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Day-case success or why still in hospital after total hip, total knee, and medial unicompartmental knee arthroplasties? 全髋关节、全膝关节和内侧单隔间膝关节置换术后是日间手术成功还是仍需住院?
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-11-05 DOI: 10.1302/2633-1462.511.BJO-2024-0125.R1
Oddrún Danielsen, Christian B Jensen, Claus Varnum, Thomas Jakobsen, Mikkel R Andersen, Manuel J Bieder, Søren Overgaard, Christoffer C Jørgensen, Henrik Kehlet, Kirill Gromov, Martin Lindberg-Larsen

Aims: Day-case success rates after primary total hip arthroplasty (THA), total knee arthroplasty (TKA), and medial unicompartmental knee arthroplasty (mUKA) may vary, and detailed data are needed on causes of not being discharged. The aim of this study was to analyze the association between surgical procedure type and successful day-case surgery, and to analyze causes of not being discharged on the day of surgery when eligible and scheduled for day-case THA, TKA, and mUKA.

Methods: A multicentre, prospective consecutive cohort study was carried out from September 2022 to August 2023. Patients were screened for day-case eligibility using well defined inclusion and exclusion criteria, and discharged when fulfilling predetermined discharge criteria. Day-case eligible patients were scheduled for surgery with intended start of surgery before 1.00 pm.

Results: Of 6,142 primary hip and knee arthroplasties, eligibility rates for day-case surgery were 34% for THA (95% CI 32% to 36%), 34% for TKA (95% CI 32% to 36%), and 52% for mUKA (95% CI 49% to 55%). Surgery before 1.00 pm was achieved in 85% of eligible patients. The day-case success rate among patients with surgery before 1.00 pm was 59% (95% CI 55% to 62%) for THA, 61% (95% CI 57% to 65%) for TKA, and 72% (95% CI 68% to 76%) for mUKA. Overall day-case success rates (eligible and non-eligible) were 19% (95% CI 17% to 20%) for THA, 20% (95% CI 18% to 21%) for TKA, and 42% (95% CI 39% to 45%) for mUKA. Adjusted analysis confirmed higher day-case success in eligible mUKA patients (odds ratio 1.9 (1.6 to 2.3)) compared to TKA and THA patients. Primary causes for day-case failure were mobilization issues (9% to 12% between procedures), prolonged spinal anaesthesia (4% to 9%), and postoperative nausea and vomiting (PONV) (4% to 14%).

Conclusion: THA and TKA patients showed comparable eligibility (34%) with similar day-case success rates (59 to 61%), whereas mUKA patients demonstrated higher eligibility (52%) and day-case success (72%). Mobilization issues, prolonged spinal anaesthesia, and PONV were the most frequent causes for not being discharged.

目的:初级全髋关节置换术(THA)、全膝关节置换术(TKA)和内侧单间室膝关节置换术(mUKA)术后的日间手术成功率可能会有所不同,因此需要有关未出院原因的详细数据。本研究旨在分析手术类型与日间手术成功率之间的关系,并分析符合条件并计划进行日间THA、TKA和mUKA手术的患者在手术当天未能出院的原因:方法:2022 年 9 月至 2023 年 8 月期间开展了一项多中心、前瞻性连续队列研究。采用明确界定的纳入和排除标准对患者进行日间手术资格筛选,符合预定出院标准的患者即可出院。符合日间手术条件的患者被安排在下午1点之前开始手术:在 6,142 例初级髋关节和膝关节置换术中,符合日间手术条件的患者比例分别为:THA 34% (95% CI 32% to 36%)、TKA 34% (95% CI 32% to 36%)、mUKA 52% (95% CI 49% to 55%)。85%的合格患者在下午 1:00 之前完成了手术。在下午 1:00 之前进行手术的患者中,THA 的日间手术成功率为 59%(95% CI 55% 至 62%),TKA 为 61%(95% CI 57% 至 65%),mUKA 为 72%(95% CI 68% 至 76%)。总体日间手术成功率(符合条件和不符合条件)分别为:THA 19% (95% CI 17% to 20%), TKA 20% (95% CI 18% to 21%), mUKA 42% (95% CI 39% to 45%)。调整分析证实,与TKA和THA患者相比,符合条件的mUKA患者的日间手术成功率更高(几率比1.9(1.6至2.3))。日间手术失败的主要原因是活动问题(手术间隙9%至12%)、脊髓麻醉时间过长(4%至9%)以及术后恶心和呕吐(PONV)(4%至14%):THA和TKA患者的合格率(34%)相当,日间成功率(59%至61%)相似,而MUKA患者的合格率(52%)和日间成功率(72%)更高。移动问题、脊髓麻醉时间过长和 PONV 是导致患者无法出院的最常见原因。
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引用次数: 0
Prediction of humeral shaft fracture healing using the Radiographic Union Score for HUmeral Fractures (RUSHU). 使用肱骨骨干骨折放射学愈合评分(RUSHU)预测肱骨骨干骨折愈合情况。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-11-04 DOI: 10.1302/2633-1462.511.BJO-2024-0134.R1
Cyrill Suter, Henrik Mattila, Thomas Ibounig, Bakir O Sumrein, Antti Launonen, Teppo L N Järvinen, Tuomas Lähdeoja, Lasse Rämö

Aims: Though most humeral shaft fractures heal nonoperatively, up to one-third may lead to nonunion with inferior outcomes. The Radiographic Union Score for HUmeral Fractures (RUSHU) was created to identify high-risk patients for nonunion. Our study evaluated the RUSHU's prognostic performance at six and 12 weeks in discriminating nonunion within a significantly larger cohort than before.

Methods: Our study included 226 nonoperatively treated humeral shaft fractures. We evaluated the interobserver reliability and intraobserver reproducibility of RUSHU scoring using intraclass correlation coefficients (ICCs). Additionally, we determined the optimal cut-off thresholds for predicting nonunion using the receiver operating characteristic (ROC) method.

Results: The RUSHU demonstrated good interobserver reliability with an ICC of 0.78 (95% CI 0.72 to 0.83) at six weeks and 0.77 (95% CI 0.71 to 0.82) at 12 weeks. Intraobserver reproducibility was good or excellent for all analyses. Area under the curve in the ROC analysis was 0.83 (95% CI 0.77 to 0.88) at six weeks and 0.89 (95% CI 0.84 to 0.93) at 12 weeks, indicating excellent discrimination. The optimal cut-off values for predicting nonunion were ≤ eight points at six weeks and ≤ nine points at 12 weeks, providing the best specificity-sensitivity trade-off.

Conclusion: The RUSHU proves to be a reliable and reproducible radiological scoring system that aids in identifying patients at risk of nonunion at both six and 12 weeks post-injury during non-surgical treatment of humeral shaft fractures. The statistically optimal cut-off values for predicting nonunion are ≤ eight at six weeks and ≤ nine points at 12 weeks post-injury.

目的:虽然大多数肱骨轴骨折都能非手术愈合,但多达三分之一的骨折可能会导致不愈合,造成不良后果。肱骨骨折放射学愈合评分(RUSHU)的创立是为了识别高风险的不愈合患者。我们的研究评估了 RUSHU 在 6 周和 12 周时的预后性能,它能在比以前大得多的队列中鉴别骨折不愈合:我们的研究包括 226 例未经手术治疗的肱骨轴骨折。我们使用类内相关系数(ICC)评估了RUSHU评分的观察者间可靠性和观察者内可重复性。此外,我们还使用接收器操作特征(ROC)方法确定了预测不愈合的最佳临界值:RUSHU显示出良好的观察者间可靠性,6周时的ICC为0.78(95% CI 0.72至0.83),12周时的ICC为0.77(95% CI 0.71至0.82)。所有分析的观察者内部再现性均为良好或极佳。在 ROC 分析中,6 周时的曲线下面积为 0.83(95% CI 0.77 至 0.88),12 周时为 0.89(95% CI 0.84 至 0.93),表明辨别能力极佳。预测骨不连的最佳临界值为:6周时≤8点,12周时≤9点,这提供了最佳的特异性-敏感性权衡:事实证明,RUSHU 是一种可靠且可重复的放射学评分系统,有助于在非手术治疗肱骨轴骨折的过程中,识别伤后 6 周和 12 周有不愈合风险的患者。从统计学角度来看,预测骨折不愈合的最佳临界值为:伤后六周时≤8分,伤后12周时≤9分。
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引用次数: 0
Bridging the gap: enhancing orthopaedic outcomes through qualitative research integration. 缩小差距:通过整合定性研究提高骨科成果。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1302/2633-1462.511.BJO-2024-0145.R1
Louise E Mew, Vanessa Heaslip, Tikki Immins, Arul Ramasamy, Thomas W Wainwright

Aims: The evidence base within trauma and orthopaedics has traditionally favoured quantitative research methodologies. Qualitative research can provide unique insights which illuminate patient experiences and perceptions of care. Qualitative methods reveal the subjective narratives of patients that are not captured by quantitative data, providing a more comprehensive understanding of patient-centred care. The aim of this study is to quantify the level of qualitative research within the orthopaedic literature.

Methods: A bibliometric search of journals' online archives and multiple databases was undertaken in March 2024, to identify articles using qualitative research methods in the top 12 trauma and orthopaedic journals based on the 2023 impact factor and SCImago rating. The bibliometric search was conducted and reported in accordance with the preliminary guideline for reporting bibliometric reviews of the biomedical literature (BIBLIO).

Results: Of the 7,201 papers reviewed, 136 included qualitative methods (0.1%). There was no significant difference between the journals, apart from Bone & Joint Open, which included 21 studies using qualitative methods, equalling 4% of its published articles.

Conclusion: This study demonstrates that there is a very low number of qualitative research papers published within trauma and orthopaedic journals. Given the increasing focus on patient outcomes and improving the patient experience, it may be argued that there is a requirement to support both quantitative and qualitative approaches to orthopaedic research. Combining qualitative and quantitative methods may effectively address the complex and personal aspects of patients' care, ensuring that outcomes align with patient values and enhance overall care quality.

目的:创伤和矫形外科的证据基础历来偏重于定量研究方法。定性研究可以提供独特的见解,阐明病人的经历和对护理的看法。定性方法揭示了定量数据无法捕捉的患者主观叙述,从而更全面地了解以患者为中心的护理。本研究旨在量化骨科文献中定性研究的水平:方法:2024 年 3 月,我们对期刊的在线档案和多个数据库进行了文献计量学检索,根据 2023 年的影响因子和 SCImago 评级,在排名前 12 位的创伤和骨科期刊中找出使用定性研究方法的文章。文献计量学检索是根据生物医学文献文献计量学综述报告初步指南(BIBLIO)进行和报告的:在审查的 7201 篇论文中,有 136 篇采用了定性方法(0.1%)。除了《骨与关节》(Bone & Joint Open)收录了21项使用定性方法的研究,相当于其已发表文章的4%之外,其他期刊之间没有明显差异:这项研究表明,在创伤和骨科期刊上发表的定性研究论文数量很少。鉴于人们越来越关注患者的治疗效果和改善患者的就医体验,可以说骨科研究需要同时支持定量和定性方法。将定性和定量方法结合起来可有效解决患者护理中复杂的个人问题,确保结果符合患者的价值观并提高整体护理质量。
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引用次数: 0
Association of MRI findings with intra-articular tumour extension. 核磁共振成像结果与关节内肿瘤扩展的关联。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-10-25 DOI: 10.1302/2633-1462.510.BJO-2024-0047.R2
Lorenzo Deveza, Mohammed A El Amine, Anton S Becker, John Nolan, Sinchun Hwang, Meera Hameed, Max Vaynrub

Aims: Treatment of high-grade limb bone sarcoma that invades a joint requires en bloc extra-articular excision. MRI can demonstrate joint invasion but is frequently inconclusive, and its predictive value is unknown. We evaluated the diagnostic accuracy of direct and indirect radiological signs of intra-articular tumour extension and the performance characteristics of MRI findings of intra-articular tumour extension.

Methods: We performed a retrospective case-control study of patients who underwent extra-articular excision for sarcoma of the knee, hip, or shoulder from 1 June 2000 to 1 November 2020. Radiologists blinded to the pathology results evaluated preoperative MRI for three direct signs of joint invasion (capsular disruption, cortical breach, cartilage invasion) and indirect signs (e.g. joint effusion, synovial thickening). The discriminatory ability of MRI to detect intra-articular tumour extension was determined by receiver operating characteristic analysis.

Results: Overall, 49 patients underwent extra-articular excision. The area under the curve (AUC) ranged from 0.65 to 0.76 for direct signs of joint invasion, and was 0.83 for all three combined. In all, 26 patients had only one to two direct signs of invasion, representing an equivocal result. In these patients, the AUC was 0.63 for joint effusion and 0.85 for synovial thickening. When direct signs and synovial thickening were combined, the AUC was 0.89.

Conclusion: MRI provides excellent discrimination for determining intra-articular tumour extension when multiple direct signs of invasion are present. When MRI results are equivocal, assessment of synovial thickening increases MRI's discriminatory ability to predict intra-articular joint extension. These results should be interpreted in the context of the study's limitations. The inclusion of only extra-articular excisions enriched the sample for true positive cases. Direct signs likely varied with tumour histology and location. A larger, prospective study of periarticular bone sarcomas with spatial correlation of histological and radiological findings is needed to validate these results before their adoption in clinical practice.

目的:治疗侵犯关节的高级别肢体骨肉瘤需要进行关节外整体切除。核磁共振成像可显示关节受侵,但常常不能得出结论,其预测价值尚不清楚。我们评估了肿瘤向关节内扩展的直接和间接放射学征象的诊断准确性,以及核磁共振成像发现肿瘤向关节内扩展的表现特征:我们对2000年6月1日至2020年11月1日期间因膝关节、髋关节或肩关节肉瘤接受关节外切除术的患者进行了一项回顾性病例对照研究。对病理结果保密的放射科医生对术前核磁共振成像进行了评估,以确定关节受侵的三种直接征象(关节囊破坏、皮质破损、软骨受侵)和间接征象(如关节积液、滑膜增厚)。通过接收器操作特征分析确定了核磁共振成像检测关节内肿瘤扩展的判别能力:结果:共有49名患者接受了关节外切除术。对于关节侵犯的直接征象,曲线下面积(AUC)为 0.65 至 0.76,三者合计为 0.83。总共有 26 名患者只有一到两个直接侵犯征象,结果不明确。在这些患者中,关节积液的 AUC 为 0.63,滑膜增厚的 AUC 为 0.85。将直接征象和滑膜增厚合并计算,AUC 为 0.89:当存在多种直接侵袭征象时,核磁共振成像在确定关节内肿瘤扩展方面具有极佳的鉴别力。当核磁共振成像结果不明确时,对滑膜增厚的评估可提高核磁共振成像预测关节内扩展的鉴别能力。在解释这些结果时应考虑到研究的局限性。只纳入关节外切除的病例丰富了真正阳性病例的样本。直接征象可能因肿瘤组织学和位置而异。在将这些结果应用于临床实践之前,需要对关节周围骨肉瘤进行更大规模的前瞻性研究,并对组织学和放射学结果进行空间相关性分析,以验证这些结果。
{"title":"Association of MRI findings with intra-articular tumour extension.","authors":"Lorenzo Deveza, Mohammed A El Amine, Anton S Becker, John Nolan, Sinchun Hwang, Meera Hameed, Max Vaynrub","doi":"10.1302/2633-1462.510.BJO-2024-0047.R2","DOIUrl":"https://doi.org/10.1302/2633-1462.510.BJO-2024-0047.R2","url":null,"abstract":"<p><strong>Aims: </strong>Treatment of high-grade limb bone sarcoma that invades a joint requires en bloc extra-articular excision. MRI can demonstrate joint invasion but is frequently inconclusive, and its predictive value is unknown. We evaluated the diagnostic accuracy of direct and indirect radiological signs of intra-articular tumour extension and the performance characteristics of MRI findings of intra-articular tumour extension.</p><p><strong>Methods: </strong>We performed a retrospective case-control study of patients who underwent extra-articular excision for sarcoma of the knee, hip, or shoulder from 1 June 2000 to 1 November 2020. Radiologists blinded to the pathology results evaluated preoperative MRI for three direct signs of joint invasion (capsular disruption, cortical breach, cartilage invasion) and indirect signs (e.g. joint effusion, synovial thickening). The discriminatory ability of MRI to detect intra-articular tumour extension was determined by receiver operating characteristic analysis.</p><p><strong>Results: </strong>Overall, 49 patients underwent extra-articular excision. The area under the curve (AUC) ranged from 0.65 to 0.76 for direct signs of joint invasion, and was 0.83 for all three combined. In all, 26 patients had only one to two direct signs of invasion, representing an equivocal result. In these patients, the AUC was 0.63 for joint effusion and 0.85 for synovial thickening. When direct signs and synovial thickening were combined, the AUC was 0.89.</p><p><strong>Conclusion: </strong>MRI provides excellent discrimination for determining intra-articular tumour extension when multiple direct signs of invasion are present. When MRI results are equivocal, assessment of synovial thickening increases MRI's discriminatory ability to predict intra-articular joint extension. These results should be interpreted in the context of the study's limitations. The inclusion of only extra-articular excisions enriched the sample for true positive cases. Direct signs likely varied with tumour histology and location. A larger, prospective study of periarticular bone sarcomas with spatial correlation of histological and radiological findings is needed to validate these results before their adoption in clinical practice.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"5 10","pages":"944-952"},"PeriodicalIF":2.8,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11503032/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142509480","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}
引用次数: 0
Five- and ten-year follow-up of medial unicompartmental knee arthroplasties in obese and non-obese patients. 肥胖和非肥胖患者内侧单室膝关节置换术的五年和十年随访。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-10-22 DOI: 10.1302/2633-1462.510.BJO-2024-0124.R1
Reinhold H Gregor, Gary J Hooper, Christopher Frampton

Aims: The aim of this study was to determine whether obesity had a detrimental effect on the long-term performance and survival of medial unicompartmental knee arthroplasties (UKAs).

Methods: This study reviewed prospectively collected functional outcome scores and revision rates of all medial UKA patients with recorded BMI performed in Christchurch, New Zealand, from January 2011 to September 2021. Patient-reported outcome measures (PROMs) were the primary outcome of this study, with all-cause revision rate analyzed as a secondary outcome. PROMs were taken preoperatively, at six months, one year, five years, and ten years postoperatively. There were 873 patients who had functional scores recorded at five years and 164 patients had scores recorded at ten years. Further sub-group analysis was performed based on the patient's BMI. Revision data were available through the New Zealand Joint Registry for 2,323 UKAs performed during this time period.

Results: Obese patients (BMI > 30 kg/m2) were 3.1 years younger than non-obese patients (BMI < 30 kg/m2) at the time of surgery (mean age of obese patients 65.5 years (SD 9.7) and mean age of non-obese patients 68.6 years (SD 10.1)). Preoperatively, obese patients tended to have significantly lower functional scores than non-obese patients, which continued at five and ten years postoperatively. At these timepoints, obese patients had significantly lower scores for most PROMs measured compared to non-obese patients. However, there was no significant difference in the improvement of any of these scores after surgery between obese and non-obese patients. There was no significant difference in revision rates between obese and non-obese patients at any time. All-cause revision rate for obese patients was 0.73 per 100 observed component years compared to 0.67 in non-obese patients at ten years. There was also no significant difference in the aseptic loosening rate between groups.

Conclusion: Our study supports the use of UKAs in obese patients, with similar benefit and survival compared to non-obese patients at ten years.

目的:本研究旨在确定肥胖是否会对内侧单间室膝关节置换术(UKA)的长期效果和存活率产生不利影响:本研究回顾了前瞻性收集的2011年1月至2021年9月期间在新西兰克赖斯特彻奇进行的有BMI记录的所有内侧UKA患者的功能结果评分和翻修率。患者报告结局指标(PROMs)是本研究的主要结果,全因翻修率则作为次要结果进行分析。PROM分别在术前、术后六个月、一年、五年和十年进行测量。有 873 名患者在术后五年时获得了功能评分,164 名患者在术后十年时获得了评分。根据患者的体重指数进行了进一步的分组分析。新西兰关节登记处提供了在此期间进行的2323例UKA的翻修数据:手术时,肥胖患者(体重指数大于 30 kg/m2)比非肥胖患者(体重指数小于 30 kg/m2)年轻 3.1 岁(肥胖患者的平均年龄为 65.5 岁(标准差为 9.7 岁),非肥胖患者的平均年龄为 68.6 岁(标准差为 10.1 岁))。术前,肥胖患者的功能评分往往明显低于非肥胖患者,这种情况在术后五年和十年仍在持续。在这些时间点上,与非肥胖患者相比,肥胖患者的大多数 PROMs 评分都明显较低。不过,肥胖患者和非肥胖患者术后在这些评分的改善程度上没有明显差异。肥胖患者和非肥胖患者在任何时候的翻修率都没有明显差异。肥胖患者的全因复发率为 0.73/100,而非肥胖患者的全因复发率为 0.67/10。两组患者的无菌性松动率也无明显差异:我们的研究支持在肥胖患者中使用UKAs,与非肥胖患者相比,肥胖患者在十年内的获益和存活率相似。
{"title":"Five- and ten-year follow-up of medial unicompartmental knee arthroplasties in obese and non-obese patients.","authors":"Reinhold H Gregor, Gary J Hooper, Christopher Frampton","doi":"10.1302/2633-1462.510.BJO-2024-0124.R1","DOIUrl":"10.1302/2633-1462.510.BJO-2024-0124.R1","url":null,"abstract":"<p><strong>Aims: </strong>The aim of this study was to determine whether obesity had a detrimental effect on the long-term performance and survival of medial unicompartmental knee arthroplasties (UKAs).</p><p><strong>Methods: </strong>This study reviewed prospectively collected functional outcome scores and revision rates of all medial UKA patients with recorded BMI performed in Christchurch, New Zealand, from January 2011 to September 2021. Patient-reported outcome measures (PROMs) were the primary outcome of this study, with all-cause revision rate analyzed as a secondary outcome. PROMs were taken preoperatively, at six months, one year, five years, and ten years postoperatively. There were 873 patients who had functional scores recorded at five years and 164 patients had scores recorded at ten years. Further sub-group analysis was performed based on the patient's BMI. Revision data were available through the New Zealand Joint Registry for 2,323 UKAs performed during this time period.</p><p><strong>Results: </strong>Obese patients (BMI > 30 kg/m<sup>2</sup>) were 3.1 years younger than non-obese patients (BMI < 30 kg/m<sup>2</sup>) at the time of surgery (mean age of obese patients 65.5 years (SD 9.7) and mean age of non-obese patients 68.6 years (SD 10.1)). Preoperatively, obese patients tended to have significantly lower functional scores than non-obese patients, which continued at five and ten years postoperatively. At these timepoints, obese patients had significantly lower scores for most PROMs measured compared to non-obese patients. However, there was no significant difference in the improvement of any of these scores after surgery between obese and non-obese patients. There was no significant difference in revision rates between obese and non-obese patients at any time. All-cause revision rate for obese patients was 0.73 per 100 observed component years compared to 0.67 in non-obese patients at ten years. There was also no significant difference in the aseptic loosening rate between groups.</p><p><strong>Conclusion: </strong>Our study supports the use of UKAs in obese patients, with similar benefit and survival compared to non-obese patients at ten years.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"5 10","pages":"937-943"},"PeriodicalIF":2.8,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11495132/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142476449","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}
引用次数: 0
The greater tuberosity version angle: a novel method of acquiring humeral alignment during intramedullary nailing. 大结节版本角:一种在髓内钉钉入过程中获得肱骨对齐的新方法。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-10-22 DOI: 10.1302/2633-1462.510.BJO-2024-0105
Jose M Gutierrez-Naranjo, Luis M Salazar, Vaibhav A Kanawade, Emam E Abdel Fatah, Mohamed Mahfouz, Nicholas W Brady, Anil K Dutta

Aims: This study aims to describe a new method that may be used as a supplement to evaluate humeral rotational alignment during intramedullary nail (IMN) insertion using the profile of the perpendicular peak of the greater tuberosity and its relation to the transepicondylar axis. We called this angle the greater tuberosity version angle (GTVA).

Methods: This study analyzed 506 cadaveric humeri of adult patients. All humeri were CT scanned using 0.625 × 0.625 × 0.625 mm cubic voxels. The images acquired were used to generate 3D surface models of the humerus. Next, 3D landmarks were automatically calculated on each 3D bone using custom-written C++ software. The anatomical landmarks analyzed were the transepicondylar axis, the humerus anatomical axis, and the peak of the perpendicular axis of the greater tuberosity. Lastly, the angle between the transepicondylar axis and the greater tuberosity axis was calculated and defined as the GTVA.

Results: The value of GTVA was 20.9° (SD 4.7°) (95% CI 20.47° to 21.3°). Results of analysis of variance revealed that females had a statistically significant larger angle of 21.95° (SD 4.49°) compared to males, which were found to be 20.49° (SD 4.8°) (p = 0.001).

Conclusion: This study identified a consistent relationship between palpable anatomical landmarks, enhancing IMN accuracy by utilizing 3D CT scans and replicating a 20.9° angle from the greater tuberosity to the transepicondylar axis. Using this angle as a secondary reference may help mitigate the complications associated with malrotation of the humerus following IMN. However, future trials are needed for clinical validation.

目的:本研究旨在描述一种新方法,该方法可在髓内钉(IMN)插入过程中,利用大结节垂直峰的轮廓及其与跨肱骨髁轴的关系,作为评估肱骨旋转对位的补充。我们将这一角度称为大结节角度(GTVA):本研究分析了 506 例成年患者的肱骨尸体。所有肱骨均使用 0.625 × 0.625 × 0.625 毫米立方体体素进行 CT 扫描。获得的图像用于生成肱骨的三维表面模型。然后,使用定制的 C++ 软件自动计算每块三维骨骼上的三维地标。分析的解剖地标包括横髁轴、肱骨解剖轴和大结节垂直轴的峰值。最后,计算横髁轴线与大结节轴线之间的夹角,并将其定义为 GTVA:GTVA值为20.9°(SD 4.7°)(95% CI 20.47°至21.3°)。方差分析结果显示,与男性的 20.49°(SD 4.8°)相比,女性的 21.95°(SD 4.49°)具有显著的统计学意义(P = 0.001):这项研究确定了可触摸的解剖地标之间的一致关系,通过利用三维 CT 扫描和复制从大结节到横髁轴的 20.9° 角度,提高了 IMN 的准确性。将这一角度作为辅助参考,可能有助于减轻 IMN 后与肱骨旋转不良相关的并发症。不过,还需要未来的试验进行临床验证。
{"title":"The greater tuberosity version angle: a novel method of acquiring humeral alignment during intramedullary nailing.","authors":"Jose M Gutierrez-Naranjo, Luis M Salazar, Vaibhav A Kanawade, Emam E Abdel Fatah, Mohamed Mahfouz, Nicholas W Brady, Anil K Dutta","doi":"10.1302/2633-1462.510.BJO-2024-0105","DOIUrl":"10.1302/2633-1462.510.BJO-2024-0105","url":null,"abstract":"<p><strong>Aims: </strong>This study aims to describe a new method that may be used as a supplement to evaluate humeral rotational alignment during intramedullary nail (IMN) insertion using the profile of the perpendicular peak of the greater tuberosity and its relation to the transepicondylar axis. We called this angle the greater tuberosity version angle (GTVA).</p><p><strong>Methods: </strong>This study analyzed 506 cadaveric humeri of adult patients. All humeri were CT scanned using 0.625 × 0.625 × 0.625 mm cubic voxels. The images acquired were used to generate 3D surface models of the humerus. Next, 3D landmarks were automatically calculated on each 3D bone using custom-written C++ software. The anatomical landmarks analyzed were the transepicondylar axis, the humerus anatomical axis, and the peak of the perpendicular axis of the greater tuberosity. Lastly, the angle between the transepicondylar axis and the greater tuberosity axis was calculated and defined as the GTVA.</p><p><strong>Results: </strong>The value of GTVA was 20.9° (SD 4.7°) (95% CI 20.47° to 21.3°). Results of analysis of variance revealed that females had a statistically significant larger angle of 21.95° (SD 4.49°) compared to males, which were found to be 20.49° (SD 4.8°) (p = 0.001).</p><p><strong>Conclusion: </strong>This study identified a consistent relationship between palpable anatomical landmarks, enhancing IMN accuracy by utilizing 3D CT scans and replicating a 20.9° angle from the greater tuberosity to the transepicondylar axis. Using this angle as a secondary reference may help mitigate the complications associated with malrotation of the humerus following IMN. However, future trials are needed for clinical validation.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"5 10","pages":"929-936"},"PeriodicalIF":2.8,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11493473/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142476464","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}
引用次数: 0
Implant design influences the joint-specific outcome after total knee arthroplasty. 植入物设计影响全膝关节置换术后的关节特异性结果。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-10-21 DOI: 10.1302/2633-1462.510.BJO-2024-0111.R1
Nick Clement, Deborah J MacDonald, David F Hamilton, Paul Gaston

Aims: The aims were to assess whether joint-specific outcome after total knee arthroplasty (TKA) was influenced by implant design over a 12-year follow-up period, and whether patient-related factors were associated with loss to follow-up and mortality risk.

Methods: Long-term follow-up of a randomized controlled trial was undertaken. A total of 212 patients were allocated a Triathlon or a Kinemax TKA. Patients were assessed preoperatively, and one, three, eight, and 12 years postoperatively using the Oxford Knee Score (OKS). Reasons for patient lost to follow-up, mortality, and revision were recorded.

Results: A total of 94 patients completed 12-year functional follow-up (62 females, mean age 66 years (43 to 82) at index surgery). There was a clinically significantly greater improvement in the OKS at one year (mean difference (MD) 3.0 (95% CI 0.4 to 5.7); p = 0.027) and three years (MD 4.7 (95% CI 1.9 to 7.5); p = 0.001) for the Triathlon group, but no differences were observed at eight (p = 0.331) or 12 years' (p = 0.181) follow-up. When assessing the OKS in the patients surviving to 12 years, the Triathlon group had a clinically significantly greater improvement in the OKS (marginal mean 3.8 (95% CI 0.2 to 7.4); p = 0.040). Loss to functional follow-up (53%, n = 109/204) was independently associated with older age (p = 0.001). Patient mortality was the major reason (56.4%, n = 62/110) for loss to follow-up. Older age (p < 0.001) and worse preoperative OKS (p = 0.043) were independently associated with increased mortality risk. An age at time of surgery of ≥ 72 years was 75% sensitive and 74% specific for predicting mortality with an area under the curve of 78.1% (95% CI 70.9 to 85.3; p < 0.001).

Conclusion: The Triathlon TKA was associated with clinically meaningful greater improvement in knee-specific outcome when compared to the Kinemax TKA. Loss to follow-up at 12 years was a limitation, and studies planning longer-term functional assessment could limit their cohort to patients aged under 72 years.

目的:旨在评估在12年的随访期内,全膝关节置换术(TKA)后的关节特异性结果是否受植入物设计的影响,以及患者相关因素是否与随访失败和死亡风险有关:方法:对一项随机对照试验进行了长期随访。共有212名患者被分配使用Triathlon或Kinemax TKA。使用牛津膝关节评分(OKS)对患者进行术前评估、术后1年、3年、8年和12年的评估。记录了患者失去随访的原因、死亡率和翻修率:共有94名患者完成了为期12年的功能随访(62名女性,指数手术时的平均年龄为66岁(43至82岁))。铁人三项组在一年(平均差异(MD)为 3.0(95% CI 0.4 至 5.7);p = 0.027)和三年(MD 为 4.7(95% CI 1.9 至 7.5);p = 0.001)时的 OKS 有明显改善,但在八年(p = 0.331)或十二年(p = 0.181)的随访中未观察到差异。在对存活 12 年的患者的 OKS 进行评估时,铁人三项组患者的 OKS 改善幅度明显更大(边际平均值为 3.8 (95% CI 0.2 至 7.4);p = 0.040)。失去功能随访(53%,n = 109/204)与年龄较大有独立关联(p = 0.001)。患者死亡是失去随访的主要原因(56.4%,n = 62/110)。年龄较大(p < 0.001)和术前 OKS 较差(p = 0.043)与死亡风险增加有独立关联。手术时年龄≥72岁对预测死亡率的敏感度为75%,特异度为74%,曲线下面积为78.1% (95% CI 70.9 to 85.3; p < 0.001):结论:与Kinemax TKA相比,Triathlon TKA对膝关节特异性结果的改善更具有临床意义。12年的随访损失是一个限制因素,计划进行更长期功能评估的研究可将其队列限制在72岁以下的患者。
{"title":"Implant design influences the joint-specific outcome after total knee arthroplasty.","authors":"Nick Clement, Deborah J MacDonald, David F Hamilton, Paul Gaston","doi":"10.1302/2633-1462.510.BJO-2024-0111.R1","DOIUrl":"10.1302/2633-1462.510.BJO-2024-0111.R1","url":null,"abstract":"<p><strong>Aims: </strong>The aims were to assess whether joint-specific outcome after total knee arthroplasty (TKA) was influenced by implant design over a 12-year follow-up period, and whether patient-related factors were associated with loss to follow-up and mortality risk.</p><p><strong>Methods: </strong>Long-term follow-up of a randomized controlled trial was undertaken. A total of 212 patients were allocated a Triathlon or a Kinemax TKA. Patients were assessed preoperatively, and one, three, eight, and 12 years postoperatively using the Oxford Knee Score (OKS). Reasons for patient lost to follow-up, mortality, and revision were recorded.</p><p><strong>Results: </strong>A total of 94 patients completed 12-year functional follow-up (62 females, mean age 66 years (43 to 82) at index surgery). There was a clinically significantly greater improvement in the OKS at one year (mean difference (MD) 3.0 (95% CI 0.4 to 5.7); p = 0.027) and three years (MD 4.7 (95% CI 1.9 to 7.5); p = 0.001) for the Triathlon group, but no differences were observed at eight (p = 0.331) or 12 years' (p = 0.181) follow-up. When assessing the OKS in the patients surviving to 12 years, the Triathlon group had a clinically significantly greater improvement in the OKS (marginal mean 3.8 (95% CI 0.2 to 7.4); p = 0.040). Loss to functional follow-up (53%, n = 109/204) was independently associated with older age (p = 0.001). Patient mortality was the major reason (56.4%, n = 62/110) for loss to follow-up. Older age (p < 0.001) and worse preoperative OKS (p = 0.043) were independently associated with increased mortality risk. An age at time of surgery of ≥ 72 years was 75% sensitive and 74% specific for predicting mortality with an area under the curve of 78.1% (95% CI 70.9 to 85.3; p < 0.001).</p><p><strong>Conclusion: </strong>The Triathlon TKA was associated with clinically meaningful greater improvement in knee-specific outcome when compared to the Kinemax TKA. Loss to follow-up at 12 years was a limitation, and studies planning longer-term functional assessment could limit their cohort to patients aged under 72 years.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"5 10","pages":"911-919"},"PeriodicalIF":2.8,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491871/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142476450","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}
引用次数: 0
Protocol for a prospective randomized trial of surgical versus conservative management for unstable fractures of the distal radius in patients aged 65 years and older. 针对 65 岁及以上患者桡骨远端不稳定骨折的手术治疗与保守治疗的前瞻性随机试验方案。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-10-21 DOI: 10.1302/2633-1462.510.BJO-2024-0044
Katrina R Bell, William M Oliver, Timothy O White, Samuel G Molyneux, Catriona Graham, Nick D Clement, Andrew D Duckworth

Aims: The primary aim of this study is to quantify and compare outcomes following a dorsally displaced fracture of the distal radius in elderly patients (aged ≥ 65 years) who are managed conservatively versus with surgical fixation (open reduction and internal fixation). Secondary aims are to assess and compare upper limb-specific function, health-related quality of life, wrist pain, complications, grip strength, range of motion, radiological parameters, healthcare resource use, and cost-effectiveness between the groups.

Methods: A prospectively registered (ISRCTN95922938) randomized parallel group trial will be conducted. Elderly patients meeting the inclusion criteria with a dorsally displaced distal radius facture will be randomized (1:1 ratio) to either conservative management (cast without further manipulation) or surgery. Patients will be assessed at six, 12, 26 weeks, and 52 weeks post intervention. The primary outcome measure and endpoint will be the Patient-Rated Wrist Evaluation (PRWE) at 52 weeks. In addition, the abbreviated version of the Disabilities of Arm, Shoulder and Hand questionnaire (QuickDASH), EuroQol five-dimension questionnaire, pain score (visual analogue scale 1 to 10), complications, grip strength (dynamometer), range of motion (goniometer), and radiological assessments will be undertaken. A cost-utility analysis will be performed to assess the cost-effectiveness of surgery. We aim to recruit 89 subjects per arm (total sample size 178).

Discussion: The results of this study will help guide treatment of dorsally displaced distal radial fractures in the elderly and assess whether surgery offers functional benefit to patients. This is an important finding, as the number of elderly distal radial fractures is estimated to increase in the future due to the ageing population. Evidence-based management strategies are therefore required to ensure the best outcome for the patient and to optimize the use of increasingly scarce healthcare resources.

目的:本研究的主要目的是量化和比较老年患者(年龄≥ 65 岁)桡骨远端背侧移位骨折后保守治疗与手术固定(切开复位内固定)的疗效。次要目的是评估和比较两组患者的上肢特异性功能、健康相关生活质量、腕痛、并发症、握力、活动范围、放射学参数、医疗资源使用和成本效益:将进行一项前瞻性注册(ISRCTN95922938)的随机平行分组试验。符合纳入标准的桡骨远端背侧移位的老年患者将被随机分配(1:1 的比例)接受保守治疗(石膏固定,无需进一步操作)或手术治疗。患者将在干预后 6 周、12 周、26 周和 52 周接受评估。主要结果测量和终点是 52 周时的患者腕部评分(Patient-Rated Wrist Evaluation,PRWE)。此外,还将进行手臂、肩部和手部残疾问卷缩略版(QuickDASH)、EuroQol 五维问卷、疼痛评分(视觉模拟量表 1 至 10)、并发症、握力(测力计)、活动范围(动态关节角度计)和放射学评估。我们还将进行成本效益分析,以评估手术的成本效益。我们的目标是每臂招募 89 名受试者(样本总数为 178):本研究的结果将有助于指导老年人桡骨远端骨折背侧移位的治疗,并评估手术是否能为患者带来功能上的益处。这是一个重要的发现,因为随着人口老龄化的加剧,预计未来老年人桡骨远端骨折的数量还会增加。因此,我们需要基于证据的管理策略,以确保患者获得最佳治疗效果,并优化利用日益稀缺的医疗资源。
{"title":"Protocol for a prospective randomized trial of surgical versus conservative management for unstable fractures of the distal radius in patients aged 65 years and older.","authors":"Katrina R Bell, William M Oliver, Timothy O White, Samuel G Molyneux, Catriona Graham, Nick D Clement, Andrew D Duckworth","doi":"10.1302/2633-1462.510.BJO-2024-0044","DOIUrl":"10.1302/2633-1462.510.BJO-2024-0044","url":null,"abstract":"<p><strong>Aims: </strong>The primary aim of this study is to quantify and compare outcomes following a dorsally displaced fracture of the distal radius in elderly patients (aged ≥ 65 years) who are managed conservatively versus with surgical fixation (open reduction and internal fixation). Secondary aims are to assess and compare upper limb-specific function, health-related quality of life, wrist pain, complications, grip strength, range of motion, radiological parameters, healthcare resource use, and cost-effectiveness between the groups.</p><p><strong>Methods: </strong>A prospectively registered (ISRCTN95922938) randomized parallel group trial will be conducted. Elderly patients meeting the inclusion criteria with a dorsally displaced distal radius facture will be randomized (1:1 ratio) to either conservative management (cast without further manipulation) or surgery. Patients will be assessed at six, 12, 26 weeks, and 52 weeks post intervention. The primary outcome measure and endpoint will be the Patient-Rated Wrist Evaluation (PRWE) at 52 weeks. In addition, the abbreviated version of the Disabilities of Arm, Shoulder and Hand questionnaire (QuickDASH), EuroQol five-dimension questionnaire, pain score (visual analogue scale 1 to 10), complications, grip strength (dynamometer), range of motion (goniometer), and radiological assessments will be undertaken. A cost-utility analysis will be performed to assess the cost-effectiveness of surgery. We aim to recruit 89 subjects per arm (total sample size 178).</p><p><strong>Discussion: </strong>The results of this study will help guide treatment of dorsally displaced distal radial fractures in the elderly and assess whether surgery offers functional benefit to patients. This is an important finding, as the number of elderly distal radial fractures is estimated to increase in the future due to the ageing population. Evidence-based management strategies are therefore required to ensure the best outcome for the patient and to optimize the use of increasingly scarce healthcare resources.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"5 10","pages":"920-928"},"PeriodicalIF":2.8,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491869/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142476453","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}
引用次数: 0
Concurrent validity of the Single Assessment Numerical Evaluation and hip-specific patient-reported outcome measures. 单一评估数字评价和髋关节特异性患者报告结果测量的并发有效性。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-10-18 DOI: 10.1302/2633-1462.510.BJO-2024-0094.R1
Elizabeth M Bergman, Edward P Mulligan, Rupal M Patel, Joel Wells

Aims: The Single Assessment Numerical Evalution (SANE) score is a pragmatic alternative to longer patient-reported outcome measures (PROMs). The purpose of this study was to investigate the concurrent validity of the SANE and hip-specific PROMs in a generalized population of patients with hip pain at a single timepoint upon initial visit with an orthopaedic surgeon who is a hip preservation specialist. We hypothesized that SANE would have a strong correlation with the 12-question International Hip Outcome Tool (iHOT)-12, the Hip Outcome Score (HOS), and the Hip disability and Osteoarthritis Outcome Score (HOOS), providing evidence for concurrent validity of the SANE and hip-specific outcome measures in patients with hip pain.

Methods: This study was a cross-sectional retrospective database analysis at a single timepoint. Data were collected from 2,782 patients at initial evaluation with a hip preservation specialist using the iHOT-12, HOS, HOOS, and SANE. Outcome scores were retrospectively analyzed using Pearson correlation coefficients.

Results: Mean raw scores were iHOT-12 67.01 (SD 29.52), HOS 58.42 (SD 26.26), HOOS 86.85 (SD 32.94), and SANE 49.60 (SD 27.92). SANE was moderately correlated with the iHOT-12 (r = -0.4; 95% CI -0.35 to -0.44; p < 0.001), HOS (r = 0.57; 95% CI 0.53 to 0.60; p < 0.001), and HOOS (r = -0.55; 95% CI -0.51 to -0.58; p < 0.001). The iHOT-12 and HOOS were recorded as a lower score, indicating better function, which accounts for the negative r values.

Conclusion: This study was the first to investigate the relationship between the SANE and the iHOT-12, HOS, and HOOS in a population of patients with hip pain at the initial evaluation with an orthopaedic surgeon, and found moderate correlation between SANE and the iHOT-12, HOS, and HOOS. The SANE may be a pragmatic alternative for clinical benchmarking in a general population of patients with hip pain. The construct validity of the SANE should be questioned compared to legacy measures whose content validity has been more rigorously investigated.

目的:单次评估数字评价(SANE)评分是一种实用的患者报告结果测量法(PROM)的替代方法。本研究的目的是在髋关节疼痛患者中调查 SANE 和髋关节特异性 PROMs 的并发有效性,调查对象是髋关节疼痛患者在初次就诊时的单一时间点。我们假设 SANE 与 12 个问题的国际髋关节结果工具 (iHOT)-12、髋关节结果评分 (HOS) 以及髋关节残疾和骨关节炎结果评分 (HOOS) 有很强的相关性,从而为髋关节疼痛患者的 SANE 和髋关节特异性结果测量的并发有效性提供证据:本研究是一项单一时间点的横断面回顾性数据库分析。研究收集了 2782 名患者的数据,这些患者在接受髋关节保护专家的初步评估时使用了 iHOT-12、HOS、HOOS 和 SANE。使用皮尔逊相关系数对结果评分进行回顾性分析:平均原始得分分别为:iHOT-12 67.01 (SD 29.52)、HOS 58.42 (SD 26.26)、HOOS 86.85 (SD 32.94)、SANE 49.60 (SD 27.92)。SANE 与 iHOT-12 (r = -0.4; 95% CI -0.35 to -0.44; p < 0.001)、HOS (r = 0.57; 95% CI 0.53 to 0.60; p < 0.001) 和 HOOS (r = -0.55; 95% CI -0.51 to -0.58; p < 0.001) 呈中度相关。iHOT-12和HOOS的得分越低,表明功能越好,这也是r值为负的原因:本研究首次调查了骨科医生对髋关节疼痛患者进行初步评估时 SANE 与 iHOT-12、HOS 和 HOOS 之间的关系,发现 SANE 与 iHOT-12、HOS 和 HOOS 之间存在适度的相关性。SANE 可能是髋关节疼痛患者临床基准的一种实用替代方法。与传统的测量方法相比,SANE 的构造效度应该受到质疑,因为传统测量方法的内容效度已经过更严格的研究。
{"title":"Concurrent validity of the Single Assessment Numerical Evaluation and hip-specific patient-reported outcome measures.","authors":"Elizabeth M Bergman, Edward P Mulligan, Rupal M Patel, Joel Wells","doi":"10.1302/2633-1462.510.BJO-2024-0094.R1","DOIUrl":"https://doi.org/10.1302/2633-1462.510.BJO-2024-0094.R1","url":null,"abstract":"<p><strong>Aims: </strong>The Single Assessment Numerical Evalution (SANE) score is a pragmatic alternative to longer patient-reported outcome measures (PROMs). The purpose of this study was to investigate the concurrent validity of the SANE and hip-specific PROMs in a generalized population of patients with hip pain at a single timepoint upon initial visit with an orthopaedic surgeon who is a hip preservation specialist. We hypothesized that SANE would have a strong correlation with the 12-question International Hip Outcome Tool (iHOT)-12, the Hip Outcome Score (HOS), and the Hip disability and Osteoarthritis Outcome Score (HOOS), providing evidence for concurrent validity of the SANE and hip-specific outcome measures in patients with hip pain.</p><p><strong>Methods: </strong>This study was a cross-sectional retrospective database analysis at a single timepoint. Data were collected from 2,782 patients at initial evaluation with a hip preservation specialist using the iHOT-12, HOS, HOOS, and SANE. Outcome scores were retrospectively analyzed using Pearson correlation coefficients.</p><p><strong>Results: </strong>Mean raw scores were iHOT-12 67.01 (SD 29.52), HOS 58.42 (SD 26.26), HOOS 86.85 (SD 32.94), and SANE 49.60 (SD 27.92). SANE was moderately correlated with the iHOT-12 (<i>r</i> = -0.4; 95% CI -0.35 to -0.44; p < 0.001), HOS (<i>r</i> = 0.57; 95% CI 0.53 to 0.60; p < 0.001), and HOOS (<i>r</i> = -0.55; 95% CI -0.51 to -0.58; p < 0.001). The iHOT-12 and HOOS were recorded as a lower score, indicating better function, which accounts for the negative r values.</p><p><strong>Conclusion: </strong>This study was the first to investigate the relationship between the SANE and the iHOT-12, HOS, and HOOS in a population of patients with hip pain at the initial evaluation with an orthopaedic surgeon, and found moderate correlation between SANE and the iHOT-12, HOS, and HOOS. The SANE may be a pragmatic alternative for clinical benchmarking in a general population of patients with hip pain. The construct validity of the SANE should be questioned compared to legacy measures whose content validity has been more rigorously investigated.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"5 10","pages":"904-910"},"PeriodicalIF":2.8,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11486539/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142476448","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}
引用次数: 0
Sensitivity and specificity of electrodiagnostic parameters in diagnosing carpal tunnel syndrome. 诊断腕管综合征的电诊断参数的敏感性和特异性。
IF 2.8 Q1 ORTHOPEDICS Pub Date : 2024-10-17 DOI: 10.1302/2633-1462.510.BJO-2024-0025.R1
Shahir Mazaheri, Jalal Poorolajal, Alireza Mazaheri

Aims: The sensitivity and specificity of electrodiagnostic parameters in diagnosing carpal tunnel syndrome (CTS) have been reported differently, and this study aims to address this gap.

Methods: This case-control study was conducted on 57 cases with CTS and 58 controls without complaints, such as pain or paresthesia on the median nerve. The main assessed electrodiagnostic parameters were terminal latency index (TLI), residual latency (RL), median ulnar F-wave latency difference (FdifMU), and median sensory latency-ulnar motor latency difference (MSUMLD).

Results: The mean age in cases and controls were 50.7 years (SD 9.9) and 47.9 years (SD 12.1), respectively. The CTS severity was mild in 20 patients (34.4%), moderate in 19 patients (32.8%), and severe in 19 patients (32.8%). The sensitivity and specificity of the electrodiagnostic parameters in diagnosing CTS were as follows: TLI 75.4% and 87.8%; RL 85.9% and 82.5%; FdifMU 87.9% and 82.9%; and MSUMLD 94.8% and 60.0%, respectively.

Conclusion: Our findings indicated that electrodiagnostic parameters are significantly associated with the clinical manifestation of CTS, and are associated with high diagnostic accuracy in CTS diagnosis. However, further studies are required to highlight the role of electrodiagnostic parameters and their combination in CTS detection.

目的:电诊断参数在诊断腕管综合征(CTS)方面的敏感性和特异性有不同的报道,本研究旨在弥补这一不足:这项病例对照研究的对象是 57 名 CTS 患者和 58 名无正中神经疼痛或麻痹等主诉的对照者。评估的主要电诊断参数包括终末潜伏期指数(TLI)、残余潜伏期(RL)、正中尺神经F波潜伏期差值(FdifMU)和正中感觉潜伏期-尺神经运动潜伏期差值(MSUMLD):病例和对照组的平均年龄分别为 50.7 岁(SD 9.9)和 47.9 岁(SD 12.1)。20 名患者的 CTS 严重程度为轻度(34.4%),19 名患者为中度(32.8%),19 名患者为重度(32.8%)。电诊断参数对诊断 CTS 的敏感性和特异性如下:TLI分别为75.4%和87.8%;RL分别为85.9%和82.5%;FdifMU分别为87.9%和82.9%;MSUMLD分别为94.8%和60.0%:我们的研究结果表明,电诊断参数与 CTS 的临床表现显著相关,在 CTS 诊断中具有较高的诊断准确性。然而,还需要进一步的研究来强调电诊断参数及其组合在 CTS 检测中的作用。
{"title":"Sensitivity and specificity of electrodiagnostic parameters in diagnosing carpal tunnel syndrome.","authors":"Shahir Mazaheri, Jalal Poorolajal, Alireza Mazaheri","doi":"10.1302/2633-1462.510.BJO-2024-0025.R1","DOIUrl":"https://doi.org/10.1302/2633-1462.510.BJO-2024-0025.R1","url":null,"abstract":"<p><strong>Aims: </strong>The sensitivity and specificity of electrodiagnostic parameters in diagnosing carpal tunnel syndrome (CTS) have been reported differently, and this study aims to address this gap.</p><p><strong>Methods: </strong>This case-control study was conducted on 57 cases with CTS and 58 controls without complaints, such as pain or paresthesia on the median nerve. The main assessed electrodiagnostic parameters were terminal latency index (TLI), residual latency (RL), median ulnar F-wave latency difference (FdifMU), and median sensory latency-ulnar motor latency difference (MSUMLD).</p><p><strong>Results: </strong>The mean age in cases and controls were 50.7 years (SD 9.9) and 47.9 years (SD 12.1), respectively. The CTS severity was mild in 20 patients (34.4%), moderate in 19 patients (32.8%), and severe in 19 patients (32.8%). The sensitivity and specificity of the electrodiagnostic parameters in diagnosing CTS were as follows: TLI 75.4% and 87.8%; RL 85.9% and 82.5%; FdifMU 87.9% and 82.9%; and MSUMLD 94.8% and 60.0%, respectively.</p><p><strong>Conclusion: </strong>Our findings indicated that electrodiagnostic parameters are significantly associated with the clinical manifestation of CTS, and are associated with high diagnostic accuracy in CTS diagnosis. However, further studies are required to highlight the role of electrodiagnostic parameters and their combination in CTS detection.</p>","PeriodicalId":34103,"journal":{"name":"Bone & Joint Open","volume":"5 10","pages":"898-903"},"PeriodicalIF":2.8,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11485627/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142476463","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}
引用次数: 0
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