Pub Date : 2025-12-17DOI: 10.1007/s43390-025-01246-1
Hannah G Geoffroy, Richard M Schwend, David B Bumpass, Paige L Seiler, Jason E O Muka, Richard E McCarthy
Purpose: To present our experience using Shilla Growth Guidance System (SGGS) technology with a solid pelvic foundation in patients with severe early-onset neuromuscular spine deformity.
Methods: The surgical procedure involved a solid instrumented fusion from L5 to the pelvis with iliac screws, with minimal dissection of the spine from L4 to T4, leaving the longitudinal para-spinal muscles intact. Alternating SGGS screws were sequentially placed from L4 to T4 with fluoroscopy and/or computer navigation. This retrospective study from two institutions included surgeries performed by three surgeons. The primary outcomes were the number of revision surgeries and the complication rate; T1-S1 height increase was a secondary outcome.
Results: For 34 patients, the average age at the initial surgery was 5.9 years and the follow-up was 10 years for surviving patients. Eleven patients were tracheostomy- and ventilator-dependent. The average total number of surgeries/patients was 2.3. The revision surgery rate was 53% (45 revision surgeries in 18 patients, average of 2.5 revision surgeries/patient). 20 patients (59%) had a major complication (modified Clavien-Sink-Dindo classification 3a-5). Nine (26%) had a deep surgical-site (SSI) infection requiring irrigation, debridement, and implant exchange. Thirteen patients died at an average age of 10.7 years, average 4.7 years post-operative, a 38% 10-year mortality and representing the frail nature of this population. Ten of these 13 (77%) deceased patients had no additional surgery after their index surgery, which was one of the major goals of the procedure. Nine of the 34 patients (26%) had a final fusion. The T1-S1 height increased by a mean of 6.7 cm (p < 0.01).
Conclusions: SGGS with a solid pelvic foundation is an option for addressing severe spinal deformity for patients with early-onset neuromuscular scoliosis who are too immature for a definitive fusion. For 47% of these patients, only the initial surgical procedure was necessary, thus avoiding serial surgical or clinic lengthening procedures. However, the revision rate of 53% and complication rate of 59% demonstrates the high risks of this procedure in this extremely frail population.
目的:介绍新罗生长引导系统(SGGS)技术与坚实骨盆基础治疗严重早发性神经肌肉脊柱畸形的经验。方法:采用髂骨螺钉对L5至骨盆进行固定融合术,对L4至T4椎体进行最小程度的剥离,使纵脊旁肌保持完整。在透视和/或计算机导航下,从L4到T4依次放置交替的SGGS螺钉。本回顾性研究来自两家机构,包括三位外科医生的手术。主要观察结果为翻修手术次数和并发症发生率;T1-S1高度增高是次要结局。结果:34例患者初次手术时平均年龄为5.9岁,存活患者随访10年。11例患者依赖气管切开术和呼吸机。平均总手术次数为2.3次/例。翻修率为53%(18例45例,平均2.5例/例)。20例患者(59%)出现主要并发症(改良Clavien-Sink-Dindo分类3a-5)。9例(26%)有深部手术部位(SSI)感染,需要冲洗、清创和植入物置换。13例患者死亡,平均年龄为10.7岁,平均术后4.7年,10年死亡率为38%,代表了这一人群的脆弱本质。这13例死亡患者中有10例(77%)在首次手术后没有进行其他手术,这是手术的主要目标之一。34例患者中有9例(26%)最终融合。T1-S1高度平均增加6.7 cm (p)。结论:SGGS结合坚实的骨盆基础是解决早发性神经肌肉性脊柱侧凸患者严重脊柱畸形的一种选择。其中47%的患者只需要进行初始手术,从而避免了一系列手术或临床延长手术。然而,53%的翻修率和59%的并发症率表明,在这个极度虚弱的人群中,这种手术的风险很高。
{"title":"Shilla growth guidance system (SGGS) instrumentation with pelvic foundation for severe early-onset neuromuscular spine deformity.","authors":"Hannah G Geoffroy, Richard M Schwend, David B Bumpass, Paige L Seiler, Jason E O Muka, Richard E McCarthy","doi":"10.1007/s43390-025-01246-1","DOIUrl":"https://doi.org/10.1007/s43390-025-01246-1","url":null,"abstract":"<p><strong>Purpose: </strong>To present our experience using Shilla Growth Guidance System (SGGS) technology with a solid pelvic foundation in patients with severe early-onset neuromuscular spine deformity.</p><p><strong>Methods: </strong>The surgical procedure involved a solid instrumented fusion from L5 to the pelvis with iliac screws, with minimal dissection of the spine from L4 to T4, leaving the longitudinal para-spinal muscles intact. Alternating SGGS screws were sequentially placed from L4 to T4 with fluoroscopy and/or computer navigation. This retrospective study from two institutions included surgeries performed by three surgeons. The primary outcomes were the number of revision surgeries and the complication rate; T1-S1 height increase was a secondary outcome.</p><p><strong>Results: </strong>For 34 patients, the average age at the initial surgery was 5.9 years and the follow-up was 10 years for surviving patients. Eleven patients were tracheostomy- and ventilator-dependent. The average total number of surgeries/patients was 2.3. The revision surgery rate was 53% (45 revision surgeries in 18 patients, average of 2.5 revision surgeries/patient). 20 patients (59%) had a major complication (modified Clavien-Sink-Dindo classification 3a-5). Nine (26%) had a deep surgical-site (SSI) infection requiring irrigation, debridement, and implant exchange. Thirteen patients died at an average age of 10.7 years, average 4.7 years post-operative, a 38% 10-year mortality and representing the frail nature of this population. Ten of these 13 (77%) deceased patients had no additional surgery after their index surgery, which was one of the major goals of the procedure. Nine of the 34 patients (26%) had a final fusion. The T1-S1 height increased by a mean of 6.7 cm (p < 0.01).</p><p><strong>Conclusions: </strong>SGGS with a solid pelvic foundation is an option for addressing severe spinal deformity for patients with early-onset neuromuscular scoliosis who are too immature for a definitive fusion. For 47% of these patients, only the initial surgical procedure was necessary, thus avoiding serial surgical or clinic lengthening procedures. However, the revision rate of 53% and complication rate of 59% demonstrates the high risks of this procedure in this extremely frail population.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145769015","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-17DOI: 10.1007/s43390-025-01255-0
Tanmay S Mehta, Manjot Singh, Michael J Farias, Joseph E Nassar, Nicolas L Carayannopoulos, Zvipo M Chisango, Alan H Daniels, Bassel G Diebo
Purpose: Adult spinal deformity (ASD) is a chronic musculoskeletal condition characterized by abnormal spinal curvature and adverse psychological well-being. However, the mental health burden of ASD remains poorly characterized. This retrospective cross-sectional cohort study compared the prevalence and odds of mental health conditions in the ASD population to a matched general population cohort using the nationally representative All of Us Research Program.
Methods: ASD patients (n = 6531) were identified using ICD-9/10. Using 1:1 nearest neighbor propensity matching without replacement (caliper = 0.05), 6396 ASD patients were matched to 6396 general population controls. Logistic regression was performed to compute odds ratios (OR) and 95% confidence-intervals (CI) for mental health outcomes.
Results: After matching, mean age was 58.0 and 76% were female. Compared to the general population, ASD patients had higher unadjusted rates of depression (37.6% vs. 11.3%), anxiety (41.6% vs. 12.1%), post-traumatic stress disorder (PTSD) (7.2% vs. 2.2%), bipolar disorder (7.1% vs. 2.1%), schizophrenia/psychosis (2.4% vs. 0.9%), substance use disorders (24.3% vs. 9.7%), eating disorders (1.4% vs. 0.4%), and attention-deficit hyperactivity disorder (ADHD) (5.3% vs. 1.4%). On logistic regression, ASD patients had higher odds of depression (OR = 2.06, CI = 1.90-2.23, P < 0.001), anxiety (OR = 2.24, CI = 2.07-2.43, P < 0.001), and ADHD (OR = 2.87, CI = 2.32-3.54, P < 0.001). ASD patients also exhibited significantly elevated odds for eating disorders, bipolar disorder, PTSD, and substance use disorder (P < 0.05).
Conclusions: ASD patients in the United States have a substantially elevated mental health burden than the general populace. Routine mental health screenings and psychological assessments can be beneficial for this vulnerable population.
目的:成人脊柱畸形(ASD)是一种以脊柱弯曲异常和不良心理健康为特征的慢性肌肉骨骼疾病。然而,ASD的心理健康负担仍然缺乏特征。这项回顾性横断面队列研究使用全国代表性的“我们所有人”研究项目,比较了ASD人群中精神健康状况的患病率和几率与匹配的普通人群队列。方法:采用ICD-9/10对6531例ASD患者进行分类。采用无置换的1:1最近邻倾向匹配(caliper = 0.05), 6396例ASD患者与6396例普通人群对照进行匹配。采用逻辑回归计算心理健康结果的比值比(OR)和95%置信区间(CI)。结果:配对后平均年龄58.0岁,女性占76%。与一般人群相比,ASD患者有更高的未经调整的抑郁症(37.6%比11.3%)、焦虑症(41.6%比12.1%)、创伤后应激障碍(PTSD)(7.2%比2.2%)、双相情感障碍(7.1%比2.1%)、精神分裂症/精神病(2.4%比0.9%)、物质使用障碍(24.3%比9.7%)、饮食失调(1.4%比0.4%)和注意缺陷多动障碍(ADHD)(5.3%比1.4%)。logistic回归分析显示,ASD患者患抑郁症的几率更高(OR = 2.06, CI = 1.90-2.23, P)。结论:美国ASD患者的心理健康负担明显高于普通人群。常规的心理健康检查和心理评估对这些弱势群体是有益的。
{"title":"National mental health burden in adults with spinal deformity: a propensity-matched analysis using the All of Us Research Program.","authors":"Tanmay S Mehta, Manjot Singh, Michael J Farias, Joseph E Nassar, Nicolas L Carayannopoulos, Zvipo M Chisango, Alan H Daniels, Bassel G Diebo","doi":"10.1007/s43390-025-01255-0","DOIUrl":"https://doi.org/10.1007/s43390-025-01255-0","url":null,"abstract":"<p><strong>Purpose: </strong>Adult spinal deformity (ASD) is a chronic musculoskeletal condition characterized by abnormal spinal curvature and adverse psychological well-being. However, the mental health burden of ASD remains poorly characterized. This retrospective cross-sectional cohort study compared the prevalence and odds of mental health conditions in the ASD population to a matched general population cohort using the nationally representative All of Us Research Program.</p><p><strong>Methods: </strong>ASD patients (n = 6531) were identified using ICD-9/10. Using 1:1 nearest neighbor propensity matching without replacement (caliper = 0.05), 6396 ASD patients were matched to 6396 general population controls. Logistic regression was performed to compute odds ratios (OR) and 95% confidence-intervals (CI) for mental health outcomes.</p><p><strong>Results: </strong>After matching, mean age was 58.0 and 76% were female. Compared to the general population, ASD patients had higher unadjusted rates of depression (37.6% vs. 11.3%), anxiety (41.6% vs. 12.1%), post-traumatic stress disorder (PTSD) (7.2% vs. 2.2%), bipolar disorder (7.1% vs. 2.1%), schizophrenia/psychosis (2.4% vs. 0.9%), substance use disorders (24.3% vs. 9.7%), eating disorders (1.4% vs. 0.4%), and attention-deficit hyperactivity disorder (ADHD) (5.3% vs. 1.4%). On logistic regression, ASD patients had higher odds of depression (OR = 2.06, CI = 1.90-2.23, P < 0.001), anxiety (OR = 2.24, CI = 2.07-2.43, P < 0.001), and ADHD (OR = 2.87, CI = 2.32-3.54, P < 0.001). ASD patients also exhibited significantly elevated odds for eating disorders, bipolar disorder, PTSD, and substance use disorder (P < 0.05).</p><p><strong>Conclusions: </strong>ASD patients in the United States have a substantially elevated mental health burden than the general populace. Routine mental health screenings and psychological assessments can be beneficial for this vulnerable population.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145768961","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-16DOI: 10.1007/s43390-025-01253-2
Carl-Eric Aubin, Lawrence G Lenke, Michael Vitale, Justin S Smith, Virginie Lafage, Michelle C Welborn, A Noelle Larson, Takashi Kaito, Peter O Newton, Jeffrey Mullin, Christiane Caouette, Brice Ilharreborde
Purpose: Adolescent idiopathic scoliosis (AIS) is a complex three-dimensional (3D) spinal deformity, with transverse plane rotational components increasingly targeted by modern surgical techniques. Yet, clinical evaluation remains predominantly based on 2D radiographic parameters, including the widely used Lenke classification. In response, the 3D Classification Task Force of the Scoliosis Research Society (SRS) developed a comprehensive, clinically relevant classification system that remains intuitive, reproducible, and readily applicable by spine surgeons. This manuscript introduces the proposed SRS-Lenke-Aubin 3D classification and evaluates its ability to provide a structured and clinically meaningful 3D characterization of spinal deformities in AIS.
Methods: To maintain continuity with standard clinical practices, the system builds upon the established Lenke classification and introduces two complementary 3D descriptors: the orientation of the regional plane of deformation (ORPD) and the apical vertebral rotation (AVR). These indices capture transverse plane deformities at the regional and local levels, respectively. Each was independently assessed for the proximal thoracic (PT), main thoracic (MT), and thoracolumbar/lumbar (TL/L) regions using calibrated 3D reconstructions from biplanar radiographs. A population-representative cohort of 285 AIS surgical cases was used to evaluate the system. ORPD and AVR values were translated into categorical modifiers using predefined clinical thresholds.
Results: The new SRS-Lenke-Aubin 3D AIS classification adds two transverse plane modifiers per spinal region-the ORPD and AVR-yielding a modular 3-tiered, 4-modifier system: Curve type (1-6), Lumbar spine modifier (A, B, C), Thoracic sagittal profile modifier (-, N, +), Transverse plane regional modifier (ORPD: 1-3) and Transverse plane local modifier (AVR: s, m, l). A broad range of ORPD × AVR combinations was observed across the cohort, reflecting the system's ability to capture transverse plane heterogeneity. Notably, similar coronal curve types often exhibited divergent transverse morphologies, underscoring the added value of these 3D descriptors in identifying clinically relevant variation.
Conclusions: The SRS-Lenke-Aubin 3D classification enriches the existing Lenke framework by incorporating practical transverse plane descriptors compatible with standard imaging workflows. This system offers a clinically meaningful step toward more complete 3D characterization of AIS, with potential applications in improving surgical planning, assessing outcomes, and supporting future integration with automated 3D tools.
目的:青少年特发性脊柱侧凸(AIS)是一种复杂的三维(3D)脊柱畸形,现代外科技术越来越多地针对横平面旋转部件。然而,临床评估仍然主要基于二维影像学参数,包括广泛使用的Lenke分类。作为回应,脊柱侧凸研究协会(SRS)的3D分类工作组开发了一个全面的、临床相关的分类系统,该系统保持直观、可重复性,并且易于脊柱外科医生使用。本文介绍了拟议的SRS-Lenke-Aubin 3D分类,并评估其提供AIS脊柱畸形结构化和临床有意义的3D表征的能力。方法:为了保持与标准临床实践的连续性,该系统建立在已建立的Lenke分类的基础上,并引入了两个互补的3D描述符:区域变形平面的方向(ORPD)和椎体根尖旋转(AVR)。这些指标分别在区域和局部水平上捕获横向平面畸形。使用双平面x线片校准的3D重建,分别独立评估近段胸椎(PT)、主胸椎(MT)和胸腰椎/腰椎(TL/L)区域。采用具有人口代表性的285例AIS手术病例队列来评估该系统。ORPD和AVR值使用预定义的临床阈值转化为分类修饰符。结果:新的SRS-Lenke-Aubin 3D AIS分类为每个脊柱区域增加了两个横向平面修饰符- ORPD和AVR-从而形成一个模块化的3层4个修饰符系统:曲线型(1-6)、腰椎修饰符(a、B、C)、胸椎矢状面修饰符(-、N、+)、横向平面区域修饰符(ORPD: 1-3)和横向平面局部修饰符(AVR: s、m、l)。在整个队列中观察到广泛的ORPD × AVR组合,反映了系统捕获横向平面异质性的能力。值得注意的是,相似的冠状曲线类型通常表现出不同的横向形态,强调了这些3D描述符在识别临床相关变异方面的附加价值。结论:SRS-Lenke-Aubin三维分类通过纳入与标准成像工作流程兼容的实用横向平面描述符,丰富了现有的Lenke框架。该系统为AIS更完整的3D表征提供了具有临床意义的一步,在改进手术计划、评估结果和支持未来与自动化3D工具的集成方面具有潜在的应用前景。
{"title":"The SRS-Lenke-Aubin 3D classification of adolescent idiopathic scoliosis.","authors":"Carl-Eric Aubin, Lawrence G Lenke, Michael Vitale, Justin S Smith, Virginie Lafage, Michelle C Welborn, A Noelle Larson, Takashi Kaito, Peter O Newton, Jeffrey Mullin, Christiane Caouette, Brice Ilharreborde","doi":"10.1007/s43390-025-01253-2","DOIUrl":"https://doi.org/10.1007/s43390-025-01253-2","url":null,"abstract":"<p><strong>Purpose: </strong>Adolescent idiopathic scoliosis (AIS) is a complex three-dimensional (3D) spinal deformity, with transverse plane rotational components increasingly targeted by modern surgical techniques. Yet, clinical evaluation remains predominantly based on 2D radiographic parameters, including the widely used Lenke classification. In response, the 3D Classification Task Force of the Scoliosis Research Society (SRS) developed a comprehensive, clinically relevant classification system that remains intuitive, reproducible, and readily applicable by spine surgeons. This manuscript introduces the proposed SRS-Lenke-Aubin 3D classification and evaluates its ability to provide a structured and clinically meaningful 3D characterization of spinal deformities in AIS.</p><p><strong>Methods: </strong>To maintain continuity with standard clinical practices, the system builds upon the established Lenke classification and introduces two complementary 3D descriptors: the orientation of the regional plane of deformation (ORPD) and the apical vertebral rotation (AVR). These indices capture transverse plane deformities at the regional and local levels, respectively. Each was independently assessed for the proximal thoracic (PT), main thoracic (MT), and thoracolumbar/lumbar (TL/L) regions using calibrated 3D reconstructions from biplanar radiographs. A population-representative cohort of 285 AIS surgical cases was used to evaluate the system. ORPD and AVR values were translated into categorical modifiers using predefined clinical thresholds.</p><p><strong>Results: </strong>The new SRS-Lenke-Aubin 3D AIS classification adds two transverse plane modifiers per spinal region-the ORPD and AVR-yielding a modular 3-tiered, 4-modifier system: Curve type (1-6), Lumbar spine modifier (A, B, C), Thoracic sagittal profile modifier (-, N, +), Transverse plane regional modifier (ORPD: 1-3) and Transverse plane local modifier (AVR: s, m, l). A broad range of ORPD × AVR combinations was observed across the cohort, reflecting the system's ability to capture transverse plane heterogeneity. Notably, similar coronal curve types often exhibited divergent transverse morphologies, underscoring the added value of these 3D descriptors in identifying clinically relevant variation.</p><p><strong>Conclusions: </strong>The SRS-Lenke-Aubin 3D classification enriches the existing Lenke framework by incorporating practical transverse plane descriptors compatible with standard imaging workflows. This system offers a clinically meaningful step toward more complete 3D characterization of AIS, with potential applications in improving surgical planning, assessing outcomes, and supporting future integration with automated 3D tools.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145763913","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-13DOI: 10.1007/s43390-025-01251-4
Utsav Kapoor, Jennifer M Bauer, Burt Yaszay, Scott Yang
Purpose: Advances in operative and recovery protocols such as the rapid recovery pathway (RRP) in the last decade have shortened inpatient stays for adolescent idiopathic scoliosis (AIS). This study aimed to evaluate the impact of these national trends on length of stay (LOS), complication rates, and costs in patients with AIS undergoing posterior spinal fusion (PSF) using a large, nationally representative dataset.
Methods: A retrospective review of 10,081 patients requiring PSF for AIS was conducted using the Healthcare Cost and Utilization Project's (HCUP) Kids' Inpatient Database (KID) in the latest available year prior to the popularity of protocols like RRP (2012) and most recently (2019). Patients and complications were identified via ICD-9 and ICD-10 codes. Multivariate linear and logistic regression analyses were performed to assess the impact of year of surgery while adjusting for demographic variables.
Results: Average LOS decreased in 2019 vs. 2012 (3.9 days vs. 5.4 days, p < 0.001), year of surgery (β = -1.4 days, p < 0.001), and absence of complications (β = -2.8 days, p < 0.001) were the largest predictors of LOS. Overall complication rates declined from 12.8% to 6.5% (p < 0.001). Year of surgery showed significantly increased charges after inflation adjustment (β = $12,452.6, p < 0.001), though other demographic variables demonstrated larger impact on cost.
Conclusions: More recent surgical year resulted in reduced hospital stays with fewer complications and without substantial increases in cost. These findings support continued adoption and refinement of operative and recovery protocols in pediatric spine surgery.
{"title":"Recent national improvements in length of stay and complications after posterior spinal fusion for adolescent idiopathic scoliosis: a database analysis and review of literature.","authors":"Utsav Kapoor, Jennifer M Bauer, Burt Yaszay, Scott Yang","doi":"10.1007/s43390-025-01251-4","DOIUrl":"https://doi.org/10.1007/s43390-025-01251-4","url":null,"abstract":"<p><strong>Purpose: </strong>Advances in operative and recovery protocols such as the rapid recovery pathway (RRP) in the last decade have shortened inpatient stays for adolescent idiopathic scoliosis (AIS). This study aimed to evaluate the impact of these national trends on length of stay (LOS), complication rates, and costs in patients with AIS undergoing posterior spinal fusion (PSF) using a large, nationally representative dataset.</p><p><strong>Methods: </strong>A retrospective review of 10,081 patients requiring PSF for AIS was conducted using the Healthcare Cost and Utilization Project's (HCUP) Kids' Inpatient Database (KID) in the latest available year prior to the popularity of protocols like RRP (2012) and most recently (2019). Patients and complications were identified via ICD-9 and ICD-10 codes. Multivariate linear and logistic regression analyses were performed to assess the impact of year of surgery while adjusting for demographic variables.</p><p><strong>Results: </strong>Average LOS decreased in 2019 vs. 2012 (3.9 days vs. 5.4 days, p < 0.001), year of surgery (β = -1.4 days, p < 0.001), and absence of complications (β = -2.8 days, p < 0.001) were the largest predictors of LOS. Overall complication rates declined from 12.8% to 6.5% (p < 0.001). Year of surgery showed significantly increased charges after inflation adjustment (β = $12,452.6, p < 0.001), though other demographic variables demonstrated larger impact on cost.</p><p><strong>Conclusions: </strong>More recent surgical year resulted in reduced hospital stays with fewer complications and without substantial increases in cost. These findings support continued adoption and refinement of operative and recovery protocols in pediatric spine surgery.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145752112","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-12DOI: 10.1007/s43390-025-01240-7
Leta Ashebo, Constantine D Mavroudis, Angie Kuang, Patrick J Cahill, Jason B Anari
Purpose: One factor that may lead to the development of early-onset scoliosis (EOS) is chest wall procedures during infancy, which are common for patients with Trisomy 21 requiring cardiothoracic intervention involving thoracotomies. Studies examining scoliosis incidence in patients with prior thoracotomy demonstrate a wide incidence range. Our study aimed to assess if scoliosis prevalence is higher in patients with Trisomy 21 who underwent prior thoracotomy compared to patients who underwent sternotomy for congenital heart disease repair.
Methods: An IRB-approved, single-center retrospective review included patients aged 9 years or older with Trisomy 21 who underwent prior cardiothoracic surgery. Exclusion criteria included other trisomy diagnoses, no cardiothoracic surgical history, unavailable operative records, and ages 0-8 years. Medical chart review examined demographics, surgical details, and scoliosis diagnosis and management. Statistical analyses included chi-square, z test, one-way ANOVA, and descriptive statistics.
Results: Of 301 total patients, 12.6% were eventually diagnosed with scoliosis (n = 38). Common cardiothoracic procedures included atrioventricular canal repair (n = 141/301, 46.8%) and ventricular septal defect repair (n = 67/301, 22.3%). Thoracotomies were required in 7.0% (n = 21/301) at a median age of 1 month (IQR:0-15), most commonly for patent ductus arteriosus ligation (n = 8/21, 38.0%). Among thoracotomy patients, 28.6% developed scoliosis (n = 6/21), compared to 11.4% of sternotomy patients (n = 32/280) (p = 0.023). Among all patients with scoliosis (n = 38), 36.8% required intervention in the form of non-operative (i.e. bracing) or surgical treatment due to curve presentation and/or progression (n = 14); and 13.2% ultimately required spinal fusion (n = 5).
Conclusion: Our study demonstrates that trisomy 21 patients requiring early CT intervention have greater scoliosis prevalence following thoracotomy than sternotomy. While the prevalence is greater in the thoracotomy group, the evidence suggests both cohorts must closely be monitored for spinal deformity development to intervene early and prevent progression to an operative magnitude scoliosis.
{"title":"Cardiothoracic surgical incision type and later scoliosis development in trisomy 21 patients following infant cardiothoracic surgical procedures.","authors":"Leta Ashebo, Constantine D Mavroudis, Angie Kuang, Patrick J Cahill, Jason B Anari","doi":"10.1007/s43390-025-01240-7","DOIUrl":"https://doi.org/10.1007/s43390-025-01240-7","url":null,"abstract":"<p><strong>Purpose: </strong>One factor that may lead to the development of early-onset scoliosis (EOS) is chest wall procedures during infancy, which are common for patients with Trisomy 21 requiring cardiothoracic intervention involving thoracotomies. Studies examining scoliosis incidence in patients with prior thoracotomy demonstrate a wide incidence range. Our study aimed to assess if scoliosis prevalence is higher in patients with Trisomy 21 who underwent prior thoracotomy compared to patients who underwent sternotomy for congenital heart disease repair.</p><p><strong>Methods: </strong>An IRB-approved, single-center retrospective review included patients aged 9 years or older with Trisomy 21 who underwent prior cardiothoracic surgery. Exclusion criteria included other trisomy diagnoses, no cardiothoracic surgical history, unavailable operative records, and ages 0-8 years. Medical chart review examined demographics, surgical details, and scoliosis diagnosis and management. Statistical analyses included chi-square, z test, one-way ANOVA, and descriptive statistics.</p><p><strong>Results: </strong>Of 301 total patients, 12.6% were eventually diagnosed with scoliosis (n = 38). Common cardiothoracic procedures included atrioventricular canal repair (n = 141/301, 46.8%) and ventricular septal defect repair (n = 67/301, 22.3%). Thoracotomies were required in 7.0% (n = 21/301) at a median age of 1 month (IQR:0-15), most commonly for patent ductus arteriosus ligation (n = 8/21, 38.0%). Among thoracotomy patients, 28.6% developed scoliosis (n = 6/21), compared to 11.4% of sternotomy patients (n = 32/280) (p = 0.023). Among all patients with scoliosis (n = 38), 36.8% required intervention in the form of non-operative (i.e. bracing) or surgical treatment due to curve presentation and/or progression (n = 14); and 13.2% ultimately required spinal fusion (n = 5).</p><p><strong>Conclusion: </strong>Our study demonstrates that trisomy 21 patients requiring early CT intervention have greater scoliosis prevalence following thoracotomy than sternotomy. While the prevalence is greater in the thoracotomy group, the evidence suggests both cohorts must closely be monitored for spinal deformity development to intervene early and prevent progression to an operative magnitude scoliosis.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145743884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-11DOI: 10.1007/s43390-025-01250-5
Ally A Yang, Anthony E Seddio, Dominick A Tuason
Introduction: Posterior segmental instrumented fusion (PSIF) is considered the gold standard surgical treatment for adolescent idiopathic scoliosis (AIS), as it leads to immediate deformity correction and predictable long-term outcomes. Extended inpatient length of stay (LOS) following this intervention has been associated with greater morbidity, healthcare cost, and reoperation rates. Therefore, there is a growing impetus to reduce LOS through previously described accelerated discharge protocols. However, there is a paucity of literature characterizing perioperative factors associated with extended LOS in patients undergoing PSIF for AIS. Additionally, it remains unclear whether postoperative patient-reported outcomes are superior in patients with shorter LOS after AIS surgery.
Methods: A single institution's longitudinally maintained database was queried from a large academic medical center to identify patients with AIS who underwent PSIF by a single fellowship-trained pediatric spine surgeon between 2019 and 2024. Perioperative factors including age, sex, height, weight, race, ethnicity, insurance plan, language spoken at home, Risser stage, curve magnitude, training level of first assistant, intraoperative time, levels fused, navigation assistance, estimated blood loss, and Scoliosis Research Society (SRS) scores were assessed to determine potential associations with extended LOS.
Results: Of the 118 AIS patients who underwent PSIF, the mean LOS was 3.1 ± 0.8. Perioperative factors associated with longer LOS included only greater levels fused (p = 0.023). Longer LOS was associated with higher postoperative SRS mental health scores (p = 0.022), with a trend toward greater satisfaction (p = 0.055) and pain (p = 0.072) scores after adjustment for baseline values. No other perioperative factors or specific SRS domains were associated with LOS (p > 0.05 for all).
Conclusion: Greater number of levels (more than 11 segments) fused in surgery was associated with longer length of stay for AIS patients who underwent PSIF. With growing focus on minimizing inpatient LOS duration following PSIF for AIS patients, our findings of higher postoperative patient-reported SRS scores after longer inpatient stay may warrant prospective analysis and should be further considered in the perioperative care of AIS patients.
{"title":"Higher postoperative Scoliosis Research Society (SRS) scores and number of levels fused associated with extended length of stay following posterior segmental instrumented fusion for adolescent idiopathic scoliosis.","authors":"Ally A Yang, Anthony E Seddio, Dominick A Tuason","doi":"10.1007/s43390-025-01250-5","DOIUrl":"https://doi.org/10.1007/s43390-025-01250-5","url":null,"abstract":"<p><strong>Introduction: </strong>Posterior segmental instrumented fusion (PSIF) is considered the gold standard surgical treatment for adolescent idiopathic scoliosis (AIS), as it leads to immediate deformity correction and predictable long-term outcomes. Extended inpatient length of stay (LOS) following this intervention has been associated with greater morbidity, healthcare cost, and reoperation rates. Therefore, there is a growing impetus to reduce LOS through previously described accelerated discharge protocols. However, there is a paucity of literature characterizing perioperative factors associated with extended LOS in patients undergoing PSIF for AIS. Additionally, it remains unclear whether postoperative patient-reported outcomes are superior in patients with shorter LOS after AIS surgery.</p><p><strong>Methods: </strong>A single institution's longitudinally maintained database was queried from a large academic medical center to identify patients with AIS who underwent PSIF by a single fellowship-trained pediatric spine surgeon between 2019 and 2024. Perioperative factors including age, sex, height, weight, race, ethnicity, insurance plan, language spoken at home, Risser stage, curve magnitude, training level of first assistant, intraoperative time, levels fused, navigation assistance, estimated blood loss, and Scoliosis Research Society (SRS) scores were assessed to determine potential associations with extended LOS.</p><p><strong>Results: </strong>Of the 118 AIS patients who underwent PSIF, the mean LOS was 3.1 ± 0.8. Perioperative factors associated with longer LOS included only greater levels fused (p = 0.023). Longer LOS was associated with higher postoperative SRS mental health scores (p = 0.022), with a trend toward greater satisfaction (p = 0.055) and pain (p = 0.072) scores after adjustment for baseline values. No other perioperative factors or specific SRS domains were associated with LOS (p > 0.05 for all).</p><p><strong>Conclusion: </strong>Greater number of levels (more than 11 segments) fused in surgery was associated with longer length of stay for AIS patients who underwent PSIF. With growing focus on minimizing inpatient LOS duration following PSIF for AIS patients, our findings of higher postoperative patient-reported SRS scores after longer inpatient stay may warrant prospective analysis and should be further considered in the perioperative care of AIS patients.</p><p><strong>Level of evidence: </strong>Level III.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145724931","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-11DOI: 10.1007/s43390-025-01252-3
Davide Palombi, Paolo Brigato, Alberto Benato, Sergio De Salvatore, Pier Francesco Costici, Timothee de Saint Denis, Eleftherios Archavlis, Luca Massimi, Leoanrdo Oggiano, Gianpiero Tamburrini
Purpose: Chiari I Malformation (CIM) is occasionally associated with scoliosis, especially in the presence of syringomyelia (SyM). While posterior fossa decompression (PFD) is often performed before spinal fusion, its impact on scoliosis progression remains unclear. Some studies report curve stabilization or improvement, while others show continued progression. This systematic review and meta-analysis aim to evaluate whether PFD influences CIM patients' scoliosis outcomes and identify predictive factors for curve behavior, improving multidisciplinary surgical management.
Methods: A systematic literature search was conducted in PubMed, Cochrane, Embase, Medline, Scopus, and Web of Science up to June 2025, following PRISMA guidelines. Inclusion criteria included pediatric patients (< 19 years) diagnosed with CIM who underwent PFD as the first treatment and had concurrent scoliosis (major curve angle > 10°). Data from 11 retrospective studies comprising 380 patients were analyzed. Pooled proportions of improvement, stability, and progression were calculated using random-effects models. Subgroup analyses were performed for duroplasty, and metaregression explored predictors, including age at surgery and baseline Cobb angle.
Results: The mean age at PFD was 10.3 years, with a mean preoperative curve of 37°. Syringomyelia was present in 92.6% of patients. After PFD, 55% (95% CI 46-63%) of curves improved or stabilized, while 45% (95% CI 37-54%) progressed. In the duroplasty subgroup (6 studies, 189 patients), success and progression rates were similar to the overall cohort (54% vs. 46%). Syrinx improvement was observed in 94% (95% CI 82-98%), with higher rates in duroplasty cases (97%). Metaregression demonstrated that older age at surgery (OR per year = 1.24, 95% CI 1.10-1.39; p < 0.001) and greater baseline Cobb angle (OR per + 5° = 0.79, 95% CI 0.65-0.96; p = 0.012) were independent predictors of scoliosis progression. Ultimately, 37.8% of patients required spinal fusion.
Conclusion: This meta-analysis suggests that PFD is associated with scoliosis improvement in nearly half of pediatric patients with CIM, but a significant proportion still experiences curve progression. Younger age at surgery and lower preoperative major curve angle are associated with better outcomes. Future prospective studies with standardized criteria and extended follow-up periods are needed to refine treatment strategies.
目的:Chiari I型畸形(CIM)偶尔与脊柱侧凸相关,特别是在脊髓空洞(SyM)的存在下。虽然后窝减压(PFD)通常在脊柱融合前进行,但其对脊柱侧凸进展的影响尚不清楚。一些研究报告曲线稳定或改善,而另一些则显示持续的进展。本系统综述和荟萃分析旨在评估PFD是否会影响CIM患者脊柱侧凸的预后,并确定弯曲行为的预测因素,从而改善多学科外科治疗。方法:根据PRISMA指南,在PubMed、Cochrane、Embase、Medline、Scopus和Web of Science中进行系统的文献检索,检索时间截止到2025年6月。纳入标准包括儿科患者(10°)。我们分析了11项包括380例患者的回顾性研究的数据。使用随机效应模型计算改善、稳定和进展的合并比例。对硬膜成形术进行亚组分析,并采用回归分析探讨预测因素,包括手术年龄和基线Cobb角。结果:PFD的平均年龄为10.3岁,平均术前曲线为37°。92.6%的患者存在脊髓空洞。PFD后,55% (95% CI 46-63%)的曲线改善或稳定,45% (95% CI 37-54%)的曲线进展。在硬膜成形术亚组(6项研究,189例患者),成功率和进展率与整体队列相似(54%对46%)。94% (95% CI 82-98%)的患者鼻窦改善,而硬膜成形术患者的鼻窦改善率更高(97%)。荟萃分析显示,手术年龄较大(OR每年= 1.24,95% CI 1.10-1.39; p)。结论:该荟萃分析表明,在近一半的CIM患儿中,PFD与脊柱侧凸改善相关,但仍有很大比例出现曲线进展。手术年龄越小,术前主曲线角度越小,预后越好。未来的前瞻性研究需要标准化的标准和延长的随访期,以完善治疗策略。
{"title":"Scoliosis associated with Chiari I malformation after posterior fossa decompression: a systematic review and meta-analysis of 380 pediatric patients.","authors":"Davide Palombi, Paolo Brigato, Alberto Benato, Sergio De Salvatore, Pier Francesco Costici, Timothee de Saint Denis, Eleftherios Archavlis, Luca Massimi, Leoanrdo Oggiano, Gianpiero Tamburrini","doi":"10.1007/s43390-025-01252-3","DOIUrl":"https://doi.org/10.1007/s43390-025-01252-3","url":null,"abstract":"<p><strong>Purpose: </strong>Chiari I Malformation (CIM) is occasionally associated with scoliosis, especially in the presence of syringomyelia (SyM). While posterior fossa decompression (PFD) is often performed before spinal fusion, its impact on scoliosis progression remains unclear. Some studies report curve stabilization or improvement, while others show continued progression. This systematic review and meta-analysis aim to evaluate whether PFD influences CIM patients' scoliosis outcomes and identify predictive factors for curve behavior, improving multidisciplinary surgical management.</p><p><strong>Methods: </strong>A systematic literature search was conducted in PubMed, Cochrane, Embase, Medline, Scopus, and Web of Science up to June 2025, following PRISMA guidelines. Inclusion criteria included pediatric patients (< 19 years) diagnosed with CIM who underwent PFD as the first treatment and had concurrent scoliosis (major curve angle > 10°). Data from 11 retrospective studies comprising 380 patients were analyzed. Pooled proportions of improvement, stability, and progression were calculated using random-effects models. Subgroup analyses were performed for duroplasty, and metaregression explored predictors, including age at surgery and baseline Cobb angle.</p><p><strong>Results: </strong>The mean age at PFD was 10.3 years, with a mean preoperative curve of 37°. Syringomyelia was present in 92.6% of patients. After PFD, 55% (95% CI 46-63%) of curves improved or stabilized, while 45% (95% CI 37-54%) progressed. In the duroplasty subgroup (6 studies, 189 patients), success and progression rates were similar to the overall cohort (54% vs. 46%). Syrinx improvement was observed in 94% (95% CI 82-98%), with higher rates in duroplasty cases (97%). Metaregression demonstrated that older age at surgery (OR per year = 1.24, 95% CI 1.10-1.39; p < 0.001) and greater baseline Cobb angle (OR per + 5° = 0.79, 95% CI 0.65-0.96; p = 0.012) were independent predictors of scoliosis progression. Ultimately, 37.8% of patients required spinal fusion.</p><p><strong>Conclusion: </strong>This meta-analysis suggests that PFD is associated with scoliosis improvement in nearly half of pediatric patients with CIM, but a significant proportion still experiences curve progression. Younger age at surgery and lower preoperative major curve angle are associated with better outcomes. Future prospective studies with standardized criteria and extended follow-up periods are needed to refine treatment strategies.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145743854","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-09DOI: 10.1007/s43390-025-01239-0
Malvika Choudhari, Mark Belio, Di Hu, Stuart L Mitchell, Joseph D Stone, Erik D Hanson, Feng-Chang Lin, Stephanie D Davis, James O Sanders
<p><strong>Purpose: </strong>The primary concerning outcome in early onset scoliosis (EOS), pulmonary function, is challenging to measure in children. Surrogate measures, including thoracic length and curve magnitude, poorly predict patient outcomes. Activity capacity as determined by Metabolic Equivalents of Task (MET) is a potentially useful alternative or adjunct since it more directly reflects the tasks being performed. The objective of this pilot study was to assess MET values for varying intensity activities in children with EOS and explore their relationship to pulmonary function indices, scoliosis characteristics, and patient-reported outcome measures.</p><p><strong>Methods: </strong>For this pilot study, basal metabolic rate and physical activity MET values were measured using indirect calorimetry. MET values were assessed while performing video games representing low (bowling), moderate (boxing), and high intensity (active running) activities, and treadmill walking at low, moderate, and high intensity. MET values were compared to age-matched standardized energy expenditure values in youth (METy) for similar tasks. Pulmonary function testing was assessed using spirometry with percent predicted values based on arm span. Patient outcomes were obtained for each participant through the 24-question Early-Onset Scoliosis Questionnaire (EOSQ-24) and select assessments from the Patient-Reported Outcomes Measurement Information System (PROMIS). A linear mixed model assessed differences between groups. Spearman correlation coefficients assessed relationships between variables.</p><p><strong>Results: </strong>Eight children (ages 6-16y, 50% female) completed testing. Etiologies for scoliosis were congenital (n = 3), syndromic (n = 3), and idiopathic (n = 2). Five had spirometry suggestive of severe restriction (FVC and FEV<sub>1</sub> < 50% predicted). Children with EOS had a 0.6 lower mean MET video game value compared to published METy values (p < 0.001). Increased intensity corresponded with increased MET values comparing hard to moderate and low intensities (P < 0.001). Average percent predicted MET values across all tasks revealed a negative correlation with FEV<sub>1</sub>/FVC (R = - 0.927, p = 0.024). All eight children completed the low-intensity treadmill and low and moderate-intensity videogames; seven completed the moderate-intensity treadmill and high intensity videogame. Only five completed the high-intensity treadmill.</p><p><strong>Conclusion: </strong>MET values in children with EOS were directionally similar to values in normal children. Children unable to generate higher MET values appear to self-limit their activity. The relationship between MET and pulmonary function is complex and requires further exploration. Children with EOS and pulmonary impairment appear unable to generate the energy required for more vigorous activities. This could be due to poor pulmonary function, deconditioning from their underlying condition, or limit
{"title":"Activity capacity in children with early onset scoliosis compared to pulmonary function (spirometry) and patient-reported outcomes.","authors":"Malvika Choudhari, Mark Belio, Di Hu, Stuart L Mitchell, Joseph D Stone, Erik D Hanson, Feng-Chang Lin, Stephanie D Davis, James O Sanders","doi":"10.1007/s43390-025-01239-0","DOIUrl":"https://doi.org/10.1007/s43390-025-01239-0","url":null,"abstract":"<p><strong>Purpose: </strong>The primary concerning outcome in early onset scoliosis (EOS), pulmonary function, is challenging to measure in children. Surrogate measures, including thoracic length and curve magnitude, poorly predict patient outcomes. Activity capacity as determined by Metabolic Equivalents of Task (MET) is a potentially useful alternative or adjunct since it more directly reflects the tasks being performed. The objective of this pilot study was to assess MET values for varying intensity activities in children with EOS and explore their relationship to pulmonary function indices, scoliosis characteristics, and patient-reported outcome measures.</p><p><strong>Methods: </strong>For this pilot study, basal metabolic rate and physical activity MET values were measured using indirect calorimetry. MET values were assessed while performing video games representing low (bowling), moderate (boxing), and high intensity (active running) activities, and treadmill walking at low, moderate, and high intensity. MET values were compared to age-matched standardized energy expenditure values in youth (METy) for similar tasks. Pulmonary function testing was assessed using spirometry with percent predicted values based on arm span. Patient outcomes were obtained for each participant through the 24-question Early-Onset Scoliosis Questionnaire (EOSQ-24) and select assessments from the Patient-Reported Outcomes Measurement Information System (PROMIS). A linear mixed model assessed differences between groups. Spearman correlation coefficients assessed relationships between variables.</p><p><strong>Results: </strong>Eight children (ages 6-16y, 50% female) completed testing. Etiologies for scoliosis were congenital (n = 3), syndromic (n = 3), and idiopathic (n = 2). Five had spirometry suggestive of severe restriction (FVC and FEV<sub>1</sub> < 50% predicted). Children with EOS had a 0.6 lower mean MET video game value compared to published METy values (p < 0.001). Increased intensity corresponded with increased MET values comparing hard to moderate and low intensities (P < 0.001). Average percent predicted MET values across all tasks revealed a negative correlation with FEV<sub>1</sub>/FVC (R = - 0.927, p = 0.024). All eight children completed the low-intensity treadmill and low and moderate-intensity videogames; seven completed the moderate-intensity treadmill and high intensity videogame. Only five completed the high-intensity treadmill.</p><p><strong>Conclusion: </strong>MET values in children with EOS were directionally similar to values in normal children. Children unable to generate higher MET values appear to self-limit their activity. The relationship between MET and pulmonary function is complex and requires further exploration. Children with EOS and pulmonary impairment appear unable to generate the energy required for more vigorous activities. This could be due to poor pulmonary function, deconditioning from their underlying condition, or limit","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145709314","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-08DOI: 10.1007/s43390-025-01228-3
Ahmed Baseem Ismail, Dima Hisham Fikry, Khaled A Elmenawi, Mohamed Moustafa, Ahmed Said Abdelwahed, Mohanad Abdelfattah, Sarah Ahmed Metwally, Mennatullah Shaker Arafat, Laial Al-Twisi, Aya Shebl Elnaggar, Khaled Ashraf Mohamed
Purpose: This systematic review and meta-analysis aim to investigate the prevalence of cardiac abnormalities in patients with idiopathic scoliosis.
Methods: A systematic search on PubMed, Embase, Scopus, and Web of Science was conducted, covering studies published from their inception up to February 2024. Peer-reviewed studies that used echocardiograms to screen for cardiac abnormalities were included. Nine thousand five hundred fifty-four cases met the inclusion criteria and were included in the final data synthesis. A meta-analysis was performed to calculate the pooled prevalence of cardiac abnormalities and a 95% confidence interval (CI). Results were divided into subgroups to reveal the prevalence of each cardiac abnormality for further consideration.
Results: 7.5% had cardiac abnormalities. Valvular diseases are the most common cardiac abnormalities. Tricuspid regurgitation (TR) is the most prevalent, accounting for 24.4% of cases. This is followed by mitral regurgitation (MR) at 17%, mitral valve prolapse (MVP) at 8%, aortic regurgitation (AR) at 3.8%, and pulmonary insufficiency at 1.9%. In addition, other valvular diseases collectively make up 22% of the findings. Congenital heart diseases (CHD) were also included in the results, with atrial septal defect (ASD) being the most prominent at 1.5%, followed by ventricular septal defect (VSD) at 1.4%, and other CHD comprising 2.5%. Pulmonary hypertension accounts for a substantial portion of the results, representing 16.8%. A dilated aortic root and pericardial effusion were observed in 2.4% and 0.9% of cases, respectively.
Conclusion: Cardiovascular abnormalities are prevalent in patients with idiopathic scoliosis. This highlights the need for thorough cardiovascular screening of these patients before surgical intervention.
目的:本系统综述和荟萃分析旨在调查特发性脊柱侧凸患者心脏异常的患病率。方法:系统检索PubMed、Embase、Scopus和Web of Science,涵盖从成立到2024年2月发表的研究。使用超声心动图筛查心脏异常的同行评议研究也包括在内。95,554例病例符合纳入标准,并纳入最终数据综合。进行荟萃分析以计算心脏异常的总患病率和95%置信区间(CI)。结果被分成亚组,以揭示每种心脏异常的患病率,以供进一步考虑。结果:7.5%有心脏异常。瓣膜病是最常见的心脏异常。三尖瓣反流(TR)最为常见,占24.4%。其次是二尖瓣反流(MR) 17%,二尖瓣脱垂(MVP) 8%,主动脉反流(AR) 3.8%,肺功能不全(1.9%)。此外,其他瓣膜疾病总共占所有发现的22%。先天性心脏病(CHD)也包括在结果中,房间隔缺损(ASD)最突出,占1.5%,其次是室间隔缺损(VSD),占1.4%,其他冠心病占2.5%。肺动脉高压占结果的很大一部分,占16.8%。主动脉根扩张和心包积液分别占2.4%和0.9%。结论:心血管异常在特发性脊柱侧凸患者中普遍存在。这强调了在手术干预前对这些患者进行彻底的心血管筛查的必要性。
{"title":"Prevalence of cardiac abnormalities in patients with idiopathic scoliosis: a systematic review and meta-analysis.","authors":"Ahmed Baseem Ismail, Dima Hisham Fikry, Khaled A Elmenawi, Mohamed Moustafa, Ahmed Said Abdelwahed, Mohanad Abdelfattah, Sarah Ahmed Metwally, Mennatullah Shaker Arafat, Laial Al-Twisi, Aya Shebl Elnaggar, Khaled Ashraf Mohamed","doi":"10.1007/s43390-025-01228-3","DOIUrl":"https://doi.org/10.1007/s43390-025-01228-3","url":null,"abstract":"<p><strong>Purpose: </strong>This systematic review and meta-analysis aim to investigate the prevalence of cardiac abnormalities in patients with idiopathic scoliosis.</p><p><strong>Methods: </strong>A systematic search on PubMed, Embase, Scopus, and Web of Science was conducted, covering studies published from their inception up to February 2024. Peer-reviewed studies that used echocardiograms to screen for cardiac abnormalities were included. Nine thousand five hundred fifty-four cases met the inclusion criteria and were included in the final data synthesis. A meta-analysis was performed to calculate the pooled prevalence of cardiac abnormalities and a 95% confidence interval (CI). Results were divided into subgroups to reveal the prevalence of each cardiac abnormality for further consideration.</p><p><strong>Results: </strong>7.5% had cardiac abnormalities. Valvular diseases are the most common cardiac abnormalities. Tricuspid regurgitation (TR) is the most prevalent, accounting for 24.4% of cases. This is followed by mitral regurgitation (MR) at 17%, mitral valve prolapse (MVP) at 8%, aortic regurgitation (AR) at 3.8%, and pulmonary insufficiency at 1.9%. In addition, other valvular diseases collectively make up 22% of the findings. Congenital heart diseases (CHD) were also included in the results, with atrial septal defect (ASD) being the most prominent at 1.5%, followed by ventricular septal defect (VSD) at 1.4%, and other CHD comprising 2.5%. Pulmonary hypertension accounts for a substantial portion of the results, representing 16.8%. A dilated aortic root and pericardial effusion were observed in 2.4% and 0.9% of cases, respectively.</p><p><strong>Conclusion: </strong>Cardiovascular abnormalities are prevalent in patients with idiopathic scoliosis. This highlights the need for thorough cardiovascular screening of these patients before surgical intervention.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145709283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-04DOI: 10.1007/s43390-025-01243-4
Alyssa Barré, Andrew Kirk, Ryan Muchow, Aamir Kadri, Vishwas Talwalkar, Christopher Montgomery, Vincent W Prusick
Background: Severe adolescent idiopathic scoliosis (AIS) may be associated with cardiopulmonary issues, including previously undiagnosed congenital cardiac anomalies, valvular disease, and pulmonary hypertension. Many centers routinely refer patients with coronal Cobb angles ≥ 70° for pre-operative cardiology evaluation prior to posterior spinal fusion (PSF). The clinical utility of this practice remains uncertain.
Methods: A retrospective review was conducted of AIS patients undergoing PSF at a single pediatric orthopedic center from 2017 to 2024. All patients received pre-operative anesthesia evaluations including history, auscultation, and electrocardiogram (EKG). Cardiology referral was made for patients with Cobb angles ≥ 70° or for those with cardiac symptoms, murmurs, or EKG abnormalities. Data collected included cardiology referral status, echocardiogram (TTE) findings, need for intervention or follow-up, surgical delays, and perioperative cardiac complications. Comparative analysis was performed between patients with Cobb angles ≥ 70° and < 70°.
Results: Of 151 patients (mean age 14.5 years [range 11-20] 75% female), 51 had Cobb angles ≥ 70°. These patients were more likely to report cardiac symptoms (20% vs. 3%, p = 0.0012) and have murmurs (10% vs. 1%, p = 0.017). 35 patients with Cobb ≥ 70° patients were referred to cardiology, and 17 underwent TTE. Nine had abnormal but largely benign findings; only three required follow-ups. No patient in either group experienced surgical delays or perioperative cardiac complications.
Conclusions: Although AIS patients with Cobb angles ≥ 70° demonstrate higher rates of symptoms and murmurs, routine cardiology referral based on Cobb angle alone rarely uncovers clinically significant findings or impacts surgical timing. A targeted referral strategy incorporating symptoms, exam findings, and EKG abnormalities may optimize patient safety while reducing unnecessary testing and cost.
{"title":"Low utility of pre-operative cardiology referrals in adolescent idiopathic scoliosis using a cutoff of Cobb > 70 degrees.","authors":"Alyssa Barré, Andrew Kirk, Ryan Muchow, Aamir Kadri, Vishwas Talwalkar, Christopher Montgomery, Vincent W Prusick","doi":"10.1007/s43390-025-01243-4","DOIUrl":"https://doi.org/10.1007/s43390-025-01243-4","url":null,"abstract":"<p><strong>Background: </strong>Severe adolescent idiopathic scoliosis (AIS) may be associated with cardiopulmonary issues, including previously undiagnosed congenital cardiac anomalies, valvular disease, and pulmonary hypertension. Many centers routinely refer patients with coronal Cobb angles ≥ 70° for pre-operative cardiology evaluation prior to posterior spinal fusion (PSF). The clinical utility of this practice remains uncertain.</p><p><strong>Methods: </strong>A retrospective review was conducted of AIS patients undergoing PSF at a single pediatric orthopedic center from 2017 to 2024. All patients received pre-operative anesthesia evaluations including history, auscultation, and electrocardiogram (EKG). Cardiology referral was made for patients with Cobb angles ≥ 70° or for those with cardiac symptoms, murmurs, or EKG abnormalities. Data collected included cardiology referral status, echocardiogram (TTE) findings, need for intervention or follow-up, surgical delays, and perioperative cardiac complications. Comparative analysis was performed between patients with Cobb angles ≥ 70° and < 70°.</p><p><strong>Results: </strong>Of 151 patients (mean age 14.5 years [range 11-20] 75% female), 51 had Cobb angles ≥ 70°. These patients were more likely to report cardiac symptoms (20% vs. 3%, p = 0.0012) and have murmurs (10% vs. 1%, p = 0.017). 35 patients with Cobb ≥ 70° patients were referred to cardiology, and 17 underwent TTE. Nine had abnormal but largely benign findings; only three required follow-ups. No patient in either group experienced surgical delays or perioperative cardiac complications.</p><p><strong>Conclusions: </strong>Although AIS patients with Cobb angles ≥ 70° demonstrate higher rates of symptoms and murmurs, routine cardiology referral based on Cobb angle alone rarely uncovers clinically significant findings or impacts surgical timing. A targeted referral strategy incorporating symptoms, exam findings, and EKG abnormalities may optimize patient safety while reducing unnecessary testing and cost.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145678786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}