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Defining Targets for Case Minimum Requirements During Accreditation Council for Graduate Medical Education Accredited Pediatric Orthopaedic Surgery Fellowship Training. 在研究生医学教育认证委员会认可的儿科骨科奖学金培训期间确定病例最低要求的目标。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-10-16 DOI: 10.1097/BPO.0000000000003138
Jason Silvestre, Pooya Hosseinzadeh, Wudbhav N Sankar, John M Flynn

Background: Increasingly, professional societies and accrediting bodies in orthopaedic surgery recognize the role of case minimum requirements to assess and enhance fellowship training. This study analyzes targets for case minimum requirements during Accreditation Council for Graduate Medical Education (ACGME)-accredited pediatric orthopaedic surgery fellowship training.

Methods: This was a cross-sectional study of ACGME-accredited pediatric orthopaedic surgery fellows who graduated between 2018 and 2024. Means, SDs, and percentiles for recorded case volumes were calculated across ACGME-defined case categories. Variability was defined as the fold-difference between the 90th and 10th percentiles of case volume. Potential targets for case minimum requirements were identified through sensitivity analyses.

Results: There were 258 ACGME-accredited pediatric orthopaedic surgery fellows included in this study. Mean annual case volume increased over the study period (254.9±70 to 285.2±82, P =0.456). The most frequently reported cases were in spine deformity (19%), foot and ankle deformity (16%), hip reconstruction (13%), and limb deformity (12%). Variability in total reported case volume was 2.0 and was greatest in clubfoot (78.4), soft tissue: transfer, lengthen, release (15.4), and treatment of infection (10.6). The 10th and 30th percentiles of fellows reported 18 and 26 hip reconstruction cases, 17 and 30 foot and ankle deformity cases, 14 and 23 limb deformity cases, 12 and 25 spine deformity cases, 11 and 19 trauma lower limb cases, and 8 and 14 trauma upper limb cases before graduation, respectively.

Conclusions: Case volumes of recently graduated fellows may help inform future case minimum requirements for ACGME-accredited pediatric orthopaedic surgery fellowship training. Future investigation is needed to refine proposed targets for case minimum requirements through elucidation of surgical learning curves and other clinical competency metrics.

Clinical relevance: Case minimum requirements may facilitate operative training during pediatric orthopaedic surgery fellowship training and promote greater standardization across programs. Case minimum requirements may also promote clinical competency assessments and patient safety in pediatric orthopaedic surgery.

背景:越来越多的骨科专业协会和认证机构认识到病例最低要求在评估和加强奖学金培训中的作用。本研究分析了研究生医学教育认证委员会(ACGME)认可的儿科骨科奖学金培训期间病例最低要求的目标。方法:这是一项对2018年至2024年毕业的acgme认证的儿科骨科研究员的横断面研究。计算acgme定义的病例类别中记录病例量的平均值、标准差和百分位数。变异被定义为病例量的第90百分位和第10百分位之间的倍差。通过敏感性分析确定了病例最低要求的潜在目标。结果:258名经acgme认证的儿科骨科医师被纳入本研究。在研究期间,年平均病例量增加(254.9±70至285.2±82,P=0.456)。最常见的病例是脊柱畸形(19%)、足部和踝关节畸形(16%)、髋关节重建(13%)和肢体畸形(12%)。报告病例总数的变异率为2.0例,其中最大的是内翻足(78.4例)、软组织:转移、延长、释放(15.4例)和感染治疗(10.6例)。第10百分位和第30百分位的学生毕业前分别报告髋关节重建18例和26例,足部和踝关节畸形17例和30例,肢体畸形14例和23例,脊柱畸形12例和25例,下肢创伤11例和19例,上肢创伤8例和14例。结论:最近毕业的研究人员的病例量可能有助于告知acgme认证的儿科骨科研究人员培训的未来病例最低要求。未来的研究需要通过阐明手术学习曲线和其他临床能力指标来完善病例最低要求的拟议目标。临床相关性:病例最低要求可以促进儿科骨科奖学金培训期间的手术培训,并促进整个项目的更大标准化。病例最低要求也可以促进儿科骨科手术的临床能力评估和患者安全。
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引用次数: 0
First Assistant Training Level Does Not Impact Postoperative Outcomes and Complications Following Varus Derotational Osteotomy in Patients With Cerebral Palsy. 第一助理训练水平不影响脑瘫患者内翻旋转截骨术后的预后和并发症。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-10-06 DOI: 10.1097/BPO.0000000000003119
Amith Umesh, Mathangi Sridharan, Gabrielle Noullet, Aura M Elias, Charlotte F Wahle, Michaela L Juels, Nakul Talathi, Rachel M Thompson

Introduction: The influence of the first assistant's training level on outcomes of orthopaedic surgery in children with cerebral palsy (CP) remains unknown. As such, this study aims to evaluate the effects of first assistant training level (resident vs. fellow) on perioperative and postoperative outcomes following proximal femoral varus derotational osteotomy (VDRO) in children with CP.

Methods: Pediatric patients (age <18 y) with CP who underwent VDRO by a single fellowship-trained pediatric orthopaedic surgeon between 2017 and 2021 were retrospectively reviewed. Patients with a minimum of 2-year follow-up were included. Demographic data, training level of first assistant, and perioperative surgical characteristics (operative time, operating room time, estimated blood loss, length of stay, and peri- and postoperative complications) were recorded. Acute complications (≤ 90 d postoperatively) included medical complications, surgical site infection (SSI), peri-prosthetic fractures, emergency department visits, hospital readmission, and revision surgery. Long-term complications (>90 d postoperatively) included delayed/nonunion, re-subluxation, SSI, symptomatic hardware, and revision surgery. Preoperative and minimum 1-year postoperative migration percentages (MPs) were collected. t tests, χ 2 test, and Fisher exact test were used to detect differences between complication rates and outcomes between resident-assisted (group A) and fellow-assisted (group B) cases.

Results: Sixty-nine patients were included for analysis (group A: 27; group B: 42). Demographic data, medical comorbidities, and surgical complexity were comparable between groups. Perioperative surgical characteristics, acute complications, and long-term complications were equivalent between groups ( P >0.05). Minimum 1-year postoperative MPs were lower in group A than group B (1% vs. 7.5%, P <0.001). No patients had MP≥40% at 1-year postoperatively in either group.

Conclusion: Despite the high surgical and medical complexity of osseous hip reconstructions for children with CP, postoperative outcomes are not impacted by the first assistant's training level. While postoperative MPs were slightly lower for patients in the resident-assisted group, these differences were not clinically significant, and 1-year radiographic outcomes were comparable. Resident surgeons should be encouraged to participate in VDRO cases, and families should be reassured that resident participation will not negatively affect outcomes.

导读:目前尚不清楚第一助理的培训水平对脑瘫(CP)患儿骨科手术疗效的影响。因此,本研究旨在评估第一助理培训水平(住院医师与专科医师)对cp患儿股骨近端内翻旋转截骨术(VDRO)围手术期和术后预后的影响。方法:儿童患者(术后90 d)包括延迟/不愈合、再半脱位、SSI、症状性硬体和翻修手术。收集术前和术后最少1年的迁移百分比(MPs)。采用t检验、χ2检验和Fisher精确检验检验住院医师辅助(A组)和同事辅助(B组)患者并发症发生率和预后的差异。结果:69例患者纳入分析,其中A组27例,B组42例。人口统计数据、医疗合并症和手术复杂性在两组之间具有可比性。两组围手术期手术特征、急性并发症及远期并发症相当(P < 0.05)。A组术后1年最低MPs低于B组(1% vs. 7.5%)。结论:尽管CP患儿骨性髋关节重建的手术和医疗复杂性较高,但第一助理的训练水平并不影响术后结果。虽然住院医师辅助组患者术后MPs略低,但这些差异没有临床意义,并且1年的放射学结果具有可比性。应鼓励住院医生参与VDRO病例,并应向家属保证住院医生的参与不会对结果产生负面影响。
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引用次数: 0
Impact of Pediatric Neuropsychiatric Disorders on Postoperative Outcomes Following Common Nonspine Orthopedic Surgeries. 儿童神经精神疾病对普通非脊柱骨科手术后预后的影响。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-10-14 DOI: 10.1097/BPO.0000000000003131
Levi M Travis, Soumil Prasad, Faaris A Khan, Aneesh V Samineni, Christine Mei, Brian Grottkau

Background: Pediatric fractures are common injuries, and the increasing prevalence of neuropsychiatric conditions like ADHD, autism, anxiety, and depression may complicate postoperative outcomes. Understanding how these diagnoses affect surgical recovery is essential for optimizing care in this vulnerable population.

Methods: This study analyzed data from the 2019 and 2022 Kids Inpatient Database. Children undergoing common nonspine orthopedic procedures were identified and matched one-to-one by age, sex, ethnicity, and severity of illness. Primary outcomes included postoperative complications, such as infection and mechanical implant failures; secondary outcomes were length of stay and total hospital charges. Logistic regression models were used to adjust for potential confounders.

Results: Among 4931 ADHD-matched pairs, patients with ADHD had longer mean hospital stays (5.07 vs. 4.69 d, P=0.041) and significantly increased risk of osteomyelitis (OR: 1.42, P=0.0017) and soft tissue infection (OR: 1.39, P=0.009). For 5673 anxiety-matched pairs, anxiety correlated with higher mean length of stay (7.16 vs. 5.54 d, P<0.01) and elevated odds of soft tissue infections (OR: 1.55, P<0.01), mechanical implant complications (OR: 1.28, P=0.036), and constipation (OR: 2.03, P<0.01). Depression (2950 matched pairs) was associated with longer stays (8.31 vs. 6.00 d, P<0.01) and greater risk of osteomyelitis (OR: 2.04, P<0.01). Among 2322 autism-matched pairs, autism did not significantly impact length of stay but increased pneumonia risk (OR: 1.76, P=0.025) and postoperative ileus (OR: 1.71, P=0.040).

Conclusion: These findings demonstrate the significant impact of neuropsychiatric comorbidities on pediatric orthopedic recovery. Behavioral factors, such as impulsivity or anxiety-driven movement avoidance, and physiological mechanisms, including altered immune function, may drive elevated complication rates. Tailored perioperative management, including mental health screening, specialized communication strategies, and enhanced caregiver support, could improve adherence and reduce morbidity for these patients. Further research should focus on targeted interventions, medication considerations, and strategies that foster cooperation among orthopedic, mental health, and rehabilitative services. Addressing these challenges can ultimately enhance the quality of care and reduce disparities for pediatric patients with coexisting orthopedic injuries and neuropsychiatric diagnoses.

Level of evidence: Level III-retrospective comparative study.

背景:儿童骨折是一种常见的损伤,神经精神疾病如ADHD、自闭症、焦虑和抑郁的患病率增加可能使术后结果复杂化。了解这些诊断如何影响手术恢复对于优化这一弱势群体的护理至关重要。方法:本研究分析了2019年和2022年儿童住院患者数据库的数据。接受普通非脊柱整形手术的儿童按年龄、性别、种族和疾病严重程度进行一对一匹配。主要结局包括术后并发症,如感染和机械植入失败;次要结局是住院时间和总住院费用。使用逻辑回归模型来调整潜在的混杂因素。结果:4931对ADHD配对患者中,ADHD患者平均住院时间较长(5.07 vs 4.69 d, P=0.041),骨髓炎(OR: 1.42, P=0.0017)和软组织感染(OR: 1.39, P=0.009)的风险显著增加。在5673对焦虑匹配的患者中,焦虑与较高的平均住院时间相关(7.16天vs. 5.54天)。结论:这些发现表明神经精神合并症对儿童骨科康复有显著影响。行为因素,如冲动或焦虑驱动的运动回避,以及生理机制,包括免疫功能改变,可能导致并发症发生率升高。量身定制的围手术期管理,包括心理健康筛查、专门的沟通策略和增强的护理人员支持,可以提高这些患者的依从性并降低发病率。进一步的研究应侧重于有针对性的干预措施、药物考虑以及促进骨科、心理健康和康复服务之间合作的策略。解决这些挑战最终可以提高护理质量,减少小儿患者共存的骨科损伤和神经精神诊断的差异。证据等级:iii级——回顾性比较研究。
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引用次数: 0
Type IV Hereditary Sensory and Autonomic Neuropathy: Challenges and Functional Outcomes. IV型遗传性感觉和自主神经病变:挑战和功能结局。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-08-18 DOI: 10.1097/BPO.0000000000003084
Ahmed Dudic, Paul Van Schuyver, Dane Van Tassel, Mohan V Belthur

Background: Type IV Hereditary Sensory and Autonomic Neuropathy (HSAN IV) is an exceedingly rare autosomal recessive disease classically characterized by generalized loss of temperature/pain sensation, intellectual disability, and anhidrosis. HSAN IV patients are subject to repeated orthopaedic injuries and complications. There is some data on the clinical presentation, but limited data on the diagnostic and treatment challenges, and functional outcomes with HSAN IV.

Methods: This is a retrospective case series of 4 siblings with HSAN IV. Medical records were reviewed for data regarding presentation, diagnosis, and management. Functional outcomes were assessed using the Pediatric Outcomes Data Collection Instrument, with historical normative data used as a control. The 2 populations were evaluated with a Welch-modified 2-sample t test to explore the alternative hypothesis that HSAN IV patients are significantly functionally impaired.

Results: Our study included 4 siblings, 2 males and 2 females, aged 3, 8, 12, and 21 years, respectively. The average time to diagnosis was 53 months, and each diagnosis was confirmed through whole-exome sequencing. The challenges faced included delayed diagnosis, diverse clinical presentations, unestablished treatment guidelines, and unnecessary healthcare utilization before definitive diagnosis. The comparison of means between the normative population and the HSAN IV patients revealed a significant difference in sports/play ( T -score =-4.14, P =0.025) and global function ( T -score =-3.19, P =0.049) but no significant difference in upper extremity function ( P =0.216), transfer mobility ( P =0.164), pain/comfort ( P =0.955), and happiness ( P =0.995).

Conclusions: HSAN IV is a rare genetic condition with protean clinical manifestations that can result in significant deficits in play and global function. The clinical manifestations are varied, including multiple fractures, delayed/abnormal fracture healing, bone deformity, osteomyelitis, and various other non-orthopaedic manifestations. Whole-exome sequencing is a useful tool that, when combined with a high index of clinical suspicion, can expedite the diagnostic process for HSAN IV. Patients can benefit from earlier diagnosis and earlier access to education to prevent functional deterioration and repeat medical interventions.

Level of evidence: IV-case series.

背景:IV型遗传性感觉和自主神经病变(HSAN IV)是一种极其罕见的常染色体隐性遗传病,典型特征为全身发热/疼痛感觉丧失、智力残疾和无汗。HSAN IV患者易发生反复的骨科损伤和并发症。有一些关于临床表现的数据,但关于HSAN IV的诊断和治疗挑战以及功能结局的数据有限。方法:这是一个回顾性的病例系列,有4个HSAN IV的兄弟姐妹,回顾了有关表现、诊断和管理的数据。使用儿科结局数据收集工具评估功能结局,以历史规范数据作为对照。采用welch修正的双样本t检验对这两个人群进行评估,以探索HSAN IV患者存在显著功能受损的另一种假设。结果:本研究纳入兄弟姐妹4例,男2例,女2例,年龄分别为3岁、8岁、12岁和21岁。平均诊断时间为53个月,每次诊断均通过全外显子组测序得到证实。面临的挑战包括诊断延迟、临床表现多样化、未建立的治疗指南以及在明确诊断之前不必要的医疗保健使用。正常人群与HSAN IV患者在运动/游戏(T-score =-4.14, P=0.025)和整体功能(T-score =-3.19, P=0.049)方面差异有统计学意义,但在上肢功能(P=0.216)、转移能力(P=0.164)、疼痛/舒适(P=0.955)和幸福感(P=0.995)方面差异无统计学意义。结论:HSAN IV是一种罕见的遗传性疾病,临床表现为变异性,可导致显著的功能和整体功能缺陷。临床表现多种多样,包括多发骨折、骨折延迟/异常愈合、骨畸形、骨髓炎以及其他各种非骨科表现。全外显子组测序是一种有用的工具,当与高临床怀疑指数相结合时,可以加快HSAN IV的诊断过程。患者可以从早期诊断和早期教育中受益,以防止功能恶化和重复医疗干预。证据级别:iv -病例系列。
{"title":"Type IV Hereditary Sensory and Autonomic Neuropathy: Challenges and Functional Outcomes.","authors":"Ahmed Dudic, Paul Van Schuyver, Dane Van Tassel, Mohan V Belthur","doi":"10.1097/BPO.0000000000003084","DOIUrl":"10.1097/BPO.0000000000003084","url":null,"abstract":"<p><strong>Background: </strong>Type IV Hereditary Sensory and Autonomic Neuropathy (HSAN IV) is an exceedingly rare autosomal recessive disease classically characterized by generalized loss of temperature/pain sensation, intellectual disability, and anhidrosis. HSAN IV patients are subject to repeated orthopaedic injuries and complications. There is some data on the clinical presentation, but limited data on the diagnostic and treatment challenges, and functional outcomes with HSAN IV.</p><p><strong>Methods: </strong>This is a retrospective case series of 4 siblings with HSAN IV. Medical records were reviewed for data regarding presentation, diagnosis, and management. Functional outcomes were assessed using the Pediatric Outcomes Data Collection Instrument, with historical normative data used as a control. The 2 populations were evaluated with a Welch-modified 2-sample t test to explore the alternative hypothesis that HSAN IV patients are significantly functionally impaired.</p><p><strong>Results: </strong>Our study included 4 siblings, 2 males and 2 females, aged 3, 8, 12, and 21 years, respectively. The average time to diagnosis was 53 months, and each diagnosis was confirmed through whole-exome sequencing. The challenges faced included delayed diagnosis, diverse clinical presentations, unestablished treatment guidelines, and unnecessary healthcare utilization before definitive diagnosis. The comparison of means between the normative population and the HSAN IV patients revealed a significant difference in sports/play ( T -score =-4.14, P =0.025) and global function ( T -score =-3.19, P =0.049) but no significant difference in upper extremity function ( P =0.216), transfer mobility ( P =0.164), pain/comfort ( P =0.955), and happiness ( P =0.995).</p><p><strong>Conclusions: </strong>HSAN IV is a rare genetic condition with protean clinical manifestations that can result in significant deficits in play and global function. The clinical manifestations are varied, including multiple fractures, delayed/abnormal fracture healing, bone deformity, osteomyelitis, and various other non-orthopaedic manifestations. Whole-exome sequencing is a useful tool that, when combined with a high index of clinical suspicion, can expedite the diagnostic process for HSAN IV. Patients can benefit from earlier diagnosis and earlier access to education to prevent functional deterioration and repeat medical interventions.</p><p><strong>Level of evidence: </strong>IV-case series.</p>","PeriodicalId":16945,"journal":{"name":"Journal of Pediatric Orthopaedics","volume":" ","pages":"e282-e287"},"PeriodicalIF":1.5,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144873723","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Various Corrective Osteotomy Techniques for Cubitus Varus in Children: Systematic Review. 儿童肘内翻的各种矫正截骨技术:系统综述。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-11-25 DOI: 10.1097/BPO.0000000000003101
Aryadi Kurniawan, Indah S Widyahening, Bram Swandika, Witantra D Hutami

Background: Supracondylar humerus fractures are common in children, often leading to malunion and cubitus varus. Corrective osteotomy techniques for cubitus varus include lateral closing-wedge, step-cut, dome, distraction osteogenesis, and computer-assisted multiplanar 3D osteotomies. This study seeks to determine the most effective corrective osteotomy technique for pediatric malunion of the supracondylar humerus through a systematic review, as there is currently no up-to-date review on this topic.

Methods: A literature search was conducted across the PubMed, EMBASE, ProQuest, Scopus, and Cochrane Library databases on April 2, 2023, following the PRISMA guidelines. Selected articles underwent a review process by 2 independent reviewers to reassess their eligibility based on predefined inclusion criteria. The quality and potential biases of each article were assessed utilizing the Newcastle-Ottawa Scale (NOS) for nonrandomized studies and the Cochrane Risk of Bias Tool for randomized studies.

Results: This systematic review included 39 out of 754 articles, involving 863 patients who underwent various osteotomies. The patients were followed up for an average of 27.3 months, and data on range of motion, angle correction, and clinical outcomes were collected. Different assessment criteria were used for functional outcomes. Complications included infections, nerve injuries, reoperations, residual deformity, and absence of lateral condyle prominence. The systematic review revealed a shortage of randomized controlled trials (RCTs) due to challenges in randomization, surgical technique variations, and ethical considerations.

Conclusions: Various osteotomy techniques can be used to achieve favourable outcomes in cases of pediatric supracondylar malunion. These techniques include lateral closing wedge osteotomy, step-cut osteotomy, dome osteotomy, distraction osteogenesis, and multiplanar 3D osteotomy. Each osteotomy technique has its own advantages and disadvantages for specific outcomes. Lateral closing wedge osteotomy is recommended for patients with preoperative range of motion deficits. Step-cut osteotomy excels in correcting the humerus-elbow-wrist angle. A meta-analysis favoured the lateral closing wedge over the dome osteotomy for satisfactory outcomes.

Level of evidence: Level III.

背景:儿童肱骨髁上骨折很常见,常导致骨不愈合和肘内翻。肘内翻的矫正截骨技术包括外侧闭合楔形、阶梯切割、穹顶、牵张成骨和计算机辅助的多平面三维截骨术。本研究旨在通过系统综述来确定治疗儿童肱骨髁上畸形愈合最有效的截骨技术,因为目前还没有关于该主题的最新综述。方法:按照PRISMA指南,于2023年4月2日在PubMed、EMBASE、ProQuest、Scopus和Cochrane Library数据库中进行文献检索。选定的文章经过2名独立审稿人的审查过程,以根据预定义的纳入标准重新评估其资格。非随机研究采用纽卡斯尔-渥太华量表(NOS),随机研究采用Cochrane偏倚风险工具,对每篇文章的质量和潜在偏倚进行评估。结果:本系统综述纳入了754篇文章中的39篇,涉及863例接受各种截骨术的患者。患者平均随访27.3个月,收集活动范围、角度矫正和临床结果的数据。功能结果采用不同的评估标准。并发症包括感染、神经损伤、再手术、残留畸形和外侧髁突缺失。系统评价显示,由于随机化、手术技术变化和伦理考虑方面的挑战,随机对照试验(rct)缺乏。结论:小儿髁上畸形愈合可采用多种截骨术,获得良好的治疗效果。这些技术包括外侧闭合楔形截骨术、阶梯截骨术、圆顶截骨术、牵张成骨术和多平面三维截骨术。每一种截骨术都有其优缺点。外侧闭合楔形截骨术推荐用于术前活动范围不足的患者。阶梯截骨术在矫正肱骨-肘关节-腕关节角度方面效果显著。一项荟萃分析表明外侧闭合楔骨比穹窿截骨更能获得令人满意的结果。证据等级:三级。
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引用次数: 0
The Effect of Immediate Weight Bearing After Planovalgus Foot Reconstruction in Ambulatory Children With Cerebral Palsy. 脑性瘫痪患儿平外翻足重建术后即刻负重的效果。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-11-03 DOI: 10.1097/BPO.0000000000003147
Chris Church, Hannah Scott, Madison Lennon, Jose J Salazar-Torres, Jason J Howard, Nancy Lennon, M Wade Shrader, Christina P Herrero, Rachel L Lenhart, Hannah Popper, Abigail Helms, Arianna Trionfo

Background: Planovalgus is a common foot deformity in children with cerebral palsy (CP). Orthopaedic surgery is widely established as an effective treatment for planovalgus deformity, but postoperative protocols vary without a clear rationale. Immediate weight bearing (WB) after planovalgus foot correction may accelerate recovery; however, concerns about complications cause reluctance. This study aimed to determine the prevalence of complications after planovalgus correction in children with CP with early WB versus non-WB (NWB).

Methods: This retrospective cohort study included ambulatory children (Gross Motor Function Classification System I to III) with CP and planovalgus foot deformity who underwent reconstructive surgery and pre- and postoperative gait analyses. Complications were defined in 3 timeframes: (1) short-term, within 6 months of surgery, by radiograph review for nonunion, hardware failure, or infection requiring return to surgery; (2) mid-term, at 1 to 3 years, by pedobarographic assessment; and (3) long-term, >3 years, by recurrence requiring surgical revision. Fisher's exact tests compared the prevalence of complications between the immediate WB and NWB groups. Regression analysis was used to evaluate the relationship between complications and child, surgical, and postoperative factors.

Results: One hundred thirty-five children with CP (Gross Motor Function Classification System I-12%, II-58%, III-30%) underwent 140 surgical events (224 feet) at age 12.7±2.8 years. Following surgery, 84% of children followed an immediate WB protocol; 16% were NWB for 6 weeks. The prevalence of short-term complications between the WB and NWB groups was not different (nonunion/hardware failure/infection: WB, 3%/1%/0%; NWB, 0%/3%/0%; P >0.9). No differences existed between groups in midterm correction status (undercorrected/corrected/overcorrected: WB, 31%/45%/24%; NWB, 32%/54%/14%; P >0.9). The prevalence of long-term recurrence necessitating surgery was not significantly different (WB/NWB, 3%/11%; 8.5±2.8 years postoperatively; P >0.9). WB status was not a significant predictor of correction status or long-term recurrence requiring revision ( P ≥0.11).

Conclusions: There were no significant differences in complications between groups who followed immediate WB versus NWB postoperative protocols. Immediate WB after planovalgus foot correction surgery should be encouraged in children with CP, as early WB may prevent disuse muscle weakness and promote recovery.

Level of evidence: Level III-retrospective cohort study.

背景:平外翻是脑瘫患儿常见的足部畸形。骨科手术被广泛认为是平外翻畸形的有效治疗方法,但术后方案各不相同,没有明确的基本原理。平外翻足矫正后立即负重(WB)可加速恢复;然而,对并发症的担忧导致了不情愿。本研究旨在确定早期白斑患儿与非白斑患儿(NWB)平外翻矫正后并发症的发生率。方法:这项回顾性队列研究包括患有CP和平外翻足畸形的门诊儿童(大运动功能分类系统I至III),他们接受了重建手术并进行了术前和术后步态分析。并发症在3个时间范围内定义:(1)短期,手术6个月内,通过x线片检查不愈合,硬件故障或需要返回手术的感染;(2)中期,1至3年,通过儿童地理学评估;(3)长期,3年以上,因复发需要手术翻修。Fisher的精确测试比较了即时WB组和非WB组之间并发症的发生率。采用回归分析评估并发症与儿童、手术和术后因素的关系。结果:135名患有CP(大运动功能分类系统I-12%, II-58%, III-30%)的儿童在12.7±2.8岁时接受了140次手术(224英尺)。手术后,84%的儿童遵循了立即WB方案;16%的患者连续6周无尿路。WB组和NWB组的短期并发症发生率无差异(骨不连/硬体故障/感染:WB组,3%/1%/0%;NWB组,0%/3%/0%;P>0.9)。中期矫正状态组间无差异(未矫正/矫正/过度矫正:WB, 31%/45%/24%; NWB, 32%/54%/14%; P < 0.9)。需要手术的长期复发率差异无统计学意义(WB/NWB, 3%/11%;术后8.5±2.8年;P>0.9)。WB状态不是矫正状态或需要修正的长期复发的显著预测因子(P≥0.11)。结论:术后立即WB组与非WB组的并发症无显著差异。对于患有CP的儿童,应鼓励在平外翻足矫正手术后立即WB,因为早期WB可以预防废用性肌无力并促进康复。证据等级:iii级回顾性队列研究。
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引用次数: 0
Comparison of Medial/Lateral Pinning Versus All Lateral Pinning in Treatment of Pediatric Supracondylar Humerus Fractures. 内侧/外侧固定与全外侧固定治疗小儿肱骨髁上骨折的比较。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-10-23 DOI: 10.1097/BPO.0000000000003127
Nicole Lange, Joshua A Whitmore, Madelyn J Hill, Michael C Albert

Objective: Supracondylar humerus fracture is a common elbow injury sustained in the pediatric population. Percutaneous pinning, whether all lateral or medial-lateral, is the mainstay of operative management for these injuries. There has been much debate on the safety of medial-sided pinning, with the literature indicating that medial-sided pinning can lead to iatrogenic ulnar nerve injury. Thus, the goal of our study is to describe the rates of nerve injuries (radial, median, and ulnar), loss of reduction, and range of motion between all lateral and medial-lateral treatment groups.

Methods: Patients aged 1 to 18 years presenting at a pediatric hospital for a single, isolated supracondylar humerus fracture and treated with percutaneous pinning between 2018 and 2023 were reviewed. Patients with concurrent surgical treatment at the time of pinning, who presented with multiple injuries, had an open reduction, had an open fracture, or were lost to follow-up, were excluded. Age, sex, Gartland fracture classification, pinning method, nerve injury, range of motion, loss of reduction, and duration of follow-up were collected. Descriptive statistics were analyzed for variables of interest.

Results: A total of 406 pediatric patients were included. The average (SD) age at presentation was 5.7 (2.3) years, with 179 (44.1%) patients presenting with Type II fracture and 227 (55.9%) with Type III or IV. There were 131 (32.3%) patients treated with a medial-lateral pinning approach and 275 (67.7%) patients treated with an all-lateral pinning approach. Patients treated with a medial-lateral pinning experienced no new ulnar, radial, or median nerve injuries postoperatively. There was 1 (0.8%) patient with a loss of reduction, and 68.4% of patients with a medial pin had a full range of motion at their last follow-up. Patients treated with an all-lateral pinning approach experienced a new median nerve injury (n=1) and a new ulnar nerve injury (n=1) postoperatively. No patients with an all-lateral pinning approach had a loss of reduction, and 70.7% had a full range of motion at the last follow-up.

Conclusions: This study demonstrated no occurrence of an ulnar nerve injury while utilizing the medial entry pins in the treatment of supracondylar fractures. Strict adherence to surgical principles pertaining to medial entry pins is crucial to avoid ulnar nerve injury and should be included in orthopaedic surgeon's armamentarium when treating unstable supracondylar fractures.

目的:肱骨髁上骨折是儿童常见的肘部损伤。经皮钉钉,无论是外侧还是中外侧,都是这些损伤的主要手术治疗方法。关于内侧侧固定的安全性存在很多争论,文献表明内侧侧固定可导致医源性尺神经损伤。因此,我们研究的目的是描述所有外侧治疗组和中外侧治疗组之间神经损伤(桡骨、正中骨和尺骨)、复位丧失和活动范围的发生率。方法:回顾2018年至2023年在儿科医院就诊的1至18岁的单例孤立性肱骨髁上骨折并经皮穿刺钉钉治疗的患者。排除在钉钉时同时进行手术治疗的患者,包括多发损伤、开放性复位、开放性骨折或无法随访的患者。收集患者的年龄、性别、Gartland骨折分型、钉钉方式、神经损伤、活动范围、复位损失、随访时间。对感兴趣的变量进行描述性统计分析。结果:共纳入406例儿科患者。平均(SD)年龄为5.7(2.3)岁,其中179例(44.1%)为II型骨折,227例(55.9%)为III型或IV型骨折。131例(32.3%)患者采用内侧外侧固定入路,275例(67.7%)患者采用全外侧固定入路。接受内外侧固定治疗的患者术后没有出现新的尺神经、桡骨神经或正中神经损伤。有1例(0.8%)患者复位丧失,68.4%的内固定针患者在最后一次随访时活动范围完整。采用全外侧钉入路治疗的患者术后出现新的正中神经损伤(n=1)和新的尺神经损伤(n=1)。采用全外侧固定入路的患者没有复位丧失,70.7%的患者在最后一次随访时活动范围完整。结论:本研究表明,在使用内侧入针治疗髁上骨折时,没有发生尺神经损伤。严格遵守与内侧入针相关的手术原则对于避免尺神经损伤至关重要,在治疗不稳定的髁上骨折时,应将其纳入骨科医生的装备中。
{"title":"Comparison of Medial/Lateral Pinning Versus All Lateral Pinning in Treatment of Pediatric Supracondylar Humerus Fractures.","authors":"Nicole Lange, Joshua A Whitmore, Madelyn J Hill, Michael C Albert","doi":"10.1097/BPO.0000000000003127","DOIUrl":"10.1097/BPO.0000000000003127","url":null,"abstract":"<p><strong>Objective: </strong>Supracondylar humerus fracture is a common elbow injury sustained in the pediatric population. Percutaneous pinning, whether all lateral or medial-lateral, is the mainstay of operative management for these injuries. There has been much debate on the safety of medial-sided pinning, with the literature indicating that medial-sided pinning can lead to iatrogenic ulnar nerve injury. Thus, the goal of our study is to describe the rates of nerve injuries (radial, median, and ulnar), loss of reduction, and range of motion between all lateral and medial-lateral treatment groups.</p><p><strong>Methods: </strong>Patients aged 1 to 18 years presenting at a pediatric hospital for a single, isolated supracondylar humerus fracture and treated with percutaneous pinning between 2018 and 2023 were reviewed. Patients with concurrent surgical treatment at the time of pinning, who presented with multiple injuries, had an open reduction, had an open fracture, or were lost to follow-up, were excluded. Age, sex, Gartland fracture classification, pinning method, nerve injury, range of motion, loss of reduction, and duration of follow-up were collected. Descriptive statistics were analyzed for variables of interest.</p><p><strong>Results: </strong>A total of 406 pediatric patients were included. The average (SD) age at presentation was 5.7 (2.3) years, with 179 (44.1%) patients presenting with Type II fracture and 227 (55.9%) with Type III or IV. There were 131 (32.3%) patients treated with a medial-lateral pinning approach and 275 (67.7%) patients treated with an all-lateral pinning approach. Patients treated with a medial-lateral pinning experienced no new ulnar, radial, or median nerve injuries postoperatively. There was 1 (0.8%) patient with a loss of reduction, and 68.4% of patients with a medial pin had a full range of motion at their last follow-up. Patients treated with an all-lateral pinning approach experienced a new median nerve injury (n=1) and a new ulnar nerve injury (n=1) postoperatively. No patients with an all-lateral pinning approach had a loss of reduction, and 70.7% had a full range of motion at the last follow-up.</p><p><strong>Conclusions: </strong>This study demonstrated no occurrence of an ulnar nerve injury while utilizing the medial entry pins in the treatment of supracondylar fractures. Strict adherence to surgical principles pertaining to medial entry pins is crucial to avoid ulnar nerve injury and should be included in orthopaedic surgeon's armamentarium when treating unstable supracondylar fractures.</p>","PeriodicalId":16945,"journal":{"name":"Journal of Pediatric Orthopaedics","volume":" ","pages":"e218-e222"},"PeriodicalIF":1.5,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145345877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Children With Presumed Early-Onset Idiopathic Scoliosis and Treated in Cast May Have Delayed Ambulation. 推定为早发性特发性脊柱侧凸并在石膏内治疗的儿童可能会延迟行走。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-11-11 DOI: 10.1097/BPO.0000000000003151
Oliver X Dong, Bryan O Ren, Peter Sturm, Sumeet Garg, Joshua Pahys, Michael P Glotzbecker

Background: Serial casting is a safe and effective treatment for early-onset idiopathic scoliosis (I-EOS). However, its impact on a child's ability to walk has not been previously described. This study evaluates the influence of serial casting on ambulatory age in I-EOS patients.

Methods: A retrospective multicenter review was conducted on I-EOS patients who received their first casts before 18 months of age. Excluded were patients who were ambulatory at the first visit or had incomplete records. Data collected included sex, age at first visit and cast application, number of casts, precast/postcast coronal and kyphosis curves, age at final cast removal, total duration in cast, and age at first change in recorded ambulatory status. Patients were grouped by first recorded change in ambulatory status: ≤18 months, 19 to 24 months, and >24 months. Differences were assessed using ANOVA.

Results: Of the 203 patients, 148 were preambulatory at first visit. One hundred fourteen patients had sufficient documentation and of these, 30 ambulated by 18 months, 44 at 19 to 24 months, and 40 after 24 months. Significant differences were found in terms of sex ( P =0.012), precast major curve ( P =0.025), precast minor curve ( P =0.011), age at cast removal ( P =0.011), and casting duration ( P =0.007). Ambulators after 24 months had larger precast major curves compared with those at 19 to 24 months (47 vs. 36 degrees, P =0.019). Ambulators after 24 months also were older at age of cast removal (34 vs. 23 mo, P =0.008) and had longer casting duration (22 vs. 10 mo, P =0.007) versus ambulators at ≤18 months. No other statistical differences were observed.

Conclusion: In I-EOS patients treated with serial casting, delayed ambulators were more likely to be male, have greater magnitude initial major curves, a later age of cast removal, or longer total cast duration. There is an apparent association of casting with later ambulatory status; however, it is impossible to separate the impact of casting from the potential differences in underlying condition.

Level of evidence: Level III-retrospective chart review.

背景:连续铸造是一种安全有效的治疗早发性特发性脊柱侧凸的方法。然而,它对儿童行走能力的影响以前没有被描述过。本研究评估连续铸造对I-EOS患者门诊年龄的影响。方法:对18个月前首次使用石膏的I-EOS患者进行回顾性多中心评价。排除了第一次就诊时走动或记录不完整的患者。收集的数据包括性别、首次就诊时的年龄和使用石膏的年龄、石膏数量、预制/后石膏冠状和后凸曲线、最终拆除石膏时的年龄、石膏总持续时间以及记录的门诊状态中首次改变的年龄。根据首次记录的活动状态变化对患者进行分组:≤18个月,19至24个月和bb0 24个月。采用方差分析评估差异。结果:203例患者中148例首次就诊时可走动。114个病人有足够的文件,其中30个在18个月时走动,44个在19到24个月时走动,40个在24个月后走动。在性别(P=0.012)、预制件主曲线(P=0.025)、预制件次曲线(P=0.011)、拆模年龄(P=0.011)和浇铸时间(P=0.007)方面存在显著差异。与19 ~ 24个月时相比,24个月后的步行器的预制主曲线更大(47度vs. 36度,P=0.019)。与≤18个月的行走器相比,24个月后的行走器在拆除石膏时年龄也更大(34个月对23个月,P=0.008),并且铸造持续时间更长(22个月对10个月,P=0.007)。未观察到其他统计学差异。结论:在连续铸造治疗的I-EOS患者中,延迟行走器更可能是男性,具有更大的初始主要曲线,更晚的拔模年龄,或更长的总铸造时间。铸造与后期的流动状态有明显的联系;然而,不可能将铸造的影响与潜在条件的潜在差异分开。证据等级:iii级——回顾性图表回顾。
{"title":"Children With Presumed Early-Onset Idiopathic Scoliosis and Treated in Cast May Have Delayed Ambulation.","authors":"Oliver X Dong, Bryan O Ren, Peter Sturm, Sumeet Garg, Joshua Pahys, Michael P Glotzbecker","doi":"10.1097/BPO.0000000000003151","DOIUrl":"10.1097/BPO.0000000000003151","url":null,"abstract":"<p><strong>Background: </strong>Serial casting is a safe and effective treatment for early-onset idiopathic scoliosis (I-EOS). However, its impact on a child's ability to walk has not been previously described. This study evaluates the influence of serial casting on ambulatory age in I-EOS patients.</p><p><strong>Methods: </strong>A retrospective multicenter review was conducted on I-EOS patients who received their first casts before 18 months of age. Excluded were patients who were ambulatory at the first visit or had incomplete records. Data collected included sex, age at first visit and cast application, number of casts, precast/postcast coronal and kyphosis curves, age at final cast removal, total duration in cast, and age at first change in recorded ambulatory status. Patients were grouped by first recorded change in ambulatory status: ≤18 months, 19 to 24 months, and >24 months. Differences were assessed using ANOVA.</p><p><strong>Results: </strong>Of the 203 patients, 148 were preambulatory at first visit. One hundred fourteen patients had sufficient documentation and of these, 30 ambulated by 18 months, 44 at 19 to 24 months, and 40 after 24 months. Significant differences were found in terms of sex ( P =0.012), precast major curve ( P =0.025), precast minor curve ( P =0.011), age at cast removal ( P =0.011), and casting duration ( P =0.007). Ambulators after 24 months had larger precast major curves compared with those at 19 to 24 months (47 vs. 36 degrees, P =0.019). Ambulators after 24 months also were older at age of cast removal (34 vs. 23 mo, P =0.008) and had longer casting duration (22 vs. 10 mo, P =0.007) versus ambulators at ≤18 months. No other statistical differences were observed.</p><p><strong>Conclusion: </strong>In I-EOS patients treated with serial casting, delayed ambulators were more likely to be male, have greater magnitude initial major curves, a later age of cast removal, or longer total cast duration. There is an apparent association of casting with later ambulatory status; however, it is impossible to separate the impact of casting from the potential differences in underlying condition.</p><p><strong>Level of evidence: </strong>Level III-retrospective chart review.</p>","PeriodicalId":16945,"journal":{"name":"Journal of Pediatric Orthopaedics","volume":" ","pages":"129-132"},"PeriodicalIF":1.5,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145489051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Popliteal Fossa Infection, Septic Arthritis of the Knee, Pyomyositis, and Deep Vein Thrombosis Risk in Children. 儿童腘窝感染、化脓性膝关节炎、化脓性肌炎和深静脉血栓形成风险。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-10-06 DOI: 10.1097/BPO.0000000000003123
Piers D Mitchell, Jose Blanco, Mariusz Chomicki, Alastair Littlewood

Background: Our aim is to investigate the association between soft tissue infection in the popliteal fossa and hamstring muscles to determine the risk of DVT formation in children with infections in the knee and posterior thigh.

Methods: This prospective cohort study (the Peterborough Paediatric Musculoskeletal Infection Study) has gathered data for 181 children aged 0 to 15 years with infection of their limbs or spine. Those with MRI evidence for infection of the popliteal fossa of the knee were identified, as well as those with thrombosis in the venous system.

Results: Popliteal fossa infection was present in 15 children (8% of the 181 in the entire study). Most were associated with septic arthritis of the knee (80%), but some were due to pyomyositis of the hamstrings or calf (20%). Venous thrombosis was noted in 1.1% of the entire 181 study group, but 13% of those with popliteal fossa infection, a 12-fold difference (Fisher exact test statistic 0.0064, P <0.01). One of those with a DVT died from pulmonary embolism a few hours after their MRI scan had been performed.

Conclusion: Thirteen percent of children with popliteal fossa infection had an associated DVT, so it may be an independent risk factor for thrombosis. To minimize the risk of DVT and its serious complications, we recommend that children presenting to the Emergency Department with pain in the knee, thigh or calf and raised inflammatory markers (CRP/ESR) suspicious for musculoskeletal infection should have their popliteal fossa examined, and if tender, an urgent Doppler ultrasound should be organised. On MRI, attention should be paid to the popliteal fossa on axial STIR images, and if oedema is present around the popliteal vessels, then prophylactic dose anticoagulation should be started, while those with a dilated popliteal vein on MRI should receive treatment dose anticoagulation.

Level of evidence: Level II. A lesser quality prospective study with patients enrolled at different points in their disease.

背景:我们的目的是研究腘窝和腘绳肌软组织感染之间的关系,以确定膝和大腿后部感染的儿童DVT形成的风险。方法:这项前瞻性队列研究(彼得伯勒儿童肌肉骨骼感染研究)收集了181名0至15岁的四肢或脊柱感染儿童的数据。那些有MRI证据表明膝关节腘窝感染,以及那些有静脉系统血栓形成。结果:15例儿童腘窝感染(占整个研究181例的8%)。大多数与化脓性膝关节炎有关(80%),但有些是由于腿筋或小腿的化脓性肌炎(20%)。在整个181个研究组中,静脉血栓发生率为1.1%,而腘窝感染发生率为13%,差异为12倍(Fisher精确检验统计量为0.0064,p)。结论:13%腘窝感染患儿合并DVT,可能是血栓形成的独立危险因素。为了尽量减少深静脉血栓及其严重并发症的风险,我们建议到急诊科就诊的儿童,如果出现膝盖、大腿或小腿疼痛,炎症标志物(CRP/ESR)升高,怀疑是肌肉骨骼感染,应检查腘窝,如果有触痛,应组织紧急多普勒超声检查。MRI上应注意轴位STIR图像上的腘窝,如果腘窝血管周围出现水肿,则应开始预防性剂量抗凝治疗,MRI上腘静脉扩张者应接受治疗剂量抗凝治疗。证据等级:二级。一项较低质量的前瞻性研究,患者在疾病的不同阶段入组。
{"title":"Popliteal Fossa Infection, Septic Arthritis of the Knee, Pyomyositis, and Deep Vein Thrombosis Risk in Children.","authors":"Piers D Mitchell, Jose Blanco, Mariusz Chomicki, Alastair Littlewood","doi":"10.1097/BPO.0000000000003123","DOIUrl":"10.1097/BPO.0000000000003123","url":null,"abstract":"<p><strong>Background: </strong>Our aim is to investigate the association between soft tissue infection in the popliteal fossa and hamstring muscles to determine the risk of DVT formation in children with infections in the knee and posterior thigh.</p><p><strong>Methods: </strong>This prospective cohort study (the Peterborough Paediatric Musculoskeletal Infection Study) has gathered data for 181 children aged 0 to 15 years with infection of their limbs or spine. Those with MRI evidence for infection of the popliteal fossa of the knee were identified, as well as those with thrombosis in the venous system.</p><p><strong>Results: </strong>Popliteal fossa infection was present in 15 children (8% of the 181 in the entire study). Most were associated with septic arthritis of the knee (80%), but some were due to pyomyositis of the hamstrings or calf (20%). Venous thrombosis was noted in 1.1% of the entire 181 study group, but 13% of those with popliteal fossa infection, a 12-fold difference (Fisher exact test statistic 0.0064, P <0.01). One of those with a DVT died from pulmonary embolism a few hours after their MRI scan had been performed.</p><p><strong>Conclusion: </strong>Thirteen percent of children with popliteal fossa infection had an associated DVT, so it may be an independent risk factor for thrombosis. To minimize the risk of DVT and its serious complications, we recommend that children presenting to the Emergency Department with pain in the knee, thigh or calf and raised inflammatory markers (CRP/ESR) suspicious for musculoskeletal infection should have their popliteal fossa examined, and if tender, an urgent Doppler ultrasound should be organised. On MRI, attention should be paid to the popliteal fossa on axial STIR images, and if oedema is present around the popliteal vessels, then prophylactic dose anticoagulation should be started, while those with a dilated popliteal vein on MRI should receive treatment dose anticoagulation.</p><p><strong>Level of evidence: </strong>Level II. A lesser quality prospective study with patients enrolled at different points in their disease.</p>","PeriodicalId":16945,"journal":{"name":"Journal of Pediatric Orthopaedics","volume":" ","pages":"e271-e275"},"PeriodicalIF":1.5,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145232892","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Response to the Letter to the Editor. 对给编辑的信的回应。
IF 1.5 3区 医学 Q3 ORTHOPEDICS Pub Date : 2026-03-01 Epub Date: 2025-12-24 DOI: 10.1097/BPO.0000000000003201
Antti J Saarinen, Ilkka Helenius
{"title":"Response to the Letter to the Editor.","authors":"Antti J Saarinen, Ilkka Helenius","doi":"10.1097/BPO.0000000000003201","DOIUrl":"10.1097/BPO.0000000000003201","url":null,"abstract":"","PeriodicalId":16945,"journal":{"name":"Journal of Pediatric Orthopaedics","volume":" ","pages":"e297"},"PeriodicalIF":1.5,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145819802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Pediatric Orthopaedics
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