Pub Date : 2025-11-05DOI: 10.1302/2633-1462.611.BJO-2025-0188.R1
Anna Bridgens, Deborah M Eastwood, James G Wright, Jason Mavrotas, Alpesh Kothari, Luiz R Agrizzi de Angeli, Alaric Aroojis, Yael Gelfer, Donato G Leo, Deepika Pinto, Hannah Coulton, Cristina Rafter
Aims: Orthopaedic interventions in spinal dysraphism (SD) are frequently required to address a wide spectrum of musculoskeletal deformities. The outcomes used to assess treatment, however, are heterogeneous and most fail to incorporate patient/family perceptions. The aim of this study was to identify the minimum set of outcomes to be collected in clinical practice and research settings following orthopaedic intervention in ambulatory and non-ambulatory children with SD.
Methods: The study was based on Core Outcome Measures in Effectiveness trials (COMET) initiative. A list of individual clinical outcomes (ICOs) and outcome measurement tools (OMTs) were obtained from a systematic literature review (SR) and from patients and families through an interview and questionnaire. Core outcomes were rated for importance in a two-round Delphi process that included international orthopaedic surgeons, physiotherapists, orthotists, patients, and families. Outcomes that did not reach consensus during the Delphi process were resolved with a final consensus meeting.
Results: In total, 88 statements, including ICOs and OMTs, were scored during the Delphi process for ambulatory and non-ambulatory children. A total of 35 items were resolved in the final consensus meeting. The final core outcome set (COS) is goal-based and includes 28 outcome parameters to be collected a minimum of one year after any orthopaedic intervention and at subsequent set points during childhood. The COS incorporates clinical examination, mobility and functional assessment, patient-reported outcome measures, and investigations with the Goal Attainment Score recommended for goal setting.
Conclusion: A minimum set of outcomes to evaluate the orthopaedic treatment of SD was created thereby enabling consistency in reporting among centres and studies.
{"title":"A global core outcome set for orthopaedic interventions in children with spinal dysraphism : aiming to enhance research quality and patient outcomes.","authors":"Anna Bridgens, Deborah M Eastwood, James G Wright, Jason Mavrotas, Alpesh Kothari, Luiz R Agrizzi de Angeli, Alaric Aroojis, Yael Gelfer, Donato G Leo, Deepika Pinto, Hannah Coulton, Cristina Rafter","doi":"10.1302/2633-1462.611.BJO-2025-0188.R1","DOIUrl":"10.1302/2633-1462.611.BJO-2025-0188.R1","url":null,"abstract":"<p><strong>Aims: </strong>Orthopaedic interventions in spinal dysraphism (SD) are frequently required to address a wide spectrum of musculoskeletal deformities. The outcomes used to assess treatment, however, are heterogeneous and most fail to incorporate patient/family perceptions. The aim of this study was to identify the minimum set of outcomes to be collected in clinical practice and research settings following orthopaedic intervention in ambulatory and non-ambulatory children with SD.</p><p><strong>Methods: </strong>The study was based on Core Outcome Measures in Effectiveness trials (COMET) initiative. A list of individual clinical outcomes (ICOs) and outcome measurement tools (OMTs) were obtained from a systematic literature review (SR) and from patients and families through an interview and questionnaire. Core outcomes were rated for importance in a two-round Delphi process that included international orthopaedic surgeons, physiotherapists, orthotists, patients, and families. Outcomes that did not reach consensus during the Delphi process were resolved with a final consensus meeting.</p><p><strong>Results: </strong>In total, 88 statements, including ICOs and OMTs, were scored during the Delphi process for ambulatory and non-ambulatory children. A total of 35 items were resolved in the final consensus meeting. The final core outcome set (COS) is goal-based and includes 28 outcome parameters to be collected a minimum of one year after any orthopaedic intervention and at subsequent set points during childhood. The COS incorporates clinical examination, mobility and functional assessment, patient-reported outcome measures, and investigations with the Goal Attainment Score recommended for goal setting.</p><p><strong>Conclusion: </strong>A minimum set of outcomes to evaluate the orthopaedic treatment of SD was created thereby enabling consistency in reporting among centres and studies.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 11","pages":"1371-1381"},"PeriodicalIF":3.1,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12585783/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145446085","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 : 2025-11-04DOI: 10.1302/2633-1462.611.BJO-2024-0153.R1
Sarah McColm, Philip Ackerman, Victoria Graham, David F Hamilton
Aims: Knee osteoarthritis (OA) is a leading cause of pain and disability, impacting quality of life. There are various conservative (non-surgical, non-pharmacological) management approaches suggested to support those with knee OA and multiple international clinical practice guidelines to inform patient care. This study contrasts the consistency of these management recommendations across the currently available guidelines.
Methods: Systematic search of CINAHL, MEDLINE, Science Direct, and the Guideline International Network website applying PRISMA guidance. Clinical practice guidelines from representative bodies relating to the conservative management of knee OA were included. Quality assessment was completed using the International Centre for Allied Health Evidence (iCAHE) tool.
Results: The search returned 750 records, from which 13 current clinical practice guidelines from national and international medical, surgical, and professional associations were identified. Quality of guideline construction was high. Recommendations for core knee OA management were broadly consistent; entailing exercise, self-management advice and education, and weight management; however, detail as to the proposed delivery of these interventions was lacking. Notable variation was evident between guidelines recommendation for all other interventions, such as manual therapy, bracing/orthotics and acupuncture, related to how the guideline groups interpreted generally low levels of evidence.
Conclusion: There is broad consistency across clinical practice guidelines regarding core conservative management of knee OA which should direct and support patient care. Differences in evidence interpretation as to effect of alternative treatments result in different recommendations which may be confusing for patients, physiotherapists and medical personnel referring to these services.
目的:膝关节骨关节炎(OA)是疼痛和残疾的主要原因,影响生活质量。有多种保守(非手术、非药物)治疗方法被建议用于支持膝关节OA患者,并有多个国际临床实践指南为患者护理提供指导。本研究对比了这些管理建议在现有指南中的一致性。方法:应用PRISMA指南系统检索CINAHL、MEDLINE、Science Direct和guidelines International Network网站。来自代表性机构的关于膝关节OA保守治疗的临床实践指南被纳入。使用国际联合卫生证据中心(iCAHE)工具完成了质量评估。结果:检索返回750份记录,从中确定了13份来自国家和国际医学、外科和专业协会的现行临床实践指南。指南构建质量高。膝关节核心OA管理的建议大致一致;包括锻炼、自我管理建议和教育,以及体重管理;但是,缺乏关于拟议实施这些干预措施的细节。指南推荐的所有其他干预措施(如手工治疗、支具/矫形器和针灸)之间存在明显差异,这与指南组如何解释普遍低水平的证据有关。结论:对于膝关节OA的核心保守治疗,临床实践指南具有广泛的一致性,指导和支持患者护理。关于替代治疗效果的证据解释的差异导致不同的建议,这可能会使患者、物理治疗师和提及这些服务的医务人员感到困惑。
{"title":"Consistency of advice for the conservative management of knee osteoarthritis across international clinical practice guidelines.","authors":"Sarah McColm, Philip Ackerman, Victoria Graham, David F Hamilton","doi":"10.1302/2633-1462.611.BJO-2024-0153.R1","DOIUrl":"10.1302/2633-1462.611.BJO-2024-0153.R1","url":null,"abstract":"<p><strong>Aims: </strong>Knee osteoarthritis (OA) is a leading cause of pain and disability, impacting quality of life. There are various conservative (non-surgical, non-pharmacological) management approaches suggested to support those with knee OA and multiple international clinical practice guidelines to inform patient care. This study contrasts the consistency of these management recommendations across the currently available guidelines.</p><p><strong>Methods: </strong>Systematic search of CINAHL, MEDLINE, Science Direct, and the Guideline International Network website applying PRISMA guidance. Clinical practice guidelines from representative bodies relating to the conservative management of knee OA were included. Quality assessment was completed using the International Centre for Allied Health Evidence (iCAHE) tool.</p><p><strong>Results: </strong>The search returned 750 records, from which 13 current clinical practice guidelines from national and international medical, surgical, and professional associations were identified. Quality of guideline construction was high. Recommendations for core knee OA management were broadly consistent; entailing exercise, self-management advice and education, and weight management; however, detail as to the proposed delivery of these interventions was lacking. Notable variation was evident between guidelines recommendation for all other interventions, such as manual therapy, bracing/orthotics and acupuncture, related to how the guideline groups interpreted generally low levels of evidence.</p><p><strong>Conclusion: </strong>There is broad consistency across clinical practice guidelines regarding core conservative management of knee OA which should direct and support patient care. Differences in evidence interpretation as to effect of alternative treatments result in different recommendations which may be confusing for patients, physiotherapists and medical personnel referring to these services.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 11","pages":"1358-1370"},"PeriodicalIF":3.1,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12582647/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145439228","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 : 2025-11-03DOI: 10.1302/2633-1462.611.BJO-2025-0178.R1
Mohammad Aryaie, Jonathan T Evans, Cliff L Shelton, Antony Johansen, Toby O Smith, Michael R Whitehouse, Dawn Goodwin, Alex Bottle
Aims: Postoperative periprosthetic femoral fractures (POPFFs) following hip and knee arthroplasty are increasing. They often have poor outcomes. We have limited understanding of the predictors of these outcomes, which this study addresses.
Methods: We extracted administrative hospital data for patients aged 18 years and above with admissions to NHS hospitals in England with a primary diagnosis of POPFF between April 2016 and December 2022, including demographic characteristics, comorbidities, surgery for POPFF, admission source, outpatient department (OPD) appointments, and pre-POPFF admissions. Data were linked to the national death register. The most relevant available hospital-level key performance indicators (KPIs) were taken from the National Hip Fracture Database (NHFD). We used multilevel models with random intercepts for hospitals to predict in-hospital death, 30-day death, length of stay (LOS) above the upper quartile, and 30-day emergency readmission.
Results: A total of 33,728 patients were included, with a median age of 82 years (IQR 73 to 88); 65.9% were female. In total, 1,510 deaths occurred within 30 days of admission. In multiple regression models, age was associated with higher mortality and longer LOS. Females showed lower odds of mortality and 30-day readmission. Congestive heart failure and liver disease were more strongly linked to all adverse outcomes than were other comorbidities. Fixation (odds ratio (OR) 0.72, 95% CI 0.64 to 0.81) and revision (OR 0.78, 95% CI 0.68 to 0.91) were associated with lower 30-day mortality but longer hospital stays than having neither procedure. Previous hip fracture was associated with 30-day readmission and longer LOS but not with mortality. Admission from a care home was associated with higher 30-day mortality (OR 1.70, 95% CI 1.31 to 2.39), but shorter LOS. Previous any-cause emergency admissions and missed outpatient appointments were associated with worse outcomes. Hospital-level NHFD KPIs for POPFF and admission numbers for POPFF were not associated with any outcome.
Conclusion: We identified several patient factors, but no hospital factors, associated with adverse short-term outcomes following POPFF admission.
目的:髋关节和膝关节置换术后股骨假体周围骨折(POPFFs)的发生率越来越高。他们的结果往往很糟糕。我们对这些结果的预测因素了解有限,这是本研究要解决的问题。方法:我们提取了2016年4月至2022年12月期间在英国NHS医院就诊的18岁及以上初步诊断为POPFF的患者的行政医院数据,包括人口统计学特征、合并症、POPFF手术、入院来源、门诊预约和POPFF前入院情况。数据与国家死亡登记册相关联。最相关的医院级关键绩效指标(kpi)来自国家髋部骨折数据库(NHFD)。我们使用具有随机截距的医院多层模型来预测院内死亡、30天死亡、高于上四分位数的住院时间(LOS)和30天的急诊再入院。结果:共纳入33,728例患者,中位年龄为82岁(IQR 73 ~ 88);65.9%为女性。总共有1 510人在入院后30天内死亡。在多元回归模型中,年龄与较高的死亡率和较长的LOS相关。女性患者的死亡率和30天再入院率较低。与其他合并症相比,充血性心力衰竭和肝脏疾病与所有不良结果的关联更强。固定手术(优势比(OR) 0.72, 95% CI 0.64 ~ 0.81)和翻修手术(OR 0.78, 95% CI 0.68 ~ 0.91)与不进行手术相比,30天死亡率较低,但住院时间较长。既往髋部骨折与30天再入院和更长的LOS相关,但与死亡率无关。从护理院入院与较高的30天死亡率(OR 1.70, 95% CI 1.31至2.39)相关,但与较短的LOS相关。先前的任何原因急诊入院和错过门诊预约与较差的结果相关。医院级别的NHFD关键绩效指标和POPFF入院人数与任何结果无关。结论:我们确定了几个患者因素,但没有医院因素,与POPFF入院后的不良短期结果相关。
{"title":"Predictors of short-term outcomes after postoperative periprosthetic femoral fracture : a UK linked data analysis.","authors":"Mohammad Aryaie, Jonathan T Evans, Cliff L Shelton, Antony Johansen, Toby O Smith, Michael R Whitehouse, Dawn Goodwin, Alex Bottle","doi":"10.1302/2633-1462.611.BJO-2025-0178.R1","DOIUrl":"10.1302/2633-1462.611.BJO-2025-0178.R1","url":null,"abstract":"<p><strong>Aims: </strong>Postoperative periprosthetic femoral fractures (POPFFs) following hip and knee arthroplasty are increasing. They often have poor outcomes. We have limited understanding of the predictors of these outcomes, which this study addresses.</p><p><strong>Methods: </strong>We extracted administrative hospital data for patients aged 18 years and above with admissions to NHS hospitals in England with a primary diagnosis of POPFF between April 2016 and December 2022, including demographic characteristics, comorbidities, surgery for POPFF, admission source, outpatient department (OPD) appointments, and pre-POPFF admissions. Data were linked to the national death register. The most relevant available hospital-level key performance indicators (KPIs) were taken from the National Hip Fracture Database (NHFD). We used multilevel models with random intercepts for hospitals to predict in-hospital death, 30-day death, length of stay (LOS) above the upper quartile, and 30-day emergency readmission.</p><p><strong>Results: </strong>A total of 33,728 patients were included, with a median age of 82 years (IQR 73 to 88); 65.9% were female. In total, 1,510 deaths occurred within 30 days of admission. In multiple regression models, age was associated with higher mortality and longer LOS. Females showed lower odds of mortality and 30-day readmission. Congestive heart failure and liver disease were more strongly linked to all adverse outcomes than were other comorbidities. Fixation (odds ratio (OR) 0.72, 95% CI 0.64 to 0.81) and revision (OR 0.78, 95% CI 0.68 to 0.91) were associated with lower 30-day mortality but longer hospital stays than having neither procedure. Previous hip fracture was associated with 30-day readmission and longer LOS but not with mortality. Admission from a care home was associated with higher 30-day mortality (OR 1.70, 95% CI 1.31 to 2.39), but shorter LOS. Previous any-cause emergency admissions and missed outpatient appointments were associated with worse outcomes. Hospital-level NHFD KPIs for POPFF and admission numbers for POPFF were not associated with any outcome.</p><p><strong>Conclusion: </strong>We identified several patient factors, but no hospital factors, associated with adverse short-term outcomes following POPFF admission.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 11","pages":"1349-1357"},"PeriodicalIF":3.1,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12579994/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145432442","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 : 2025-11-01DOI: 10.1302/2633-1462.611.BJO-2025-0171.R1
Haodong Tian, Weixin Zheng, Yi Li, Xinwen Wang
Aims: Varus ankle arthritis with excessive talar tilt (TT) angle often has unsatisfactory outcomes after supramalleolar osteotomy (SMOT) surgery. These patients have a 3D deformity involving the hind foot as well as the ankle. Thus, adjuvant correction of the hind foot component may contribute to the TT angle. This study aimed to explore whether calcaneal osteotomy combined with SMOT could effectively correct the hindfoot alignment to treat varus ankle arthritis with a large TT angle.
Methods: In total, 26 patients diagnosed with varus ankle arthritis with excessive TT angle were included in this study. Calcaneal osteotomy was combined with SMOT to correct the hindfoot alignment. Thus, a combination of supramalleolar and subtalar corrections was performed to improve the alignment of the lower limbs. Anterior and lateral radiographs of the weightbearing ankle were performed preoperatively and postoperatively. The tibial anterior surface angle, the tibial lateral surface angle, and TT angle were measured. The clinical efficacy was evaluated according to the American Orthopaedic Foot and Ankle Society scoring system and pain visual analogue scale.
Results: Preoperative varus hindfoot alignment was corrected to nearly normal via SMOT combined with calcaneal osteotomy. Radiological parameters demonstrated that SMOT combined with calcaneal osteotomy could significantly improve varus ankle arthritis and correct excessive TT angle. Moreover, the clinical outcomes of the patients were significantly improved and the pain was significantly relieved after the surgery.
Conclusion: We found that SMOT combined with calcaneal osteotomy significantly improved varus ankle arthritis with a significant reduction in TT angle. Therefore, with the correction of the subtalar alignment and the displacement of the talus centre, the hindfoot alignment can recovery effectively and the TT angle can be significantly reduced. This suggests that SMOT combined with calcaneal osteotomy is a practical surgical approach for varus ankle arthritis with excessive TT angle.
{"title":"Supramalleolar osteotomy combined with calcaneal osteotomy for the treatment of varus ankle arthritis with excessive talar tilt angle.","authors":"Haodong Tian, Weixin Zheng, Yi Li, Xinwen Wang","doi":"10.1302/2633-1462.611.BJO-2025-0171.R1","DOIUrl":"10.1302/2633-1462.611.BJO-2025-0171.R1","url":null,"abstract":"<p><strong>Aims: </strong>Varus ankle arthritis with excessive talar tilt (TT) angle often has unsatisfactory outcomes after supramalleolar osteotomy (SMOT) surgery. These patients have a 3D deformity involving the hind foot as well as the ankle. Thus, adjuvant correction of the hind foot component may contribute to the TT angle. This study aimed to explore whether calcaneal osteotomy combined with SMOT could effectively correct the hindfoot alignment to treat varus ankle arthritis with a large TT angle.</p><p><strong>Methods: </strong>In total, 26 patients diagnosed with varus ankle arthritis with excessive TT angle were included in this study. Calcaneal osteotomy was combined with SMOT to correct the hindfoot alignment. Thus, a combination of supramalleolar and subtalar corrections was performed to improve the alignment of the lower limbs. Anterior and lateral radiographs of the weightbearing ankle were performed preoperatively and postoperatively. The tibial anterior surface angle, the tibial lateral surface angle, and TT angle were measured. The clinical efficacy was evaluated according to the American Orthopaedic Foot and Ankle Society scoring system and pain visual analogue scale.</p><p><strong>Results: </strong>Preoperative varus hindfoot alignment was corrected to nearly normal via SMOT combined with calcaneal osteotomy. Radiological parameters demonstrated that SMOT combined with calcaneal osteotomy could significantly improve varus ankle arthritis and correct excessive TT angle. Moreover, the clinical outcomes of the patients were significantly improved and the pain was significantly relieved after the surgery.</p><p><strong>Conclusion: </strong>We found that SMOT combined with calcaneal osteotomy significantly improved varus ankle arthritis with a significant reduction in TT angle. Therefore, with the correction of the subtalar alignment and the displacement of the talus centre, the hindfoot alignment can recovery effectively and the TT angle can be significantly reduced. This suggests that SMOT combined with calcaneal osteotomy is a practical surgical approach for varus ankle arthritis with excessive TT angle.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"6 11","pages":"1343-1348"},"PeriodicalIF":3.1,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12580771/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145423000","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 : 2025-10-28DOI: 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}