The purpose of the study was to determine the rate of conversion from RSA to THR in a number of Canadian centers performing resurfacings Retrospective review was undertaken in 12 Canadian Centers to determine the rate of revision and reason for conversion from RSA to THR. Averages and cross-tabulation with Chi-Squared analysis was performed. kaplan Meier survivorship was calculated.Purpose
Method
To identify any difference in clinical outcome between Intra-Capsular facet (IF) and Peri-facet (PF) injections in patients with low back pain (LBP). IF and PF joint steroid injections have been used for treatment of LBP with varied reports of pain relief for many years. Patients randomised into IF and PF groups. Bilateral L4/5 and L5/S1 levels injected. 40mg of Depo-Medrone with Lignocaine (total 1ml) in IF group. 80mg of Depo-Medrone with 1ml of 0.5% Chirocaine (total 3ml) in PF group. Pain visual analogue score (VAS) and analgesic chart – completed till six months.Objective
Methods
Thirty-six patients had MRI at 2 years. Using paired t test we noted statistically significant increase in mean dural sac area in all four positions mentioned above. There was clinical improvement in 26 and some or no improvement in 10 patients. Number with increase in canal cross sectional area was 28 and that with reduced area was 8. Clinical and canal area improvement was seen in 20 (56%) patients and clinical improvement with reduced canal area was seen in 5 (14%). Some or no clinical improvement with canal area improvement occurred in 8 (22%) patients and no significant clinical or canal area improvement in 3 (8%).
Majority of patients (56%) showed clinical and cross sectional area improvement at 2 years. One patient with no clinical improvement had subsequent decompression surgery (this patient had dural cross sectional area improvement). 64% patients had similar clinical and dural cross sectional area changes but there is not a clear-cut correlation between clinical outcome and change in canal cross-sectional area.
Radiologically, BAC-MS and cartilage thickness at three months had no significant difference between treatment and placebo groups (p-value = 0.81 and 0.88 respectively). The change in BAC-MS and cartilage thickness at 3 months was also not significant (p-value = 0.09 and 0.41 respectively).
Clinical outcome was assessed by Zurich claudication questionnaire (ZCQ), visual analogue score (VAS), Oswestery disability index (ODI) and SF36 questionnaires preoperatively and at 2 years. ZCQ has three components- symptom severity, physical function and patient satisfaction. ZCQ is considered the most precise, reliable and condition specific questionnaire for lumbar canal stenosis. Out of 57 patients, 2 died due to unrelated causes, 3 withdrew from study and 3 had the device removed within 2 years. Forty-five, 44, 42 and 48 completed ZCQ, ODI, SF-36 and VAS respectively at 24 months.
The mean ODI improved by 6.5 in single level and 10.8 in double level cases. The SF-36 showed improvement in physical function, role physical, bodily pain and vitality social domain. Average hospital stay for the procedure was 1.6 days. One patient stayed for 10 days for investigation unrelated to the procedure. There were no major complications.
There is little evidence from the literature regarding the timing of hip fracture surgery for patients who are on the antiplatelet agent clopidogrel bisulphate (Plavix) (1). We report the results of a retrospective case control study of 40 patients comparing the timing of surgery for patients taking clopidogrel against a control group of those not taking an antiplatelet agent. Time to surgery, length of stay, transfusion requirements, wound problems and other post operative complications were examined. Within the study group of patients taking clopidogrel, we also compared those who underwent surgery within four days of stopping the clopidogrel and after four days. The transfusion requirements were greater in those patients on clopidogrel prior to admission. Wound healing and post operative complications were similar between the two groups. Total length of hospital stay and post operative length of stay were longer in the clopidogrel group. There was an increase in transfusion requirements and post operative length of stay in patients on clopidogrel undergoing early surgery (within 4 days) compared to the group where surgery was delayed. We conclude that, in this small study, transfusion requirements and length of stay were greater in patients on clopidogrel. Transfusion requirements and post operative length of stay were also greater if surgery was performed within four days of omitting clopidogrel. Further studies are required to determine optimal timing of surgery following discontinuation of clopidogrel.
The patients were divided into two groups, A and B. The first, Group A, in which only Dynesys was used and the second, Group B, in which Dynesys was used adjacent to one or more fused segments.
The ROM of the end plate angle at the instrumented segments in Group A reduced from 5.72o to 1.44o{difference 4.28o(p=0.005)} and in Group B reduced from 6.00o to 2.17o,{difference 3.83o(p=0.001)}. The ROM of the end plate angle at the level above instrumentation in Group A reduced from 8.2o to 5.1o {reduction 3.1o(p=0.085)}, while in group-B increased from 7.3o to 7.5o, a difference of 0.2o (p=0.877). The mean anterior disc height in Group A reduced by 2.1mm (p<
0.001) from 9.59mm to 7.44mm. The posterior disc height also reduced from 6.56mm to 6.26mm, a difference of 0.3mm, (p=0.434). In Group B, the anterior disc height reduced by 1.98mm (pre-op=9.04mm, post-op= 7.06mm, p=0.001) and the posterior height by 0.35mm (pre-op 6.14mm to post op 5.79mm, p=0.443)
The patients were divided into two groups, A and B. The first, Group A, in which only Dynesys was used and the second, Group B, in which Dynesys was used adjacent to one or more fused segments.
The ROM of the end plate angle at the instrumented segments in Group A reduced from 5.72o to 1.44o{difference 4.28o(p=0.005)} and in Group B reduced from 6.00o to 2.17o,{difference 3.83o(p=0.001)}. The ROM of the end plate angle at the level above instrumentation in Group A reduced from 8.2o to 5.1o {reduction 3.1o(p=0.085)}, while in group-B increased from 7.3o to 7.5o, a difference of 0.2o (p=0.877). The mean anterior disc height in Group A reduced by 2.1mm (p<
0.001) from 9.59mm to 7.44mm. The posterior disc height also reduced from 6.56mm to 6.26mm, a difference of 0.3mm, (p=0.434). In Group B, the anterior disc height reduced by 1.98mm (pre-op=9.04mm, post-op= 7.06mm, p=0.001) and the posterior height by 0.35mm (pre-op 6.14mm to post op 5.79mm, p=0.443)
Thirty patients with were treated with Dynesys system. All had discography and positional MRI preoperatively and nine months post-operatively. The patients were divided in to two groups. The first in which only Dynesys was used and the second in which Dynesys was used with fusion.
The ROM of the end plate angle at the instrumented segments in group-A reduced from 5.24o to 2.18o{difference 3.06o(p<
0.005)} and in group-B reduced from 6.69o to 2.46o,{difference 4.23o(p=0.008)}. The ROM of the end plate angle at adjacent level in group-A changed from 8.26o to 7.0o {reduction 1.26o(p=0.388)},while in group-B increased from 6.91o to 8.64o, {difference 1.73o(p=0.149)} The mean anterior disc height in-group A reduced by 1.43mm (p<
0.005) from 9.75mm to 8.32mm, and the posterior one was increased from 6.27mm to 6.77mm {difference of 0.5mm,(p=0.008)}. In group-B the anterior disc height reduced by 1.11mm (pre-op=10.44mm,post-op= 9.33mm,p=0.049) and the posterior one by 0.16mm (pre-op 6.98mm to post-op 6.82mm,p=0.714).
A retrospective study of one hundred and nineteen unicompartmental knee arthroplasties was performed. Outcome measures were the Oxford twelve-item knee questionnaire, the Short Musculoskeletal Functional Assessment (SMFA) and the WOMAC. Regression analysis was performed in order to determine predictors of outcome. After an average follow up period of four years, the mean scores indicated a good to excellent functional outcome. The only predictor of outcome identified was gender, with women obtaining a better functional outcome than men. Other variables that did not influence functional outcome included age, weight, stage of disease, previous HTO and bilateral procedures. The purpose of this study was to determine
the functional outcome of unicompartmental knee arthroplasty and predictors of outcome. Although unicompartmental knee arthroplasty is becoming more widely accepted as a treatment option for degenerative osteoarthritis, there are very few studies in the literature that systematically investigate the predictors of outcome for this procedure. This is a retrospective study of one hundred and nineteen unicompartmental knee arthroplasties perfomed at a university hospital by a single surgeon. The outcome measures used were the Oxford twelve-item knee questionnaire, the Short Musculoskeletal Function Assessment (SMFA) and the Western Ontario and McMaster (WOMAC) functional indices. Multiple regression analysis was performed to determine predictors of outcome from chart derived variables. After a mean follow-up of four years the mean Oxford Knee Score was thirty-nine and the mean SMFA and WOMAC functional scores were eight and seven respectively, indicating a good to excellent functional outcome. Regression analysis revealed gender as a predictor of outcome however other variables including age (range 49–84 yrs), weight (range 55–225 kgs), previous ORIF, preoperative varus/valgus (range 0–16 degrees), joint subluxation (range 0–13mm), radiographic stage of disease (Kellgren and Lawrence), as well as previous HTO and bilateral (simultaneous or staged) unicompartmental knee arthroplasty were found to not correlate with functional outcome. Good to excellent functional outcome scores can be achieved with unicompartmental knee replacement. Previous HTO or bilateral procedures as well as weight, pre-operative varus/valgus <
sixteen degrees or radiographic stage of disease were not predictive of outcome.
This study measures the changes in the lumbar spine in different postures, pre- and after insertion of the device.
All had a positional MRI preoperatively and nine months post-operatively in flexion-extension-lateral bending. The patients were divided in to two groups: Group(A) with 8 patients in which Dynesys was used with fusion (disc-height<
40 %) Group(B) with 12 patients was the Dynesys-only group (disc-height=40–90%).
The changes in the anterior disc height was (mean= −1.18)(p<
0.05) and to the posterior (mean=0.37)(p=0.134). In bending were (mean=−0.87°)(p=0.18) for left and (mean=−0.24°)(p=0.75) for the right
21 patients (11 males; 10 females) were included in the study. Age ranged from 57 – 88 years. All had symptomatic lumbar spinal stenosis- single level- 13 (L2/3-1; L3/4-3; L4/5-9); double level 8(L3/4, L4/5 – 7; L4/5, L5/ S1 – 1).
This study measures the changes in the lumbar spine in different postures, pre- and after insertion of the device. Methods In our study 25 patients with dominant low back pain, with or without leg pain, were treated with Dynesys system, 14 females and 11 males with mean age 43.5 yrs. Discography was done to evaluate the symptomatic painful level. All patients had a positional magnetic resonance imaging (pMRI) scans preoperatively and nine months post-operatively in standing; sitting flexion and extension, and left and right bending postures. The patients were initially divided into two groups. The first (Group A) with 14 patients in which only Dynesys was used (disc height 40–90%) and the second (group B) with 11 patients in which Dynesys was used with fusion (disc height <
40 %).
The range of movement of the end plate angle at the instrumented segments in group A reduced from 5.6° preoperatively to 2.6° with a difference of 3.0° (p=0.016) while in group B it reduced from 6.7° to 2.5° postoperatively with a difference of 4.2°(p=0.008). The range of movement of the end plate angle at adjacent level in group A changed from 8.8° preop. to 7.2° with a reduction of 1.6° (p=0.427) while in group B it increased from 6.9° to 8.6°, difference of 1.7° (p=0.149) The mean anterior disc height in group A reduced by 1.2mm (p<
0.005) from 10.1mm to 8.9mm postoperatively, and the posterior one was increased from 6.5mm to 8.9mm with a difference of 0.6mm (p= 0.013). In group B the anterior disc height was reduced by 1.1mm (pre-op 10.4mm to post-op 9.3mm; p=0.049) and the posterior one by 0.16mm (pre-op 6.98mm to post-op 6.82mm; p=0.714)
Introduction: Given the timing and nature of adolescent-onset idiopathic scoliosis (AIS), this progressively deforming condition is highly likely to have a significant psychosocial impact. Body image dissatisfaction is a frequent finding in AIS patients, which is of concern, as there is a well-documented causative link between body image disturbance and the formation of disordered eating behaviour, reflected in the theoretical models for this area of psychopathology. However, although AIS patients have frequently been observed to exhibit disturbed body image, there has been no previous attempt to assess indications of disordered eating behaviour. Given the prevalence of AIS in adolescent females and the possible medical consequences of disordered eating, this study aimed to investigate whether AIS patients have an increased likelihood of low body weight. Methods and Results: Patients were recruited over a four month period from the regional scoliosis out-patient clinic at St James’ University Hospital; 44 female scoliosis patients participated, with a mean age of 16 (range 13 to 19). All those meeting the inclusion criteria (diagnosed with AIS, not diagnosed with any other serious medical condition), and attending clinic over the data collection period were asked to participate. Weight, height, and BMI (weight (kg)/height(m)2) measurements taken from AIS participants were compared to age and gender-adjusted normative data. No uncoiling correction was made for the scoliosis in terms of body height. The International Classification of Diseases (ICD-10) body mass criterion for eating pathology was used to determine how many AIS participants were within the range considered eating disordered. Independent-sample t-tests revealed that, when compared to the normative data, the AIS group did not differ significantly in terms of height (p=0.646). However, they were significantly lighter (p<
0.001), and had significantly lower BMI scores (p<
0.001); 25% of the sample had a BMI score within the range considered anorectic. Of these low-BMI patients, the mean index score was 15.6 (range 12.9–17.5). The mean weight was 40.25 kg (6st 4lbs), with a range from 31.5 to 49 kg (4st 13lbs – 7st 11lbs). The body mass data for this low-BMI group, both in terms of range and severity, is not within ‘normal’ body shape variation, and would not be expected in healthy adolescent females. Conclusion: The relationship between a diagnosis of AIS and low body weight may indicate disordered eating behaviour and is thus a cause for considerable concern. This is of particular relevance in the light of the well-established relationship between eating psychopathology and osteoporosis, which may result if disordered eating produces a reduced peak bone mass. Organic health consequences may need to be added to a matter previously considered to be one of cosmetic deformation.
This prospective study was carried out to correlate findings of magnetic resonance imaging (MRI) and discography. Fifty-five consecutive patients with degenerative disc disease not responding to non-operative treatment were included in the study. There were 19 men and 36 women and the mean age was 45 years. Discography was carried out on 131 disc levels. The discograms were classified using modified Adams’s classification and pain recorded into three grades. MRI scans were graded using a new classification system based on parasagittal and axial images by two independent observers blinded to discography findings. There was good intraobserver (kappa 0. 74) and interobserver (kappa 0. 70) agreement for the classification system. There was a significant correlation in the morphology of discs as determined by discograms and MRI classification (p<
0. 001). Each disc was graded on MRI scan as painful or painless on basis of defined criteria. Concordant discography pain was considered as the gold standard. The sensitivity and specificity of MRI in predicting symptomatic disc using defined criteria was 94% and 77%. The sensitivities and specificity of high intensity zones was 27% and 87% and for end plate changes was 32% and 98% respectively. In 14 patients (25%) the findings of MRI and discography did not correlate. In conclusion though MRI is an excellent investigation for assessing disc morphology it should be interpreted along with discography findings before planning fusion surgery. The proposed MRI classification is a useful aid in predicting painful degenerative disc. The utility of high intensity zones and end plate changes is limited due to low sensitivity.
The quantification of local bone blood flow in man has not previously been possible, despite its importance in the study of normal and pathological bone. We report the use of positron emission tomography, using 15O-labelled water, to measure bone blood flow in patients with closed unilateral fractures of the tibia. We compared fractured and unfractured limbs; alterations in blood flow paralleled those found in animal models. There was increased tibial blood flow at the fracture site as early as 24 hours after fracture, reaching up to 14 times that in the normal limb at two weeks. Blood flow increase was less in displaced than in undisplaced fractures. The muscle to bone ratios of blood flow were similar to those in previous animal work using other techniques. Positron emission tomography will allow study of human bone blood flow in vivo in a wide variety of pathological conditions.