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Journal of Hand Surgery-American Volume最新文献

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Perioperative Patient Experience in Office-Based Wide-Awake Hand Surgery. 办公室宽醒手部手术的围手术期患者体验。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-22 DOI: 10.1016/j.jhsa.2024.10.009
Shafic Sraj, Brendan J Farley, John S Taras, Andrea B Lese, B Joseph Prud'homme, Richard Gross, Wing Yan Vien Cheung, Stephanie Cox

Purpose: Office-based surgery, is a safe, well-tolerated option associated with high patient satisfaction. However, some patients remain hesitant due to concerns of being awake during surgery. Preoperative anxiety may be linked to poorer postoperative outcomes. The purpose of this study was to examine patients' distress prior to, during, and following office-based hand surgery under local anesthesia and to identify patient variables associated with distress.

Methods: This study included 57 patients, 19 of whom had a history of anxiety and/or depression. Each patient completed the Amsterdam Preoperative Anxiety and Information Scale (APAIS) before surgery; patients completed the Subjective Units of Disturbance Scale (SUDS) before surgery, immediately after surgery, and at their first postoperative visit. They rated their SUDS with respect to the following distress domains: Being Awake During Surgery, Needlestick, Surgical Pain, and Discomfort.

Results: The average distress experienced was less than the patients' preoperative expectations across all domains, and most patients rated their experiences to be equivalent to or better than expected (81 to 96% of patients, depending on the domain). Patients with elevated APAIS scores were more likely to have less distress (a better experience) than expected compared to those who were not.

Conclusions: Average distress levels experienced were better than expected. Patients with higher APAIS had less distress (better experiences) than they expected.

Type of study/level of evidence: Prognosis II.

目的:办公室手术是一种安全、耐受性好、患者满意度高的选择。然而,一些患者由于担心手术过程中保持清醒而犹豫不决。术前焦虑可能与较差的术后效果有关。本研究的目的是检查患者在局部麻醉下进行诊室手部手术之前、期间和之后的痛苦,并确定与痛苦相关的患者变量:本研究包括 57 名患者,其中 19 人有焦虑和/或抑郁病史。每位患者在术前都填写了阿姆斯特丹术前焦虑和信息量表(APAIS);患者在术前、术后即刻和术后首次就诊时都填写了主观干扰单位量表(SUDS)。他们就以下困扰领域对自己的 SUDS 进行了评分:结果:结果:在所有领域中,患者经历的平均痛苦程度均低于术前预期,大多数患者对自己经历的评价相当于或优于预期(81% 至 96% 的患者,视领域而定)。APAIS评分升高的患者与未升高的患者相比,其痛苦程度(更好的经历)更有可能低于预期:结论:患者的平均痛苦程度比预期的要好。研究类型/证据级别:预后 II。
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引用次数: 0
Benefits of Sensory Nerve Transfers and Risks of Using the Superficial Radial Nerve as a Donor. 感觉神经移植的益处和使用桡侧浅神经作为供体的风险
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-21 DOI: 10.1016/j.jhsa.2024.09.027
Yamaan S Saadeh, Martijn J Malessy

Nerve transfers have re-emerged in the past several decades as a powerful tool for restoration of neurological function and are an essential part of peripheral nerve surgical practice. There is extensive literature describing outcomes from nerve transfers for the restoration of motor nerve function and describing the complication profile. Recently, interest and use of nerve transfers for restoration of sensation has increased. In this review, we highlight the limitations of the current literature on outcomes from sensory nerve transfers and showcase potential complications from their use, particularly related to use of the superficial branch of the radial nerve as a donor sensory nerve.

在过去的几十年中,神经转移作为恢复神经功能的有力工具重新崛起,成为周围神经手术实践中不可或缺的一部分。有大量文献描述了神经转移术在恢复运动神经功能方面的疗效以及并发症情况。最近,人们对用于恢复感觉的神经转移的兴趣和使用有所增加。在这篇综述中,我们强调了目前有关感觉神经转移结果的文献的局限性,并展示了使用这种方法可能出现的并发症,尤其是与使用桡神经浅支作为供体感觉神经有关的并发症。
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引用次数: 0
Outcomes of Median Nerve Release in Complex Regional Pain Syndrome Type 1 of the Hand: A Prospective Case Series. 手部 1 型复杂区域疼痛综合征的正中神经松解术疗效:前瞻性病例系列。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-21 DOI: 10.1016/j.jhsa.2024.09.024
Francisco Del Piñal

Purpose: Pain, allodynia, and stiffness in complex regional pain syndrome (CRPS) greatly affects social, vocational, and community engagement. The aim of this study was to evaluate the effect of isolated median nerve releases on the outcome of CRPS 1 of the hand.

Methods: In this prospective case series, people of any age diagnosed with and treated for CRPS 1 of the upper limb attending the author's practice were consecutively recruited. All were self-referrals dissatisfied with the treatment provided previously. Only patients who had been treated with nerve release to control their symptoms were included. Primary outcome measures were pain and Disabilities of the Arm, Shoulder, and Hand score. A secondary outcome was withdrawal from pain medication. Full resolution was defined as 0 pain, on a scale of 0-10, and total withdrawal from pain medication at the latest follow-up.

Results: Between January 2018 and December 2022, 82 participants with CRPS 1 of the hand for an average of 20 months were evaluated. Eighty-five nerve releases were performed. As per protocol, carpal tunnel release was performed in all, and three patients also received an endoscopic pronator release. Minor procedures unrelated to the pain were carried out concomitantly in 17 patients. Significant improvements were observed in pain score (mean 8.9 ± 1.2 at baseline vs 0.6 ± 1.8 at 35 months) and in Disabilities of the Arm, Shoulder, and Hand score (82 ± 13 vs 13 ± 20) for the same period. Five patients (6%) were considered failures. In contrast, 65 patients (79%) had full resolution of their symptoms.

Conclusions: This study demonstrates that a large percentage of patients diagnosed with and treated for CRPS type 1 can have full resolution of their symptoms with carpal tunnel release. Future research is needed to understand the pathophysiology and the failures.

Type of study/level of evidence: Therapeutic II.

目的:复杂性区域疼痛综合征(CRPS)的疼痛、异痛和僵硬会严重影响患者的社交、职业和社区参与。本研究旨在评估孤立正中神经松解术对手部 CRPS 1 治疗效果的影响:在这项前瞻性病例系列研究中,连续招募了在作者诊所就诊的任何年龄段的上肢 CRPS 1 患者。所有患者都是对之前的治疗不满意而自行转诊的。只有接受过神经松解术治疗以控制症状的患者才包括在内。主要结果指标是疼痛和手臂、肩部和手部残疾评分。次要结果是停用止痛药物。完全缓解的定义是,在最近一次随访中,疼痛程度为0(0-10分),且完全停用止痛药物:结果:2018 年 1 月至 2022 年 12 月期间,共有 82 名参与者接受了评估,他们患有手部 CRPS 1,平均病程为 20 个月。共进行了 85 例神经松解术。按照方案,所有患者都接受了腕管松解术,3 名患者还接受了内窥镜下的代指松解术。17名患者同时接受了与疼痛无关的小手术。疼痛评分(基线时平均为 8.9±1.2 分,35 个月时为 0.6±1.8 分)和同期手臂、肩部和手部残疾评分(82±13 分,13±20 分)均有显著改善。五名患者(6%)被视为治疗失败。相比之下,65 名患者(79%)的症状得到了完全缓解:这项研究表明,大部分被诊断为 CRPS 1 型并接受治疗的患者都能通过腕管松解术完全缓解症状。未来的研究需要了解病理生理学和失败的原因:治疗 II.
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引用次数: 0
Claims Database Research in Hand Surgery: From Data to Bedside. 手外科索赔数据库研究:从数据到床边
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-21 DOI: 10.1016/j.jhsa.2024.10.004
Thompson Zhuang, Lauren M Shapiro, Robin N Kamal

The widespread availability of administrative claims data has unlocked opportunities to answer challenging clinical questions in hand surgery, overcoming the limitations of traditional data sets. Researchers are taking advantage of claims data sets to obtain samples from broader segments of the population and achieve statistical power that was previously unattainable. Therefore, a basic understanding of claims database research is quickly becoming an invaluable tool in the surgeon's toolkit, enabling the performance of ground-breaking research and the critical evaluation of data-driven results to inform clinical practice. We provide an overview of methodological approaches to claims data analysis for hand surgery and a roadmap for analyzing and interpreting these studies in clinical practice.

行政报销数据的普及为回答手外科具有挑战性的临床问题提供了机会,克服了传统数据集的局限性。研究人员正在利用理赔数据集从更广泛的人群中获取样本,并获得以前无法实现的统计能力。因此,对索赔数据库研究的基本了解正迅速成为外科医生工具包中的一个宝贵工具,使他们能够进行突破性研究,并对数据驱动的结果进行批判性评估,为临床实践提供依据。我们概述了手外科索赔数据分析的方法论,以及在临床实践中分析和解释这些研究的路线图。
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引用次数: 0
Investigating the Effect of Triamcinolone Local Injection on Clinical Outcomes of Patients With Radial Tunnel Syndrome: A Placebo-Controlled Clinical Trial. 研究曲安奈德局部注射对桡骨隧道综合征患者临床疗效的影响:安慰剂对照临床试验。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-19 DOI: 10.1016/j.jhsa.2024.09.023
Fariba Estaji, Mahla Daliri, Shahryar Hashemi, Ali Moradi

Purpose: The role of corticosteroid injection for radial tunnel syndrome (RTS) has not been studied in a placebo-controlled clinical trial. The present clinical trial aimed to evaluate the effect of local triamcinolone injection on pain intensity, upper-extremity disability, and elbow function of patients with RTS.

Methods: Forty-nine patients clinically diagnosed with RTS were randomized into the intervention and placebo groups. The diagnosis of RTS was made based on the following criteria: activity-related pain, maximal tenderness 3 to 5 cm distal to the lateral epicondyle, pain that worsens with forearm supination, pain radiating to the dorsoradial aspect of the forearm, and a positive Lister test. To confirm RTS, patients needed to exhibit at least four of these five criteria, with the requirement that one of the criteria be the tenderness located 3-5 cm distal to the lateral epicondyle. Patients in the intervention group received local injection of a single dose of corticosteroid (0.25 mL lidocaine 1% and 1 mL triamcinolone 40 mg/mL), and the placebo group received injection of single dose of normal saline (0.25 mL lidocaine 1% and 1 mL normal saline). The clinical outcomes, including QuickDASH (Disabilities of the Arm, Shoulder, and Hand), visual analog scale for pain, and Oxford Elbow Score, were evaluated before treatment, as well as 2 weeks and 3 months after the injection.

Results: Visual analog scale pain score, QuickDASH score, and Oxford Elbow Scores were similar between the intervention and placebo groups at 2 weeks and 3 months of follow-up. However, reduction in visual analog scale pain, QuickDASH score, and Oxford Elbow Scores were statistically significant over time among both groups.

Conclusions: Triamcinolone injection does not have any superior effect on the clinical outcomes of patients with RTS, compared with placebo.

Type of study/level of evidence: Therapeutic II.

目的:安慰剂对照临床试验尚未研究皮质类固醇注射对桡骨隧道综合征(RTS)的作用。本临床试验旨在评估局部注射曲安奈德对 RTS 患者疼痛强度、上肢残疾和肘关节功能的影响:临床诊断为 RTS 的 49 名患者被随机分为干预组和安慰剂组。RTS的诊断标准如下:活动相关性疼痛、外侧上髁远端3至5厘米处最大压痛、前臂上举时疼痛加剧、疼痛向前臂背侧放射、李斯特试验阳性。要确认 RTS,患者至少需要具备上述五项标准中的四项,其中一项标准必须是位于外侧上髁远端 3-5 厘米处的压痛。干预组患者接受单剂量皮质类固醇局部注射(0.25 mL 1%利多卡因和 1 mL 40 mg/mL 曲安奈德),安慰剂组患者接受单剂量生理盐水注射(0.25 mL 1%利多卡因和 1 mL 生理盐水)。对治疗前、注射后 2 周和 3 个月的临床结果进行了评估,包括 QuickDASH(手臂、肩部和手部残疾)、疼痛视觉模拟量表和牛津肘部评分:结果:在随访 2 周和 3 个月时,干预组和安慰剂组的疼痛视觉模拟量表评分、QuickDASH 评分和牛津肘评分相似。然而,随着时间的推移,两组的视觉模拟量表疼痛评分、QuickDASH 评分和牛津肘评分均有显著的统计学意义:结论:与安慰剂相比,曲安奈德注射对RTS患者的临床疗效没有任何优越性:治疗 II.
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引用次数: 0
Complications and Outcomes of Bone-Anchored Prostheses of the Hand: A Systematic Review. 手部骨缺损假体的并发症和疗效:系统回顾。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-19 DOI: 10.1016/j.jhsa.2024.09.017
Taylor Bates, Liana J Tedesco, Janos Barrera, Adam Margalit, Michael Fitzgerald, Jacques Hacquebord, Omri Ayalon

Purpose: The purpose of this study was to conduct a systematic review evaluating the reported complications and outcomes of bone-anchored prostheses in digit and partial hand amputees.

Methods: A literature review of primary research articles on osseointegration and bone-anchored prostheses for digit and partial amputees was performed. The Medline, Embase, Scopus, and Cochrane Library databases were queried. Inclusion criteria were journal articles that evaluated osseointegration and bone-anchored prostheses in digit and partial hand amputees. The main outcome measures were reported complications and the need for revision surgery. Secondary outcomes included all reported outcome assessments.

Results: Fifteen articles were included with publication dates ranging from 1996 to 2022. The sample sizes ranged from single-patient case reports to a 13-patient retrospective study. Overall, 33 men and 16 women were reported with a mean age of 33.6 years (range: 12-68) and a total of 71 amputated digits. The median follow-up was 2.1 years (IQR: 1.1-6.8 years). A total of 24 complications were reported in 14 digits (19.7%). Complications included superficial infection in 6 digits (8.5%), abutment loosening or failure in 5 (7%), fixture aseptic loosening in 4 (5.6%), deep infection in 1 (1.4%), and soft tissue instability in 1 (1.4%). Sixteen revision surgeries or component changes were reported.

Conclusions: Bone-anchored prostheses using osseointegrated implants in the hand are associated with favorable outcomes in the limited number of low-quality studies available for review. Superficial infections and implant-related failures were the most frequently reported complications.

Type of study/level of evidence: Systematic review IV.

目的:本研究的目的是进行系统性综述,评估已报道的骨锚定假体用于数位和部分手部截肢者的并发症和结果:对有关骨结合和骨锚定假体用于截肢者和部分截肢者的主要研究文章进行了文献综述。检索了 Medline、Embase、Scopus 和 Cochrane 图书馆数据库。纳入标准是评估骨结合和骨锚定假体用于数位和部分手部截肢者的期刊文章。主要结果指标为报告的并发症和翻修手术需求。次要结果包括所有报告的结果评估:共纳入 15 篇文章,发表日期从 1996 年到 2022 年不等。样本量从单个患者的病例报告到13名患者的回顾性研究不等。总共有 33 名男性和 16 名女性接受了研究,平均年龄为 33.6 岁(范围:12-68 岁),共截肢 71 个指头。中位随访时间为 2.1 年(IQR:1.1-6.8 年)。据报告,有 14 个指头(19.7%)出现了 24 种并发症。并发症包括:6 位数(8.5%)的表皮感染、5 位数(7%)的基台松动或失败、4 位数(5.6%)的夹具无菌性松动、1 位数(1.4%)的深部感染和 1 位数(1.4%)的软组织不稳定。报告了16例翻修手术或组件更换:结论:在有限的低质量研究中,手部使用骨结合植入物的骨锚定假体具有良好的疗效。表皮感染和植入失败是最常见的并发症:系统综述 IV.
{"title":"Complications and Outcomes of Bone-Anchored Prostheses of the Hand: A Systematic Review.","authors":"Taylor Bates, Liana J Tedesco, Janos Barrera, Adam Margalit, Michael Fitzgerald, Jacques Hacquebord, Omri Ayalon","doi":"10.1016/j.jhsa.2024.09.017","DOIUrl":"https://doi.org/10.1016/j.jhsa.2024.09.017","url":null,"abstract":"<p><strong>Purpose: </strong>The purpose of this study was to conduct a systematic review evaluating the reported complications and outcomes of bone-anchored prostheses in digit and partial hand amputees.</p><p><strong>Methods: </strong>A literature review of primary research articles on osseointegration and bone-anchored prostheses for digit and partial amputees was performed. The Medline, Embase, Scopus, and Cochrane Library databases were queried. Inclusion criteria were journal articles that evaluated osseointegration and bone-anchored prostheses in digit and partial hand amputees. The main outcome measures were reported complications and the need for revision surgery. Secondary outcomes included all reported outcome assessments.</p><p><strong>Results: </strong>Fifteen articles were included with publication dates ranging from 1996 to 2022. The sample sizes ranged from single-patient case reports to a 13-patient retrospective study. Overall, 33 men and 16 women were reported with a mean age of 33.6 years (range: 12-68) and a total of 71 amputated digits. The median follow-up was 2.1 years (IQR: 1.1-6.8 years). A total of 24 complications were reported in 14 digits (19.7%). Complications included superficial infection in 6 digits (8.5%), abutment loosening or failure in 5 (7%), fixture aseptic loosening in 4 (5.6%), deep infection in 1 (1.4%), and soft tissue instability in 1 (1.4%). Sixteen revision surgeries or component changes were reported.</p><p><strong>Conclusions: </strong>Bone-anchored prostheses using osseointegrated implants in the hand are associated with favorable outcomes in the limited number of low-quality studies available for review. Superficial infections and implant-related failures were the most frequently reported complications.</p><p><strong>Type of study/level of evidence: </strong>Systematic review IV.</p>","PeriodicalId":54815,"journal":{"name":"Journal of Hand Surgery-American Volume","volume":" ","pages":""},"PeriodicalIF":2.1,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142683626","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Description of Specific Portals for Extensor Carpi Ulnaris Tenoscopy: Anatomical Safety Study. 描述用于伸拇肌腱鞘镜检查的特定入口:解剖安全性研究。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-19 DOI: 10.1016/j.jhsa.2024.10.005
Elisa de Torres-de Torres, Fernando Corella, Ricardo Kaempf de Oliveira, Montserrat Ocampos Hernández, Miguel Ángel Corella, María Teresa Vázquez-Osorio

Purpose: The objective of this study was to describe potential working portals positioned directly over the extensor carpi ulnaris (ECU) tendon and assess their safety in relation to the dorsal branch of the ulnar nerve (DBUN).

Methods: A descriptive anatomical study was conducted on 15 fresh human cadaver upper limbs. Five distinct portals over the ECU were examined, and the shortest distances from these portals to the DBUN were measured. Additionally, three distances from two portals and the ulnar styloid to the point where the DBUN crosses the ECU tendon were assessed.

Results: The measurements of the distance to the DBUN from the portal at the level of the ulnocarpal joint (UCJ) from the proximal ECU (PECU) portal and from the portals located two and three centimeters proximal to the PECU indicate that no distances fell within the high-risk category (less than 3.5 mm). Measuring from the portal at the level of the UCJ to the DBUN, only one specimen fell within the medium-risk range (3.5-4.5 mm). However, in the rest of the previously described portals, all measurements corresponded to a low-risk range (more than 4.5 mm). The measurements from the distal ECU (DECU) portal to the DBUN revealed that 4 of 15 specimens had a distance less than 3.5 mm (high-risk range), whereas 2 of 15 fell within the medium-risk range.

Conclusions: Proximal portals are safer and present a lower risk of nerve injury. Three distinct zones have been defined along the ECU based on their safety characteristics. The "green zone" is the safest area, situated 1 cm proximal to the 6R portal. The "yellow zone" encompasses the area extending from 1 cm proximal to 0.5 cm distal to the 6R portal. Finally, the "red zone" is located 0.5 cm distal to the 6R portal.

Clinical relevance: For arthroscopic procedures involving the ECU, additional portals may be necessary. This anatomical study may be valuable in developing and implementing surgical techniques tailored for ECU pathology.

目的:本研究旨在描述直接位于尺侧伸肌(ECU)肌腱上方的潜在工作门户,并评估其与尺神经背支(DBUN)的安全性:方法: 对 15 个新鲜人体尸体上肢进行了描述性解剖研究。方法:对 15 具新鲜人体尸体上肢进行了描述性解剖研究,检查了 ECU 上的五个不同门户,并测量了从这些门户到 DBUN 的最短距离。此外,还评估了从两个门户和尺骨髁到 DBUN 与 ECU 肌腱交叉点的三个距离:从尺桡关节(UCJ)水平的门户到 ECU 近端(PECU)门户,以及从 PECU 近端两厘米和三厘米处的门户到 DBUN 的距离测量结果表明,没有任何距离属于高风险类别(小于 3.5 毫米)。从 UCJ 水平的入口测量到 DBUN,只有一个标本属于中等风险范围(3.5-4.5 毫米)。然而,在之前描述的其他入口处,所有测量值都属于低风险范围(超过 4.5 毫米)。从ECU(DECU)远端门户到DBUN的测量结果显示,15个标本中有4个的距离小于3.5毫米(高风险范围),而15个标本中有2个属于中等风险范围:结论:近端门户更安全,神经损伤风险更低。根据 ECU 的安全特性,沿 ECU 划分了三个不同的区域。绿色区域 "是最安全的区域,位于6R入口近端1厘米处。黄区 "包括从 6R 门近端 1 厘米到远端 0.5 厘米的区域。最后,"红色区域 "位于 6R 门远端 0.5 厘米处:临床相关性:对于涉及 ECU 的关节镜手术,可能需要额外的入口。这项解剖学研究可能对开发和实施针对 ECU 病理的手术技术很有价值。
{"title":"Description of Specific Portals for Extensor Carpi Ulnaris Tenoscopy: Anatomical Safety Study.","authors":"Elisa de Torres-de Torres, Fernando Corella, Ricardo Kaempf de Oliveira, Montserrat Ocampos Hernández, Miguel Ángel Corella, María Teresa Vázquez-Osorio","doi":"10.1016/j.jhsa.2024.10.005","DOIUrl":"https://doi.org/10.1016/j.jhsa.2024.10.005","url":null,"abstract":"<p><strong>Purpose: </strong>The objective of this study was to describe potential working portals positioned directly over the extensor carpi ulnaris (ECU) tendon and assess their safety in relation to the dorsal branch of the ulnar nerve (DBUN).</p><p><strong>Methods: </strong>A descriptive anatomical study was conducted on 15 fresh human cadaver upper limbs. Five distinct portals over the ECU were examined, and the shortest distances from these portals to the DBUN were measured. Additionally, three distances from two portals and the ulnar styloid to the point where the DBUN crosses the ECU tendon were assessed.</p><p><strong>Results: </strong>The measurements of the distance to the DBUN from the portal at the level of the ulnocarpal joint (UCJ) from the proximal ECU (PECU) portal and from the portals located two and three centimeters proximal to the PECU indicate that no distances fell within the high-risk category (less than 3.5 mm). Measuring from the portal at the level of the UCJ to the DBUN, only one specimen fell within the medium-risk range (3.5-4.5 mm). However, in the rest of the previously described portals, all measurements corresponded to a low-risk range (more than 4.5 mm). The measurements from the distal ECU (DECU) portal to the DBUN revealed that 4 of 15 specimens had a distance less than 3.5 mm (high-risk range), whereas 2 of 15 fell within the medium-risk range.</p><p><strong>Conclusions: </strong>Proximal portals are safer and present a lower risk of nerve injury. Three distinct zones have been defined along the ECU based on their safety characteristics. The \"green zone\" is the safest area, situated 1 cm proximal to the 6R portal. The \"yellow zone\" encompasses the area extending from 1 cm proximal to 0.5 cm distal to the 6R portal. Finally, the \"red zone\" is located 0.5 cm distal to the 6R portal.</p><p><strong>Clinical relevance: </strong>For arthroscopic procedures involving the ECU, additional portals may be necessary. This anatomical study may be valuable in developing and implementing surgical techniques tailored for ECU pathology.</p>","PeriodicalId":54815,"journal":{"name":"Journal of Hand Surgery-American Volume","volume":" ","pages":""},"PeriodicalIF":2.1,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142683633","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Variation in Recommended Treatment Strategies Among American Surgeons for Actual Adult Traumatic Brachial Plexus Injury Cases. 美国外科医生对成人创伤性臂丛神经损伤实际病例推荐治疗策略的差异。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-18 DOI: 10.1016/j.jhsa.2024.10.002
Michele N Christy, Christopher J Dy, R Glenn Gaston, Bryan J Loeffler, Mihir J Desai, Steve K Lee, Harvey Chim, Jeffrey B Friedrich, Sameer K Puri, Jason H Ko

Purpose: The surgical management of adult traumatic brachial plexus injuries (BPI) is challenging, with no consensus on optimal strategies. This study aimed to gather preferred reconstructive strategies from BPI surgeons for actual cases from a multicenter cohort to identify areas of agreement.

Methods: Four case files (history, physical examination, and imaging and electrodiagnostic testing results) were distributed to eight self-designated Level IV expert BPI surgeons in the United States. Each surgeon independently reviewed the cases and provided a preferred reconstructive plan via free text response.

Results: For a pan-plexus case after blunt trauma (67 years old; 3 months from injury): three surgeons recommended nerve grafting upper trunk roots to distal targets. There was disagreement in shoulder reconstruction: one suggested early shoulder fusion, two preferred cranial nerve XI to suprascapular nerve (SSN) transfer, and two anticipated future salvage shoulder fusion. For elbow reconstruction, six surgeons preferred intercostal nerve to musculocutaneous nerve transfer. For an upper trunk injury from a motorcycle accident (33 years old; 6 months from injury), only one surgeon recommended nerve grafting, six preferred XI to SSN transfer, all recommended triceps-to-axillary transfer, and all but one favored a double fascicular transfer.

Conclusions: There is inconsistency in the use of nerve grafting for BPI patients, especially in pan-plexus injuries where options are limited. Variability exists in shoulder reconstruction and stability management, with some advocating early glenohumeral arthrodesis. Although single fascicular and triceps-to-axillary transfers are consistently favored, there is no consensus for restoring shoulder and elbow function when intraplexal transfers are unavailable.

Clinical relevance: This study highlights substantial variability in surgical approaches to BPI among experts, underscoring the need for standardized treatment protocols. Understanding these diverse strategies can inform clinical decision making and help develop more uniform guidelines to improve patient outcomes.

目的:成人创伤性臂丛神经损伤(BPI)的手术治疗极具挑战性,目前尚未就最佳策略达成共识。本研究旨在收集多中心队列中臂丛神经外科医生对实际病例的首选重建策略,以确定意见一致的领域:将四份病例档案(病史、体格检查、影像学和电子诊断测试结果)分发给美国八位自行指定的四级 BPI 外科医生。每位外科医生都独立审查了病例,并通过自由文本回复提供了首选的重建方案:对于钝性创伤后的泛神经丛病例(67 岁;受伤后 3 个月):三位外科医生建议将上干根神经移植到远端目标。在肩关节重建方面存在分歧:一名外科医生建议尽早进行肩关节融合术,两名外科医生倾向于将颅神经XI转移到肩胛上神经(SSN),还有两名外科医生预计将来会进行肩关节修复融合术。在肘部重建方面,六名外科医生倾向于肋间神经转运而非肌皮神经转运。对于因摩托车事故造成的上躯干损伤(33岁;受伤6个月),只有一名外科医生建议进行神经移植,六名外科医生倾向于XI神经与SSN神经的转移,所有外科医生都建议进行肱三头肌与腋神经的转移,除了一名外科医生外,所有外科医生都倾向于进行双筋膜转移:结论:BPI患者在使用神经移植方面存在不一致,尤其是在选择有限的泛神经损伤中。在肩部重建和稳定性管理方面也存在差异,有些人主张尽早进行盂肱关节固定术。虽然单一筋膜转移和肱三头肌至腋窝转移一直受到青睐,但在无法进行复合体内转移时,如何恢复肩部和肘部功能还没有达成共识:本研究强调了专家们在 BPI 手术方法上的巨大差异,强调了标准化治疗方案的必要性。了解这些不同的策略可为临床决策提供依据,并有助于制定更统一的指南来改善患者的预后。
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引用次数: 0
The Use of Cannabinoids in the Treatment of Peripheral Neuropathy and Neuropathic Pain: A Systematic Review. 使用大麻素治疗周围神经病变和神经性疼痛:系统综述》(The Use of Cannabinoids in the Treatment of Peripheral Neuropathy and Neuropathic Pain: A Systematic Review)。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-18 DOI: 10.1016/j.jhsa.2024.09.015
Janice Choi, Gabrielle Li, Kristen L Stephens, Michael P Timko, Brent R DeGeorge

Purpose: Peripheral neuropathies are commonly occurring conditions that are chronic and debilitating for patients. Established nonsurgical treatments have yielded mixed and patient-dependent results. Although cannabinoids have demonstrated efficacy as a treatment for central neuropathic pain, the therapeutic potential of cannabis-based medications for the management of peripheral neuropathic pain caused by nerve injury, trauma, and other noncompressive etiologies has yet to be definitively established. This study aims to determine whether cannabinoids are a potentially effective treatment for pain and symptoms associated with peripheral neuropathy.

Methods: A systematic search was conducted by two independent reviewers across PubMed, Cochrane, Ovid Medline, and CINAHL to identify studies in accordance with the predetermined inclusion/exclusion criteria. Information regarding study design, medication, dosage, effect on neuropathic pain, and other related outcomes was extracted. Meta-analysis of pain scores was performed for seven studies, and descriptive statistics were used to summarize other study findings as appropriate.

Results: Of the 927 studies identified, 14 randomized controlled trials were included. Thirteen of 14 studies (79%) observed a statistically significant decrease in neuropathic pain score following treatment with a cannabinoid. Meta-analysis yielded a mean difference of -0.67 [-0.89, -0.45]) on a 0-10 scale compared with placebo. Improvements in secondary outcomes such as sleep, sensory symptoms, and quality of life were observed.

Conclusions: Our analysis of the literature shows that cannabis-based medicines may be effective in treating the pain and symptoms of peripheral neuropathy. These findings suggest the applicability of cannabis-based medicines for peripheral neuropathy.

Type of study/level of evidence: Therapeutic IV.

目的:周围神经病是一种常见病,是一种慢性病,会使患者衰弱。既有的非手术疗法疗效参差不齐,且取决于患者的病情。虽然大麻素已被证明具有治疗中枢神经病理痛的功效,但大麻类药物在治疗神经损伤、创伤和其他非压迫性病因引起的周围神经病理痛方面的治疗潜力仍有待明确确定。本研究旨在确定大麻素是否是治疗周围神经病变相关疼痛和症状的潜在有效方法:方法:由两名独立审稿人在 PubMed、Cochrane、Ovid Medline 和 CINAHL 上进行系统检索,以确定符合预定纳入/排除标准的研究。提取了有关研究设计、药物、剂量、对神经性疼痛的影响以及其他相关结果的信息。对 7 项研究的疼痛评分进行了元分析,并酌情使用描述性统计学方法总结了其他研究结果:在确定的 927 项研究中,有 14 项随机对照试验被纳入其中。14 项研究中有 13 项(79%)观察到使用大麻素治疗后神经病理性疼痛评分有统计学意义的显著下降。元分析结果显示,与安慰剂相比,0-10 分的平均差异为-0.67 [-0.89, -0.45])。睡眠、感觉症状和生活质量等次要结果也有所改善:我们对文献的分析表明,以大麻为基础的药物可以有效治疗周围神经病变的疼痛和症状。研究类型/证据级别:治疗 IV。
{"title":"The Use of Cannabinoids in the Treatment of Peripheral Neuropathy and Neuropathic Pain: A Systematic Review.","authors":"Janice Choi, Gabrielle Li, Kristen L Stephens, Michael P Timko, Brent R DeGeorge","doi":"10.1016/j.jhsa.2024.09.015","DOIUrl":"https://doi.org/10.1016/j.jhsa.2024.09.015","url":null,"abstract":"<p><strong>Purpose: </strong>Peripheral neuropathies are commonly occurring conditions that are chronic and debilitating for patients. Established nonsurgical treatments have yielded mixed and patient-dependent results. Although cannabinoids have demonstrated efficacy as a treatment for central neuropathic pain, the therapeutic potential of cannabis-based medications for the management of peripheral neuropathic pain caused by nerve injury, trauma, and other noncompressive etiologies has yet to be definitively established. This study aims to determine whether cannabinoids are a potentially effective treatment for pain and symptoms associated with peripheral neuropathy.</p><p><strong>Methods: </strong>A systematic search was conducted by two independent reviewers across PubMed, Cochrane, Ovid Medline, and CINAHL to identify studies in accordance with the predetermined inclusion/exclusion criteria. Information regarding study design, medication, dosage, effect on neuropathic pain, and other related outcomes was extracted. Meta-analysis of pain scores was performed for seven studies, and descriptive statistics were used to summarize other study findings as appropriate.</p><p><strong>Results: </strong>Of the 927 studies identified, 14 randomized controlled trials were included. Thirteen of 14 studies (79%) observed a statistically significant decrease in neuropathic pain score following treatment with a cannabinoid. Meta-analysis yielded a mean difference of -0.67 [-0.89, -0.45]) on a 0-10 scale compared with placebo. Improvements in secondary outcomes such as sleep, sensory symptoms, and quality of life were observed.</p><p><strong>Conclusions: </strong>Our analysis of the literature shows that cannabis-based medicines may be effective in treating the pain and symptoms of peripheral neuropathy. These findings suggest the applicability of cannabis-based medicines for peripheral neuropathy.</p><p><strong>Type of study/level of evidence: </strong>Therapeutic IV.</p>","PeriodicalId":54815,"journal":{"name":"Journal of Hand Surgery-American Volume","volume":" ","pages":""},"PeriodicalIF":2.1,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142683648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Current Concepts Review: Radiation Plexopathy. 当前概念回顾:放射性神经丛病。
IF 2.1 2区 医学 Q2 ORTHOPEDICS Pub Date : 2024-11-18 DOI: 10.1016/j.jhsa.2024.09.026
Adam Mosa, David M Brogan, Christopher J Dy

Radiation induced brachial plexopathy represents a constellation of symptoms that present in a delayed manner because of peri-plexus progressive fibrosis or direct neural injury with demyelination. Symptom onset is typically delayed months to years after radiotherapy. Patients may report neuropathic pain, weakness, or extremity dysfunction associated with morbidity and diminished quality of life. Reported surgical interventions include plexus neurolysis, nerve transfers, and vascularized free tissue transfer. In this review, we aim to present the practicing hand surgeon with an update and analysis on the current state of the radiation induced brachial plexopathy literature.

放射性诱发的臂丛神经病是由于神经丛周围进行性纤维化或脱髓鞘的直接神经损伤而延迟出现的一系列症状。症状通常在放疗后数月至数年内延迟出现。患者可能会出现神经性疼痛、乏力或肢体功能障碍,并伴有发病率和生活质量下降。已报道的手术干预包括神经丛神经切除术、神经转移术和血管化游离组织转移术。在这篇综述中,我们旨在向执业手外科医生介绍辐射诱发臂丛神经病文献的最新进展和分析。
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Journal of Hand Surgery-American Volume
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