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A comparison of cancellous screws in a sliding compression configuration and angle-stable sliding compression implants for internal fixation of femoral neck fractures in the non-elderly predominantly below 65 years: a systematic review and meta-analysis. 滑动加压松质螺钉与角度稳定滑动加压植入物内固定65岁以下非老年人股骨颈骨折的比较:系统回顾和荟萃分析。
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-06-16 DOI: 10.2340/17453674.2025.44034
Michaela M Hansen, Mads S Nielsen, Per H Gundtoft, Maiken Stilling, Ming Ding, Bjarke Viberg

Background and purpose:  Internal fixation is the preferred treatment in the non-elderly with femoral neck fractures, regardless of fracture displacement. High complication rates are reported, in particular for displaced fractures. We aimed to compare cancellous screws with angle-stable sliding compression implants for internal fixation of femoral neck fractures in the non-elderly.

Methods:  A systematic search was carried out in Medline, Embase, Scopus, and Cochrane. The search results were screened by 2 reviewers using Covidence and assessed for risk of bias. All comparative studies were included. The studies reported at least 1 of the following outcomes: avascular necrosis, fixation failure/cut-out, non-union, any complication, reoperation, femoral neck shortening, or Harris Hip Score (HHS). Dichotomous outcomes are reported as risk ratio (RR) and continuous outcomes as mean difference (MD). All effect measures use a random effects model.

Results: The search yielded 23 studies eligible for inclusion: 4 randomized controlled trials (RCTs) and 19 retrospective cohort trials, including 1,844 fractures. Only 1 study had low risk of bias. The results demonstrated no difference in RCTs alone. Analysis of all studies showed superior outcomes in favor of angle-stable sliding compression implants for fixation failure/cut-out (RR 0.54, 95% confidence interval [CI] 0.31-0.94), any complication (RR 0.49, CI 0.28-0.87), shortening > 5 mm (RR 0.54, CI 0.37-0.80), and HHS 6-24 months (MD 3.1, CI 1.8-4.4).

Conclusion:  RCTs alone showed no significant differences between implant types. When including retrospective studies, angle-stable sliding compression implants demonstrated some advantages. The strength of evidence is limited by the predominance of retrospective cohort studies and high risk of bias in the included studies.

背景与目的:不论骨折移位与否,内固定是非老年股骨颈骨折的首选治疗方法。报道了高并发症发生率,特别是移位骨折。我们的目的是比较松质螺钉与角度稳定滑动加压植入物在非老年人股骨颈骨折内固定中的应用。方法:在Medline、Embase、Scopus和Cochrane中进行系统检索。搜索结果由2名审稿人使用covid进行筛选,并评估偏倚风险。所有的比较研究都包括在内。这些研究报告了以下至少1种结果:无血管坏死、固定失败/切断、不愈合、任何并发症、再手术、股骨颈缩短或Harris髋关节评分(HHS)。二分类结果报告为风险比(RR),连续结果报告为平均差(MD)。所有的效应测量都使用随机效应模型。结果:检索得到23项符合纳入条件的研究:4项随机对照试验(rct)和19项回顾性队列试验,包括1,844例骨折。只有1项研究具有低偏倚风险。结果显示单独的随机对照试验没有差异。对所有研究的分析显示,对于固定失败/断开(RR 0.54, 95%可信区间[CI] 0.31-0.94)、任何并发症(RR 0.49, CI 0.28-0.87)、缩短bbb50 mm (RR 0.54, CI 0.37-0.80)和HHS 6-24个月(MD 3.1, CI 1.8-4.4),均采用角度稳定的滑动压缩植入物。结论:单独的随机对照试验显示种植体类型之间无显著差异。当包括回顾性研究时,角度稳定的滑动加压植入物显示出一些优势。证据的强度受到回顾性队列研究的优势和纳入研究的高偏倚风险的限制。
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引用次数: 0
Effectiveness of nighttime vs full-time bracing in the treatment of moderate-grade adolescent idiopathic scoliosis: a secondary analysis of the CONTRAIS trial. 夜间与全日制支具治疗中度青少年特发性脊柱侧凸的有效性:contris试验的二次分析
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-06-09 DOI: 10.2340/17453674.2025.43706
Anastasios Charalampidis, Elias Diarbakerli, Kourosh Jalalpour, Acke Ohlin, Anna Aspberg Ahl, Hans Möller, Allan Abbott, Paul Gerdhem

Background and purpose:  Data on effectiveness of nighttime bracing compared with full-time bracing in adolescent idiopathic scoliosis is scarce. We aimed to investigate risk of curve progression and surgery with nighttime bracing vs full-time bracing for patients with moderate-grade adolescent idiopathic scoliosis.

Methods:  Skeletally immature individuals with idiopathic scoliosis (25°-40°) treated with a nighttime brace as part of a parallel-group randomized controlled trial (RCT) were compared with non-participants treated with a full-time brace. In the case of curve progression of more than 6° in the nighttime brace group individuals were offered transition to a full-time brace. Surgery was offered if curve sizes were 45° or larger.

Results: Median age at treatment start was 12.8 years (nighttime brace n = 45, full-time brace n = 44). Female sex (odds ratio [OR] 6.5, 95% confidence interval [CI] 1.1-37.4), lower Risser grade (OR 1.6, CI 1.01-2.7), and larger curve size at the beginning of brace treatment (OR 1.4, CI 1.2-1.5) increased the risk of curve progression to ≥ 45°. Major curves in the groups were similar at median 33 months' follow-up (P = 0.7). After 94 months of follow-up, 11 patients in the nighttime brace group and 6 in the full-time brace group had undergone surgery (OR 2.0, CI 0.7-6.1).

Conclusion:  Nighttime bracing, including a possibility to transition to full-time brace in the case of progression, demonstrated comparable effectiveness in preventing curve progression, but a tendency to a higher risk of surgical treatment.

背景和目的:夜间支具与全日制支具在青少年特发性脊柱侧凸治疗中的有效性比较的数据很少。我们的目的是调查中度青少年特发性脊柱侧凸患者夜间支具与全日制支具的弯曲进展和手术风险。方法:作为平行组随机对照试验(RCT)的一部分,使用夜间支架治疗的患有特发性脊柱侧凸(25°-40°)的骨骼未成熟个体与使用全日制支架治疗的非参与者进行比较。如果夜间支具组的弯曲程度超过6°,则可以向全日制支具组过渡。如果曲线大小为45°或更大,则提供手术。结果:治疗开始时的中位年龄为12.8岁(夜间支具n = 45,全日制支具n = 44)。女性(优势比[OR] 6.5, 95%可信区间[CI] 1.1-37.4)、较低的Risser分级(OR 1.6, CI 1.01-2.7)和支架治疗开始时较大的曲线尺寸(OR 1.4, CI 1.2-1.5)增加了曲线进展至≥45°的风险。在中位随访33个月时,两组的主要曲线相似(P = 0.7)。经过94个月的随访,夜间支具组11例,全日制支具组6例进行了手术(OR 2.0, CI 0.7-6.1)。结论:夜间支具,包括在进展情况下过渡到全日制支具的可能性,在预防弯曲进展方面显示出相当的有效性,但倾向于手术治疗的高风险。
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引用次数: 0
Evaluation of sonication for the detection of periprosthetic joint infection in hip revision arthroplasty: a retrospective observational single-center study of 288 episodes. 超声检测髋关节翻修置换术中假体周围关节感染的评价:288例回顾性观察性单中心研究。
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-06-09 DOI: 10.2340/17453674.2025.43679
Bernhardt Kickinger, Tor Monsen, Emma Karis, Micael Widerström, Petter Sundin, Kjell G Nilsson, Volker Otten, Sead Crnalic

Background and purpose:  Sonication fluid cultures have been proposed as a complementary diagnostic method to intraoperative tissue culture sampling for the diagnosis of periprosthetic joint infection (PJI). We evaluated whether sonication provides additional clinically relevant information in the diagnosis of PJI in hip revision.

Methods:  Episodes of hip revision performed between January 2007 and December 2016 were assigned retrospectively to the European Bone and Joint Infection Society (EBJIS) definition of periprosthetic joint infection: infection unlikely, infection likely, and infection confirmed. The inclusion criteria were a minimum of 2 perioperative tissue cultures collected at the index procedure and sonication performed on a removed implant. The results of the tissue cultures were compared with the results of the implant sonication fluid cultures (SFCs).

Results:  288 hip revision episodes in 250 patients fulfilled the inclusion criteria and were analyzed. The "infection unlikely" group included 203 episodes (178 patients), the "infection likely" group included 5 episodes (5 patients), and the "infection confirmed" group included 80 episodes (67 patients). SFC delivered additional clinical information in 15/288: 6 of 203 episodes in the "infection unlikely" group, 2 of 5 episodes in the "infection likely" group, and 7 of 80 in the "infection confirmed" group. Coagulase-negative staphylococci and Staphylococcus aureus were the dominant bacterial species in both the SFC and tissue cultures.

Conclusion:  In addition to tissue cultures, sonication fluid cultures optimized the microbiological yield in 15 out of 288 hip revision episodes.

背景与目的:超声液培养已被提出作为术中组织培养取样诊断假体周围关节感染(PJI)的补充诊断方法。我们评估超声是否为髋关节翻修中PJI的诊断提供了额外的临床相关信息。方法:2007年1月至2016年12月期间进行的髋关节翻修事件回顾性分配到欧洲骨和关节感染协会(EBJIS)对假体周围关节感染的定义:不可能感染,可能感染和确认感染。纳入标准是在索引程序中收集至少2个围手术期组织培养物,并对移除的植入物进行超声检查。将组织培养结果与植体超声液体培养(sfc)结果进行比较。结果:250例患者288次髋关节翻修符合纳入标准并进行分析。“不可能感染”组203次(178例),“可能感染”组5次(5例),“确诊感染”组80次(67例)。SFC在15/288中提供了额外的临床信息:203例中有6例为“不可能感染”组,5例中有2例为“可能感染”组,80例中有7例为“确诊感染”组。凝固酶阴性葡萄球菌和金黄色葡萄球菌是SFC和组织培养的优势菌种。结论:除组织培养外,超声液体培养在288例髋关节翻修中有15例优化了微生物产量。
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引用次数: 0
Comparing incomplete atypical femur fractures in patients with or without bisphosphonate treatment: radiography and bone morphology in a retrospective study of 19 cases. 比较不完全非典型股骨骨折患者接受或不接受双膦酸盐治疗:19例影像学和骨形态学回顾性研究
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-06-05 DOI: 10.2340/17453674.2025.43899
Georg Zdolsek, Hans Peter Bögl, Rickard Sand, Aneta Liszka, Anna Fahlgren, Jörg Schilcher

Background and purpose:  Atypical femur fractures (AFF) are associated with bisphosphonate (BP) treatment, although 10-50% of AFF patients have never used BPs. We aimed to compare the medical history, radiographs, and bone biopsies from the fracture site of patients with AFF with (BP group) and without BP exposure (non-BP group).

Methods: Between 2008 and 2021, we included 19 patients aged ≥ 50 years with incomplete AFF. During prophylactic nailing for thigh pain, a biopsy was taken that included the visible fracture line. Medical charts and radiographs were reviewed, and biopsies were analyzed histologically.

Results:  In the non-BP group (n = 9; mean age 70 years) patients had diseases affecting bone tissue properties (n = 3), pathological structural variations of the femur geometry or a fatigue-type mechanism (n = 3), or no identified causative patho-mechanism (n = 3). In the BP group (n = 10; mean age, 77 years) 2 patients had pathological variations of femur geometry and all used BPs. In the non-BP group, the fracture line was surrounded by bone resorption (n = 6) and cortical irregularities (n = 3), while the fracture line was restricted to a well-defined line in all patients in the BP group. The bone volume fraction (BV/TV) was on average 18% lower (95% confidence interval -35 to -1.2) in the non-BP group.

Conclusion:  AFF in the non-BP group are associated with bone metabolic diseases or deviations in whole-bone geometry and have a specific radiographic appearance at the fracture site whereas antiresorptive treatment appears to be the predominant etiological factor in the BP group.

背景和目的:非典型股骨骨折(AFF)与双膦酸盐(BP)治疗相关,尽管10-50%的AFF患者从未使用过BP。我们的目的是比较(BP组)和(非BP组)有BP暴露的AFF患者的病史、x线片和骨折部位的骨活检。方法:在2008年至2021年期间,我们纳入了19例年龄≥50岁的不完全性AFF患者。在预防性钉入大腿疼痛期间,进行了活检,包括可见的骨折线。回顾了医学图表和x线片,并对活检进行了组织学分析。结果:非bp组(n = 9;平均年龄70岁)患者患有影响骨组织特性的疾病(n = 3),股骨几何形状的病理结构变化或疲劳型机制(n = 3),或未确定的病因病理机制(n = 3)。BP组(n = 10;平均年龄77岁)2例患者股骨几何形态病理改变,均采用bp治疗。在非BP组中,骨折线被骨吸收(n = 6)和皮质不规则(n = 3)包围,而BP组中所有患者的骨折线都被限制在明确的线上。非bp组骨体积分数(BV/TV)平均降低18%(95%可信区间为-35 ~ -1.2)。结论:非BP组AFF与骨代谢性疾病或全骨几何形状偏差有关,在骨折部位具有特定的x线表现,而抗吸收治疗似乎是BP组的主要病因。
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引用次数: 0
Effect of high-dose dexamethasone on morphine use after periacetabular osteotomy for hip dysplasia: a randomized double-blind placebo-controlled single center trial. 大剂量地塞米松对髋臼周围截骨术后吗啡使用的影响:一项随机双盲安慰剂对照单中心试验
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-06-01 DOI: 10.2340/17453674.2025.43903
Viktoria Lindberg-Larsen, Martin Lindberg-Larsen, Ole Ovesen, Stine T Zwisler, Peter Lindholm, Stine Hebsgaard, Robin Christensen, Søren Overgaard

Background and purpose:  Periacetabular osteotomy (PAO) for hip dysplasia is associated with intensive pain and high opioid consumption. High doses of dexamethasone may reduce this. We aimed to compare the effect of 1 or 2 doses of dexamethasone 24 mg, relative to placebo, on postoperative morphine consumption after PAO.

Methods:  A 3-group, randomized, double-blind, placebo-controlled trial was undertaken on patients ≥ 18 years, undergoing PAO (ClinicalTrials.gov: NCT03874936). Randomization Group A received 1 preoperative dose of dexamethasone 24 mg and placebo 24 hours later; Group B received 1 dose of intravenous dexamethasone 24 mg preoperatively and a repeated dose 24 hours postoperatively; and Group C received placebo at both time points. The primary endpoint was the difference in least squares mean cumulative postoperative morphine consumption between the combined dexamethasone groups and placebo within 48 hours from baseline. Key secondary outcomes included postoperative pain intensity, nausea and vomiting, antiemetic consumption and Timed Up and Go at 24 and 48 hours postoperatively, and cumulative morphine consumption from 48 hours to day 14 post-operation.

Results:  90 patients were randomized to dexamethasone groups (n = 60) and placebo (n = 30); 58 and 28, respectively, completed the trial. Mean age was 31 years and 71 (79%) were females. In the combined dexamethasone group the mean cumulated postoperative morphine consumption within 48 hours was 92 mg vs 95 mg in the placebo group, corresponding to a between-group difference of -3 mg (95% confidence interval -27 to 21; P = 0.8). There were no differences observed between groups for any of the secondary outcomes.

Conclusion:  High-dose dexamethasone did not reduce postoperative morphine use or improve any of the secondary outcomes after PAO.

背景和目的:髋臼周围截骨术(PAO)治疗髋关节发育不良与剧烈疼痛和高阿片类药物消耗有关。高剂量的地塞米松可能会减少这种情况。我们的目的是比较1剂或2剂地塞米松24mg相对于安慰剂对PAO术后吗啡消耗的影响。方法:对≥18岁的PAO患者进行3组随机、双盲、安慰剂对照试验(ClinicalTrials.gov: NCT03874936)。A组术前给予1剂地塞米松24 mg, 24 h后给予安慰剂;B组患者术前静脉注射地塞米松1剂24 mg,术后24 h重复给药;C组在两个时间点均服用安慰剂。主要终点是联合地塞米松组和安慰剂组术后48小时内最小二乘平均累积吗啡用量的差异。主要次要结局包括术后疼痛强度、恶心和呕吐、止吐剂用量和术后24和48小时的time Up and Go,以及术后48小时至第14天的吗啡累积用量。结果:90例患者随机分为地塞米松组(n = 60)和安慰剂组(n = 30);分别有58人和28人完成了试验。平均年龄31岁,女性71例(79%)。在联合地塞米松组中,术后48小时内吗啡的平均累计用量为92 mg,而安慰剂组为95 mg,组间差异为-3 mg(95%可信区间为-27 ~ 21;P = 0.8)。在任何次要结果方面,两组之间没有观察到差异。结论:大剂量地塞米松并没有减少PAO术后吗啡的使用,也没有改善PAO术后的任何次要结局。
{"title":"Effect of high-dose dexamethasone on morphine use after periacetabular osteotomy for hip dysplasia: a randomized double-blind placebo-controlled single center trial.","authors":"Viktoria Lindberg-Larsen, Martin Lindberg-Larsen, Ole Ovesen, Stine T Zwisler, Peter Lindholm, Stine Hebsgaard, Robin Christensen, Søren Overgaard","doi":"10.2340/17453674.2025.43903","DOIUrl":"10.2340/17453674.2025.43903","url":null,"abstract":"<p><strong>Background and purpose: </strong> Periacetabular osteotomy (PAO) for hip dysplasia is associated with intensive pain and high opioid consumption. High doses of dexamethasone may reduce this. We aimed to compare the effect of 1 or 2 doses of dexamethasone 24 mg, relative to placebo, on postoperative morphine consumption after PAO.</p><p><strong>Methods: </strong> A 3-group, randomized, double-blind, placebo-controlled trial was undertaken on patients ≥ 18 years, undergoing PAO (ClinicalTrials.gov: NCT03874936). Randomization Group A received 1 preoperative dose of dexamethasone 24 mg and placebo 24 hours later; Group B received 1 dose of intravenous dexamethasone 24 mg preoperatively and a repeated dose 24 hours postoperatively; and Group C received placebo at both time points. The primary endpoint was the difference in least squares mean cumulative postoperative morphine consumption between the combined dexamethasone groups and placebo within 48 hours from baseline. Key secondary outcomes included postoperative pain intensity, nausea and vomiting, antiemetic consumption and Timed Up and Go at 24 and 48 hours postoperatively, and cumulative morphine consumption from 48 hours to day 14 post-operation.</p><p><strong>Results: </strong> 90 patients were randomized to dexamethasone groups (n = 60) and placebo (n = 30); 58 and 28, respectively, completed the trial. Mean age was 31 years and 71 (79%) were females. In the combined dexamethasone group the mean cumulated postoperative morphine consumption within 48 hours was 92 mg vs 95 mg in the placebo group, corresponding to a between-group difference of -3 mg (95% confidence interval -27 to 21; P = 0.8). There were no differences observed between groups for any of the secondary outcomes.</p><p><strong>Conclusion: </strong> High-dose dexamethasone did not reduce postoperative morphine use or improve any of the secondary outcomes after PAO.</p>","PeriodicalId":6916,"journal":{"name":"Acta Orthopaedica","volume":"96 ","pages":"413-420"},"PeriodicalIF":2.5,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12128623/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144214514","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hospital-related healthcare expenditure of impending versus completed pathological femur fractures: a propensity score matched study of 265 patients. 即将发生的病理性股骨骨折与已完成的病理性股骨骨折的医院相关医疗支出:265例患者的倾向评分匹配研究
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-05-27 DOI: 10.2340/17453674.2025.43479
Tom M De Groot, Michelle R Shimizu, David Shin, Olivier Q Groot, Stein J Janssen, Kevin A Raskin, Eric T Newman, Marco L Ferrone, Santiago A Lozano-Calderon, Joseph H Schwab, Paul C Jutte

Background and purpose:  The prevalence of metastatic bone disease as well as the accompanying societal costs are expected to increase due to advances in cancer treatment. While the literature suggests that there is economic value in prophylactic stabilization compared with the fixation of completed pathological fractures in long bone metastases, studies are limited by their small sample sizes and insufficient correction for potential confounders. We aimed to evaluate whether prophylactic treatment of an impending femur fracture was associated with lower healthcare costs compared with completed pathologic fractures. We further aimed to compare prophylactic surgical treatment with completed pathological fractures in terms of postoperative complications, discharge disposition, and postoperative length of stay.

Methods:  This is a retrospective cohort study with propensity score matching (PSM). We included clinical and financial data for 265 patients who received surgery for impending (n = 161) or completed (n = 104) femoral fractures of metastatic lesions, from 2 affiliated urban tertiary care centers between 2016 and 2020 in the United States. After PSM on 13 variables, including demographics and clinical characteristics, 100 impending fractures were matched with 100 completed fractures. The primary outcome was healthcare costs per episode of care, defined as the total cost from admission to 30 days after discharge.

Results:  We found no difference in total cost of care between patients undergoing prophylactic surgical treatment and patients who underwent surgical treatment for a completed pathological fracture (median difference 44 cost-units [CU], 95% confidence interval [CI] -294 to 262). No differences were seen when dividing total cost into cost during hospital admission (median difference -25 CUs, CI -152 to 159) and 30 days following discharge (median difference 31 CUs, CI -74 to 88). Patients with completed pathologic fractures were more often discharged to rehabilitation facilities (57/100, vs 30/100, P < 0.01).

Conclusion:  In contrast to earlier findings, we showed no difference in treatment costs between surgical management of impending and completed pathological fractures of femur metastases after adjusting for confounding factors. However, patients with completed pathological fractures were significantly more likely to require discharge to rehabilitation facilities, highlighting potential out-of-hospital costs related to extended rehabilitation, reduced mobility, and loss of independence.

背景和目的:由于癌症治疗的进步,转移性骨病的患病率以及随之而来的社会成本预计会增加。虽然文献表明,与长骨转移性病理性骨折的固定相比,预防性稳定具有经济价值,但研究样本量小,对潜在混杂因素的校正不足,限制了研究的开展。我们的目的是评估预防性治疗即将发生的股骨骨折是否与较低的医疗费用相关。我们进一步的目的是比较预防性手术治疗与完全病理性骨折的术后并发症、出院处置和术后住院时间。方法:采用倾向评分匹配法(PSM)进行回顾性队列研究。我们纳入了2016年至2020年间美国2个附属城市三级医疗中心265例因即将发生(n = 161)或已完成(n = 104)转移性股骨骨折接受手术的患者的临床和财务数据。在对包括人口统计学和临床特征在内的13个变量进行PSM后,将100例即将发生的骨折与100例已完成的骨折进行匹配。主要结局是每一次护理的医疗费用,定义为从入院到出院后30天的总费用。结果:我们发现接受预防性手术治疗的患者和接受完全病理性骨折手术治疗的患者的总护理成本没有差异(中位数差44成本单位[CU], 95%可信区间[CI] -294至262)。将总成本分为住院期间的成本(中位数差异为-25 cu, CI为-152至159)和出院后30天的成本(中位数差异为31 cu, CI为-74至88),未见差异。病理性骨折患者出院到康复机构的比例更高(57/100,比30/100,P < 0.01)。结论:与早期研究结果相反,在调整混杂因素后,我们发现手术治疗即将发生的和已完成的病理性股骨转移骨折的治疗费用没有差异。然而,完全病理性骨折的患者更有可能需要出院到康复机构,这突出了与延长康复、活动能力降低和独立性丧失相关的潜在院外费用。
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引用次数: 0
Reducing surgical trays to cut both carbon emissions and costs in total knee arthroplasty. 减少手术托盘,减少全膝关节置换术的碳排放和成本。
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-05-27 DOI: 10.2340/17453674.2025.43677
Pim W Van Egmond, Paul Lodder

Background and purpose:  Operating theatres are significant contributors to hospital waste and carbon emissions. In total knee arthroplasty (TKA), the number of surgical trays - and thus the carbon footprint - may be reduced by accurately estimating the prosthesis size preoperatively. We aimed to develop a predictive model to improve preoperative estimation of femoral prosthesis size and reduce the number of trays used in primary TKA.

Methods:  We retrospectively reviewed all primary TKA procedures performed between January 2012 and November 2022 at a single teaching hospital in the Netherlands. Using repeated hold-out cross-validation, we developed a prediction model based on routinely available demographic and anthropometric data to predict femoral component size. Rather than minimizing instruments per tray, our strategy focused on reducing the total number of trays. We used the created prediction model in combination with frequency data from our implanted TKAs to tailor surgical trays accordingly. We performed a post-hoc analysis to estimate the carbon emission cut and cost reduction.

Results:  The best-performing models utilized overlapping tray size ranges, with a practical limit of 3 sizes per tray. The final model predicted the appropriate size range with 97.4% accuracy. This enabled the elimination of 1 tray from the standard surgical setup, reducing total tray use by 11%.

Conclusion:  Accurate preoperative prediction of femoral prosthesis size facilitates surgical tray reconfiguration. We were able to reach an 11% reduction in total trays used with an estimated 1.03 kgCO2eq and a €29.6 cost reduction per reduced tray.

背景和目的:手术室是医院废物和碳排放的重要来源。在全膝关节置换术(TKA)中,通过术前准确估计假体尺寸,可以减少手术托盘的数量,从而减少碳足迹。我们的目的是建立一个预测模型,以改善术前对股骨假体大小的估计,并减少初级TKA中使用的托盘数量。方法:我们回顾性回顾了2012年1月至2022年11月在荷兰一家教学医院进行的所有初级TKA手术。通过重复交叉验证,我们建立了一个基于常规人口统计学和人体测量学数据的预测模型来预测股骨成分的大小。而不是尽量减少每个托盘的仪器,我们的策略侧重于减少托盘的总数。我们利用建立的预测模型结合植入tka的频率数据来定制相应的手术托盘。我们进行了事后分析,以估计碳排放量的减少和成本的降低。结果:表现最好的模型利用重叠的托盘尺寸范围,与实际限制3大小每个托盘。最终模型预测出合适的尺寸范围,准确率为97.4%。这使得从标准手术设置中消除了一个托盘,减少了11%的托盘使用。结论:术前准确预测股骨假体大小有助于手术托盘的重新配置。我们的托盘总量减少了11%,估计减少了1.03千克二氧化碳当量,每个减少的托盘成本降低了29.6欧元。
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引用次数: 0
The risk of complications in elective orthopedic surgeries in children and young adults with cerebral palsy: a population-based register study. 脑瘫儿童和青年选择性骨科手术并发症的风险:一项基于人群的登记研究
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-05-27 DOI: 10.2340/17453674.2025.43705
Anna Telléus, Johan Von Heideken, Fredrik Granath, Eva Broström, Gunnar Hägglund, Per Åstrand

Background and purpose: Musculoskeletal deformities in cerebral palsy (CP) may be surgically treated, but population-based studies of postoperative complications after these surgeries are rare. The aim of our study was to assess the risk of complications following elective orthopedic surgery in children and young adults with CP.

Methods: We performed a register-based cohort study of 1,514 individuals born between 1990 and 2019 who underwent 2,983 orthopedic surgical events between January 1, 1997, and December 31, 2019. Data was obtained from the CP surveillance program CPUP, the Swedish National Patient Register, and the National Cause of Death Register. We used logistic regression to calculate odds ratios (OR) with 95% confidence intervals (CI) for postoperative complications within 90 days, in relation to the Gross Motor Function Classification System (GMFCS) level, anatomic level, and type of surgery (i.e., skeletal vs. soft tissue).

Results: 13% of all surgical events had at least 1 postoperative complication (6% in soft tissue surgeries, 17% in skeletal surgeries), and 51% of these were related to infection. The complication rate was higher in individuals with GMFCS levels IV and V than in the pooled GMFCS levels I-III. The highest ORs were found in GMFCS level V (7.0, CI 3.7-13.5) vs. GMFCS I and spinal surgery (7.9, CI 3.7-13.5) vs. foot/ankle surgery. The OR for skeletal surgery was 1.6 (CI 1.2-2.1) compared with soft tissue surgery.

Conclusion: 13% of all surgical events had at least 1 postoperative complication. The risk of complications after elective orthopedic surgery was higher in children with higher GMFCS levels and in skeletal surgery compared with soft tissue surgery.

背景和目的:脑瘫(CP)的肌肉骨骼畸形可以通过手术治疗,但对这些手术后并发症的基于人群的研究很少。本研究的目的是评估患有cp的儿童和年轻人择期骨科手术后并发症的风险。方法:我们对1514名1990年至2019年出生的患者进行了一项基于登记的队列研究,这些患者在1997年1月1日至2019年12月31日期间接受了2983例骨科手术。数据来自CP监测程序CPUP、瑞典国家患者登记和国家死因登记。我们使用逻辑回归计算90天内术后并发症的95%可信区间(CI)的比值比(OR),与大运动功能分类系统(GMFCS)水平、解剖水平和手术类型(即骨骼与软组织)相关。结果:13%的手术事件至少有1种术后并发症(软组织手术为6%,骨骼手术为17%),其中51%与感染有关。IV级和V级GMFCS患者的并发症发生率高于I-III级GMFCS患者。GMFCS水平V (7.0, CI 3.7-13.5)与GMFCS水平I相比,脊柱手术(7.9,CI 3.7-13.5)与足/踝关节手术相比,or最高。与软组织手术相比,骨骼手术的OR为1.6 (CI 1.2-2.1)。结论:13%的手术事件至少有1个术后并发症。与软组织手术相比,GMFCS水平较高的儿童和骨骼手术择期骨科手术后并发症的风险更高。
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引用次数: 0
Adherence to the RSA and CT-RSA guideline items in clinical prosthesis migration studies: a systematic review. 临床假体迁移研究中遵循RSA和CT-RSA指南项目:一项系统综述。
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-05-27 DOI: 10.2340/17453674.2025.43750
Thies J N Van der Lelij, Lennard A Koster, Bart L Kaptein, Rob G H H Nelissen, Perla J Marang-van de Mheen

Background and purpose:  Standardized reporting on methodology and results in clinical RSA research papers facilitates evaluation of quality and interpretation of results. We aimed to assess the extent to which radiostereometric analysis (RSA) and computed tomography-based RSA (CT-RSA) studies adhered to the items of the new RSA reporting guideline from 2024.

Methods:  A systematic literature search was performed to identify all clinical RSA studies published between January 2012 and February 2024. Studies were eligible for inclusion if prosthesis migration over time was assessed. The adherence of studies to each applicable guideline item (full, partial, or no) was assessed.

Results:  285 studies were included, most of which assessed prosthesis migration in the hip (n = 161) or knee (n = 99). No study reported on all guideline items. The mean (full or partial) adherence of studies to all (applicable) items was 61% (standard deviation [SD] 11). Large variation between the reporting of items was found, ranging from being reported in 1% of the studies to 100%. The least reported items in studies were the mean number and SD of days between surgery and baseline RSA examination (8% of studies), mean number and SD of days between surgery and primary endpoint RSA examination (1%), and consistent- or all-marker method for RSA analysis (3%).

Conclusion:  Current studies on average reported only 61% of the items from the updated RSA guidelines. Adherence to the guidelines in clinical RSA studies on prosthesis migration should be improved, in order to improve the quality of studies and the interpretation of outcomes on implant migration.

背景和目的:临床RSA研究论文中方法和结果的标准化报告有助于质量评估和结果解释。我们的目的是评估放射立体分析(RSA)和基于计算机层析成像的RSA (CT-RSA)研究在多大程度上遵守2024年新RSA报告指南的项目。方法:系统检索2012年1月至2024年2月期间发表的所有临床RSA研究。如果评估假体随时间的迁移,则研究符合纳入条件。评估研究对每个适用指南项目(全部、部分或没有)的依从性。结果:纳入了285项研究,其中大多数评估了髋关节(n = 161)或膝关节(n = 99)的假体迁移。没有关于所有指南项目的研究报道。研究对所有(适用)项目的平均(全部或部分)依从性为61%(标准差[SD] 11)。报告项目之间存在很大差异,从1%的研究报告到100%的研究报告。研究中报告最少的项目是手术和基线RSA检查之间的平均天数和SD(8%的研究),手术和主要终点RSA检查之间的平均天数和SD(1%),以及RSA分析的一致或全部标记法(3%)。结论:目前的研究平均只报告了更新的RSA指南中61%的项目。为了提高研究质量和对种植体迁移结果的解释,临床RSA研究中对假体迁移指南的依从性应该得到提高。
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引用次数: 0
Corrigendum: The accuracy and precision of CT-RSA in arthroplasty: a systematic review and meta-analysis. 更正:CT-RSA在关节置换术中的准确性和精密度:一项系统回顾和荟萃分析。
IF 2.5 2区 医学 Q1 ORTHOPEDICS Pub Date : 2025-05-27 DOI: 10.2340/17453674.2025.43900
Sjors F Van de Vusse, Nienke N De Laat, Lennard A Koster, Bart Kaptein

To our unpleasant surprise, we discovered that we have mistakenly included incorrect values in Table 2 (Reported accuracy of CT-RSA) for the paper by De Laat et al. (2024). The paper by De Laat (2024) is from our group as well. In the draft version of the systematic review manuscript, we included data from a draft manuscript of the paper by De Laat. Before publication of De Laat (2024) we updated the values for the RMS error for accuracy in translations and rotations based on an increased number of observations. However, we have overlooked to use the updated values for Table 2 of the systematic review. We are sincerely sorry for this mistake. We believe it is important to be transparent and to ensure a correct link between the systematic review and the paper by De Laat. These requested changes do not alter our conclusions of the systematic review. On behalf of all authors Bart Kaptein.

令我们不快的是,我们发现在De Laat et al.(2024)的论文中,我们错误地在表2(报告的CT-RSA精度)中包含了不正确的值。De Laat(2024)的论文也是我们组的。在系统综述草稿中,我们纳入了De Laat论文草稿中的数据。在De Laat(2024)发表之前,我们根据观测值的增加更新了平移和旋转精度的均方根误差值。然而,我们忽略了在系统评价的表2中使用更新的值。我们对这个错误深表歉意。我们认为,重要的是保持透明,并确保系统评价与De Laat论文之间的正确联系。这些要求的改变不会改变我们对系统评价的结论。我代表所有作者巴特·卡普斯坦。
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引用次数: 0
期刊
Acta Orthopaedica
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