Francisco de Assis Ulisses Sampaio Júnior, Hetevaldo Tavares de Lira Filho, Mateus de Sousa Rodrigues, Laylla Maria Quidute Sampaio, Bartolomeu Souto Queiroz Quidute, José Cássio Falcão da Cunha, Oscar Luís Alves
Peripheral injury-induced movement disorders encompass a broad spectrum of conditions characterized by involuntary movements resulting from injuries to the peripheral nervous system. While most reported cases are associated with traumatic events-such as nerve lacerations-surgical interventions are also recognized as potential triggers of such disorders. This article aims to report a rare presentation of dancing dorsal quadrilateral syndrome (DDQS) following spinal surgery with instrumentation. A 63-year-old man presented with back pain and neck pain and was diagnosed with Scheuermann's disease. He underwent thoracic spinal fusion with pedicle screw instrumentation to correct hyperkyphosis. Six months after surgery, he began to experience a burning pain in the bilateral subscapular region along with abnormal and involuntary movements in the dorsal musculature. The motor unit potential followed an ascending-descending pattern, and these findings were compatible with dyskinesia, specifically DDQS. A joint management approach with a clinical neurologist was indicated, including the prescription of muscle relaxants and the administration of botulinum toxin in the dorsal quadrilaterals, resulting in partial improvement of the condition. Treatment options range from addressing afferent nerve injury, which can sometimes be curative in some focal dyskinesias, to the use of botulinum toxin for symptomatic relief, as presented in the above case. Additional research is warranted to better understand the pathophysiology of DDQS and to optimize treatment strategies for this uncommon but clinically significant condition.
{"title":"Dancing Dorsal Quadrilaterals: Case Report.","authors":"Francisco de Assis Ulisses Sampaio Júnior, Hetevaldo Tavares de Lira Filho, Mateus de Sousa Rodrigues, Laylla Maria Quidute Sampaio, Bartolomeu Souto Queiroz Quidute, José Cássio Falcão da Cunha, Oscar Luís Alves","doi":"10.14444/8779","DOIUrl":"10.14444/8779","url":null,"abstract":"<p><p>Peripheral injury-induced movement disorders encompass a broad spectrum of conditions characterized by involuntary movements resulting from injuries to the peripheral nervous system. While most reported cases are associated with traumatic events-such as nerve lacerations-surgical interventions are also recognized as potential triggers of such disorders. This article aims to report a rare presentation of dancing dorsal quadrilateral syndrome (DDQS) following spinal surgery with instrumentation. A 63-year-old man presented with back pain and neck pain and was diagnosed with Scheuermann's disease. He underwent thoracic spinal fusion with pedicle screw instrumentation to correct hyperkyphosis. Six months after surgery, he began to experience a burning pain in the bilateral subscapular region along with abnormal and involuntary movements in the dorsal musculature. The motor unit potential followed an ascending-descending pattern, and these findings were compatible with dyskinesia, specifically DDQS. A joint management approach with a clinical neurologist was indicated, including the prescription of muscle relaxants and the administration of botulinum toxin in the dorsal quadrilaterals, resulting in partial improvement of the condition. Treatment options range from addressing afferent nerve injury, which can sometimes be curative in some focal dyskinesias, to the use of botulinum toxin for symptomatic relief, as presented in the above case. Additional research is warranted to better understand the pathophysiology of DDQS and to optimize treatment strategies for this uncommon but clinically significant condition.</p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"565-568"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679451/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144761682","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Khanathip Jitpakdee, Chibuikem A Ikwuegbuenyi, Minaam Farooq, Fabian Sommer, Edna Gouveia, Blake I Boadi, Jessica Berger, Ibrahim Hussain, Roger Härtl
Background: Minimally invasive transforaminal lumbar interbody fusion (MIS-TLIF) often struggles to provide sufficient lordotic alignment restoration. The choice of cage design, including its height and lordotic angle, is critical. This study compares 2 expandable cage designs in MIS-TLIF: one that increases only disc height (group H) and another that expands both height and lordosis (group HL).
Methods: Seventy-five patients who underwent navigation-assisted MIS-TLIF using expandable cages were reviewed. These included 35 cases using expandable cages that increase only height (group H) and 40 cases using cages that expand both height and lordosis (group HL). Clinical outcomes, including a numeric rating scale of back pain, leg pain, and Oswestry Disability Index and radiographic parameters, including disc height, lordotic angle, subsidence, and fusion rates, were evaluated.
Results: Both groups showed significant improvements in clinical outcomes, with no differences between groups. Postoperative disc and foraminal height increased significantly. At the 1-year follow-up, group HL demonstrated greater improvements in segmental lordosis (4.0° ± 3.3° vs 1.9° ± 5.4°, P = 0.018) and disc angle (5.8° ± 4.1° vs 1.9° ± 4.2°, P < 0.001) compared with group H. The overall fusion rate was 92%, and the overall subsidence rate was 32%, which decreased to 20% after the first 20 cases. No neurological injuries occurred, and there were no significant differences in complications between the groups.
Conclusion: This study demonstrates that MIS-TLIF with expandable cages designed to increase lordosis offers superior improvement in segmental lordosis at the 1-year follow-up, compared with expandable cages that only expand disc height. Both cage designs achieved high fusion rates and showed similar clinical outcomes.
Clinical relevance: The surgeon's experience in the use of expandable cages is a critical factor in reducing the risk of cage subsidence, a complication that may adversely affect clinical outcomes.
{"title":"Comparison of 1-Year Clinical and Radiographic Outcomes Between 2 Expandable Cage Designs in Navigation-Assisted Minimally Invasive Transforaminal Lumbar Interbody Fusion.","authors":"Khanathip Jitpakdee, Chibuikem A Ikwuegbuenyi, Minaam Farooq, Fabian Sommer, Edna Gouveia, Blake I Boadi, Jessica Berger, Ibrahim Hussain, Roger Härtl","doi":"10.14444/8797","DOIUrl":"10.14444/8797","url":null,"abstract":"<p><strong>Background: </strong>Minimally invasive transforaminal lumbar interbody fusion (MIS-TLIF) often struggles to provide sufficient lordotic alignment restoration. The choice of cage design, including its height and lordotic angle, is critical. This study compares 2 expandable cage designs in MIS-TLIF: one that increases only disc height (group H) and another that expands both height and lordosis (group HL).</p><p><strong>Methods: </strong>Seventy-five patients who underwent navigation-assisted MIS-TLIF using expandable cages were reviewed. These included 35 cases using expandable cages that increase only height (group H) and 40 cases using cages that expand both height and lordosis (group HL). Clinical outcomes, including a numeric rating scale of back pain, leg pain, and Oswestry Disability Index and radiographic parameters, including disc height, lordotic angle, subsidence, and fusion rates, were evaluated.</p><p><strong>Results: </strong>Both groups showed significant improvements in clinical outcomes, with no differences between groups. Postoperative disc and foraminal height increased significantly. At the 1-year follow-up, group HL demonstrated greater improvements in segmental lordosis (4.0° ± 3.3° vs 1.9° ± 5.4°, <i>P</i> = 0.018) and disc angle (5.8° ± 4.1° vs 1.9° ± 4.2°, <i>P</i> < 0.001) compared with group H. The overall fusion rate was 92%, and the overall subsidence rate was 32%, which decreased to 20% after the first 20 cases. No neurological injuries occurred, and there were no significant differences in complications between the groups.</p><p><strong>Conclusion: </strong>This study demonstrates that MIS-TLIF with expandable cages designed to increase lordosis offers superior improvement in segmental lordosis at the 1-year follow-up, compared with expandable cages that only expand disc height. Both cage designs achieved high fusion rates and showed similar clinical outcomes.</p><p><strong>Clinical relevance: </strong>The surgeon's experience in the use of expandable cages is a critical factor in reducing the risk of cage subsidence, a complication that may adversely affect clinical outcomes.</p><p><strong>Level of evidence: 3: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"587-597"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679419/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151365","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Guntram Krzok, Shailen G Sampath, Mihaly Peca, Sanjay Konakondlam, Jian Shen, Albert E Telfeian
Hemorrhagic facet cysts are a rare condition including both synovial and ganglion cysts. Here, the authors present the first-ever reported case of a hemorrhagic ganglion cyst of the facet joint at L1 to L2 causing cauda equina syndrome. In this report, a 72-year-old woman presented with symptoms of cauda equina syndrome requiring urgent surgical consideration. Magnetic resonance imaging and computed tomography showed an extradural mass at the L1 to L2 level. Due to the giant size of the cyst, there was severe compression of the thecal sac and nerve roots. The patient underwent interlaminar contralateral decompression and cystectomy using a uniportal endoscopic approach. The patient had a quick postoperative recovery, with postoperative magnetic resonance imaging of the lumbar spine showing recovery of the facet cyst with no sign of recurrence or stenosis. This case demonstrates the successful surgical technique of interlaminar endoscopic contralateral decompression combined with cystectomy, showing that a hemorrhagic ganglion cyst at the facet at L1 to L2 can be removed completely under endoscopic view.
{"title":"Interlaminar Endoscopic Resection of Giant Hemorrhagic Ganglion Cyst of the Facet Joint at L1 to L2 Level.","authors":"Guntram Krzok, Shailen G Sampath, Mihaly Peca, Sanjay Konakondlam, Jian Shen, Albert E Telfeian","doi":"10.14444/8793","DOIUrl":"10.14444/8793","url":null,"abstract":"<p><p>Hemorrhagic facet cysts are a rare condition including both synovial and ganglion cysts. Here, the authors present the first-ever reported case of a hemorrhagic ganglion cyst of the facet joint at L1 to L2 causing cauda equina syndrome. In this report, a 72-year-old woman presented with symptoms of cauda equina syndrome requiring urgent surgical consideration. Magnetic resonance imaging and computed tomography showed an extradural mass at the L1 to L2 level. Due to the giant size of the cyst, there was severe compression of the thecal sac and nerve roots. The patient underwent interlaminar contralateral decompression and cystectomy using a uniportal endoscopic approach. The patient had a quick postoperative recovery, with postoperative magnetic resonance imaging of the lumbar spine showing recovery of the facet cyst with no sign of recurrence or stenosis. This case demonstrates the successful surgical technique of interlaminar endoscopic contralateral decompression combined with cystectomy, showing that a hemorrhagic ganglion cyst at the facet at L1 to L2 can be removed completely under endoscopic view.</p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"604-610"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679444/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145139016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Steven A Rundell, Steven M Kurtz, Hannah Spece, Jeffrey A Goldstein, Scott D Hodges, Ron V Yarbrough
Background: During lumbar total joint replacement (LTJR), component misalignment during implantation may affect the bearing surface interaction. In this study, validated computational models of the lumbar spine were used to investigate a range of clinically relevant misalignment scenarios.
Methods: A finite element model (FEM) of the LTJR, exposed to mode I (normal wear) and mode IV (impingement) wear boundary conditions, was previously validated following the ASME V&V 40 standard. The LTJR FEM was virtually implanted into a previously validated FEM of the lumbar spine (L3-L5) at L4 to L5. The model included vertebrae, major spinal ligaments, erector muscle forces, and intervertebral discs. Misalignment was introduced by adjusting the bilateral implant axial plane convergence angle (20°-40°), anterior-posterior offset (0-4 mm), and coronal plane tilt (±20°). Analyses were conducted using LS-DYNA3D (ANSYS) under boundary conditions simulating bending at the waist. Contact pressures and von Mises stresses were evaluated for each misalignment scenario and compared with those developed during mode I and mode IV impingement scenarios.
Results: Axial plane convergence angle had minimal impact on contact stress and von Mises stress magnitude and distribution. Increasing anterior-posterior offset led to higher stresses on the anteriorly shifted component but did not significantly alter the overall stress pattern. Coronal tilt had the most substantial effect on both stress magnitude and distribution.
Conclusion: Overall, polyethylene stresses in all misalignment scenarios remained below mode IV impingement levels. Contact areas remained within the intended spherical bearing surfaces without signs of impingement. LTJR contact stresses were found to be reasonably insensitive to misalignment under boundary conditions representing bending at the waist.
Clinical relevance: This work assesses the impact of clinically relevant implant misalignment scenarios on the polyethylene stresses associated with damage and wear for a novel LTJR and offers best practice guidelines for surgeons.
{"title":"Sensitivity of Lumbar Total Joint Replacement to Axial and Coronal Plane Misalignment Using Computational Modeling.","authors":"Steven A Rundell, Steven M Kurtz, Hannah Spece, Jeffrey A Goldstein, Scott D Hodges, Ron V Yarbrough","doi":"10.14444/8792","DOIUrl":"10.14444/8792","url":null,"abstract":"<p><strong>Background: </strong>During lumbar total joint replacement (LTJR), component misalignment during implantation may affect the bearing surface interaction. In this study, validated computational models of the lumbar spine were used to investigate a range of clinically relevant misalignment scenarios.</p><p><strong>Methods: </strong>A finite element model (FEM) of the LTJR, exposed to mode I (normal wear) and mode IV (impingement) wear boundary conditions, was previously validated following the ASME V&V 40 standard. The LTJR FEM was virtually implanted into a previously validated FEM of the lumbar spine (L3-L5) at L4 to L5. The model included vertebrae, major spinal ligaments, erector muscle forces, and intervertebral discs. Misalignment was introduced by adjusting the bilateral implant axial plane convergence angle (20°-40°), anterior-posterior offset (0-4 mm), and coronal plane tilt (±20°). Analyses were conducted using LS-DYNA3D (ANSYS) under boundary conditions simulating bending at the waist. Contact pressures and von Mises stresses were evaluated for each misalignment scenario and compared with those developed during mode I and mode IV impingement scenarios.</p><p><strong>Results: </strong>Axial plane convergence angle had minimal impact on contact stress and von Mises stress magnitude and distribution. Increasing anterior-posterior offset led to higher stresses on the anteriorly shifted component but did not significantly alter the overall stress pattern. Coronal tilt had the most substantial effect on both stress magnitude and distribution.</p><p><strong>Conclusion: </strong>Overall, polyethylene stresses in all misalignment scenarios remained below mode IV impingement levels. Contact areas remained within the intended spherical bearing surfaces without signs of impingement. LTJR contact stresses were found to be reasonably insensitive to misalignment under boundary conditions representing bending at the waist.</p><p><strong>Clinical relevance: </strong>This work assesses the impact of clinically relevant implant misalignment scenarios on the polyethylene stresses associated with damage and wear for a novel LTJR and offers best practice guidelines for surgeons.</p><p><strong>Level of evidence: 5: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"635-644"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679452/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145214072","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Adult isthmic spondylolisthesis often remains stable in adulthood, but progressive neural compression can occur due to scar tissue, bony overgrowth, and disc degeneration. Conventional endoscopic techniques such as the interlaminar or transforaminal approaches may be limited by anatomical constraints in adult isthmic spondylolisthesis, making complete decompression difficult.
Methods: A 70-year-old man presented with bilateral leg pain and neurogenic claudication. Imaging revealed bilateral L4 to L5 lateral recess narrowing, L5 foraminal stenosis, and a bulging L5 to S1 disc compressing the extraforaminal nerve roots. A novel craniocaudal interlaminar approach via unilateral biportal endoscopic spine surgery was used to decompress the central and contralateral foraminal regions. The residual ipsilateral extraforaminal lesion was accessed through a separate full endoscopic transforaminal approach. Three incisions of 7 mm each were used.
Results: The patient experienced immediate and significant relief of radicular symptoms and improved function and was discharged the next day. At 18-month follow-up, he remained pain-free and without new-onset back pain or signs of instability.
Conclusions: This is the first reported case combining unilateral biportal endoscopic spine surgery and full endoscopic spine surgery. The approach enabled full decompression from central to extraforaminal zones with minimal invasiveness. This dual-endoscopic strategy may serve as a model for treating complex spine cases not amenable to single-approach techniques.
{"title":"Full Decompression of Spinal Stenosis in Stable Adult Isthmic Spondylolisthesis With a Combination of Full Endoscopic Spine Surgery and Unilateral Biportal Endoscopic Spine Surgery: A Case Report.","authors":"Chien-Chieh Wang, Kin-Weng Wong, Po-Kuan Wu, Kuan-Ting Chen, Wen-Shuo Chang, Chi-Sheng Chien, Dae-Jung Choi, Tsung-Mu Wu","doi":"10.14444/8800","DOIUrl":"10.14444/8800","url":null,"abstract":"<p><strong>Background: </strong>Adult isthmic spondylolisthesis often remains stable in adulthood, but progressive neural compression can occur due to scar tissue, bony overgrowth, and disc degeneration. Conventional endoscopic techniques such as the interlaminar or transforaminal approaches may be limited by anatomical constraints in adult isthmic spondylolisthesis, making complete decompression difficult.</p><p><strong>Methods: </strong>A 70-year-old man presented with bilateral leg pain and neurogenic claudication. Imaging revealed bilateral L4 to L5 lateral recess narrowing, L5 foraminal stenosis, and a bulging L5 to S1 disc compressing the extraforaminal nerve roots. A novel craniocaudal interlaminar approach via unilateral biportal endoscopic spine surgery was used to decompress the central and contralateral foraminal regions. The residual ipsilateral extraforaminal lesion was accessed through a separate full endoscopic transforaminal approach. Three incisions of 7 mm each were used.</p><p><strong>Results: </strong>The patient experienced immediate and significant relief of radicular symptoms and improved function and was discharged the next day. At 18-month follow-up, he remained pain-free and without new-onset back pain or signs of instability.</p><p><strong>Conclusions: </strong>This is the first reported case combining unilateral biportal endoscopic spine surgery and full endoscopic spine surgery. The approach enabled full decompression from central to extraforaminal zones with minimal invasiveness. This dual-endoscopic strategy may serve as a model for treating complex spine cases not amenable to single-approach techniques.</p><p><strong>Level of evidence: 4: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"598-603"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679434/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145214096","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Dong Hyun Lee, Jin Young Lee, Sung Bum Kim, Choon Keun Park, Kang Taek Lim, Dong Chan Lee, Inbo Han, Jae-Won Jang, Dong-Geun Lee, Il-Tae Jang
Background: This study aimed to compare a 3-dimensional (3D)-printed titanium cage with a polyetheretherketone (PEEK) cage in biportal endoscopic transforaminal lumbar interbody fusion (BETLIF) using a double cage construct, evaluate differences in fusion stability and subsidence between the 2 cage types, and analyze factors influencing subsidence.
Methods: We retrospectively examined 89 patients who underwent BETLIF using a double cage (3D-printed titanium, 48 levels; PEEK, 46 levels). Fusion status and subsidence were assessed using dynamic plain lateral lumbar spine radiographs and computed tomography images at 6 months and 1 year postoperatively. Fusion was graded according to the Bridwell system, and significant subsidence was defined as ≥2 mm endplate depression on computed tomography. Demographic and clinical variables, including age, sex, body mass index, American Society of Anesthesiologists classification, history of tobacco smoking, diabetes mellitus, bone mineral density measured using dual-energy x-ray absorptiometry, cage length, and cage material, were collected and analyzed as potential risk factors.
Results: At 1-year follow-up, fusion grades were I (75.0%, 36 levels), II (20.8%, 10 levels), and III (4.2%, 2 levels) for 3D-printed titanium and I (53.2%, 25 levels), II (40.4%, 19 levels), and III (6.4%, 3 levels) for PEEK. The overall fusion rate (grades I and II) was similar for both cages (95.8% vs 93.6%, P = 0.629), but grade I was more prevalent with 3D-printed titanium than with PEEK (75.0% vs 53.2%, P = 0.027). No significant differences were observed in subsidence or complications between the 2 cages. Multivariate analysis revealed age as the only variable significantly associated with subsidence in BETLIF.
Conclusions: Both double 3D-printed titanium and PEEK cages demonstrated high fusion rates with no significant differences in overall success. However, double 3D-printed titanium cages showed better early fusion grades and comparable subsidence to that of PEEK cages. Although long-term follow-up is necessary to ascertain efficacy, these findings suggest that 3D-printed titanium cages offer advantages in early fusion quality in BETLIF. Further research is needed to optimize cage arrangement, cage design, and surgical techniques to improve outcomes.
Clinical relevance: The use of double 3D-printed titanium cages is recommended in BETLIF.
{"title":"Use of Double Cages for Biportal Endoscopic Transforaminal Lumbar Interbody Fusion: A Comparison of 3-Dimensional-Printed Titanium and Polyetheretherketone Cages.","authors":"Dong Hyun Lee, Jin Young Lee, Sung Bum Kim, Choon Keun Park, Kang Taek Lim, Dong Chan Lee, Inbo Han, Jae-Won Jang, Dong-Geun Lee, Il-Tae Jang","doi":"10.14444/8788","DOIUrl":"10.14444/8788","url":null,"abstract":"<p><strong>Background: </strong>This study aimed to compare a 3-dimensional (3D)-printed titanium cage with a polyetheretherketone (PEEK) cage in biportal endoscopic transforaminal lumbar interbody fusion (BETLIF) using a double cage construct, evaluate differences in fusion stability and subsidence between the 2 cage types, and analyze factors influencing subsidence.</p><p><strong>Methods: </strong>We retrospectively examined 89 patients who underwent BETLIF using a double cage (3D-printed titanium, 48 levels; PEEK, 46 levels). Fusion status and subsidence were assessed using dynamic plain lateral lumbar spine radiographs and computed tomography images at 6 months and 1 year postoperatively. Fusion was graded according to the Bridwell system, and significant subsidence was defined as ≥2 mm endplate depression on computed tomography. Demographic and clinical variables, including age, sex, body mass index, American Society of Anesthesiologists classification, history of tobacco smoking, diabetes mellitus, bone mineral density measured using dual-energy x-ray absorptiometry, cage length, and cage material, were collected and analyzed as potential risk factors.</p><p><strong>Results: </strong>At 1-year follow-up, fusion grades were I (75.0%, 36 levels), II (20.8%, 10 levels), and III (4.2%, 2 levels) for 3D-printed titanium and I (53.2%, 25 levels), II (40.4%, 19 levels), and III (6.4%, 3 levels) for PEEK. The overall fusion rate (grades I and II) was similar for both cages (95.8% vs 93.6%, <i>P</i> = 0.629), but grade I was more prevalent with 3D-printed titanium than with PEEK (75.0% vs 53.2%, <i>P</i> = 0.027). No significant differences were observed in subsidence or complications between the 2 cages. Multivariate analysis revealed age as the only variable significantly associated with subsidence in BETLIF.</p><p><strong>Conclusions: </strong>Both double 3D-printed titanium and PEEK cages demonstrated high fusion rates with no significant differences in overall success. However, double 3D-printed titanium cages showed better early fusion grades and comparable subsidence to that of PEEK cages. Although long-term follow-up is necessary to ascertain efficacy, these findings suggest that 3D-printed titanium cages offer advantages in early fusion quality in BETLIF. Further research is needed to optimize cage arrangement, cage design, and surgical techniques to improve outcomes.</p><p><strong>Clinical relevance: </strong>The use of double 3D-printed titanium cages is recommended in BETLIF.</p><p><strong>Level of evidence: 3: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"611-624"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679439/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144972375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Adarsh Suresh, Takashi Hirase, Scott A Buhler, Rex A W Marco
Background: There are currently no studies that directly compare the previously established 2-dimensional (2D) sagittal technique with 3-dimensional (3D) templating for C2 pedicle screw.
Objective: To verify the accuracy of sagittal radiological analysis for safe placement of a C2 pedicle screw by performing a direct comparison between 2D planning with 3D templating methods.
Methods: In this retrospective analysis, forty-six sets of computed tomography scans that contained 2-mm bony cuts and 2D reconstructions in the axial, sagittal, and coronal planes of skeletally mature patients were analyzed. StealthStation S7 (Medtronic Surgical Navigation, Minneapolis, Minnesota, United States) trajectory planning was used to plan the ideal placement, maximum diameter pedicle screw into the C2 pedicle. Based on the parameters of ≤3 mm screw diameter as high risk, >3 mm and <5 mm as moderate risk, and ≥5 mm as low risk, frequency and percentage values were calculated for the left, right, and bilateral pedicle screws.
Results: Out of the 46 patients analyzed in this study, only 1 patient (2.2%) was classified as low risk (≥5 mm) bilaterally, 5 were classified as high risk (≤3 mm) bilaterally (10.8%), and 25 patients (54.3%) showed variability in pedicle width between the left and right sides. With analysis of both left and right pedicle, 7 out of 92 pedicles (7.6%) analyzed were classified as low risk (≥5 mm), 67 out of 92 (72.8%) were at moderate risk (>3 mm and <5 mm), and 18 out of 92 (19.6%) were at high risk (≤3 mm).
Conclusion: Both the previously described 2D sagittal planning method and the current 3D templating method allow for accurate preoperative planning for the placement of ≤4 mm C2 pedicle screws, which is important given the limited availability and amount of resources utilized for the 3D templating model. However, the 3D templating method more precisely identifies C2 pedicles where 3.0 to 4.5 mm screws can feasibly be placed.
{"title":"Accuracy of 2D Sagittal Radiological Analysis vs 3D Templating for Pedicle Screw Fixation of C2 Vertebral Body.","authors":"Adarsh Suresh, Takashi Hirase, Scott A Buhler, Rex A W Marco","doi":"10.14444/8775","DOIUrl":"10.14444/8775","url":null,"abstract":"<p><strong>Background: </strong>There are currently no studies that directly compare the previously established 2-dimensional (2D) sagittal technique with 3-dimensional (3D) templating for C2 pedicle screw.</p><p><strong>Objective: </strong>To verify the accuracy of sagittal radiological analysis for safe placement of a C2 pedicle screw by performing a direct comparison between 2D planning with 3D templating methods.</p><p><strong>Methods: </strong>In this retrospective analysis, forty-six sets of computed tomography scans that contained 2-mm bony cuts and 2D reconstructions in the axial, sagittal, and coronal planes of skeletally mature patients were analyzed. StealthStation S7 (Medtronic Surgical Navigation, Minneapolis, Minnesota, United States) trajectory planning was used to plan the ideal placement, maximum diameter pedicle screw into the C2 pedicle. Based on the parameters of ≤3 mm screw diameter as high risk, >3 mm and <5 mm as moderate risk, and ≥5 mm as low risk, frequency and percentage values were calculated for the left, right, and bilateral pedicle screws.</p><p><strong>Results: </strong>Out of the 46 patients analyzed in this study, only 1 patient (2.2%) was classified as low risk (≥5 mm) bilaterally, 5 were classified as high risk (≤3 mm) bilaterally (10.8%), and 25 patients (54.3%) showed variability in pedicle width between the left and right sides. With analysis of both left and right pedicle, 7 out of 92 pedicles (7.6%) analyzed were classified as low risk (≥5 mm), 67 out of 92 (72.8%) were at moderate risk (>3 mm and <5 mm), and 18 out of 92 (19.6%) were at high risk (≤3 mm).</p><p><strong>Conclusion: </strong>Both the previously described 2D sagittal planning method and the current 3D templating method allow for accurate preoperative planning for the placement of ≤4 mm C2 pedicle screws, which is important given the limited availability and amount of resources utilized for the 3D templating model. However, the 3D templating method more precisely identifies C2 pedicles where 3.0 to 4.5 mm screws can feasibly be placed.</p><p><strong>Level of evidence: 3: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"511-516"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679415/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144592541","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Megan L Anderson, Nicholas G Rhodes, Michelle Y Hung, Ankur Khanna, William W Cross
Background: Bilateral sacroiliac joint fusion (BSIJF) is an accepted management strategy for sacroiliac joint dysfunction, though outcomes data are limited by patient number and lack of long-term follow-up. This study investigated the clinical, radiological, and patient-reported outcomes of BSIJF.
Methods: A retrospective review was conducted of all patients who underwent BSIJF with a single surgeon between 2020 and 2023. All BSIJF utilized a principles-based approach: joint decortication, bone grafting, compression, and rigid stability. Patient-reported outcomes at preoperative, 6-month, 1-year, and 2-year follow-up timepoints were recorded for the Numeric Pain Rating Scale, Oswestry Disability Index (ODI), Single Assessment Numeric Evaluation (SANE), PROMIS Pain Interference (PI), and PROMIS Physical Function (PF). Fusion grading was assessed by computed tomography after 1 and 2 years.
Results: Forty-eight patients who underwent BSIJF were included, of whom 31 (65%) were women with a mean age of 54 ± 14 years and a mean body mass index of 29 ± 5. Twenty-five patients (52%) had prior lumbar spine surgery (PLSS). One patient required revision for implant malpositioning and nerve impingement. Bridging bone across the sacroiliac joint was observed in 85% of patients. Numeric Pain Rating Scale scores dropped significantly from 7.6 preoperatively to 3.9, 3.3, and 3.7 at 6-month, 1-year, and 2-year follow-ups, respectively (P ≤ 0.004). PI and PF scores were significantly improved at all timepoints (all P < 0.001). ODI scores demonstrated sustained improvement from 52.3 preoperatively to 33.3 at 1-year follow-up and 29.3 at 2-year follow-up (P < 0.001). SANE scores were 80% at 1-year follow-up and 85% at 2-year follow-up. PI, PF, and ODI scores were significantly improved at all timepoints, independent of PLSS status. The mean SANE score in patients with PLSS was 82% ± 22% at 2-year follow-up. Patient history of hip surgery prior to BSIJF was associated with inferior postoperative ODI and SANE scores.
Conclusions: BSIJF is a safe and effective treatment that is associated with high rates of bony bridging at the sacroiliac joint and long-term clinically significant improvements in pain and function.
{"title":"Patient-Reported and Radiological Outcomes of Primary Bilateral Sacroiliac Joint Fusion Using a Principles-Based Approach.","authors":"Megan L Anderson, Nicholas G Rhodes, Michelle Y Hung, Ankur Khanna, William W Cross","doi":"10.14444/8789","DOIUrl":"10.14444/8789","url":null,"abstract":"<p><strong>Background: </strong>Bilateral sacroiliac joint fusion (BSIJF) is an accepted management strategy for sacroiliac joint dysfunction, though outcomes data are limited by patient number and lack of long-term follow-up. This study investigated the clinical, radiological, and patient-reported outcomes of BSIJF.</p><p><strong>Methods: </strong>A retrospective review was conducted of all patients who underwent BSIJF with a single surgeon between 2020 and 2023. All BSIJF utilized a principles-based approach: joint decortication, bone grafting, compression, and rigid stability. Patient-reported outcomes at preoperative, 6-month, 1-year, and 2-year follow-up timepoints were recorded for the Numeric Pain Rating Scale, Oswestry Disability Index (ODI), Single Assessment Numeric Evaluation (SANE), PROMIS Pain Interference (PI), and PROMIS Physical Function (PF). Fusion grading was assessed by computed tomography after 1 and 2 years.</p><p><strong>Results: </strong>Forty-eight patients who underwent BSIJF were included, of whom 31 (65%) were women with a mean age of 54 ± 14 years and a mean body mass index of 29 ± 5. Twenty-five patients (52%) had prior lumbar spine surgery (PLSS). One patient required revision for implant malpositioning and nerve impingement. Bridging bone across the sacroiliac joint was observed in 85% of patients. Numeric Pain Rating Scale scores dropped significantly from 7.6 preoperatively to 3.9, 3.3, and 3.7 at 6-month, 1-year, and 2-year follow-ups, respectively (<i>P</i> ≤ 0.004). PI and PF scores were significantly improved at all timepoints (all <i>P</i> < 0.001). ODI scores demonstrated sustained improvement from 52.3 preoperatively to 33.3 at 1-year follow-up and 29.3 at 2-year follow-up (<i>P</i> < 0.001). SANE scores were 80% at 1-year follow-up and 85% at 2-year follow-up. PI, PF, and ODI scores were significantly improved at all timepoints, independent of PLSS status. The mean SANE score in patients with PLSS was 82% ± 22% at 2-year follow-up. Patient history of hip surgery prior to BSIJF was associated with inferior postoperative ODI and SANE scores.</p><p><strong>Conclusions: </strong>BSIJF is a safe and effective treatment that is associated with high rates of bony bridging at the sacroiliac joint and long-term clinically significant improvements in pain and function.</p><p><strong>Level of evidence: 4: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"625-634"},"PeriodicalIF":1.7,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12679443/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145040841","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Saagar Dhanjani, Timothy Choi, Abdufarrukh Karimov, Kishan S Shah, Micah B Blais, Gregory M Mundis, Ali Bagheri, Behrooz A Akbarnia, Robert K Eastlack
Background: This study aims to determine whether single-level lateral lumbar interbody fusion (LLIF) with unilateral pedicle screw fixation (UPSF) might offer advantages over bilateral pedicle screw fixation (BPSF) in terms of radiation emission, cost, and outcomes.
Methods: The records of 101 patients who underwent single-level LLIF with percutaneous pedicle screw fixation from September 2017 to August 2024 were analyzed. Patients were divided into 2 groups: 42 with UPSF and 59 with BPSF. Demographic data, social history, comorbidities, surgical characteristics, costs (based on manufacturer prices), and radiation metrics (radiation emitted, fluoroscopy time, number of images, and magnification mode used) were collected. Clinical outcomes were assessed using the Numeric Rating Scale (NRS), the Oswestry Disability Index, and procedure satisfaction, while radiographic evaluation employed a novel fusion classification system.
Results: There were no significant differences in age, body mass index, social history, comorbidities, or operative level. However, the BPSF group included significantly more women (P = 0.002) and a higher proportion of spondylolisthesis cases (P < 0.001). Oswestry Disability Index and NRS scores were similar, except for greater improvements in NRS back pain at 1 year in the BPSF group (-4.0 vs -1.75, P = 0.008). While the total fluoroscopy time, number of images, and Mag 1 usage were greater in the BPSF group (all P < 0.001), the average radiation emitted did not significantly differ (39.38 milligray for UPSF vs 50.75 milligray for BPSF, P = 0.211). Fusion grades were comparable (P = 0.478), and UPSF costs were 27.7% lower.
Conclusions: Our study found that when used according to clinical indications, UPSF results in similar radiation emission and radiographic outcomes, while being 27.7% less expensive than BPSF for single-level LLIF. Additionally, while BPSF was associated with greater improvement in 1 year NRS back scores, no other significant differences in patient-reported outcome measures were observed between the 2 groups.
Clinical relevance: This study provides clinically relevant insights for selecting between UPSF and BPSF in single-level LLIF when both are considered appropriate.
Level of evidence: 3:
背景:本研究旨在确定单节段外侧腰椎椎体间融合术(LLIF)联合单侧椎弓根螺钉固定(UPSF)是否在放射、成本和结果方面优于双侧椎弓根螺钉固定(BPSF)。方法:分析2017年9月至2024年8月101例经皮经椎弓根螺钉内固定单节段LLIF患者的临床资料。将患者分为2组:UPSF组42例,BPSF组59例。收集了人口统计数据、社会历史、合并症、手术特征、成本(基于制造商价格)和辐射指标(辐射发射、透视时间、图像数量和使用的放大模式)。临床结果采用数字评定量表(NRS)、Oswestry残疾指数和手术满意度进行评估,而放射学评估采用一种新的融合分类系统。结果:两组患者在年龄、体重指数、社会病史、合并症、手术水平等方面无显著差异。然而,BPSF组包括更多的女性(P = 0.002)和更高比例的脊柱滑脱病例(P < 0.001)。Oswestry残疾指数和NRS评分相似,除了BPSF组1年NRS背痛的改善更大(-4.0 vs -1.75, P = 0.008)。虽然BPSF组的总透视时间、图像数量和1级显像使用更大(均P < 0.001),但平均放射量没有显著差异(UPSF组为39.38毫克,BPSF组为50.75毫克,P = 0.211)。融合等级具有可比性(P = 0.478), UPSF成本降低27.7%。结论:我们的研究发现,当根据临床适应症使用UPSF时,UPSF的辐射发射和放射学结果相似,而对于单级别LLIF, UPSF的费用比BPSF低27.7%。此外,虽然BPSF与1年NRS背部评分的更大改善相关,但在患者报告的结果测量中,两组之间没有观察到其他显著差异。临床相关性:本研究为单水平LLIF患者在UPSF和BPSF之间的选择提供了临床相关的见解。证据等级:3;
{"title":"Bilateral Pedicle Screw Fixation Vs Unilateral Pedicle Screw Fixation for Single Level Lateral Lumbar Interbody Fusion: Outcomes, Cost Analysis, and Radiation Exposure.","authors":"Saagar Dhanjani, Timothy Choi, Abdufarrukh Karimov, Kishan S Shah, Micah B Blais, Gregory M Mundis, Ali Bagheri, Behrooz A Akbarnia, Robert K Eastlack","doi":"10.14444/8794","DOIUrl":"https://doi.org/10.14444/8794","url":null,"abstract":"<p><strong>Background: </strong>This study aims to determine whether single-level lateral lumbar interbody fusion (LLIF) with unilateral pedicle screw fixation (UPSF) might offer advantages over bilateral pedicle screw fixation (BPSF) in terms of radiation emission, cost, and outcomes.</p><p><strong>Methods: </strong>The records of 101 patients who underwent single-level LLIF with percutaneous pedicle screw fixation from September 2017 to August 2024 were analyzed. Patients were divided into 2 groups: 42 with UPSF and 59 with BPSF. Demographic data, social history, comorbidities, surgical characteristics, costs (based on manufacturer prices), and radiation metrics (radiation emitted, fluoroscopy time, number of images, and magnification mode used) were collected. Clinical outcomes were assessed using the Numeric Rating Scale (NRS), the Oswestry Disability Index, and procedure satisfaction, while radiographic evaluation employed a novel fusion classification system.</p><p><strong>Results: </strong>There were no significant differences in age, body mass index, social history, comorbidities, or operative level. However, the BPSF group included significantly more women (<i>P</i> = 0.002) and a higher proportion of spondylolisthesis cases (<i>P</i> < 0.001). Oswestry Disability Index and NRS scores were similar, except for greater improvements in NRS back pain at 1 year in the BPSF group (-4.0 vs -1.75, <i>P</i> = 0.008). While the total fluoroscopy time, number of images, and Mag 1 usage were greater in the BPSF group (all <i>P</i> < 0.001), the average radiation emitted did not significantly differ (39.38 milligray for UPSF vs 50.75 milligray for BPSF, <i>P</i> = 0.211). Fusion grades were comparable (<i>P</i> = 0.478), and UPSF costs were 27.7% lower.</p><p><strong>Conclusions: </strong>Our study found that when used according to clinical indications, UPSF results in similar radiation emission and radiographic outcomes, while being 27.7% less expensive than BPSF for single-level LLIF. Additionally, while BPSF was associated with greater improvement in 1 year NRS back scores, no other significant differences in patient-reported outcome measures were observed between the 2 groups.</p><p><strong>Clinical relevance: </strong>This study provides clinically relevant insights for selecting between UPSF and BPSF in single-level LLIF when both are considered appropriate.</p><p><strong>Level of evidence: 3: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":""},"PeriodicalIF":1.7,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151388","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}
Marc Prod'homme, Maxime Saad, Jérôme Tonetti, Guillaume Cavalié, Gaël Kerschbaumer, Arun Thangavelu, Jean-Loup Gassend, Mehdi Boudissa
Background: Computerized navigation improves the accuracy of spine procedures. However, intraoperative imaging is plagued by ionizing irradiation and its cancer risk. Advanced technologies attempt to optimize the radiation dose. The goal of this study was to compare radiation exposure and screw accuracy of O-arm navigation and the Surgivisio device (SD) in pedicle screw insertion.
Methods: All patients operated on by navigated pedicle screw insertion during a 19-month period were prospectively included in 2 spine centers: the first with the O-arm and the second with the SD. Demographic, operative, and irradiation data were collected. The accuracy of the screw positioning was assessed using the Heary and Gertzbein classifications. The effective dose in millisievert (mSv) was calculated.
Results: One hundred patients were included, 50 per group. Five hundred and twelve screws were inserted, among them 228 in 120 vertebrae with the O-am and 284 in 145 vertebrae with the SD. Screw accuracy was 99.1% with the O-arm vs 93.3% with the SD (P = 0.07). Operative times were similar, with 145 vs 139 minutes respectively, P = 0.68. The effective dose was significantly higher in the O-arm group, with 5.43 vs 2.70 mSv with the SD (P < 0.01). The effective dose related to 2-dimensional imaging was significantly lower in the O-arm group than in the SD group, with 0.26 vs 1.16 mSv, respectively, P < 0.01, related to a shorter imaging duration (4 vs 109 seconds respectively, P < 0.01).
Conclusions: Accuracy of pedicle screws was higher with the O-arm than with the Surgivisio, but the latter showed less radiation exposure. Despite promising results, improvements in technology should be pursued for ergonomics and surgical safety.
Level of evidence: 4:
背景:计算机导航提高了脊柱手术的准确性。然而,术中成像受到电离辐射及其致癌风险的困扰。先进的技术试图优化辐射剂量。本研究的目的是比较o型臂导航和Surgivisio装置(SD)在椎弓根螺钉置入中的辐射暴露和螺钉精度。方法:在19个月的时间内,所有采用导航椎弓根螺钉置入手术的患者前瞻性地纳入2个脊柱中心:第一个是o型臂,第二个是SD。收集了人口学、手术和辐照数据。使用Heary和Gertzbein分类评估螺钉定位的准确性。计算了有效剂量,单位为毫西弗。结果:纳入100例患者,每组50例。共置入512枚螺钉,其中O-am椎体置入120枚228枚,SD椎体置入145枚284枚。o型臂的螺钉精度为99.1%,SD为93.3% (P = 0.07)。手术时间相似,分别为145和139分钟,P = 0.68。0组有效剂量为5.43 vs2.70 mSv (P < 0.01)。与二维成像相关的有效剂量,o组明显低于SD组,分别为0.26 vs 1.16 mSv, P < 0.01,与成像时间较短相关(4 vs 109 s, P < 0.01)。结论:o型臂固定椎弓根螺钉的准确性高于Surgivisio,但后者的辐射暴露较少。尽管有很好的结果,技术的改进应该追求人体工程学和手术安全。证据等级:4;
{"title":"O-Arm Vs Surgivisio for Pedicle Screw Insertion: A Prospective Study on Screw Accuracy and Irradiation on 100 Patients.","authors":"Marc Prod'homme, Maxime Saad, Jérôme Tonetti, Guillaume Cavalié, Gaël Kerschbaumer, Arun Thangavelu, Jean-Loup Gassend, Mehdi Boudissa","doi":"10.14444/8766","DOIUrl":"10.14444/8766","url":null,"abstract":"<p><strong>Background: </strong>Computerized navigation improves the accuracy of spine procedures. However, intraoperative imaging is plagued by ionizing irradiation and its cancer risk. Advanced technologies attempt to optimize the radiation dose. The goal of this study was to compare radiation exposure and screw accuracy of O-arm navigation and the Surgivisio device (SD) in pedicle screw insertion.</p><p><strong>Methods: </strong>All patients operated on by navigated pedicle screw insertion during a 19-month period were prospectively included in 2 spine centers: the first with the O-arm and the second with the SD. Demographic, operative, and irradiation data were collected. The accuracy of the screw positioning was assessed using the Heary and Gertzbein classifications. The effective dose in millisievert (mSv) was calculated.</p><p><strong>Results: </strong>One hundred patients were included, 50 per group. Five hundred and twelve screws were inserted, among them 228 in 120 vertebrae with the O-am and 284 in 145 vertebrae with the SD. Screw accuracy was 99.1% with the O-arm vs 93.3% with the SD (<i>P</i> = 0.07). Operative times were similar, with 145 vs 139 minutes respectively, <i>P</i> = 0.68. The effective dose was significantly higher in the O-arm group, with 5.43 vs 2.70 mSv with the SD (<i>P</i> < 0.01). The effective dose related to 2-dimensional imaging was significantly lower in the O-arm group than in the SD group, with 0.26 vs 1.16 mSv, respectively, <i>P</i> < 0.01, related to a shorter imaging duration (4 vs 109 seconds respectively, <i>P</i> < 0.01).</p><p><strong>Conclusions: </strong>Accuracy of pedicle screws was higher with the O-arm than with the Surgivisio, but the latter showed less radiation exposure. Despite promising results, improvements in technology should be pursued for ergonomics and surgical safety.</p><p><strong>Level of evidence: 4: </strong></p>","PeriodicalId":38486,"journal":{"name":"International Journal of Spine Surgery","volume":" ","pages":"383-391"},"PeriodicalIF":1.7,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12570053/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144318233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}