Pub Date : 2026-02-14DOI: 10.1007/s43390-026-01283-4
Jacob Jordan, Vincent Ruggieri, Ben Sinder, John Flynn, Patrick Cahill, Jason Anari
Introduction: Growing construct expansion surgeries in the setting of early-onset scoliosis (EOS) involve surgeon's feel to determine the optimal amount of distraction force to maximize correction and spinal length gained without compromising anchor integrity. Growing construct designs may require different amounts of distraction force to lengthen the spine or chest wall depending on the device used and various patient factors. Understanding these variations could guide appropriate force levels for the rational design for next-generation remote/external distraction devices and ultimately patient/deformity-specific lengthening forces.
Aim/objectives: The purpose of this study was to determine distraction force levels for expansion events in traditional growing rods (TGRs) and vertical expandable prosthetic titanium rib (VEPTR) constructs across patients with various anchor attachment points and etiologies of EOS.
Methods: With IRB approval, two different distraction devices (VEPTR distractor and TGR/rod distractor) were outfitted with electronic strain gauges to measure distraction force. Force data were recorded at a rate of 40 Hz during each surgery via a laptop connected to a PowerLab 8/35 data acquisition system. After each surgery, the distractor was validated on a custom calibration device. The data collected were then analyzed to determine the maximum force and average force during every distraction.
Results: From February 2019 to June 2023, a total of 146 in vivo distractions were collected on 52 patients with VEPTRs and 28 in vivo distractions were collected on 9 patients with traditional growing rods. TGR procedures required significantly higher forces than VEPTR (437.89 N vs 349.10 N, p < 0.001).
Conclusion: Modification of two different distraction devices with electronic strain gauges identified differences in distraction force between traditional growing rods and VEPTR constructs during expansion surgeries in children with EOS. Our findings highlight that implant type and potentially other factors may play significant roles in the amount of force required for lengthening the spine and chest wall. Current market implant technology (MCGR maximum force of 187 N) is likely underpowered compared to traditional technology across all construct types and disease classifications. These insights should inform the development of next-generation remote lengthening construct design.
简介:在早发性脊柱侧凸(EOS)的情况下,生长结构扩张手术涉及到外科医生的感觉,以确定最佳的牵引力量,以最大限度地矫正和脊柱长度,而不损害锚的完整性。根据所使用的器械和不同的患者因素,不断增长的结构设计可能需要不同数量的撑开力来延长脊柱或胸壁。了解这些变化可以指导合理设计下一代远程/外部牵引装置的适当力水平,并最终为患者/变形特定的延长力提供指导。目的/目的:本研究的目的是确定具有不同锚点和病因的EOS患者在传统生长棒(tgr)和垂直可膨胀假体钛肋骨(VEPTR)结构中扩展事件的牵开力水平。方法:采用经IRB批准的两种不同的牵张器(VEPTR牵张器和TGR/棒牵张器),安装电子应变计测量牵张力。在每次手术中,通过连接到PowerLab 8/35数据采集系统的笔记本电脑以40 Hz的速率记录力数据。每次手术后,牵开器在定制的校准设备上进行验证。然后对收集到的数据进行分析,以确定每次分心时的最大力和平均力。结果:2019年2月至2023年6月,对52例VEPTRs患者共收集到146个体内干扰,对9例传统生长棒患者共收集到28个体内干扰。TGR手术所需的力明显高于VEPTR (437.89 N vs 349.10 N, p < 0.001)。结论:采用电子应变片改良两种不同的牵张装置,可识别传统生长棒和VEPTR装置在小儿EOS扩张手术中的牵张力差异。我们的研究结果强调,植入物类型和潜在的其他因素可能在延长脊柱和胸壁所需的力量方面发挥重要作用。与传统技术相比,目前市场上的植入技术(MCGR最大作用力为187牛)在所有结构类型和疾病分类中都可能存在动力不足。这些见解应该为下一代远程延长结构设计的发展提供信息。
{"title":"Growing construct forces in early-onset scoliosis: How do TGR and VEPTR compare?","authors":"Jacob Jordan, Vincent Ruggieri, Ben Sinder, John Flynn, Patrick Cahill, Jason Anari","doi":"10.1007/s43390-026-01283-4","DOIUrl":"https://doi.org/10.1007/s43390-026-01283-4","url":null,"abstract":"<p><strong>Introduction: </strong>Growing construct expansion surgeries in the setting of early-onset scoliosis (EOS) involve surgeon's feel to determine the optimal amount of distraction force to maximize correction and spinal length gained without compromising anchor integrity. Growing construct designs may require different amounts of distraction force to lengthen the spine or chest wall depending on the device used and various patient factors. Understanding these variations could guide appropriate force levels for the rational design for next-generation remote/external distraction devices and ultimately patient/deformity-specific lengthening forces.</p><p><strong>Aim/objectives: </strong>The purpose of this study was to determine distraction force levels for expansion events in traditional growing rods (TGRs) and vertical expandable prosthetic titanium rib (VEPTR) constructs across patients with various anchor attachment points and etiologies of EOS.</p><p><strong>Methods: </strong>With IRB approval, two different distraction devices (VEPTR distractor and TGR/rod distractor) were outfitted with electronic strain gauges to measure distraction force. Force data were recorded at a rate of 40 Hz during each surgery via a laptop connected to a PowerLab 8/35 data acquisition system. After each surgery, the distractor was validated on a custom calibration device. The data collected were then analyzed to determine the maximum force and average force during every distraction.</p><p><strong>Results: </strong>From February 2019 to June 2023, a total of 146 in vivo distractions were collected on 52 patients with VEPTRs and 28 in vivo distractions were collected on 9 patients with traditional growing rods. TGR procedures required significantly higher forces than VEPTR (437.89 N vs 349.10 N, p < 0.001).</p><p><strong>Conclusion: </strong>Modification of two different distraction devices with electronic strain gauges identified differences in distraction force between traditional growing rods and VEPTR constructs during expansion surgeries in children with EOS. Our findings highlight that implant type and potentially other factors may play significant roles in the amount of force required for lengthening the spine and chest wall. Current market implant technology (MCGR maximum force of 187 N) is likely underpowered compared to traditional technology across all construct types and disease classifications. These insights should inform the development of next-generation remote lengthening construct design.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146195563","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 : 2026-02-14DOI: 10.1007/s43390-026-01307-z
Harsh Jain, Advith Sarikonda, Ranbir Ahluwalia, Omar Zakieh, Austin Montgomery, Walter Navid, Philip Raj, Clayton R Baker, Hani Chanbour, Iyan Younus, Tyler Zeoli, Soren Jonzzon, Autumn Zuckerman, S Bobo Tanner, Julian G Lugo-Pico, Amir M Abtahi, Byron F Stephens, Scott L Zuckerman
Purpose: Though the use of anabolic bone agents has proven effective in adult spinal deformity (ASD) surgery, prescription and approval of these medications remains a challenge. In osteopenic/osteoporotic patients undergoing ASD surgery, we sought to determine the impact of a bone optimization clinic on: (1) prescription patterns of anabolic agents, (2) mechanical complications, and (3) reoperation.
Methods: A retrospective cohort study (2009-23) was performed for osteopenic/osteoporotic patients undergoing ASD surgery with ≥ 2-year follow-up. The study period was binarized into before/after a bone optimization clinic was established (2009-19 vs. 2020-23). The primary outcomes were: (1) use of anabolic agents prior to surgery (Teriparatide, Abaloparatide, and Romosozumab-aqqg), (2) mechanical complications, and (3) reoperation. Multivariable regression controlling for age, sex, body mass index, and operative time was performed.
Results: Of 126 patients (mean age 68 ± 10yrs; 86% female) undergoing ASD surgery with osteopenia (80%) or osteoporosis (20%), 91 (72%) were before the bone optimization clinic and 35 (28%) were after. Similar rates of osteoporosis in both groups were seen (pre-21% vs. post-17%, p = 0.638). After the bone optimization clinic, more patients received preoperative anabolic therapy (54% vs. 23%, p < 0.001) and for a longer duration (98 ± 156 vs. 40 ± 109 days, p = 0.027). Overall mechanical complications decreased significantly (49% vs 81%, p < 0.001) as did reoperation for mechanical complications (6% vs. 44%, p < 0.001). Multivariable regression showed that a bone optimization clinic independently improved the use of preoperative anabolic agents (OR = 5.3, 95%CI:2.1-13.4, p < 0.001) and reduced the risk of mechanical complications (OR = 0.2 95%CI:0.1-0.5, p < 0.001) and reoperation for mechanical complications (OR = 0.1, 95%CI:0.1-0.4, p < 0.001).
Conclusion: In osteopenic/osteoporotic patients undergoing ASD surgery, a bone optimization clinic was independently associated with increased prescription rates and duration of anabolic bone agents, reduced mechanical complications, and reduced reoperation for mechanical complications.
目的:尽管在成人脊柱畸形(ASD)手术中使用合成代谢骨剂已被证明是有效的,但这些药物的处方和批准仍然是一个挑战。在接受ASD手术的骨质减少/骨质疏松患者中,我们试图确定骨优化诊所对以下方面的影响:(1)合成代谢药物的处方模式,(2)机械并发症,(3)再手术。方法:对接受ASD手术的骨质减少/骨质疏松患者进行回顾性队列研究(2009-23),随访≥2年。研究期间被二值化为骨优化诊所建立前后(2009-19 vs. 2020-23)。主要结局是:(1)术前使用合成代谢药物(Teriparatide, Abaloparatide和Romosozumab-aqqg),(2)机械并发症,(3)再次手术。采用多变量回归控制年龄、性别、体重指数和手术时间。结果:126例伴有骨质减少(80%)或骨质疏松(20%)的ASD手术患者(平均年龄68±10岁,女性86%),骨优化门诊前91例(72%),术后35例(28%)。两组骨质疏松率相似(治疗前21% vs.治疗后17%,p = 0.638)。结论:在接受ASD手术的骨质减少/骨质疏松患者中,骨优化门诊与合成代谢骨剂处方率和持续时间的增加、机械并发症的减少以及机械并发症的再手术减少独立相关。
{"title":"A bone optimization rheumatology clinic increases anabolic bone agent use and reduces mechanical complications in adult spinal deformity surgery.","authors":"Harsh Jain, Advith Sarikonda, Ranbir Ahluwalia, Omar Zakieh, Austin Montgomery, Walter Navid, Philip Raj, Clayton R Baker, Hani Chanbour, Iyan Younus, Tyler Zeoli, Soren Jonzzon, Autumn Zuckerman, S Bobo Tanner, Julian G Lugo-Pico, Amir M Abtahi, Byron F Stephens, Scott L Zuckerman","doi":"10.1007/s43390-026-01307-z","DOIUrl":"https://doi.org/10.1007/s43390-026-01307-z","url":null,"abstract":"<p><strong>Purpose: </strong>Though the use of anabolic bone agents has proven effective in adult spinal deformity (ASD) surgery, prescription and approval of these medications remains a challenge. In osteopenic/osteoporotic patients undergoing ASD surgery, we sought to determine the impact of a bone optimization clinic on: (1) prescription patterns of anabolic agents, (2) mechanical complications, and (3) reoperation.</p><p><strong>Methods: </strong>A retrospective cohort study (2009-23) was performed for osteopenic/osteoporotic patients undergoing ASD surgery with ≥ 2-year follow-up. The study period was binarized into before/after a bone optimization clinic was established (2009-19 vs. 2020-23). The primary outcomes were: (1) use of anabolic agents prior to surgery (Teriparatide, Abaloparatide, and Romosozumab-aqqg), (2) mechanical complications, and (3) reoperation. Multivariable regression controlling for age, sex, body mass index, and operative time was performed.</p><p><strong>Results: </strong>Of 126 patients (mean age 68 ± 10yrs; 86% female) undergoing ASD surgery with osteopenia (80%) or osteoporosis (20%), 91 (72%) were before the bone optimization clinic and 35 (28%) were after. Similar rates of osteoporosis in both groups were seen (pre-21% vs. post-17%, p = 0.638). After the bone optimization clinic, more patients received preoperative anabolic therapy (54% vs. 23%, p < 0.001) and for a longer duration (98 ± 156 vs. 40 ± 109 days, p = 0.027). Overall mechanical complications decreased significantly (49% vs 81%, p < 0.001) as did reoperation for mechanical complications (6% vs. 44%, p < 0.001). Multivariable regression showed that a bone optimization clinic independently improved the use of preoperative anabolic agents (OR = 5.3, 95%CI:2.1-13.4, p < 0.001) and reduced the risk of mechanical complications (OR = 0.2 95%CI:0.1-0.5, p < 0.001) and reoperation for mechanical complications (OR = 0.1, 95%CI:0.1-0.4, p < 0.001).</p><p><strong>Conclusion: </strong>In osteopenic/osteoporotic patients undergoing ASD surgery, a bone optimization clinic was independently associated with increased prescription rates and duration of anabolic bone agents, reduced mechanical complications, and reduced reoperation for mechanical complications.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146195537","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 : 2026-02-14DOI: 10.1007/s43390-026-01301-5
F D Højsager, L Borch, R Castelein, S B Christensen, A Simony
Background: Adolescent Idiopathic Scoliosis (AIS) affects over 1% of adolescents and is often diagnosed during a sensitive developmental period, with repeated radiographs, potentially increasing cancer risk. Previous studies have suggested an association between scoliosis and breast cancer, but have been limited by small cohorts, lack of matched controls, and incomplete registry data. The aim of this study, therefore, was to assess the hazard ratio (HR) of cancer among women with scoliosis compared to age-matched controls using nationwide registry data.
Methods: This observational cohort study included all Danish women born 1967-1977 with a scoliosis diagnosis (ICD-8 735.0/735.2 or ICD-10 DM411), and four age-matched controls per case, identified through national health registers. Cancer outcomes were obtained from the Danish National Cancer Register, and Cox regression was used to estimate HRs, with time at risk beginning at age 12.
Results: Among 6,217 women (1,238 (20% with scoliosis), the mean follow-up time was approximately 38 years. The HR (95% CI) for any cancer was 1.06 [0.85-1.31]. For breast cancer, HR was 1.25 [0.86-1.80], while HR for carcinoma in situ (CIS) of the breast was 13.62 [3.75-49.50]. Among 12 cases of ovarian cancer, the HR was 2.91 [0.92-9.18]. This study could not, however, discriminate between idiopathic and non-idiopathic scoliosis.
Conclusion: Women with scoliosis showed a significantly increased HR for CIS of the breast, and a non-significant trend toward increased risk of invasive breast and gynecologic cancers. Findings support further investigation into genetic or developmental links between scoliosis and cancer risk.
Key points: Women with scoliosis are at a higher risk of getting cancer, namely of the breast. Pregnancy did not appear to have a protective effect.
{"title":"Cancer risk among women with scoliosis: a nationwide danish register-based study.","authors":"F D Højsager, L Borch, R Castelein, S B Christensen, A Simony","doi":"10.1007/s43390-026-01301-5","DOIUrl":"https://doi.org/10.1007/s43390-026-01301-5","url":null,"abstract":"<p><strong>Background: </strong>Adolescent Idiopathic Scoliosis (AIS) affects over 1% of adolescents and is often diagnosed during a sensitive developmental period, with repeated radiographs, potentially increasing cancer risk. Previous studies have suggested an association between scoliosis and breast cancer, but have been limited by small cohorts, lack of matched controls, and incomplete registry data. The aim of this study, therefore, was to assess the hazard ratio (HR) of cancer among women with scoliosis compared to age-matched controls using nationwide registry data.</p><p><strong>Methods: </strong>This observational cohort study included all Danish women born 1967-1977 with a scoliosis diagnosis (ICD-8 735.0/735.2 or ICD-10 DM411), and four age-matched controls per case, identified through national health registers. Cancer outcomes were obtained from the Danish National Cancer Register, and Cox regression was used to estimate HRs, with time at risk beginning at age 12.</p><p><strong>Results: </strong>Among 6,217 women (1,238 (20% with scoliosis), the mean follow-up time was approximately 38 years. The HR (95% CI) for any cancer was 1.06 [0.85-1.31]. For breast cancer, HR was 1.25 [0.86-1.80], while HR for carcinoma in situ (CIS) of the breast was 13.62 [3.75-49.50]. Among 12 cases of ovarian cancer, the HR was 2.91 [0.92-9.18]. This study could not, however, discriminate between idiopathic and non-idiopathic scoliosis.</p><p><strong>Conclusion: </strong>Women with scoliosis showed a significantly increased HR for CIS of the breast, and a non-significant trend toward increased risk of invasive breast and gynecologic cancers. Findings support further investigation into genetic or developmental links between scoliosis and cancer risk.</p><p><strong>Key points: </strong>Women with scoliosis are at a higher risk of getting cancer, namely of the breast. Pregnancy did not appear to have a protective effect.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146195530","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 : 2026-02-13DOI: 10.1007/s43390-025-01172-2
Christopher Cheng, Connie Poe-Kochert, George H Thompson, Jochen Son-Hing, Christina K Hardesty
Purpose: Posterior spinal fusion (PSF) for scoliosis correction can be associated with substantial blood loss. Accurately characterizing risk factors and identifying strategies for minimizing blood loss are important for operative planning. Previous literature utilizes estimated blood loss (EBL), which may underestimate bleeding, and are limited in their usage of new anti-fibrinolytic medications and electrocautery technology. We sought to investigate blood loss difference in adolescent idiopathic scoliosis (AIS) and neuromuscular scoliosis (NMS) utilizing both EBL and calculated blood loss (CBL) based on height, weight, and hemoglobin values.
Methods: Retrospective review was conducted of children who underwent PSF for scoliosis correction from 2013 to 2021. EBL was determined from estimated intraoperative blood loss and measured postoperative drain output. CBL was computed as described by Foss et al. All values were further normalized based on vertebral levels fused and patient weight.
Results: Final cohort included 224 children with AIS and 76 with NMS. EBL significantly underestimated blood loss compared to CBL (882.2 ± 447.1 cc vs. 1315.0 ± 375.1 cc, P < 0.001 in AIS; 1132.9 ± 562.1 cc vs. 1455.2 ± 482.7 cc, P < 0.001 in NMS). CBL in patients with NMS was significantly higher than those with AIS (1455.2 ± 482.7 cc vs. 1215.0 ± 375.1 cc, P < 0.001). Per-level CBL, however, was lower in the NMS cohort, particularly in patients requiring fusion to pelvis.
Conclusion: EBL significantly underestimates blood loss compared to CBL. Patients with NMS have significantly greater blood loss than AIS. These differences appear to be driven by the extent of fusion. Updated guidelines would be valuable for more accurate determination of when to cross-match blood products prior to PSF for pediatric scoliosis.
Level of evidence: IV-Case series, diagnostic.
目的:脊柱侧凸矫正的后路脊柱融合术(PSF)可能与大量失血有关。准确地描述危险因素和确定减少失血的策略对手术计划很重要。以前的文献采用估计失血量(EBL),可能低估出血,并且在使用新的抗纤溶药物和电灼技术方面受到限制。我们试图利用EBL和基于身高、体重和血红蛋白值的计算失血量(CBL)来研究青少年特发性脊柱侧凸(AIS)和神经肌肉性脊柱侧凸(NMS)的失血量差异。方法:回顾性分析2013年至2021年接受PSF矫正脊柱侧凸的儿童。EBL通过估计术中出血量和测量术后引流量来确定。CBL的计算方法由Foss等人描述。根据融合的椎体水平和患者体重进一步标准化所有值。结果:最终队列包括224名AIS患儿和76名NMS患儿。与CBL相比,EBL显着低估了出血量(882.2±447.1 cc vs 1315.0±375.1 cc), P结论:EBL与CBL相比显着低估了出血量。NMS患者的出血量明显大于AIS患者。这些差异似乎是由核聚变的程度决定的。更新后的指南将有助于更准确地确定在小儿脊柱侧凸PSF治疗前何时交叉配血。证据级别:iv -病例系列,诊断性。
{"title":"Coming up short: estimated vs calculated blood loss in adolescent idiopathic and neuromuscular scoliosis surgery.","authors":"Christopher Cheng, Connie Poe-Kochert, George H Thompson, Jochen Son-Hing, Christina K Hardesty","doi":"10.1007/s43390-025-01172-2","DOIUrl":"https://doi.org/10.1007/s43390-025-01172-2","url":null,"abstract":"<p><strong>Purpose: </strong>Posterior spinal fusion (PSF) for scoliosis correction can be associated with substantial blood loss. Accurately characterizing risk factors and identifying strategies for minimizing blood loss are important for operative planning. Previous literature utilizes estimated blood loss (EBL), which may underestimate bleeding, and are limited in their usage of new anti-fibrinolytic medications and electrocautery technology. We sought to investigate blood loss difference in adolescent idiopathic scoliosis (AIS) and neuromuscular scoliosis (NMS) utilizing both EBL and calculated blood loss (CBL) based on height, weight, and hemoglobin values.</p><p><strong>Methods: </strong>Retrospective review was conducted of children who underwent PSF for scoliosis correction from 2013 to 2021. EBL was determined from estimated intraoperative blood loss and measured postoperative drain output. CBL was computed as described by Foss et al. All values were further normalized based on vertebral levels fused and patient weight.</p><p><strong>Results: </strong>Final cohort included 224 children with AIS and 76 with NMS. EBL significantly underestimated blood loss compared to CBL (882.2 ± 447.1 cc vs. 1315.0 ± 375.1 cc, P < 0.001 in AIS; 1132.9 ± 562.1 cc vs. 1455.2 ± 482.7 cc, P < 0.001 in NMS). CBL in patients with NMS was significantly higher than those with AIS (1455.2 ± 482.7 cc vs. 1215.0 ± 375.1 cc, P < 0.001). Per-level CBL, however, was lower in the NMS cohort, particularly in patients requiring fusion to pelvis.</p><p><strong>Conclusion: </strong>EBL significantly underestimates blood loss compared to CBL. Patients with NMS have significantly greater blood loss than AIS. These differences appear to be driven by the extent of fusion. Updated guidelines would be valuable for more accurate determination of when to cross-match blood products prior to PSF for pediatric scoliosis.</p><p><strong>Level of evidence: </strong>IV-Case series, diagnostic.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146182233","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 : 2026-02-10DOI: 10.1007/s43390-026-01304-2
Emily K Vallee
{"title":"Authors' response to letter to the editor: impact of preoperative mental health disorders on postoperative outcomes in patients with adolescent idiopathic scoliosis undergoing surgery.","authors":"Emily K Vallee","doi":"10.1007/s43390-026-01304-2","DOIUrl":"https://doi.org/10.1007/s43390-026-01304-2","url":null,"abstract":"","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146150532","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 : 2026-02-07DOI: 10.1007/s43390-026-01295-0
Ramana Kolady, Kevin Yoon, Cindy Wang, Linus Lee, Mark Ehioghae, Jonthan P Japa, Ruijie Yin, Mina Botros, Addisu Mesfin
Purpose: The current body of literature has examined both pediatric and adult patients in concert with respect to single- versus dual-surgeon treatment of spinal deformity; however, to our knowledge, pediatric and adult outcomes have not yet been reported independently. We hypothesize that the favorable outcomes seen in pediatric spine deformity with a dual-surgeon approach may also extend to adult spinal deformity patients.
Methods: Databases were searched for studies involving surgeries around spinal deformities and the use of dual or single surgeons. For both dual- and single-surgeon group, details on rates of complications, operating room times, lengths of stay, blood loss, rates of transfusion, and reoperation rates were recorded. Categorical variables were reported in pooled odds ratio (OR) and continuous variables were reported in standardized mean difference (SMD). Alpha value of less than 0.05 was considered significant.
Results: In adults, the dual-surgeon approach was associated with decreased risk of complications (OR = 0.31, 95% CI, 0.21-0.46; p < 0.01). In pediatrics, the dual-surgeon approach was associated with a decreased length of stay (SMD = -0.93 days, 95% CI: -1.25 - -0.61; p < 0.01) and operating time (SMD = -82.20 min, 95% CI: -114.28 - -51.32; p < 0.01).
Conclusion: The results of this study demonstrated statistically significant decrease in length of stay and operative duration with a dual-surgeon team in pediatric patients. In adults, a dual-surgeon team had correlated with a significant decreased rate of complications. There exists a lack of sufficient adult data to determine differences in operative duration, length of stay, and blood loss. Further investigation may utilize larger datasets to better understand the impacts of the dual-surgeon approach for both adult and pediatric populations.
{"title":"Single- versus dual-surgeon outcomes in adult and pediatric spinal deformity patients: systematic review and meta-analysis.","authors":"Ramana Kolady, Kevin Yoon, Cindy Wang, Linus Lee, Mark Ehioghae, Jonthan P Japa, Ruijie Yin, Mina Botros, Addisu Mesfin","doi":"10.1007/s43390-026-01295-0","DOIUrl":"https://doi.org/10.1007/s43390-026-01295-0","url":null,"abstract":"<p><strong>Purpose: </strong>The current body of literature has examined both pediatric and adult patients in concert with respect to single- versus dual-surgeon treatment of spinal deformity; however, to our knowledge, pediatric and adult outcomes have not yet been reported independently. We hypothesize that the favorable outcomes seen in pediatric spine deformity with a dual-surgeon approach may also extend to adult spinal deformity patients.</p><p><strong>Methods: </strong>Databases were searched for studies involving surgeries around spinal deformities and the use of dual or single surgeons. For both dual- and single-surgeon group, details on rates of complications, operating room times, lengths of stay, blood loss, rates of transfusion, and reoperation rates were recorded. Categorical variables were reported in pooled odds ratio (OR) and continuous variables were reported in standardized mean difference (SMD). Alpha value of less than 0.05 was considered significant.</p><p><strong>Results: </strong>In adults, the dual-surgeon approach was associated with decreased risk of complications (OR = 0.31, 95% CI, 0.21-0.46; p < 0.01). In pediatrics, the dual-surgeon approach was associated with a decreased length of stay (SMD = -0.93 days, 95% CI: -1.25 - -0.61; p < 0.01) and operating time (SMD = -82.20 min, 95% CI: -114.28 - -51.32; p < 0.01).</p><p><strong>Conclusion: </strong>The results of this study demonstrated statistically significant decrease in length of stay and operative duration with a dual-surgeon team in pediatric patients. In adults, a dual-surgeon team had correlated with a significant decreased rate of complications. There exists a lack of sufficient adult data to determine differences in operative duration, length of stay, and blood loss. Further investigation may utilize larger datasets to better understand the impacts of the dual-surgeon approach for both adult and pediatric populations.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146137650","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 : 2026-02-03DOI: 10.1007/s43390-026-01294-1
Sadegh Bagherzadeh, Faramarz Roohollahi, Natalie J Bales, Anjali Pradhan, Sawyer Bauer, Katherine E Baker, Joshua Vignolles-Jeong, Dana Saleh, Diego Soto Rubio, Patrick Kim, Waseem Aziz, Mark Greenberg, Mohsen Rostami, Puya Alikhani
Purpose: To compare radiographic outcomes, patient-reported outcomes (PROs), and complications between L5 and sacropelvic fixation as the lowest instrumented vertebra (LIV) in long-segment fusion for adult spinal deformity (ASD).
Methods: Following PRISMA 2020 guidelines, PubMed, Web of Science, Scopus, and Embase were searched for studies comparing L5 vs. pelvic fixation in ASD. Studies with Newcastle-Ottawa Scale (NOS) ≥ 7 were included. Extracted data included demographics, radiographic parameters [pelvic tilt (PT), lumbar lordosis (LL), sagittal vertical axis (SVA)], complications, and PROs [Scoliosis Research Society (SRS) and Oswestry Disability Index (OD)]. Meta-analysis used standardized mean differences (SMD) and odds ratios (OR). Heterogeneity was assessed with I2, and publication bias with Egger's test.
Results: Nine studies (1196 patients; mean age 67.5 years; mean follow-up 36.5 months) were included. Pelvic fixation achieved better sagittal correction: lower PT (SMD 0.88, p = 0.005), higher LL (SMD - 0.76, p < 0.001), and lower SVA (SMD 0.82, p = 0.016). PROs were similar at baseline and follow-up (all p > 0.05). L5 fixation had shorter operative time (SMD - 0.78, p = 0.005) but higher distal junctional failure (DJF) risk (OR 2.62, p = 0.002). Predictors of DJF with L5 LIV included older age, extensive fusion, high pelvic incidence, facet degeneration, and poor baseline sagittal balance.
Conclusions: Pelvic fixation provides superior sagittal correction with comparable PROs and overall complications, while L5 fixation carries a 2.6-fold higher DJF risk. LIV selection must be individualized; pelvic fixation is strongly recommended for patients with advanced age (> 66 years), high pelvic incidence (> 52°), or severe sagittal malalignment to mitigate mechanical failure. PROSPERO ID Number: CRD420251129518.
目的:比较L5和骶盆腔固定作为成人脊柱畸形(ASD)长节段融合术中最低固定椎体(LIV)的影像学结果、患者报告的结果(PROs)和并发症。方法:根据PRISMA 2020指南,检索PubMed、Web of Science、Scopus和Embase,比较L5与盆腔固定治疗ASD的研究。纳入纽卡斯尔-渥太华量表(NOS)≥7的研究。提取的数据包括人口统计学、影像学参数[骨盆倾斜(PT)、腰椎前凸(LL)、矢状垂直轴(SVA)]、并发症和PROs[脊柱侧凸研究会(SRS)和Oswestry残疾指数(OD)]。meta分析采用标准化平均差异(SMD)和优势比(OR)。异质性采用I2评估,发表偏倚采用Egger检验。结果:纳入9项研究(1196例患者,平均年龄67.5岁,平均随访36.5个月)。骨盆固定获得了更好的矢状面矫正:较低的PT (SMD - 0.88, p = 0.005),较高的LL (SMD - 0.76, p 0.05)。L5内固定手术时间较短(SMD = 0.78, p = 0.005),但远端结功能衰竭(DJF)风险较高(OR = 2.62, p = 0.002)。DJF合并L5 LIV的预测因素包括年龄较大、广泛融合、骨盆发生率高、关节突变性和基线矢状平衡差。结论:骨盆固定提供了更好的矢状面矫正,其PROs和总体并发症相当,而L5固定具有2.6倍的DJF风险。LIV的选择必须个性化;强烈建议高龄(> ~ 66岁)、高骨盆发生率(> ~ 52°)或严重矢状面错位的患者进行骨盆固定,以减轻机械故障。普洛斯彼罗ID号:CRD420251129518。
{"title":"L5 vs. pelvic fixation as the lowest instrumented vertebra in long-segment fusion for adult spinal deformity: a systematic review and meta-analysis.","authors":"Sadegh Bagherzadeh, Faramarz Roohollahi, Natalie J Bales, Anjali Pradhan, Sawyer Bauer, Katherine E Baker, Joshua Vignolles-Jeong, Dana Saleh, Diego Soto Rubio, Patrick Kim, Waseem Aziz, Mark Greenberg, Mohsen Rostami, Puya Alikhani","doi":"10.1007/s43390-026-01294-1","DOIUrl":"https://doi.org/10.1007/s43390-026-01294-1","url":null,"abstract":"<p><strong>Purpose: </strong>To compare radiographic outcomes, patient-reported outcomes (PROs), and complications between L5 and sacropelvic fixation as the lowest instrumented vertebra (LIV) in long-segment fusion for adult spinal deformity (ASD).</p><p><strong>Methods: </strong>Following PRISMA 2020 guidelines, PubMed, Web of Science, Scopus, and Embase were searched for studies comparing L5 vs. pelvic fixation in ASD. Studies with Newcastle-Ottawa Scale (NOS) ≥ 7 were included. Extracted data included demographics, radiographic parameters [pelvic tilt (PT), lumbar lordosis (LL), sagittal vertical axis (SVA)], complications, and PROs [Scoliosis Research Society (SRS) and Oswestry Disability Index (OD)]. Meta-analysis used standardized mean differences (SMD) and odds ratios (OR). Heterogeneity was assessed with I<sup>2</sup>, and publication bias with Egger's test.</p><p><strong>Results: </strong>Nine studies (1196 patients; mean age 67.5 years; mean follow-up 36.5 months) were included. Pelvic fixation achieved better sagittal correction: lower PT (SMD 0.88, p = 0.005), higher LL (SMD - 0.76, p < 0.001), and lower SVA (SMD 0.82, p = 0.016). PROs were similar at baseline and follow-up (all p > 0.05). L5 fixation had shorter operative time (SMD - 0.78, p = 0.005) but higher distal junctional failure (DJF) risk (OR 2.62, p = 0.002). Predictors of DJF with L5 LIV included older age, extensive fusion, high pelvic incidence, facet degeneration, and poor baseline sagittal balance.</p><p><strong>Conclusions: </strong>Pelvic fixation provides superior sagittal correction with comparable PROs and overall complications, while L5 fixation carries a 2.6-fold higher DJF risk. LIV selection must be individualized; pelvic fixation is strongly recommended for patients with advanced age (> 66 years), high pelvic incidence (> 52°), or severe sagittal malalignment to mitigate mechanical failure. PROSPERO ID Number: CRD420251129518.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146114115","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 : 2026-02-01DOI: 10.1007/s43390-026-01286-1
José María González-Ruiz, Andrea P Loayza, Stephan Rothstock
Scoliosis, the most common spinal deformity in adolescents, requires frequent radiographic follow-up, exposing patients to cumulative ionizing radiation with potential long-term risks. In response, recent efforts have explored radiation-free alternatives for Cobb angle estimation, but most fail to meet the clinical threshold of a minimum significant change of 5°. In this study, we aimed to develop and internally validate a fully automated method for predicting Cobb angle using 3D surface topography (ST) data and a linear regression model (LRM). Principal component analysis was used to reduce the dimensionality of the ST data, and several machine learning models were compared, including neural networks, XGBoost and Stacking. The LRM showed the best performance in the test set, with a mean absolute error (MAE) of 3.97°, a root Mean square error (RMSE) of 4.70°, and a strong correlation with the ground truth (r = 0.91). Residual analysis confirmed normality and homoscedasticity, supporting the robustness of the model. Importantly, the MAE fell below the clinically significant threshold of 5°, indicating the model's ability to detect minimal but critical changes in spinal curvature. These results outperform most previous non-radiographic methods and suggest that a simple, interpretable LRM, combined with open-source tools and ST data, offers a viable and scalable solution for non-invasive scoliosis monitoring. If externally validated, this method could reduce reliance on x-rays, thereby reducing radiation exposure while maintaining assessment accuracy.
{"title":"Radiation-free Cobb angle estimation in adolescent scoliosis using surface topography and a linear regression model.","authors":"José María González-Ruiz, Andrea P Loayza, Stephan Rothstock","doi":"10.1007/s43390-026-01286-1","DOIUrl":"https://doi.org/10.1007/s43390-026-01286-1","url":null,"abstract":"<p><p>Scoliosis, the most common spinal deformity in adolescents, requires frequent radiographic follow-up, exposing patients to cumulative ionizing radiation with potential long-term risks. In response, recent efforts have explored radiation-free alternatives for Cobb angle estimation, but most fail to meet the clinical threshold of a minimum significant change of 5°. In this study, we aimed to develop and internally validate a fully automated method for predicting Cobb angle using 3D surface topography (ST) data and a linear regression model (LRM). Principal component analysis was used to reduce the dimensionality of the ST data, and several machine learning models were compared, including neural networks, XGBoost and Stacking. The LRM showed the best performance in the test set, with a mean absolute error (MAE) of 3.97°, a root Mean square error (RMSE) of 4.70°, and a strong correlation with the ground truth (r = 0.91). Residual analysis confirmed normality and homoscedasticity, supporting the robustness of the model. Importantly, the MAE fell below the clinically significant threshold of 5°, indicating the model's ability to detect minimal but critical changes in spinal curvature. These results outperform most previous non-radiographic methods and suggest that a simple, interpretable LRM, combined with open-source tools and ST data, offers a viable and scalable solution for non-invasive scoliosis monitoring. If externally validated, this method could reduce reliance on x-rays, thereby reducing radiation exposure while maintaining assessment accuracy.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146097244","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 : 2026-01-31DOI: 10.1007/s43390-026-01299-w
Kishankumar Mahida, Snehal Rajendra Jagtap
{"title":"Letter to the Editor concerning \"Impact of preoperative mental health disorders on postoperative outcomes in patients with adolescent idiopathic scoliosis undergoing surgery\" by Vallee EK, et al. (Spine Deformity [2026]: doi:10.1007/s43390-026-01288-z).","authors":"Kishankumar Mahida, Snehal Rajendra Jagtap","doi":"10.1007/s43390-026-01299-w","DOIUrl":"https://doi.org/10.1007/s43390-026-01299-w","url":null,"abstract":"","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146097291","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 : 2026-01-31DOI: 10.1007/s43390-026-01293-2
Antti Juhani Saarinen
Background: The 24-item Early-Onset Scoliosis Questionnaire (EOSQ-24) is a condition-specific instrument to assess health-related quality of life in children with early-onset scoliosis (EOS). Previous studies have raised concerns regarding ceiling effects, i.e. clustering of scores at the upper limit, which may reduce the ability of the EOSQ-24 to detect clinical improvements.
Methods: A structured review of published clinical studies reporting EOSQ-24 scores was performed. Data were standardized to a 0-100 scale. For each domain weighted mean scores, standard deviations (SD), and ceiling effect percentages were calculated. A ceiling effect ≥ 15% was considered significant.
Results: Data from 16 studies were included. Significant ceiling effects were observed in the following domains: pulmonary function (28%), physical function (25%), overall satisfaction (22%), transfer (20%), financial burden (22%), daily living (18%), fatigue/energy level (18%), and emotion (16%). Lower ceiling effects were noted in general health, pain/discomfort, parental burden, and child/parent satisfaction domains.
Conclusions: Eight of EOSQ-24 domains exhibit marked ceiling effects, potentially limiting responsiveness to treatment effects in patients with high baseline function. These findings support consideration of revised scoring strategies or adjunctive measures in EOS outcome assessment. The presence of marked ceiling effect should be noted as a limitation in studies. Objective pulmonary function testing should be implemented in future studies.
{"title":"Ceiling effects in the EOSQ-24 may limit its ability to assess treatment outcomes in early-onset scoliosis.","authors":"Antti Juhani Saarinen","doi":"10.1007/s43390-026-01293-2","DOIUrl":"https://doi.org/10.1007/s43390-026-01293-2","url":null,"abstract":"<p><strong>Background: </strong>The 24-item Early-Onset Scoliosis Questionnaire (EOSQ-24) is a condition-specific instrument to assess health-related quality of life in children with early-onset scoliosis (EOS). Previous studies have raised concerns regarding ceiling effects, i.e. clustering of scores at the upper limit, which may reduce the ability of the EOSQ-24 to detect clinical improvements.</p><p><strong>Methods: </strong>A structured review of published clinical studies reporting EOSQ-24 scores was performed. Data were standardized to a 0-100 scale. For each domain weighted mean scores, standard deviations (SD), and ceiling effect percentages were calculated. A ceiling effect ≥ 15% was considered significant.</p><p><strong>Results: </strong>Data from 16 studies were included. Significant ceiling effects were observed in the following domains: pulmonary function (28%), physical function (25%), overall satisfaction (22%), transfer (20%), financial burden (22%), daily living (18%), fatigue/energy level (18%), and emotion (16%). Lower ceiling effects were noted in general health, pain/discomfort, parental burden, and child/parent satisfaction domains.</p><p><strong>Conclusions: </strong>Eight of EOSQ-24 domains exhibit marked ceiling effects, potentially limiting responsiveness to treatment effects in patients with high baseline function. These findings support consideration of revised scoring strategies or adjunctive measures in EOS outcome assessment. The presence of marked ceiling effect should be noted as a limitation in studies. Objective pulmonary function testing should be implemented in future studies.</p>","PeriodicalId":21796,"journal":{"name":"Spine deformity","volume":" ","pages":""},"PeriodicalIF":1.8,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146094024","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}