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Influence of age and severity of Lenke 5 or 6 idiopathic scoliosis on postoperative quality of life in adult patients lenke5或6特发性脊柱侧弯的年龄和严重程度对成年患者术后生活质量的影响。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2023.103742

Introduction

Thoracolumbar adolescent idiopathic scoliosis can continue to progress beyond skeletal maturity. Ideal timing of surgery remains undefined. Earlier intervention, with shorter instrumentation, incurs early partial loss of lumbar motion. Waiting for progression incurs a greater risk of extensive arthrodesis. The aim of the present study was to assess the quality-of-life impact of age and scoliosis severity at surgery.

Material and methods

Patients with Lenke 5 or 6 adolescent idiopathic scoliosis, aged 16–45 years, were analyzed based on a prospective clinical registry. Oswestry Disability Index (ODI) and Scoliosis Research Society (SRS)-22 scores were collected preoperatively and at 6 months, 1 year and 2 years. Coronal and sagittal alignments were measured on full-spine radiographs, and curve flexibility was assessed on bending radiographs. A mixed linear model was used to assess the impact of age, Cobb angle and flexibility on quality of life.

Results

Thirty-six patients were included. Mean ODI was 20.5% preoperatively and 13.8% at 2 years (p = 0.017). Mean SRS-22 was 3.2 preoperatively and 3.9 at 2 years (p < 0.001). Mean Cobb angle was 56.6° preoperatively and 23.2° at 2 years (p < 0.001), with mean preoperative reducibility of 68.1%. Age and ODI correlated preoperatively (r = 0.6; p < 0.001) and at 6 months (r = 0.5; p = 0.002), as did age and SRS-22 (r = –0.6; p < 0.001 and r = –0.6; p < 0.001, respectively). Linear regression found a significant negative correlation between thoracolumbar Cobb angle and change in SRS-22 at 6 months.

Discussion

In 16–45 year-olds with Lenke 5 or 6 idiopathic scoliosis, age influenced SRS-22 score. Younger patients had better quality of life both pre- and post-operatively. Curve magnitude influenced postoperative score. The present study suggests that early surgical correction in younger patients, where instrumentation can be shorter, does not impair quality of life.

Level of evidence

IV; prospective registry study.
引言:青少年胸腰椎特发性脊柱侧弯可以在骨骼成熟后继续发展。手术的理想时机尚未确定。早期干预,使用较短的器械,会导致腰椎运动的早期部分丧失。等待进展会带来更大的广泛关节融合术风险。本研究的目的是评估手术中年龄和脊柱侧弯严重程度对生活质量的影响。材料和方法:根据前瞻性临床登记对年龄在16-45岁的Lenke 5或6名青少年特发性脊柱侧弯患者进行分析。Oswestry残疾指数(ODI)和脊柱侧弯研究会(SRS)-22分在术前和6个月、1年和2年时收集。在全脊柱X线片上测量冠状面和矢状面对齐,在弯曲X线片上评估曲线灵活性。使用混合线性模型来评估年龄、Cobb角和灵活性对生活质量的影响。结果:纳入36例患者。平均ODI术前为20.5%,术后2年为13.8%(p=0.017)。SRS-22术前为3.2,术后两年为3.9(p讨论:在16-45岁的Lenke 5或6特发性脊柱侧弯患者中,年龄影响SRS-22评分。年轻患者术前和术后的生活质量更好。曲线幅度影响术后评分。本研究表明,年轻患者的早期手术矫正(器械可能更短)不会损害生活质量。证据水平:IV;p前瞻性注册表研究。
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引用次数: 0
Perioperative duloxetine improves postoperative outcomes after anterior talofibular ligament repair for chronic lateral ankle instability for patients with depression: A prospective randomized clinical trial 围手术期服用度洛西汀可改善抑郁症患者前距腓骨韧带修复术治疗慢性外侧踝关节不稳的术后效果:前瞻性随机临床试验。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2024.103837
<div><h3>Background</h3><div><span>Recent studies have indicated that depression is associated with persistent postoperative pain and decreased satisfaction following </span>foot and ankle surgery<span>. This study aimed to evaluate the effect of perioperative duloxetine on postoperative outcomes of anterior talofibular ligament (ATFL) surgical repair for chronic ankle instability (CAI) in patients with depression. We further sought to evaluate patients’ satisfaction and side effects related to duloxetine.</span></div></div><div><h3>Material and methods</h3><div><span>Patients undergoing ATFL repair were screened for depression preoperatively with the Patient Health Questionnaire (PHQ-9). Among 249 patients who underwent arthroscopic or open surgical Brostrom repair of the ATFL, 120 patients were identified as being “possibly depressed” and were included in the study. Sixty patients were randomly assigned to the duloxetine group (one day preoperatively and for 6 weeks postoperatively), and the other sixty were randomized to the placebo group. Painkillers and opioid consumption, pain scores, and patient satisfaction were recorded at 12, 24, 48, and 72</span> <!-->hours postoperatively and at follow-up visits 1, 3, and 6 months after surgery. Patient-reported outcome measures (PROMs) were assessed preoperatively and at 3, 6, 12 and 24 months postoperatively. Duloxetine-related side effects such as nausea/vomiting and fatigue were also recorded.</div></div><div><h3>Results</h3><div><span><span><span><span>The patients in the duloxetine group reported a significantly longer time to rescue </span>analgesic and reduced opioid requirements (including </span>celecoxib, </span>pregabalin<span>, acetaminophen, and tramadol). The patients experienced decreased pain intensity and greater satisfaction with their pain management at 24, 48, 72</span></span> <!-->h and 1 and 3 months after surgery (<em>p</em> <!--><<!--> <!-->0.05). The duloxetine group also had significantly better clinical and functional outcomes at 3 and 6 months of follow-up compared to the placebo group (<em>p</em> <!--><<!--> <!-->0.05). The occurrence and rate of symptoms of duloxetine side effects were not significant.</div></div><div><h3>Discussion</h3><div>Depression is an important factor to consider and address because its presence before surgery can predict poor postoperative outcomes, including more severe postoperative pain, persistent postoperative pain, and increased consumption of painkillers and opioids.</div></div><div><h3>Conclusion</h3><div>Perioperative administration of duloxetine following ATFL repair for CAI in patients with depression increased the time to first postoperative rescue analgesic request and reduced both opioid consumption and postoperative pain. This approach also led to a high level of patient satisfaction. In addition, duloxetine improved the quality of recovery without leading to significant side effects.</div></div><div><h3>Level of evidence</h3
背景:最近的研究表明,抑郁症与足踝手术后持续疼痛和满意度下降有关。本研究旨在评估围手术期使用度洛西汀对抑郁症患者慢性踝关节不稳(CAI)前距腓韧带(ATFL)手术修复术后疗效的影响。我们还试图评估患者对度洛西汀的满意度和副作用:对接受 ATFL 修复术的患者进行术前抑郁筛查,采用患者健康问卷 (PHQ-9)。在 249 名接受了关节镜或开放手术的 ATFL 修复术的患者中,120 名患者被确定为 "可能患有抑郁症",并被纳入研究。60名患者被随机分配到度洛西汀组(术前一天和术后6周),另外60名患者被随机分配到安慰剂组。在术后 12、24、48 和 72 小时以及术后 1、3 和 6 个月的随访中记录止痛药和阿片类药物的用量、疼痛评分和患者满意度。术前以及术后 3、6、12 和 24 个月时对患者报告的结果指标(PROMs)进行了评估。还记录了与度洛西汀相关的副作用,如恶心/呕吐和疲劳:结果:度洛西汀组患者使用镇痛抢救药物的时间明显延长,对阿片类药物(包括塞来昔布、普瑞巴林、对乙酰氨基酚和曲马多)的需求减少。术后 24、48、72 小时以及术后 1 和 3 个月,患者的疼痛强度降低,对疼痛治疗的满意度提高(P < 0.05)。与安慰剂组相比,度洛西汀组在3个月和6个月随访时的临床和功能效果也明显更好(P < 0.05)。度洛西汀副作用症状的发生率和发生率不显著:讨论:抑郁症是一个需要考虑和解决的重要因素,因为在手术前出现抑郁症可预测不良的术后结果,包括更严重的术后疼痛、持续性术后疼痛以及止痛药和阿片类药物用量的增加:结论:抑郁症患者在进行ATFL修复术治疗CAI后,围手术期使用度洛西汀能延长患者术后首次要求使用镇痛药的时间,并减少阿片类药物的用量和术后疼痛。患者对这种方法的满意度也很高。此外,度洛西汀还能提高康复质量,且不会产生明显的副作用:证据级别:I;前瞻性随机对照试验。
{"title":"Perioperative duloxetine improves postoperative outcomes after anterior talofibular ligament repair for chronic lateral ankle instability for patients with depression: A prospective randomized clinical trial","authors":"","doi":"10.1016/j.otsr.2024.103837","DOIUrl":"10.1016/j.otsr.2024.103837","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;div&gt;&lt;span&gt;Recent studies have indicated that depression is associated with persistent postoperative pain and decreased satisfaction following &lt;/span&gt;foot and ankle surgery&lt;span&gt;. This study aimed to evaluate the effect of perioperative duloxetine on postoperative outcomes of anterior talofibular ligament (ATFL) surgical repair for chronic ankle instability (CAI) in patients with depression. We further sought to evaluate patients’ satisfaction and side effects related to duloxetine.&lt;/span&gt;&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Material and methods&lt;/h3&gt;&lt;div&gt;&lt;span&gt;Patients undergoing ATFL repair were screened for depression preoperatively with the Patient Health Questionnaire (PHQ-9). Among 249 patients who underwent arthroscopic or open surgical Brostrom repair of the ATFL, 120 patients were identified as being “possibly depressed” and were included in the study. Sixty patients were randomly assigned to the duloxetine group (one day preoperatively and for 6 weeks postoperatively), and the other sixty were randomized to the placebo group. Painkillers and opioid consumption, pain scores, and patient satisfaction were recorded at 12, 24, 48, and 72&lt;/span&gt; &lt;!--&gt;hours postoperatively and at follow-up visits 1, 3, and 6 months after surgery. Patient-reported outcome measures (PROMs) were assessed preoperatively and at 3, 6, 12 and 24 months postoperatively. Duloxetine-related side effects such as nausea/vomiting and fatigue were also recorded.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;div&gt;&lt;span&gt;&lt;span&gt;&lt;span&gt;&lt;span&gt;The patients in the duloxetine group reported a significantly longer time to rescue &lt;/span&gt;analgesic and reduced opioid requirements (including &lt;/span&gt;celecoxib, &lt;/span&gt;pregabalin&lt;span&gt;, acetaminophen, and tramadol). The patients experienced decreased pain intensity and greater satisfaction with their pain management at 24, 48, 72&lt;/span&gt;&lt;/span&gt; &lt;!--&gt;h and 1 and 3 months after surgery (&lt;em&gt;p&lt;/em&gt; &lt;!--&gt;&lt;&lt;!--&gt; &lt;!--&gt;0.05). The duloxetine group also had significantly better clinical and functional outcomes at 3 and 6 months of follow-up compared to the placebo group (&lt;em&gt;p&lt;/em&gt; &lt;!--&gt;&lt;&lt;!--&gt; &lt;!--&gt;0.05). The occurrence and rate of symptoms of duloxetine side effects were not significant.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Discussion&lt;/h3&gt;&lt;div&gt;Depression is an important factor to consider and address because its presence before surgery can predict poor postoperative outcomes, including more severe postoperative pain, persistent postoperative pain, and increased consumption of painkillers and opioids.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;div&gt;Perioperative administration of duloxetine following ATFL repair for CAI in patients with depression increased the time to first postoperative rescue analgesic request and reduced both opioid consumption and postoperative pain. This approach also led to a high level of patient satisfaction. In addition, duloxetine improved the quality of recovery without leading to significant side effects.&lt;/div&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Level of evidence&lt;/h3","PeriodicalId":54664,"journal":{"name":"Orthopaedics & Traumatology-Surgery & Research","volume":"110 7","pages":"Article 103837"},"PeriodicalIF":2.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139736715","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Patient Acceptable Symptom State (PASS) after proximal and distal femoral replacement 股骨近端和远端置换术后患者可接受症状状态(PASS)。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2024.103931

Introduction

Femoral megaprostheses are used for bone reconstruction surgery in patients with local tumors or who require multiple revisions. Patient reported outcome measures (PROMs) provide a subjective result and, like patient satisfaction, have become an integral part of the outcomes in orthopedics. However, the threshold of satisfaction (PASS: Patient Acceptable Symptom State) has not yet been defined in a French population after this type of arthroplasty. This led us to carry out a retrospective study on a population of patients who received a femoral reconstruction megaprosthesis in order to 1) define the PASS for the Harris Hip Score (HHS), Knee Society Score (KSS) and the Musculoskeletal Tumor Society score (MSTS), 2) study the complications.

Hypothesis

The PASS threshold for proximal femur and distal femur reconstruction prothesis for the HHS and the KSS, respectively, will be lower than the threshold for these same scores for primary arthroplasty.

Materials and methods

Forty-four patients who were operated on between 2009 and 2020 were included: 23 received a proximal femur prosthesis and 21 received a distal femur prosthesis. The PASS threshold was defined using an anchoring strategy by analyzing ROC curves for the HSS for the proximal femur, KSS for the distal femur and the MSTS for all the prostheses. Complications were classified according to Henderson.

Results

The mean follow-up was 4.5 ± 3.6 (1–12.5) years. The PASS threshold was 47.5 (area under curve (AUC) 0.71 (0.45–0.97)) for the HHS, 69.5 (AUC 0.97 (0.92–1.0)) for the KSS knee and 62.5 (AUC 0.81 (0.61–0.99)) for the KSS function. Thirteen patients (29%) had complications, nine of whom required another surgery (20%). The most frequent were Henderson type 1 (soft tissue lesions, n = 5/44 [11%]) and type 2 (loosening, n = 5/44 [11%]) There was no relationship between satisfaction and postoperative complications (p = 0.071).

Discussion

Most of the patients who undergo femoral resection and reconstruction (59%) are satisfied with their function, albeit reduced, despite a high complication rate (29%). Our hypothesis is confirmed for the PASS threshold for the HHS (47.5 versus 93) and the KSS knee and function (69.5 and 62.5 versus 85.5 and 72.5).

Level of evidence

IV; retrospective observational single-center study.
导言:股骨巨型假体用于局部肿瘤患者或需要多次翻修的患者的骨重建手术。患者报告结果测量(PROMs)提供的是一种主观结果,与患者满意度一样,已成为骨科结果的一个组成部分。然而,在法国人群中,此类关节置换术后的满意度阈值(PASS:患者可接受的症状状态)尚未确定。因此,我们对接受股骨重建巨型假体的患者进行了一项回顾性研究,目的是:1)确定哈里斯髋关节评分(HHS)、膝关节协会评分(KSS)和肌肉骨骼肿瘤协会评分(MSTS)的PASS;2)研究并发症:假设:股骨近端和股骨远端重建假体的HHS和KSS的PASS阈值将分别低于初次关节成形术的相同评分阈值:纳入2009年至2020年间接受手术的44名患者:23名患者接受了股骨近端假体,21名患者接受了股骨远端假体。通过分析股骨近端假体的HSS、股骨远端假体的KSS和所有假体的MSTS的ROC曲线,采用锚定策略确定了PASS阈值。并发症根据亨德森分类:平均随访时间为 4.5 ± 3.6 (1-12.5) 年。HHS的PASS阈值为47.5(曲线下面积(AUC)为0.71(0.45-0.97)),KSS膝关节的PASS阈值为69.5(AUC为0.97(0.92-1.0)),KSS功能的PASS阈值为62.5(AUC为0.81(0.61-0.99))。13名患者(29%)出现并发症,其中9人需要再次手术(20%)。最常见的并发症是亨德森1型(软组织病变,n = 5/44 [11%])和2型(松动,n = 5/44 [11%]),满意度与术后并发症之间没有关系(p = 0.071):讨论:尽管并发症发生率较高(29%),但大多数接受股骨切除和重建术的患者(59%)对其功能表示满意,尽管功能有所减退。我们的假设在HHS的PASS阈值(47.5对93)以及KSS膝关节和功能(69.5和62.5对85.5和72.5)方面得到了证实:证据级别:IV;单中心回顾性观察研究。
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引用次数: 0
Long-term safety of total knee arthroplasty in patients with chronic kidney disease in Taiwan: A retrospective cohort study 台湾慢性肾病患者接受全膝关节置换术的长期安全性:一项回顾性队列研究。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2024.103847

Background

Chronic kidney disease (CKD) is a prevalent condition in Taiwan, and the incidence of total knee arthroplasty (TKA) is on the rise. This study aimed to evaluate the postoperative results of patients with different degrees of CKD after TKA, using data from the Taiwan National Health Insurance Research Database.

Methods

The study analyzed 3078 patients who received TKA from 2012 to 2017, equally divided into three groups: none-CKD, mild CKD (without dialysis), and severe CKD (with dialysis). Propensity score matching was used to minimize selection bias.

Results

After TKA, there was no significant difference in the risk of debridement surgery for infection between the three groups (adjusted HR of mild CKD: 0.71 95% CI = 0.36–1.38, p = 0.3073; adjusted HR of severe CKD: 1.14, 95% CI = 0.63–2.06, p = 0.6616). However, CKD patients requiring dialysis had a significantly higher risk of mortality (adjusted HR: 1.98, 95% CI = 1.57–2.50, p < 0.001) and readmission within 90 days of any causes (adjusted HR: 1.83, 95% CI = 1.48–2.26, p < 0.001) than non-CKD and mild CKD patients.

Conclusion

Severe CKD patients needing dialysis after TKA have a higher risk of mortality and readmission rates than that of the non-CKD or mild CKD patients. If the patient is in the early stage of CKD, their prognosis after receiving TKA is expected to be as good as non-CKD patients.

Level of evidence

IV; well-designed cohort study.
背景:慢性肾脏病(CKD)是台湾的一种流行病,而全膝关节置换术(TKA)的发病率正在上升。本研究旨在利用台湾国民健康保险研究数据库的数据,评估不同程度的 CKD 患者接受 TKA 后的术后效果:研究分析了2012年至2017年接受TKA的3078名患者,将其平均分为三组:非CKD、轻度CKD(无透析)和重度CKD(有透析)。为减少选择偏差,采用了倾向评分匹配法:TKA术后,三组患者因感染而进行清创手术的风险无明显差异(轻度CKD的调整HR为0.71,95% CI = 0.36 - 1.38,P = 0.3073;重度CKD的调整HR为1.14,95% CI = 0.63 - 2.06,P = 0.6616)。然而,与非 CKD 和轻度 CKD 患者相比,需要透析的 CKD 患者的死亡风险(调整后 HR 1.98,95% CI = 1.57 - 2.50,P < 0.001)和 90 天内因任何原因再次入院的风险(调整后 HR 1.83,95% CI = 1.48 - 2.26,P < 0.001)明显更高:结论:与非 CKD 或轻度 CKD 患者相比,TKA 术后需要透析的重度 CKD 患者的死亡率和再入院率风险更高。如果患者处于 CKD 早期,接受 TKA 后的预后预计与非 CKD 患者一样好:证据级别:IV;精心设计的队列研究。
{"title":"Long-term safety of total knee arthroplasty in patients with chronic kidney disease in Taiwan: A retrospective cohort study","authors":"","doi":"10.1016/j.otsr.2024.103847","DOIUrl":"10.1016/j.otsr.2024.103847","url":null,"abstract":"<div><h3>Background</h3><div>Chronic kidney disease<span> (CKD) is a prevalent condition in Taiwan, and the incidence of total knee arthroplasty (TKA) is on the rise. This study aimed to evaluate the postoperative results of patients with different degrees of CKD after TKA, using data from the Taiwan National Health Insurance Research Database.</span></div></div><div><h3>Methods</h3><div>The study analyzed 3078 patients who received TKA from 2012 to 2017, equally divided into three groups: none-CKD, mild CKD (without dialysis), and severe CKD (with dialysis). Propensity score matching was used to minimize selection bias.</div></div><div><h3>Results</h3><div><span>After TKA, there was no significant difference in the risk of debridement surgery for infection between the three groups (adjusted HR of mild CKD: 0.71 95% CI</span> <!-->=<!--> <!-->0.36–1.38, <em>p</em> <!-->=<!--> <!-->0.3073; adjusted HR of severe CKD: 1.14, 95% CI<!--> <!-->=<!--> <!-->0.63–2.06, <em>p</em> <!-->=<!--> <!-->0.6616). However, CKD patients requiring dialysis had a significantly higher risk of mortality (adjusted HR: 1.98, 95% CI<!--> <!-->=<!--> <!-->1.57–2.50, <em>p</em> <!-->&lt;<!--> <!-->0.001) and readmission within 90<!--> <!-->days of any causes (adjusted HR: 1.83, 95% CI<!--> <!-->=<!--> <!-->1.48–2.26, <em>p</em> <!-->&lt;<!--> <!-->0.001) than non-CKD and mild CKD patients.</div></div><div><h3>Conclusion</h3><div>Severe CKD patients needing dialysis after TKA have a higher risk of mortality and readmission rates than that of the non-CKD or mild CKD patients. If the patient is in the early stage of CKD, their prognosis after receiving TKA is expected to be as good as non-CKD patients.</div></div><div><h3>Level of evidence</h3><div>IV; well-designed cohort study.</div></div>","PeriodicalId":54664,"journal":{"name":"Orthopaedics & Traumatology-Surgery & Research","volume":"110 7","pages":"Article 103847"},"PeriodicalIF":2.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139991866","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Does inverse kinematic alignment coupled with robot-assisted TKA optimize patellofemoral clinical and radiological results? 反向运动对位配合机器人辅助 TKA 是否能优化髌骨的临床和放射学效果?
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2024.103880

Introduction

With a satisfaction rate of 80%, total knee arthroplasty (TKA) surgery has seen significant improvements in recent decades. The 20% of poor results may be explained by the alignment technique used for implant placement, which can influence patellofemoral kinematics. The objective of this study was to demonstrate that the use of inverse kinematic alignment makes it possible to obtain satisfactory clinical and radiological patellar scores in robotic TKA.

Hypothesis

The inverse kinematic alignment technique coupled with robotic surgery makes it possible to restore the native kinematics of the patella.

Materials and methods

This prospective study including 100 TKAs with a primary TKA performed using the Stryker Mako™ robotic surgery system, and the inverse kinematic alignment technique. Patients who underwent patella resurfacing were excluded. Clinical and radiological scores were recorded preoperatively and 1 year postoperatively.

Results

At one year, the specific patellar clinical scores were excellent with an average Kujala score of 85.69 and an average HSS Patellar score 88.15. The average patellar lateralization index was 0.15 and the average patellar tilt was 5.1°, showing no significant difference compared to preoperation (p = 0.45 and p = 0.18). The average external rotation of the femoral implant was 0.47 ± 0.6° [–1.9; 2.1].

Discussion

The patellofemoral clinical results were excellent. The use of the robotic arm coupled with this alignment technique makes it possible to obtain a controlled external rotation of the femoral implant as well as an optimized orientation of the tibial component, favoring good restitution of the alignment of the extensor apparatus. This study did not demonstrate any radiological correction of patellar tilt and lateralization.

Conclusion

The combined use of robotic surgery with the inverse kinematic alignment technique seems effective on specific clinical results of the patellofemoral joint.

Level of evidence

II; prospective cohort.
导言:近几十年来,全膝关节置换术(TKA)手术的满意率高达 80%,取得了显著的进步。20%的手术效果不佳可能是由于植入假体时使用的对位技术影响了髌股关节运动学。本研究的目的是证明在机器人TKA手术中使用逆运动学对位可以获得令人满意的临床和放射学髌骨评分:假设:逆运动学对位技术与机器人手术相结合,可恢复髌骨的原生运动学:这项前瞻性研究包括100例使用史赛克Mako™机器人手术系统和逆运动学配准技术进行的初级TKA。接受髌骨复位手术的患者除外。术前和术后一年记录临床和放射学评分:术后一年,患者的髌骨临床评分非常好,Kujala评分平均为85.69分,HSS髌骨评分平均为88.15分。髌骨外侧化指数平均为0.15,髌骨倾斜度平均为5.1°,与手术前相比无显著差异(P=0.45和P=0.18)。股骨假体的平均外旋度为0.47±0.6°[-1.9; 2.1]:讨论:髌骨股骨的临床效果非常好。讨论:髌骨的临床效果非常好,机器人手臂的使用加上这种对位技术,使得股骨假体的外旋得到了控制,胫骨组件的方向也得到了优化,有利于外展装置对位的良好恢复。本研究未显示任何髌骨倾斜和外侧化的放射学校正:结论:机器人手术与逆运动学对位技术的结合使用似乎对髌股关节的具体临床效果有效:II级;前瞻性队列
{"title":"Does inverse kinematic alignment coupled with robot-assisted TKA optimize patellofemoral clinical and radiological results?","authors":"","doi":"10.1016/j.otsr.2024.103880","DOIUrl":"10.1016/j.otsr.2024.103880","url":null,"abstract":"<div><h3>Introduction</h3><div><span>With a satisfaction rate of 80%, total knee arthroplasty (TKA) surgery has seen significant improvements in recent decades. The 20% of poor results may be explained by the alignment technique used for </span>implant placement, which can influence patellofemoral kinematics. The objective of this study was to demonstrate that the use of inverse kinematic alignment makes it possible to obtain satisfactory clinical and radiological patellar scores in robotic TKA.</div></div><div><h3>Hypothesis</h3><div>The inverse kinematic alignment technique coupled with robotic surgery<span> makes it possible to restore the native kinematics of the patella.</span></div></div><div><h3>Materials and methods</h3><div>This prospective study including 100 TKAs with a primary TKA performed using the Stryker Mako™ robotic surgery system, and the inverse kinematic alignment technique. Patients who underwent patella resurfacing were excluded. Clinical and radiological scores were recorded preoperatively and 1 year postoperatively.</div></div><div><h3>Results</h3><div>At one year, the specific patellar clinical scores were excellent with an average Kujala score of 85.69 and an average HSS Patellar score 88.15. The average patellar lateralization index was 0.15 and the average patellar tilt was 5.1°, showing no significant difference compared to preoperation (<em>p</em> <!-->=<!--> <!-->0.45 and <em>p</em> <!-->=<!--> <!-->0.18). The average external rotation of the femoral implant was 0.47<!--> <!-->±<!--> <!-->0.6° [–1.9; 2.1].</div></div><div><h3>Discussion</h3><div>The patellofemoral clinical results were excellent. The use of the robotic arm coupled with this alignment technique makes it possible to obtain a controlled external rotation of the femoral implant as well as an optimized orientation of the tibial component, favoring good restitution of the alignment of the extensor apparatus. This study did not demonstrate any radiological correction of patellar tilt and lateralization.</div></div><div><h3>Conclusion</h3><div>The combined use of robotic surgery with the inverse kinematic alignment technique seems effective on specific clinical results of the patellofemoral joint.</div></div><div><h3>Level of evidence</h3><div>II; prospective cohort.</div></div>","PeriodicalId":54664,"journal":{"name":"Orthopaedics & Traumatology-Surgery & Research","volume":"110 7","pages":"Article 103880"},"PeriodicalIF":2.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140867832","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lumbar scoliosis and stenosis: What outcomes for which treatment? Analysis of three surgical techniques in 154 patients with minimum two-year follow-up 腰椎侧弯和狭窄:哪种治疗方法有什么效果?对 154 例至少随访两年的患者采用的三种手术技术进行分析。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2023.103632

Study design

Prospective multicentric study.

Objective

This study goal was to analyze the clinical and radiographic outcomes of lumbar stenosis and scoliosis (LSS) patients, treated with lumbar decompression (LD), short fusion and decompression (SF) or long fusion with deformity correction (LF).

Hypothesis

Procedures without correction lead to poorer long-term outcomes.

Methods

Consecutive patients with two-year minimum follow-up, older than 50, with lumbar scoliosis (Cobb angle > 15°), and symptomatic lumbar stenosis were included. Age, gender, Lumbar and Radicular Visual Analog Scale, ODI, SF12 and SRS30 were collected. Main and adjacent curves Cobb angles, C7 coronal tilt (C7CT), spinopelvic parameters, and spino-sacral angle (SSA) were measured preoperatively, at one and two years. Patients were sorted into surgery type groups.

Results

In total, 154 patients were included, with respectively 18, 58 and 78 patients in LD, SF and LF groups. Mean age was 69, 85% were women. Clinical scores improved in each group at one year, but only LF group exhibited persistent improvement at 2 years. A significant fractional Cobb angle increase was noted in the SF group at 2 years (from 12 ± 11° to 18 ± 14°). C7CT significantly increased in the LD group at 2 years (from 2.5 ± 1.3° to 5.1 ± 3.5°). LF group presented the highest complication rate (45%, 19% for SF and 0% for LD). The overall revision rate was 14% in SF group and 30% in LF group.

Conclusion

LSS is a complex pathology requiring custom-made surgical treatment. LD, SF and LF allow satisfactory clinical outcome, with a better and more sustained clinical improvement for LF despite higher complication and revision rates.

Level of evidence

IV.
研究设计前瞻性多中心研究:研究目的:分析腰椎管狭窄症和脊柱侧弯症(LSS)患者的临床和影像学结果,这些患者接受了腰椎减压术(LD)、短融合减压术(SF)或长融合畸形矫正术(LF)治疗:假设:未进行畸形矫正的手术会导致较差的长期疗效:方法:纳入至少随访两年、年龄超过 50 岁、患有腰椎侧弯(Cobb 角>15°)和无症状腰椎管狭窄的连续患者。收集年龄、性别、腰椎和脊柱视觉模拟量表、ODI、SF12 和 SRS30。在术前、术后一年和两年测量主要和邻近曲线的 Cobb 角、C7 冠状位倾斜度(C7CT)、脊柱骨盆参数和脊骶角度(SSA)。患者按手术类型分组:共纳入 154 名患者,其中 LD、SF 和 LF 组分别有 18、58 和 78 名患者。平均年龄为69岁,85%为女性。各组患者的临床评分在一年后均有改善,但只有低频组在两年后有持续改善。SF组在2年后Cobb角明显增加(从12±11°增加到18±14°)。LD 组的 C7CT 在 2 年后明显增加(从 2.5±1.3° 增加到 5.1±3.5°)。LF 组的并发症发生率最高(45%,SF 组为 19%,LD 组为 0%)。SF组的总体翻修率为14%,LF组为30%:结论:LSS是一种复杂的病理,需要个性化的手术治疗。尽管并发症和翻修率较高,但 LD、SF 和 LF 的临床疗效令人满意,其中 LF 的临床疗效更好、更持久:证据等级:IV。
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引用次数: 0
Patellar resurfacing might not be mandatory in contralateral second total knee replacement even if performed during replacement of the first knee 在对侧第二次全膝关节置换术中,即使在置换第一个膝关节时进行了髌骨复位,也不一定必须进行髌骨复位。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2024.103857

Introduction

The appropriateness or necessity of patellar resurfacing in total knee arthroplasty (TKA) is not clearly established. The objective of the present study was to compare the clinical and functional results of patients with bilateral involvement, operated on in one knee by TKA with patellar resurfacing and in the other knee by TKA without resurfacing. The hypothesis was that there was no difference in results between the two sides.

Method

This was a retrospective cohort of patients operated on by TKA without patellar resurfacing in a second osteoarthritic knee after contralateral TKA with patellar resurfacing. Twenty consecutive patients who underwent second primary TKA constituted their own control group (40 knees). Iwano scores were comparable. Mean age was 75.9 ± 6.2 years. Mean time between the two procedures was 20.6 ± 11.9 months.

Results

There were no differences in SF-36, KOOS or Lille patellofemoral scores between the right and left knees. Sixty-five percent of patients were unable to differentiate the performance of their knees in activities of daily living.

Conclusion

The present study did not differentiate results according to patellar resurfacing, showing the limitations of resurfacing for early functional gain after primary TKA. Resurfacing might thus not be essential, even if it was performed in replacement of the first knee.

Level of evidence

IV; retrospective cohort study.
导言:在全膝关节置换术(TKA)中进行髌骨复位是否合适或必要,目前尚无明确定论。本研究的目的是比较双侧受累患者的临床和功能结果,其中一侧膝关节接受了髌骨复位的全膝关节置换术,另一侧膝关节则未接受髌骨复位的全膝关节置换术。假设两侧手术效果无差异:这是一项回顾性队列研究,研究对象是在对侧进行髌骨复位的TKA手术后,在第二个膝关节骨性关节炎的膝关节上进行TKA手术但不进行髌骨复位的患者。连续接受第二次初级 TKA 手术的 20 名患者组成对照组(40 个膝关节)。伊瓦诺评分具有可比性。平均年龄为 75.9 ± 6.2 岁。两次手术的平均间隔时间为(20.6 ± 11.9)个月:结果:左右膝关节的 SF-36、KOOS 或里尔髌骨评分没有差异。65%的患者无法区分膝关节在日常生活活动中的表现:本研究并未根据髌骨复位的情况对结果进行区分,这表明髌骨复位在初次TKA术后早期功能恢复方面存在局限性。证据等级:IV;回顾性队列研究:证据级别:IV;回顾性队列研究。
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引用次数: 0
Pregnancy and childbirth after adolescent idiopathic scoliosis surgery: A study of 80 pregnancies 青少年特发性脊柱侧弯手术后的妊娠和分娩:对80例妊娠的研究。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2023.103711

Background

Adolescent idiopathic scoliosis (AIS) is a common spinal disease affecting 2% of adolescents, and women in 90% of the cases. When a surgical treatment is opted for, many questions are frequently asked by families and patients about the course of pregnancy and childbirth after the spinal fusion. This subject remains little studied in the literature, especially with modern instrumentation techniques.

Hypothesis

The goal was to describe pregnancy and childbirth after AIS surgery in terms of access to epidural analgesia, need for cesarean section (c-section), and low back pain during and after pregnancy. We thus hypothesized that women undergoing spinal surgery for AIS have subsequently uncomplicated pregnancies and childbirths, and have access to epidural analgesia as women without AIS do.

Patients and methods

In this retrospective multicenter study, 198 women who underwent surgery between 1984 and 2014 were reviewed from two university hospitals. Among them, 50 women became pregnant, for a total of 80 pregnancies. Surgical data were collected [approach, uppermost and lowermost instrumented vertebra (UIV, LIV)]. Pregnancy characteristics were evaluated: time between surgery and pregnancy, number of births, mode of analgesia, type of delivery, weight gain. Occurrence of low back pain during pregnancy and at follow-up was recorded using ODI.

Results

Of the 50 women, 34 had posterior surgery and 16 had anterior surgery. Deliveries took place from 1988 to 2018. Of the 80 pregnancies, 81% were delivered by vaginal route (n = 65/80), and an effective epidural anesthesia was performed for 49% of them (n = 39/80). Epidural analgesia failed in 9% of pregnancies (n = 7/80), and was denied in 35% of cases (n = 28/80), half of the time by anesthesiologists (n = 15/80). Patients refused epidural in 13 pregnancies (16%, n = 13/80). A general anesthesia was used in six pregnancies (8%, n = 6/80), for c-sections only. Back pain was reported in 48% of the pregnancies (n = 38/80). The level of fusion was correlated with c-section, and conversely with epidural anesthesia.

Discussion

A normal pregnancy with vaginal delivery seems to be the rule for women undergoing spinal fusion for AIS. The c-section rate in AIS women was similar to the general population (19%). Yet, access to epidural anesthesia still seems problematic with only 49% of births in this series, compared with 81% in the French population.

Level of evidence

IV, retrospective cohort.
背景:青少年特发性脊柱侧弯(AIS)是一种常见的脊柱疾病,影响2%的青少年,90%的病例为女性。当选择手术治疗时,家庭和患者经常会询问许多关于脊柱融合术后怀孕和分娩过程的问题。这一主题在文献中很少被研究,尤其是在现代仪器技术方面。假设:目的是描述AIS手术后的妊娠和分娩,包括硬膜外镇痛的途径、剖宫产(剖腹产)的需要以及妊娠期间和之后的腰痛。因此,我们假设接受AIS脊柱手术的女性随后怀孕和分娩都没有并发症,并且可以像没有AIS的女性一样获得硬膜外镇痛。患者和方法:在这项回顾性多中心研究中,对1984年至2014年间从两所大学医院接受手术的198名女性进行了回顾。其中,有50名妇女怀孕,总共有80名妇女怀孕。收集手术数据(入路、最上面和最下面的器械椎骨(UIV、LIV))。评估妊娠特征:手术与妊娠之间的时间、分娩次数、镇痛方式、分娩类型、体重增加。使用ODI记录怀孕期间和随访时腰痛的发生情况。结果:50名女性中,34名接受了后部手术,16名接受了前部手术。交付时间为1988年至2018年。在80例妊娠中,81%通过阴道途径分娩(N=65/80),其中49%采用了有效的硬膜外麻醉(N=39/80)。硬膜外镇痛在9%的妊娠中失败(N=7/80),在35%的妊娠中被拒绝(N=28/80),一半的时间被麻醉师拒绝(N=15/80)。13例妊娠患者拒绝硬膜外麻醉(16%,N=13/80)。全身麻醉用于6例妊娠(8%,N=6/80),仅用于剖腹产。据报道,48%的孕妇出现背痛(N=38/80)。融合程度与剖腹产相关,与硬膜外麻醉相反。讨论:阴道分娩的正常妊娠似乎是接受AIS脊柱融合术的女性的规则。AIS妇女的剖腹产率与普通人群相似(19%)。然而,硬膜外麻醉似乎仍然存在问题,在这一系列中,只有49%的新生儿出生,而法国人口的这一比例为81%。证据水平:IV,回顾性队列。
{"title":"Pregnancy and childbirth after adolescent idiopathic scoliosis surgery: A study of 80 pregnancies","authors":"","doi":"10.1016/j.otsr.2023.103711","DOIUrl":"10.1016/j.otsr.2023.103711","url":null,"abstract":"<div><h3>Background</h3><div>Adolescent idiopathic scoliosis<span> (AIS) is a common spinal disease affecting 2% of adolescents, and women in 90% of the cases. When a surgical treatment is opted for, many questions are frequently asked by families and patients about the course of pregnancy and childbirth<span> after the spinal fusion. This subject remains little studied in the literature, especially with modern instrumentation techniques.</span></span></div></div><div><h3>Hypothesis</h3><div><span>The goal was to describe pregnancy and childbirth after AIS surgery in terms of access to epidural analgesia, need for </span>cesarean section (c-section), and low back pain during and after pregnancy. We thus hypothesized that women undergoing spinal surgery for AIS have subsequently uncomplicated pregnancies and childbirths, and have access to epidural analgesia as women without AIS do.</div></div><div><h3>Patients and methods</h3><div><span>In this retrospective multicenter study, 198 women who underwent surgery between 1984 and 2014 were reviewed from two university hospitals. Among them, 50 women became pregnant, for a total of 80 pregnancies. Surgical data were collected [approach, uppermost and lowermost instrumented vertebra (UIV, LIV)]. Pregnancy characteristics were evaluated: time between surgery and pregnancy, number of births, mode of analgesia, type of delivery, weight gain. Occurrence of low back pain during pregnancy and at follow-up was recorded using </span>ODI.</div></div><div><h3>Results</h3><div>Of the 50 women, 34 had posterior surgery and 16 had anterior surgery. Deliveries took place from 1988 to 2018. Of the 80 pregnancies, 81% were delivered by vaginal route (<em>n</em> <!-->=<!--> <span>65/80), and an effective epidural anesthesia was performed for 49% of them (</span><em>n</em> <!-->=<!--> <!-->39/80). Epidural analgesia failed in 9% of pregnancies (<em>n</em> <!-->=<!--> <!-->7/80), and was denied in 35% of cases (<em>n</em> <!-->=<!--> <!-->28/80), half of the time by anesthesiologists (<em>n</em> <!-->=<!--> <!-->15/80). Patients refused epidural in 13 pregnancies (16%, <em>n</em> <!-->=<!--> <span>13/80). A general anesthesia was used in six pregnancies (8%, </span><em>n</em> <!-->=<!--> <span>6/80), for c-sections only. Back pain was reported in 48% of the pregnancies (</span><em>n</em> <!-->=<!--> <!-->38/80). The level of fusion was correlated with c-section, and conversely with epidural anesthesia.</div></div><div><h3>Discussion</h3><div>A normal pregnancy with vaginal delivery seems to be the rule for women undergoing spinal fusion for AIS. The c-section rate in AIS women was similar to the general population (19%). Yet, access to epidural anesthesia still seems problematic with only 49% of births in this series, compared with 81% in the French population.</div></div><div><h3>Level of evidence</h3><div>IV, retrospective cohort.</div></div>","PeriodicalId":54664,"journal":{"name":"Orthopaedics & Traumatology-Surgery & Research","volume":"110 7","pages":"Article 103711"},"PeriodicalIF":2.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49685051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retroarticular drilling for osteochondritis dissecans of the talus: A systematic review 后关节钻孔治疗距骨软骨炎:系统性综述。
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2024.103834

Background

Opinions differ on the optimal treatment for stable talar osteochondritis dissecans (OCD) with intact cartilage. Some recommend conservative management, while others prefer surgical care, which includes debridement and micro-fractures, transarticular drilling through a direct or medial malleolus approach and retroarticular drilling. The rationale behind retroarticular drilling is to induce bone marrow healing without touching the intact cartilage. The goal of this systematic review is to summarize the clinical outcomes of retroarticular drilling as a standalone procedure for stable talar OCD with intact cartilage.

Patients and methods

A systematic review of the literature prospectively registered in the PROSPERO register was performed along the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Medline, EMBASE and Evidence-Based Medicine databases were searched from inception to December 2021 for retroarticular drilling for stable talar OCD with an intact cartilage. Two independent evaluators screened the search results, selected the articles to be included in the analysis and assessed the methodological quality of all included articles with the Newcastle-Ottawa Scale (NOS).

Results

Twelve studies, on 99 patients were included in the final analysis. Methodological quality was poor for all the included studies. High heterogeneity prevented any pooling or meta-analysis, but favorable clinical results were reported according to excellent post-intervention scores on the American Orthopedic Foot and Anke Score (AOFAS), ranging from 88.9 to 100. There was also significant improvement in pain as measured by the Visual Analog Scale (VAS), ranging between 2.3 and 5.9.

Discussion

Favorable results seem to be achieved with retroarticular drilling without grafting for stable talar OCD with intact cartilage, but more powered comparative studies between surgical options and conservative management are needed to establish the gold standard treatment.

Level of evidence

IV.
背景:对于软骨完整的稳定型距骨软骨炎(OCD)的最佳治疗方法众说纷纭。一些人建议保守治疗,而另一些人则倾向于手术治疗,包括清创和微骨折、通过直接或内侧踝骨途径进行经关节钻孔以及后关节钻孔。后关节钻孔的原理是在不接触完整软骨的情况下诱导骨髓愈合。本系统性综述的目的是总结后关节钻孔作为一种独立手术治疗稳定的距骨OCD且软骨完好的临床结果:根据系统综述和荟萃分析首选报告项目(PRISMA)指南,对在PROSPERO注册中心登记的前瞻性文献进行了系统综述。在 Medline、EMBASE 和循证医学数据库中检索了从开始到 2021 年 12 月期间有关后关节钻孔治疗稳定的距骨 OCD 且软骨完好的文献。两名独立评估员对检索结果进行了筛选,选出了纳入分析的文章,并采用纽卡斯尔-渥太华量表(NOS)对所有纳入文章的方法学质量进行了评估:最终分析共纳入了 12 项研究,涉及 99 名患者。所有纳入研究的方法学质量均较差。由于异质性较高,因此无法进行汇总或荟萃分析,但根据美国骨科足踝评分(AOFAS)显示,干预后的评分从 88.9 分到 100 分不等,临床效果良好。用视觉模拟量表(VAS)测量,疼痛也有明显改善,从 2.3 到 5.9 不等:讨论:对于软骨完好的稳定型距骨OCD,后关节钻孔而不植骨似乎能取得良好的效果,但需要对手术方案和保守治疗进行更多的研究,以确定金标准治疗方法:证据等级:IV。
{"title":"Retroarticular drilling for osteochondritis dissecans of the talus: A systematic review","authors":"","doi":"10.1016/j.otsr.2024.103834","DOIUrl":"10.1016/j.otsr.2024.103834","url":null,"abstract":"<div><h3>Background</h3><div><span>Opinions differ on the optimal treatment for stable talar osteochondritis dissecans (OCD) with intact cartilage. Some recommend conservative management, while others prefer surgical care, which includes </span>debridement<span><span> and micro-fractures, transarticular drilling through a direct or medial malleolus approach and retroarticular drilling. The rationale behind retroarticular drilling is to induce bone marrow healing without touching the intact cartilage. The goal of this </span>systematic review is to summarize the clinical outcomes of retroarticular drilling as a standalone procedure for stable talar OCD with intact cartilage.</span></div></div><div><h3>Patients and methods</h3><div>A systematic review of the literature prospectively registered in the PROSPERO register was performed along the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Medline, EMBASE and Evidence-Based Medicine databases were searched from inception to December 2021 for retroarticular drilling for stable talar OCD with an intact cartilage. Two independent evaluators screened the search results, selected the articles to be included in the analysis and assessed the methodological quality of all included articles with the Newcastle-Ottawa Scale (NOS).</div></div><div><h3>Results</h3><div>Twelve studies, on 99 patients were included in the final analysis. Methodological quality was poor for all the included studies. High heterogeneity prevented any pooling or meta-analysis, but favorable clinical results were reported according to excellent post-intervention scores on the American Orthopedic<span> Foot and Anke Score (AOFAS), ranging from 88.9 to 100. There was also significant improvement in pain as measured by the Visual Analog Scale (VAS), ranging between 2.3 and 5.9.</span></div></div><div><h3>Discussion</h3><div>Favorable results seem to be achieved with retroarticular drilling without grafting for stable talar OCD with intact cartilage, but more powered comparative studies between surgical options and conservative management are needed to establish the gold standard treatment.</div></div><div><h3>Level of evidence</h3><div>IV.</div></div>","PeriodicalId":54664,"journal":{"name":"Orthopaedics & Traumatology-Surgery & Research","volume":"110 7","pages":"Article 103834"},"PeriodicalIF":2.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139716681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
MPFL reconstruction with proximal rather than distal femoral tunnel position leads to less favorable short-term results 采用股骨隧道近端而非远端位置进行 MPFL 重建,短期效果较差
IF 2.3 3区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-01 DOI: 10.1016/j.otsr.2024.103816

Background

This study aimed to compare the clinical and radiological outcomes of medial patellofemoral ligament (MPFL) reconstruction (MPFLR) between anatomic femoral tunnel positions: proximal (near adductor tubercle [AT]) and distal (near medial epicondyle [ME]).

Hypothesis

MPFLR with the proximal femoral tunnel position has worse clinical and radiological outcomes than those with the distal femoral tunnel position.

Patients and methods

Fifty-five patients who underwent isolated MPFLR with proximal or distal femoral tunnels with at least 2 years of follow-up were retrospectively analyzed. Based on postoperative CT images, 28 patients were classified as group AT and the remaining 27 patients were classified as group ME. The International Knee Documentation Committee, Lysholm, Tegner, Kujala scores, and complications were evaluated. Radiologically, the Caton-Deschamps Index (CDI), patellar tilt angle, patellofemoral osteoarthritis (PFOA), patellofemoral cartilage status by the International Cartilage Repair Society (ICRS) grade, bone contusion, and MPFL graft signal intensity were evaluated.

Results

All clinical scores significantly improved in both groups (p < 0.01). No statistically significant difference was noted between the two groups in regards to their preoperative demographic data, postoperative clinical scores, complications, or radiological findings (CDI, patellar tilt angle, PFOA, bone contusion, and graft signal intensity). The group AT had worse cartilage status on the medial facet of the patella (p = 0.02). The ICRS grade for the medial facet of the patella statistically progressed in group AT compared to group ME (p = 0.04) as well.

Discussion

Both groups showed significantly improved clinical outcomes. However, for the medial facet of the patella, MPFLR with the proximal femoral tunnel position had worse cartilage status and ICRS grade progression than those with the distal femoral tunnel position.

Level of evidence

III; retrospective comparative study.
背景:本研究旨在比较股骨隧道近端(靠近内收肌结节[AT])和远端(靠近内上髁[ME])解剖位置的髌股内侧韧带(MPFL)重建术(MPFLR)的临床和放射学结果:假设:股骨隧道近端位置的 MPFLR 比股骨隧道远端位置的 MPFLR 的临床和放射学结果更差:回顾性分析了55例接受股骨近端或远端隧道孤立性MPFLR手术且随访至少2年的患者。根据术后CT图像,28名患者被分为AT组,其余27名患者被分为ME组。对国际膝关节文献委员会、Lysholm、Tegner、Kujala 评分和并发症进行了评估。在放射学方面,对卡顿-德尚指数(CDI)、髌骨倾斜角、髌股骨关节炎(PFOA)、国际软骨修复学会(ICRS)分级的髌股软骨状况、骨挫伤和 MPFL 移植信号强度进行了评估:结果:两组患者的所有临床评分均有明显改善(p <0.01)。两组在术前人口统计学数据、术后临床评分、并发症或放射学结果(CDI、髌骨倾斜角、PFOA、骨挫伤和移植物信号强度)方面均无统计学差异。AT 组髌骨内侧面软骨状况较差(P = 0.02)。与ME组相比,AT组髌骨内侧面的ICRS分级在统计学上也有所提高(P = 0.04):讨论:两组的临床疗效均有明显改善。然而,就髌骨内侧面而言,股骨隧道近端位置的 MPFLR 比股骨隧道远端位置的 MPFLR 的软骨状况和 ICRS 分级进展更差:证据级别:III;回顾性比较研究。
{"title":"MPFL reconstruction with proximal rather than distal femoral tunnel position leads to less favorable short-term results","authors":"","doi":"10.1016/j.otsr.2024.103816","DOIUrl":"10.1016/j.otsr.2024.103816","url":null,"abstract":"<div><h3>Background</h3><div>This study aimed to compare the clinical and radiological outcomes of medial patellofemoral ligament (MPFL) reconstruction (MPFLR) between anatomic femoral tunnel positions: proximal (near adductor tubercle [AT]) and distal (near medial epicondyle [ME]).</div></div><div><h3>Hypothesis</h3><div>MPFLR with the proximal femoral tunnel position has worse clinical and radiological outcomes than those with the distal femoral tunnel position.</div></div><div><h3>Patients and methods</h3><div>Fifty-five patients who underwent isolated MPFLR with proximal or distal femoral tunnels with at least 2 years of follow-up were retrospectively analyzed. Based on postoperative CT images, 28 patients were classified as group AT and the remaining 27 patients were classified as group ME. The International Knee Documentation Committee, Lysholm, Tegner, Kujala scores, and complications were evaluated. Radiologically, the Caton-Deschamps Index (CDI), patellar tilt angle, patellofemoral osteoarthritis (PFOA), patellofemoral cartilage status by the International Cartilage Repair Society (ICRS) grade, bone contusion, and MPFL graft signal intensity were evaluated.</div></div><div><h3>Results</h3><div>All clinical scores significantly improved in both groups (<em>p</em> <!-->&lt;<!--> <span>0.01). No statistically significant difference was noted between the two groups in regards to their preoperative demographic data, postoperative clinical scores, complications, or radiological findings<span> (CDI, patellar tilt angle, PFOA, bone contusion, and graft signal intensity). The group AT had worse cartilage status on the medial facet of the patella (</span></span><em>p</em> <!-->=<!--> <!-->0.02). The ICRS grade for the medial facet of the patella statistically progressed in group AT compared to group ME (<em>p</em> <!-->=<!--> <!-->0.04) as well.</div></div><div><h3>Discussion</h3><div>Both groups showed significantly improved clinical outcomes. However, for the medial facet of the patella, MPFLR with the proximal femoral tunnel position had worse cartilage status and ICRS grade progression than those with the distal femoral tunnel position.</div></div><div><h3>Level of evidence</h3><div>III; retrospective comparative study.</div></div>","PeriodicalId":54664,"journal":{"name":"Orthopaedics & Traumatology-Surgery & Research","volume":"110 7","pages":"Article 103816"},"PeriodicalIF":2.3,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139508046","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Orthopaedics & Traumatology-Surgery & Research
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