group with a mean follow-up of 70.8 months (range 2 to 328). The median overall survival was 47 months and the mean of 70.8months. The rate of local recurrence is comparable to reports in the literature in which patients had their entire pre-chemotherapy tumour volume treated by radiation and/or surgery. Similarly, two-year overall survival for our patient cohort is not significantly different from previous studies in which more aggressive local control measures were employed. Resecting the post-chemotherapy tumour volume in Ewing Sarcoma without the use of (neo)adjuvant radiotherapy does not appear to increase the risk of local recurrence or negatively impact overall survival. This approach should be studied further as it reduces the risk of short and long-term complications for this patient population.”


Orthopaedic Proceedings
Vol. 101-B, Issue SUPP_4 | Pages 147 - 147
1 Apr 2019
Frankel W Navarro S Haeberle H Mont M Ramkumar P
Full Access

BACKGROUND. High-volume surgeons and hospital systems have been shown to deliver higher value care in several studies. However, no evidence-based volume thresholds for cost currently exist in total hip arthroplasty (THA). The objective of this study was to establish clinically meaningful volume thresholds based on cost for surgeons and hospitals performing THA. A secondary objective was to analyze the relative market share of THAs among the newly defined surgeon and hospital volume strata. METHODS. Using 136,501 patients from the New York State Department of Health's SPARCS database undergoing total hip arthroplasty, we used stratum-specific likelihood ratio (SSLR) analysis of a receiver operating characteristic (ROC) curve to generate volume thresholds predictive of increased costs for both surgeons and hospitals. Additionally, we examined the relative proportion of annual THA cases performed by each of these surgeon and hospital volume strata we had established. RESULTS. SSLR analysis of cost by annual surgeon THA volume produced stratifications at: 0–73 (low), 74–123 (medium), and 124 or more (high) (Figure 1). Analysis by annual hospital THA volume produced stratifications at: 0–121 (low), 122–309 (medium), and 310 or more (high) (Figure 2). Hospital costs decreased significantly (P < .05) in progressively higher volume stratifications. The largest proportion of THA cases are performed at high-volume hospitals (48.6%); however, low-volume surgeons perform the greatest share of these cases (44.6%) (Figure 3). CONCLUSIONS. Our study establishes economies of scale in total hip arthroplasty by demonstrating a direct relationship between volume and cost reduction. High volume hospitals are performing the greatest proportion of total hip arthroplasties; however, low volume, surgeons perform the largest share of these cases, which highlights a potential area for enhanced value in the care of patients undergoing total hip arthroplasty


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_6 | Pages 18 - 18
1 Mar 2017
Stratton-Powell A Tipper J Williams S Redmond A Brockett C
Full Access

Introduction. Total ankle replacement (TAR) is less successful than other joint replacements with a 77% survivorship at 10 years. Predominant indications for revision include: Insert dislocation, soft tissue impingement and pain/stiffness. Insert edge-loading may be both a product and cause of these indications and was reported to affect 22% of patients with the, now withdrawn from market, Ankle Evolutive System (AES) TAR (Transysteme, Nimes, France). Compressive forces up to seven times body weight over a relatively small contact area (∼6.0 to 9.2 cm. 2. ), in combination with multi-directional motion potentially causes significant polyethylene wear and deformation in mobile-bearing TAR designs. Direct methods of measuring component volume (e.g. pycnometer) use Archimedes' principle but cannot identify spatial changes in volume or form indicative of wear/deformation. Quantitative methods for surface analysis bridge this limitation and may advance methods for analysing the edge loading phenomena in TAR. Aim. Determine the frequency of edge loading in a cohort of explanted total ankle replacements and compare the quantitative surface characteristics using a novel explant analysis method. Methods. Thirty-two AES TAR devices were implanted and retrieved by the same surgeon (UK Health Research Authority approval: 09/H1307/60). Mean implantation time was 7.8 years (1.5 to 12.1 range). Pain and/or loosening were the primary indications for revision. An Alicona Infinite microscope measured the entire superior surface of each insert (10× mag; 1.76µm lateral resolution). Abbott-Firestone curves were produced per insert to quantify the deviation of the insert surface from flat. Peak material volume (Vmp), core material volume (Vmc), core void volume (Vvc) and dale void volume (Vvv) were measured. Edge loading was identified visually by a depressed area in the insert surface indicative of articulation with the edge of the tibial component. Inserts were identified as either edge-loaded or not edge-loaded and the above analyses compared. Results. Seventeen inserts (53%) showed edge loading. Peak material volume (Vmp) was significantly increased for the edge loaded inserts 5.64 ± 5.42µm compared to the normal inserts 1.29 ± 0.954µm (Independent T-Test, P=0.005). No difference was found for the other volume parameters (Figure 2). A progressive change in insert form, beginning at the edges of the superior insert surface, was evident (Figure 1). Machining marks identified at the centre of several components supported this observation. Discussion. Insert edge loading affected 53% of TAR explants. The volume parameters showed a statistically significant inflection of material at the inserts' edge for the affected ankles. Spatial changes to insert form progressed over time in-vivo. Machining marks at the centre of several inserts remained which indicated the deformation/wear process commenced at the periphery of the insert. Normal ranges of volume change/redistribution are not established for TAR devices and the implications of insert form change are not yet understood. However, edge-loaded components composed over half of this cohort, which reflects the conflict between design simplicity and kinematic complexity. For any figures or tables, please contact authors directly (see Info & Metrics tab above).


Orthopaedic Proceedings
Vol. 95-B, Issue SUPP_34 | Pages 570 - 570
1 Dec 2013
Boudt P Piepers I Van Der Straeten C Van Tongel A De Wilde L
Full Access

Background:. The balance between the subscapularis muscle and the infraspinatus/teres minor muscles, often referred to as the rotator cuff ‘force couple’, has been proposed to be critical component for glenohumeral stability. Function of these muscles can be estimated with the evaluation of muscle atrophy. In clinical practice, muscle cross-sectional area (CSA) rather than 3D muscle volume measurement have been used because it is less time consuming. Because combined anthropometric measures of length and width more accurately define the muscular volume it seems logical to study the transversal rotator cuff force couple in the transversal plane an not in the sagittal plane of the body because both parameters can be included. But is it not clear which transversal CSA has the best correlation with muscle volume. Purpose:. To determine the optimal transversal CSA that has the best correlation with muscle volume. Material and Methods:. A total of 30 CT images containing the full scapula were used. Using Mimics® and 3-Matic® the correlation between CSA's and volume has been evaluated. Two methods have been evaluated. The first method was the CSA measured on transversal plane without 3D editing. The second method is a CSA measured on a new defined transversal plane using 3D reconstruction and reslice editing techniques. Results. Both techniques showed a very high inter and intraobserver reliability (ICC for single measures in both techniques > 0.97, p < 0.001). Correlation of the muscle volume/CSA of the subscapularis showed a high correlation in both the non-reconstructed (ρ = 0,699, p = 0,002) and reconstructed technique (ρ = 0,842, p < 0,001). Correlation of the muscle volume/CSA of the infraspinatus/teres minor showed a moderate correlation in the non-reconstructed (ρ = 0,591, p = 0,013) and a high correlation in reconstructed technique (ρ = 0,779, p < 0,001). There is a significant higher correlation with the volume with the reconstructed technique compared to the non-reconstructed technique (ρ = 0.638, p < 0.001 for the conventional transversal section versus ρ = 0.818, p < 0.001 for the resliced section). Conclusion. Muscular volume of the rotator cuff force couple can be quantified using a non-reconstructed CSA, but is significant more accurately quantified by a 3D reconstructed technique. In the future, balance of the force couple in different shoulder pathologies can be quantified with this measurement technique


Orthopaedic Proceedings
Vol. 95-B, Issue SUPP_1 | Pages 197 - 197
1 Jan 2013
Baker P Critchley R Jameson S Hodgson S Reed M Gregg P Deehan D
Full Access

Background. Both surgeon and hospital volume influence patient outcomes following revision knee arthroplasty. Purpose. To audit all centres performing revision knee procedures in England and Wales over a 2-year period. All centres were audited against two pre-defined standards linked to hospital volume. Operative volume should be greater than 10 revisions per year;. More than 2.5 revisions should be performed for every 100 primary arthroplasties implanted. Methods. Data for 9659 knee revisions performed in 359 different centres between 01/07/08 and 30/06/10 was accessed from the National Joint Registry for England and Wales. For each centre information on the volume of primary and revision knee procedures undertaken during this period was available and was used as the basis for audit. Results. During the 2-year study period 396 different centres performed 153133 primary knee arthroplasties. Of these 359 (91%) performed 9659 knee revisions, equivalent to 6.2 revisions for every 100 primary arthroplasties performed. Revision centres included 208 (58%) NHS hospitals performing 8148 revisions, 141 (39%) independent hospitals performing 1258 revisions and 10 (3%) Independent Sector Treatment Centres (ISTC) performing 253 revisions. The median number of revisions performed per hospital was 7 per year (Range 1 to 144). Volume differed dependent upon hospital type (NHS=14/year vs. Independent=3/year, p< 0.001). Two hundred and twelve (59%) centres performed < 10 revisions per year and thus fell below the audit standard. Eighty of these centres also performed < 2.5 revisions per 100 primaries. Of the 141 independent hospitals 128 (91%) fell below the suggested standards for revision volume. Conclusions. A significant number of institutions are performing only a small volume of knee revision procedures. To ensure safe and sustainable practice with better outcomes, consideration should be given to rationalising the revision service in fewer centres


Bone & Joint Open
Vol. 1, Issue 6 | Pages 261 - 266
12 Jun 2020
Fahy S Moore J Kelly M Flannery O Kenny P

Aims. Europe has found itself at the epicentre of the COVID-19 pandemic. Naturally, this has placed added strain onto healthcare systems internationally. It was feared that the impact of the COVID-19 pandemic could overrun the Irish healthcare system. As such, the Irish government opted to introduce a national lockdown on the 27 March 2020 in an attempt to stem the flow of admissions to hospitals. Similar lockdowns in the UK and New Zealand have resulted in reduced emergency department presentations and trauma admissions. The aim of this study is to assess the effect of the national lockdown on trauma presentations to a model-3 hospital in Dublin, Ireland. Methods. A retrospective study was conducted. All emergency department presentations between 27 March 2019 to 27 April 2020 and 27 March 2020 to 27 April 2020 were cross-referenced against the National Integrated Medical Imaging System-Picture Archiving Communication System (NIMIS-PACS) radiology system to identify those with radiologically proven skeletal trauma. These patients were grouped according to sex, age, discharge outcome, mechanism of injury, and injury location. Results. A 21% decrease in radiologically proven trauma was observed on comparison with the same time-period last year. Additionally, a 40% reduction in trauma admissions was observed during the COVID-19 lockdown. A 60% reduction in sports-related injuries and road traffic accident-related injuries was noted during the national lockdown. However, a 17% increase was observed in patients sustaining trauma because of domestic accidents. Conclusion. Variation was observed in both the volume and nature of trauma presentations during the COVID-19 lockdown. As would be expected, a reduction was seen in the number of injuries resulting from outdoor activities. Interestingly, increased rates of domestic injuries were seen during this period which could represent an unintended consequence of the prolonged period of lockdown. Cite this article: Bone Joint Open 2020;1-6:261–266


Orthopaedic Proceedings
Vol. 103-B, Issue SUPP_15 | Pages 58 - 58
1 Dec 2021
Ayoglu N Karaismailoglu B Botanlioglu H
Full Access

Aim. The diagnosis of septic arthritis mostly relies on clinical examination, several blood parameters including white blood cell count, C-reactive protein, sedimentation, and the analysis of the joint aspiration. However, the diagnosis can be difficult when the symptoms are vague and the information obtained from laboratory might be insufficient for definitive diagnosis. This study aimed to evaluate several ratios obtained from routine blood tests for a possible use in the diagnosis of septic arthritis. Method. The adult patients who were operated in our clinic due to septic arthritis between 2014–2020 were identified and retrospectively evaluated. The patients with any blood disorders or missing file information were excluded. A total of 36 patients were found to be eligible for inclusion. The control group included 40 patients without any sign of infection who underwent total knee arthroplasty due to knee osteoarthritis. Preoperative blood tests of each patients were examined. In addition to CRP and sedimentation values, neutrophil-lymphocyte, monocyte-lymphocyte, platelet-lymphocyte, and platelet count-mean platelet volume were calculated and receiving operating characteristics (ROC) curve analysis was made to determine the sensitivity, specificity and area under curve (AUC) values of these parameters. Results. The distribution of affected joint in septic arthritis group was as follow; 22 knees, 6 hips, 4 shoulders, 2 elbows, 1 wrist and 1 ankle. The cultures of joint aspiration yielded positive result in 19 patients while the cultures were negative in 17 patients. All of the analyzed parameters were significantly different between the groups (p<0.001). ROC curve analysis results are given in detail, in Table 1 and Figure 1. The AUC value was 97.3 when only CRP and sedimentation values were used but increased to 98.6 when neutrophile/ lymphocyte ratio was added and increased to 100 when all analyzed parameters were included. Conclusions. The analyzed parameters were found to increase the overall sensitivity and specificity when used together with acute phase reactants. However, when evaluated separately, CRP and sedimentation were still found as the most valuable parameters in the diagnosis of septic arthritis. In the diagnosis of septic arthritis, 35 mm/hr cut-off value for sedimentation and 10 mg/L cut-off value for CRP were found more sensitive and specific compared to standard laboratory cut-off values of 20 mm/hr and 5 mg/L. For any tables or figures, please contact the authors directly


Orthopaedic Proceedings
Vol. 104-B, Issue SUPP_1 | Pages 2 - 2
1 Jan 2022
Boktor J Alshahwani A El-Bahi A Banerjee2 P Ahuja S
Full Access

Abstract. Background. Cauda equina syndrome (CES) is a rare serious condition that, if missed at initial presentation, can lead to serious disability. Early diagnosis is crucial for a favourable outcome. Few studies included urodynamic test and measurement of post-void residual urine (PVR) as an adjunct screening tool for acute CES before proceeding to MRI scan, yet there are differences in the cut-off point as a threshold volume to be considered as a red flag for doing MRI amongst these studies. Aim. Meta-analysis and systematic review of literature that included PVR as a predictive tool in CES to identify the reliability of PVR and the optimal numerical value to be considered as red flag. Material & Methods. A comprehensive literature search was undertaken in PubMed, Medline, and Embase databases using our search strategy. Meta-analysis of collated data. Results. A total of seven studies were included with a total of 938 patients. The number of cases suitable for meta-analysis was 714. CES was confirmed in 73. urodynamic testing and PVR diagnosed 86 and excluded 426. The sensitivity of PVR>100ml was 64% (CI 97.5%: 0.44–0.80), specificity 59.2% (CI 97.5%: 0.46 – 0.711), while PVR >200 showed more predictive figures, with sensitivity improved to 83.1% (CI 97.5%: 0.62–0.94) and specificity to 93.5% (CI 97.5%: 0.50–0.99). Conclusions. Urodynamics test is an essential tool in CES assessment. Authors recommend PVR > 200 ml as the numerical cut-off point to be considered as a red flag that if present with other clinical red flags, urgent MRI is recommended in suspected CES


Orthopaedic Proceedings
Vol. 102-B, Issue SUPP_6 | Pages 44 - 44
1 Jul 2020
Wallace R Xie S Simpson H
Full Access

Trabecular bone is a multiscale hierarchical composite material that is known to display time-dependant properties. However, most biomechanical models treat this material as time independent. Time-dependant properties, such as creep and relaxation, are thought to play an important role in many clinically relevant orthopaedic issues: implant loosening, vertebral collapse, and non-traumatic fractures. In this study compressive multiple-load-creep-unload-recovery (MLCUR) tests were applied to human trabecular bone specimens. 15 female femoral heads were harvested, with full ethical approval and patient consent, at the time of total hip replacement. Central cores were extracted and cut parallel under constant irrigation. Specimens were embedded in end caps using surgical cement, an epoxy tube was secured around the end caps and filled with phosphate buffered saline (PBS) to ensure the specimens remained hydrated throughout. Embedded samples were scanned by microCT (SkyScan 1172, Bruker) at a resolution of 17µm to determine microarchitecture. Bone volume fraction (BVF) was used to represent microarchitecture. Specimens had an effective length of 16.37mm (±1.90SD) with diameter of 8.08mm (±0.05SD), and BVF of 19.22% (±5.61SD). The compressive MLCUR tests were conducted at 5 strain levels, 2000µε, 4000µε, 6000µε, 8000µε and 10000µε. At each strain level, the load required to maintain each strain was held for 200s (creep) then unloaded to 1N for 600s (recovery). The instantaneous, creep, unloading and recovered strains can be easily obtained from the strain-time curves. Stress-strain plots revealed the Young's modulus. Data was modelled using line of best fit with appropriate curve fitting. R2 values were used to indicate association. Mechanical testing demonstrated the expected time independent relationship between BVF and stiffness: higher stiffness was found for specimen with higher BVF and this was consistent for all strain levels. Creep strain was found to depend on instantaneous strain and BVF. At low levels of instantaneous strain, there was a greater amount of creep strain in low BVF samples (R2 = 0.524). This relationship was no longer apparent at higher strain levels (R2 = 0.058). Residual strain also depended on the applied instantaneous strain and BVF: at low levels of strain, residual strain was similar with all BVF (R2 = 0.108) and at high levels of strain, residual strain was greater in low BVF samples (R2 = 0.319). The amount of instantaneous strain applied to each sample is constant, variations in stiffness result in different applied loads. In low BVF bone, the stiffness is also low, therefore the stress required to reach designed strain is also lower: yet, there is more creep and less recovery. We have demonstrated that even at loads below recognised yield levels, time-dependence affects the mechanical response and residual strain is present. In cases of low BVF, deflection due to creep, and increased irrecoverable strain could have clinically relevant consequences, such as implant loosening and vertebral collapse. The role of time-dependant properties of bone is seldom considered. This data could be developed into a constitutive model allowing these time-dependant behaviours to be incorporated in finite element modelling, leading to better predictions of implant loosening, especially for lower quality bone


Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_II | Pages 9 - 9
1 Feb 2012
McGrath L
Full Access

The effects of wear particles on artificial hip joints are well documented. Aseptic loosening has been demonstrated to be dependent on both particle numbers and particle size. This study investigated the effects of stem material and surface finish on particles produced at the stem/cement interface in cemented artificial hips. Three commonly used implant materials of different hardness were investigated: cobalt chrome, the hardest of the three materials, stainless steel and titanium alloy which was the softest material tested. The surfaces of three femoral stems with different surface finishes were measured and used as templates; the Exeter which is highly polished, the Charnley which is moderately rough and the Capital which is very rough. Test plates were manufactured in each material and with each surface finish making 9 sets of plates in all. The plates were opposed to cement pins (CMW) in a sliding wear tester. The volume of debris produced was calculated from measurements of the pins pre- and post-test. The debris was collected, filtered and examined under the electron microscope, which allowed particle sizes of a representative sample of debris to be measured. From this mean particle size was calculated. Volume of debris: for all three materials the roughest surface produced the greatest volume of debris and the smoothest surface the least. For any given surface finish the softest material produced the greatest volume of debris and the hardest material the least. Size of particles: for all three materials the roughest surfaces produced the largest particles and the smoothest surface the smallest particles. For any given surface finish the hardest material produced the smallest particles and the softest material produced the largest particles


Orthopaedic Proceedings
Vol. 98-B, Issue SUPP_8 | Pages 117 - 117
1 May 2016
Kohan L Kerr D Farah S Field C Nguyen D
Full Access

Aim. Adverse tissue reactions have been a concern in relation to metal components, particularly in hip replacements. We look at a possible correlation between hip joint effusion and metal ion levels. Materials and methods. 56 patients,(42M, 14F) agreed to the study. All had metal-on-mental arthroplasties. Average age was 64.2 (SD 9.8). All patients were asymptomatic. Ultrasound examination performed by one ultrasonographer, using a Sonosite M-Turbo machine with a C60X/5-2 MHz transducer. Cobalt levels were assessed using an inductively coupled plasma mass spectrometer. Chromium levels were assessed using a graphite furnace atomic absorption spectrometer. Results. Average blood ion levels were:. Cobalt 39.02 nmol/L. (SD41.18) range 3 to 215. Chromium 52.51 nmol/L (SD47.48) range 5 to 284. Average Volume: 10.38ml (SD21.3) Range 0 to 219. Conclusion. There was no statistically significant correlation between joint effusion and metal ion levels


Orthopaedic Proceedings
Vol. 95-B, Issue SUPP_19 | Pages 27 - 27
1 Apr 2013
Karuppal R
Full Access

Introduction. Epidural steroid injection is an established treatment modality for intervertebral disc prolapse. It is a low-risk alternative to surgical intervention in some patients for whom noninvasive treatment has failed. Caudal epidural steroid injection is one of the most widely used methods for pain relief. The aim of this study was to determine the significance of same dose in different volume of caudal epidural steroid injection in the treatment of lumbar degenerative disc disease. Material/Methods. Prospective study was conducted during 2007 to 2009. 100 Patients were randomized in to two groups, of which 50 % (group A) received 4 ml of steroid with isotonic saline and remaining 50 % (group B) received 12 ml. Injection was given in prone position through a 22-G needle in to the epidural space through the sacral hiatus. The average follow-up was 18 months. Outcomes scores included the SF-36, Oswestry disability index and pain VAS and were recorded in the pre and post injection periods. Results. In group A, 18 patients had significant pain relief and 32 had no relief during the early period. Whereas in group B, 22 had significant pain relief and 28 had no relief. The quality of pain relief of 50% or greater was considered as significant. Follow up after 1 year does not show much difference. Group B had significant decrease in symptoms in the initial post injection period (P<0.05). Conclusions. The volume of steroid solution in the treatment of lumbar degenerative disc disease is significant in the early post injection period only


Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_XLIV | Pages 16 - 16
1 Oct 2012
Smith E Al-Sanawi H Gammon B St. John P Pichora D Ellis R
Full Access

Primary internal fixation of uncomplicated scaphoid fractures is growing in popularity due to its advantages over conventional cast fixation. Performing the procedure percutaneously reduces the risk of infection and soft tissue damage, but can be tricky because of the small size and complex three-dimensional (3D) shape of this bone. Computer-assisted navigation has been an invaluable tool in other pin insertion procedures. This in-vitro study aimed to evaluate two different rendering techniques for our navigation interface: (i) 3D volume rendering of the CBCT image to show digitally-reconstructed radiographs of the anatomy, and (ii) volume-slicing, analogous to CT-images. As the shape of the scaphoid is highly variable, a plastic model of the wrist was constructed in order to provide consistency that would not be possible in a cadaver-based study. The plastic model featured a removable scaphoid such that a new one was replaced between trials. Three surgeons each performed eight trials using each of the two navigated techniques (yielding a total of 48 trials for analysis). Central placement of scaphoid fixation has been linked with mechanical stability and improved clinical outcomes, thus the surgical goal was to place a K-wire to maximise both depth from the surface and length of the drill path. The wire was drilled through the scaphoid, from distal to proximal, allowing for post-trial analysis of the drill path. A ceiling-mounted OptoTrak Certus camera (Northern Digital Inc., Canada) and a floor-mounted isocentric 3D CBCT C-arm (Innova 4100, GE Healthcare, France) permitted a registration transformation between the tracking and imaging systems to be computed preoperatively, before each trial, using a custom calibration device. Optical local coordinate reference bodies were attached to the wrist model and a custom drill guide for tracking with the Certus camera. During each trial, a 3D spin image of the wrist model was acquired, and rendered according to the technique under study. For 3D volume rendering, the spin image was rendered as a digitally-reconstructed radiograph (DRR) that could be rotated in three dimensions. In the planning phase, the surgeon positioned a desired drill path on the images. Anterior-posterior and lateral views of the 3D volume rendering were used for navigation during the drilling phase. The real-time orientation of the drill guide was shown relative to these images and the plan on an overhead. For volume-sliced (VS) navigation, the spin image was volume-rendered and sliced along the principal planes (axial, coronal, sagittal) for planning. A slider interface allowed the surgeon to scroll through the slices in each of the planes, as if they were looking at individual CT slices. Once the desired drill path was positioned, the volume-sliced views were reconfigured to show slices along the oblique planes of the planned path for navigation. Following all trials, model scaphoids with wire intact were imaged using CT with a slice thickness of 0.625 mm. The CT series were segmented and used to construct 3D digital models of the wire and drilled scaphoid. Algorithms were developed to determine the minimum distance from the centerline of the wire and the scaphoid surface, and to compute the length of the drill path. Screw breach should be avoided as it disrupts the articular surface and may lead to a sequela of cartilage deterioration and osteoarthritic changes. The shortest distance measure was extrapolated to assess whether a standard fixation screw (Accutrak Mini, 1.78 mm radius) would have breached the scaphoid surface. There were three screw breaches noted in the 3D DRR trials, while only one occurred using volume-slicing. The minimum distance from the centerline of the wire to the scaphoid surface can also be thought of as a “safe zone” for screw breach. Although no difference in the mean distance (μ) was noted between groups (μ. DRR. = 2.3 mm, μ. VS. = 2.2 mm), the standard deviation (σ) was significantly higher for the DRR trials (σ. DRR. = 0.50 mm, σ. VS. = 0.37 mm, p < 0.1), suggesting a higher reliability of central placement using VS for navigation. In contrast, the length of the drill paths were significantly longer for the DRR trials (μ = 28.7 mm, σ = 0.66 mm) than for VS-navigation (μ = 28.3 mm, σ = 0.62 mm) at p < 0.1. The surgical goal was to pick a path that maximised both the length of the path, as well as the minimum distance from the scaphoid surface. Algorithms were developed to find the paths that would maximise: (i) the length and (ii) the distance from the surface of the model scaphoid used in this study. The maximum possible length was 29.8mm (with a minimum distance of 2.2mm from the scaphoid surface), and the maximum distance was 3.3mm (with a length of 27.5mm). Therefore, the set of optimal drill paths had length > 27.5 mm, and distance > 2.8 mm. Of the DRR-navigated trials, 11 were below the minimum optimal depth, and only one trial was below the optimal length; 13 of the 24 trials (54%) were of both optimal length and depth. Of the VS-navigated trials, nine were below the minimal optimal distance, and four were below the minimum optimal length; 11 out of 24 trials (46%) were within both the optimal length and depth. From this comparative study, we conclude that VS-navigation was superior in locating a central location for the fixation wire, while DRRs were superior in maximising the depth of the drill path. Thus, we propose a hybrid interface, incorporating both volume-slicing and DRRs, in order to maximise the effectiveness of navigation for percutaneous scaphoid pinning


Bone & Joint Open
Vol. 2, Issue 8 | Pages 655 - 660
2 Aug 2021
Green G Abbott S Vyrides Y Afzal I Kader D Radha S

Aims

Elective orthopaedic services have had to adapt to significant system-wide pressures since the emergence of COVID-19 in December 2019. Length of stay is often recognized as a key marker of quality of care in patients undergoing arthroplasty. Expeditious discharge is key in establishing early rehabilitation and in reducing infection risk, both procedure-related and from COVID-19. The primary aim was to determine the effects of the COVID-19 pandemic length of stay following hip and knee arthroplasty at a high-volume, elective orthopaedic centre.

Methods

A retrospective cohort study was performed. Patients undergoing primary or revision hip or knee arthroplasty over a six-month period, from 1 July to 31 December 2020, were compared to the same period in 2019 before the COVID-19 pandemic. Demographic data, American Society of Anesthesiologists (ASA) grade, wait to surgery, COVID-19 status, and length of hospital stay were recorded.


Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_XXXVIII | Pages 125 - 125
1 Sep 2012
Turgeon TR Petrak M Slobodian L Bohm E
Full Access

Purpose. Current practice requires all post-operative hip and knee arthroplasty patients complete a series of clinical questionnaires at each visit. The patients responses to these questionnaires are used as a clinical evaluation tool for the surgeons to assess functionality, satisfaction and pain at routine pre and post-operative visits. The recent installation of 4 touch screen computer terminals, located in the patient waiting area, has created the opportunity to have the patients complete these questionnaires by using only the touch screen entry system. This eliminates the need for clinic staff to manually enter the patients responses into the clinics database, eliminate potential data entry errors, and will significantly reduce the amount of time and paper required to prepare questionnaires for each patient. In addition to possibly increasing the volume of data we can collect in our clinic, this also allows the surgeon to have immediate access to the patients responses which can be reviewed prior to seeing the patient in the office. Our goal was to determine the overall level of patient satisfaction with using the new touch screen direct entry system, the efficiency of completion and the quality of data entry occurring from the direct entry system. Method. During the month of April, 2010, a consecutive series of 100 patients entering the orthopaedic clinic, were directed to the touch screen kiosks to complete the required questionnaires (SF-12, Oxford Knee/Hip, Harris Hip/Knee Society Score, and the Patient Satisfaction Survey). Once the patients completed the touch screen questionnaires they were asked to complete a paper copy of the Touch Screen Satisfaction Questionnaire. This questionnaire asked 6 questions regarding their satisfaction with the touch-screen system, the ease/difficulty of use, and which method they would prefer to complete such questionnaires if given a choice. Results. Our sample resulted in a mean age of 68.5 years (range 41.7 to 93.8 years), with 53 females and 47 males. Ninety-six percent of patients who used this system reported they had never used a touch-screen for health purposes, 71% found it very easy to use, and 49% reported that it was very quick to use. When polled about their preferences regarding questionnaires, 82% of patients preferred to use the touch-screen system, over filling out paper copies (2%), using an external internet site from home (1%) and 15% reported having no real preference for any of these methods. Patients were unable to continue without answering all questions, therefore this method of data collection prevents the occurrence of missing values and incomplete records. Conclusion. Our results support our initial hypothesis that the new touch-screen system is a superior tool for obtaining clinically relevant patient information regarding function, pain and satisfaction in an effective and timely manner. These findings support our decision to integrate touch-screen systems into the information flow in an orthopaedic clinic