首页 > 最新文献

Foot & Ankle Orthopaedics最新文献

英文 中文
Validation of Foot Angular Measurements Using Intraoperative Simulated Weightbearing Fluoroscopic Images. 利用术中模拟负重透视图像验证足部角度测量。
Pub Date : 2026-02-12 eCollection Date: 2026-01-01 DOI: 10.1177/24730114261417690
Troye J Joseph, Nikiforos P Saragas, Michael de Buys, Paulo N F Ferrao

Background: Weightbearing foot and ankle radiographs are essential because skeletal geometry changes under load. Radiographic measurements, which guide management decisions, have been validated using weightbearing radiographs. Simulation of weightbearing intraoperatively would be ideal and may improve the accuracy of deformity correction in foot and ankle surgery. This study aims to validate the accuracy of angular measurements on intraoperative simulated weightbearing fluoroscopic foot images.

Methods: A prospective study of 50 patients with a mean age of 51.3 years undergoing elective foot surgery at a single institution was performed. A simulation of weightbearing was performed intraoperatively and fluoroscopic anteroposterior and lateral images were obtained. Six angular measurements were performed on the standard preoperative weightbearing radiographs and compared to the intraoperative simulated weightbearing fluoroscopic images, by 4 researchers at 2 intervals.

Results: The mean differences for the hallux valgus angle (HVA), intermetatarsal angle (IMA), interphalangeal angle (IPA), 4-5 intermetatarsal angle (4-5 IMA), calcaneal pitch (CP), and talocalcaneal angle (TCA) were +0.02, -1.79, +1.13, -0.01, +4.80, and -1.41 degrees, respectively. Of the anteroposterior and lateral measurements, the HVA, IPA, 4-5 IMA, and TCA showed no statistically significant mean difference (paired t test), and inter- and intraobserver reliability was good to excellent. The IMA and CP showed a mean difference that was statistically significant; however, this mean difference was clinically negligible (IMA: -1.79 ± 1.68 degrees; CP: 4.8 ± 3.4 degrees). A good inter- and intraobserver reliability was found between researchers. Regression analyses showed strong correlations for the HVA, IMA, 4-5 IMA, and CP and fair correlations for the TCA and IPA.

Conclusion: The study suggests the technique we use for intraoperative simulated weightbearing fluoroscopic imaging correlates with standard preoperative weightbearing foot radiographs and may facilitate a more accurate, real time assessment of alignment during foot deformity correction surgery.

Level of evidence: Level II, diagnostic.

背景:负重足部和踝关节x线片是必要的,因为骨骼几何形状在负荷下发生变化。用于指导管理决策的放射测量已通过负重x线片进行验证。术中负重模拟是理想的,可以提高足部和踝关节手术畸形矫正的准确性。本研究旨在验证术中模拟负重透视足部图像角度测量的准确性。方法:对50例平均年龄51.3岁、在同一医院接受择期足部手术的患者进行前瞻性研究。术中进行负重模拟,并获得透视正位和侧位图像。4名研究人员在术前标准负重x线片上进行了6次角度测量,并与术中模拟负重透视图像进行了对比。结果:拇外翻角(HVA)、跖间角(IMA)、指间角(IPA)、4-5跖间角(4-5 IMA)、跟距角(CP)、距跟角(TCA)的平均差异分别为+0.02度、-1.79度、+1.13度、-0.01度、+4.80度、-1.41度。在正位和侧位测量中,HVA、IPA、4-5 IMA和TCA没有统计学上显著的平均差异(配对t检验),观察者之间和观察者内部的信度从良好到优秀。IMA和CP的平均差异有统计学意义;然而,这一平均差异在临床上可以忽略不计(IMA: -1.79±1.68度;CP: 4.8±3.4度)。研究者之间具有良好的观察者之间和观察者内部的信度。回归分析显示HVA、IMA、4-5 IMA和CP有很强的相关性,TCA和IPA有一定的相关性。结论:本研究表明,术中模拟负重透视成像技术与标准的术前负重足部x线片相关,可能有助于更准确、实时地评估足部畸形矫正手术中的对齐情况。证据等级:II级,诊断性。
{"title":"Validation of Foot Angular Measurements Using Intraoperative Simulated Weightbearing Fluoroscopic Images.","authors":"Troye J Joseph, Nikiforos P Saragas, Michael de Buys, Paulo N F Ferrao","doi":"10.1177/24730114261417690","DOIUrl":"10.1177/24730114261417690","url":null,"abstract":"<p><strong>Background: </strong>Weightbearing foot and ankle radiographs are essential because skeletal geometry changes under load. Radiographic measurements, which guide management decisions, have been validated using weightbearing radiographs. Simulation of weightbearing intraoperatively would be ideal and may improve the accuracy of deformity correction in foot and ankle surgery. This study aims to validate the accuracy of angular measurements on intraoperative simulated weightbearing fluoroscopic foot images.</p><p><strong>Methods: </strong>A prospective study of 50 patients with a mean age of 51.3 years undergoing elective foot surgery at a single institution was performed. A simulation of weightbearing was performed intraoperatively and fluoroscopic anteroposterior and lateral images were obtained. Six angular measurements were performed on the standard preoperative weightbearing radiographs and compared to the intraoperative simulated weightbearing fluoroscopic images, by 4 researchers at 2 intervals.</p><p><strong>Results: </strong>The mean differences for the hallux valgus angle (HVA), intermetatarsal angle (IMA), interphalangeal angle (IPA), 4-5 intermetatarsal angle (4-5 IMA), calcaneal pitch (CP), and talocalcaneal angle (TCA) were +0.02, -1.79, +1.13, -0.01, +4.80, and -1.41 degrees, respectively. Of the anteroposterior and lateral measurements, the HVA, IPA, 4-5 IMA, and TCA showed no statistically significant mean difference (paired <i>t</i> test), and inter- and intraobserver reliability was good to excellent. The IMA and CP showed a mean difference that was statistically significant; however, this mean difference was clinically negligible (IMA: -1.79 ± 1.68 degrees; CP: 4.8 ± 3.4 degrees). A good inter- and intraobserver reliability was found between researchers. Regression analyses showed strong correlations for the HVA, IMA, 4-5 IMA, and CP and fair correlations for the TCA and IPA.</p><p><strong>Conclusion: </strong>The study suggests the technique we use for intraoperative simulated weightbearing fluoroscopic imaging correlates with standard preoperative weightbearing foot radiographs and may facilitate a more accurate, real time assessment of alignment during foot deformity correction surgery.</p><p><strong>Level of evidence: </strong>Level II, diagnostic.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114261417690"},"PeriodicalIF":0.0,"publicationDate":"2026-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12901831/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146200710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Temporary Transarticular Screw Fixation for Traumatic Peritalar Instability After Talar Fracture-Dislocation. 临时经关节螺钉固定治疗距骨骨折脱位后外伤性髂骨不稳。
Pub Date : 2026-02-12 eCollection Date: 2026-01-01 DOI: 10.1177/24730114261417683
Serge Andreou, Najeeb Baig, Rumyah Rafique, Ameen Suhrawardy, Pranav Khambete, Robert Meehan

Background: Traumatic peritalar instability following talar fracture-dislocation is a complex surgical challenge with no consensus on adjunctive stabilization. Current strategies can involve extensive soft tissue dissection or external fixation. We report a retrospective case series evaluating temporary transarticular screw fixation as an adjunct to open reduction and internal fixation (ORIF).

Methods: We conducted a retrospective case series of 9 patients (10 extremities) treated at a single tertiary institution between 2015 and 2024 for traumatic peritalar instability persisting after ORIF. After primary ORIF of the talus, persistent subtalar instability was addressed with one or two 4.0-mm cortical screws placed across the subtalar joint. Screws were removed after radiographic evidence of fracture union. Primary outcomes were resolution of instability judged by intraoperative resolution of dislocation/subluxation with maintenance of joint congruity to injury resolution. Secondary outcomes were incidence of complications, including avascular necrosis (AVN) and posttraumatic arthritis (PTA).

Results: The cohort included 9 patients (mean age 37 years) with a mean follow-up of 27 months. All 10 operative extremities achieved full resolution of peritalar instability. Three extremities required subsequent arthrodesis because of PTA and/or AVN. Two extremities developed AVN, with 2 of the 3 arthrodeses following AVN development. One patient did not have the transarticular screw removed because of articular surface damage at the time of index injury. Three extremities developed infections: 2 superficial infections resolved with oral antibiotics, and 1 deep infection necessitated tibiotalar and subtalar arthrodesis using an antibiotic-coated intramedullary nail due to osteomyelitis, with infection resolution and return to activity. Nine extremities exhibited some form of PTA in the peritalar articulations. Four of 10 patients underwent Achilles tendon lengthening for contracture. Eight of 9 patients returned to unprotected weightbearing and full activity at the most recent follow-up; 6 resumed work and could perform a double-leg heel rise, and 2 required bracing.

Conclusion: Temporary transarticular screw fixation appears safe in this limited series and effective for resolving traumatic peritalar instability. The observed AVN rate (20%) is lower than many published series but should be interpreted cautiously given the small sample size. PTA rates remain high but are consistent with the expected results because of the severity of the initial injury. This technique may serve as a valuable, minimally invasive adjunct in the management of complex talar trauma.

Level of evidence: Level IV, retrospective case series.

背景:距骨骨折脱位后的外伤性椎体周围不稳定是一个复杂的外科挑战,在辅助稳定方面尚无共识。目前的策略包括广泛的软组织剥离或外固定。我们报告了一个回顾性病例系列,评估临时经关节螺钉固定作为切开复位内固定(ORIF)的辅助手段。方法:我们对2015年至2024年间在同一所高等医疗机构治疗的9例(10条肢体)创伤性椎体周围不稳定的回顾性病例进行了分析。距骨原发性ORIF术后,通过在距下关节上放置一枚或两枚4.0 mm皮质螺钉来解决持续的距下不稳定问题。在x线片显示骨折愈合后取下螺钉。主要结局是通过术中脱位/半脱位的消退来判断不稳定的消退,并维持关节与损伤消退的一致性。次要结局是并发症的发生率,包括无血管坏死(AVN)和创伤后关节炎(PTA)。结果:该队列包括9例患者,平均年龄37岁,平均随访27个月。所有10个手术肢体均完全解决了椎体周围不稳定。由于PTA和/或AVN,三个肢体需要随后的关节融合术。2个肢体发生AVN, 3个关节中有2个发生AVN。1例患者在食指损伤时因关节面损伤未取下经关节螺钉。三个肢体发生感染:2例浅表感染通过口服抗生素解决,1例深部感染由于骨髓炎需要使用抗生素包被的髓内钉进行胫距和距下关节融合术,感染消退并恢复活动。九只肢体在肱骨周围关节处表现出某种形式的PTA。10例患者中有4例因挛缩而行跟腱延长术。在最近一次随访中,9例患者中有8例恢复无保护的负重和充分活动;6人恢复工作,可以进行双腿跟抬,2人需要支撑。结论:临时经关节螺钉固定在这个有限的系列中是安全的,并且可以有效地解决外伤性髂骨周围不稳定。观察到的AVN率(20%)低于许多已发表的系列,但考虑到样本量小,应谨慎解释。由于初始损伤的严重性,PTA率仍然很高,但与预期结果一致。该技术可作为一种有价值的微创辅助治疗复杂距骨创伤。证据级别:四级,回顾性病例系列。
{"title":"Temporary Transarticular Screw Fixation for Traumatic Peritalar Instability After Talar Fracture-Dislocation.","authors":"Serge Andreou, Najeeb Baig, Rumyah Rafique, Ameen Suhrawardy, Pranav Khambete, Robert Meehan","doi":"10.1177/24730114261417683","DOIUrl":"10.1177/24730114261417683","url":null,"abstract":"<p><strong>Background: </strong>Traumatic peritalar instability following talar fracture-dislocation is a complex surgical challenge with no consensus on adjunctive stabilization. Current strategies can involve extensive soft tissue dissection or external fixation. We report a retrospective case series evaluating temporary transarticular screw fixation as an adjunct to open reduction and internal fixation (ORIF).</p><p><strong>Methods: </strong>We conducted a retrospective case series of 9 patients (10 extremities) treated at a single tertiary institution between 2015 and 2024 for traumatic peritalar instability persisting after ORIF. After primary ORIF of the talus, persistent subtalar instability was addressed with one or two 4.0-mm cortical screws placed across the subtalar joint. Screws were removed after radiographic evidence of fracture union. Primary outcomes were resolution of instability judged by intraoperative resolution of dislocation/subluxation with maintenance of joint congruity to injury resolution. Secondary outcomes were incidence of complications, including avascular necrosis (AVN) and posttraumatic arthritis (PTA).</p><p><strong>Results: </strong>The cohort included 9 patients (mean age 37 years) with a mean follow-up of 27 months. All 10 operative extremities achieved full resolution of peritalar instability. Three extremities required subsequent arthrodesis because of PTA and/or AVN. Two extremities developed AVN, with 2 of the 3 arthrodeses following AVN development. One patient did not have the transarticular screw removed because of articular surface damage at the time of index injury. Three extremities developed infections: 2 superficial infections resolved with oral antibiotics, and 1 deep infection necessitated tibiotalar and subtalar arthrodesis using an antibiotic-coated intramedullary nail due to osteomyelitis, with infection resolution and return to activity. Nine extremities exhibited some form of PTA in the peritalar articulations. Four of 10 patients underwent Achilles tendon lengthening for contracture. Eight of 9 patients returned to unprotected weightbearing and full activity at the most recent follow-up; 6 resumed work and could perform a double-leg heel rise, and 2 required bracing.</p><p><strong>Conclusion: </strong>Temporary transarticular screw fixation appears safe in this limited series and effective for resolving traumatic peritalar instability. The observed AVN rate (20%) is lower than many published series but should be interpreted cautiously given the small sample size. PTA rates remain high but are consistent with the expected results because of the severity of the initial injury. This technique may serve as a valuable, minimally invasive adjunct in the management of complex talar trauma.</p><p><strong>Level of evidence: </strong>Level IV, retrospective case series.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114261417683"},"PeriodicalIF":0.0,"publicationDate":"2026-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12901916/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146200609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pilot, Randomized Comparison of Traditionally Fabricated Custom Foot Orthoses vs HP Arize 3D-Printed Orthoses for Plantar Fasciitis. 传统制作定制足部矫形器与HP 3d打印足底筋膜炎矫形器的试验,随机比较。
Pub Date : 2026-02-10 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251413246
J Benjamin Jackson, Kaleb Eaton, Harley T Davis, Emily McKinney, Tyler A Gonzalez

Background: Plantar fasciitis is the most common cause of plantar heel pain and the use of custom foot orthosis is a well-supported treatment modality. Traditional custom orthoses are fabricated using foam impressions and manual techniques, but these methods are time-intensive and susceptible to variability in fit and quality. The HP Arize platform applies high-resolution 3D laser scanning with algorithm-driven modeling to streamline fabrication of custom foot orthoses. Although early reports suggest comparable comfort and durability to traditional devices, clinical data evaluating patient-reported outcomes remain limited.

Methods: This prospective pilot, randomized study assigned 34 adults diagnosed with plantar fasciitis to receive either traditionally fabricated custom orthoses (n = 18) or HP Arize 3D-printed orthoses (n = 16). Primary analyses used a modified intention‑to‑treat cohort (n = 30) comprising participants who received an insert and completed baseline assessments. Patient-Reported Outcomes Measurement Information System (PROMIS) physical function, pain interference, and mobility scores were collected at baseline, 4 weeks, and 8 weeks. Secondary measures included patient satisfaction, frequency of orthotic use, and adverse effects. Statistical comparisons were performed using Fisher exact test and Student t test or Wilcoxon signed-rank test, with significance set at P < .05.

Results: Baseline demographic and clinical characteristics did not differ between groups. At 4 weeks, satisfaction with customization, fit, and comfort was high across both groups (median 4.0-5.0). Traditional orthosis users reported greater daily use (P = .04) but also higher rates of rubbing/discomfort (P = .047). By 8 weeks, side effects were not statistically significantly different. Exploratory comparisons suggested higher mean PROMIS physical function (49.0 vs 41.9, Δ 7.1; P = .008) and mobility scores (46.9 vs 41.4, Δ 5.5; P = .02) at 8 weeks in the traditional group, whereas pain interference scores did not differ.

Conclusion: Both traditionally fabricated and HP Arize 3D-printed custom orthoses were associated with high satisfaction and functional improvement. Although traditional devices showed greater early compliance and superior 8-week functional outcomes, the HP Arize system demonstrated fewer adverse effects and offers a scalable, efficient alternative. As an exploratory pilot study, these findings are preliminary and intended to inform feasibility and effect‑size estimation for future trials.

Level of evidence: Level IV, pilot prospective comparative study.

Type of study: Quasi-experimental pre-post study.

背景:足底筋膜炎是足底后跟疼痛最常见的原因,使用定制足部矫形器是一种得到良好支持的治疗方式。传统的定制矫形器是使用泡沫压模和手工技术制造的,但这些方法耗时长,而且易受适合度和质量变化的影响。HP alize平台采用高分辨率3D激光扫描和算法驱动的建模,简化了定制足部矫形器的制造。尽管早期的报告显示,与传统设备相比,其舒适度和耐用性相当,但评估患者报告结果的临床数据仍然有限。方法:这项前瞻性的随机研究将34名诊断为足底筋膜炎的成年人分配到传统制作的定制矫形器(n = 18)或HP Arize 3d打印矫形器(n = 16)。初步分析使用了修改后的意向治疗队列(n = 30),包括接受插入并完成基线评估的参与者。在基线、4周和8周收集患者报告的预后测量信息系统(PROMIS)的身体功能、疼痛干扰和活动能力评分。次要测量包括患者满意度、矫形器使用频率和不良反应。采用Fisher精确检验、Student t检验或Wilcoxon sign -rank检验进行统计学比较,显著性设置为P。结果:组间基线人口学和临床特征无差异。在第4周,两组对定制、合身和舒适度的满意度都很高(中位数为4.0-5.0)。传统矫形器使用者报告了更多的日常使用(P = 0.04),但也有更高的摩擦/不适感(P = 0.047)。8周时,两组不良反应差异无统计学意义。探索性比较表明PROMIS物理功能平均值更高(49.0 vs 41.9, Δ 7.1; P =。008)和活动能力评分(46.9 vs 41.4, Δ 5.5;传统组疼痛干扰评分差异无统计学意义(p < 0.05)。结论:传统制造和HP 3d打印定制矫形器均具有较高的满意度和功能改善。尽管传统设备表现出更高的早期依从性和更好的8周功能结果,但HP Arize系统显示出更少的不良反应,并提供了一种可扩展的、高效的替代方案。作为一项探索性试点研究,这些发现是初步的,旨在为未来试验的可行性和效应大小估计提供信息。证据等级:四级,试点前瞻性比较研究。研究类型:准实验前后研究。
{"title":"Pilot, Randomized Comparison of Traditionally Fabricated Custom Foot Orthoses vs HP Arize 3D-Printed Orthoses for Plantar Fasciitis.","authors":"J Benjamin Jackson, Kaleb Eaton, Harley T Davis, Emily McKinney, Tyler A Gonzalez","doi":"10.1177/24730114251413246","DOIUrl":"10.1177/24730114251413246","url":null,"abstract":"<p><strong>Background: </strong>Plantar fasciitis is the most common cause of plantar heel pain and the use of custom foot orthosis is a well-supported treatment modality. Traditional custom orthoses are fabricated using foam impressions and manual techniques, but these methods are time-intensive and susceptible to variability in fit and quality. The HP Arize platform applies high-resolution 3D laser scanning with algorithm-driven modeling to streamline fabrication of custom foot orthoses. Although early reports suggest comparable comfort and durability to traditional devices, clinical data evaluating patient-reported outcomes remain limited.</p><p><strong>Methods: </strong>This prospective pilot, randomized study assigned 34 adults diagnosed with plantar fasciitis to receive either traditionally fabricated custom orthoses (n = 18) or HP Arize 3D-printed orthoses (n = 16). Primary analyses used a modified intention‑to‑treat cohort (n = 30) comprising participants who received an insert and completed baseline assessments. Patient-Reported Outcomes Measurement Information System (PROMIS) physical function, pain interference, and mobility scores were collected at baseline, 4 weeks, and 8 weeks. Secondary measures included patient satisfaction, frequency of orthotic use, and adverse effects. Statistical comparisons were performed using Fisher exact test and Student <i>t</i> test or Wilcoxon signed-rank test, with significance set at <i>P</i> < .05.</p><p><strong>Results: </strong>Baseline demographic and clinical characteristics did not differ between groups. At 4 weeks, satisfaction with customization, fit, and comfort was high across both groups (median 4.0-5.0). Traditional orthosis users reported greater daily use (<i>P</i> = .04) but also higher rates of rubbing/discomfort (<i>P</i> = .047). By 8 weeks, side effects were not statistically significantly different. Exploratory comparisons suggested higher mean PROMIS physical function (49.0 vs 41.9, Δ 7.1; <i>P</i> = .008) and mobility scores (46.9 vs 41.4, Δ 5.5; <i>P</i> = .02) at 8 weeks in the traditional group, whereas pain interference scores did not differ.</p><p><strong>Conclusion: </strong>Both traditionally fabricated and HP Arize 3D-printed custom orthoses were associated with high satisfaction and functional improvement. Although traditional devices showed greater early compliance and superior 8-week functional outcomes, the HP Arize system demonstrated fewer adverse effects and offers a scalable, efficient alternative. As an exploratory pilot study, these findings are preliminary and intended to inform feasibility and effect‑size estimation for future trials.</p><p><strong>Level of evidence: </strong>Level IV, pilot prospective comparative study.</p><p><strong>Type of study: </strong>Quasi-experimental pre-post study.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251413246"},"PeriodicalIF":0.0,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12891397/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146178411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Combination Endoscopic Plantar Fasciotomy and Gastrocnemius Recession in the Treatment of Recalcitrant Plantar Fasciitis: Clinical Outcomes From a Case Series. 联合内镜下足底筋膜切开术和腓肠肌收缩治疗顽固性足底筋膜炎:来自病例系列的临床结果。
Pub Date : 2026-02-10 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251412894
Andrew G Beauperthuy, Lauren Homolka, Patrick Waldron, Peter A Falgiano, Robert J Rowland, Gino Mercadal, Alejandro Pino

Background: Classically, the gold standard surgical management of recalcitrant plantar fasciitis has been plantar fasciotomy. Recent research has established a correlation between posterior leg tightness and plantar fasciitis. As a result, surgeons are increasingly performing a gastrocnemius recession to manage this condition. The purpose of this report was to assess clinical outcomes in patients undergoing a combined endoscopic partial plantar fasciotomy and a gastrocnemius recession for the treatment of plantar fasciitis.

Methods: Surgery was performed on 37 feet (35 patients), of which 31 (29 patients) were retrospectively reviewed. Preoperative and follow-up measures of pain, limitations on daily activities, and maximum walking distance were assessed. Patient satisfaction, complications, and recovery time were recorded.

Results: The mean follow-up was 3.02 (range, 1-6.67) years. The mean visual analog score for pain decreased from 9.3 preoperatively to 1.5 at final follow-up. At the most recent follow-up, 21 of 31 (67.6%) patients were completely pain free, and 28 of 31 (90.3%) were very satisfied or satisfied with the surgery. Twenty-eight of 31 patients (90.3%) returned to activity without any limitations. Complications were seen in 5 patients, including 3 patients with persistent pain.

Conclusion: Our study demonstrated that endoscopic partial plantar fasciotomy combined with gastrocnemius recession was associated with improved pain and function in this case series. However these findings should be considered preliminary; prospective comparative studies are needed.

Level of evidence: Level IV, case series.

背景:传统上,治疗顽固性足底筋膜炎的金标准手术是足底筋膜切开术。最近的研究证实了后肢紧绷和足底筋膜炎之间的相关性。因此,外科医生越来越多地采用腓肠肌收缩术来治疗这种情况。本报告的目的是评估联合内镜下部分足底筋膜切开术和腓肠肌切除术治疗足底筋膜炎的临床结果。方法:对37例(35例)足部进行手术治疗,其中31例(29例)进行回顾性分析。评估术前和随访疼痛测量、日常活动限制和最大步行距离。记录患者满意度、并发症及恢复时间。结果:平均随访时间3.02年(1 ~ 6.67年)。疼痛的平均视觉模拟评分从术前9.3下降到最终随访时的1.5。在最近的随访中,31例患者中有21例(67.6%)完全无疼痛,31例患者中有28例(90.3%)对手术非常满意或满意。31例患者中有28例(90.3%)无任何限制地恢复活动。并发症5例,其中持续性疼痛3例。结论:我们的研究表明,在这个病例系列中,内镜下部分足底筋膜切开术联合腓肠肌收缩与疼痛和功能的改善有关。然而,这些发现应被视为初步的;需要前瞻性的比较研究。证据等级:四级,案例系列。
{"title":"Combination Endoscopic Plantar Fasciotomy and Gastrocnemius Recession in the Treatment of Recalcitrant Plantar Fasciitis: Clinical Outcomes From a Case Series.","authors":"Andrew G Beauperthuy, Lauren Homolka, Patrick Waldron, Peter A Falgiano, Robert J Rowland, Gino Mercadal, Alejandro Pino","doi":"10.1177/24730114251412894","DOIUrl":"10.1177/24730114251412894","url":null,"abstract":"<p><strong>Background: </strong>Classically, the gold standard surgical management of recalcitrant plantar fasciitis has been plantar fasciotomy. Recent research has established a correlation between posterior leg tightness and plantar fasciitis. As a result, surgeons are increasingly performing a gastrocnemius recession to manage this condition. The purpose of this report was to assess clinical outcomes in patients undergoing a combined endoscopic partial plantar fasciotomy and a gastrocnemius recession for the treatment of plantar fasciitis.</p><p><strong>Methods: </strong>Surgery was performed on 37 feet (35 patients), of which 31 (29 patients) were retrospectively reviewed. Preoperative and follow-up measures of pain, limitations on daily activities, and maximum walking distance were assessed. Patient satisfaction, complications, and recovery time were recorded.</p><p><strong>Results: </strong>The mean follow-up was 3.02 (range, 1-6.67) years. The mean visual analog score for pain decreased from 9.3 preoperatively to 1.5 at final follow-up. At the most recent follow-up, 21 of 31 (67.6%) patients were completely pain free, and 28 of 31 (90.3%) were very satisfied or satisfied with the surgery. Twenty-eight of 31 patients (90.3%) returned to activity without any limitations. Complications were seen in 5 patients, including 3 patients with persistent pain.</p><p><strong>Conclusion: </strong>Our study demonstrated that endoscopic partial plantar fasciotomy combined with gastrocnemius recession was associated with improved pain and function in this case series. However these findings should be considered preliminary; prospective comparative studies are needed.</p><p><strong>Level of evidence: </strong>Level IV, case series.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251412894"},"PeriodicalIF":0.0,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12891392/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146178895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association of Morbid Obesity (BMI ≥40) With Postoperative Complications and Pain After Insertional Achilles Tendinopathy Achilles Splitting Surgical Treatment. 病态肥胖(BMI≥40)与插入性跟腱病跟腱分裂手术治疗后并发症和疼痛的关系
Pub Date : 2026-02-10 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251413603
Charles C Hower, Wesley J Manz, Param J Desai, Rishin J Kadakia, Jason T Bariteau

Background: Insertional Achilles tendinopathy (IAT) is a common cause of posterior heel pain and is often managed surgically when conservative treatment fails. Wound complications are common after Achilles surgery. Obesity is a known risk factor for such complications; however, evidence on morbid obesity (body mass index [BMI] ≥ 40) and outcomes after IAT repair is limited. This study evaluates the incidence of complications and pain relief in patients undergoing IAT surgery by BMI group.

Methods: This is a retrospective cohort study. All patients with an established diagnosis of IAT who underwent an Achilles central splitting, detachment, debridement, and reattachment surgery between 2015 and 2023 were included. Patient demographics, surgical outcomes, and reported pain (visual analog scale for pain [VAS] scores) were collected. Patients were categorized into 2 BMI groups: <40 and ≥40. Statistical analysis included independent t test, Fisher exact, and χ2 testing.

Results: There were 123 patients in this study, of which 90 had BMI <40 and 33 had a BMI ≥40. The mean age was 53.6 ± 10.6 years. Twenty-four had documented complications: higher in the morbidly obese group (30.3%) than in non-morbidly obese patients (15.6%, P = .077), with a significantly increased rate of wound dehiscence (24.2% vs 8.9%, P = .035; relative risk 2.72, 95% CI 1.11-6.67). VAS scores were highest in patients with BMI ≥40 compared to BMI <40 both preoperatively (P = .003) and at their final follow-up appointment (P = .006). No difference was found in change in VAS scores from preoperative to final follow-up visits (P = .818).

Conclusion: Morbid obesity was associated with increased wound complications and higher levels of pain in this retrospective cohort undergoing IAT surgical repair. However, VAS reduction after surgery was comparable across BMI groups.

Level of evidence: Level III, retrospective cohort.

背景:插入性跟腱病(IAT)是引起后脚跟疼痛的常见原因,保守治疗失败后通常采用手术治疗。跟腱手术后伤口并发症很常见。肥胖是导致这些并发症的已知危险因素;然而,关于病态肥胖(身体质量指数[BMI]≥40)和IAT修复后预后的证据有限。本研究评估BMI组IAT手术患者并发症发生率及疼痛缓解情况。方法:回顾性队列研究。所有确诊为IAT的患者均在2015年至2023年间接受了跟腱中心分裂、脱离、清创和再附着手术。收集患者人口统计资料、手术结果和报告的疼痛(视觉模拟疼痛量表[VAS]评分)。将患者分为2组:t检验、Fisher精确检验和χ2检验。结果:本组患者123例,其中BMI P = 90例。077),伤口裂开率显著增加(24.2% vs 8.9%, P = 0.035;相对危险度2.72,95% CI 1.11-6.67)。与BMI P =相比,BMI≥40的患者VAS评分最高。003)和最后一次随访预约(P = .006)。术前与最终随访时VAS评分无差异(P = .818)。结论:在接受IAT手术修复的回顾性队列中,病态肥胖与伤口并发症增加和疼痛水平升高有关。然而,手术后VAS降低在BMI组之间具有可比性。证据等级:III级,回顾性队列。
{"title":"Association of Morbid Obesity (BMI ≥40) With Postoperative Complications and Pain After Insertional Achilles Tendinopathy Achilles Splitting Surgical Treatment.","authors":"Charles C Hower, Wesley J Manz, Param J Desai, Rishin J Kadakia, Jason T Bariteau","doi":"10.1177/24730114251413603","DOIUrl":"10.1177/24730114251413603","url":null,"abstract":"<p><strong>Background: </strong>Insertional Achilles tendinopathy (IAT) is a common cause of posterior heel pain and is often managed surgically when conservative treatment fails. Wound complications are common after Achilles surgery. Obesity is a known risk factor for such complications; however, evidence on morbid obesity (body mass index [BMI] ≥ 40) and outcomes after IAT repair is limited. This study evaluates the incidence of complications and pain relief in patients undergoing IAT surgery by BMI group.</p><p><strong>Methods: </strong>This is a retrospective cohort study. All patients with an established diagnosis of IAT who underwent an Achilles central splitting, detachment, debridement, and reattachment surgery between 2015 and 2023 were included. Patient demographics, surgical outcomes, and reported pain (visual analog scale for pain [VAS] scores) were collected. Patients were categorized into 2 BMI groups: <40 and ≥40. Statistical analysis included independent <i>t</i> test, Fisher exact, and χ<sup>2</sup> testing.</p><p><strong>Results: </strong>There were 123 patients in this study, of which 90 had BMI <40 and 33 had a BMI ≥40. The mean age was 53.6 ± 10.6 years. Twenty-four had documented complications: higher in the morbidly obese group (30.3%) than in non-morbidly obese patients (15.6%, <i>P</i> = .077), with a significantly increased rate of wound dehiscence (24.2% vs 8.9%, <i>P</i> = .035; relative risk 2.72, 95% CI 1.11-6.67). VAS scores were highest in patients with BMI ≥40 compared to BMI <40 both preoperatively (<i>P</i> = .003) and at their final follow-up appointment (<i>P</i> = .006). No difference was found in change in VAS scores from preoperative to final follow-up visits (<i>P</i> = .818).</p><p><strong>Conclusion: </strong>Morbid obesity was associated with increased wound complications and higher levels of pain in this retrospective cohort undergoing IAT surgical repair. However, VAS reduction after surgery was comparable across BMI groups.</p><p><strong>Level of evidence: </strong>Level III, retrospective cohort.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251413603"},"PeriodicalIF":0.0,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12891377/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146178875","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Percutaneous Zadek Osteotomy and Sural Nerve Proximity: A Cadaveric Anatomical Mapping Study. 经皮Zadek截骨术与腓肠神经邻近:尸体解剖图研究。
Pub Date : 2026-02-06 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251412344
Paolo Ivan Fiore, Alice Montagna, Enrico Pozzessere, Tyler A Gonzalez, Jonathan R M Kaplan, Ettore Vulcano

Background: The Zadek osteotomy, a dorsal closing-wedge procedure of the calcaneus, is commonly used in the surgical treatment of insertional Achilles tendinopathy, particularly in patients unresponsive to conservative measures. Although minimally invasive surgical (MIS) techniques offer potential benefits such as reduced soft tissue trauma and faster recovery, concerns persist regarding the risk of iatrogenic injury to the sural nerve because of limited visualization. This cadaveric study aims to provide a detailed anatomical assessment of the sural nerve and its branches in relation to the entry point of the MIS Zadek osteotomy, with the goal of quantifying their proximity and offering data that may help reduce the risk of nerve injury during the procedure.

Methods: Twenty fresh-frozen human lower limb specimens were subjected to a standardized MIS Zadek osteotomy using a 3 × 30-mm Shannon burr. The osteotomy was guided fluoroscopically and performed through a lateral percutaneous approach. Post-procedure, meticulous anatomical dissections were conducted to identify the sural nerve and measure its distance from the anterior and posterior arms of the osteotomy using digital calipers with 0.1-mm precision. Measurements were independently recorded by 2 observers to ensure accuracy.

Results: The sural nerve was successfully identified in all specimens. No instances of sural nerve transection or gross anatomical disruption were observed. The mean distance from the osteotomy to the sural nerve was 11.95 mm, with a range of 8.3 to 15.4 mm and an SD of 2.18 mm. These findings suggest that when performed within the defined anatomical parameters, the MIS Zadek osteotomy maintains a safe distance from the sural nerve.

Conclusion: In our cadaver study, we found that the MIS Zadek osteotomy maintained a mean distance of 11.95 mm from the sural nerve. These findings define anatomical proximity; clinical safety requires prospective validation.

Clinical relevance: Our study defines a reproducible anatomical margin for MIS Zadek osteotomy; clinical safety needs prospective validation.

背景:Zadek截骨术是一种跟骨背侧闭合楔形手术,常用于手术治疗插入性跟腱病,特别是对保守措施无反应的患者。尽管微创手术(MIS)技术提供了潜在的好处,如减少软组织创伤和更快的恢复,但由于有限的可视化,人们仍然担心医源性腓肠神经损伤的风险。本尸体研究旨在提供与MIS Zadek截骨术切入点相关的腓肠神经及其分支的详细解剖评估,目的是量化它们的接近程度,并提供有助于降低手术过程中神经损伤风险的数据。方法:20例新鲜冷冻的人下肢标本使用3 × 30 mm Shannon burr进行标准化MIS Zadek截骨术。在透视引导下,经外侧经皮入路行截骨术。术后进行细致的解剖解剖,以确定腓肠神经,并使用0.1 mm精度的数字卡尺测量其与截骨前后臂的距离。测量由两名观察员独立记录,以确保准确性。结果:所有标本均成功鉴定出腓肠神经。没有观察到腓肠神经横断或大体解剖破坏的情况。截骨至腓肠神经的平均距离为11.95 mm,范围8.3 ~ 15.4 mm, SD为2.18 mm。这些结果表明,当在规定的解剖参数内进行时,MIS Zadek截骨术与腓肠神经保持安全距离。结论:在我们的尸体研究中,我们发现MIS Zadek截骨术与腓肠神经的平均距离为11.95 mm。这些发现确定了解剖学上的接近性;临床安全性需要前瞻性验证。临床相关性:我们的研究定义了MIS Zadek截骨术的可复制解剖边缘;临床安全性需要前瞻性验证。
{"title":"Percutaneous Zadek Osteotomy and Sural Nerve Proximity: A Cadaveric Anatomical Mapping Study.","authors":"Paolo Ivan Fiore, Alice Montagna, Enrico Pozzessere, Tyler A Gonzalez, Jonathan R M Kaplan, Ettore Vulcano","doi":"10.1177/24730114251412344","DOIUrl":"10.1177/24730114251412344","url":null,"abstract":"<p><strong>Background: </strong>The Zadek osteotomy, a dorsal closing-wedge procedure of the calcaneus, is commonly used in the surgical treatment of insertional Achilles tendinopathy, particularly in patients unresponsive to conservative measures. Although minimally invasive surgical (MIS) techniques offer potential benefits such as reduced soft tissue trauma and faster recovery, concerns persist regarding the risk of iatrogenic injury to the sural nerve because of limited visualization. This cadaveric study aims to provide a detailed anatomical assessment of the sural nerve and its branches in relation to the entry point of the MIS Zadek osteotomy, with the goal of quantifying their proximity and offering data that may help reduce the risk of nerve injury during the procedure.</p><p><strong>Methods: </strong>Twenty fresh-frozen human lower limb specimens were subjected to a standardized MIS Zadek osteotomy using a 3 × 30-mm Shannon burr. The osteotomy was guided fluoroscopically and performed through a lateral percutaneous approach. Post-procedure, meticulous anatomical dissections were conducted to identify the sural nerve and measure its distance from the anterior and posterior arms of the osteotomy using digital calipers with 0.1-mm precision. Measurements were independently recorded by 2 observers to ensure accuracy.</p><p><strong>Results: </strong>The sural nerve was successfully identified in all specimens. No instances of sural nerve transection or gross anatomical disruption were observed. The mean distance from the osteotomy to the sural nerve was 11.95 mm, with a range of 8.3 to 15.4 mm and an SD of 2.18 mm. These findings suggest that when performed within the defined anatomical parameters, the MIS Zadek osteotomy maintains a safe distance from the sural nerve.</p><p><strong>Conclusion: </strong>In our cadaver study, we found that the MIS Zadek osteotomy maintained a mean distance of 11.95 mm from the sural nerve. These findings define anatomical proximity; clinical safety requires prospective validation.</p><p><strong>Clinical relevance: </strong>Our study defines a reproducible anatomical margin for MIS Zadek osteotomy; clinical safety needs prospective validation.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251412344"},"PeriodicalIF":0.0,"publicationDate":"2026-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12881311/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146141572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unable to Heel: The Clinical Journey of a Traumatic Near-Total Calcanectomy With 54 Years of Follow-up. 不能跟:创伤性近全跟骨切除术的临床历程与54年的随访。
Pub Date : 2026-02-05 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251413583
Serge Andreou, Najeeb Baig, Rumyah Rafique, Ameen Suhrawardy, Pranav Khambete, Robert Meehan

Graphical Abstract.

图形抽象。
{"title":"Unable to Heel: The Clinical Journey of a Traumatic Near-Total Calcanectomy With 54 Years of Follow-up.","authors":"Serge Andreou, Najeeb Baig, Rumyah Rafique, Ameen Suhrawardy, Pranav Khambete, Robert Meehan","doi":"10.1177/24730114251413583","DOIUrl":"10.1177/24730114251413583","url":null,"abstract":"<p><p>Graphical Abstract.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251413583"},"PeriodicalIF":0.0,"publicationDate":"2026-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12876634/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146141535","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Metatarsophalangeal Arthrodesis: Risk Factors for Nonunion in a 10-Year Retrospective Cohort. 跖趾关节融合术:10年回顾性队列中骨不连的危险因素。
Pub Date : 2026-01-31 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251413590
Caroline M Dingler, Charles C Hower, Kevin T Kane, Alicia G Edwards, Rishin J Kadakia, Jason T Bariteau

Background: First metatarsophalangeal (MTP) joint fusion is a common surgical procedure to treat hallux rigidus and malalignment at the MTP joint. Nonunion after first MTP arthrodesis can cause continued pain and limitation in function. The present study aims to provide a single-site analysis of nonunion risk factors after first MTP fusion. We hypothesized that diabetes, smoking, and a body mass index (BMI) ≥30 are associated with increased risk of nonunion.

Methods: This is a retrospective cohort study. All patients who underwent first MTP fusion performed by 3 orthopaedic foot and ankle surgeons between September 20, 2013, and September 20, 2023, were included. Patient demographics, comorbidities, intraoperative medications, and postoperative complications were collected. Relationships to nonunion were evaluated using the multivariable logistic regression (a < 0.05) and both odds ratio (OR) and adjusted odds ratio (aOR) were calculated.

Results: A total of 417 patients (450 feet) were included. Average BMI was 27.94 ± 6.79. There were 25 nonunions, which did not statistically differ in sex or age. Per-patient models identified idiopathic peripheral neuropathy and bilateral surgeries as independent predictors, with BMI ≥30 showing a trend toward significance. Diagnosis of peripheral neuropathy was subdivided into diabetic and idiopathic peripheral neuropathy, with increased nonunion rates in the idiopathic group. Osteoporosis, bisphosphonate use, and smoking history showed no statistical difference in nonunion rates. BMI and diabetes showed statistical differences with univariate logistic regression but were deemed insignificant on multivariate analysis.

Conclusion: In this single-institution cohort, idiopathic peripheral neuropathy and bilateral MTP fusions were associated with higher odds of nonunion; findings for BMI ≥30 and diabetes should be interpreted prudently, given the limited events and wide CIs.

Level of evidence: Level III, retrospective cohort study.

背景:第一跖趾(MTP)关节融合术是治疗拇趾僵硬和MTP关节错位的常用手术方法。首次MTP关节融合术后不愈合可引起持续疼痛和功能限制。本研究旨在对首次MTP融合后的骨不连危险因素进行单位点分析。我们假设糖尿病、吸烟和体重指数(BMI)≥30与骨不连风险增加相关。方法:回顾性队列研究。所有在2013年9月20日至2023年9月20日期间由3名骨科足踝外科医生进行首次MTP融合术的患者纳入研究。收集患者统计资料、合并症、术中用药和术后并发症。使用多变量逻辑回归评估与骨不连的关系(a结果:共纳入417例患者(450英尺)。平均BMI为27.94±6.79。有25例骨不连,在性别和年龄上没有统计学差异。每例患者模型确定特发性周围神经病变和双侧手术为独立预测因素,BMI≥30有显著性趋势。周围神经病变的诊断被细分为糖尿病和特发性周围神经病变,特发性组的不愈合率增加。骨质疏松、双膦酸盐使用和吸烟史在骨不连发生率上无统计学差异。BMI和糖尿病在单因素logistic回归中有统计学差异,但在多因素分析中不显著。结论:在这个单机构队列中,特发性周围神经病变和双侧MTP融合与较高的不愈合几率相关;考虑到有限的事件和广泛的ci, BMI≥30和糖尿病的发现应谨慎解释。证据等级:III级,回顾性队列研究。
{"title":"Metatarsophalangeal Arthrodesis: Risk Factors for Nonunion in a 10-Year Retrospective Cohort.","authors":"Caroline M Dingler, Charles C Hower, Kevin T Kane, Alicia G Edwards, Rishin J Kadakia, Jason T Bariteau","doi":"10.1177/24730114251413590","DOIUrl":"10.1177/24730114251413590","url":null,"abstract":"<p><strong>Background: </strong>First metatarsophalangeal (MTP) joint fusion is a common surgical procedure to treat hallux rigidus and malalignment at the MTP joint. Nonunion after first MTP arthrodesis can cause continued pain and limitation in function. The present study aims to provide a single-site analysis of nonunion risk factors after first MTP fusion. We hypothesized that diabetes, smoking, and a body mass index (BMI) ≥30 are associated with increased risk of nonunion.</p><p><strong>Methods: </strong>This is a retrospective cohort study. All patients who underwent first MTP fusion performed by 3 orthopaedic foot and ankle surgeons between September 20, 2013, and September 20, 2023, were included. Patient demographics, comorbidities, intraoperative medications, and postoperative complications were collected. Relationships to nonunion were evaluated using the multivariable logistic regression (a < 0.05) and both odds ratio (OR) and adjusted odds ratio (aOR) were calculated.</p><p><strong>Results: </strong>A total of 417 patients (450 feet) were included. Average BMI was 27.94 ± 6.79. There were 25 nonunions, which did not statistically differ in sex or age. Per-patient models identified idiopathic peripheral neuropathy and bilateral surgeries as independent predictors, with BMI ≥30 showing a trend toward significance. Diagnosis of peripheral neuropathy was subdivided into diabetic and idiopathic peripheral neuropathy, with increased nonunion rates in the idiopathic group. Osteoporosis, bisphosphonate use, and smoking history showed no statistical difference in nonunion rates. BMI and diabetes showed statistical differences with univariate logistic regression but were deemed insignificant on multivariate analysis.</p><p><strong>Conclusion: </strong>In this single-institution cohort, idiopathic peripheral neuropathy and bilateral MTP fusions were associated with higher odds of nonunion; findings for BMI ≥30 and diabetes should be interpreted prudently, given the limited events and wide CIs.</p><p><strong>Level of evidence: </strong>Level III, retrospective cohort study.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251413590"},"PeriodicalIF":0.0,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12861394/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146104577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Radiographic and Clinical Outcomes of Intermetatarsal Screw Fixation in First Tarsometatarsal Arthrodesis for Hallux Valgus. 拇外翻第一跗跖关节融合术中跖间螺钉固定的影像学及临床效果。
Pub Date : 2026-01-29 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251413242
Ashley N Kimbel, Robin M Litten, Allison D Desforges, Robert W Rutz, Michael D Johnson

Background: First tarsometatarsal (TMT) arthrodesis is a surgical option for moderate to severe hallux valgus, particularly in the setting of first-ray instability. The use of a supplemental intermetatarsal screw (IMS) has emerged as a technique intended to enhance transverse plane stability and may help maintain correction; however, limited clinical data exist regarding its radiographic and complication profile. This study compared radiographic correction, maintenance of alignment, and postoperative complications following TMT arthrodesis with vs without IMS fixation.

Methods: A retrospective review was performed of adult patients who underwent first TMT arthrodesis for hallux valgus from 2013 to 2023 at a tertiary academic center. Patients undergoing additional midfoot fusion or with <6-month follow-up were excluded. Patients were grouped by whether supplemental IMS fixation was used, which was determined at surgeon discretion. Demographic, operative, and clinical data were recorded. Radiographic measurements included intermetatarsal angle (IMA) and relative first metatarsal (MT) length preoperatively, immediately postoperatively, and at latest follow-up.

Results: Eighty-nine patients met criteria (51 IMS; 38 no IMS). Baseline demographics and comorbidities were similar between groups. Immediately postoperatively, the IMS cohort demonstrated a smaller IMA (5.8 vs 7.8 degrees, P = .010), which persisted at latest follow-up (7.3 vs 9.3 degrees, P = .015). The IMS group demonstrated a greater reduction in IMA from preoperative to final follow-up (6.9 vs 3.9 degrees, P = .001). Relative first MT length remained greater in the IMS cohort across all time points (P ≤ .045) but change‑score (Postop-Preop) differences in length were not statistically significant. Complication rates, including nonunion (2.0% vs 2.6%), revision surgery (9.8% vs 18.4%), and hardware-related complications (7.8% vs 2.6%), did not differ significantly between groups (P > .05).

Conclusion: Supplemental IMS fixation in first tarsometatarsal arthrodesis for hallux valgus was associated with greater maintenance of radiographic correction without observed differences in complication rates. These findings support IMS augmentation as a potential adjunct in appropriately selected patients.

Level of evidence: Level III, retrospective review.

背景:第一跗跖骨(TMT)关节融合术是治疗中度至重度拇外翻的手术选择,特别是在一线不稳定的情况下。使用补充跖骨间螺钉(IMS)已成为一种旨在增强横平面稳定性并有助于维持矫正的技术;然而,关于其放射学和并发症的临床资料有限。本研究比较了有与无IMS固定的TMT关节融合术的x线矫正、对齐维持和术后并发症。方法:回顾性分析2013年至2023年在某三级学术中心接受首次拇外翻TMT关节融合术的成年患者。结果:89例患者符合标准(51例IMS, 38例无IMS)。两组之间的基线人口统计学和合并症相似。即刻术后,IMS队列显示IMA较小(5.8 vs 7.8度,P =。010),在最近的随访中持续存在(7.3度vs 9.3度,P = 0.015)。IMS组从术前到最终随访期间IMA降低幅度更大(6.9度vs 3.9度,P = 0.001)。IMS队列在所有时间点上的相对第一次MT长度仍然较大(P≤0.045),但变化评分(术后-术前)长度差异无统计学意义。并发症发生率,包括骨不连(2.0% vs 2.6%)、翻修手术(9.8% vs 18.4%)和硬件相关并发症(7.8% vs 2.6%),两组间无显著差异(P < 0.05)。结论:拇外翻第一跗跖关节融合术中补充IMS固定与更大程度的影像学矫正维持相关,且并发症发生率无明显差异。这些发现支持IMS增强在适当选择的患者中作为潜在的辅助手段。证据等级:III级,回顾性审查。
{"title":"Radiographic and Clinical Outcomes of Intermetatarsal Screw Fixation in First Tarsometatarsal Arthrodesis for Hallux Valgus.","authors":"Ashley N Kimbel, Robin M Litten, Allison D Desforges, Robert W Rutz, Michael D Johnson","doi":"10.1177/24730114251413242","DOIUrl":"10.1177/24730114251413242","url":null,"abstract":"<p><strong>Background: </strong>First tarsometatarsal (TMT) arthrodesis is a surgical option for moderate to severe hallux valgus, particularly in the setting of first-ray instability. The use of a supplemental intermetatarsal screw (IMS) has emerged as a technique intended to enhance transverse plane stability and may help maintain correction; however, limited clinical data exist regarding its radiographic and complication profile. This study compared radiographic correction, maintenance of alignment, and postoperative complications following TMT arthrodesis with vs without IMS fixation.</p><p><strong>Methods: </strong>A retrospective review was performed of adult patients who underwent first TMT arthrodesis for hallux valgus from 2013 to 2023 at a tertiary academic center. Patients undergoing additional midfoot fusion or with <6-month follow-up were excluded. Patients were grouped by whether supplemental IMS fixation was used, which was determined at surgeon discretion. Demographic, operative, and clinical data were recorded. Radiographic measurements included intermetatarsal angle (IMA) and relative first metatarsal (MT) length preoperatively, immediately postoperatively, and at latest follow-up.</p><p><strong>Results: </strong>Eighty-nine patients met criteria (51 IMS; 38 no IMS). Baseline demographics and comorbidities were similar between groups. Immediately postoperatively, the IMS cohort demonstrated a smaller IMA (5.8 vs 7.8 degrees, <i>P</i> = .010), which persisted at latest follow-up (7.3 vs 9.3 degrees, <i>P</i> = .015). The IMS group demonstrated a greater reduction in IMA from preoperative to final follow-up (6.9 vs 3.9 degrees, <i>P</i> = .001). Relative first MT length remained greater in the IMS cohort across all time points (<i>P</i> ≤ .045) but change‑score (Postop-Preop) differences in length were not statistically significant. Complication rates, including nonunion (2.0% vs 2.6%), revision surgery (9.8% vs 18.4%), and hardware-related complications (7.8% vs 2.6%), did not differ significantly between groups (<i>P</i> > .05).</p><p><strong>Conclusion: </strong>Supplemental IMS fixation in first tarsometatarsal arthrodesis for hallux valgus was associated with greater maintenance of radiographic correction without observed differences in complication rates. These findings support IMS augmentation as a potential adjunct in appropriately selected patients.</p><p><strong>Level of evidence: </strong>Level III, retrospective review.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251413242"},"PeriodicalIF":0.0,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12855761/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146104628","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Peroneus Brevis Allograft Reconstruction: Clinical Outcomes and Complications. 腓骨短肌异体移植物重建:临床结果和并发症。
Pub Date : 2026-01-29 eCollection Date: 2026-01-01 DOI: 10.1177/24730114251412848
Walter C Hembree, Smitha E Mathew, Casey Kuripla, Michelle M Coleman, Jingyi Shao, Gregory P Guyton

Background: Clinical data are limited for allograft reconstruction of peroneus brevis tears, and its complication profile remains poorly defined.

Methods: Retrospective chart review was conducted for patients with peroneus brevis tears who underwent tendon reconstruction with semitendinosus allograft at a single tertiary center between March 2010 and July 2019. A total of 68 patients (69 feet), 24 men and 44 women, were identified with mean age at surgery 51.8 (range, 23-74) years and mean follow-up 20.2 (range, 3.4-71.4) months. At the time of chart review, patients were contacted by phone to assess satisfaction, brace use, and work status.

Results: Visual analog scale (VAS) pain score was significantly lower postoperatively (4.0 ± 2.7 vs 2.4 ± 2.8, P = .0018) in the 54 patients with VAS pain data. A total of 40 (58%) feet had at least 1 complication. The most common complications were sural neuralgia in 18 (26%) feet and allograft failure in 7 (10%) feet. Fifteen feet (21%) required reoperation, including 7 for graft failure. In the 30 feet with prior peroneal tendon surgery, there was no association between prior surgery and complications (P = .21). Of the 24 (35%) patients available for phone survey, 20 (83%) were employed prior to surgery and 18 (90%) of these employed patients returned to work and 14 (58%) did not use an assistive device at final follow-up. Sixteen (67%) of the 24 patients contacted reported being very satisfied or satisfied with the procedure.

Conclusion: This is the largest case series to date, demonstrating significant pain improvement and high return-to-work rates in complex cases, but also a 58% overall complication rate and 10% graft failure. Allograft reconstruction may be effective when few options exist, yet careful patient selection and awareness of technical challenges are essential.Level of Evidence: Level IV, case series.

背景:同种异体腓骨短肌撕裂重建的临床资料有限,其并发症概况仍不明确。方法:回顾性分析2010年3月至2019年7月在单一三级中心行同种异体半腱肌肌腱重建腓骨短肌撕裂患者的病历。共有68名患者(69英尺),24名男性和44名女性,手术时平均年龄51.8岁(范围23-74),平均随访20.2个月(范围3.4-71.4)。在回顾病历时,通过电话联系患者评估满意度、支具使用情况和工作状态。结果:术后视觉模拟评分(VAS)疼痛评分明显低于对照组(4.0±2.7 vs 2.4±2.8,P =;0018) 54例患者的VAS疼痛数据。总共有40只脚(58%)至少有1个并发症。最常见的并发症是18(26%)只脚的腓肠神经痛和7(10%)只脚的同种异体移植失败。15英尺(21%)需要再次手术,其中7英尺因移植物失败。在30英尺既往腓骨肌腱手术中,既往手术与并发症之间没有关联(P = 0.21)。在24例(35%)可接受电话调查的患者中,20例(83%)在手术前受雇,其中18例(90%)受雇患者重返工作岗位,14例(58%)在最终随访时未使用辅助装置。接触的24名患者中有16名(67%)报告对手术非常满意或满意。结论:这是迄今为止最大的病例系列,显示出明显的疼痛改善和复杂病例的高重返工作率,但也有58%的总并发症率和10%的移植物失败。同种异体移植物重建在选择很少的情况下可能是有效的,但谨慎的患者选择和对技术挑战的认识是必不可少的。证据等级:四级,案例系列。
{"title":"Peroneus Brevis Allograft Reconstruction: Clinical Outcomes and Complications.","authors":"Walter C Hembree, Smitha E Mathew, Casey Kuripla, Michelle M Coleman, Jingyi Shao, Gregory P Guyton","doi":"10.1177/24730114251412848","DOIUrl":"10.1177/24730114251412848","url":null,"abstract":"<p><strong>Background: </strong>Clinical data are limited for allograft reconstruction of peroneus brevis tears, and its complication profile remains poorly defined.</p><p><strong>Methods: </strong>Retrospective chart review was conducted for patients with peroneus brevis tears who underwent tendon reconstruction with semitendinosus allograft at a single tertiary center between March 2010 and July 2019. A total of 68 patients (69 feet), 24 men and 44 women, were identified with mean age at surgery 51.8 (range, 23-74) years and mean follow-up 20.2 (range, 3.4-71.4) months. At the time of chart review, patients were contacted by phone to assess satisfaction, brace use, and work status.</p><p><strong>Results: </strong>Visual analog scale (VAS) pain score was significantly lower postoperatively (4.0 ± 2.7 vs 2.4 ± 2.8, <i>P</i> = .0018) in the 54 patients with VAS pain data. A total of 40 (58%) feet had at least 1 complication. The most common complications were sural neuralgia in 18 (26%) feet and allograft failure in 7 (10%) feet. Fifteen feet (21%) required reoperation, including 7 for graft failure. In the 30 feet with prior peroneal tendon surgery, there was no association between prior surgery and complications (<i>P</i> = .21). Of the 24 (35%) patients available for phone survey, 20 (83%) were employed prior to surgery and 18 (90%) of these employed patients returned to work and 14 (58%) did not use an assistive device at final follow-up. Sixteen (67%) of the 24 patients contacted reported being very satisfied or satisfied with the procedure.</p><p><strong>Conclusion: </strong>This is the largest case series to date, demonstrating significant pain improvement and high return-to-work rates in complex cases, but also a 58% overall complication rate and 10% graft failure. Allograft reconstruction may be effective when few options exist, yet careful patient selection and awareness of technical challenges are essential.<b>Level of Evidence:</b> Level IV, case series.</p>","PeriodicalId":12429,"journal":{"name":"Foot & Ankle Orthopaedics","volume":"11 1","pages":"24730114251412848"},"PeriodicalIF":0.0,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12855776/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146104542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Foot & Ankle Orthopaedics
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1