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Patients with a history of lumbar fusion have a higher risk of revision arthroscopy and conversion to total hip arthroplasty after primary hip arthroscopy. 有腰椎融合术病史的患者在初次髋关节镜手术后进行关节镜翻修和转为全髋关节置换术的风险较高。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-29 DOI: 10.1016/j.arthro.2024.08.026
Abhinaba Chatterjee, Kaisen Yao, Matthew H Nasra, Thun Itthipanichpong, Gregory Galano, Anil S Ranawat

Purpose: To characterize the risk of revision hip arthroscopy or conversion to total hip arthroplasty (THA) among patients with a history of lumbar fusion undergoing primary hip arthroscopy.

Methods: We used the Statewide Planning and Research Cooperative System, an administrative database including all ambulatory and inpatient surgery encounters in New York (NY), to identify all patients who underwent hip arthroscopy for FAI between 2010-2020. Patients with prior lumbar fusion were identified using CPT and ICD 9th/10th Revision coding definitions. Patients with and without prior fusion were matched in a 1:5 ratio according to age and comorbidity burden. The number of levels fused was defined in the following fashion: i) no fusion, ii) 1-2 levels, or iii) ≥3 levels. Patients were followed for two years to evaluate the rate of revision hip arthroscopy or conversion to THA. Multivariable logistic regression models were used to measure the association between number of levels fused and revision hip arthroscopy or conversion to THA.

Results: Between 2010-2020, there were 23,277 patients that underwent primary hip arthroscopy in NY state. Of these, 348 (1.4%) had a prior lumbar fusion. After matching for age and comorbidities, the composite rate of revision hip arthroscopy or conversion to THA was higher in patients with prior lumbar fusion compared to patients without (16.5% vs. 8.5%; P < 0.001). This risk increased with the number of levels fused (1-2 levels: 15.1%; aOR, 1.8; 95% CI, 1.3-2.6; vs. ≥3 levels: 26.3%; aOR, 3.4; 95% CI, 1.7-7.0).

Conclusion: Patients with a history of lumbar fusion had significantly higher rates of revision hip arthroscopy and conversion to THA compared to patients without prior fusion. The risk of revision hip arthroscopy or conversion to THA was increased approximately 2-fold in patients with 1-2 levels fused and 3-fold in patients with 3 or more levels fused.

Level of evidence: Level III, prognostic retrospective matched comparative case series.

目的:分析有腰椎融合史的患者接受初次髋关节镜手术后进行髋关节镜翻修或转为全髋关节置换术(THA)的风险:我们利用全州规划与研究合作系统(Statewide Planning and Research Cooperative System)这一包括纽约州(NY)所有门诊和住院手术病例的行政数据库,确定了 2010-2020 年间因 FAI 接受髋关节镜手术的所有患者。使用 CPT 和 ICD 第 9/10 次修订版编码定义确定了既往接受过腰椎融合术的患者。根据年龄和合并症负担,将既往接受过腰椎融合术和未接受过腰椎融合术的患者按 1:5 的比例进行配对。融合的水平数定义如下:i) 无融合,ii) 1-2 水平,或 iii) ≥3 水平。对患者进行为期两年的随访,以评估髋关节镜翻修率或转为 THA 的比率。多变量逻辑回归模型用于测量融合水平数与髋关节镜翻修或转为THA之间的关系:2010-2020年间,纽约州共有23277名患者接受了初次髋关节镜手术。其中,348人(1.4%)曾接受过腰椎融合术。在对年龄和合并症进行匹配后,既往接受过腰椎融合术的患者与未接受过腰椎融合术的患者相比,髋关节镜翻修或转为 THA 的复合率更高(16.5% 对 8.5%;P < 0.001)。这一风险随融合的水平数增加而增加(1-2个水平:15.1%;aOR,1.8;95% CI,1.3-2.6;与≥3个水平相比:26.3%;aOR,3.4;95% CI,1.7-7.0):结论:与无腰椎融合术史的患者相比,有腰椎融合术史的患者接受髋关节镜翻修手术和转为 THA 的比例明显更高。髋关节镜翻修或转为THA的风险在1-2级融合的患者中增加了约2倍,在3级或3级以上融合的患者中增加了3倍:III级,预后回顾性匹配比较病例系列。
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引用次数: 0
Editorial Commentary: Arthroscopic Subacromial Balloon Spacer for Massive Rotator Cuff Tears Results in Fast Recovery and Lasting Pain Relief. 编辑评论:关节镜下肩峰下球囊垫片治疗肩袖大面积撕裂,恢复快,疼痛缓解持久。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-29 DOI: 10.1016/j.arthro.2024.08.028
Nikhil N Verma

Repair of rotator cuff tear is challenging because poor biologic factors can negatively impact tendon healing and risk complications. Sometimes, instead of attempting complex procedures with a guarded prognosis to reconstruct or replace rotator cuff like tissue, less is more. Minimally invasive, arthroscopic subacromial balloon spacer (SBS) for massive rotator cuff tears, demonstrates excellent long-term outcomes. Radiographically, SBS outcomes may be concerning, but clinically, patients do well. If pain is the primary complaint and function is maintained, the balloon spacer is an excellent option with a fast recovery. However, if function is deficient, or if the patient prioritizes strength recovery as their primary desired outcome, then more invasive procedures are often indicated.

肩袖撕裂的修复具有挑战性,因为不良的生物因素会对肌腱愈合产生负面影响,并带来并发症风险。有时,与其在预后不佳的情况下尝试复杂的手术来重建或替换类似肩袖的组织,不如以少胜多。微创、关节镜下肩峰下球囊垫片(SBS)治疗大面积肩袖撕裂的长期疗效极佳。从影像学角度看,SBS 的疗效可能令人担忧,但从临床角度看,患者的疗效很好。如果疼痛是主要主诉,且功能得以维持,球囊垫片是一种恢复快的极佳选择。但是,如果功能不足,或者患者将力量恢复作为主要期望结果,则通常需要进行更具创伤性的手术。
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引用次数: 0
Preoperative Increases in T2-Weighted Fat-Suppressed MRI Signal Intensities Associated with Advanced Tissue Degeneration and Mitochondrial Dysfunction in Rotator Cuff Tears. 术前 T2 加权脂肪抑制磁共振成像信号强度的增加与肩袖撕裂的晚期组织变性和线粒体功能障碍有关。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-28 DOI: 10.1016/j.arthro.2024.08.019
Masaya Kusunose, Yutaka Mifune, Atsuyuki Inui, Kohei Yamaura, Takahiro Furukawa, Tatuso Kato, Ryosuke Kuroda

Purpose: The purpose of this study was to investigate the relationship between magnetic resonance imaging (MRI) signal intensities and mitochondrial function in patients undergoing arthroscopic rotator cuff repair, assessed through histological and genetic profiling of tendon tissue.

Methods: This study, conducted between April 2022 and January 2023, included 20 patients undergoing rotator cuff repair for atraumatic/degenerative tears. Rotator cuff tendon edge samples were obtained during arthroscopic rotator cuff repair. Patients were classified based on signal intensity from preoperative T2-weighted fat suppressed MRI. Specifically, they were categorized as having either high or low signal intensity at the rotator cuff tendon edge, with the deltoid muscle serving as a reference. Comparative analyses specifically compared the histological features and genetic profiles of the tendon tissue at the rotator cuff tendon edge. Histological evaluation of harvested tendon specimens during arthroscopic rotator cuff repair employed the modified Bonar score. Real-time polymerase chain reaction was used to assess expression of various mitochondrial and apoptosis-related genes. The mitochondrial morphology of the rotator cuff torn site was examined using electron microscopy.

Results: The higher signal intensity group showed significantly higher modified Bonar scores (p=0.0068), decreased mitochondrial gene expression, increased TUNEL-positive cells (p=0.032), lower SOD activity (p=0.011), reduced ATP5A (p=0.031), and increased cleaved caspase-9 activity (p=0.026) when compared to the lower signal intensity group. Electron microscopy revealed fewer mitochondrial cristae in the higher signal intensity group.

Conclusion: Our results suggest correlations between high MRI signal intensities and the presence of degeneration, mitochondrial dysfunction, and increased apoptosis in rotator cuff tissues. This underscores the utility of MRI signal intensity as an indicator of tissue condition.

Clinical relevance: Building on the established premise that elevated preoperative MRI signal intensities may indicate higher rates of postoperative rotator cuff re-tears, the current study substantiates these findings from a mitochondrial function perspective.

目的:本研究的目的是通过肌腱组织的组织学和基因分析评估接受关节镜下肩袖修复术的患者的磁共振成像(MRI)信号强度与线粒体功能之间的关系:本研究于 2022 年 4 月至 2023 年 1 月间进行,包括 20 名因创伤性/退行性撕裂而接受肩袖修复术的患者。肩袖肌腱边缘样本是在关节镜下肩袖修复术中获取的。根据术前 T2 加权脂肪抑制磁共振成像的信号强度对患者进行分类。具体来说,他们被分为肩袖肌腱边缘信号强度高和信号强度低两类,三角肌作为参照物。对比分析特别比较了肩袖肌腱边缘肌腱组织的组织学特征和基因特征。在关节镜下肩袖修复过程中对采集的肌腱标本进行组织学评估时,采用了改良的博纳尔评分法。实时聚合酶链反应用于评估各种线粒体和凋亡相关基因的表达。使用电子显微镜检查了肩袖撕裂部位的线粒体形态:结果:与较低信号强度组相比,较高信号强度组的改良博纳尔评分明显升高(p=0.0068),线粒体基因表达减少,TUNEL阳性细胞增加(p=0.032),SOD活性降低(p=0.011),ATP5A减少(p=0.031),裂解caspase-9活性增加(p=0.026)。电子显微镜显示,信号强度较高组的线粒体嵴较少:我们的研究结果表明,高磁共振成像信号强度与肩袖组织变性、线粒体功能障碍和凋亡增加之间存在相关性。这强调了核磁共振成像信号强度作为组织状况指标的实用性:基于术前磁共振成像信号强度升高可能预示着术后肩袖再次撕裂的发生率较高这一既定前提,本研究从线粒体功能的角度证实了这些发现。
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引用次数: 0
Improved Acromiohumeral Distance Independently Predicts Better Outcomes After Arthroscopic Superior Capsular Reconstruction Graft Tears. 肱骨喙突距离的改善可独立预测关节镜下上睑囊重建移植物撕裂术后的更好疗效。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-28 DOI: 10.1016/j.arthro.2024.08.017
Hui Ben, Erica Kholinne, Jia Guo, Seung Min Ryu, Jian Loong Ling, Kyoung Hwan Koh, In-Ho Jeon

Purpose: To identify independent factors responsible for the poor outcomes after a graft tear after arthroscopic superior capsular reconstruction (ASCR).

Methods: Patients who underwent ASCR for massive rotator cuff tears between January 2013 and July 2021were reviewed. Based on the achievement of the minimal clinically important differences for clinical outcome measures at the final follow up, patients were divided into the good outcome (GO) and poor outcome (PO) groups. The minimal clinically important differences were calculated as the values equal to one-half of the standard deviation of the changes in outcome scores between the preoperative baseline and the latest follow-up. Pre- and final follow-up variables included demographics, American Shoulder and Elbow Surgeons (ASES) score, Constant score, visual analog scale (VAS) score, range of motion, Preoperative and postoperative 1-year radiological variables were analyzed using MRIs, including anteroposterior (AP) and mediolateral (ML) tear sizes, subscapularis tear, acromiohumeral distance (AHD), and degree of fatty degeneration. Logistic regression analysis was performed to identify the significant predictors of poor outcomes.

Results: A total of 33 patients who underwent ASCR presented with graft tears, which were confirmed by postoperative 1-year magnetic resonance imaging (MRI), and had a minimum follow-up duration of 2 years after surgery were enrolled. The GO group demonstrated significantly greater improvements in functional outcomes compared with the PO group (ASES: 83.5 ± 11.8 vs. 64.0 ± 20.4, P = 0.004; Constant: 67.6 ± 5.7 vs. 57.1 ± 9.8, P <0.001; and VAS: 0.9 ± 1.2 vs. 2.4 ± 2.0, P = 0.026). The postoperative 1-year AHD showed significant improvement in the GO group (3.1 ± 1.2 vs. 6.1 ± 1.4, P <0.001) but no change in the PO group (3.4 ± 1.3 vs. 4.2 ± 0.9, P = 0.074) postoperatively. Multivariate logistic regression analysis indicated that a decreased postoperative 1-year AHD (OR, 0.145; P = 0.019) was associated with a poor outcome after a graft tear.

Conclusion: A narrow postoperative 1-year AHD was identified as the most importantindependent risk factor indicating poor clinical outcomes after a graft tear post-ASCR, which was related to a larger tear and loss of integrity between the grafts and infraspinatus at 1 year postoperatively.

Level of evidence: Level IV.

目的:确定导致关节镜上关节囊重建术(ASCR)后移植物撕裂不良后果的独立因素:回顾性分析2013年1月至2021年7月期间因肩袖大面积撕裂而接受ASCR的患者。根据最终随访时临床结局指标的最小临床重要差异,将患者分为良好结局(GO)组和不良结局(PO)组。最小临床重要差异的计算方法是,术前基线与最近一次随访之间结果评分变化的标准差的二分之一。术前和最终随访变量包括人口统计学、美国肩肘外科医生(ASES)评分、康斯坦茨评分、视觉模拟量表(VAS)评分、活动范围、术前和术后1年的放射学变量(包括前后(AP)和内外侧(ML)撕裂大小、肩胛下撕裂、肩峰肱骨距离(AHD)和脂肪变性程度)。为确定不良预后的重要预测因素,进行了逻辑回归分析:共有33名接受ASCR手术的患者出现移植物撕裂,并经术后1年磁共振成像(MRI)证实,且术后随访时间至少为2年。与 PO 组相比,GO 组的功能结果改善明显(ASES:83.5±11.8 vs. 64.0±20.4,P = 0.004;Constant:67.6±5.7 vs. 57.1±9.8,P 结论:GO 组术后 1 年的 AH 值较 PO 组窄:术后1年AHD变窄被认为是ASCR术后移植物撕裂后临床效果不佳的最重要的独立风险因素,这与术后1年移植物和冈下肌之间撕裂面积增大和完整性丧失有关:证据等级:IV 级。
{"title":"Improved Acromiohumeral Distance Independently Predicts Better Outcomes After Arthroscopic Superior Capsular Reconstruction Graft Tears.","authors":"Hui Ben, Erica Kholinne, Jia Guo, Seung Min Ryu, Jian Loong Ling, Kyoung Hwan Koh, In-Ho Jeon","doi":"10.1016/j.arthro.2024.08.017","DOIUrl":"https://doi.org/10.1016/j.arthro.2024.08.017","url":null,"abstract":"<p><strong>Purpose: </strong>To identify independent factors responsible for the poor outcomes after a graft tear after arthroscopic superior capsular reconstruction (ASCR).</p><p><strong>Methods: </strong>Patients who underwent ASCR for massive rotator cuff tears between January 2013 and July 2021were reviewed. Based on the achievement of the minimal clinically important differences for clinical outcome measures at the final follow up, patients were divided into the good outcome (GO) and poor outcome (PO) groups. The minimal clinically important differences were calculated as the values equal to one-half of the standard deviation of the changes in outcome scores between the preoperative baseline and the latest follow-up. Pre- and final follow-up variables included demographics, American Shoulder and Elbow Surgeons (ASES) score, Constant score, visual analog scale (VAS) score, range of motion, Preoperative and postoperative 1-year radiological variables were analyzed using MRIs, including anteroposterior (AP) and mediolateral (ML) tear sizes, subscapularis tear, acromiohumeral distance (AHD), and degree of fatty degeneration. Logistic regression analysis was performed to identify the significant predictors of poor outcomes.</p><p><strong>Results: </strong>A total of 33 patients who underwent ASCR presented with graft tears, which were confirmed by postoperative 1-year magnetic resonance imaging (MRI), and had a minimum follow-up duration of 2 years after surgery were enrolled. The GO group demonstrated significantly greater improvements in functional outcomes compared with the PO group (ASES: 83.5 ± 11.8 vs. 64.0 ± 20.4, P = 0.004; Constant: 67.6 ± 5.7 vs. 57.1 ± 9.8, P <0.001; and VAS: 0.9 ± 1.2 vs. 2.4 ± 2.0, P = 0.026). The postoperative 1-year AHD showed significant improvement in the GO group (3.1 ± 1.2 vs. 6.1 ± 1.4, P <0.001) but no change in the PO group (3.4 ± 1.3 vs. 4.2 ± 0.9, P = 0.074) postoperatively. Multivariate logistic regression analysis indicated that a decreased postoperative 1-year AHD (OR, 0.145; P = 0.019) was associated with a poor outcome after a graft tear.</p><p><strong>Conclusion: </strong>A narrow postoperative 1-year AHD was identified as the most importantindependent risk factor indicating poor clinical outcomes after a graft tear post-ASCR, which was related to a larger tear and loss of integrity between the grafts and infraspinatus at 1 year postoperatively.</p><p><strong>Level of evidence: </strong>Level IV.</p>","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Decreasing Incidence of Anterior Cruciate Ligament Tears, Increasing Utilization of Anterior Cruciate Ligament Reconstruction in the United States from 2010-2020. 2010-2020 年美国前十字韧带撕裂的发生率下降,前十字韧带重建的使用率上升。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-28 DOI: 10.1016/j.arthro.2024.08.018
Victoria E Bergstein, Uzoma Ahiarakwe, Mark Haft, Henry Fox, Matthew J Best

Purpose: The present study aimed to characterize the incidence of anterior cruciate ligament (ACL) tears, ACL reconstruction (ACLR), and ACL non-operative management from 2010-2020, stratifying by age, biological sex, and Charlson Comorbidity Index (CCI) score.

Methods: A retrospective cohort analysis was performed using the PearlDiver national insurance claims database. Cohorts of patients with ACL tears, ACLR, and non-operative management were identified using ICD-9/10, and CPT codes between 2010-2020. All patients with ACL tears were included. Patients were stratified by age, sex, and CCI. Compound Annual Growth Rate (CAGR) analysis, T tests, and Cohen's d tests were performed to analyze trends and demographic variables.

Results: Of 931,186 ACL tears during the study period, 196,589 were managed with ACLR and 734,597 were managed non-operatively. The cumulative incidence of ACL tears was 75.19 tears per 100,000 person-years. There was a modest decrease in the incidence of ACL tears, ACLR, and non-operative management from 2010-2020, with CAGRs of -3.43%, -3.55%, and -5.35%, respectively. The relative utilization of ACLR compared to non-operative management increased from 2010-2020 (CAGR 2.15%). Patients aged 10-19 accounted for the majority of ACL tears (22.31%) and ACLRs (30.97%). A slight majority of ACL tears (51.2%, p<0.001), ACLR (50.7%, p<0.001), and ACL tears with non-operative management (51.6%, p<0.001) occurred in female patients. The mean CCI of patients who underwent ACLR (mean=0.32; SD=0.77) was significantly lower than that of the general ACL tear cohort (mean=0.54; SD=1.19; p=0.005), and the non-operative management cohort (mean=0.64; SD 1.32; p=0.0004).

Conclusion: The overall decrease in ACL tears, ACLR, and non-operative management found in this study is a reversal from trends reported in the literature from previous decades.

Level of evidence: 4 (Retrospective Case Series).

目的:本研究旨在描述 2010-2020 年前交叉韧带(ACL)撕裂、ACL 重建(ACLR)和 ACL 非手术治疗的发病率,并根据年龄、生理性别和夏尔森综合症指数(CCI)评分进行分层:利用 PearlDiver 国家保险理赔数据库进行了一项回顾性队列分析。使用 ICD-9/10 和 CPT 编码确定了 2010-2020 年间前交叉韧带撕裂、前交叉韧带重建和非手术治疗患者的队列。所有前交叉韧带撕裂患者均被纳入其中。根据年龄、性别和 CCI 对患者进行分层。通过复合年增长率 (CAGR) 分析、T 检验和 Cohen's d 检验来分析趋势和人口统计学变量:在研究期间的 931,186 例前交叉韧带撕裂中,196,589 例接受了前交叉韧带重建术,734,597 例接受了非手术治疗。前交叉韧带撕裂的累计发生率为每 10 万人年 75.19 例。2010-2020 年间,前交叉韧带撕裂、前交叉韧带置换术和非手术治疗的发病率略有下降,年均复合增长率分别为-3.43%、-3.55% 和-5.35%。与非手术治疗相比,前交叉韧带重建的相对使用率在 2010-2020 年间有所上升(CAGR 2.15%)。在前交叉韧带撕裂(22.31%)和前交叉韧带重建(30.97%)中,10-19 岁的患者占大多数。前交叉韧带撕裂患者略占多数(51.2%,pConclusion):本研究发现,前交叉韧带撕裂、前交叉韧带重建和非手术治疗的总体下降趋势与前几十年文献报道的趋势相反:4(回顾性病例系列)
{"title":"Decreasing Incidence of Anterior Cruciate Ligament Tears, Increasing Utilization of Anterior Cruciate Ligament Reconstruction in the United States from 2010-2020.","authors":"Victoria E Bergstein, Uzoma Ahiarakwe, Mark Haft, Henry Fox, Matthew J Best","doi":"10.1016/j.arthro.2024.08.018","DOIUrl":"https://doi.org/10.1016/j.arthro.2024.08.018","url":null,"abstract":"<p><strong>Purpose: </strong>The present study aimed to characterize the incidence of anterior cruciate ligament (ACL) tears, ACL reconstruction (ACLR), and ACL non-operative management from 2010-2020, stratifying by age, biological sex, and Charlson Comorbidity Index (CCI) score.</p><p><strong>Methods: </strong>A retrospective cohort analysis was performed using the PearlDiver national insurance claims database. Cohorts of patients with ACL tears, ACLR, and non-operative management were identified using ICD-9/10, and CPT codes between 2010-2020. All patients with ACL tears were included. Patients were stratified by age, sex, and CCI. Compound Annual Growth Rate (CAGR) analysis, T tests, and Cohen's d tests were performed to analyze trends and demographic variables.</p><p><strong>Results: </strong>Of 931,186 ACL tears during the study period, 196,589 were managed with ACLR and 734,597 were managed non-operatively. The cumulative incidence of ACL tears was 75.19 tears per 100,000 person-years. There was a modest decrease in the incidence of ACL tears, ACLR, and non-operative management from 2010-2020, with CAGRs of -3.43%, -3.55%, and -5.35%, respectively. The relative utilization of ACLR compared to non-operative management increased from 2010-2020 (CAGR 2.15%). Patients aged 10-19 accounted for the majority of ACL tears (22.31%) and ACLRs (30.97%). A slight majority of ACL tears (51.2%, p<0.001), ACLR (50.7%, p<0.001), and ACL tears with non-operative management (51.6%, p<0.001) occurred in female patients. The mean CCI of patients who underwent ACLR (mean=0.32; SD=0.77) was significantly lower than that of the general ACL tear cohort (mean=0.54; SD=1.19; p=0.005), and the non-operative management cohort (mean=0.64; SD 1.32; p=0.0004).</p><p><strong>Conclusion: </strong>The overall decrease in ACL tears, ACLR, and non-operative management found in this study is a reversal from trends reported in the literature from previous decades.</p><p><strong>Level of evidence: </strong>4 (Retrospective Case Series).</p>","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Studies with Direct Industry Affiliation are More Likely to Report Positive Results in Randomized Controlled Trials for Platelet-Rich Plasma Use in Rotator Cuff Pathology: A Systematic Review. 在将富血小板血浆用于治疗肩袖病变的随机对照试验中,与企业有直接关联的研究更有可能报告阳性结果:系统回顾。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-28 DOI: 10.1016/j.arthro.2024.08.025
Jacob L Kotlier, Amir Fathi, Eric Lin, Ryan D Freshman, Ioanna K Bolia, Joseph N Liu, Frank A Petrigliano

Purpose: To perform a systematic review to evaluate the effect of industry affiliation on the outcomes of randomized controlled trials (RCTs) for platelet-rich plasma (PRP) injections in rotator cuff tears.

Methods: PubMed, SPORTdiscus, and Scopus databases were searched from 2010 to the present for terms "rotator cuff" and "platelet-rich plasma." Inclusion criteria were RCTs comparing PRP to controls for treatment of rotator cuff tears and exclusion criteria were systematic reviews, meta-analyses, case reports, cohort studies, basic science studies, other level 3 and below studies, and studies not in English. Degree of industry affiliation was categorized into three groups: direct, indirect, and not affiliated. Direct affiliation required the study or its authors to receive financial support from the company manufacturing the devices used in the study to prepare or administer PRP. Indirect affiliation required financial association with a different company that produces or administers PRP than the one used in the study. Studies were classified as favorable if study outcomes achieved significance (p < 0.05) of PRP over the control, or analogous if there was no statistical significance between PRP and control. Data was analyzed using chi-squared and fisher's exact tests.

Results: Of the 47 studies selected for analysis, 8 (17.0%) had no direct industry affiliation, 9 (19.1%) indirect affiliation and 30 (63.8%) no industry affiliation. 22 (46.8%) studies reported favorable results with PRP compared to the control and 25 (53.2%) showed analogous results between PRP and control. Degree of industry affiliation was significantly associated with increased likelihood of reporting favorable study outcomes (p = 0.041). Directly affiliated studies had a significantly increased likelihood of reporting favorable results (p = 0.024) compared to indirectly affiliated.

Conclusions: Studies that used PRP produced by companies that directly fund the study or were financially affiliated with the authors were significantly more likely to report favorable results.

Level of evidence: Systematic review of Level I and II studies.

目的:对富血小板血浆(PRP)注射治疗肩袖撕裂的随机对照试验(RCT)结果的行业归属影响进行系统性回顾评估:方法:以 "肩袖 "和 "富血小板血浆 "为关键词,检索了 2010 年至今的 PubMed、SPORTdiscus 和 Scopus 数据库。纳入标准为将 PRP 与治疗肩袖撕裂的对照组进行比较的 RCT,排除标准为系统综述、荟萃分析、病例报告、队列研究、基础科学研究、其他 3 级及以下研究以及非英语研究。行业隶属程度分为三类:直接隶属、间接隶属和非隶属。直接隶属关系要求研究或其作者从研究中使用的制备或管理 PRP 设备的生产公司获得资金支持。间接隶属关系要求与研究中使用的 PRP 生产或管理公司有财务关联。如果研究结果显示 PRP 与对照组相比具有显著性(P < 0.05),则将研究归类为有利研究;如果 PRP 与对照组之间没有统计学意义,则将研究归类为类似研究。数据采用卡方检验和费氏精确检验进行分析:在被选中进行分析的 47 项研究中,8 项(17.0%)没有直接的行业隶属关系,9 项(19.1%)有间接隶属关系,30 项(63.8%)没有行业隶属关系。22项(46.8%)研究报告了 PRP 与对照组相比的良好结果,25 项(53.2%)研究报告了 PRP 与对照组之间的类似结果。行业隶属程度与报告有利研究结果的可能性增加显著相关(p = 0.041)。与间接关联研究相比,直接关联研究报告有利结果的可能性明显增加(p = 0.024):结论:使用由直接资助研究的公司或与作者有经济关联的公司生产的 PRP 的研究,报告有利结果的可能性明显增加:证据级别:I级和II级研究的系统综述。
{"title":"Studies with Direct Industry Affiliation are More Likely to Report Positive Results in Randomized Controlled Trials for Platelet-Rich Plasma Use in Rotator Cuff Pathology: A Systematic Review.","authors":"Jacob L Kotlier, Amir Fathi, Eric Lin, Ryan D Freshman, Ioanna K Bolia, Joseph N Liu, Frank A Petrigliano","doi":"10.1016/j.arthro.2024.08.025","DOIUrl":"https://doi.org/10.1016/j.arthro.2024.08.025","url":null,"abstract":"<p><strong>Purpose: </strong>To perform a systematic review to evaluate the effect of industry affiliation on the outcomes of randomized controlled trials (RCTs) for platelet-rich plasma (PRP) injections in rotator cuff tears.</p><p><strong>Methods: </strong>PubMed, SPORTdiscus, and Scopus databases were searched from 2010 to the present for terms \"rotator cuff\" and \"platelet-rich plasma.\" Inclusion criteria were RCTs comparing PRP to controls for treatment of rotator cuff tears and exclusion criteria were systematic reviews, meta-analyses, case reports, cohort studies, basic science studies, other level 3 and below studies, and studies not in English. Degree of industry affiliation was categorized into three groups: direct, indirect, and not affiliated. Direct affiliation required the study or its authors to receive financial support from the company manufacturing the devices used in the study to prepare or administer PRP. Indirect affiliation required financial association with a different company that produces or administers PRP than the one used in the study. Studies were classified as favorable if study outcomes achieved significance (p < 0.05) of PRP over the control, or analogous if there was no statistical significance between PRP and control. Data was analyzed using chi-squared and fisher's exact tests.</p><p><strong>Results: </strong>Of the 47 studies selected for analysis, 8 (17.0%) had no direct industry affiliation, 9 (19.1%) indirect affiliation and 30 (63.8%) no industry affiliation. 22 (46.8%) studies reported favorable results with PRP compared to the control and 25 (53.2%) showed analogous results between PRP and control. Degree of industry affiliation was significantly associated with increased likelihood of reporting favorable study outcomes (p = 0.041). Directly affiliated studies had a significantly increased likelihood of reporting favorable results (p = 0.024) compared to indirectly affiliated.</p><p><strong>Conclusions: </strong>Studies that used PRP produced by companies that directly fund the study or were financially affiliated with the authors were significantly more likely to report favorable results.</p><p><strong>Level of evidence: </strong>Systematic review of Level I and II studies.</p>","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115165","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Postoperative Effusion-Synovitis is Associated With Poor Clinical Outcomes in Patients With Femoroacetabular Impingement Syndrome: a Consecutive Magnetic Resonance Imaging Study. 股骨髋臼撞击综合征患者术后渗出-滑膜炎与临床疗效不佳有关:一项连续磁共振成像研究。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-28 DOI: 10.1016/j.arthro.2024.08.021
Yichuan Zhu, Hongli Wang, Kesheng Wu, Shuo Luan, Yanni Zhang, Guanying Gao, Yan Xu
<p><strong>Purpose: </strong>(1) to investigate the consecutive changes in effusion-synovitis following primary arthroscopic treatment for patients with femoroacetabular impingement syndrome (FAIS), and (2) to determine the effect of postoperative effusion-synovitis on clinical outcomes.</p><p><strong>Methods: </strong>Data between March 2021 and January 2022 was reviewed. Patients diagnosed with FAIS and undergoing hip arthroscopic treatment were included. Exclusion criteria were incomplete magnetic resonance imaging (MRI) data, prior history of hip surgery, labral reconstruction, and concomitant hip conditions. MRI (non-contrast 3.0 T) was performed preoperatively and 3, 6, 12-month postoperatively, and the measurement of the largest femoral neck fluid thickness (FTM) and cross-sectional area (CSA) of the effusion-synovitis were collected. Preoperative and a minimum of 2-year postoperative patient-reported outcome (PRO) scores including Visual Analog pain Scale (VAS), modified Harris Hip Score (mHHS), and international Hip Outcome Tool, 12-component form (iHOT-12) were collected and compared. Postoperative Tegner activity scale was also collected. The PROs and achievements of minimal clinically important difference (MCID) and patient acceptable symptom state (PASS) were compared between patients with and without postoperative effusion-synovitis. Multivariate linear regression analysis was performed to determine the effect of the effusion-synovitis size on PROs.</p><p><strong>Results: </strong>A total of 61 patients (61 hips) were included in the study. The 3-month postoperative FTM, CSA and grade of effusion-synovitis presented a significant increase compared to the preoperative values (all with P < .05). No significant differences were observed in the 6-month postoperative measurements compared to the preoperative values (all with P > .05). At the 12-month follow-up, although there was a significant decrease in all measurements compared to the preoperative values (all with P < .001), 39 patients (63.9%) still presented effusion-synovitis. Compared to the other 22 patients (36.1%) without effusion-synovitis, these patients presented inferior mHHS, iHOT-12 (all with P < .05), as well as lower achievement of PASS of mHHS (82.1% vs 100%, P = .035) and iHOT-12 (38.5% vs 81.8%, P = .001). The achievement of MCID of mHHS (79.5% vs 77.3%, P = .839) and iHOT-12 (89.7% vs 95.5%, P = .839) were comparable between patients with and without effusion-synovitis. The postoperative sagittal CSA (Beta = -.302, P = .039) were negatively related to mHHS in the regression analysis.</p><p><strong>Conclusion: </strong>After arthroscopic treatment for FAIS, the level of effusion-synovitis presented an initial increase, then followed by a subsequent decrease. Effusion-synovitis was significantly alleviated at 12 months compared to the preoperative level. Patients with postoperative effusion-synovitis had inferior clinical outcomes and lower achievement of PASS compare
目的:(1)研究股骨髋臼撞击综合征(FAIS)患者在接受初次关节镜治疗后积液-鞘膜炎的连续变化;(2)确定术后积液-鞘膜炎对临床疗效的影响:方法:回顾 2021 年 3 月至 2022 年 1 月期间的数据。方法:回顾 2021 年 3 月至 2022 年 1 月期间的数据,纳入确诊为 FAIS 并接受髋关节镜治疗的患者。排除标准为磁共振成像(MRI)数据不完整、既往髋关节手术史、唇瓣重建术以及并发髋关节疾病。术前、术后3个月、6个月、12个月进行核磁共振成像(非对比3.0 T),并收集股骨颈积液最大厚度(FTM)和积液-滑膜炎横截面积(CSA)的测量数据。收集并比较术前和术后至少两年的患者报告结果(PRO)评分,包括视觉模拟疼痛量表(VAS)、改良哈里斯髋关节评分(mHHS)和国际髋关节结果工具 12 要素表(iHOT-12)。此外,还收集了术后泰格纳活动量表。比较了有术后渗出-滑膜炎和无术后渗出-滑膜炎患者的PROs和最小临床重要差异(MCID)及患者可接受症状状态(PASS)。进行了多变量线性回归分析,以确定渗出-滑膜炎大小对PROs的影响:研究共纳入了61名患者(61个髋关节)。与术前相比,术后 3 个月的 FTM、CSA 和渗出-滑膜炎分级均有显著增加(均为 P <.05)。术后 6 个月的测量结果与术前相比无明显差异(均为 P > .05)。在 12 个月的随访中,虽然所有测量值与术前值相比都有显著下降(均为 P < .001),但仍有 39 名患者(63.9%)出现了渗出性滑膜炎。与其他 22 例(36.1%)无流出液-滑膜炎的患者相比,这些患者的 mHHS 和 iHOT-12 均较差(均为 P <.05),mHHS(82.1% vs 100%,P = .035)和 iHOT-12 (38.5% vs 81.8%,P = .001)的 PASS 值也较低。mHHS(79.5% vs 77.3%,P = .839)和iHOT-12(89.7% vs 95.5%,P = .839)的MCID达标率在有渗出-滑膜炎和无渗出-滑膜炎患者之间相当。在回归分析中,术后矢状面CSA(Beta = -.302, P = .039)与mHHS呈负相关:结论:关节镜治疗 FAIS 后,渗出-滑膜炎的水平最初会升高,随后会降低。与术前水平相比,12 个月后渗出性滑膜炎明显减轻。与没有渗出性滑膜炎的患者相比,术后有渗出性滑膜炎的患者临床疗效较差,PASS的达标率也较低:证据级别:IV级;回顾性病例系列。
{"title":"Postoperative Effusion-Synovitis is Associated With Poor Clinical Outcomes in Patients With Femoroacetabular Impingement Syndrome: a Consecutive Magnetic Resonance Imaging Study.","authors":"Yichuan Zhu, Hongli Wang, Kesheng Wu, Shuo Luan, Yanni Zhang, Guanying Gao, Yan Xu","doi":"10.1016/j.arthro.2024.08.021","DOIUrl":"https://doi.org/10.1016/j.arthro.2024.08.021","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Purpose: &lt;/strong&gt;(1) to investigate the consecutive changes in effusion-synovitis following primary arthroscopic treatment for patients with femoroacetabular impingement syndrome (FAIS), and (2) to determine the effect of postoperative effusion-synovitis on clinical outcomes.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Data between March 2021 and January 2022 was reviewed. Patients diagnosed with FAIS and undergoing hip arthroscopic treatment were included. Exclusion criteria were incomplete magnetic resonance imaging (MRI) data, prior history of hip surgery, labral reconstruction, and concomitant hip conditions. MRI (non-contrast 3.0 T) was performed preoperatively and 3, 6, 12-month postoperatively, and the measurement of the largest femoral neck fluid thickness (FTM) and cross-sectional area (CSA) of the effusion-synovitis were collected. Preoperative and a minimum of 2-year postoperative patient-reported outcome (PRO) scores including Visual Analog pain Scale (VAS), modified Harris Hip Score (mHHS), and international Hip Outcome Tool, 12-component form (iHOT-12) were collected and compared. Postoperative Tegner activity scale was also collected. The PROs and achievements of minimal clinically important difference (MCID) and patient acceptable symptom state (PASS) were compared between patients with and without postoperative effusion-synovitis. Multivariate linear regression analysis was performed to determine the effect of the effusion-synovitis size on PROs.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;A total of 61 patients (61 hips) were included in the study. The 3-month postoperative FTM, CSA and grade of effusion-synovitis presented a significant increase compared to the preoperative values (all with P &lt; .05). No significant differences were observed in the 6-month postoperative measurements compared to the preoperative values (all with P &gt; .05). At the 12-month follow-up, although there was a significant decrease in all measurements compared to the preoperative values (all with P &lt; .001), 39 patients (63.9%) still presented effusion-synovitis. Compared to the other 22 patients (36.1%) without effusion-synovitis, these patients presented inferior mHHS, iHOT-12 (all with P &lt; .05), as well as lower achievement of PASS of mHHS (82.1% vs 100%, P = .035) and iHOT-12 (38.5% vs 81.8%, P = .001). The achievement of MCID of mHHS (79.5% vs 77.3%, P = .839) and iHOT-12 (89.7% vs 95.5%, P = .839) were comparable between patients with and without effusion-synovitis. The postoperative sagittal CSA (Beta = -.302, P = .039) were negatively related to mHHS in the regression analysis.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;After arthroscopic treatment for FAIS, the level of effusion-synovitis presented an initial increase, then followed by a subsequent decrease. Effusion-synovitis was significantly alleviated at 12 months compared to the preoperative level. Patients with postoperative effusion-synovitis had inferior clinical outcomes and lower achievement of PASS compare","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
No Clinically Significant Differences in Outcomes after Anterior Cruciate Ligament Reconstruction When Comparing Quadriceps, Bone Patellar Tendon Bone, and Hamstring Autografts of 9mm or Greater. 比较股四头肌自体移植物、髌腱骨自体移植物和9毫米或更大的腘绳肌自体移植物,前交叉韧带重建术后的疗效无明显临床差异。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-27 DOI: 10.1016/j.arthro.2024.08.015
Giovanna Medina, Natalie A Lowenstein, Jamie E Collins, Elizabeth G Matzkin

Purpose: The purpose of this study was to determine if there are patient-reported outcome differences in bone-patellar-tendon-bone (BTB), quadriceps tendon (QT), and hamstring (HS) grafts of comparable size.

Methods: We performed a retrospective analysis of global registry data to include all patients that had an ACL reconstruction with BTB, QT, or HS autograft of at least 9mm diameter between 2010 and 2021 with complete 1- and 2-year outcome scores. We compared 1- and 2-year postoperative outcome scores (VAS, KOOS pain, MARS, VR-12) between BTB, QT and HS of the same size graft.

Results: 2318 subjects were included in the analysis and all graft types showed improved PROMs at 1- and 2-years postoperatively when compared to baseline. The KOOS pain score for the BTB group was significantly better than the HS (between-group difference = 2.71, p<0.01) and QT (between-group difference = 2.51, p<0.01) groups at 1-year, and the BTB group was better than HS (between-group difference = 1.88, p<0.01) at 2-years. However, the differences were small and not clinically meaningful. When comparing graft type there were no differences in the percentage of patients who reached MCID, or clinical scores VAS, MARS at 2-years follow-up.

Conclusion: There is no clinically meaningful difference in KOOS-pain, VR-12, VAS, and MARS at 1- and 2-years postoperatively in patients having anterior cruciate ligament reconstruction with BTB, HS or QT if graft size is at least 9mm in diameter.

Level of evidence: III (Retrospective Comparative Study).

目的:本研究的目的是确定骨-髌腱-骨(BTB)、股四头肌腱(QT)和腘绳肌(HS)移植物在大小相当的情况下是否存在患者报告的结果差异:我们对全球登记数据进行了回顾性分析,纳入了所有在 2010 年至 2021 年期间使用直径至少为 9 毫米的 BTB、QT 或 HS 自体移植物进行前交叉韧带重建且 1 年和 2 年结果评分完整的患者。我们比较了相同大小的 BTB、QT 和 HS 自体移植物的术后 1 年和 2 年结果评分(VAS、KOOS 疼痛、MARS、VR-12)。结果:2318 名受试者参与了分析,与基线相比,所有移植物类型在术后 1 年和 2 年的 PROMs 都有所改善。BTB 组的 KOOS 疼痛评分明显优于 HS 组(组间差异 = 2.71,p 结论:BTB 组与 HS 组的疼痛评分没有临床意义上的差异:如果移植物的直径至少为 9 毫米,则使用 BTB、HS 或 QT 进行前交叉韧带重建的患者在术后 1 年和 2 年的 KOOS 疼痛、VR-12、VAS 和 MARS 评分没有临床意义的差异:III(回顾性比较研究)。
{"title":"No Clinically Significant Differences in Outcomes after Anterior Cruciate Ligament Reconstruction When Comparing Quadriceps, Bone Patellar Tendon Bone, and Hamstring Autografts of 9mm or Greater.","authors":"Giovanna Medina, Natalie A Lowenstein, Jamie E Collins, Elizabeth G Matzkin","doi":"10.1016/j.arthro.2024.08.015","DOIUrl":"https://doi.org/10.1016/j.arthro.2024.08.015","url":null,"abstract":"<p><strong>Purpose: </strong>The purpose of this study was to determine if there are patient-reported outcome differences in bone-patellar-tendon-bone (BTB), quadriceps tendon (QT), and hamstring (HS) grafts of comparable size.</p><p><strong>Methods: </strong>We performed a retrospective analysis of global registry data to include all patients that had an ACL reconstruction with BTB, QT, or HS autograft of at least 9mm diameter between 2010 and 2021 with complete 1- and 2-year outcome scores. We compared 1- and 2-year postoperative outcome scores (VAS, KOOS pain, MARS, VR-12) between BTB, QT and HS of the same size graft.</p><p><strong>Results: </strong>2318 subjects were included in the analysis and all graft types showed improved PROMs at 1- and 2-years postoperatively when compared to baseline. The KOOS pain score for the BTB group was significantly better than the HS (between-group difference = 2.71, p<0.01) and QT (between-group difference = 2.51, p<0.01) groups at 1-year, and the BTB group was better than HS (between-group difference = 1.88, p<0.01) at 2-years. However, the differences were small and not clinically meaningful. When comparing graft type there were no differences in the percentage of patients who reached MCID, or clinical scores VAS, MARS at 2-years follow-up.</p><p><strong>Conclusion: </strong>There is no clinically meaningful difference in KOOS-pain, VR-12, VAS, and MARS at 1- and 2-years postoperatively in patients having anterior cruciate ligament reconstruction with BTB, HS or QT if graft size is at least 9mm in diameter.</p><p><strong>Level of evidence: </strong>III (Retrospective Comparative Study).</p>","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115145","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Posterior Tibial Slope Measurements of the Medial and Lateral Plateaus Vary Widely Between Magnetic Resonance Imaging And Computed Tomography. 磁共振成像和计算机断层扫描对胫骨内侧和外侧平台后斜坡的测量结果差别很大。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-27 DOI: 10.1016/j.arthro.2024.08.016
Deborah Wen, Hunter Bohlen, Scott Mahanty, Dean Wang

Purpose: This study aims to compare posterior tibial slope (PTS) measurements of the medial tibial plateau (MTP) and lateral tibial plateau (LTP) on magnetic resonance imaging (MRI) versus computed tomography (CT) to determine the agreement of measurement between imaging modalities.

Methods: Patients aged 15-65 years with concurrent MRI and CT imaging were initially included. Knees with significant arthrosis (Kellgren-Lawrence grade >2), proximal tibia fracture, or artifact obscuring visualization were excluded. Two independent raters measured PTS of the MTP and LTP on paired MRI and CT. Interrater and intrarater reliability were assessed using the intraclass correlation coefficient (ICC). Intermethod agreement was assessed using ICC and Bland-Altman analyses. An acceptable Bland-Altman limit of agreement (LOA) was set at ±2°, requiring 95% of measurement differences between imaging modalities to fall between ±2° for an acceptable level of agreement.

Results: 46 knees in 45 patients met final inclusion criteria. Interrater reliability was good for MRI (ICC 0.78-0.83) and moderate-to-good for CT (ICC 0.64-0.80) studies. Intrarater reliability was moderate-to-excellent (ICC 0.64-0.94). Intermethod agreement between MRI and CT was poor at the MTP (ICC 0.34-0.42) and moderate at the LTP (ICC 0.59-0.70). Bland-Altman analysis demonstrated high variability of PTS measurements between MRI and CT: 0.16° (95% LOA -6.10-6.41°) for MTP for Rater 1; 0.22° (95% LOA -5.01-5.45°) for LTP for Rater 1; -0.95° (95% LOA -7.22-5.33°) for MTP for Rater 2; -0.99° (95% LOA -6.48-4.85°) for LTP for Rater 2, with only 47.83 to 60.87% of measurement differences falling within the predetermined acceptable LOA of ±2°.

Conclusion: Although the interrater and intrarater reliability was moderate-to-excellent, the degree of agreement between PTS measurements on MRI and CT was highly variable at both medial and lateral plateaus. Although some variability may have been due to the study's limitations, PTS measurements at individual plateaus may not be interchangeable between MRI and CT.

Level of evidence: Level III, retrospective cohort study.

目的:本研究旨在比较磁共振成像(MRI)与计算机断层扫描(CT)对胫骨内侧平台(MTP)和胫骨外侧平台(LTP)的胫骨后斜坡(PTS)测量结果,以确定不同成像模式之间测量结果的一致性:首先纳入同时接受核磁共振成像和计算机断层扫描成像的 15-65 岁患者。排除有明显关节病(Kellgren-Lawrence分级>2)、胫骨近端骨折或伪影遮挡视野的膝关节。两名独立的评分员在成对的 MRI 和 CT 上测量 MTP 和 LTP 的 PTS。使用类内相关系数(ICC)评估评定者之间和评定者内部的可靠性。使用 ICC 和 Bland-Altman 分析评估方法间的一致性。可接受的布兰-阿尔特曼一致性界限(LOA)设定为±2°,要求成像模式之间95%的测量差异在±2°之间,这才是可接受的一致性水平:结果:45 名患者的 46 个膝关节符合最终纳入标准。MRI(ICC 0.78-0.83)和CT(ICC 0.64-0.80)研究的相互间可靠性分别为良好和中等至良好。研究者之间的可靠性为中等至优秀(ICC 0.64-0.94)。MRI 和 CT 的方法间一致性在 MTP 较差(ICC 0.34-0.42),在 LTP 中等(ICC 0.59-0.70)。Bland-Altman分析表明,MRI和CT的PTS测量结果之间存在很大差异:Rater 1的MTP测量结果为0.16°(95% LOA -6.10-6.41°);Rater 1的LTP测量结果为0.22°(95% LOA -5.01-5.45°);Rater 1的MTP测量结果为-0.95°(95% LOA -7.22-5.33°)。22-5.33°);评分者 2 的 LTP 为-0.99°(95% LOA -6.48-4.85°),只有 47.83% 至 60.87% 的测量差异在预定的可接受 LOA ±2° 范围内:结论:虽然评分者之间和评分者内部的可靠性为中等至优秀,但在内侧和外侧平台部,MRI 和 CT 的 PTS 测量值之间的一致性差异很大。虽然有些差异可能是由于研究的局限性造成的,但MRI和CT在个别平台部的PTS测量值可能无法互换:证据等级:III级,回顾性队列研究。
{"title":"Posterior Tibial Slope Measurements of the Medial and Lateral Plateaus Vary Widely Between Magnetic Resonance Imaging And Computed Tomography.","authors":"Deborah Wen, Hunter Bohlen, Scott Mahanty, Dean Wang","doi":"10.1016/j.arthro.2024.08.016","DOIUrl":"https://doi.org/10.1016/j.arthro.2024.08.016","url":null,"abstract":"<p><strong>Purpose: </strong>This study aims to compare posterior tibial slope (PTS) measurements of the medial tibial plateau (MTP) and lateral tibial plateau (LTP) on magnetic resonance imaging (MRI) versus computed tomography (CT) to determine the agreement of measurement between imaging modalities.</p><p><strong>Methods: </strong>Patients aged 15-65 years with concurrent MRI and CT imaging were initially included. Knees with significant arthrosis (Kellgren-Lawrence grade >2), proximal tibia fracture, or artifact obscuring visualization were excluded. Two independent raters measured PTS of the MTP and LTP on paired MRI and CT. Interrater and intrarater reliability were assessed using the intraclass correlation coefficient (ICC). Intermethod agreement was assessed using ICC and Bland-Altman analyses. An acceptable Bland-Altman limit of agreement (LOA) was set at ±2°, requiring 95% of measurement differences between imaging modalities to fall between ±2° for an acceptable level of agreement.</p><p><strong>Results: </strong>46 knees in 45 patients met final inclusion criteria. Interrater reliability was good for MRI (ICC 0.78-0.83) and moderate-to-good for CT (ICC 0.64-0.80) studies. Intrarater reliability was moderate-to-excellent (ICC 0.64-0.94). Intermethod agreement between MRI and CT was poor at the MTP (ICC 0.34-0.42) and moderate at the LTP (ICC 0.59-0.70). Bland-Altman analysis demonstrated high variability of PTS measurements between MRI and CT: 0.16° (95% LOA -6.10-6.41°) for MTP for Rater 1; 0.22° (95% LOA -5.01-5.45°) for LTP for Rater 1; -0.95° (95% LOA -7.22-5.33°) for MTP for Rater 2; -0.99° (95% LOA -6.48-4.85°) for LTP for Rater 2, with only 47.83 to 60.87% of measurement differences falling within the predetermined acceptable LOA of ±2°.</p><p><strong>Conclusion: </strong>Although the interrater and intrarater reliability was moderate-to-excellent, the degree of agreement between PTS measurements on MRI and CT was highly variable at both medial and lateral plateaus. Although some variability may have been due to the study's limitations, PTS measurements at individual plateaus may not be interchangeable between MRI and CT.</p><p><strong>Level of evidence: </strong>Level III, retrospective cohort study.</p>","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115161","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Patients With Dysplasia Achieve Similar Outcomes and Survivorship As Non-Dysplastic Patients 10 Years Following Hip Arthroscopy for Femoroacetabular Impingement. 髋关节镜治疗股骨髋臼撞击术后 10 年,发育不良患者的疗效和存活率与非发育不良患者相似。
IF 4.4 1区 医学 Q1 ORTHOPEDICS Pub Date : 2024-08-27 DOI: 10.1016/j.arthro.2024.08.022
Karen Mullins, David Filan, Patrick Carton

Purpose: To determine the long-term outcomes of hip arthroscopy (HA) for femoroacetabular impingement (FAI) in the presence of concomitant lateral rim dysplasia compared to a matched control group.

Methods: Patients undergoing HA between January 2009 and October 2013 with minimum 10-year follow up were reviewed. Inclusion criteria consisted of hip arthroscopy patients for FAI with evidence of lateral rim dysplasia (LCEA of <25o). Patients with lateral rim dysplasia, were matched to patients with a LCEA >30o, based on sex, Tonnis grade and age. Outcomes included survival (avoidance of total hip replacement {THR}), repeat-HA and patient-reported outcomes. Survivorship was assessed using a Kaplan-Meier curve and Log ranks test, while revision rates between groups were assessed using Chi Squared analysis. Between and within group analysis for PROs were conducted using Mann Whitney U and Wilcoxon signed ranks respectively. The proportion of cases achieving the patient acceptable symptom state (PASS) was compared between groups using Chi squared analysis.

Results: Forty-six dysplasia and 90 control cases were reported on. There was no statistical difference between groups for baseline metrics apart from the LCEA (p<0.001), Sharp angle (p<0.001) and Tonnis angle (p<0.001). By 10 years, 9% of dysplasia cases and 4% of control cases converted to THR. There was no statistical difference between groups for survival or revision rates. Both groups reported improvements in PROs and there was no difference between PRO scores at either timepoint. Excluding those undergoing THR, 84% and 83% of dysplasia and control cases respectively achieved PASS.

Conclusion: Hip arthroscopy for symptomatic femoroacetabular impingement (FAI) is a successful treatment in cases where dysplasia is present. Low complication rates, comparable outcomes to those without lateral rim dysplasia, and a high survivorship rate of 91% at minimum 10-year follow up are observed. Increasing Tonnis angle preoperatively may increase the risk of THR conversion.

Level of evidence: IV Retrospective Cohort Study.

目的:与配对对照组相比,确定伴有外侧缘发育不良的股骨髋臼撞击症(FAI)患者接受髋关节镜手术(HA)的长期疗效:对2009年1月至2013年10月期间接受HA手术且随访至少10年的患者进行回顾性研究。纳入标准包括有外侧缘发育不良证据(LCEA为o)的髋关节镜治疗FAI患者。根据性别、Tonnis分级和年龄,将外侧缘发育不良的患者与LCEA>30o的患者进行配对。结果包括存活率(避免全髋关节置换术{THR})、重复髋关节置换术(repeat-HA)和患者报告的结果。存活率采用卡普兰-梅耶曲线和对数秩检验进行评估,组间翻修率采用卡普兰-梅耶曲线和对数秩检验进行评估,组间翻修率采用卡普兰-梅耶曲线和对数秩检验进行评估。PROs的组间和组内分析分别采用Mann Whitney U和Wilcoxon符号秩进行。采用卡方分析比较了组间达到患者可接受症状状态(PASS)的病例比例:报告了 46 例发育不良病例和 90 例对照病例。结果:共报告了 46 例发育不良病例和 90 例对照病例,除 LCEA 外,各组间基线指标无统计学差异(p 结论:髋关节镜手术治疗髋关节症状的效果非常好:髋关节镜治疗有症状的股骨髋臼撞击症(FAI)在发育不良的病例中是一种成功的治疗方法。并发症发生率低,疗效与无外侧缘发育不良的病例相当,且在至少10年的随访中存活率高达91%。术前增大Tonnis角可能会增加THR转换的风险:IV 回顾性队列研究。
{"title":"Patients With Dysplasia Achieve Similar Outcomes and Survivorship As Non-Dysplastic Patients 10 Years Following Hip Arthroscopy for Femoroacetabular Impingement.","authors":"Karen Mullins, David Filan, Patrick Carton","doi":"10.1016/j.arthro.2024.08.022","DOIUrl":"https://doi.org/10.1016/j.arthro.2024.08.022","url":null,"abstract":"<p><strong>Purpose: </strong>To determine the long-term outcomes of hip arthroscopy (HA) for femoroacetabular impingement (FAI) in the presence of concomitant lateral rim dysplasia compared to a matched control group.</p><p><strong>Methods: </strong>Patients undergoing HA between January 2009 and October 2013 with minimum 10-year follow up were reviewed. Inclusion criteria consisted of hip arthroscopy patients for FAI with evidence of lateral rim dysplasia (LCEA of <25<sup>o</sup>). Patients with lateral rim dysplasia, were matched to patients with a LCEA >30<sup>o</sup>, based on sex, Tonnis grade and age. Outcomes included survival (avoidance of total hip replacement {THR}), repeat-HA and patient-reported outcomes. Survivorship was assessed using a Kaplan-Meier curve and Log ranks test, while revision rates between groups were assessed using Chi Squared analysis. Between and within group analysis for PROs were conducted using Mann Whitney U and Wilcoxon signed ranks respectively. The proportion of cases achieving the patient acceptable symptom state (PASS) was compared between groups using Chi squared analysis.</p><p><strong>Results: </strong>Forty-six dysplasia and 90 control cases were reported on. There was no statistical difference between groups for baseline metrics apart from the LCEA (p<0.001), Sharp angle (p<0.001) and Tonnis angle (p<0.001). By 10 years, 9% of dysplasia cases and 4% of control cases converted to THR. There was no statistical difference between groups for survival or revision rates. Both groups reported improvements in PROs and there was no difference between PRO scores at either timepoint. Excluding those undergoing THR, 84% and 83% of dysplasia and control cases respectively achieved PASS.</p><p><strong>Conclusion: </strong>Hip arthroscopy for symptomatic femoroacetabular impingement (FAI) is a successful treatment in cases where dysplasia is present. Low complication rates, comparable outcomes to those without lateral rim dysplasia, and a high survivorship rate of 91% at minimum 10-year follow up are observed. Increasing Tonnis angle preoperatively may increase the risk of THR conversion.</p><p><strong>Level of evidence: </strong>IV Retrospective Cohort Study.</p>","PeriodicalId":55459,"journal":{"name":"Arthroscopy-The Journal of Arthroscopic and Related Surgery","volume":null,"pages":null},"PeriodicalIF":4.4,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115147","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Arthroscopy-The Journal of Arthroscopic and Related Surgery
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