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Can surgeons predict how much compensation is needed to correct glenoid inclination in reverse shoulder arthroplasty? 外科医生能否预测在反向肩关节置换术中矫正肩关节倾斜需要多少补偿?
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.06.005
Mark Mouchantaf MD , Gregorio Secci MD , Manon Biegun MD , Mikael Chelli MD , Philipp Schippers MD , Pascal Boileau MD, PhD

Background

Correction of superior glenoid inclination, with a neutral reverse shoulder arthroplasty RSA angle, is crucial for achieving optimal outcomes and avoiding complications in RSA. This study aimed to assess the compensation distance (CD) required to correct the RSA angle without medialization. We hypothesized that measuring the RSA angle could provide a viable and simple method to estimate the extent of superior glenoid bone erosion and predict the CD needed to achieve neutral inclination of the baseplate during RSA.

Methods

We analyzed 101 preoperative computed tomography (CT) scans from 101 consecutive patients (mean age 76 ± 9 years) undergoing RSA for cuff tear arthropathy (84) or massive rotator cuff tear (MRCT = 17). Using validated 3-dimensional (3D) planning software, the baseplate was positioned inferiorly, tangent to the inferior glenoid rim (6 o'clock position), and adjusted to achieve neutral inclination (RSA angle = 0°). The CDs (the distance between the backside of the baseplate and the native glenoid) were measured at 2 levels: the superior edge of the baseplate (superior compensation distance [SCD]) and the center of the baseplate (CCD = central compensation distance). Univariate regression models were used to analyze the relationships between the RSA angle, glenoid inclination, and CDs. Predicted CDs for specific RSA angles were also calculated.

Results

The mean global glenoid inclination was 9° ± 6° (range: 0–27°), and the mean RSA angle was 15° ± 5.6° (range: 4–28°). There was a strong linear correlation between the RSA angle and the CDs: the higher the RSA angle, the greater the CDs. CCD had a correlation coefficient (ρ) of 0.83 (R2 = 0.688; P < .001), while SCD showed a stronger correlation with ρ = 0.93 (R2 = 0.874; P < .001). Subgroup analysis revealed no statistically significant differences between baseplate diameters (25 mm vs 29 mm) in their relationship with the RSA angle (interaction terms: P = .291 for CCD and P = .500 for SCD). Regression models demonstrated that SCD is approximately half the RSA angle: 5 mm for 10°, 7.5 mm for 15°, 10 mm for 20°, and 12.5 mm for 25°.

Conclusion

By measuring the RSA angle, surgeons can estimate the SCD (ie, the thickness of bone graft or metal augment) required to achieve neutral inclination of the baseplate. The value of SCD is approximately half the RSA angle value and is independent of the baseplate diameter (25 mm vs 29 mm).
背景:采用中性反向肩关节置换术RSA角度矫正上盂倾斜,对于获得最佳结果和避免RSA并发症至关重要。本研究的目的是评估补偿距离(CD)需要纠正的RSA角度没有中介。我们假设测量RSA角度可以提供一种可行和简单的方法来估计上盂骨侵蚀的程度,并预测在RSA期间实现基板中性倾斜所需的CD。方法对101例连续接受肩袖撕裂性关节病(84例)或大面积肩袖撕裂(17例)行RSA手术的患者(平均年龄76±9岁)的101例术前CT扫描结果进行分析。使用经过验证的三维(3D)规划软件,将底板置于下方,与下盂缘相切(6点钟位置),并调整至中性倾斜(RSA角= 0°)。在2个水平测量CDs(基底后侧与关节盂间的距离):基底上边缘(上部补偿距离[SCD])和基底中心(CCD =中心补偿距离)。采用单变量回归模型分析RSA角度、关节盂倾角和cd之间的关系。还计算了特定RSA角度下的预测CDs。结果关节盂整体倾角平均值为9°±6°(范围:0 ~ 27°),RSA角度平均值为15°±5.6°(范围:4 ~ 28°)。RSA角度和cd之间有很强的线性相关性:RSA角度越高,cd越大。CCD的相关系数(ρ)为0.83 (R2 = 0.688; P < .001), SCD的相关系数(ρ)为0.93 (R2 = 0.874; P < .001)。亚组分析显示,基板直径(25 mm vs 29 mm)与RSA角度的关系无统计学差异(相互作用项:CCD P = 0.291, SCD P = 0.500)。回归模型表明,SCD大约是RSA角的一半:10°为5 mm, 15°为7.5 mm, 20°为10 mm, 25°为12.5 mm。结论通过测量RSA角度,外科医生可以估计达到中性基底倾斜所需的SCD(即植骨或金属增强物的厚度)。SCD值大约是RSA角值的一半,与底板直径(25mm vs 29mm)无关。
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引用次数: 0
Study on stability of resurfacing total elbow arthroplasty: a cadaver study 全肘关节表面置换术稳定性的尸体研究
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.06.002
Hiromasa Wakita MD , Yusuke Matsuura MD, PhD , Yohei Shimada MD, PhD , Shinji Taniguchi MD, PhD , Takane Suzuki MD, PhD , Mitsuyasu Iwasawa MD, PhD , Yoshihiko Tabira MD, PhD , Yuichi Nagase MD, PhD , Koji Fujita MD, PhD , Jun Hirose MD, PhD , Yasuhiro Ozasa MD, PhD , Seiji Ohtori MD, PhD (Professor)

Background

Although excellent clinical results have been reported for resurfacing total elbow arthroplasty, also known as K-elbow, there are still reports of complications due to postoperative instability of the elbow joint. Appropriate implant selection, proper implant placement, and establishment of soft tissue repair methods are necessary to prevent complications, but these requirements have not fully undergone scientific verification. Surgical techniques such as the extent of bone resection of the distal humerus and soft tissue repair methods require technical skill, but the extent to which these techniques contribute to joint stability is unclear. This study aimed to investigate the factors contributing to elbow joint stability after elbow arthroplasty using K-elbow and fresh-frozen cadavers.

Methods

Six upper limbs of fresh-frozen cadavers were used in this study. The resurfaced unlinked-type elbow prosthesis (K-elbow) was placed using a posterior approach. The distal humerus was resected at 0 mm, 2 mm, and 4 mm on the articular surface, and the artificial elbow joint was installed. Anchors were inserted into the olecranon, the biceps tuberosity, and the coronoid process to simulate the triceps, biceps, and brachialis muscles, and traction forces of 20 N, 10 N, and 10 N, respectively, were applied. In addition, a digital angle meter was attached to the forearm, and varus and valgus stress tests were performed at all elbow joint ranges of motion using forearm weight to evaluate the spacer effect. Furthermore, a stress test was performed for each soft tissue repair process at the 2-mm bone resection site to evaluate the stability of the procedure.

Results

As the extent of bone resection of the distal humerus increased, the extension angle tended to improve. Furthermore, as the extent of bone resection increased, elbow joint instability due to varus and valgus stress increased. Soft tissue repair did not affect elbow instability due to varus stress, but it tended to reduce elbow instability due to valgus stress. In addition, the triceps fascia suture reduced the external rotation angle of the elbow joint in response to valgus stress.

Conclusion

This cadaver study demonstrated that bone resection of the distal humerus significantly affects both the range of motion and stability of the elbow joint after K-elbow arthroplasty. The triceps fascia suture was identified as the most critical soft tissue repair procedure for ensuring elbow joint stability, particularly against valgus stress.
背景:尽管有报道称全肘关节置换术(也称为k -肘关节)有良好的临床效果,但仍有报道称由于肘关节术后不稳定而引起并发症。选择合适的种植体,选择合适的种植体,建立软组织修复方法是预防并发症的必要条件,但这些要求还没有得到充分的科学验证。手术技术,如肱骨远端骨切除的程度和软组织修复方法需要技术技能,但这些技术对关节稳定性的贡献程度尚不清楚。本研究旨在探讨影响k -肘关节置换术和新鲜冷冻尸体置换术后肘关节稳定性的因素。方法采用6例新鲜冷冻尸体上肢标本进行实验研究。采用后路放置表面无连接型肘关节假体(k -肘关节)。在关节面0 mm、2 mm、4 mm处切除肱骨远端,安装人工肘关节。将锚钉插入鹰嘴、二头肌粗隆和冠突,模拟肱三头肌、二头肌和肱肌,分别施加20牛、10牛和10牛的牵引力。此外,将一个数字角度计连接到前臂,并使用前臂重量在所有肘关节运动范围内进行内翻和外翻应力测试,以评估间隔器的效果。此外,在2毫米骨切除部位对每个软组织修复过程进行应力测试,以评估手术的稳定性。结果随着肱骨远端骨切除程度的增加,肱骨外展角有改善的趋势。此外,随着骨切除程度的增加,肘关节因内翻和外翻应力而不稳定增加。软组织修复对肘关节内翻应力不稳定无影响,但对肘关节外翻应力不稳定有减轻作用。此外,三头肌筋膜缝合可降低肘关节外翻应力下的外旋角度。结论本尸体研究表明,肱骨远端骨切除对k型肘关节置换术后肘关节的活动范围和稳定性有显著影响。三头肌筋膜缝合被认为是最关键的软组织修复程序,以确保肘关节的稳定性,特别是对抗外翻应力。
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引用次数: 0
Is anatomical radial head arthroplasty more effective for acute or for chronic traumatic lesions? A retrospective cohort study 解剖性桡骨头置换术对急性或慢性创伤性病变更有效?回顾性队列研究
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.05.004
Giuseppe Bardellini MD , Biagio Abate MD , Clelia Rota MD , Andrea Pautasso MD , Andrea Celli MD , Luigi Celli MD

Background

Radial head arthroplasty (RHA) can achieve favorable outcomes in patients with radial head (RH) and neck fractures. Notably, it has proved effective in treating both acute fractures and traumatic injuries, where delayed treatment can lead to secondary degenerative changes, soft tissue contractures, and altered biomechanics. Yet, the outcomes of RHA performed in these two groups have never been compared. Anatomical RHA is designed to replicate the native RH geometry, providing stable elbow kinematics and correct load distribution. This study compares the clinical and radiographic results of anatomical RHA in patients with acute lesions and chronic post-traumatic conditions.

Methods

We reviewed the data of 52 consecutive patients who were managed by anatomical RHA (Anatomical Radial Head; Acumed, Hillsboro, OR, USA) for acute RH fracture or chronic sequelae of traumatic injury at our institution. Assessments included range of motion and stability using the Mayo Elbow Performance Score, Quick Disabilities of the Arm, Shoulder, and Hand score, Visual Analog Scale score, and overall patient satisfaction. Radiographs were analyzed for signs of loosening, periarticular ossification, and degenerative changes of the ulnohumeral joint and capitellum.

Results

At a mean follow-up of 70 months, 23 (44%) patients had achieved excellent outcomes with a Mayo Elbow Performance Score greater than 90 points and a mean Quick Disabilities of the Arm, Shoulder, and Hand score of 7 (range, 0-18.2). The mean range of motion was 111° in flexion–extension (range, 70°-140°) and 144° in pronation–supination (range, 100°-160°). There were 13 (25%) complications requiring secondary surgery in the first 29 months. The implant revision rate was 7.7%. At the last follow-up, 42/52 patients (81%) were satisfied with their outcome. The clinical and radiological outcomes between the groups were not significantly different.

Conclusion

The anatomical RH system is a viable option for acute and chronic trauma patients. Despite these encouraging results, prospective studies with larger sample sizes are required to validate them.
背景桡骨头置换术(RHA)对桡骨头(RH)和颈部骨折患者可获得良好的治疗效果。值得注意的是,它已被证明对治疗急性骨折和外伤性损伤有效,其中延迟治疗可能导致继发性退行性改变,软组织挛缩和生物力学改变。然而,这两组RHA的结果从未进行过比较。解剖RHA的设计是为了复制原始的RH几何形状,提供稳定的肘关节运动学和正确的负荷分布。本研究比较了急性病变和慢性创伤后疾病患者解剖性RHA的临床和影像学结果。方法我们回顾了52例连续在我院接受解剖桡骨头(解剖桡骨头;Acumed, Hillsboro, OR, USA)治疗急性桡骨头骨折或创伤性损伤慢性后遗症的患者的资料。评估包括运动范围和稳定性,使用Mayo肘部表现评分,手臂、肩膀和手的快速残疾评分,视觉模拟量表评分和总体患者满意度。x线片分析松动、关节周围骨化、肱骨尺关节和肱骨小头退行性改变的迹象。结果在平均70个月的随访中,23例(44%)患者获得了良好的结果,Mayo肘关节功能评分大于90分,手臂、肩膀和手的平均快速残疾评分为7分(范围0-18.2)。屈伸关节的平均活动范围为111°(范围,70°-140°),旋前关节的平均活动范围为144°(范围,100°-160°)。在前29个月有13例(25%)并发症需要二次手术。种植体翻修率为7.7%。末次随访时,52例患者中有42例(81%)对治疗结果满意。两组间临床及影像学结果无显著差异。结论解剖RH系统是治疗急慢性创伤患者的可行选择。尽管这些令人鼓舞的结果,需要更大样本量的前瞻性研究来验证它们。
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引用次数: 0
Glucagon-like peptide-1 receptor agonist use is not associated with reduced postoperative complications in obese patients after total shoulder arthroplasty 胰高血糖素样肽-1受体激动剂的使用与全肩关节置换术后肥胖患者术后并发症的减少无关
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.05.006
Mark F. Megerian MD , Rajiv P. Reddy MD , Billy I. Kim MD , Alexander E. White MD , Miles Miller BS, MPH , Lawrence V. Gulotta MD , Michael C. Fu MD , Samuel A. Taylor MD

Background

The use of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) has increased substantially in the orthopedic patient population, necessitating investigation into their perioperative safety profile. Limited studies have investigated the use of GLP-1 RAs in the setting of total shoulder arthroplasty (TSA). Therefore, the purpose of this study was to evaluate the 90-day and 2-year postoperative outcomes in patients with body mass index >30 kg/m2 who received GLP-1 RA medication prior to primary TSA (reverse TSA or anatomic total shoulder arthroplasty [aTSA]) compared to matched controls.

Methods

A national administrative claims database was retrospectively reviewed from 2010 to 2022. Obese patients (body mass index >30 kg/m2) with GLP-1 RA use within the 90 days preceding their TSA were identified and compared to a propensity score matched cohort without GLP-1 RA use (1:4 ratio). The database was queried using International Classification of Diseases, ninth and tenth revisions, and Current Procedural Terminology codes to identify the study cohort. Outcomes were compared via univariate analysis and included 90-day postoperative medical and surgical complications, 90-day readmissions, and 2-year surgical complications. P values were adjusted for multiple comparisons using the Bonferroni method.

Results

Ninety-day outcomes were obtained for 518 GLP-1 RA users and 2,070 matched nonusers and 2-year outcomes were available for 359 GLP-1 RA users and 1,436 matched nonusers. In the 90-day and 2-year postoperative period, there were no differences in the rates of medical complications, surgical complications, readmissions, or reoperations between GLP-1 RA users and nonusers. GLP-1 RA users experienced a higher rate of acute kidney injury in the 90-day postoperative period (14.1% vs. 3.7%) and a decreased rate of rotator cuff tear (8% vs. 13.6%) at 2 years as compared to nonusers, though these trends were not significant.

Conclusion

There was no difference in rate of medical or surgical complications after primary TSA (aTSA and reverse TSA) in obese patients taking GLP-1 RA medication as compared to matched controls. There were nonsignificant trends toward increased acute kidney injury rate at 90 days following TSA and decreased rotator cuff tear rate at 2 years following aTSA in GLP-1 RA users.
背景胰高血糖素样肽-1受体激动剂(GLP-1 RAs)在骨科患者群体中的使用大幅增加,有必要对其围手术期安全性进行调查。有限的研究调查了GLP-1 RAs在全肩关节置换术(TSA)中的应用。因此,本研究的目的是评估体重指数为30 kg/m2的患者在首次TSA(反向TSA或解剖性全肩关节置换术[aTSA])前接受GLP-1 RA药物治疗的90天和2年的术后结果。方法回顾性分析2010 - 2022年国家行政索赔数据库。确定在TSA前90天内使用GLP-1 RA的肥胖患者(体重指数>;30 kg/m2),并将其与倾向评分匹配的未使用GLP-1 RA的队列进行比较(1:4比例)。使用《国际疾病分类》第九版和第十版以及现行程序术语代码对数据库进行查询,以确定研究队列。结果通过单因素分析进行比较,包括术后90天的内科和外科并发症、90天的再入院和2年的手术并发症。使用Bonferroni方法调整P值以进行多重比较。结果518名GLP-1 RA使用者和2070名匹配的非使用者获得了90天的结果,359名GLP-1 RA使用者和1436名匹配的非使用者获得了2年的结果。在术后90天和2年的时间里,GLP-1 RA使用者和非使用者的医疗并发症、手术并发症、再入院或再手术率没有差异。与非GLP-1 RA使用者相比,GLP-1 RA使用者在术后90天内急性肾损伤的发生率更高(14.1%对3.7%),2年内肩袖撕裂的发生率降低(8%对13.6%),尽管这些趋势并不显著。结论肥胖患者服用GLP-1类RA药物后原发性TSA (aTSA和反向TSA)的内科和外科并发症发生率与对照组相比无差异。GLP-1 RA使用者在TSA后90天急性肾损伤发生率增加,在aTSA后2年肩袖撕裂率下降的趋势不显著。
{"title":"Glucagon-like peptide-1 receptor agonist use is not associated with reduced postoperative complications in obese patients after total shoulder arthroplasty","authors":"Mark F. Megerian MD ,&nbsp;Rajiv P. Reddy MD ,&nbsp;Billy I. Kim MD ,&nbsp;Alexander E. White MD ,&nbsp;Miles Miller BS, MPH ,&nbsp;Lawrence V. Gulotta MD ,&nbsp;Michael C. Fu MD ,&nbsp;Samuel A. Taylor MD","doi":"10.1053/j.sart.2025.05.006","DOIUrl":"10.1053/j.sart.2025.05.006","url":null,"abstract":"<div><h3>Background</h3><div>The use of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) has increased substantially in the orthopedic patient population, necessitating investigation into their perioperative safety profile. Limited studies have investigated the use of GLP-1 RAs in the setting of total shoulder arthroplasty (TSA). Therefore, the purpose of this study was to evaluate the 90-day and 2-year postoperative outcomes in patients with body mass index &gt;30 kg/m<sup>2</sup> who received GLP-1 RA medication prior to primary TSA (reverse TSA or anatomic total shoulder arthroplasty [aTSA]) compared to matched controls.</div></div><div><h3>Methods</h3><div>A national administrative claims database was retrospectively reviewed from 2010 to 2022. Obese patients (body mass index &gt;30 kg/m<sup>2</sup>) with GLP-1 RA use within the 90 days preceding their TSA were identified and compared to a propensity score matched cohort without GLP-1 RA use (1:4 ratio). The database was queried using International Classification of Diseases, ninth and tenth revisions, and Current Procedural Terminology codes to identify the study cohort. Outcomes were compared via univariate analysis and included 90-day postoperative medical and surgical complications, 90-day readmissions, and 2-year surgical complications. <em>P</em> values were adjusted for multiple comparisons using the Bonferroni method.</div></div><div><h3>Results</h3><div>Ninety-day outcomes were obtained for 518 GLP-1 RA users and 2,070 matched nonusers and 2-year outcomes were available for 359 GLP-1 RA users and 1,436 matched nonusers. In the 90-day and 2-year postoperative period, there were no differences in the rates of medical complications, surgical complications, readmissions, or reoperations between GLP-1 RA users and nonusers. GLP-1 RA users experienced a higher rate of acute kidney injury in the 90-day postoperative period (14.1% vs. 3.7%) and a decreased rate of rotator cuff tear (8% vs. 13.6%) at 2 years as compared to nonusers, though these trends were not significant.</div></div><div><h3>Conclusion</h3><div>There was no difference in rate of medical or surgical complications after primary TSA (aTSA and reverse TSA) in obese patients taking GLP-1 RA medication as compared to matched controls. There were nonsignificant trends toward increased acute kidney injury rate at 90 days following TSA and decreased rotator cuff tear rate at 2 years following aTSA in GLP-1 RA users.</div></div>","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 591-598"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685857","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of baseplate augmentation on humeral offset and clinical outcomes in reverse shoulder arthroplasty 反向肩关节置换术中钢板增强对肱骨偏移的影响及临床结果
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.06.003
Matthew Como BS, Rajiv P. Reddy MD, MS, Fritz Steuer MD, Ehab M. Nazzal MD, Romano Sebastiani MD, Confidence Njoku-Austin MD, Anya Singh-Varma MD, Warren P. Austin BS, Albert Lin MD

Background

Metallic augmented baseplates have increasingly been used to correct glenoid deformity during reverse shoulder arthroplasty (RSA). However, few studies have examined their clinical outcomes and effect on humeral offset. The purpose of this study was to evaluate clinical outcomes and change in humeral offset from preoperative anatomic baseline of RSA performed with an augmented baseplate (aRSA) to RSA without baseplate augmentation. We hypothesized that aRSA would yield similar outcomes and complication rates to non-aRSA but result in a greater increase in global lateralization from preoperative to postoperative measurements.

Methods

This was a retrospective review of consecutive patients who underwent RSA between 2015 and 2021 at a single institution with a minimum 12-month follow-up. RSA performed with an augmented baseplate (aRSA) was compared to RSA performed without augmentation (control). Baseline demographics, and pre/postoperative humeral offset and glenoid version and inclination were obtained. Pre/postoperative range of motion (ROM) and patient reported outcomes including visual analog scale (VAS), subjective shoulder value (SSV), and American Shoulder and Elbow Surgeons scores, and complications were recorded. Independent sample t-tests and Chi-squared and Fisher's exact test were utilized for continuous and binary variables, respectively. Statistical significance was set at P < .05.

Results

There were 58 patients in the aRSA cohort and 86 patients in the control cohort with similar mean follow-up times (22.16 vs. 19.65 months; P = .373). On average, the aRSA cohort had a greater absolute difference between preoperative and postoperative humeral offset than the control cohort (7.4 ± 4.2 vs. 5.9 ± 3.9 mm; P = .041). In both cohorts, all patient-reported outcomes and ROM parameters were significantly improved from preoperative baselines. At final follow-up, the aRSA cohort had slightly greater pain scores (1.2 ± 2.3 vs. 0.5 ± 1.0; P = .038) than the control cohort but SSV and American Shoulder and Elbow Surgeons were similar. Similar ROM was achieved between the cohorts. The control cohort had significantly greater improvements in VAS (7.0 ± 2.3 vs. 5.8 ± 3.1; P = .050) and SSV (59.3 ± 25.5 vs. 44.5 ± 22.4; P < .001) compared to the aRSA cohort. There were no differences in complications.

Conclusion

RSA with metallic augmented baseplates achieves comparable overall clinical outcomes to non-aRSA at 12-month follow-up, with low revision and complication rates. However, the control cohort demonstrated greater gains in SSV and VAS, whereas the augmented group exhibited greater changes in humeral offset.
背景金属增强基板越来越多地用于矫正肩关节置换(RSA)期间的关节盂畸形。然而,很少有研究检查其临床结果和对肱骨偏移的影响。本研究的目的是评估临床结果和肱骨偏移量的变化,从术前解剖基线的RSA进行增强基板(aRSA)到RSA没有增强基板。我们假设aRSA会产生与非aRSA相似的结果和并发症发生率,但从术前到术后测量,aRSA会导致更大的整体偏侧增加。方法:本研究对2015年至2021年间在一家机构接受RSA治疗的连续患者进行回顾性研究,随访时间至少为12个月。将增强基板(aRSA)的RSA与未增强基板(对照组)的RSA进行比较。基线人口统计数据,以及术前/术后肱骨偏移和肩关节内倾角。术前/术后活动范围(ROM)和患者报告的结果包括视觉模拟评分(VAS)、主观肩关节值(SSV)和美国肩关节外科医生评分,并记录并发症。对连续变量和二元变量分别采用独立样本t检验和卡方检验和Fisher精确检验。差异有统计学意义,P < 0.05。结果aRSA组58例,对照组86例,平均随访时间相似(22.16个月对19.65个月,P = 0.373)。平均而言,aRSA组术前和术后肱骨偏移的绝对差异大于对照组(7.4±4.2 vs 5.9±3.9 mm; P = 0.041)。在这两个队列中,所有患者报告的结果和ROM参数均较术前基线显著改善。在最后随访时,aRSA组的疼痛评分略高于对照组(1.2±2.3 vs. 0.5±1.0;P = 0.038),但SSV组和American Shoulder and肘部外科医生的疼痛评分相似。在队列之间获得了类似的ROM。与aRSA组相比,对照组VAS(7.0±2.3比5.8±3.1,P = 0.050)和SSV(59.3±25.5比44.5±22.4,P < 0.001)的改善明显更大。并发症发生率无差异。结论金属增强基板rsa在12个月的随访中获得了与非arsa相当的总体临床结果,翻修率低,并发症发生率低。然而,对照组在SSV和VAS方面表现出更大的增益,而增强组在肱骨偏移方面表现出更大的变化。
{"title":"Effect of baseplate augmentation on humeral offset and clinical outcomes in reverse shoulder arthroplasty","authors":"Matthew Como BS,&nbsp;Rajiv P. Reddy MD, MS,&nbsp;Fritz Steuer MD,&nbsp;Ehab M. Nazzal MD,&nbsp;Romano Sebastiani MD,&nbsp;Confidence Njoku-Austin MD,&nbsp;Anya Singh-Varma MD,&nbsp;Warren P. Austin BS,&nbsp;Albert Lin MD","doi":"10.1053/j.sart.2025.06.003","DOIUrl":"10.1053/j.sart.2025.06.003","url":null,"abstract":"<div><h3>Background</h3><div>Metallic augmented baseplates have increasingly been used to correct glenoid deformity during reverse shoulder arthroplasty (RSA). However, few studies have examined their clinical outcomes and effect on humeral offset. The purpose of this study was to evaluate clinical outcomes and change in humeral offset from preoperative anatomic baseline of RSA performed with an augmented baseplate (aRSA) to RSA without baseplate augmentation. We hypothesized that aRSA would yield similar outcomes and complication rates to non-aRSA but result in a greater increase in global lateralization from preoperative to postoperative measurements.</div></div><div><h3>Methods</h3><div>This was a retrospective review of consecutive patients who underwent RSA between 2015 and 2021 at a single institution with a minimum 12-month follow-up. RSA performed with an augmented baseplate (aRSA) was compared to RSA performed without augmentation (control). Baseline demographics, and pre/postoperative humeral offset and glenoid version and inclination were obtained. Pre/postoperative range of motion (ROM) and patient reported outcomes including visual analog scale (VAS), subjective shoulder value (SSV), and American Shoulder and Elbow Surgeons scores, and complications were recorded. Independent sample <em>t</em>-tests and Chi-squared and Fisher's exact test were utilized for continuous and binary variables, respectively. Statistical significance was set at <em>P</em> &lt; .05.</div></div><div><h3>Results</h3><div>There were 58 patients in the aRSA cohort and 86 patients in the control cohort with similar mean follow-up times (22.16 vs. 19.65 months; <em>P</em> = .373). On average, the aRSA cohort had a greater absolute difference between preoperative and postoperative humeral offset than the control cohort (7.4 ± 4.2 vs. 5.9 ± 3.9 mm; <em>P</em> = .041). In both cohorts, all patient-reported outcomes and ROM parameters were significantly improved from preoperative baselines. At final follow-up, the aRSA cohort had slightly greater pain scores (1.2 ± 2.3 vs. 0.5 ± 1.0; <em>P</em> = .038) than the control cohort but SSV and American Shoulder and Elbow Surgeons were similar. Similar ROM was achieved between the cohorts. The control cohort had significantly greater improvements in VAS (7.0 ± 2.3 vs. 5.8 ± 3.1; <em>P</em> = .050) and SSV (59.3 ± 25.5 vs. 44.5 ± 22.4; <em>P</em> &lt; .001) compared to the aRSA cohort. There were no differences in complications.</div></div><div><h3>Conclusion</h3><div>RSA with metallic augmented baseplates achieves comparable overall clinical outcomes to non-aRSA at 12-month follow-up, with low revision and complication rates. However, the control cohort demonstrated greater gains in SSV and VAS, whereas the augmented group exhibited greater changes in humeral offset.</div></div>","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 620-627"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685812","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Single-stage revision of periprosthetic shoulder arthroplasty infection is more cost effective than two-stage revision: a break-even cost analysis 单阶段翻修假体周围肩关节置换术感染比两阶段翻修更具成本效益:盈亏平衡成本分析
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.04.012
Mathangi J. Sridharan MD, Al-Hassan Dajani BS, Andrew R. Jensen MD, MBE

Background

Periprosthetic joint infections (PJIs) of the shoulder carry significant financial and functional burdens. No consensus exists on whether a single-stage or two-stage revision surgery protocol is optimal for treatment of shoulder PJI. In this study, we performed a break-even cost analysis to guide clinical decision making between performing single- vs. two-stage revision surgery in treating shoulder PJI.

Methods

Institutional cost data were collected for all primary and revision shoulder arthroplasties performed at a single institution from January 2018 to June 2023. A break-even cost analysis equation was used to solve for the reinfection rate at which the cost of a single-stage revision surgery protocol breaks even with the cost of a two-stage revision surgery protocol. Cost variables were derived from institutional data. Rates of complications, both infectious and aseptic, were derived from published studies.

Results

The modified equation demonstrated that a 58% reinfection rate of a single-stage revision protocol would be necessary to financially break-even with a two-stage revision surgery protocol. Rates of complications were varied across published ranges to account for clinical variability and demonstrate the breadth of the equation. These variations again yielded break-even rates between 54% and 62%.

Conclusion

The reinfection rate at which a single-stage revision surgery for shoulder PJI breaks even with a two-stage revision is approximately 58%, which far exceeds the reinfection rate seen in clinical practice with single-stage revisions. Thus, strictly from a cost perspective, single-stage revision arthroplasty for PJI after shoulder arthroplasty is more cost-effective than a two-stage revision.
肩部假体周围关节感染(PJIs)带来了巨大的经济和功能负担。单期或两期翻修手术方案是治疗肩部PJI的最佳方案,目前尚无共识。在这项研究中,我们进行了盈亏平衡成本分析,以指导临床决策在单阶段翻修手术与两阶段翻修手术治疗肩部PJI之间的选择。方法收集2018年1月至2023年6月在同一家机构进行的所有原发性和翻修性肩关节置换术的机构成本数据。采用盈亏平衡成本分析方程求解单阶段翻修手术方案成本与两阶段翻修手术方案成本盈亏平衡时的再感染率。成本变量来源于机构数据。感染性和无菌性并发症的发生率来源于已发表的研究。结果修正后的方程表明,单阶段翻修方案的再感染率为58%,需要两阶段翻修手术方案的经济收支平衡。并发症的发生率在公布的范围内有所不同,以说明临床变异性,并证明方程的广度。这些差异再次产生了54%至62%之间的盈亏平衡率。结论肩关节PJI单期翻修与两期翻修相平衡的再感染率约为58%,远高于临床单期翻修的再感染率。因此,严格从成本角度来看,肩关节置换术后PJI单期翻修关节置换术比两期翻修更具成本效益。
{"title":"Single-stage revision of periprosthetic shoulder arthroplasty infection is more cost effective than two-stage revision: a break-even cost analysis","authors":"Mathangi J. Sridharan MD,&nbsp;Al-Hassan Dajani BS,&nbsp;Andrew R. Jensen MD, MBE","doi":"10.1053/j.sart.2025.04.012","DOIUrl":"10.1053/j.sart.2025.04.012","url":null,"abstract":"<div><h3>Background</h3><div><span>Periprosthetic joint infections (PJIs) of the shoulder carry significant financial and functional burdens. No consensus exists on whether a single-stage or two-stage revision surgery protocol is optimal for treatment of shoulder PJI. In this study, we performed a break-even </span>cost analysis to guide clinical decision making between performing single- vs. two-stage revision surgery in treating shoulder PJI.</div></div><div><h3>Methods</h3><div>Institutional cost data were collected for all primary and revision shoulder arthroplasties performed at a single institution from January 2018 to June 2023. A break-even cost analysis equation was used to solve for the reinfection rate at which the cost of a single-stage revision surgery protocol breaks even with the cost of a two-stage revision surgery protocol. Cost variables were derived from institutional data. Rates of complications, both infectious and aseptic, were derived from published studies.</div></div><div><h3>Results</h3><div>The modified equation demonstrated that a 58% reinfection rate of a single-stage revision protocol would be necessary to financially break-even with a two-stage revision surgery protocol. Rates of complications were varied across published ranges to account for clinical variability and demonstrate the breadth of the equation. These variations again yielded break-even rates between 54% and 62%.</div></div><div><h3>Conclusion</h3><div>The reinfection rate at which a single-stage revision surgery for shoulder PJI breaks even with a two-stage revision is approximately 58%, which far exceeds the reinfection rate seen in clinical practice with single-stage revisions. Thus, strictly from a cost perspective, single-stage revision arthroplasty for PJI after shoulder arthroplasty is more cost-effective than a two-stage revision.</div></div>","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 547-552"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison of internal rotation strength after reverse total shoulder arthroplasty without subscapularis repair: lateralized vs. medialized prosthesis design 无肩胛下肌修复的反向全肩关节置换术后内旋强度的比较:外侧与内侧假体设计
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.06.006
Chang Hee Baek MD, Chaemoon Lim MD, Jung Gon Kim MD, Bo Taek Kim MD, Seung Jin Kim MS

Background

Reverse total shoulder arthroplasty (rTSA) is an effective treatment option for rotator cuff tear arthropathy. It was reported that lateralized rTSA showed no significant difference whether subscapularis (SSC) was repaired or not. On the other hand, SSC repair has been associated with a lower rate of dislocation and improved internal rotation (IR) in medialized rTSA. To date, no study has directly compared lateralized and medialized rTSA without SSC repair, aiming to clarify the specific effect of lateralized rTSA in this context. The purpose of this retrospective clinical comparative study is to compare the clinical outcomes focused on IR strength between medialized and lateralized rTSA without SSC repair.

Methods

This study included patients who underwent rTSA between January 2014 and December 2016, in whom SSC repair was not performed. Among them, patients who received medialized rTSA prosthesis were classified into medialized rTSA group, while those who received lateralized rTSA prosthesis were classified into lateralized rTSA group. Clinical outcomes were assessed using pain scores, patient-reported outcome measures (PROMs), active range of motion, active range of motion strength, and toileting ability. Radiologic outcomes were evaluated as the presence of acromial stress fractures, scapular notching, and loosening of the implanted components on plain radiographs. For comparison of mid-term outcomes, clinical and radiologic outcomes between the two groups were compared at 5 years postoperatively.

Results

Fifty-six patients of medialized rTSA group and 58 patients of lateralized rTSA group were included for study population. The clinical results were significantly improved in both groups. There was no significant difference in visual analog scale score and patient-reported outcome measures. Although both groups showed significant improvements in rage of motion, the lateralized rTSA group had significantly better mean postoperative IR at the back (6.8 ± 1.8 vs. 5.7 ± 1.7, P = .001). Although there was no significant difference in the ability to perform toileting activities between the two groups, 69.6% of medialized rTSA group and 69.0% of lateralized rTSA group had a difficulty. Moreover, there was no significant improvement of external rotation strength and IR strength in both groups.

Conclusion

Both medialized and lateralized rTSA without SSC repair had no improvement of IR strength, and showed significant difficulty in IR related toileting activities. As a result, lateralized rTSA prosthesis had no advantage in IR strength and IR-related toileting activities in case of SSC nonrepair.
背景:逆行全肩关节置换术(rTSA)是治疗肩袖撕裂性关节病的有效方法。据报道,侧化rTSA在肩胛下肌(SSC)是否修复方面无显著差异。另一方面,SSC修复与中位rTSA中较低的脱位率和改善的内旋(IR)有关。迄今为止,还没有研究直接比较没有SSC修复的侧化rTSA和中介化rTSA,旨在阐明侧化rTSA在这种情况下的具体作用。本回顾性临床比较研究的目的是比较未进行SSC修复的中枢性和偏侧性rTSA的临床结果。方法本研究纳入2014年1月至2016年12月期间未行SSC修复术的rTSA患者。其中,接受中位rTSA假体的患者分为中位rTSA组,接受偏侧rTSA假体的患者分为偏侧rTSA组。临床结果通过疼痛评分、患者报告的结果测量(PROMs)、活动范围、活动范围强度和如厕能力进行评估。影像学结果评估为平片上肩峰应力性骨折、肩胛骨缺口和植入物松动的存在。为了比较中期预后,比较两组术后5年的临床和影像学结果。结果纳入中位rTSA组56例,侧位rTSA组58例。两组临床疗效均有明显改善。视觉模拟量表评分和患者报告的结果测量没有显著差异。虽然两组的运动范围均有显著改善,但侧边rTSA组术后背部平均IR明显更好(6.8±1.8比5.7±1.7,P = 0.001)。虽然两组在如厕能力上无显著差异,但中位rTSA组69.6%和侧位rTSA组69.0%存在如厕困难。此外,两组外旋强度和IR强度均无明显改善。结论未进行SSC修复的中位化和侧位化rTSA均未改善IR强度,且在IR相关的如厕活动中表现出明显困难。结果表明,在SSC未修复的情况下,侧侧rTSA假体在IR强度和IR相关的如厕活动方面没有优势。
{"title":"Comparison of internal rotation strength after reverse total shoulder arthroplasty without subscapularis repair: lateralized vs. medialized prosthesis design","authors":"Chang Hee Baek MD,&nbsp;Chaemoon Lim MD,&nbsp;Jung Gon Kim MD,&nbsp;Bo Taek Kim MD,&nbsp;Seung Jin Kim MS","doi":"10.1053/j.sart.2025.06.006","DOIUrl":"10.1053/j.sart.2025.06.006","url":null,"abstract":"<div><h3>Background</h3><div>Reverse total shoulder arthroplasty (rTSA) is an effective treatment option for rotator cuff tear arthropathy. It was reported that lateralized rTSA showed no significant difference whether subscapularis (SSC) was repaired or not. On the other hand, SSC repair has been associated with a lower rate of dislocation and improved internal rotation (IR) in medialized rTSA. To date, no study has directly compared lateralized and medialized rTSA without SSC repair, aiming to clarify the specific effect of lateralized rTSA in this context. The purpose of this retrospective clinical comparative study is to compare the clinical outcomes focused on IR strength between medialized and lateralized rTSA without SSC repair.</div></div><div><h3>Methods</h3><div>This study included patients who underwent rTSA between January 2014 and December 2016, in whom SSC repair was not performed. Among them, patients who received medialized rTSA prosthesis were classified into medialized rTSA group, while those who received lateralized rTSA prosthesis were classified into lateralized rTSA group. Clinical outcomes were assessed using pain scores, patient-reported outcome measures (PROMs), active range of motion, active range of motion strength, and toileting ability. Radiologic outcomes were evaluated as the presence of acromial stress fractures, scapular notching, and loosening of the implanted components on plain radiographs. For comparison of mid-term outcomes, clinical and radiologic outcomes between the two groups were compared at 5 years postoperatively.</div></div><div><h3>Results</h3><div>Fifty-six patients of medialized rTSA group and 58 patients of lateralized rTSA group were included for study population. The clinical results were significantly improved in both groups. There was no significant difference in visual analog scale score and patient-reported outcome measures. Although both groups showed significant improvements in rage of motion, the lateralized rTSA group had significantly better mean postoperative IR at the back (6.8 ± 1.8 vs. 5.7 ± 1.7, <em>P</em> = .001). Although there was no significant difference in the ability to perform toileting activities between the two groups, 69.6% of medialized rTSA group and 69.0% of lateralized rTSA group had a difficulty. Moreover, there was no significant improvement of external rotation strength and IR strength in both groups.</div></div><div><h3>Conclusion</h3><div>Both medialized and lateralized rTSA without SSC repair had no improvement of IR strength, and showed significant difficulty in IR related toileting activities. As a result, lateralized rTSA prosthesis had no advantage in IR strength and IR-related toileting activities in case of SSC nonrepair.</div></div>","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 645-653"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685813","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rate of improvement following reverse shoulder arthroplasty: a comparison of primary and revision reverse shoulder arthroplasty 肩关节置换术后的改善率:初次肩关节置换术和翻修肩关节置换术的比较
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.07.001
Ali A. Mohamed BS, MS , Devin Q. John MD , Garrett R. Jackson MD , Aghdas Movassaghi BS , Diego J.L. Lima MD , Howard Routman DO , Vani J. Sabesan MD
<div><h3>Background</h3><div>As the incidence of reverse shoulder arthroplasty (rTSA) increases, so do the expected revision rates. Despite this, little is known about postoperative recovery rates following revision rTSA. This study aimed to determine the rate of improvement for patients who underwent revision rTSA compared to patients who underwent primary rTSA.</div></div><div><h3>Methods</h3><div>A retrospective review of 476 patients who underwent rTSA by a single fellowship-trained shoulder surgeon was conducted. In this cohort, 386 patients underwent primary rTSA and 90 patients underwent revision rTSA. Demographics, range of motion, and outcome scores—including the Simple Shoulder Test, Constant–Murray Score, University of California at Los Angeles Shoulder Score, Shoulder Pain and Disability Index (SPADI), Shoulder Arthroplasty Smart score, and American Shoulder and Elbow Surgeons scores—were collected preoperatively and postoperatively for both cohorts. Outcome scores were collected at 6 weeks, 3 months, 6 months, 12 months, and 24 months. The rate of improvement in each outcome measure was quantified and compared between primary rTSA and revision rTSA, and final follow-up scores were compared between the two groups.</div></div><div><h3>Results</h3><div>A total of 476 patients (primary rTSA = 386 patients, revision rTSA = 90 patients) were included in the final analysis. Preoperatively, no baseline differences were observed in patient-reported outcome measures or functional scores between the revision and primary rTSA groups. Postoperatively, both groups demonstrated improvements in outcome scores from their preoperative assessments. When postoperative outcomes were evaluated over time, revision rTSA patients showed lower scores than the primary rTSA cohort as early as 3 months in SPADI (46.6 vs. 58.6; <em>P</em> = .03) and 6 months for forward elevation (126.3 vs. 141; <em>P</em> = .04). Between 12 and 24 months, analysis revealed no significant changes in improvement trends for both revision rTSA and primary rTSA groups (<em>P</em> > .05), indicating that recovery stabilizes after the first year. However, postoperative outcomes collected at final follow-up visit demonstrated that the revision rTSA cohort achieved less favorable results compared to the primary rTSA group. Specifically, the revision rTSA group did not achieve the same level of improvement in Simple Shoulder Test (6.8 vs. 9.2, d = 0.67, <em>P</em> < .01), University of California at Los Angeles (25.2 vs. 29.8, d = 0.60, <em>P</em> < .01), American Shoulder and Elbow Surgeons (62.6 vs. 77, d = 0.61, <em>P</em> = .01), SPADI (50 vs. 30.8, d = 0.60, <em>P</em> = .01), and Shoulder Arthroplasty Smart (63.2 vs. 71.8, d = 0.53, <em>P</em> = .02) as observed in the primary rTSA cohort.</div></div><div><h3>Conclusion</h3><div>Although revision rTSA shows an early recovery pace comparable to primary rTSA, it plateaus at lower absolute patient-reported outcome measure and
背景:随着逆行肩关节置换术(rTSA)发生率的增加,预期翻修率也在增加。尽管如此,对rTSA改良后的术后恢复率知之甚少。本研究旨在确定接受改良rTSA的患者与接受原发性rTSA的患者的改善率。方法回顾性分析476例接受肩外科医生rTSA治疗的患者。在该队列中,386例患者接受了原发性rTSA, 90例患者接受了改良rTSA。术前和术后收集两组人群的人口统计数据、活动范围和结果评分,包括简单肩关节测试、Constant-Murray评分、加州大学洛杉矶分校肩关节评分、肩关节疼痛和残疾指数(SPADI)、肩关节置换术智能评分和美国肩关节外科医生评分。在6周、3个月、6个月、12个月和24个月时收集结果评分。每个结果测量的改善率被量化,并在初次rTSA和修订rTSA之间进行比较,并在两组之间比较最终随访评分。结果共纳入476例患者,其中原发性rTSA = 386例,改进性rTSA = 90例。术前,在改良组和原rTSA组之间,没有观察到患者报告的结果测量或功能评分的基线差异。术后,两组的预后评分均较术前评估有所改善。随着时间的推移评估术后结果,改良rTSA患者早在SPADI的3个月(46.6比58.6,P = 0.03)和前抬高的6个月(126.3比141,P = 0.04)的评分就低于原始rTSA队列。在12至24个月之间,分析显示,改良rTSA组和初级rTSA组的改善趋势没有显著变化(P > 0.05),表明第一年之后恢复稳定。然而,在最后的随访中收集的术后结果表明,与最初的rTSA组相比,修订后的rTSA组取得了较差的结果。修订rTSA集团特别没有达到同样水平的提高简单的肩膀测试(6.8 vs 9.2 d = 0.67, P & lt; . 01),加州大学洛杉矶分校(25.2 vs 29.8 d = 0.60, P & lt; . 01),美国的肩部和肘部的外科医生(62.6 vs 77 d = 0.61, P = . 01), SPADI(50和30.8 d = 0.60, P = . 01),和肩膀关节成形术智能(63.2 vs 71.8 d = 0.53, P = .02点)作为主要观察rTSA队列。结论:虽然改良rTSA的早期恢复速度与原发性rTSA相当,但在6个月后,它在较低的患者报告的绝对结果测量值和活动范围值上达到稳定。外科医生应利用这些数据,在患者咨询和随访期间为长期功能恢复和疼痛缓解设定切合实际的期望。
{"title":"Rate of improvement following reverse shoulder arthroplasty: a comparison of primary and revision reverse shoulder arthroplasty","authors":"Ali A. Mohamed BS, MS ,&nbsp;Devin Q. John MD ,&nbsp;Garrett R. Jackson MD ,&nbsp;Aghdas Movassaghi BS ,&nbsp;Diego J.L. Lima MD ,&nbsp;Howard Routman DO ,&nbsp;Vani J. Sabesan MD","doi":"10.1053/j.sart.2025.07.001","DOIUrl":"10.1053/j.sart.2025.07.001","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;div&gt;As the incidence of reverse shoulder arthroplasty (rTSA) increases, so do the expected revision rates. Despite this, little is known about postoperative recovery rates following revision rTSA. This study aimed to determine the rate of improvement for patients who underwent revision rTSA compared to patients who underwent primary rTSA.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;div&gt;A retrospective review of 476 patients who underwent rTSA by a single fellowship-trained shoulder surgeon was conducted. In this cohort, 386 patients underwent primary rTSA and 90 patients underwent revision rTSA. Demographics, range of motion, and outcome scores—including the Simple Shoulder Test, Constant–Murray Score, University of California at Los Angeles Shoulder Score, Shoulder Pain and Disability Index (SPADI), Shoulder Arthroplasty Smart score, and American Shoulder and Elbow Surgeons scores—were collected preoperatively and postoperatively for both cohorts. Outcome scores were collected at 6 weeks, 3 months, 6 months, 12 months, and 24 months. The rate of improvement in each outcome measure was quantified and compared between primary rTSA and revision rTSA, and final follow-up scores were compared between the two groups.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;A total of 476 patients (primary rTSA = 386 patients, revision rTSA = 90 patients) were included in the final analysis. Preoperatively, no baseline differences were observed in patient-reported outcome measures or functional scores between the revision and primary rTSA groups. Postoperatively, both groups demonstrated improvements in outcome scores from their preoperative assessments. When postoperative outcomes were evaluated over time, revision rTSA patients showed lower scores than the primary rTSA cohort as early as 3 months in SPADI (46.6 vs. 58.6; &lt;em&gt;P&lt;/em&gt; = .03) and 6 months for forward elevation (126.3 vs. 141; &lt;em&gt;P&lt;/em&gt; = .04). Between 12 and 24 months, analysis revealed no significant changes in improvement trends for both revision rTSA and primary rTSA groups (&lt;em&gt;P&lt;/em&gt; &gt; .05), indicating that recovery stabilizes after the first year. However, postoperative outcomes collected at final follow-up visit demonstrated that the revision rTSA cohort achieved less favorable results compared to the primary rTSA group. Specifically, the revision rTSA group did not achieve the same level of improvement in Simple Shoulder Test (6.8 vs. 9.2, d = 0.67, &lt;em&gt;P&lt;/em&gt; &lt; .01), University of California at Los Angeles (25.2 vs. 29.8, d = 0.60, &lt;em&gt;P&lt;/em&gt; &lt; .01), American Shoulder and Elbow Surgeons (62.6 vs. 77, d = 0.61, &lt;em&gt;P&lt;/em&gt; = .01), SPADI (50 vs. 30.8, d = 0.60, &lt;em&gt;P&lt;/em&gt; = .01), and Shoulder Arthroplasty Smart (63.2 vs. 71.8, d = 0.53, &lt;em&gt;P&lt;/em&gt; = .02) as observed in the primary rTSA cohort.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;div&gt;Although revision rTSA shows an early recovery pace comparable to primary rTSA, it plateaus at lower absolute patient-reported outcome measure and ","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 662-668"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685807","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Does social deprivation status affect the complication profile among patients undergoing total shoulder arthroplasty? A matched cohort analysis 社会剥夺状态是否影响全肩关节置换术患者的并发症?配对队列分析
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.06.004
Akhil Katakam MD , Tej Joshi MD , Tuckerman Jones MD , Daniella Ogilvie MD , Amanda Azer MD , Sefy A. Paulose MD , Eitan M. Kohan MD , Francis G. Alberta MD

Background

Employment, living status, and income level are a few examples of social determinants of health (SDoH). Patients determined to be suffering in any of these SDoH have been previously identified as being socially deprived, which has been associated with numerous poor outcomes following total shoulder arthroplasty (TSA). This study aimed to further clarify the relationship between SDoH and medical and operative outcomes following TSA. We hypothesized that patients classified as being socially deprived would suffer higher medical and orthopedic complications compared to patients without a history of social deprivation.

Methods

A retrospective cohort study was conducted using the TriNetX Research Network database to identify patients with a history of social deprivation who underwent TSA. These patients were propensity score–matched to TSA patients without this exposure using several demographic and comorbidity-related variables. Outcomes assessed included multiple surgery-related, implant-related, and medical-related complications. Kaplan–Meier survival analysis and chi-square testing were used to evaluate outcomes, with results reported as hazard ratios (HRs), 95% confidence intervals, and P values, with significance set at P < .05.

Results

A total of 2,808 propensity-matched patients (1,404 in each cohort) were analyzed. Within 30 days of surgery, hospital readmissions (HR 1.74, P < .001) and emergency department (ED) visits (HR 1.83, P < .001) were higher in the social deprivation group. Rates of acute kidney injury (AKI) (HR 2.115, P = .004) and urinary tract infections (UTIs) (HR 2.70, P < .001) were also higher within 30 days in the social deprivation group. Dislocation rate was also higher in socially deprived group at 30 days (HR 11.09, P = .004). Readmissions, ED visits, AKI, and UTI rates were also higher at 90 days in this cohort. There was no association with higher adverse postoperative outcomes at 1 year, 2 year, and any time in the socially deprived group.

Conclusion

Patients who were classified as socially deprived were associated with more readmissions, ED visits, a higher dislocation rate, and medical complications, including UTI and AKI especially in the short-term postoperative period compared to those who were not classified in this category. This study indicates a link between SDoH and patient postoperative outcomes in the setting of TSA, underscoring the need for surgeon awareness regarding these factors when treating patients.
就业、生活状况和收入水平是健康(SDoH)社会决定因素的几个例子。被确定患有这些SDoH的患者以前被确定为社会剥夺,这与全肩关节置换术(TSA)后的许多不良结果有关。本研究旨在进一步阐明SDoH与TSA后医疗和手术结果之间的关系。我们假设,与没有社会剥夺史的患者相比,被归类为社会剥夺的患者会遭受更高的医疗和骨科并发症。方法使用TriNetX研究网络数据库进行回顾性队列研究,以确定有社会剥夺史的TSA患者。使用几个人口统计学和合并症相关变量,这些患者的倾向评分与没有这种暴露的TSA患者相匹配。评估的结果包括多种手术相关、植入物相关和医学相关并发症。Kaplan-Meier生存分析和卡方检验用于评价结果,以风险比(hr)、95%置信区间和P值报告结果,显著性设置为P <; 05。结果共分析2808例倾向匹配患者(每组1404例)。在手术30天内,社会剥夺组的住院率(HR 1.74, P < 0.001)和急诊科(ED)就诊率(HR 1.83, P < 0.001)更高。社会剥夺组30天内的急性肾损伤(AKI)发生率(HR 2.115, P = 0.004)和尿路感染(uti)发生率(HR 2.70, P < 0.001)也较高。社会剥夺组30天脱位率较高(HR 11.09, P = 0.004)。在该队列中,90天的再入院率、急诊科就诊率、AKI率和UTI率也较高。在社会剥夺组中,术后1年、2年和任何时间的不良预后均无较高的相关性。结论与非社会剥夺患者相比,社会剥夺患者的再入院率、急诊科就诊率、脱位率以及包括UTI和AKI在内的医疗并发症(尤其是在术后短期内)均较高。该研究表明,在TSA环境下,SDoH与患者术后结果之间存在联系,强调了外科医生在治疗患者时对这些因素的认识的必要性。
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引用次数: 0
Perioperative glucagon-like peptide-1 receptor agonist use is not associated with increased complications in obese patients undergoing total shoulder arthroplasty: a propensity-matched large database study 围手术期使用胰高血糖素样肽-1受体激动剂与接受全肩关节置换术的肥胖患者并发症增加无关:一项倾向匹配的大型数据库研究
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.06.001
Argen Omurzakov BA , Arsen M. Omurzakov BA , Rajiv P. Reddy MD , Mark Megerian MD , Alexander E. White MD , Miles Miller BS, MPH , John M. Apostolakos MD, MPH , Samuel A. Taylor MD

Background

Obesity significantly impacts outcomes in shoulder arthroplasty, leading to higher complication rates. Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are increasingly prescribed for weight loss and glycemic control, but their perioperative safety in shoulder arthroplasty remains unclear.

Methods

This retrospective cohort study used the TriNetX Network to analyze obese patients (body mass index [BMI] >30 kg/m2) undergoing anatomic or reverse shoulder arthroplasty across 67 health care organizations. Patients were categorized by preoperative GLP-1 RA use and matched 1:1 using propensity scores to balance the cohorts based on demographic variables and comorbid conditions such as age, race, ethnicity, BMI, diabetes, and hypertension. Outcomes assessed at 90 days and 1 year included revision surgery, emergency department visits, readmission, deep vein thrombosis (DVT), pulmonary embolism (PE), acute kidney injury, prosthetic joint stiffness, postoperative rotator cuff tear, mechanical complications, periprosthetic fracture, prosthetic joint infection, surgical site infection, airway aspiration, cardiac arrest, transfusion, and prosthetic joint dislocation.

Results

After matching, there were no statistically significant differences between GLP-1 RA users (n = 2,132) and controls at both time points of comparison. Rates of DVT, PE, revision surgery, prosthetic joint stiffness, readmission, emergency department utilization, airway aspiration, and other complications were comparable between groups.

Conclusion

Perioperative GLP-1 RA use prior to primary shoulder arthroplasty in obese patients (BMI >30 kg/m2) was not associated with increased risk of DVT, PE, airway aspiration, or other postoperative complications at 90-day or 1-year follow-up. These findings support the perioperative safety of GLP-1 RAs in obese patients.
背景:肥胖显著影响肩关节置换术的结果,导致更高的并发症发生率。胰高血糖素样肽-1受体激动剂(GLP-1 RAs)越来越多地被用于减肥和血糖控制,但其在肩关节置换术中的围手术期安全性尚不清楚。方法本回顾性队列研究采用TriNetX网络对67家医疗机构接受解剖或反向肩关节置换术的肥胖患者(体重指数[BMI] >;30 kg/m2)进行分析。根据术前GLP-1 RA使用情况对患者进行分类,并根据人口统计学变量和合并症(如年龄、种族、民族、BMI、糖尿病和高血压)使用倾向评分进行1:1匹配,以平衡队列。在90天和1年内评估的结果包括翻修手术、急诊就诊、再入院、深静脉血栓形成(DVT)、肺栓塞(PE)、急性肾损伤、假体关节僵硬、术后肩袖撕裂、机械并发症、假体周围骨折、假体关节感染、手术部位感染、气道误吸、心脏骤停、输血和假体关节脱位。结果匹配后,GLP-1 RA使用者(n = 2132)与对照组在两个时间点的比较无统计学差异。DVT、PE、翻修手术、假体关节僵硬、再入院率、急诊科使用率、气道误吸率和其他并发症在两组之间具有可比性。结论肥胖患者(BMI≤30 kg/m2)在初次肩关节置换术前围手术期使用GLP-1 RA与90天或1年随访时DVT、PE、气道误吸或其他术后并发症的风险增加无关。这些发现支持GLP-1 RAs在肥胖患者围手术期的安全性。
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Seminars in Arthroplasty
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