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Orthopaedic Proceedings
Vol. 105-B, Issue SUPP_16 | Pages 41 - 41
17 Nov 2023
Samir A Abdelghany A Metwally A
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Abstract. Objectives. To compare the effectiveness of phonophoresis (PH) and conventional therapeutic ultrasound (US) on the functional and pain outcomes of patients with knee osteoarthritis. Methods. We conducted an electronic search through PubMed, Cochrane Central Register of Clinical Trials (CENTRAL), Web of Science (WOS), and Scopus databases. We screened the retrieved articles to include only English full-text randomized controlled trials that examined the effect of phonophoresis versus conventional therapeutic ultrasound on patients with knee osteoarthritis. Two reviewers screened, extracted the data, and independently assessed the quality of the included articles. Results. A total of five randomized controlled trials met our inclusion criteria out of 267 studies screened. Our results showed no statistically significant differences between the PH and US groups (1), (2), (3),(4), and (5). The PH group demonstrated more significant effects than the UT group in reducing VAS pain scores (P=0.009) and improving WOMAC scores, although this did not reach the level of significance (P=0.143) (5). In the long term, PH therapy was found to be superior to US in improving painless walking duration and distance VAS scores (p=0.034, 0.017) respectively, as well as walking and resting walking VAS scores (p=0.03, 0.007) respectively, which were found to be permanent (3). Conclusions. Both therapies improve pain and function. However, we suggest conducting more high-quality trials with larger sample sizes and do not recommend the use of these therapies in clinical practice due to limitations in gender selection and high risk of bias. Declaration of Interest. (b) declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported:I declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research project


Orthopaedic Proceedings
Vol. 103-B, Issue SUPP_13 | Pages 109 - 109
1 Nov 2021
Rigney B Casey C Donald CM Pomeroy E Cleary M
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Introduction and Objective. Wide awake local anaesthetic no tourniquet (WALANT) is being used for a wide variety of hand and wrist surgery. It has recently been used in distal radius fracture fixation. The purpose of this systematic review and meta-analysis was to assess the effectiveness of the WALANT technique in open reduction internal fixation. Materials and Methods. Pubmed, Embase, and Scopus databases were searched on 02/03/21 with the following search terms: radius, WALANT, local anesthetic, wide awake surgery. The primary outcome measure was conversion to general anaesthetic and mean intra-operative visual analogue scale (VAS) pain scores. Secondary measures were operative times, mean intraoperative blood loss, post-operative functional and radiological outcomes. Results. 110 articles were identified; eight studies were deemed eligible with 212 in the WALANT group and 247 in the comparative groups of regional anaesthesia and general Anaesthesia (GA). Two patients in the WALANT group required conversion to general anaesthesia due to anxiety rather than pain. Intra-operative VAS pain scores in the WALANT and regional anaesthetic group were 1.75 and 2.86 respectively (p<0.001). There was no statistically significant difference in Q-DASH scores, range of motion or radiological outcomes. There was a slight increase in mean blood loss in the WALANT group compared with those given a GA or regional anaesthetic with tourniquet (22.5ml vs 12.15ml, p<0.001). Conclusions. The WALANT technique is a viable option for anaesthetic when performing distal radius fracture fixation. It is well tolerated, giving similar post-operative outcomes to other anaesthetic methods. It is a potentially useful technique in a centre with an underresourced anaesthetic department or for patients who may not tolerate regional and general anaesthetic methods. Adequate patient counselling prior to the procedure should be performed with appropriate patient selection


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_9 | Pages 61 - 61
1 May 2017
Mijnes J Heyligers I Grimm B
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Background. Complete and reliable outcome assessment is important for clinical quality control and research evidence. Online questionnaires offer the opportunity to perform follow-up at distance and desired frequency saving efforts and cost to patients and hospitals increasingly not reimbursed for this service. Patients in this unique study have been invited by mail (not at visit or by phone) and were asked to complete both methods (online, paper) instead of only one option. For the first time, response, completion and reliability of the HOOS, KOOS-PS and New-KSS, popular patient-reported outcomes (PROM's) in TJA were measured. Methods. Patients (n=107) were invited pre-operative by mail to register at atriumproms.nl (Interactive Studios, Netherlands) and complete PROM's online, followed by a second invitation three days later to complete the same on paper. THA patients (n=48) completed EQ-5D-3L, VAS pain and HOOS. TKA (n=59) questionnaires consisted of KOOS-PS, VAS pain and New-KSS. Reliability was assessed using intraclass correlation coefficient (ICC). ICC was considered excellent >0.75 according to literature. Results. Overall response rate was 77.6% (83/107) with no difference between THA (77.1%) and TKA (79.3%). Paper had a higher response rate (70.1% vs. 34.9%, p<0.01, Fisher Exact test). However, completion rate was higher online (95%) than on paper (54%, p<0.01). Age had a significant influence on online response rates (<70yrs: 43%, >=70yrs: 23%, p=0.03). Reliability was excellent in the THA group (ICC: 0.84 – 0.95) except for the EQ-5D-3L (ICC: 0.72). The TKA group showed excellent reliability for VAS-pain (0.92). However, for New-KSS reliability was only good (0.60) or poor for KOOS-PS (0.39). Conclusions. A high response rate shows patient cooperation making distance follow-up by mail feasible. Online PROM's were only half as popular as paper questionnaires but achieve twice the completion rate. Taking scores online has excellent reliability. Only when conversions are performed (KOOS-PS, EQ-5D) reliability suffers


Orthopaedic Proceedings
Vol. 100-B, Issue SUPP_3 | Pages 52 - 52
1 Apr 2018
Huish E Coury J Ummel J Casey J Cohen J
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Introduction. Management of the patellofemoral surface in total knee arthroplasty (TKA) remains a topic of debate. Incidence of anterior knee pain and incidence of repeat operation have been the focus of several recent meta-analyses, however there is little recent data regarding patients” subjective ability to kneel effectively after TKA. The purpose of this study was to compare patient reported outcomes, including reported ability to kneel, after total knee arthroplasty with and without patellar resurfacing. Methods. Retrospective chart review of 84 consecutive patients who underwent primary TKA with patella resurfacing (56 knees) or without patella resurfacing (28 knees) having a minimum of 2.5 year follow up was performed. Oxford knee scores (OKS), visual analog pain scores (VAS), and questionnaires regarding ability to kneel were evaluated from both groups. Inability to kneel was defined as patients reporting inability or extreme difficulty with kneeling. Shapiro-Wilk test was used to determine normality of data. Mann Whitney U test was used to compare the OKS and VAS between groups. Chi square test was used to compare kneeling ability between groups. Statistical analysis was performed with SPSS version 23 (IBM, Aramonk, NY). Results. The 84 patients included 26 males and 58 females with average age 66.5 (range 46–91). Average follow up was 51 months (range 30–85). There was no significant difference in the percentage of female patients (64% vs 79%), age (67.8 vs 63.8), or reoperation rate (4% vs 7%) between the resurfaced and non-resurfaced groups. There was significantly longer follow up in the non-resurfaced group (57 vs 48 months). There was no statistically significant difference between the resurfacing and non-resurfacing group in terms of OKS (39 vs 38) or VAS (2.5 vs 3.0). However, those patients who did not have their patellofemoral joint resurfaced were more likely to report ability to kneel when compared to the resurfacing group (64% vs 39%, p=0.035). Kneeling ability was not correlated with duration of follow up, patient age or VAS. Kneeling ability was higher in female patients (57%) than males (27%), p=0.017. Discussion. There is concern for increased anterior knee pain and reoperation in patients whose patellae are not resurfaced. However, their failure to imnprove after revision to a resurfaced patella has left some room for depate as to whether or not the lack of resurfacing is the cause of their problems. This study did not show any increase in knee pain or reoperation between groups. There was an increased subjective ability to kneel in paients whose patellae were not resurfaced. This may have implications for the subset of paeitnts whose work or hobbies may require kneeling. There have been previous reports that subjective ability to kneel and actual ability may differ, and also that kneeling can be taught by a therapist. Our data also shows that female gender had a higher reported rate of kneeling


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_9 | Pages 101 - 101
1 May 2017
Jordan R Aparajit P Docker C El-Shazly M
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Introduction. Osteonecrosis of the knee encompasses three conditions; spontaneous osteonecrosis of the knee, secondary osteonecrosis (ON) and post-arthroscopic ON. Early stage lesions can be managed by non-operative measures that include protected weight-bearing and analgesia. The aim of this study was to report the experience of the authors in managing early stages of knee ON by analysing the functional outcome and need for surgical intervention. Methods. All patients treated for osteonecrosis of the knee between 1st August 2001 and 1st April 2014 were prospectively collected. Treatment consisted of touch-down weight bearing for four to six weeks. The cases were retrospectively reviewed. MR imaging was evaluated for the stage of disease according to Koshino's Classification system, the condyles involved and the time taken for resolution. Tegner Activity Scale, VAS pain, Lysholm, WOMAC and IKDC scores were recorded at presentation and final follow up. Results. 51 cases were treated for knee ON at our centre; 40 cases of SONK, seven secondary ON and four post-arthroscopic ON. Of the seven cases of secondary osteonecrosis; 5 were secondary to self-reported high ethanol intake and two secondary to corticosteroid treatment. The mean age of the group was 56.9 years and 68.7% were male. The medial femoral condyle was the most commonly affected (54.9%). 86% reported resolution of clinical symptoms and a statistically significant improvement was reported in all functional outcome measures. Four patients required total knee arthroplasty; three in the post-arthroscopic group within 15 months and one following ON secondary to corticosteroids performed at 5 months. Conclusion. Early stage spontaneous osteonecrosis of the knee can be managed successfully without surgery if diagnosed early. Although secondary and post-arthroscopic ON seem to be more resistant. Larger studies are required to confirm or refute this. Level of Evidence. IV – a case series. Conflict of Interests. The authors confirm that they have no relevant financial disclosures or conflicts of interest. Ethical approval was not sought as this was a systematic review


Orthopaedic Proceedings
Vol. 100-B, Issue SUPP_4 | Pages 89 - 89
1 Apr 2018
Stoffels A Lipperts M van Hemert W Rijkers K Grimm B
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Introduction. Limited physical activity (PA) is one indication for orthopaedic intervention and restoration of PA a treatment goal. However, the objective assessment of PA is not routinely performed and in particular the effect of spinal pathology on PA is hardly known. It is the purpose of this study using wearable accelerometers to measure if, by how much and in what manner spinal stenosis affects PA compared to age-matched healthy controls. Patients & Methods. Nine patients (m/f= 5/4, avg. age: 67.4 ±7.7 years, avg. BMI: 29.2 ±3.5) diagnosed with spinal stenosis but without decompressive surgery or other musculoskeletal complaints were measured. These patients were compared to 28 age-matched healthy controls (m/f= 17/11, avg. age: 67.4 ±7.6 years, avg. BMI: 25.3±2.9). PA was measured using a wearable accelerometer (GCDC X8M-3) worn during waking hours on the lateral side of the right leg for 4 consecutive days. Data was analyzed using previously validated activity classification algorithms in MATLAB to identify the type, duration and event counts of postures or PA like standing, sitting, walking or cycling. In addition, VAS pain and OSWESTRY scores were taken. Groups were compared using the t-test or Mann-Whitney U-test where applicable. Correlations between PA and clinical scores were tested using Pearson”s r. Results. Spinal stenosis patients showed much lower PA than healthy controls regarding all parameters like e.g. daily step count (2946 vs 8039, −63%, p<0.01) or the relative daily time-on-feet (%) (8.6% vs 28.3%, −70%, p<0.01) which is matched with increased sitting durations (80.3% vs 58.8%, p<0.01). Also qualitative parameters such as walking cadence was reduced in stenosis patients (83.7 vs 97.8 steps/min). With stenosis no patient ever walked >1000 steps without interruption. Also the number of walking bouts between 250–1000 steps was 4.5 times lower than in healthy controls (p<0.01). When the relative distribution of walking bout length was calculated, it became visible that stenosis patients showed more short walking bouts of 10–50 steps (p<0.05). There were no strong and significant correlations between the clinical scores and PA parameters. Discussion & Conclusions. Spinal stenosis greatly reduced physical activity to levels below WHO guidelines (e.g. <5000 steps= sedentary lifestyle) where the risk for general health (overall mortality), cardiovascular or endocrinological health is significantly increased. Activity levels are lower than reported for end-stage hip or knee osteoarthritis. Therefore, spinal stenosis patients should not only receive pain medication, but be made aware of their limited PA and its detrimental health effects, participate in activation programs, or be considered for surgical intervention. The absence of long walking bouts and the relatively more frequent short walking bouts seem indicative of intermittent claudication as typical in spinal stenosis


Orthopaedic Proceedings
Vol. 96-B, Issue SUPP_11 | Pages 99 - 99
1 Jul 2014
Morsi E Eid T Hadhoud M Elseedy A
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Summary Statement. This work proved by prospective clinical and radiological controlled study that the best regimen for treatment of early KOA is combination of NSAIDS, physiotherapy, vasoprotective and vasodilator drugs, and alendronate. Introduction. There is controversy in the literatures regarding the best treatment for early knee osteoarthritis because there is a more controversy regarding the initiating factor of KOA The Objectives of this work were to evaluate the efficacy of various treatment regimens for the prevention of progression of early knee osteoarthritis (KOA). Also, to elucidate the factors for initiation and progression of KOA. Patients and Methods. Four groups of 50 patients with early KOA were treated with four treatment regimens. The first group (control) received analgesics as needed for one year. The second group received non steroidal anti-inflammatory drugs (NSAIDS) plus physiotherapy for one month; with analgesics as needed for the rest of the year. The third group received NSAIDS plus physiotherapy, plus vasoprotective and vasodilator drugs for one month; vasoprotective and vasodilator drugs for the next six months, and analgesics as needed for the rest of the year. The fourth group received NSAIDS plus physiotherapy, plus vasoprotective and vasodilator drugs plus alendronate for one month; vasoprotective and vasodilator drugs plus alendronate for the next six months; and analgesics as needed for the rest of the year. The age of the patients was from 40 to45years. There were 25 males and 25 females in each group. Patients with causes of secondary KOA (e.g. rheumatoid, gouty, traumatic, etc.) were excluded. All patients were subjected to Pre- and post treatment regimens clinical and radiological evaluation Clinical evaluation included history of progressive knee pain for 3–6weeks, limping, Visual analog pain score, tenderness, and knee range of motion. Radiological evaluation included 1.0 T MRI which was performed using proton density-weighted, fat-suppressed sequences. BML size and cartilage status were scored in the same sub regions according to the WORMS system. Results. Progression of KOA in the first, second, third, and fourth group were 66%, 55%, 25%, and 19% of patients respectively No sex difference was detected. Conclusion. The best treatment regimen for early KOA is combination of NSAIDS, physiotherapy, vasoprotective and vasodilator drugs, and alendronate. Vascular and local osteoporotic factors may play a major role in progression of KOA


Orthopaedic Proceedings
Vol. 95-B, Issue SUPP_17 | Pages 18 - 18
1 Apr 2013
Jeevathol A Odedra A Strutton P
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Background. Alterations in the neural drive to trunk muscles have been implicated in low back pain (LBP). This is supported by evidence of reduced corticospinal excitability, delayed muscle activation, reduced endurance and enhanced fatigability of these muscles; whether these changes persist during pain free periods remain unclear. Neural drive (or voluntary activation-VA) can be measured using twitch interpolation and the aim of this study is to investigate if subjects with a history of LBP show reduced VA. Methods. Twenty five subjects participated (13 with a history of LBP, 12 controls). Back extensor torque was measured using a dynamometer and bilateral electromyographic (EMG) activity was recorded from erector spinae and rectus abdominis. Transcranial magnetic stimulation of the motor cortex was applied while the subject, lying prone, performed graded voluntary back extensions. VA was calculated from the size of the twitches evoked by the TMS and EMG data were analysed for evidence of altered neural drive. Results. The LBP typical VAS pain scores were 3.39±1.76(SD), with worst pain being 5.92±2.29. There were no differences in the physical activity scores between the groups. EMG data revealed no differences in the evoked responses at varying levels of voluntary torque. VA was not significantly different between the LBP and control groups (LBP: 85.30±6.45% vs C: 80.14±11.40%). Discussion. These data show that in our cohort of subjects with a history of LBP, their ability to fully activate their back muscles maximally is not reduced. Whether subjects with current LBP exhibit reduced VA remains to be established. No conflicts of interest. Funded by Imperial College London. This abstract has not been previously published in whole or substantial part nor has it been presented previously at a national meeting


Bone & Joint 360
Vol. 3, Issue 4 | Pages 35 - 38
1 Aug 2014
Hammerberg EM