Mederic M. Hall, Ruth L. Chimenti, Jessica F. Danielson, Timothy R. Fleagle
Ultrasound-guided tenotomy and debridement is a minimally invasive treatment with a low risk of complications for individuals with chronic Achilles tendinopathy. Yet the benefits of this procedure on pain, function, and pain-related psychological factors, as well as predictors of treatment success, remain understudied. A total of 56 individuals with chronic Achilles tendinopathy (mean (SD): age = 55.9 (11) years, BMI = 34.8 (8.2) kg/m2, women = 68%) underwent baseline ultrasonography, followed by ultrasound-guided tenotomy and debridement, and rehabilitation. Participants reported pain (0–10), function (Foot and Ankle Ability Measure—ADL), kinesiophobia (Tampa Scale of Kinesiophobia-17), and pain catastrophizing (Pain Catastrophizing Scale) at baseline and for a year following the procedure. Baseline pain was 6.1 (2.2), kinesiophobia was 40.8 (7.1), pain catastrophizing was 13.7 (10.2), and function was 55.9 (17.3). By 6 weeks, there were decreases in pain (mean change (95% CI): −1.9 (−1.1 to −2.6), function: 14.4 (9.3–19.5), kinesiophobia: −5 (−3.2 to −6.9), and pain catastrophizing: −7 (−4.9 to −9.1)). Patient-reported outcomes were similar at 52 weeks (pain: −2.99 (−2.2 to −3.8), function: 25.1 (19.6–30.7), kinesiophobia: −7.5 (−6.1 to −11.4), catastrophizing: −8.5 (−6.1 to −10.8)) following the procedure. Haglund deformity (β: −13.1 (−0.6 to −25.5)) and intratendinous calcifications (β: −14.7 (−1.4 to −28.1)) were associated with smaller improvements in function. No procedure-related complications were reported. Clinical significance: Ultrasound-guided tenotomy and debridement for chronic Achilles tendinopathy may provide positive outcomes for pain, function, and pain-related psychological factors at 6-week and 1-year follow-up. Haglund deformity and tendon calcifications were associated with smaller improvements in function.
{"title":"Effects of Ultrasound-Guided Tenotomy and Debridement on Pain, Function, and Psychological Factors for Achilles Tendinopathy: A Prospective Cohort Study","authors":"Mederic M. Hall, Ruth L. Chimenti, Jessica F. Danielson, Timothy R. Fleagle","doi":"10.1002/jor.70071","DOIUrl":"10.1002/jor.70071","url":null,"abstract":"<p>Ultrasound-guided tenotomy and debridement is a minimally invasive treatment with a low risk of complications for individuals with chronic Achilles tendinopathy. Yet the benefits of this procedure on pain, function, and pain-related psychological factors, as well as predictors of treatment success, remain understudied. A total of 56 individuals with chronic Achilles tendinopathy (mean (SD): age = 55.9 (11) years, BMI = 34.8 (8.2) kg/m<sup>2</sup>, women = 68%) underwent baseline ultrasonography, followed by ultrasound-guided tenotomy and debridement, and rehabilitation. Participants reported pain (0–10), function (Foot and Ankle Ability Measure—ADL), kinesiophobia (Tampa Scale of Kinesiophobia-17), and pain catastrophizing (Pain Catastrophizing Scale) at baseline and for a year following the procedure. Baseline pain was 6.1 (2.2), kinesiophobia was 40.8 (7.1), pain catastrophizing was 13.7 (10.2), and function was 55.9 (17.3). By 6 weeks, there were decreases in pain (mean change (95% CI): −1.9 (−1.1 to −2.6), function: 14.4 (9.3–19.5), kinesiophobia: −5 (−3.2 to −6.9), and pain catastrophizing: −7 (−4.9 to −9.1)). Patient-reported outcomes were similar at 52 weeks (pain: −2.99 (−2.2 to −3.8), function: 25.1 (19.6–30.7), kinesiophobia: −7.5 (−6.1 to −11.4), catastrophizing: −8.5 (−6.1 to −10.8)) following the procedure. Haglund deformity (<i>β</i>: −13.1 (−0.6 to −25.5)) and intratendinous calcifications (<i>β</i>: −14.7 (−1.4 to −28.1)) were associated with smaller improvements in function. No procedure-related complications were reported. Clinical significance: Ultrasound-guided tenotomy and debridement for chronic Achilles tendinopathy may provide positive outcomes for pain, function, and pain-related psychological factors at 6-week and 1-year follow-up. Haglund deformity and tendon calcifications were associated with smaller improvements in function.</p>","PeriodicalId":16650,"journal":{"name":"Journal of Orthopaedic Research®","volume":"44 2","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12856796/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145182045","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Miriam G. E. Oldhoff, Anne M. L. Meesters, Joep Kraeima, Mehool R. Acharya, Kaj ten Duis, Jean-Paul P. M. de Vries, Bram B. J. Merema, Frank F. A. IJpma
The aim of the study was to design a standardized mechanical test setup and a corresponding finite element analysis to assess the stability and strength of both patient-specific and conventional implants for posterior wall acetabular fractures. Ten synthetic hemi-pelves with posterior wall fractures were biomechanically tested with two types of implants: a patient-specific implant (PSI) and a seven-hole plate conventional implant. 3D-printed guides ensured reproducibility. The models were tested using an Instron machine. The protocol involved 10,000 cyclic load cycles with static tests at 3200 N before and after to simulate early postoperative weightbearing conditions. Construct stiffness, stiffness over cyclic loading and fracture gapping were measured and compared. A finite element analysis was created with similar conditions to investigate stresses within the synthetic bone and fixation materials. The mechanical tests showed comparable stiffness for PSI (1.75 kN/mm) and the conventional implant (1.71 kN/mm, p = 0.47). Stability over 10,000 cycles was similar, and fracture gapping remained minimal (0.0–0.8 mm) without significant differences. No failure or plastic deformation occurred under 3200 N loading. Finite element analysis confirmed that von Mises stresses remained below the yield stress. This study introduces a reproducible workflow for biomechanical testing of acetabular fractures using synthetic bone models and 3D-printed guides. It serves as a step-by-step guideline and standard reference for pelvic biomechanical testing. Both patient-specific and conventional implants, using a seven-hole plate construct with one or two screws through the plate in the fracture fragment, provide stable fixation for large posterior wall fragments.
本研究的目的是设计一个标准化的力学测试装置和相应的有限元分析,以评估髋臼后壁骨折患者特异性植入物和常规植入物的稳定性和强度。对10例后壁骨折的合成半骨盆进行生物力学测试,采用两种类型的植入物:患者专用植入物(PSI)和七孔钢板常规植入物。3d打印导轨确保了再现性。使用Instron机器对模型进行了测试。该方案包括在3200 N的静态测试前后进行10,000次循环载荷循环,以模拟术后早期的负重条件。对结构刚度、循环加载刚度和断裂间隙进行了测量和比较。在类似的条件下创建了有限元分析来研究合成骨和固定材料内的应力。力学测试显示PSI (1.75 kN/mm)和常规种植体(1.71 kN/mm, p = 0.47)的刚度相当。超过10,000次循环的稳定性相似,裂缝间隙保持最小(0.0-0.8 mm),没有显着差异。在3200n载荷下,未发生破坏和塑性变形。有限元分析证实,von Mises应力保持在屈服应力以下。本研究介绍了一种可重复的工作流程,用于使用合成骨模型和3d打印导板进行髋臼骨折的生物力学测试。它作为骨盆生物力学测试的一步一步的指导和标准参考。患者特异性植入物和常规植入物均采用7孔钢板结构,在骨折碎片中通过钢板置入1或2颗螺钉,可为较大的后壁碎片提供稳定的固定。
{"title":"Mechanical Evaluation of Posterior Wall Acetabular Facture Fixation: Patient-Specific Implants Versus Conventional Implants","authors":"Miriam G. E. Oldhoff, Anne M. L. Meesters, Joep Kraeima, Mehool R. Acharya, Kaj ten Duis, Jean-Paul P. M. de Vries, Bram B. J. Merema, Frank F. A. IJpma","doi":"10.1002/jor.70062","DOIUrl":"10.1002/jor.70062","url":null,"abstract":"<p>The aim of the study was to design a standardized mechanical test setup and a corresponding finite element analysis to assess the stability and strength of both patient-specific and conventional implants for posterior wall acetabular fractures. Ten synthetic hemi-pelves with posterior wall fractures were biomechanically tested with two types of implants: a patient-specific implant (PSI) and a seven-hole plate conventional implant. 3D-printed guides ensured reproducibility. The models were tested using an Instron machine. The protocol involved 10,000 cyclic load cycles with static tests at 3200 N before and after to simulate early postoperative weightbearing conditions. Construct stiffness, stiffness over cyclic loading and fracture gapping were measured and compared. A finite element analysis was created with similar conditions to investigate stresses within the synthetic bone and fixation materials. The mechanical tests showed comparable stiffness for PSI (1.75 kN/mm) and the conventional implant (1.71 kN/mm, <i>p</i> = 0.47). Stability over 10,000 cycles was similar, and fracture gapping remained minimal (0.0–0.8 mm) without significant differences. No failure or plastic deformation occurred under 3200 N loading. Finite element analysis confirmed that von Mises stresses remained below the yield stress. This study introduces a reproducible workflow for biomechanical testing of acetabular fractures using synthetic bone models and 3D-printed guides. It serves as a step-by-step guideline and standard reference for pelvic biomechanical testing. Both patient-specific and conventional implants, using a seven-hole plate construct with one or two screws through the plate in the fracture fragment, provide stable fixation for large posterior wall fragments.</p>","PeriodicalId":16650,"journal":{"name":"Journal of Orthopaedic Research®","volume":"44 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jor.70062","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145125050","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}