Pub Date : 2025-10-28DOI: 10.1302/2633-1462.610.BJO-2025-0098.R1
Katrina R Bell, William M Oliver, Timothy O White, Samuel G Molyneux, Nicholas D Clement, Andrew D Duckworth
Aims: This systematic review and meta-analysis aimed to compare the patient-reported outcomes of operative and nonoperative management in adults with a fracture of the distal radius, with a focus on the outcomes in older patients (aged ≥ 65 years).
Methods: Randomized controlled trials comparing operative and nonoperative management of patients aged ≥ 18 years with dorsally displaced distal radius fractures were included. Operative management included open reduction and internal fixation (ORIF), manipulation and Kirschner-wiring, or external fixation. Nonoperative management included cast/splint immobilization with or without closed reduction. Primary outcome was the 12-month Patient-Rated Wrist Evaluation (PRWE). Additional outcomes included the Disabilities of Arm, Shoulder and Hand (DASH), pain, complications, and radiological parameters. A sub-group analysis was undertaken for studies that reported outcomes in older adults (aged ≥ 65 years).
Results: After screening 1,635 studies, 19 trials with 2,178 patients (mean age 63 years (18 to 98), 74% female) were included. Seven studies reported outcomes in older patients (n = 773). There were statistical but not clinically significant differences favouring surgery for PRWE at three months (mean difference (MD) -8.70, 95% CI -14.45 to -2.95; p = 0.003) and 12 months (MD -2.96, 95% CI -5.15 to -0.77; p = 0.008). There was a statistical but not clinically significant difference in DASH at three months (MD -10.58, 95% CI -13.15 to -8.01; p < 0.00001) and 12 months (MD -4.17, 95% CI -6.05 to -2.30; p < 0.001) favouring surgery. There was no difference in complications (odds ratio (OR) 0.95, 95% CI 0.52 to 1.76; p = 0.880). For older adults, there was no difference in the PRWE at three months (MD -8.53, 95% CI -18.13 to 1.07; p = 0.080) or 12 months (MD -2.13, 95% CI -4.60 to 0.33; p = 0.090), with no difference in complications (OR 0.73, 95% CI 0.21 to 2.49; p = 0.620).
Conclusion: Operative management of adult dorsally displaced distal radius fractures was associated with superior functional outcomes according to the PRWE and DASH, but whether these are clinically meaningful is debatable. However, in older adults there was no significant or clinically meaningful benefit of surgery.
目的:本系统综述和荟萃分析旨在比较成人桡骨远端骨折手术和非手术治疗的患者报告结果,重点关注老年患者(年龄≥65岁)的结果。方法:纳入随机对照试验,比较手术和非手术治疗年龄≥18岁桡骨远端背侧移位骨折患者。手术治疗包括切开复位内固定(ORIF)、手法加克氏针或外固定。非手术治疗包括带或不带闭合复位的石膏/夹板固定。主要终点为12个月患者腕关节评估(PRWE)。其他结果包括手臂、肩膀和手的残疾(DASH)、疼痛、并发症和放射学参数。对报告老年人(年龄≥65岁)结局的研究进行亚组分析。结果:在筛选了1635项研究后,纳入了19项试验,2178例患者(平均年龄63岁(18 - 98岁),74%为女性)。7项研究报告了老年患者的结果(n = 773)。3个月时PRWE患者接受手术治疗有统计学差异,但无临床意义(平均差异(MD) -8.70, 95% CI -14.45 ~ -2.95;p = 0.003)和12个月(MD -2.96, 95% CI -5.15 ~ -0.77; p = 0.008)。3个月时(MD -10.58, 95% CI -13.15 ~ -8.01, p < 0.00001)和12个月时(MD -4.17, 95% CI -6.05 ~ -2.30, p < 0.001),偏爱手术的患者DASH差异有统计学意义,但无临床意义。并发症发生率无差异(优势比(OR) 0.95, 95% CI 0.52 ~ 1.76;P = 0.880)。对于老年人,3个月(MD -8.53, 95% CI -18.13至1.07;p = 0.080)或12个月(MD -2.13, 95% CI -4.60至0.33;p = 0.090)的PRWE无差异,并发症无差异(or 0.73, 95% CI 0.21至2.49;p = 0.620)。结论:根据PRWE和DASH,成人桡骨远端背侧移位骨折的手术处理与良好的功能预后相关,但这些是否具有临床意义尚存争议。然而,在老年人中,手术没有显著的或有临床意义的益处。
{"title":"Operative management of displaced fractures of the distal radius is associated with improved function but not in older adults : systematic review and meta-analysis of randomized controlled trials.","authors":"Katrina R Bell, William M Oliver, Timothy O White, Samuel G Molyneux, Nicholas D Clement, Andrew D Duckworth","doi":"10.1302/2633-1462.610.BJO-2025-0098.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0098.R1","url":null,"abstract":"<p><strong>Aims: </strong>This systematic review and meta-analysis aimed to compare the patient-reported outcomes of operative and nonoperative management in adults with a fracture of the distal radius, with a focus on the outcomes in older patients (aged ≥ 65 years).</p><p><strong>Methods: </strong>Randomized controlled trials comparing operative and nonoperative management of patients aged ≥ 18 years with dorsally displaced distal radius fractures were included. Operative management included open reduction and internal fixation (ORIF), manipulation and Kirschner-wiring, or external fixation. Nonoperative management included cast/splint immobilization with or without closed reduction. Primary outcome was the 12-month Patient-Rated Wrist Evaluation (PRWE). Additional outcomes included the Disabilities of Arm, Shoulder and Hand (DASH), pain, complications, and radiological parameters. A sub-group analysis was undertaken for studies that reported outcomes in older adults (aged ≥ 65 years).</p><p><strong>Results: </strong>After screening 1,635 studies, 19 trials with 2,178 patients (mean age 63 years (18 to 98), 74% female) were included. Seven studies reported outcomes in older patients (n = 773). There were statistical but not clinically significant differences favouring surgery for PRWE at three months (mean difference (MD) -8.70, 95% CI -14.45 to -2.95; p = 0.003) and 12 months (MD -2.96, 95% CI -5.15 to -0.77; p = 0.008). There was a statistical but not clinically significant difference in DASH at three months (MD -10.58, 95% CI -13.15 to -8.01; p < 0.00001) and 12 months (MD -4.17, 95% CI -6.05 to -2.30; p < 0.001) favouring surgery. There was no difference in complications (odds ratio (OR) 0.95, 95% CI 0.52 to 1.76; p = 0.880). For older adults, there was no difference in the PRWE at three months (MD -8.53, 95% CI -18.13 to 1.07; p = 0.080) or 12 months (MD -2.13, 95% CI -4.60 to 0.33; p = 0.090), with no difference in complications (OR 0.73, 95% CI 0.21 to 2.49; p = 0.620).</p><p><strong>Conclusion: </strong>Operative management of adult dorsally displaced distal radius fractures was associated with superior functional outcomes according to the PRWE and DASH, but whether these are clinically meaningful is debatable. However, in older adults there was no significant or clinically meaningful benefit of surgery.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1330-1342"},"PeriodicalIF":3.1,"publicationDate":"2025-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12560059/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145378786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-23DOI: 10.1302/2633-1462.610.BJO-2025-0177.R1
Sophie Donoghue, Clara Miller, Karen Chui, Hannah Sevenoaks, Deborah M Eastwood
Aims: To evaluate the accessibility and utility of current radiation personal protective equipment (PPE) provision and understand the experiences and radiation protection practices offered to all levels of Trauma & Orthopaedic (T&O) surgeons in the UK.
Methods: An incentivized electronic survey was sent to all UK T&O surgeons during a six-week period in 2024. Responses to 27 multiple-choice questions were collected and free-text responses analyzed by theme.
Results: A total of 677 responses from 196 UK NHS hospitals were received: 228 recepients (33%) were female, 455 (67%) were resident doctors, and 222 (33%) were consultants, representing a response rate of 38% (341/897) for trainees and 11% (222/2114) for consultants. Overall, 171 (25%) agreed they could find appropriate lead gown PPE; 80 (12%) had been given dosimeters, although few had received feedback; 173 (26%) received mandatory training, but many more (328, 48%) had sought training individually. When undertaken, it was felt useful. Symptoms attributed to ill-fitting PPE were common and more likely to be reported by females (odds ratio 2.5). In total, 372 (55%) did not feel protected by their current PPE, and 569 (84%) were concerned about the effects of ionizing radiation (IR) on their health. Thematic analysis confirmed concerns relating to PPE availability, education, and inconsistent advice and guidance across hospitals. Health concerns and poor morale were also highlighted.
Conclusion: Employers must address the lack of compliance with the UK legislation, IR Regulations 2017 (IRR17), in relation to access to PPE, training, and monitoring. There is a need for standardized national guidelines and training.
{"title":"Evaluation of X-ray Personal protective equipment for Orthopaedic Surgeons in theatrE (EXPOSEd) study : a national survey of Trauma & Orthopaedic surgeons.","authors":"Sophie Donoghue, Clara Miller, Karen Chui, Hannah Sevenoaks, Deborah M Eastwood","doi":"10.1302/2633-1462.610.BJO-2025-0177.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0177.R1","url":null,"abstract":"<p><strong>Aims: </strong>To evaluate the accessibility and utility of current radiation personal protective equipment (PPE) provision and understand the experiences and radiation protection practices offered to all levels of Trauma & Orthopaedic (T&O) surgeons in the UK.</p><p><strong>Methods: </strong>An incentivized electronic survey was sent to all UK T&O surgeons during a six-week period in 2024. Responses to 27 multiple-choice questions were collected and free-text responses analyzed by theme.</p><p><strong>Results: </strong>A total of 677 responses from 196 UK NHS hospitals were received: 228 recepients (33%) were female, 455 (67%) were resident doctors, and 222 (33%) were consultants, representing a response rate of 38% (341/897) for trainees and 11% (222/2114) for consultants. Overall, 171 (25%) agreed they could find appropriate lead gown PPE; 80 (12%) had been given dosimeters, although few had received feedback; 173 (26%) received mandatory training, but many more (328, 48%) had sought training individually. When undertaken, it was felt useful. Symptoms attributed to ill-fitting PPE were common and more likely to be reported by females (odds ratio 2.5). In total, 372 (55%) did not feel protected by their current PPE, and 569 (84%) were concerned about the effects of ionizing radiation (IR) on their health. Thematic analysis confirmed concerns relating to PPE availability, education, and inconsistent advice and guidance across hospitals. Health concerns and poor morale were also highlighted.</p><p><strong>Conclusion: </strong>Employers must address the lack of compliance with the UK legislation, IR Regulations 2017 (IRR17), in relation to access to PPE, training, and monitoring. There is a need for standardized national guidelines and training.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1321-1329"},"PeriodicalIF":3.1,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12543439/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1302/2633-1462.610.BJO-2025-0099.R1
Raymond Tellefsen, Torbjørn B Kristensen, Eva H Dybvik, Jan-Erik Gjertsen, Lars Nordsletten, Terje Ugland, Håvard Visnes, Lene B Solberg
Aims: The aim of this study was to compare the direct lateral approach (DLA) with the anterolateral approach (ALA) and posterior approach (PA) using data on hemiarthroplasties (HAs) reported to the Norwegian Hip Fracture Register. The primary endpoint was reoperations within 12 months post-surgery. Secondary endpoints included mortality, patient-reported outcome measures (PROMs; EuroQol five-dimension three-level questionnaire (EQ-5D-3L) and EuroQol visual analogue scale (EQ-VAS)), and intraoperative complications.
Methods: A total of 39,905 HA patients aged 60 years or older who were operated on using DLA from January 2005 to December 2023 were compared to 2,813 patients operated on with ALA and 5,504 with PA in the same period. Hazard rate ratios (HRRs) for reoperations and mortality were calculated using Cox regression adjusted for age, sex, American Society of Anesthesiologists classification, cognitive status, and fixation method. Patients reported EQ-5D-3L and EQ-VAS 12 months postoperatively.
Results: The reoperation rate was 3.7% for DLA, 3.0% for ALA (HRR 0.79 (0.64 to 0.99)), and 5.9% for PA (HRR 1.54 (1.37 to 1.74)). PA was associated with an increased dislocation rate compared to DLA (HRR 3.92 (3.28 to 4.67)). Fewer infections were observed with ALA (1.5%, HRR 0.68 (0.50 to 0.93)) and PA (1.6%, HRR 0.74 (0.59 to 0.92)) compared to DLA (2.2%). Similar 30-day mortality rates were found for all approaches and marginally lower one-year mortality was found for the PA. Patients operated on with the DLA reported significantly lower EQ-5D-3L index score and EQ-VAS at 12 months post-surgery compared to ALA and PA. Fewer intraoperative fractures were found using the PA.
Conclusion: This study indicates that PA is associated with a higher reoperation rate after HA compared to the two other approaches. This is primarily due to high dislocation rate, despite a higher infection rate with DLA. EQ-5D-3L and EQ-VAS appear to favour ALA and PA 12 months post-surgery. Based on this study, traditional PA should be avoided in this patient group. ALA seems to be a safe alternative to the DLA.
{"title":"Surgical approaches in hemiarthroplasty for hip fracture : results of 48,222 hemiarthroplasties in the Norwegian Hip Fracture Register.","authors":"Raymond Tellefsen, Torbjørn B Kristensen, Eva H Dybvik, Jan-Erik Gjertsen, Lars Nordsletten, Terje Ugland, Håvard Visnes, Lene B Solberg","doi":"10.1302/2633-1462.610.BJO-2025-0099.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0099.R1","url":null,"abstract":"<p><strong>Aims: </strong>The aim of this study was to compare the direct lateral approach (DLA) with the anterolateral approach (ALA) and posterior approach (PA) using data on hemiarthroplasties (HAs) reported to the Norwegian Hip Fracture Register. The primary endpoint was reoperations within 12 months post-surgery. Secondary endpoints included mortality, patient-reported outcome measures (PROMs; EuroQol five-dimension three-level questionnaire (EQ-5D-3L) and EuroQol visual analogue scale (EQ-VAS)), and intraoperative complications.</p><p><strong>Methods: </strong>A total of 39,905 HA patients aged 60 years or older who were operated on using DLA from January 2005 to December 2023 were compared to 2,813 patients operated on with ALA and 5,504 with PA in the same period. Hazard rate ratios (HRRs) for reoperations and mortality were calculated using Cox regression adjusted for age, sex, American Society of Anesthesiologists classification, cognitive status, and fixation method. Patients reported EQ-5D-3L and EQ-VAS 12 months postoperatively.</p><p><strong>Results: </strong>The reoperation rate was 3.7% for DLA, 3.0% for ALA (HRR 0.79 (0.64 to 0.99)), and 5.9% for PA (HRR 1.54 (1.37 to 1.74)). PA was associated with an increased dislocation rate compared to DLA (HRR 3.92 (3.28 to 4.67)). Fewer infections were observed with ALA (1.5%, HRR 0.68 (0.50 to 0.93)) and PA (1.6%, HRR 0.74 (0.59 to 0.92)) compared to DLA (2.2%). Similar 30-day mortality rates were found for all approaches and marginally lower one-year mortality was found for the PA. Patients operated on with the DLA reported significantly lower EQ-5D-3L index score and EQ-VAS at 12 months post-surgery compared to ALA and PA. Fewer intraoperative fractures were found using the PA.</p><p><strong>Conclusion: </strong>This study indicates that PA is associated with a higher reoperation rate after HA compared to the two other approaches. This is primarily due to high dislocation rate, despite a higher infection rate with DLA. EQ-5D-3L and EQ-VAS appear to favour ALA and PA 12 months post-surgery. Based on this study, traditional PA should be avoided in this patient group. ALA seems to be a safe alternative to the DLA.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1311-1320"},"PeriodicalIF":3.1,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12539978/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348936","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-21DOI: 10.1302/2633-1462.610.BJO-2025-0106.R1
Ben Tyas, Sameer K Khan, Alex Sims, Nicholas R Parsons, Andrew Chaplin, Dominic Scott Inman, Timothy G Petheram, Mike R Reed
Aims: The WHiTE3:HEMI trial recruited patients with an intracapsular hip fracture to be randomized to receive the Thompson hemiarthroplasty or the Exeter stem and Unitrax modular head. Results demonstrated no difference in mortality or health-related quality of life at four months. The aim of this study was to review outcomes at eight years for patients recruited into the WHiTE3:HEMI trial at our institution.
Methods: Dates of readmission, reoperation, and death were recorded from our local Trust universal clinical system for clinical noting, results, and radiology imaging. These data are concordant with the NHS Spine Personal Demographic Service and those submitted to the National Hip Fracture Database. Patient characteristics, incidence of periprosthetic fracture (PPF), reoperation, revision, and mortality were compared between the two groups. Patients were analyzed 'as randomized'.
Results: In total, 135 Thompson patients were compared with 143 Exeter Unitrax patients. There were no differences in age, sex, American Society of Anesthesiologists grade, Abbreviated Mental Test Score, Nottingham Hip Fracture Score, grade of operating surgeon, or residence on admission. In the Thompson group, there were 13/135 (9.6%) surgical complications, 6/135 (4.4%) reoperations, and 1/135 (0.7%) PPF. In the Exeter Unitrax group, there were 10/143 (7.0%) surgical complications (p = 0.425), 5/143 (3.5%) reoperations (p = 0.685), and 2/143 (1.4%) PPFs (p = 0.596). Eight-year Thompson cumulative implant survivorship was 96.9% (95% CI 90.4 to 99.0) and Exeter Unitrax 96.5% (95% CI 90.6 to 98.7) (p = 0.954). There were no differences in 30-day or four-month mortality rates. One-year mortality rates were 37.0% in Thompson and 20.3% in Unitrax (difference 16.7%, 95% CI 1.1 to 31.8, p = 0.002). Pooled mortality at eight years was 86.3% with no difference between the two groups (p = 0.612).
Conclusion: At one year, a significantly higher mortality rate was noted in the Thompson group. At long-term follow-up, Thompson and Exeter Unitrax demonstrated equivalent and low reoperation rates and excellent implant survivorship. Further studies may look to validate these findings.
目的:WHiTE3:HEMI试验招募髋关节囊内骨折患者,随机接受Thompson半关节置换术或Exeter柄和Unitrax模块化头。结果显示,在4个月时,死亡率或与健康相关的生活质量没有差异。本研究的目的是回顾我们机构招募的WHiTE3:HEMI试验患者8年的结果。方法:从我们当地的信托通用临床系统中记录再入院、再手术和死亡的日期,以进行临床记录、结果和放射影像学检查。这些数据与NHS脊柱个人人口统计服务和提交给国家髋部骨折数据库的数据一致。比较两组患者特征、假体周围骨折(PPF)发生率、再手术、翻修和死亡率。对患者进行“随机”分析。结果:共有135名Thompson患者与143名Exeter Unitrax患者进行了比较。年龄、性别、美国麻醉医师学会分级、简略智力测验评分、诺丁汉髋部骨折评分、手术医师等级、住院时居住地均无差异。Thompson组手术并发症13/135例(9.6%),再手术6/135例(4.4%),PPF 1/135例(0.7%)。Exeter Unitrax组手术并发症发生率为10/143例(7.0%)(p = 0.425),再手术发生率为5/143例(3.5%)(p = 0.685), ppf发生率为2/143例(1.4%)(p = 0.596)。8年Thompson种植体累积成活率为96.9% (95% CI 90.4 ~ 99.0), Exeter Unitrax为96.5% (95% CI 90.6 ~ 98.7) (p = 0.954)。30天或4个月的死亡率没有差异。Thompson组的1年死亡率为37.0%,Unitrax组为20.3%(差异16.7%,95% CI 1.1 ~ 31.8, p = 0.002)。8年总死亡率为86.3%,两组间无差异(p = 0.612)。结论:一年后,汤普森组的死亡率明显高于对照组。在长期随访中,Thompson和Exeter Unitrax显示出相同的低再手术率和良好的种植体成活率。进一步的研究可能会验证这些发现。
{"title":"Eight-year outcomes from the WHiTE3 HEMI trial : comparing the Thompson hemiarthroplasty with the Exeter polished tapered stem and Unitrax modular head in the treatment of displaced intracapsular hip fractures at a single centre.","authors":"Ben Tyas, Sameer K Khan, Alex Sims, Nicholas R Parsons, Andrew Chaplin, Dominic Scott Inman, Timothy G Petheram, Mike R Reed","doi":"10.1302/2633-1462.610.BJO-2025-0106.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0106.R1","url":null,"abstract":"<p><strong>Aims: </strong>The WHiTE3:HEMI trial recruited patients with an intracapsular hip fracture to be randomized to receive the Thompson hemiarthroplasty or the Exeter stem and Unitrax modular head. Results demonstrated no difference in mortality or health-related quality of life at four months. The aim of this study was to review outcomes at eight years for patients recruited into the WHiTE3:HEMI trial at our institution.</p><p><strong>Methods: </strong>Dates of readmission, reoperation, and death were recorded from our local Trust universal clinical system for clinical noting, results, and radiology imaging. These data are concordant with the NHS Spine Personal Demographic Service and those submitted to the National Hip Fracture Database. Patient characteristics, incidence of periprosthetic fracture (PPF), reoperation, revision, and mortality were compared between the two groups. Patients were analyzed 'as randomized'.</p><p><strong>Results: </strong>In total, 135 Thompson patients were compared with 143 Exeter Unitrax patients. There were no differences in age, sex, American Society of Anesthesiologists grade, Abbreviated Mental Test Score, Nottingham Hip Fracture Score, grade of operating surgeon, or residence on admission. In the Thompson group, there were 13/135 (9.6%) surgical complications, 6/135 (4.4%) reoperations, and 1/135 (0.7%) PPF. In the Exeter Unitrax group, there were 10/143 (7.0%) surgical complications (p = 0.425), 5/143 (3.5%) reoperations (p = 0.685), and 2/143 (1.4%) PPFs (p = 0.596). Eight-year Thompson cumulative implant survivorship was 96.9% (95% CI 90.4 to 99.0) and Exeter Unitrax 96.5% (95% CI 90.6 to 98.7) (p = 0.954). There were no differences in 30-day or four-month mortality rates. One-year mortality rates were 37.0% in Thompson and 20.3% in Unitrax (difference 16.7%, 95% CI 1.1 to 31.8, p = 0.002). Pooled mortality at eight years was 86.3% with no difference between the two groups (p = 0.612).</p><p><strong>Conclusion: </strong>At one year, a significantly higher mortality rate was noted in the Thompson group. At long-term follow-up, Thompson and Exeter Unitrax demonstrated equivalent and low reoperation rates and excellent implant survivorship. Further studies may look to validate these findings.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1302-1310"},"PeriodicalIF":3.1,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12537065/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145337743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-20DOI: 10.1302/2633-1462.610.BJO-2025-0121.R1
Eline M Steggink, Anthranilla E Leeuwesteijn, Denise Telgt, Karin Veerman
Aims: Nonunion after foot and ankle arthrodesis is a major complication, which can lead to revision arthrodesis with increased risk of morbidity. Multiple factors can contribute to developing a nonunion, including a low-grade infection. The aim of this study is to investigate the rate of unsuspected low-grade infection in revision surgery for nonunion after foot and ankle arthrodesis. We also analyzed the difference in outcome of revision arthrodesis for patients with or without infection.
Methods: We conducted a retrospective study in the Sint Maartenskliniek, the Netherlands. All patients who underwent a revision arthrodesis (index surgery) for assumed aseptic nonunion after foot and ankle arthrodesis between January 2019 and July 2021 were included. Patients were excluded if fewer than five tissue samples were obtained during index surgery, or if infection was suspected before or during the index surgery. The causative microorganisms, antibiotic susceptibility, treatment, and outcome were assessed.
Results: In total, 105 revision arthrodeses due to nonunion were performed, of which 77 patients were included. In 17 patients (22.1%), an infection was diagnosed based on culture results of tissue samples taken during index arthrodesis. The causative bacteria identified were Cutibacterium acnes (n = 11), Staphylococcus spp. (n = 7), and Acinetobacter spp. (n = 1). After two years of follow-up, the success rate of the infection group was 77% compared with 88% for the patients with negative cultures (p = 0.451).
Conclusion: Low-grade infection should be considered as a possible explanation of a nonunion, despite the lack of local inflammatory signs. As 22% of the nonunions were unexpectedly caused by low-grade infection, we strongly recommend obtaining at least five tissue samples for culture during revision arthrodesis. The success rate of revision surgery followed by targeted antibiotics in patients with a low-grade infection is 77%, which is lower than the outcome in revision surgery for patients without infection (88%), although not significant (p = 0.451).
{"title":"Unsuspected low-grade infection in revision surgery for nonunion in foot and ankle arthrodesis : incidence, causative microorganisms, and treatment.","authors":"Eline M Steggink, Anthranilla E Leeuwesteijn, Denise Telgt, Karin Veerman","doi":"10.1302/2633-1462.610.BJO-2025-0121.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0121.R1","url":null,"abstract":"<p><strong>Aims: </strong>Nonunion after foot and ankle arthrodesis is a major complication, which can lead to revision arthrodesis with increased risk of morbidity. Multiple factors can contribute to developing a nonunion, including a low-grade infection. The aim of this study is to investigate the rate of unsuspected low-grade infection in revision surgery for nonunion after foot and ankle arthrodesis. We also analyzed the difference in outcome of revision arthrodesis for patients with or without infection.</p><p><strong>Methods: </strong>We conducted a retrospective study in the Sint Maartenskliniek, the Netherlands. All patients who underwent a revision arthrodesis (index surgery) for assumed aseptic nonunion after foot and ankle arthrodesis between January 2019 and July 2021 were included. Patients were excluded if fewer than five tissue samples were obtained during index surgery, or if infection was suspected before or during the index surgery. The causative microorganisms, antibiotic susceptibility, treatment, and outcome were assessed.</p><p><strong>Results: </strong>In total, 105 revision arthrodeses due to nonunion were performed, of which 77 patients were included. In 17 patients (22.1%), an infection was diagnosed based on culture results of tissue samples taken during index arthrodesis. The causative bacteria identified were <i>Cutibacterium acnes</i> (n = 11), <i>Staphylococcus spp</i>. (n = 7), and <i>Acinetobacter spp</i>. (n = 1). After two years of follow-up, the success rate of the infection group was 77% compared with 88% for the patients with negative cultures (p = 0.451).</p><p><strong>Conclusion: </strong>Low-grade infection should be considered as a possible explanation of a nonunion, despite the lack of local inflammatory signs. As 22% of the nonunions were unexpectedly caused by low-grade infection, we strongly recommend obtaining at least five tissue samples for culture during revision arthrodesis. The success rate of revision surgery followed by targeted antibiotics in patients with a low-grade infection is 77%, which is lower than the outcome in revision surgery for patients without infection (88%), although not significant (p = 0.451).</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1295-1301"},"PeriodicalIF":3.1,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12535800/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145329935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-17DOI: 10.1302/2633-1462.610.BJO-2025-0025.R1
John M Abrahams, Boopalan Ramasamy, Xiangyu Dong, Daud Tai Shan Chou, Kerry Costi, Lucian Bogdan Solomon, Stuart Adam Callary
Aims: The aim of this study was to determine the early stability of acetabular components of total hip arthroplasty (THA) treating acute acetabular fractures through a replace-in-situ technique, using standard radiological assessment techniques as well as radiostereometric analysis (RSA), the gold standard for assessment of implant stability.
Methods: We prospectively investigated 29 patients who underwent THA to manage an acute acetabular fracture in which patients underwent postoperative in-clinic radiological assessment of acetabular component stability, and detailed measurements using both RSA and manual techniques. The latter were performed based on pelvic reference landmarks located below and above the fracture. Greater than 3 mm of proximal translation and/or 5° of rotation around the sagittal axis were considered diagnostic of a loose acetabular component.
Results: The median proximal translation and sagittal rotation of the cohort was 0.5 mm (IQR 0.3 to 0.9) and 0.8° (IQR -0.6° to 1.1°), respectively, as measured by RSA at two years. Acetabular components in the most unstable acetabular fracture patterns were found to migrate more immediately post-surgery. There was a disparity between different measurement techniques. Accurate RSA measurements correctly identified two components that were deemed to be clinically loose, and the diagnostic performance of RSA migration measurements was improved when migration within the first six months was excluded. Visual assessment of radiographs in clinic underestimated - and manual radiological measurements overestimated - acetabular component loosening in these complex cases.
Conclusion: The replace-in-situ technique led to acceptable early acetabular component stability in the majority of cases (27/29, 93%), a good result considering the complexity of these reconstructions. Accurate measurements of acetabular component migration are recommended in these cases, as pelvic landmark identification on consecutive plain radiographs is influenced by both pelvic projection on plain radiographs and fracture fragment migration during healing.
目的:本研究的目的是通过原位置换技术确定全髋关节置换术(THA)治疗急性髋臼骨折髋臼假体的早期稳定性,采用标准放射学评估技术和放射立体分析(RSA),这是评估假体稳定性的金标准。方法:我们前瞻性地调查了29例接受THA治疗急性髋臼骨折的患者,其中患者术后接受髋臼部件稳定性的临床放射学评估,并使用RSA和手工技术进行详细测量。后者是基于位于骨折下方和上方的骨盆参考标志进行的。近端移位大于3mm和/或围绕矢状轴旋转5°被认为是髋臼部件松动的诊断。结果:通过两年的RSA测量,该队列的中位近端平移和矢状面旋转分别为0.5 mm (IQR 0.3至0.9)和0.8°(IQR -0.6°至1.1°)。在大多数不稳定的髋臼骨折类型中,发现髋臼成分在术后更容易移位。不同的测量技术之间存在差异。准确的RSA测量可以正确识别临床上被认为是松动的两个组成部分,当排除前六个月内的迁移时,RSA迁移测量的诊断性能得到了提高。在这些复杂的病例中,临床x线片的视觉评估低估了髋臼部件松动,而手工放射测量高估了髋臼部件松动。结论:原位置换技术在大多数病例(27/ 29,93%)的早期髋臼假体稳定性尚可,考虑到这些重建的复杂性,这是一个很好的结果。在这些病例中,建议准确测量髋臼构件的移动,因为连续x线平片上骨盆地标的识别受到x线平片上骨盆投影和愈合过程中骨折碎片移动的影响。
{"title":"Total hip arthroplasty for acute acetabular fractures through the replace-in-situ philosophy : radiological assessment of component stability.","authors":"John M Abrahams, Boopalan Ramasamy, Xiangyu Dong, Daud Tai Shan Chou, Kerry Costi, Lucian Bogdan Solomon, Stuart Adam Callary","doi":"10.1302/2633-1462.610.BJO-2025-0025.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0025.R1","url":null,"abstract":"<p><strong>Aims: </strong>The aim of this study was to determine the early stability of acetabular components of total hip arthroplasty (THA) treating acute acetabular fractures through a replace-in-situ technique, using standard radiological assessment techniques as well as radiostereometric analysis (RSA), the gold standard for assessment of implant stability.</p><p><strong>Methods: </strong>We prospectively investigated 29 patients who underwent THA to manage an acute acetabular fracture in which patients underwent postoperative in-clinic radiological assessment of acetabular component stability, and detailed measurements using both RSA and manual techniques. The latter were performed based on pelvic reference landmarks located below and above the fracture. Greater than 3 mm of proximal translation and/or 5° of rotation around the sagittal axis were considered diagnostic of a loose acetabular component.</p><p><strong>Results: </strong>The median proximal translation and sagittal rotation of the cohort was 0.5 mm (IQR 0.3 to 0.9) and 0.8° (IQR -0.6° to 1.1°), respectively, as measured by RSA at two years. Acetabular components in the most unstable acetabular fracture patterns were found to migrate more immediately post-surgery. There was a disparity between different measurement techniques. Accurate RSA measurements correctly identified two components that were deemed to be clinically loose, and the diagnostic performance of RSA migration measurements was improved when migration within the first six months was excluded. Visual assessment of radiographs in clinic underestimated - and manual radiological measurements overestimated - acetabular component loosening in these complex cases.</p><p><strong>Conclusion: </strong>The replace-in-situ technique led to acceptable early acetabular component stability in the majority of cases (27/29, 93%), a good result considering the complexity of these reconstructions. Accurate measurements of acetabular component migration are recommended in these cases, as pelvic landmark identification on consecutive plain radiographs is influenced by both pelvic projection on plain radiographs and fracture fragment migration during healing.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1282-1294"},"PeriodicalIF":3.1,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12530900/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145309393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aims: To assess the rates of relapse and risk factors for release and surgical intervention in patients with idiopathic clubfoot.
Methods: A retrospective review of all patients with idiopathic clubfoot and initiation of Ponseti treatment between February 2005 and December 2015 was conducted. All patients with successful initial Ponseti casting treatment at the study institution and one year of follow-up were included. Rates of relapse, surgery, and types of surgical procedures performed were collected.
Results: The final cohort included 268 children with 397 idiopathic clubfeet, consisting of 98 females (36.6%) and 170 males (63.4%). The successfully Ponseti-treated group without relapse was composed of 171 children with 252 feet (63.5% of total cohort). A total of 97 patients (36.2%) had a relapse and required further intervention (relapse group). There was a greater proportion of patients with complex-type clubfoot in the relapse group (18.6% vs 4.7%, p = 0.001). Patients who never relapsed presented at a median age of 33.7 days (IQR 40.8), while those who relapsed presented at a significantly younger age, at a median of 25.1 days (IQR 17.2) (p < 0.001). Children in the no-relapse group required significantly fewer casts to achieve correction, with a mean of 4.3 compared with 5.2 in patients with relapse (p < 0.001). Children in the no-relapse group showed a significantly higher rate of good adherence compared with those in the relapse-group (94.9% vs 62.3%, p < 0.001). In total, 24 children (23 feet, 5.8% of total cohort) underwent surgery, whereas 74 had a relapse but did not require surgery. The most common surgical procedures performed were tibialis anterior tendon transfer (n = 25) and open tendoachilles lengthening (n = 21).
Conclusion: We confirm that a higher number of casts to achieve correction in the initial Ponseti series, younger age at presentation, complex clubfoot features, and poor brace adherence may be correlated with risk of relapse and surgery. The need for joint invasive surgery is rarely indicated.
目的:评估特发性内翻足患者的复发率和危险因素的释放和手术干预。方法:回顾性分析2005年2月至2015年12月间所有特发性内翻足并开始庞塞提治疗的患者。所有在研究机构接受成功的初始庞氏铸造治疗并随访一年的患者均被纳入研究。收集复发率、手术和手术类型。结果:最终队列纳入268例特发性内翻足患儿397例,其中女性98例(36.6%),男性170例(63.4%)。ponseti治疗成功且无复发的组由171名252英尺的儿童组成(占总队列的63.5%)。复发组共97例(36.2%)复发并需要进一步干预。复发组复杂型内翻足患者比例更高(18.6% vs 4.7%, p = 0.001)。未复发患者的中位年龄为33.7天(IQR为40.8),而复发患者的中位年龄明显较低,为25.1天(IQR为17.2)(p < 0.001)。无复发组儿童需要更少的石膏实现矫正,平均4.3次,而复发组为5.2次(p < 0.001)。无复发组患儿的良好依从率明显高于复发组患儿(94.9% vs 62.3%, p < 0.001)。共有24名儿童(23英尺,占总队列的5.8%)接受了手术,而74名复发但不需要手术。最常见的手术是胫骨前肌腱转移(n = 25)和开放腱腱延长(n = 21)。结论:我们证实,在最初的Ponseti系列患者中,为了实现矫正而使用的石膏数量较多,出现时年龄较小,复杂的内翻足特征,以及不良的支具依从性可能与复发和手术的风险相关。很少有必要进行关节侵入性手术。
{"title":"Rate and predictors of relapse and surgery in idiopathic clubfeet after successful Ponseti treatment in infancy : a single centre, retrospective, comparative study.","authors":"Ruth Gremminger, Caroline Cristofaro, Marwah Sadat, Maryse Bouchard","doi":"10.1302/2633-1462.610.BJO-2025-0170.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0170.R1","url":null,"abstract":"<p><strong>Aims: </strong>To assess the rates of relapse and risk factors for release and surgical intervention in patients with idiopathic clubfoot.</p><p><strong>Methods: </strong>A retrospective review of all patients with idiopathic clubfoot and initiation of Ponseti treatment between February 2005 and December 2015 was conducted. All patients with successful initial Ponseti casting treatment at the study institution and one year of follow-up were included. Rates of relapse, surgery, and types of surgical procedures performed were collected.</p><p><strong>Results: </strong>The final cohort included 268 children with 397 idiopathic clubfeet, consisting of 98 females (36.6%) and 170 males (63.4%). The successfully Ponseti-treated group without relapse was composed of 171 children with 252 feet (63.5% of total cohort). A total of 97 patients (36.2%) had a relapse and required further intervention (relapse group). There was a greater proportion of patients with complex-type clubfoot in the relapse group (18.6% vs 4.7%, p = 0.001). Patients who never relapsed presented at a median age of 33.7 days (IQR 40.8), while those who relapsed presented at a significantly younger age, at a median of 25.1 days (IQR 17.2) (p < 0.001). Children in the no-relapse group required significantly fewer casts to achieve correction, with a mean of 4.3 compared with 5.2 in patients with relapse (p < 0.001). Children in the no-relapse group showed a significantly higher rate of good adherence compared with those in the relapse-group (94.9% vs 62.3%, p < 0.001). In total, 24 children (23 feet, 5.8% of total cohort) underwent surgery, whereas 74 had a relapse but did not require surgery. The most common surgical procedures performed were tibialis anterior tendon transfer (n = 25) and open tendoachilles lengthening (n = 21).</p><p><strong>Conclusion: </strong>We confirm that a higher number of casts to achieve correction in the initial Ponseti series, younger age at presentation, complex clubfoot features, and poor brace adherence may be correlated with risk of relapse and surgery. The need for joint invasive surgery is rarely indicated.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1275-1281"},"PeriodicalIF":3.1,"publicationDate":"2025-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12527565/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145303681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aims: The aim of this study was to explore the relationship between the femoral head diameter (FHD) and the degree of subluxation in developmental dysplasia of the hip (DDH) patients, and develop a machine-learning model for predicting acetabular component size in total hip arthroplasty (THA) according to demographic data and FHD.
Methods: The FHD of 469 DDH patients from Longwood Valley medical database was measured, after excluding those with severe femoral head destruction, bone grafting, or augments. Its distribution and difference across Crowe and Hartofilakidis classifications were also assessed. Five machine-learning algorithms were developed to predict the size of the acetabular component, and the best model was determined according to the mean square error (MSE), root mean square error (RMSE), and R-squared values. The accuracy of the best model's cup size prediction was validated by comparing it with acetate templating and CT-based planning in a consecutive cohort from an independent institution.
Results: The FHD gradually decreased with increasing Crowe and Hartofilakidis classifications. The Pearson correlation coefficient between FHD and the size of the acetabular component was 0.60, indicating a moderate correlation. In the test set, the random forest model outperformed the other four models in terms of MSE (0.904), RMSE (0.951), and R-squared (0.919). In the external validation, the accuracy of this model was not significantly different from CT-based planning (80.0% vs 87.5%, p > 0.05), but outperformed acetate templating (80.0% vs 52.5%, p < 0.05), particularly for Crowe Type IV (81.8% vs 27.3%, p < 0.05).
Conclusion: The FHD decreases with increasing degree of subluxation in DDH patients. The machine-learning model constructed by combining demographic parameters and FHD demonstrates significantly higher accuracy in acetabular component size planning compared to templating methods. This approach serving as an effective auxiliary tool or alternative when CT is unavailable.
{"title":"Femoral head diameter varies widely in hips with developmental dysplasia and predicts acetabular component size in total hip arthroplasty.","authors":"Songlin Li, Xingyu Liu, Wenwei Qian, Yiling Zhang, Qunshan Lu, Peilai Liu","doi":"10.1302/2633-1462.610.BJO-2025-0075.R2","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0075.R2","url":null,"abstract":"<p><strong>Aims: </strong>The aim of this study was to explore the relationship between the femoral head diameter (FHD) and the degree of subluxation in developmental dysplasia of the hip (DDH) patients, and develop a machine-learning model for predicting acetabular component size in total hip arthroplasty (THA) according to demographic data and FHD.</p><p><strong>Methods: </strong>The FHD of 469 DDH patients from Longwood Valley medical database was measured, after excluding those with severe femoral head destruction, bone grafting, or augments. Its distribution and difference across Crowe and Hartofilakidis classifications were also assessed. Five machine-learning algorithms were developed to predict the size of the acetabular component, and the best model was determined according to the mean square error (MSE), root mean square error (RMSE), and R-squared values. The accuracy of the best model's cup size prediction was validated by comparing it with acetate templating and CT-based planning in a consecutive cohort from an independent institution.</p><p><strong>Results: </strong>The FHD gradually decreased with increasing Crowe and Hartofilakidis classifications. The Pearson correlation coefficient between FHD and the size of the acetabular component was 0.60, indicating a moderate correlation. In the test set, the random forest model outperformed the other four models in terms of MSE (0.904), RMSE (0.951), and R-squared (0.919). In the external validation, the accuracy of this model was not significantly different from CT-based planning (80.0% vs 87.5%, p > 0.05), but outperformed acetate templating (80.0% vs 52.5%, p < 0.05), particularly for Crowe Type IV (81.8% vs 27.3%, p < 0.05).</p><p><strong>Conclusion: </strong>The FHD decreases with increasing degree of subluxation in DDH patients. The machine-learning model constructed by combining demographic parameters and FHD demonstrates significantly higher accuracy in acetabular component size planning compared to templating methods. This approach serving as an effective auxiliary tool or alternative when CT is unavailable.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1266-1274"},"PeriodicalIF":3.1,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12520792/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145293956","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-14DOI: 10.1302/2633-1462.610.BJO-2025-0195.R1
Fatih Ozel, Ipek Isik, Barlas Goker, Emre Unal, Turkmen T Ciftci, Devrim Akinci, Mehmet Ayvaz
Aims: This research aims to review the long-term outcomes of CT-guided radiofrequency thermal ablation (RFA) in managing patients with osteoid osteoma (OO).
Methods: A total of 210 patients, with a mean age of 16.6 years, treated with CT-guided RFA between January 2005 and December 2022, were retrospectively studied. The research assessed patients' post-procedure clinical follow-up, recording treatment success and complications. Cox regression analysis, conducted in both univariate and multiple models, examined the impact of independent variables on recurrence time.
Results: The average follow-up was 103.7 months. In the first 24 hours after the treatment, all patients had less OO pain. Successful outcomes without recurrence were achieved in 200 out of 210 patients (95.2%). Univariate analysis indicated that sex did not have a significant impact on recurrence (p = 0.657); however, recurrence was significantly associated with younger age (p = 0.004).
Conclusion: This research shows that CT-guided RFA for OO patients relieves pain quickly, has low recurrence rates, and minimal complications. Younger patients should be monitored for an extended duration due to the influence of age on recurrence rates.
{"title":"Long-term results of CT-guided radiofrequency ablation therapy in patients with osteoid osteoma : retrospective outcome analysis.","authors":"Fatih Ozel, Ipek Isik, Barlas Goker, Emre Unal, Turkmen T Ciftci, Devrim Akinci, Mehmet Ayvaz","doi":"10.1302/2633-1462.610.BJO-2025-0195.R1","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0195.R1","url":null,"abstract":"<p><strong>Aims: </strong>This research aims to review the long-term outcomes of CT-guided radiofrequency thermal ablation (RFA) in managing patients with osteoid osteoma (OO).</p><p><strong>Methods: </strong>A total of 210 patients, with a mean age of 16.6 years, treated with CT-guided RFA between January 2005 and December 2022, were retrospectively studied. The research assessed patients' post-procedure clinical follow-up, recording treatment success and complications. Cox regression analysis, conducted in both univariate and multiple models, examined the impact of independent variables on recurrence time.</p><p><strong>Results: </strong>The average follow-up was 103.7 months. In the first 24 hours after the treatment, all patients had less OO pain. Successful outcomes without recurrence were achieved in 200 out of 210 patients (95.2%). Univariate analysis indicated that sex did not have a significant impact on recurrence (p = 0.657); however, recurrence was significantly associated with younger age (p = 0.004).</p><p><strong>Conclusion: </strong>This research shows that CT-guided RFA for OO patients relieves pain quickly, has low recurrence rates, and minimal complications. Younger patients should be monitored for an extended duration due to the influence of age on recurrence rates.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1260-1265"},"PeriodicalIF":3.1,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12517971/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145287390","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-13DOI: 10.1302/2633-1462.610.BJO-2025-0084.R2
Henry A Claireaux, Helen S M Smith, Andrew M Edwards, Julian R Jones, Arul Ramasamy
Aims: Osteomyelitis and infected nonunion cause devastating morbidity and are difficult to treat. Antimicrobial resistance further complicates musculoskeletal infection and is a significant global problem, including in low- and middle-income countries. Extensively drug-resistant bacteria and high rates of musculoskeletal infection have been identified during the Russian-Ukrainian war. Biomaterials with antimicrobial properties unrelated to antibiotics represent a potential solution. Bioactive glass, for example, has shown promise as a bone void filler. It binds to bone, stimulates bone formation, causes no harmful immune response, and has antimicrobial properties. This systematic review appraises the evidence for bioactive glass as a treatment for osteomyelitis and infected nonunion.
Methods: A comprehensive search of MEDLINE and EMBASE was performed with research librarian guidance. Articles were screened and assessed for risk of bias by two blinded authors. No date limitations were used. Methodology was guided by the Cochrane Handbook and the PRISMA statement. Data were compiled and narratively synthesized.
Results: We included 24 observational studies on 957 patients. Reported outcomes were heterogeneous, with patient-reported outcome measures available in only one study. Most studies were small and at considerable risk of bias. Studies supported bioactive glass use with high rates of bone healing and infection resolution. Comparative studies found non-inferiority with established treatments such as antibiotic-containing calcium sulphate and polymethylmethacrylate cement spacers. Few significant bioactive glass-related complications were reported.
Conclusion: This review demonstrates the potential of bioactive glass as a treatment for osteomyelitis and infected nonunion. Widespread uptake over established treatments is likely to require further supporting evidence, such as high-quality randomized controlled trials, to understand the role of biomaterials in treating these challenging conditions. Future work should examine 3D-printed bioactive glass hybrids, which may have biomechanical advantages for large bone defects.
{"title":"A systematic review on bioactive glass as a treatment for limb osteomyelitis and infected nonunion.","authors":"Henry A Claireaux, Helen S M Smith, Andrew M Edwards, Julian R Jones, Arul Ramasamy","doi":"10.1302/2633-1462.610.BJO-2025-0084.R2","DOIUrl":"10.1302/2633-1462.610.BJO-2025-0084.R2","url":null,"abstract":"<p><strong>Aims: </strong>Osteomyelitis and infected nonunion cause devastating morbidity and are difficult to treat. Antimicrobial resistance further complicates musculoskeletal infection and is a significant global problem, including in low- and middle-income countries. Extensively drug-resistant bacteria and high rates of musculoskeletal infection have been identified during the Russian-Ukrainian war. Biomaterials with antimicrobial properties unrelated to antibiotics represent a potential solution. Bioactive glass, for example, has shown promise as a bone void filler. It binds to bone, stimulates bone formation, causes no harmful immune response, and has antimicrobial properties. This systematic review appraises the evidence for bioactive glass as a treatment for osteomyelitis and infected nonunion.</p><p><strong>Methods: </strong>A comprehensive search of MEDLINE and EMBASE was performed with research librarian guidance. Articles were screened and assessed for risk of bias by two blinded authors. No date limitations were used. Methodology was guided by the Cochrane Handbook and the PRISMA statement. Data were compiled and narratively synthesized.</p><p><strong>Results: </strong>We included 24 observational studies on 957 patients. Reported outcomes were heterogeneous, with patient-reported outcome measures available in only one study. Most studies were small and at considerable risk of bias. Studies supported bioactive glass use with high rates of bone healing and infection resolution. Comparative studies found non-inferiority with established treatments such as antibiotic-containing calcium sulphate and polymethylmethacrylate cement spacers. Few significant bioactive glass-related complications were reported.</p><p><strong>Conclusion: </strong>This review demonstrates the potential of bioactive glass as a treatment for osteomyelitis and infected nonunion. Widespread uptake over established treatments is likely to require further supporting evidence, such as high-quality randomized controlled trials, to understand the role of biomaterials in treating these challenging conditions. Future work should examine 3D-printed bioactive glass hybrids, which may have biomechanical advantages for large bone defects.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 10","pages":"1248-1259"},"PeriodicalIF":3.1,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12515516/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145281306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}