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Are orthopedic shoulder and elbow surgeons at risk for noise-induced hearing loss? 骨科肩部和肘部外科医生有噪音性听力损失的风险吗?
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.05.007
Matthew J. Schultz DO , William T. DiCiurcio III DO , Stephanie A. Kwan DO , Jeffrey C. Lynch DO , Dennis DeBernardis DO , Luke Austin MD

Background

Exposure to noise levels greater than 85 decibels [dB] is associated with increased incidence of hearing loss. However, the risk that occupational noise exposure poses to orthopedic shoulder and elbow (S&E) surgeons is poorly understood. This study aims to (1) quantify the noise exposure of S&E surgeons in the operating room to determine if they are exposed to harmful noise levels and (2) identify which procedures pose the greatest risk of noise-induced hearing loss.

Methods

Intraoperative audio recordings were collected during S&E procedures via a wearable microphone worn under standard sterile surgical garb. S&E procedures were characterized as open reduction and internal fixation, arthroscopic soft tissue procedures, open soft tissue procedures, and arthroplasty. The highest sound pressure level (maximum dB levels [MDLs]) and the average dB level projected over an 8-h period (time-weighted average) were reported. The percentage of allowable daily noise dose was reported as “dose,” and the measured dose projected for over 8-h was reported as “projected dose.”

Results

We collected 116 recordings consisting of 65 arthroplasties, 5 open reduction and internal fixation, 11 open soft tissue procedures (distal bicep tendon repairs), and 35 arthroscopic soft tissue procedures. The average MDL was greater than the average control MDL for all S&E procedures and ranged from 88.7 to 112.6 dB. Shoulder arthroplasty had the highest average dose (1.4%), projected dose (8.4%), and time-weighted average (64.6 dB).

Conclusion

All recorded procedure types exposed surgeons to MDLs greater than 85 dB. Shoulder arthroplasty demonstrated the highest average exposure to harmful doses of noise and appears to pose the greatest risk for occupational noise exposure. Strategies should be considered to minimize the risk of noise-induced hearing loss amongst surgeons.
暴露在大于85分贝(dB)的噪音水平中与听力损失的发生率增加有关。然而,职业性噪声暴露对肩关节和肘关节整形外科医生的风险了解甚少。本研究旨在(1)量化S&;E外科医生在手术室中的噪音暴露,以确定他们是否暴露于有害的噪音水平;(2)确定哪些手术对噪音性听力损失的风险最大。方法在标准无菌手术服下佩戴可穿戴式麦克风,收集手术中录音。S&;E手术的特点是切开复位和内固定、关节镜下软组织手术、切开软组织手术和关节成形术。报告了最高声压级(maximum dB levels [MDLs])和8 h内预测的平均dB级(时间加权平均值)。每日允许噪声剂量的百分比报告为“剂量”,预计超过8小时的测量剂量报告为“预计剂量”。结果我们收集了116例记录,包括65例关节置换术,5例切开复位内固定,11例切开软组织手术(肱二头肌远端肌腱修复)和35例关节镜下软组织手术。所有S&;E程序的平均MDL大于平均对照MDL,范围从88.7到112.6 dB。肩关节置换术的平均剂量最高(1.4%),预计剂量最高(8.4%),时间加权平均值最高(64.6 dB)。结论所有记录的手术类型对外科医生的mdl均大于85 dB。肩关节置换术显示出最高的有害噪声平均暴露剂量,似乎对职业性噪声暴露构成最大的风险。外科医生应考虑将噪声性听力损失风险降至最低的策略。
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引用次数: 0
Anatomic total shoulder arthroplasty using a short humeral stem and a non-augmented, minimally cemented all-polyethylene glenoid: minimum 2-year outcome and predictors of clinical failure 解剖性全肩关节置换术采用短肱骨柄和非增长、最低限度骨水泥全聚乙烯肩关节:至少2年的结果和临床失败的预测因素
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.04.007
Brian P. Kurcz MD , Dennis A. DeBernardis DO , Aaron Roberts DO , Peter Regala MD , Carl J. Replogle , Cassie M. Fleckenstein MS , Joseph Nolan PhD , Samer S. Hasan MD, PhD
<div><h3>Background</h3><div>Anatomic total shoulder arthroplasty (aTSA) using standard (non-augmented) glenoid implants has demonstrated excellent clinical results, but concerns have been raised regarding their use in patients with posterior glenoid wear. The primary purpose of this study is to investigate short-term patient-reported outcomes (PROs) and overall active range of motion in patients who underwent aTSA using short humeral stems and standard glenoid implants for glenohumeral arthritis with minimal or concentric wear and with posterior glenoid wear. The secondary purpose was to the determine predictors of an inferior outcome or reoperation following aTSA using this construct.</div></div><div><h3>Methods</h3><div>Patients in this study underwent aTSA with minimal glenoid reaming to achieve >90% contact of a pegged, all-polyethylene standard glenoid implant, inserted with minimal cement. Plain radiographs, active range of motion, and PROs—comprising American Shoulder and Elbow Surgeons (ASES), simple shoulder test, and visual analog scale pain scores—were obtained preoperatively and at final follow-up.</div></div><div><h3>Results</h3><div>One hundred twenty-eight consecutive aTSAs in 122 patients (75 males) with mean age of 66 years (range 48-84) were reviewed. Thirteen patients were lost to follow-up, 6 patients were deceased or had cognitive impairment precluding evaluation, and 5 patients underwent early revision for subscapularis failure, leaving 104 aTSAs for evaluation at minimum 2-year follow-up (mean 3 years, range 2-5.6 years). Twenty-four shoulders had undergone previous surgery. Fifty-nine patients had posterior glenoid wear (Walch B2 or B3) and 47 had concentric or minimal glenoid wear (Walch A1, A2, or B1). Forward elevation improved from 101° ± 25° to 147° ± 17°, abduction from 87° ± 26° to 145° ± 23°, external rotation from 21° ± 15° to 45° ± 13°, and internal rotation from the sacrum to thoracolumbar junction (<em>P</em> < .001 for all). Overall, ASES improved from 41 ± 20 to 89 ± 13, simple shoulder test from 4.5 ± 2.9 to 10.2 ± 2.5, and visual analog scale pain from 5.5 ± 2.5 to 0.7 ± 1.3 (<em>P</em> < .001). Ten patients had a final ASES score <70, which was associated with a history of previous surgery (<em>P</em> = .03). The degree of posterior glenoid wear did not influence any outcome score. Eight patients underwent subsequent ipsilateral shoulder surgery including 5 (4%) undergoing revision to reverse shoulder arthroplasty for subscapularis insufficiency (2 following traumatic injury). No revisions for prosthetic joint infection or humeral or glenoid implant loosening were performed.</div></div><div><h3>Conclusion</h3><div>aTSA using a minimally cemented standard glenoid implant following partial version correction for Walch B2 and B3 glenoids leads to marked improvements in ROM and PROs, regardless of glenoid wear pattern. No reoperations were performed for glenoid or humeral loosening or infection at
背景:使用标准(非增强)肩关节假体的原子全肩关节置换术(aTSA)已显示出良好的临床效果,但对其在肩关节后磨损患者中的应用提出了担忧。本研究的主要目的是调查短期患者报告的结果(PROs)和总体活动范围,这些患者使用短肱骨柄和标准肩关节植入物治疗肩关节关节炎,伴有轻微或同心磨损和后肩关节磨损。次要目的是使用该结构确定aTSA后不良预后或再手术的预测因素。方法在本研究中,患者接受了aTSA手术,并进行了最小的关节盂扩孔,使全聚乙烯标准关节盂假体与骨水泥的接触达到90%。术前和最终随访时获得x线平片、活动范围和pro(包括美国肩关节外科医生(ase)、简单肩关节测试和视觉模拟疼痛评分)。结果122例患者(男性75例),平均年龄66岁(48 ~ 84岁),连续128例atsa。13例患者失去随访,6例患者死亡或有认知障碍,无法进行评估,5例患者因肩胛下肌衰竭进行了早期翻修,在至少2年的随访(平均3年,范围2-5.6年)中,留下104例atsa进行评估。24个肩膀之前做过手术。59例患者为后关节盂磨损(Walch B2或B3), 47例为同心圆或轻度关节盂磨损(Walch A1、A2或B1)。前俯仰从101°±25°提高到147°±17°,外展从87°±26°提高到145°±23°,外旋从21°±15°提高到45°±13°,内旋从骶骨到胸腰椎连接处(P < 0.001)。总体而言,asa从41±20改善到89±13,简单肩部测试从4.5±2.9改善到10.2±2.5,视觉模拟疼痛从5.5±2.5改善到0.7±1.3 (P < .001)。10例患者的最终as评分为70分,与既往手术史相关(P = .03)。后关节盂磨损程度不影响任何结果评分。8例患者接受了随后的同侧肩关节手术,其中5例(4%)因肩胛下肌功能不全接受了复位肩关节置换术(2例因外伤性损伤)。假体关节感染或肱骨或关节盂内植入物松动均未进行翻修。结论:无论关节盂磨损模式如何,在Walch B2和B3关节盂部分矫正后,采用微创骨水泥标准关节盂内种植体的atsa可显著改善ROM和PROs。在最近的随访中,没有因肩关节或肱骨松动或感染而再次手术。既往手术史预测临床预后较差。
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引用次数: 0
Does bisphosphonate use in osteoporotic patients undergoing total shoulder arthroplasty have a protective effect? A propensity-matched analysis 双膦酸盐在接受全肩关节置换术的骨质疏松患者中使用是否有保护作用?倾向匹配分析
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.05.003
Akhil Katakam MD , Tej Joshi MD , Tuckerman Jones MD , Amanda Azer MD , Daniella Ogilvie MD , Sefy A. Paulose MD , Eitan M. Kohan MD , Francis G. Alberta MD

Background

Osteoporosis and its associated complications, such as fractures, place a significant burden on health care systems. Bisphosphonates are a standard treatment for osteoporosis, shown to maintain bone mineral density and reduce fracture risk. However, their role in patients undergoing reverse total shoulder arthroplasty (rTSA) remains unclear, particularly regarding complications like acromial stress fractures and other prosthesis-related outcomes. This study investigates the impact of bisphosphonate usage on postoperative outcomes in osteoporotic patients undergoing rTSA.

Methods

A retrospective cohort study was conducted using the TriNetX Research Network database to identify patients with osteoporosis who underwent rTSA. Patients were stratified into two cohorts based on preoperative bisphosphonate usage. Propensity score matching (1:1) was utilized to balance demographic characteristics, comorbidities, prior surgery, and medication use. Outcomes assessed included acromial stress fractures, revision rates, aseptic loosening, and periprosthetic fractures at 1 year postoperatively.

Results

A total of 1,208 propensity-matched patients (604 in each cohort) were analyzed. In the bisphosphonate group, 25 (4.1%) of patients were diagnosed with an acromial stress fracture compared to 23 (3.6%) in the control group (odds ratio 1.142, 95% confidence interval 0.637-2.049, P = .655). No significant differences were observed in revision rates (P = .712), aseptic loosening (P = 1.000), or periprosthetic fractures (P = 1.000) between cohorts.

Conclusion

Bisphosphonate usage does not decrease the incidence of acromial stress fractures in osteoporotic patients undergoing rTSA. Future studies should focus on the potential additional interventions to mitigate the risk of acromial stress fracture in osteoporotic patients undergoing rTSA.
背景:骨质疏松症及其相关并发症,如骨折,给卫生保健系统带来了沉重负担。双膦酸盐是治疗骨质疏松症的标准药物,可维持骨密度,降低骨折风险。然而,它们在逆行全肩关节置换术(rTSA)患者中的作用尚不清楚,特别是在肩峰应力性骨折等并发症和其他假体相关结果方面。本研究探讨双膦酸盐对骨质疏松患者行rTSA术后预后的影响。方法利用TriNetX研究网络数据库进行回顾性队列研究,以确定接受rTSA治疗的骨质疏松患者。根据术前双膦酸盐的使用情况将患者分为两组。倾向评分匹配(1:1)用于平衡人口统计学特征、合并症、既往手术和药物使用。评估的结果包括肩峰应力性骨折、翻修率、无菌性松动和术后1年假体周围骨折。结果共分析1208例倾向匹配患者(每组604例)。在双膦酸盐组中,25例(4.1%)患者被诊断为肩峰应力性骨折,对照组为23例(3.6%)(优势比1.142,95%可信区间0.637-2.049,P = 0.655)。在翻修率(P = .712)、无菌性松动(P = 1.000)或假体周围骨折(P = 1.000)方面,各组间无显著差异。结论双膦酸盐的使用并不能降低骨质疏松患者肩峰应力性骨折的发生率。未来的研究应侧重于潜在的其他干预措施,以减轻骨质疏松患者接受rTSA时肩峰应力性骨折的风险。
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引用次数: 0
Introduction of a new outcome measure for total shoulder arthroplasty: subjective patient outcome tracker (SPOT) 引入一种新的全肩关节置换术结果测量方法:主观患者结果跟踪器(SPOT)
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.05.001
B. Gage Griswold MD, Brian P. Davis MD, Hayden B. Schuette DO, Benjamin W. Sears MD, Andrea Stapleford BS, Libby Mauter MSPT, Jacqueline Bader MS, Mallory Boyd MS, Armodios M. Hatzidakis MD

Background

Patient-reported outcome measures (PROMs) provide a quantifiable rating of a patient's subjective symptoms prior to and following treatment of shoulder pathology. Shoulder Subjective Patient Outcome Tracker (SPOT) is a novel outcomes measure with 10 satisfaction domains to pinpoint shoulder-specific functions. The purpose of this study is to introduce and demonstrate the utility of SPOT for patients undergoing total shoulder arthroplasty. The authors hypothesize SPOT will demonstrate high correlations to existing PROMs with a corresponding large effect size.

Methods

Over a 1-year evaluation period, SPOT, American Shoulder and Elbow Surgeons (ASES) assessment, and Single Assessment Numeric Evaluation (SANE) scores were administered preoperatively and at 2 years postoperatively for patients undergoing anatomic total shoulder arthroplasty (aTSA) and reverse shoulder arthroplasty (rTSA). Additionally, nonsurgical patients with glenohumeral osteoarthritis were administered SPOT at 2 separate time points. Interoutcome agreement, correlation, and sensitivity of SPOT to ASES and SANE were evaluated, and the floor/ceiling effect of SPOT was assessed. Test-retest reliability was conducted on the nonsurgical cohort.

Results

A total of 139 patients were included with 73 postoperative aTSA and 66 postoperative rTSA patients. Twelve patients managed nonoperatively were included in test-retest analysis. Preoperatively, there was low correlation between SPOT and ASES and moderate correlation between SPOT and SANE. At 2 years postoperatively, there was high correlation between SPOT and ASES and between SPOT and SANE. There was good agreement between SPOT and ASES in both aTSA and rTSA cohorts and between SPOT and SANE in the aTSA cohort. Additionally, the large effect size of SPOT was similar to the effect size of ASES and SANE. There was high correlation in the test-retest evaluation in a nonoperative cohort indicating reliability of SPOT at the 2 time points assessed.

Conclusion

SPOT is a shoulder-specific, effective PROM with a low administrative burden, tailored for patients undergoing aTSA or rTSA. It demonstrates high reliability, strong correlations, and a large effect size comparable to established shoulder-specific PROMs. SPOT is more discriminatory and specific than the SANE score, offering valuable, detailed insights into patients’ perceived deficits before and after shoulder arthroplasty.
背景:患者报告的结果测量(PROMs)提供了患者在肩部病理治疗前后主观症状的可量化评分。肩部主观患者结果跟踪器(SPOT)是一种新颖的结果测量方法,有10个满意域来精确定位肩部特定功能。本研究的目的是介绍和证明SPOT在接受全肩关节置换术患者中的应用。作者假设SPOT将显示出与现有prom的高相关性,并具有相应的大效应大小。方法对解剖性全肩关节置换术(aTSA)和反向肩关节置换术(rTSA)患者进行术前和术后2年的SPOT、American Shoulder and Elbow Surgeons (ASES)评估和Single assessment Numeric evaluation (SANE)评分,为期1年的评估期。此外,肩关节骨性关节炎的非手术患者在2个不同的时间点接受SPOT治疗。评估了结果间一致性、相关性和SPOT对as和SANE的敏感性,并评估了SPOT的下限/上限效应。对非手术队列进行重测信度。结果共纳入139例患者,其中术后aTSA 73例,术后rTSA 66例。12例非手术治疗的患者纳入复试分析。术前,SPOT与ASES的相关性较低,SPOT与SANE的相关性中等。术后2年,SPOT与ASES、SPOT与SANE的相关性较高。在aTSA和rTSA队列中,SPOT和ase之间以及在aTSA队列中,SPOT和SANE之间存在良好的一致性。此外,SPOT的大效应量与ASES和SANE的效应量相似。在非手术队列中,测试-再测试评估有很高的相关性,表明SPOT在评估的2个时间点上的可靠性。结论spot是一种肩部特异性的、有效的、管理负担低的PROM,适合于接受aTSA或rTSA的患者。它证明了高可靠性、强相关性和与已建立的肩部特异性prom相当的大效应大小。SPOT评分比SANE评分更具歧视性和特异性,为患者在肩关节置换术前后的感知缺陷提供了有价值的、详细的见解。
{"title":"Introduction of a new outcome measure for total shoulder arthroplasty: subjective patient outcome tracker (SPOT)","authors":"B. Gage Griswold MD,&nbsp;Brian P. Davis MD,&nbsp;Hayden B. Schuette DO,&nbsp;Benjamin W. Sears MD,&nbsp;Andrea Stapleford BS,&nbsp;Libby Mauter MSPT,&nbsp;Jacqueline Bader MS,&nbsp;Mallory Boyd MS,&nbsp;Armodios M. Hatzidakis MD","doi":"10.1053/j.sart.2025.05.001","DOIUrl":"10.1053/j.sart.2025.05.001","url":null,"abstract":"<div><h3>Background</h3><div>Patient-reported outcome measures (PROMs) provide a quantifiable rating of a patient's subjective symptoms prior to and following treatment of shoulder pathology. Shoulder Subjective Patient Outcome Tracker (SPOT) is a novel outcomes measure with 10 satisfaction domains to pinpoint shoulder-specific functions. The purpose of this study is to introduce and demonstrate the utility of SPOT for patients undergoing total shoulder arthroplasty<span>. The authors hypothesize SPOT will demonstrate high correlations to existing PROMs with a corresponding large effect size.</span></div></div><div><h3>Methods</h3><div><span>Over a 1-year evaluation period, SPOT, American Shoulder and Elbow Surgeons (ASES) assessment, and Single Assessment Numeric Evaluation (SANE) scores were administered preoperatively and at 2 years postoperatively for patients undergoing anatomic total shoulder arthroplasty<span> (aTSA) and reverse shoulder arthroplasty (rTSA). Additionally, nonsurgical patients with glenohumeral </span></span>osteoarthritis were administered SPOT at 2 separate time points. Interoutcome agreement, correlation, and sensitivity of SPOT to ASES and SANE were evaluated, and the floor/ceiling effect of SPOT was assessed. Test-retest reliability was conducted on the nonsurgical cohort.</div></div><div><h3>Results</h3><div>A total of 139 patients were included with 73 postoperative aTSA and 66 postoperative rTSA patients. Twelve patients managed nonoperatively were included in test-retest analysis. Preoperatively, there was low correlation between SPOT and ASES and moderate correlation between SPOT and SANE. At 2 years postoperatively, there was high correlation between SPOT and ASES and between SPOT and SANE. There was good agreement between SPOT and ASES in both aTSA and rTSA cohorts and between SPOT and SANE in the aTSA cohort. Additionally, the large effect size of SPOT was similar to the effect size of ASES and SANE. There was high correlation in the test-retest evaluation in a nonoperative cohort indicating reliability of SPOT at the 2 time points assessed.</div></div><div><h3>Conclusion</h3><div>SPOT is a shoulder-specific, effective PROM with a low administrative burden, tailored for patients undergoing aTSA or rTSA. It demonstrates high reliability, strong correlations, and a large effect size comparable to established shoulder-specific PROMs. SPOT is more discriminatory and specific than the SANE score, offering valuable, detailed insights into patients’ perceived deficits before and after shoulder arthroplasty.</div></div>","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 553-560"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685809","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
Preoperative deltoid muscle volume correlates with early postoperative range of motion in flexion after reverse shoulder arthroplasty 术前三角肌体积与肩关节置换术后早期屈曲活动范围相关
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.07.003
Jun Kawamata MD , Shoji Fukuta MD, PhD , Daisuke Nakai MD, PhD , Kohei Yoshikawa MD , Koichi Sairyo MD, PhD

Background

After reverse shoulder arthroplasty (RSA), the deltoid muscle is the main source of kinematic force, and muscle strength is essential for movement of the shoulder joint. The purpose of this study was to assess the correlation of preoperative deltoid muscle volume with clinical outcomes after RSA. Our hypothesis was that preoperative deltoid muscle volume would be associated with range of motion (ROM), especially in forward flexion.

Methods

The study included 49 patients who underwent RSA for cuff tear arthropathy. The mean follow-up duration was 3.3 years. Preoperative deltoid muscle volume was measured in 3 dimensions on computed tomography scans. Postoperative clinical outcomes were evaluated by active ROM and the University of California, Los Angeles shoulder rating scale score. Correlations of deltoid muscle volume with clinical outcomes were investigated. Cases were classified according to whether flexion was 135° or more (the ≥135 group) or less than 135° (the <135 group) at the final observation. Logistic regression analysis was used to identify predictors of more than 135° of flexion. The cutoff value for deltoid muscle volume was determined by receiver operating characteristic curve analysis.

Results

Preoperative deltoid volume was correlated with flexion (6 weeks, r = 0.45, P = .003; 3 months, r = 0.33, P = .023; 6 months, r = 0.31, P = .027; 1 year, r = 0.31, P = .033; final observation, r = 0.33, P = .022) and internal rotation at 1 year (r = −0.29 P = .042). Univariable analysis identified statistically significant between-group differences in preoperative external rotation (<135 group, 10.3 ± 20.1°; ≥135 group, 28.0 ± 27.6°; P = .03), preoperative pain score (2.9 ± 1.7 points and 4.3 ± 2.6 points, respectively; P = .45), and preoperative deltoid volume (169.0 ± 62.5 ml and 223.2 ± 59.1 ml; P = .008). Logistic regression analysis identified preoperative factors associated with ≥135° of flexion to be deltoid volume (odds ratio 1.02, 95% confidence interval 1.00-1.03, P = .017) and preoperative external rotation (odds ratio 1.03, 95% confidence interval 1.00-1.05, P = .04). Receiver operating characteristic curve analysis identified a deltoid volume of 204.6 ml (area under the curve 0.737, sensitivity 0.64, specificity 0.81) as the cutoff value for a final ROM in flexion of ≥135°.

Conclusion

A correlation was observed between preoperative deltoid muscle volume and ROM in flexion after RSA, especially in the early postoperative stage.
背景:在反向肩关节置换术(RSA)后,三角肌是运动力的主要来源,肌肉力量对于肩关节的运动是必不可少的。本研究的目的是评估术前三角肌体积与RSA术后临床结果的相关性。我们的假设是术前三角肌体积与活动范围(ROM)有关,尤其是前屈。方法本研究纳入49例采用RSA治疗袖带撕裂性关节病的患者。平均随访时间为3.3年。术前通过计算机断层扫描三维测量三角肌体积。术后临床结果通过活动度ROM和加州大学洛杉矶分校肩部评定量表评分进行评估。研究三角肌体积与临床预后的相关性。根据最后观察时屈曲度≥135°(≥135组)或小于135°(<;135组)进行分类。使用逻辑回归分析来确定超过135°屈曲的预测因子。通过受试者工作特征曲线分析确定三角肌体积的临界值。结果术前三角肌体积与屈曲(6周,r = 0.45, P = 0.003; 3个月,r = 0.33, P = 0.023; 6个月,r = 0.31, P = 0.027; 1年,r = 0.31, P = 0.033;最后观察,r = 0.33, P = 0.022)和1年内旋(r = - 0.29, P = 0.042)相关。单变量分析发现,两组患者术前外旋度(≥135组,10.3±20.1°;≥135组,28.0±27.6°,P = 0.03)、术前疼痛评分(分别为2.9±1.7分和4.3±2.6分,P = 0.45)、术前三角肌容积(169.0±62.5 ml和223.2±59.1 ml, P = 0.008)差异均有统计学意义。Logistic回归分析发现术前因素与三角肌体积屈曲≥135°相关(优势比1.02,95%可信区间1.00-1.03,P = 0.017)和术前外旋相关(优势比1.03,95%可信区间1.00-1.05,P = 0.04)。受试者工作特征曲线分析确定三角肌体积为204.6 ml(曲线下面积0.737,灵敏度0.64,特异性0.81)作为屈曲≥135°时最终ROM的临界值。结论术前三角肌体积与RSA术后屈曲的ROM相关,尤其是术后早期。
{"title":"Preoperative deltoid muscle volume correlates with early postoperative range of motion in flexion after reverse shoulder arthroplasty","authors":"Jun Kawamata MD ,&nbsp;Shoji Fukuta MD, PhD ,&nbsp;Daisuke Nakai MD, PhD ,&nbsp;Kohei Yoshikawa MD ,&nbsp;Koichi Sairyo MD, PhD","doi":"10.1053/j.sart.2025.07.003","DOIUrl":"10.1053/j.sart.2025.07.003","url":null,"abstract":"<div><h3>Background</h3><div>After reverse shoulder arthroplasty (RSA), the deltoid muscle is the main source of kinematic force, and muscle strength is essential for movement of the shoulder joint. The purpose of this study was to assess the correlation of preoperative deltoid muscle volume with clinical outcomes after RSA. Our hypothesis was that preoperative deltoid muscle volume would be associated with range of motion (ROM), especially in forward flexion.</div></div><div><h3>Methods</h3><div>The study included 49 patients who underwent RSA for cuff tear arthropathy. The mean follow-up duration was 3.3 years. Preoperative deltoid muscle volume was measured in 3 dimensions on computed tomography scans. Postoperative clinical outcomes were evaluated by active ROM and the University of California, Los Angeles shoulder rating scale score. Correlations of deltoid muscle volume with clinical outcomes were investigated. Cases were classified according to whether flexion was 135° or more (the ≥135 group) or less than 135° (the &lt;135 group) at the final observation. Logistic regression analysis was used to identify predictors of more than 135° of flexion. The cutoff value for deltoid muscle volume was determined by receiver operating characteristic curve analysis.</div></div><div><h3>Results</h3><div>Preoperative deltoid volume was correlated with flexion (6 weeks, r = 0.45, <em>P</em> = .003; 3 months, r = 0.33, <em>P</em> = .023; 6 months, r = 0.31, <em>P</em> = .027; 1 year, r = 0.31, <em>P</em> = .033; final observation, r = 0.33, <em>P</em> = .022) and internal rotation at 1 year (r = −0.29 <em>P</em> = .042). Univariable analysis identified statistically significant between-group differences in preoperative external rotation (&lt;135 group, 10.3 ± 20.1°; ≥135 group, 28.0 ± 27.6°; <em>P</em> = .03), preoperative pain score (2.9 ± 1.7 points and 4.3 ± 2.6 points, respectively; <em>P</em> = .45), and preoperative deltoid volume (169.0 ± 62.5 ml and 223.2 ± 59.1 ml; <em>P</em> = .008). Logistic regression analysis identified preoperative factors associated with ≥135° of flexion to be deltoid volume (odds ratio 1.02, 95% confidence interval 1.00-1.03, <em>P</em> = .017) and preoperative external rotation (odds ratio 1.03, 95% confidence interval 1.00-1.05, <em>P</em> = .04). Receiver operating characteristic curve analysis identified a deltoid volume of 204.6 ml (area under the curve 0.737, sensitivity 0.64, specificity 0.81) as the cutoff value for a final ROM in flexion of ≥135°.</div></div><div><h3>Conclusion</h3><div>A correlation was observed between preoperative deltoid muscle volume and ROM in flexion after RSA, especially in the early postoperative stage.</div></div>","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 678-684"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685750","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
Trends in extended oral antibiotic prophylaxis after primary total shoulder arthroplasty, 2010-2021 2010-2021年原发性全肩关节置换术后扩大口服抗生素预防的趋势
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.06.007
Arman Kishan MBBS , Sanjay Kubsad BS , Jeffrey Y. Wang BS , Duc Nguyen MD , Santiago A. Lozano-Calderón MD, PhD , Umasuthan Srikumaran MD, MBA, MPH , Matthew J. Best MD

Background

The absence of national guidelines on the use of extended oral antibiotic (EOA) prophylaxis has led to inconsistent use of EOA to prevent prosthetic joint infection after total shoulder arthroplasty (TSA). Our investigation aimed to determine temporal trends and prescription patterns in the use of EOA prophylaxis after TSA from 2010 to 2021, particularly for patients considered at high risk for infection.

Methods

Using the PearlDiver database, we identified 289,908 patients who underwent primary TSA from 2010 to 2021. EOA was defined as antibiotic use initiated before, during, or immediately after surgery and continued for 2 days or more postoperatively. Compounded annual growth rate and linear regression were used for trend analysis. Stratification measures were demographic variables, geographic location, insurance type, and risk factors for infection.

Results

Among primary TSA patients, 3.8% received EOA after TSA. Antibiotic use after TSA increased by a compounded annual growth rate of 6.2% from 2010 to 2021. Associations were observed between EOA prescription patterns and factors such as age, sex, Charlson Comorbidity Index value, geographic region, and insurance type. Cephalexin was the most frequently prescribed antibiotic, but prescriptions of cephalexin declined during the study period, while doxycycline prescriptions increased. Most patients received EOA for 2-7 days. Patients at high risk for infection, including those with diabetes, a history of tobacco use, chronic kidney disease, and autoimmune disorders, were more likely to receive EOAs compared to those without these factors.

Conclusion

This study provides insights into the dynamic landscape of EOA prophylaxis after TSA. The observed changes during the study period—namely, the increase in EOA prescriptions, demographic variation in prescription patterns, and shifting antibiotic preferences—highlight the evolving nature of clinical practice in the absence of standardized national guidelines. Continued research is needed to improve prophylactic strategies for patients with risk factors for infection. Surgeons can use this information to establish their own guidelines tailored to their patients, considering factors such as age, comorbid conditions, and regional practices, while closely monitoring for adverse effects and antibiotic resistance patterns.
背景:由于缺乏关于使用延长口服抗生素(EOA)预防的国家指南,导致在全肩关节置换术(TSA)后使用EOA预防假关节感染的情况不一致。我们的调查旨在确定2010年至2021年TSA后EOA预防使用的时间趋势和处方模式,特别是对于被认为是感染高风险的患者。方法使用PearlDiver数据库,我们确定了2010年至2021年期间接受原发性TSA的289,908例患者。EOA被定义为在手术前、手术中或手术后立即开始使用抗生素,并在术后持续2天或更长时间。采用复合年增长率和线性回归进行趋势分析。分层措施是人口统计学变量、地理位置、保险类型和感染的危险因素。结果原发性TSA患者中,3.8%的患者在TSA后接受了EOA。从2010年到2021年,TSA后抗生素使用的复合年增长率为6.2%。结果表明,年龄、性别、Charlson合并症指数、地理区域、保险类型等因素与EOA处方模式存在相关性。头孢氨苄是最常用的抗生素,但在研究期间头孢氨苄的处方减少,而强力霉素的处方增加。大多数患者接受EOA治疗2-7天。与没有这些因素的患者相比,感染高危患者,包括糖尿病患者、有烟草使用史的患者、慢性肾脏疾病患者和自身免疫性疾病患者更有可能接受eoa。结论本研究提供了TSA后EOA预防的动态景观。在研究期间观察到的变化——即EOA处方的增加、处方模式的人口统计学变化和抗生素偏好的变化——突出了在缺乏标准化国家指南的情况下临床实践的演变性质。需要继续进行研究,以改进具有感染危险因素的患者的预防策略。外科医生可以利用这些信息,在密切监测不良反应和抗生素耐药性模式的同时,根据患者的年龄、合并症和地区实践等因素,制定适合他们自己的指导方针。
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引用次数: 0
Determining the minimal clinically important difference and substantial clinical benefit following revision reverse shoulder arthroplasty 确定翻修后反向肩关节置换术的最小临床重要差异和实质性临床获益
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.07.004
Ali A. Mohamed MS , Anna Redden BS , Jacob Calpey BS , Aghdas Movassaghi BS , Garrett R. Jackson MD , Howard Routman DO , Diego J.L. Lima MD , Vani J. Sabesan MD

Background

Total shoulder arthroplasty (TSA) has become a more common procedure due to its expanded indications and successful outcomes. The concern with this growth is the increased number of complications that may lead to more revision surgery. Given revision surgery has increased complexity and difficulty in recovery for patients, understanding outcomes can help guide patients and surgeons in decision-making. This study aimed to establish the minimum clinically important difference (MCID) and substantial clinical benefit (SCB) for reverse TSA performed as a revision procedure for failed prior shoulder arthroplasty types.

Methods

A retrospective review of all patients who underwent revision reverse TSA (rTSA) performed as a revision procedure for failed prior shoulder arthroplasty from 2007 to 2020 by a single fellowship-trained orthopedic surgeon was performed. Patient demographics, range of motion, and patient-reported outcome measures including Simple Shoulder Test (SST), Constant-Murley, American Shoulder and Elbow Surgeons (ASES) score, University of California at Los Angeles (UCLA), Shoulder Pain and Disability Index (SPADI), and Shoulder Arthroplasty Smart (SAS), were collected preoperatively and postoperatively at the last follow-up visit. MCID and SCB were calculated using the anchor-based method. Analyses were performed using paired- and independent-sample t-tests and logistic regressions were used to identify potential predictors for meeting MCID and SCB.

Results

A total of 91 patients were included in this analysis. The cohort had a mean age of 67.8 years and a mean body mass index of 29.7 kg/m2. A majority of the cohort was male (51.7%) and Caucasian (93.2%). The MCID was found to be 3.5 for SST, 30.6 for Constant-Murley Score, 25.3 for ASES, 11.2 for UCLA, −42.1 for SPADI, 17.4 for SAS, 56.4° for forward flexion, 47.6° for abduction and 11.7° for external rotation. The SCB was found to be 6.3 for SST, 34.3 for CMS, 45.6 for ASES, 17.6 for UCLA, −56.8 for SPADI, 30.1 for SAS, 78.4° for forward flexion, 66.8° for abduction and 7.9° for external rotation. MCID was achieved by 72.5% of patients and 43.9% (n = 40) met SCB at final follow-up. Age, sex, and body mass index were not found to be significantly associated with meeting MCID or SCB.

Conclusions

This study establishes MCID and SCB thresholds for rTSA performed as a revision procedure for failed prior shoulder arthroplasties, providing valuable benchmarks for assessing patient outcomes. Most patients achieved meaningful improvements (MCID), and a significant portion reached SCB. These findings help set recovery expectations and highlight that patient-specific factors have a limited impact on outcomes after rTSA performed as a revision surgery.
背景:全肩关节置换术(TSA)由于其适应症的扩大和成功的结果,已成为更常见的手术。这种增长的担忧是并发症的增加,可能导致更多的翻修手术。鉴于翻修手术增加了患者恢复的复杂性和难度,了解结果可以帮助指导患者和外科医生做出决策。本研究旨在建立最小临床重要差异(MCID)和实际临床获益(SCB),将反向TSA作为先前失败的肩关节置换术类型的翻修手术。方法回顾性分析2007年至2020年期间,由一名培训过的骨科医生对所有失败的肩关节置换术患者进行rTSA翻修手术。术前和术后最后一次随访时收集患者人口统计数据、活动范围和患者报告的结果测量,包括简单肩部测试(SST)、Constant-Murley、美国肩关节外科医生(ASES)评分、加州大学洛杉矶分校(UCLA)、肩部疼痛和残疾指数(SPADI)和肩关节成形术智能(SAS)。采用锚定法计算MCID和SCB。使用配对和独立样本t检验进行分析,并使用逻辑回归来确定满足MCID和SCB的潜在预测因素。结果共纳入91例患者。该队列的平均年龄为67.8岁,平均体重指数为29.7 kg/m2。大多数队列为男性(51.7%)和白种人(93.2%)。SST的MCID为3.5,Constant-Murley Score为30.6,ASES为25.3,UCLA为11.2,SPADI为- 42.1,SAS为17.4,前屈为56.4°,外展为47.6°,外旋为11.7°。SST的SCB为6.3,CMS为34.3,ASES为45.6,UCLA为17.6,SPADI为- 56.8,SAS为30.1,前屈为78.4°,外展为66.8°,外旋为7.9°。72.5%的患者达到MCID, 43.9% (n = 40)的患者在最终随访时达到SCB。年龄、性别和身体质量指数与满足MCID或SCB没有显著相关性。本研究建立了MCID和SCB阈值,rTSA作为先前肩关节置换术失败的修正程序,为评估患者预后提供了有价值的基准。大多数患者获得了有意义的改善(MCID),很大一部分达到了SCB。这些发现有助于设定恢复预期,并强调患者特异性因素对rTSA作为翻修手术后的结果影响有限。
{"title":"Determining the minimal clinically important difference and substantial clinical benefit following revision reverse shoulder arthroplasty","authors":"Ali A. Mohamed MS ,&nbsp;Anna Redden BS ,&nbsp;Jacob Calpey BS ,&nbsp;Aghdas Movassaghi BS ,&nbsp;Garrett R. Jackson MD ,&nbsp;Howard Routman DO ,&nbsp;Diego J.L. Lima MD ,&nbsp;Vani J. Sabesan MD","doi":"10.1053/j.sart.2025.07.004","DOIUrl":"10.1053/j.sart.2025.07.004","url":null,"abstract":"<div><h3>Background</h3><div>Total shoulder arthroplasty (TSA) has become a more common procedure due to its expanded indications and successful outcomes. The concern with this growth is the increased number of complications that may lead to more revision surgery. Given revision surgery has increased complexity and difficulty in recovery for patients, understanding outcomes can help guide patients and surgeons in decision-making. This study aimed to establish the minimum clinically important difference (MCID) and substantial clinical benefit (SCB) for reverse TSA performed as a revision procedure for failed prior shoulder arthroplasty types.</div></div><div><h3>Methods</h3><div>A retrospective review of all patients who underwent revision reverse TSA (rTSA) performed as a revision procedure for failed prior shoulder arthroplasty from 2007 to 2020 by a single fellowship-trained orthopedic surgeon was performed. Patient demographics, range of motion, and patient-reported outcome measures including Simple Shoulder Test (SST), Constant-Murley, American Shoulder and Elbow Surgeons (ASES) score, University of California at Los Angeles (UCLA), Shoulder Pain and Disability Index (SPADI), and Shoulder Arthroplasty Smart (SAS), were collected preoperatively and postoperatively at the last follow-up visit. MCID and SCB were calculated using the anchor-based method. Analyses were performed using paired- and independent-sample t-tests and logistic regressions were used to identify potential predictors for meeting MCID and SCB.</div></div><div><h3>Results</h3><div>A total of 91 patients were included in this analysis. The cohort had a mean age of 67.8 years and a mean body mass index of 29.7 kg/m<sup>2</sup>. A majority of the cohort was male (51.7%) and Caucasian (93.2%). The MCID was found to be 3.5 for SST, 30.6 for Constant-Murley Score, 25.3 for ASES, 11.2 for UCLA, −42.1 for SPADI, 17.4 for SAS, 56.4° for forward flexion, 47.6° for abduction and 11.7° for external rotation. The SCB was found to be 6.3 for SST, 34.3 for CMS, 45.6 for ASES, 17.6 for UCLA, −56.8 for SPADI, 30.1 for SAS, 78.4° for forward flexion, 66.8° for abduction and 7.9° for external rotation. MCID was achieved by 72.5% of patients and 43.9% (n = 40) met SCB at final follow-up. Age, sex, and body mass index were not found to be significantly associated with meeting MCID or SCB.</div></div><div><h3>Conclusions</h3><div>This study establishes MCID and SCB thresholds for rTSA performed as a revision procedure for failed prior shoulder arthroplasties, providing valuable benchmarks for assessing patient outcomes. Most patients achieved meaningful improvements (MCID), and a significant portion reached SCB. These findings help set recovery expectations and highlight that patient-specific factors have a limited impact on outcomes after rTSA performed as a revision surgery.</div></div>","PeriodicalId":39885,"journal":{"name":"Seminars in Arthroplasty","volume":"35 4","pages":"Pages 685-691"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685858","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
Preoperative 3-dimensional planning optimizes glenoid retroversion correction in shoulder arthroplasty using hemi-wedged augmented baseplates 术前三维规划优化肩关节置换术中使用半楔形增强基板的盂后翻矫正
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.05.002
Luis Navas MD , Sebastian Schmidt MD , Carolina Vogel MD , Thorsten Guehring MD, PhD

Background

Glenoid version and inclination can be corrected with an augmented baseplate during reverse shoulder arthroplasty (rTSA) procedures. To achieve an optimal correction of both glenoid version and inclination, this study investigated whether the preoperative use of a 3-dimensional planning system improved the correction of glenoid anatomy in terms of glenoid version (0°) and inclination (rTSA 0°).

Methods

We measured preoperative and postoperative glenoid version and inclination by rTSA angle by x-ray and computed tomography scans in 50 prospective cases of rTSA with wedged baseplates. All patients underwent an rTSA due to osteoarthritis and rotator cuff insufficiency. All 50 patients underwent rTSA with the use of a hemi-wedge to correct the glenoid morphology. Twenty five patients additionally underwent a preoperative planning with the Signature ONE Planner to determine the exact rotational position of the hemi-wedge. rTSA angle was determined in preoperative and postoperative x-rays, and glenoid version was determined in preoperative and postoperative computed tomography scans at 3 different glenoid levels. The Signature ONE Planner system determined the rotation, position, and size of the hemi-wedge (10°, 20°, or 30°). A control group of 25 patients underwent hemi-wedge rTSA without preoperative planning. The position of the sphere and the sphere bone overhang distance (mm) was determined in both groups.

Results

In all 50 patients, the inclination was almost corrected anatomically from a preoperative rTSA angle of 16.2° ± 6.4° to 2.4° ± 3.5° postoperatively, irrespective of the use of Signature ONE Planner. In comparison, the average correction of retroversion was worse and achieved to a lower degree but the use of Signature ONE Planner significantly improved the correction of retroversion in all 3 parts of the glenoid to an almost anatomical level (P < .0001). In both groups, the sphere bone overhang distance was between 4 and 5 mm without scapular notching.

Discussion and Conclusion

The anatomical correction of a retroverted glenoid with a hemi-wedge baseplate can be considerably improved by the preoperative use of the Signature ONE planning system. Preoperative planning can thus help surgeons to achieve an optimal baseplate position and may thus improve the correction of the glenoid retroversion after rTSA.
背景:在反向肩关节置换术(rTSA)过程中,关节盂的变形和倾斜可以用增强的底板矫正。为了实现最佳的关节盂形态和倾角矫正,本研究探讨了术前使用三维规划系统是否能改善关节盂形态(0°)和倾角(rTSA 0°)的关节盂解剖矫正。方法通过x线和ct扫描测量50例楔形基板rTSA患者术前和术后关节盂内径和关节盂内倾。所有患者均因骨关节炎和肩袖功能不全接受了rTSA。所有50例患者均接受了rTSA,并使用半楔骨矫正肩关节形态。另外,25例患者接受了Signature ONE Planner的术前计划,以确定半楔形的确切旋转位置。术前和术后x线确定rTSA角度,术前和术后3个不同关节盂的计算机断层扫描确定关节盂形态。Signature ONE Planner系统可确定半楔的旋转、位置和尺寸(10°、20°或30°)。对照组25例患者行半楔形rTSA,无术前计划。测定两组球的位置及球骨悬垂距离(mm)。结果50例患者术前rTSA角度为16.2°±6.4°至术后2.4°±3.5°,与使用Signature ONE Planner无关,均得到解剖矫正。相比之下,关节后倾的平均矫正效果较差,矫正程度较低,但Signature ONE Planner的使用显著改善了关节盂所有3个部位的后倾矫正,使其几乎达到解剖水平(P < .0001)。两组球骨悬垂距离均在4 ~ 5mm之间,无肩胛骨切迹。讨论与结论术前使用Signature ONE计划系统可显著改善半楔型关节臼内翻的解剖矫正。因此,术前计划可以帮助外科医生获得最佳的底板位置,从而改善rTSA后关节盂内翻的矫正。
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引用次数: 0
Safety of rapid discharge after total shoulder arthroplasty in septuagenarian and octogenarian patients 七八十岁患者全肩关节置换术后快速出院的安全性
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.05.005
Keneth R. Granados BS , Marco E. Guareschi BS , John W. Moore BS , Alexander S. Guareschi MD , Brandon L. Rogalski MD , Richard J. Friedman MD, FRCSC

Background

There is limited literature assessing whether patients older than age 70 can be safely discharged within a day (ie, rapid discharge [RD]), following primary total shoulder arthroplasty (TSA). The purpose of this study is to assess postoperative outcomes following TSA with RD (RD-TSA) in septuagenarian and octogenarian patients compared to those with lengthier hospital stays (LD-TSA).

Methods

The National Surgical Quality Improvement Program database was queried from 2006 to 2019 to identify patients who underwent elective primary TSA. Septuagenarian and octogenarian patients who underwent RD-TSA were compared to septuagenarian and octogenarian patients who underwent TSA with lengthier hospital stays (LD-TSA). Demographics, preoperative comorbidities, and rates of complications, readmission, reoperation, and mortality within 30 days of surgery were compared between RD-TSA and LD-TSA patients.

Results

Septuagenarian and octogenarian patients who underwent RD-TSA were less likely to be female (P < .001) and had a lower mean age (P < .001) and body mass index (P < .001). RD-TSA patients were more likely to be functionally independent (P < .001) with lower American Society of Anesthesiologists classifications (P < .001) when compared to LD-TSA patients. Patients aged 70 years and older who underwent RD-TSA exhibited lower rates of any adverse events (P = .001) and bleeding requiring transfusion (P < .001) compared to LD-TSA patients. Septuagenarian and octogenarian patients who underwent RD-TSA were less likely to have hypertension (P < .001) and diabetes mellitus (P < .001) compared to LD-TSA patients. The average total operating time (P < .001) was significantly lower for RD-TSA compared to LD-TSA, without a notable difference in readmission rates between the groups.

Conclusion

Septuagenarian and octogenarian patients who underwent RD-TSA exhibited significantly fewer postoperative complications compared to septuagenarian and octogenarian patients who underwent LD-TSA. Patients aged 70 years and older who received RD-TSA were less likely to have diabetes, hypertension requiring medication, and bleeding requiring transfusion compared to LD-TSA. These findings indicate that RD-TSA is safe and efficacious when utilized in appropriately selected septuagenarian and octogenarian patient populations.
背景:对于70岁以上患者在初次全肩关节置换术(TSA)后能否在一天内安全出院(即快速出院[RD])的评估文献有限。本研究的目的是评估70多岁和80多岁患者与住院时间较长的患者(LD-TSA)相比,TSA合并RD (RD-TSA)的术后结果。方法查询2006年至2019年国家外科质量改进计划数据库,以确定接受选择性原发性TSA的患者。将70多岁和80多岁接受RD-TSA的患者与70多岁和80多岁接受住院时间较长的TSA (LD-TSA)的患者进行比较。比较RD-TSA和LD-TSA患者的人口统计学特征、术前合并症、并发症、再入院、再手术率和手术后30天内的死亡率。结果70岁和80岁接受RD-TSA的患者中女性较少(P < 0.001),平均年龄(P < 0.001)和体重指数(P < 0.001)较低。与LD-TSA患者相比,RD-TSA患者更有可能功能独立(P < .001),美国麻醉医师学会分类较低(P < .001)。与LD-TSA患者相比,70岁及以上接受RD-TSA的患者表现出较低的不良事件发生率(P = 0.001)和需要输血的出血发生率(P < 0.001)。与LD-TSA患者相比,接受RD-TSA的70多岁和80多岁患者患高血压(P < 0.001)和糖尿病(P < 0.001)的可能性较低。RD-TSA组的平均总手术时间明显低于LD-TSA组(P < 0.001),两组再入院率无显著差异。结论70、80岁高龄的RD-TSA患者术后并发症明显少于LD-TSA患者。与LD-TSA相比,接受RD-TSA的70岁及以上患者患糖尿病、需要药物治疗的高血压和需要输血的出血的可能性更小。这些发现表明,RD-TSA是安全有效的,当使用适当选择的70岁和80岁的患者人群。
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引用次数: 0
Examining the structure of the American Academy of Orthopaedic Surgeons appropriateness criteria for persons with shoulder osteoarthritis, an intact rotator cuff, and glenoid retroversion 检查美国骨科医师学会对肩骨关节炎、完整肩袖和肩关节后翻患者的适当标准的结构
Q4 Medicine Pub Date : 2025-12-01 DOI: 10.1053/j.sart.2025.07.002
Daniel L. Riddle PT, PhD, FAPTA , Levent Dumenci PhD

Background

The American Academy of Orthopaedic Surgeons has led an effort to develop RAND/University of California Los Angeles appropriateness criteria for a variety of musculoskeletal surgical treatments. A recently developed appropriateness system is the shoulder osteoarthritis (OA) appropriateness system. The purpose of our study was to examine the structure of this appropriateness system and determine contributions of each predictive criterion to final decisions of appropriate, may be appropriate, or rarely appropriate for 5 surgical treatments for shoulder OA.

Methods

All 48 clinical vignettes were used. All predictors (age classified as young or older/elderly; physiologic demand as low or high; degree of glenoid retroversion as >20°-30°, >30°; glenoid classification as type B2, type B3, type C; and preoperative shoulder active elevation as > 90° or less than 90°) were used in the vignettes. Multivariable logistic regression and a chi-square automatic interaction detection decision tree approach were used to determine the system structure and contribution of each predictor variable used to rate appropriateness.

Results

For each of 5 treatments (2 types of anatomic shoulder arthroplasty, reverse shoulder arthroplasty, hemiarthroplasty, and arthroscopic débridement), multivariable logistic regression and chi-square automatic interaction detection are reported. For example, for reverse shoulder arthroplasty, the predictors with the largest odds ratios (ORs) for vignettes rated as “may be appropriate” as compared to “appropriate” were high physiological demand (OR = 2.63 × 1015) and glenoid type C (OR = 81.50 × 104). For anatomic shoulder arthroplasty, predictors with the largest ORs for vignettes rated as “may be appropriate” as compared to “appropriate” were glenoid type C (OR = 24.74), greater than 30° retroversion, and <90° active shoulder elevation (both OR = 24.74).

Conclusion

The American Academy of Orthopaedic Surgeons shoulder OA system has substantial limitations. It uses a limited number of vignettes, with a consequent lack of symptom spectrum representation, an absence of “appropriate” or “rarely appropriate” ratings for all treatments and an absence of critically important patient-centered measures of pain and functional loss. Alternative published appropriateness criteria appear to have greater potential for clinical use and should be considered for future study.
美国矫形外科医师学会(American Academy of Orthopaedic Surgeons)领导了一项工作,旨在为各种肌肉骨骼手术治疗制定兰德/加州大学洛杉矶分校(RAND/University of California Los Angeles)的适当标准。最近发展的适当系统是肩骨关节炎(OA)适当系统。我们研究的目的是检查这个适当性系统的结构,并确定每个预测标准对最终决定是否适合、可能合适或很少合适的5种肩部OA手术治疗的贡献。方法采用48例临床试验。所有的预测指标(年龄分类为年轻或老年/老年;生理需求低或高;肩关节后倾程度为20°-30°、30°;肩关节分类为B2型、B3型、C型;术前肩关节主动抬高为90°或小于90°)都被用于小研究中。使用多变量逻辑回归和卡方自动交互检测决策树方法来确定用于评估适当性的每个预测变量的系统结构和贡献。结果5种治疗方法(2种解剖式肩关节置换术、反向肩关节置换术、半关节置换术和关节镜内关节镜内关节移植术)均采用多变量logistic回归和卡方自动交互检测。例如,对于反向肩关节置换术,与“合适”相比,被评为“可能合适”的小目标具有最大优势比(OR)的预测因子是高生理需求(OR = 2.63 × 1015)和关节盂C型(OR = 81.50 × 104)。对于解剖性肩关节置换术,与“适当”相比,被评为“可能合适”的小关节的OR值最大的预测因子是关节盂C型(OR = 24.74),大于30°的后倾和<;90°的主动肩部抬高(OR = 24.74)。结论美国骨科学会肩关节OA系统存在一定的局限性。它使用了有限数量的小插曲,因此缺乏症状谱表示,缺乏对所有治疗的“适当”或“很少适当”评级,缺乏以患者为中心的疼痛和功能丧失的至关重要的措施。其他已发表的适宜性标准似乎具有更大的临床应用潜力,应在未来的研究中加以考虑。
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Seminars in Arthroplasty
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