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CORR Insights®: Is Ocular Safety in Orthopaedics Overlooked? A Systematic Review of Annual Ocular Radiation Exposure and Protective Measures. CORR Insights®:矫形外科的眼部安全是否被忽视?年度眼部辐射暴露和防护措施的系统回顾。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-20 DOI: 10.1097/CORR.0000000000003233
David Gendelberg
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引用次数: 0
CORR Insights®: No Difference in 10-year Clinical or Radiographic Outcomes Between Kinematic and Mechanical Alignment in TKA: A Randomized Trial. CORR Insights®:TKA 运动学对齐与机械对齐的 10 年临床或影像学结果无差异:随机试验。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-19 DOI: 10.1097/CORR.0000000000003229
Yoshinobu Watanabe
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引用次数: 0
What Is the Incidence of and Outcomes After Debridement, Antibiotics, and Implant Retention (DAIR) for the Treatment of Periprosthetic Joint Infections in the AJRR Population? 在 AJRR 群体中,清创、抗生素和植入物保留(DAIR)治疗假体周围关节感染的发生率和效果如何?
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-19 DOI: 10.1097/CORR.0000000000003138
Ayushmita De, Brian P Chalmers, Bryan D Springer, James A Browne, David G Lewallen, Jeffrey B Stambough
<p><strong>Background: </strong>Debridement, antibiotics, and implant retention (DAIR) is used to manage acute periprosthetic joint infections (PJIs) after total joint arthroplasty (TJA). Given the uncertain success of single or multiple DAIR attempts and possible long-term deleterious effects this treatment can create when trying to treat persistent infection, it is important to understand the frequency with which surgeons in the United States are attempting multiple debridements for PJI and whether those procedures are achieving the desired goal.</p><p><strong>Question/purposes: </strong>In the context of the American Joint Replacement Registry (AJRR), we asked: (1) What proportion of patients who undergo DAIR have only one DAIR, and what percentage of those patients have more than one? (2) Of the patients who undergo one or more DAIR procedures, what is the proportion who progress to additional surgical procedures? (3) What is the cumulative incidence of medical or surgical endpoints related to infection on the affected leg (other than additional DAIR procedures)?</p><p><strong>Methods: </strong>DAIR procedures to treat PJI, defined by ICD-9/10 and CPT (Current Procedural Technology) codes, reported to the AJRR from 2012 to 2020 were merged with Centers for Medicare and Medicaid Services (CMS) data from 2012 to 2020 to determine the incidence of patients aged 65 and older who underwent additional PJI-related procedures on the same joint. Linking to CMS ensures no loss to follow-up or patient migration to a non-AJRR site. As of 2021, the AJRR captures roughly 35% of all arthroplasty procedures performed in the United States. Of the total 2.2 million procedures in the AJRR, only 0.2% of the procedures were eligible based on our inclusion criteria. Additionally, 61% of the total population is Medicare eligible, and thus, these patients are linked to CMS. Of the 5029 DAIR attempts after a TKA, 46% (2318) were performed in female patients. Similarly, there were a total of 798 DAIR attempts after a THA, and 50% (398) were performed in female patients. For the purposes of decreasing confounding factors, bilateral THAs and TKAs were excluded from the study population. When querying for eligible procedures from 2012 to 2020, the patient population was limited to those 65 years and older, and a subsequent reoperation for infection had to be reported after a primary TJA. This limited the patient population as most infections reported to AJRR resulted in a revision, and we were searching for DAIRs. Although 5827 TJAs were identified as a primary TJA with a subsequent infectious event, more than 65% (3788) of that population did not have a reported event. The following conditions were queried as secondary outcomes after the first DAIR: sepsis, cellulitis, postoperative infection, endocarditis, amputation, knee fusion, resection, drainage, arthrotomy, and debridement. To answer our first and second study questions, we used frequency testing from the availab
背景:清创、抗生素和植入物留置(DAIR)用于处理全关节成形术(TJA)后的急性假体周围关节感染(PJI)。鉴于单次或多次尝试 DAIR 的成功率不确定,以及这种治疗方法在试图治疗持续感染时可能产生的长期有害影响,了解美国外科医生尝试多次清创治疗 PJI 的频率以及这些手术是否达到了预期目标非常重要:在美国关节置换登记处(AJRR)的背景下,我们提出了以下问题:(1)接受 DAIR 的患者中只有一次 DAIR 的比例是多少?(2) 在接受一次或多次 DAIR 手术的患者中,进展到其他外科手术的比例是多少?(3) 与患腿感染相关的医疗或手术终点(额外的 DAIR 手术除外)的累积发生率是多少?将 2012 年至 2020 年向 AJRR 报告的用于治疗 PJI 的 DAIR 手术(以 ICD-9/10 和 CPT(现行手术技术)代码定义)与美国医疗保险与医疗补助服务中心(CMS)2012 年至 2020 年的数据合并,以确定 65 岁及以上患者在同一关节上接受其他 PJI 相关手术的发生率。与 CMS 的链接可确保患者不会失去随访或转移到非 AJRR 站点。截至 2021 年,AJRR 记录了美国约 35% 的关节成形术。在 AJRR 的 220 万例手术中,只有 0.2% 的手术符合我们的纳入标准。此外,61% 的总人口符合医疗保险资格,因此这些患者与 CMS 有关联。在 5029 例 TKA 术后 DAIR 尝试中,46%(2318 例)为女性患者。同样,THA 后共进行了 798 次 DAIR 尝试,其中 50%(398 次)为女性患者。为了减少混杂因素,双侧 THA 和 TKAs 均未纳入研究人群。在查询 2012 年至 2020 年期间符合条件的手术时,患者人群仅限于 65 岁及以上的患者,并且必须报告初次 TJA 后因感染而进行的后续再手术。这就限制了患者人群,因为向 AJRR 报告的大多数感染都导致了翻修,而我们正在搜索 DAIR。虽然有 5827 例 TJA 被确定为初诊 TJA 后发生感染事件,但其中超过 65% 的患者(3788 例)没有报告感染事件。在第一次 DAIR 之后,我们将以下情况作为次要结果进行了查询:败血症、蜂窝组织炎、术后感染、心内膜炎、截肢、膝关节融合术、切除术、引流术、关节切开术和清创术。为了回答第一个和第二个研究问题,我们利用现有的 AJRR 数据进行了频率测试。由于存在竞争风险和数据不完整的问题,我们使用累积发生率函数来评估研究问题 3 的具体结果:在接受 DAIR 的患者中,93%(5827 例中的 5406 例)接受过一次 DAIR,8%(5827 例中的 421 例)接受过一次以上 DAIR。在接受 DAIR 的人群中,至少有 35% 的 TKAs 和 38% 的 THAs 被确定为发生过额外的 PJI 相关事件(在同一关节上进行了额外的外科手术、在关联的 CMS-AJRR 数据集中出现了感染终点,或者他们已经死亡)。与最初发生 DAIR 的关节相关的其他内科或外科疾病的累积发生率如下:TKA发生DAIR后8年的累计发生率为48%(95% CI为42%至54%),THA发生DAIR后4年的累计发生率为42%(95% CI为37%至46%)。TKA和THA的时间点不同,因为TKA的DAIR手术纵向数据比THA的多:在这项研究中,我们利用 AJRR 的数据评估了单次和多次 DAIR 尝试的发生率以及其他手术和感染相关后遗症的发生率。我们需要继续调查,以确定接受DAIR的感染关节的最终结局。未来有必要使用大型数据集进行横断面研究,以评估功能预后,并更准确地确定DAIR后持续感染的风险:证据等级:III级,治疗性研究。
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引用次数: 0
Residency Diary: Tranq. 驻校日记:Tranq.
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-19 DOI: 10.1097/CORR.0000000000003211
Lisa G M Friedman
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引用次数: 0
Taper Junction Subsidence Occurs in Modular Tumor Endoprostheses: How Concerned Should We Be? 模块化肿瘤内固定器出现锥形接合处下陷:我们应该有多担心?
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-19 DOI: 10.1097/CORR.0000000000003205
Anas Nooh, Ahmed Aoude, Adam Hart, Michael Tanzer, Robert E Turcotte
<p><strong>Background: </strong>Advancements in musculoskeletal oncologic treatment have allowed for longer survival of patients with malignant bone tumors and the associated longer use of tumor endoprostheses in those who have had such reconstructions. Several studies have reported on increased serum metal ions with the use of such implants. Modularity in these implants introduces the risk of taper junction corrosion and subsidence resulting in metal wear particle release that may cause an adverse local tissue reaction or systemic toxicity. Additionally, these implants contain a large surface area of cobalt and chromium. It is unclear whether the source of the increased serum ion levels was due to the taper junction corrosion or the implant itself. To our knowledge, no prior study has reported on taper junction subsidence.</p><p><strong>Questions/purposes: </strong>In this study we sought (1) to determine survivorship free from radiographic taper junction subsidence in a femoral modular tumor endoprosthesis, and (2) to identify the implant characteristics in the endoprostheses associated with taper subsidence.</p><p><strong>Methods: </strong>Between January 1996 and February 2020, the senior author performed 150 proximal or distal femur replacements following resections of soft tissue or bone tumors of the thigh and femur. Of those, 6% (9 of 150) of patients were lost to follow-up before 2 years, 25% (37 of 150) could not be analyzed due to absence of plain radiographs during follow-up, and 13% (20 of 150) died before 2 years follow-up, leaving 56% (84 of 150) for analysis in this retrospective study, with a median time for analysis of 14 years (range 2 to 31 years) after the index resection and endoprosthetic reconstruction for patients with distal femur replacements and 5 years (range 2 to 19 years) for patients with proximal femur replacement. Radiographs involving the entire implant were evaluated for the presence or absence of subsidence of the taper junction that was evident and clear to see if present. The association between the number of taper junctions, the length of resection, the number of collapsed junctions, and the time to collapse from the initial surgery were examined using regression analysis.</p><p><strong>Results: </strong>Overall, 14% (12 of 84) patients with a distal femur replacement had radiographic collapse of at least one of the modular tapers. Survivorship free from taper subsidence was 91% (95% CI 86% to 96%) at 10 years and 84% (95% CI 78% to 90%) at 20 years. All patients were in the distal femur replacement group. The median follow-up of patients with subsidence was 15 years (range 5 to 26). Fifty-eight percent (7 of 12) of patients had two junctions involved, 25% (3 of 12) had three junctions, and 17% (2 of 12) had one junction involved. All but one patient had subsidence in a single junction. The median time to subsidence was 15 years (range 4.5 to 24.0 years). The subsidence was progressive in all patients who d
背景:随着肌肉骨骼肿瘤治疗技术的进步,恶性骨肿瘤患者的存活时间延长了,因此,接受过此类重建手术的患者使用肿瘤内假体的时间也相应延长了。一些研究报告显示,使用此类植入物会导致血清金属离子增加。这些植入体的模块化设计带来了锥形接合点腐蚀和下沉的风险,导致金属磨损颗粒释放,可能引起局部组织不良反应或全身中毒。此外,这些植入物含有大量的钴和铬。目前还不清楚血清离子水平升高的原因是锥体连接处腐蚀还是植入物本身。据我们所知,之前还没有关于锥体连接处沉降的研究报告:在这项研究中,我们试图(1)确定股骨模块化肿瘤内假体无放射学锥形接合处下沉的存活率,(2)确定与锥形接合处下沉相关的内假体植入特征:方法:1996年1月至2020年2月期间,资深作者进行了150例大腿和股骨软组织或骨肿瘤切除术后的股骨近端或远端假体置换手术。其中,6%的患者(150例中的9例)在随访2年之前就失去了随访机会,25%的患者(150例中的37例)由于在随访期间没有拍摄X光平片而无法进行分析,13%的患者(150例中的20例)在随访2年之前死亡,剩下56%的患者(150例中的84例)可以在这项回顾性研究中进行分析、股骨远端置换术和人工关节内重建术患者的中位分析时间为手术后14年(2至31年),股骨近端置换术患者的中位分析时间为手术后5年(2至19年)。对整个假体的X光片进行评估,看是否存在明显的锥体交界处下陷。使用回归分析法研究了锥形连接点的数量、切除长度、塌陷连接点的数量以及从最初手术到塌陷的时间之间的关联:总的来说,股骨远端置换术患者中有14%(84人中有12人)至少有一个模块锥体出现了放射学上的塌陷。10年后无锥体下陷的存活率为91%(95% CI为86%至96%),20年后为84%(95% CI为78%至90%)。所有患者都属于股骨远端置换组。股骨下沉患者的中位随访时间为15年(5至26年不等)。58%的患者(12例中的7例)有两个关节受累,25%的患者(12例中的3例)有三个关节受累,17%的患者(12例中的2例)有一个关节受累。除一名患者外,其他所有患者的下陷均发生在单个交界处。中位沉降时间为 15 年(4.5 至 24.0 年不等)。所有出现下沉的患者都是渐进式下沉。75%的患者(12 例中的 9 例)锥体交界处完全下陷,25%的患者(12 例中的 3 例)部分下陷。单变量和多变量回归分析表明,我们研究的风险因素与下陷无关。两名交界处下陷的患者接受了手术,其中一名患者因锥体骨折而接受了手术,另一名患者则因远端交界处下陷而在总线交换过程中接受了手术:结论:股骨远端置换术后出现锥体损伤并伴有晚期和进行性交界处下陷的情况并不少见。这种并发症的影响尚不清楚。进一步的研究应检查长期结果,并将其与金属离子水平联系起来:证据等级:三级,治疗性研究。
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引用次数: 0
Are There Differences in Performance Among Femoral Stem Brands Utilized in Cementless Hemiarthroplasty for Treatment of Geriatric Femoral Neck Fractures? 在治疗老年股骨颈骨折的无水泥半关节成形术中,不同品牌的股骨柄性能是否存在差异?
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-15 DOI: 10.1097/CORR.0000000000003222
Ishan Shah, Heather A Prentice, Kanu Okike, Ronald A Navarro, Brian H Fasig, Elizabeth W Paxton, Christopher D Grimsrud

Background: For the vast majority of displaced femoral neck fractures in older patients, cemented femoral fixation is indicated because it is associated with a lower risk of periprosthetic fracture than cementless fixation. Nevertheless, cementless fixation continues to be utilized with high frequency for hip fractures in the United States. It is therefore helpful to understand the performance of individual cementless brands and models. Although prior studies have compared femoral stems by design type or stem geometry, there may still be a difference in revision risk according to femoral stem brand given the potential differences within design groupings with regard to manufacturing, implantation systems, and implant design nuances among vendors.

Questions/purposes: (1) Is there a difference in aseptic revision risk among femoral stem brands in patients ≥ 60 years of age who have displaced femoral neck fractures treated with cementless hemiarthroplasty? (2) Is there a difference in revision for periprosthetic fracture among femoral stem brands in patients ≥ 60 years of age with displaced femoral neck fractures treated with cementless hemiarthroplasty?

Methods: A retrospective, comparative, large-database cohort study was conducted using data from Kaiser Permanente's Hip Fracture Registry. This integrated healthcare system covers more than 12 million members throughout eight regions in the United States; membership has been found to be representative of the general population in the areas served. The Hip Fracture Registry collects details on all patients who undergo hip fracture repair within the organization. These patients are then longitudinally monitored for outcomes after their repair, and all identified outcomes are manually validated through chart review. Patients ages ≥ 60 years who underwent unilateral hemiarthroplasty treatment of a displaced femoral neck fracture from 2009 to 2021 were identified (n = 22,248). Hemiarthroplasties for polytrauma, pathologic or open fractures, or patients who had additional surgeries at other body sites during the same stay, as well as those with prior procedures in the same hip, were excluded (21.4% [4768]). Cemented procedures and those with missing or inconsistent implant information (for example, cement used but cementless implant recorded) were further excluded (47.1% [10,485]). To allow for enough events for evaluation, the study sample was restricted to seven stems for which there were at least 300 hemiarthroplasties performed, including four models from DePuy Synthes (Corail®, Summit®, Summit Basic, and Tri-Lock®) and three from Zimmer Biomet (Medial-Lateral [M/L] Taper®, Trabecular Metal®, and Versys® Low Demand Fracture [LD/FX]). The final sample included 5676 cementless hemiarthroplasties: 653 Corail, 402 M/L Taper, 1699 Summit, 1590 Summit Basic, 384 Tri-Lock, 637 Trabecular Metal, and 311 Versys LD/FX. Procedures were performed b

背景:与无骨水泥固定相比,有骨水泥股骨固定发生假体周围骨折的风险较低,因此适用于绝大多数老年患者的移位性股骨颈骨折。然而,在美国,无骨水泥固定仍被频繁用于髋部骨折的治疗。因此,了解各个无骨水泥品牌和型号的性能很有帮助。问题/目的:(1) 年龄≥60岁的股骨颈移位骨折患者接受无骨水泥半关节成形术治疗后,不同品牌股骨柄的无菌翻修风险是否存在差异?(2)对于年龄≥60岁、接受无骨水泥半人工关节置换术治疗的股骨颈移位性骨折患者,不同股骨柄品牌的假体周围骨折翻修率是否存在差异?利用凯泽医疗集团(Kaiser Permanente)髋部骨折登记处的数据,进行了一项回顾性、比较性、大数据库队列研究。该综合医疗保健系统覆盖美国 8 个地区的 1200 多万名会员,其会员人数在所服务地区的总人口中具有代表性。髋部骨折登记处收集在该机构内接受髋部骨折修复手术的所有患者的详细资料。然后对这些患者修复后的疗效进行纵向监测,并通过病历审查对所有已确定的疗效进行人工验证。2009年至2021年期间,年龄≥60岁、因股骨颈骨折移位而接受单侧半关节置换术治疗的患者均被识别出来(n = 22248)。排除了因多发性创伤、病理性或开放性骨折而接受半关节成形术的患者,或在同一住院期间在其他身体部位接受过额外手术的患者,以及曾在同一髋部接受过手术的患者(21.4% [4768])。此外,还排除了骨水泥植入手术和植入信息缺失或不一致的手术(例如,使用了骨水泥但记录了无骨水泥植入)(47.1% [10,485])。为了有足够的事件进行评估,研究样本仅限于至少进行过 300 例半关节成形术的七种柄,包括 DePuy Synthes 的四种型号(Corail®、Summit®、Summit Basic 和 Tri-Lock®)和 Zimmer Biomet 的三种型号(Medial-Lateral [M/L] Taper®、Trabecular Metal® 和 Versys® Low Demand Fracture [LD/FX])。最终样本包括 5676 个无骨水泥半关节假体:其中,Corail 653 例、M/L Taper 402 例、Summit 1699 例、Summit Basic 1590 例、Tri-Lock 384 例、Trabecular Metal 637 例和 Versys LD/FX 311 例。手术由 35 家医院的 396 名外科医生完成。组群的平均年龄和体重指数分别为 81 岁和 24 kg/m2;大多数为女性(66% [5676 例中的 3733 例])和白人(79% [5676 例中的 4488 例])。根据标准化的平均差异,我们对七个骨干组的年龄、种族/人种、美国麻醉医师协会(ASA)分类、麻醉技术、手术年份、外科医生半关节置换术的年均手术量和手术年份进行了控制。在5676名患者中,有7%的患者(5676人中有378人)在中位1.6年的会员资格终止后失去了随访机会,56%的患者(5676人中有3194人)在随访期间死亡。采用多变量特定病因 Cox 比例危险度回归模型评估无菌性翻修的风险,并对年龄、性别、ASA 分级、抑郁、手术医生、缺血性贫血、入院到手术的时间以及外科医生年均半关节成形术量进行调整。此外,还加入了随机截距,以消除由同一外科医生实施的半关节置换术的影响。因假体周围骨折而进行翻修的风险也作为次要结果进行了评估:在调整后的分析中,与Summit相比,Summit Basic (HR 1.91 [95% 置信区间 1.34 to 2.72]; p < 0.001)、M/L Taper (HR 1.91 [95% CI 1.15 to 3.15]; p = 0.01)和Versys LD/FX (HR 2.12 [95% CI 1.25 to 3.61]; p = 0.005)在随访期间的无菌翻修风险更高。与Summit相比,Corail(HR 0.57 [95% CI 0.29至1.10];p = 0.09)、Tri-Lock(HR 1.13 [95% CI 0.62至2.07];p = 0.68)或Trabecular Metal(HR 1.14 [95% CI 0.69至1.89];p = 0.61)均无差异。与Summit相比,M/L Taper(HR 2.43 [95% CI 1.29 to 4.58];p = 0.006)和Summit Basic(随访3个月内:HR 1.16 [95% CI 0.60 to 2.25];p = 0.66;随访3个月后:HR 2.84 [95% CI 1.36 to 5.94];p = 0.006)基台因假体周围骨折而翻修的风险更高。
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引用次数: 0
CORR Insights®: Comparing Open and Arthroscopic Grafting for Scaphoid Nonunion: Is There Truly a Noticeable Difference? CORR Insights®:比较肩胛骨骨不连的开放和关节镜植骨术:真的有明显区别吗?
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-14 DOI: 10.1097/CORR.0000000000003207
Shafic Sraj
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引用次数: 0
CORR Insights®: Is Quantitative Radiographic Measurement of Acetabular Version Reliable in Anteverted and Retroverted Hips? CORR Insights®:髋关节前倾和后倾时,髋臼外形的定量 X 射线测量可靠吗?
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-14 DOI: 10.1097/CORR.0000000000003208
Kawan S Rakhra
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引用次数: 0
No Difference in 10-year Clinical or Radiographic Outcomes Between Kinematic and Mechanical Alignment in TKA: A Randomized Trial. TKA 运动学对齐与机械对齐的 10 年临床或放射学结果无差异:一项随机试验。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-14 DOI: 10.1097/CORR.0000000000003193
John P Gibbons, Nina Zeng, Ali Bayan, Matthew L Walker, Bill Farrington, Simon W Young

Background: There is continuing debate about the ideal philosophy for component alignment in TKA. However, there are limited long-term functional and radiographic data on randomized comparisons of kinematic alignment versus mechanical alignment.

Questions/purposes: We present the 10-year follow-up findings of a single-center, multisurgeon randomized controlled trial (RCT) comparing these two alignment philosophies in terms of the following questions: (1) Is there a difference in PROM scores? (2) Is there a difference in survivorship free from revision or reoperation for any cause? (3) Is there a difference in survivorship free from radiographic loosening?

Methods: Ninety-nine patients undergoing primary TKA for osteoarthritis were randomized to either the mechanical alignment (n = 50) or kinematic alignment (n = 49) group. Eligibility for the study was patients undergoing unilateral TKA for osteoarthritis who were suitable for a cruciate-retaining TKA and could undergo MRI. Patients who had previous osteotomy, coronal alignment > 15° from neutral, a fixed flexion deformity > 15°, or instability whereby constrained components were being considered were excluded. Computer navigation was used in the mechanical alignment group, and patient-specific cutting blocks were used in the kinematic alignment group. At 10 years, 86% (43) of the patients in the mechanical alignment group and 80% (39) in the kinematic alignment group were available for follow-up performed as a per-protocol analysis. The PROMs that we assessed included the Knee Society Score, Oxford Knee Score, WOMAC, Forgotten Joint Score, and EuroQol 5-Dimension score. Kaplan-Meier analysis was used to assess survivorship free from reoperation (any reason) and revision (change or addition of any component). A single blinded observer assessed radiographs for signs of aseptic loosening (as defined by the presence of progressive radiolucent lines in two or more zones), which was reported as survivorship free from loosening.

Results: At 10 years, there was no difference in any PROM score measured between the groups. Ten-year survivorship free from revision (components removed or added) likewise did not differ between the groups (96% [95% CI 91% to 99%] for the mechanical alignment group and 91% [95% CI 83% to 99%] for the kinematic alignment group; p = 0.38). There were two revisions in the mechanical alignment group (periprosthetic fracture, deep infection) and four in the kinematic alignment group (two secondary patella resurfacings, two deep infections). There was no statistically significant difference in reoperations for any cause between the two groups. There was no difference with regard to survivorship free from loosening on radiographic review (χ2 = 1.3; p = 0.52) (progressive radiolucent lines seen at 10 years were 0% for mechanical alignment and 3% for kinematic alignment).

Conclusion:

背景:关于 TKA 中组件对位的理想理念一直存在争议。然而,关于运动学对位与机械对位的随机比较的长期功能和放射学数据十分有限:我们介绍了一项单中心、多外科医师随机对照试验(RCT)的 10 年随访结果,该试验从以下几个方面对这两种对位理念进行了比较:(1)PROM 评分是否存在差异? 2)无翻修或无任何原因再手术的存活率是否存在差异?(3)无放射学松动的存活率是否有差异?将接受初次TKA治疗的99名骨关节炎患者随机分为机械对位组(50人)或运动对位组(49人)。研究对象为因骨关节炎接受单侧 TKA 手术的患者,这些患者适合接受十字韧带固定 TKA 手术,并能接受核磁共振成像检查。曾接受过截骨手术、冠状位对位偏离中立位>15°、固定屈曲畸形>15°或考虑使用约束组件的不稳定患者不在研究范围内。机械对位组使用计算机导航,运动对位组使用患者特制的切割块。10年后,机械对位组和运动对位组分别有86%(43例)和80%(39例)的患者接受了按方案分析的随访。我们评估的PROMs包括膝关节社会评分、牛津膝关节评分、WOMAC、遗忘关节评分和EuroQol 5维评分。Kaplan-Meier 分析用于评估无再次手术(任何原因)和翻修(更换或增加任何组件)的存活率。由一名单盲观察者评估X光片上的无菌性松动迹象(定义为两个或两个以上区域出现进行性放射线),并将其报告为无松动存活率:10年后,两组的PROM评分均无差异。10年无翻修(移除或添加组件)存活率在两组之间同样没有差异(机械式对位组为96% [95% CI 91% to 99%],运动式对位组为91% [95% CI 83% to 99%];P = 0.38)。机械对位组有两次翻修(假体周围骨折、深度感染),运动学对位组有四次翻修(两次二次髌骨翻修、两次深度感染)。两组患者因任何原因再次手术的比例在统计学上没有明显差异。在放射学检查中,两组在无松动的存活率方面没有差异(χ2 = 1.3; p = 0.52)(10年时,机械对位组的渐进性放射线为0%,运动对位组的渐进性放射线为3%):结论:与之前报告的2年和5年结果一样,该研究的10年随访结果表明,机械对位和运动对位TKA在功能和放射学结果上没有差异。运动学对位的预期功能优势并未得到证实,两组患者在10年的无翻修存活率也没有差异。鉴于运动学对位对植入物位置(尤其是胫骨组件变位)的长期影响尚不清楚,我们必须得出结论,机械对位仍是TKA的参考标准。在10年的随访中,我们无法证明运动学对位有任何优势:证据级别:I级,治疗性研究。
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引用次数: 0
Electric Scooter-related Injuries Are Becoming More Frequent and Costly in Denver, CO. 在科罗拉多州丹佛市,与电动滑板车有关的伤害事故越来越频繁,代价也越来越高。
IF 4.2 2区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-13 DOI: 10.1097/CORR.0000000000003212
Riley Kahan, Sean Higinbotham, Kassra Garoosi, Alexander Lauder

Background: Electric scooters (e-scooters) have become a widely adopted form of transportation. Information regarding the timing, conditions, and context associated with increased frequency of e-scooter-related injuries could inform policy that may potentially reduce associated injuries and healthcare costs. However, this information is lacking, as most research to date has focused on the injury patterns sustained while using e-scooters rather than context. We sought to evaluate these factors in an urban setting and describe how these are evolving over time, as such information may help guide future safety initiatives.

Questions/purposes: (1) How has the epidemiology of e-scooter-related injuries in Denver, CO, USA, changed over time? (2) What are the associated hospital charges to treat patients with these injuries? (3) What circumstances are associated with an increased frequency of e-scooter-related injuries and higher accompanying hospital charges?

Methods: A retrospective study at a Level 1 trauma center in Denver, CO, USA, examined trends in e-scooter-related injuries from January 1, 2020, to November 1, 2023. Patients were identified by the key terms "e-scooter crash" or "scooter" within their emergency department/urgent care visit notes. Patient demographic and injury characteristics and hospital data (admission and hospital charges) were analyzed. Patients who sustained injuries from devices other than stand-up e-scooters or who did not have complete records available for analysis were excluded. The epidemiologic data on e-scooter-related injuries were quantified for each year within the study period, and descriptive analyses were performed to assess patient and injury characteristics, including age, gender, and fracture characteristics. Hospital charges were calculated using the mean annual sum of hospital charges associated with the treatment for e-scooter-related injuries. Circumstances influencing the frequency of injury and magnitude of hospital charges were assessed based on the timing of presentation to the emergency department or urgent care. We recognize that charge may have little or no direct relationship to true cost, but we believe that within one hospital system it represents a reasonable metric for comparative resource utilization. Injury frequency by time of the day and day of the week were compared using chi-square goodness-of-fit analyses. The value of hospital charges associated with e-scooter-related injuries was compared between patients presenting with alcohol intoxication and those who were not intoxicated.

Results: In all, 2424 patients were identified as having e-scooter-related injuries (58% [1405] men, 42% [1019] women, median (IQR) age 30 years [25 to 37 years]). The number of annual e-scooter-related injuries during the years 2020 to 2023 were 273 in 2020, 736 in 2021, 758 in 2022, and 657 in 2023 (only 10 months). From 2

背景:电动滑板车(e-scooters)已成为一种被广泛采用的交通工具。有关电动滑板车相关伤害发生频率增加的时间、条件和背景的信息可为制定政策提供参考,从而有可能减少相关伤害和医疗费用。然而,由于迄今为止的大多数研究都集中在使用电动滑板车时的受伤模式而非背景情况,因此缺乏这方面的信息。问题/目的:(1)美国科罗拉多州丹佛市与电动滑板车相关的伤害流行病学随着时间的推移发生了怎样的变化?(2)治疗这些受伤病人的相关医院费用是多少?(3)哪些情况与电动滑板车相关伤害的发生频率增加及相应的住院费用增加有关?美国科罗拉多州丹佛市的一家一级创伤中心开展了一项回顾性研究,调查了 2020 年 1 月 1 日至 2023 年 11 月 1 日期间与电动摩托车相关的伤害趋势。研究人员通过患者急诊科/急诊就诊记录中的关键术语 "电动滑板车碰撞 "或 "电动滑板车 "来识别患者。对患者的人口统计学特征、受伤特征和医院数据(入院和住院费用)进行了分析。排除了因站立式电动滑板车以外的设备受伤或没有完整记录可供分析的患者。对研究期间每年的电动滑板车相关伤害流行病学数据进行了量化,并进行了描述性分析,以评估患者和伤害特征,包括年龄、性别和骨折特征。住院费用是根据治疗电动滑板车相关损伤的年平均住院费用总和计算得出的。根据患者到急诊科或紧急护理中心就诊的时间评估了影响受伤频率和住院费用的因素。我们认识到,收费可能与真实成本几乎没有直接关系,但我们相信,在一个医院系统内,收费是比较资源利用率的合理指标。我们使用卡方拟合优度分析比较了一天中不同时间和一周中不同日期的受伤频率。对与电动滑板车相关的受伤住院费用进行了比较,并对酒精中毒和未酒精中毒的患者进行了比较:共有 2424 名患者被确认为与电动摩托车相关的伤害(58% [1405] 为男性,42% [1019] 为女性,中位数(IQR)年龄为 30 岁 [25 至 37 岁])。2020 年至 2023 年期间,每年与电动摩托车相关的受伤人数分别为:2020 年 273 人,2021 年 736 人,2022 年 758 人,2023 年 657 人(仅 10 个月)。从 2020 年到 2023 年,治疗电动摩托车相关伤害的医院年平均收费总和为 1040 万美元;2020 年为 640 万美元,2021 年为 1150 万美元,2022 年为 1190 万美元,2023 年为 1090 万美元(仅 10 个月)。在为期4年的研究期间,与电动摩托车相关的骨科伤害住院费平均每年为360万美元;2020年为150万美元,2021年为390万美元,2022年为450万美元,2023年为410万美元(仅10个月)。在所有与电动摩托车相关的伤害中,45%(1098 起)发生在晚上 7 点至凌晨 3 点之间,44%(1064 起)发生在周末。与清晨(4973 美元 [1178 至 11671])或白天(4871 美元 [1059 至 11673];P < 0.001),或在患者醉酒时(13,404美元 [10,346至22,525])与未醉酒者(6132美元 [2612至13,620];P < 0.001)相比:与电动滑板车相关的伤害事故日益频繁,且多发生在夜间和周末时段。治疗这些伤害的医院总费用也在逐年增加,其中晚间时段和酒精中毒患者的费用最高。这些结果可能有助于为电动滑板车宣传活动和政策改革提供信息,从而在受伤频率和医疗费用最高的时段限制电动滑板车的使用。还需要进一步研究电动摩托车限制措施的实施效果。未来对受伤时间与就诊时间进行评估的观察性研究将有助于更准确地了解这些伤害的流行病学:证据等级:IV 级,预后研究。
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