TY - JOUR
T1 - Fusions ending above the sagittal stable vertebrae in adolescent idiopathic scoliosis
T2 - does it matter?
AU - Harms Study Group
AU - Segal, Dale N.
AU - Orland, Keith J.
AU - Yoon, Eric
AU - Bastrom, Tracey
AU - Fletcher, Nicholas D.
AU - Buckland, Aaron
AU - Samdani, Amer
AU - Jain, Amit
AU - Lonner, Baron
AU - Roye, Benjamin
AU - Yaszay, Burt
AU - Reilly, Chris
AU - Hedequist, Daniel
AU - Sucato, Daniel
AU - Clements, David
AU - Miyanji, Firoz
AU - Shufflebarger, Harry
AU - Flynn, Jack
AU - Asghar, Jahangir
AU - Thiong, Jean Marc Mac
AU - Pahys, Joshua
AU - Harms, Juergen
AU - Bachmann, Keith
AU - Lenke, Larry
AU - Abel, Mark
AU - Glotzbecker, Michael
AU - Kelly, Michael
AU - Vitale, Michael
AU - Marks, Michelle
AU - Gupta, Munish
AU - Fletcher, Nicholas
AU - Cahill, Patrick
AU - Sponseller, Paul
AU - Gabos, Peter
AU - Newton, Peter
AU - Sturm, Peter
AU - Betz, Randal
AU - Lehman, Ron
AU - Parent, Stefan
AU - George, Stephen
AU - Hwang, Steven
AU - Shah, Suken
AU - Errico, Tom
AU - Upasani, Vidyadhar
N1 - Funding Information:
Harms Study Group: Grants were received from DePuy Synthes Spine to the Setting Scoliosis Straight Foundation in support of Harms Study Group research Nicholas D. Fletcher: reports grants from Harrison Foundation, personal fees from Orthopaediatrics, personal fees from Medtronic Spine, personal fees from Nuvasive, personal fees from Zimmer Biomet, outside the submitted work. This study was supported in part by grants to the Setting Scoliosis Straight Foundation in support of Harms Study Group research from DePuy Synthes Spine, EOS imaging, K2M, Medtronic, NuVasive and Zimmer Biomet.
Funding Information:
Harms Study Group: Grants were received from DePuy Synthes Spine to the Setting Scoliosis Straight Foundation in support of Harms Study Group research Nicholas D. Fletcher: reports grants from Harrison Foundation, personal fees from Orthopaediatrics, personal fees from Medtronic Spine, personal fees from Nuvasive, personal fees from Zimmer Biomet, outside the submitted work. This study was supported in part by grants to the Setting Scoliosis Straight Foundation in support of Harms Study Group research from DePuy Synthes Spine, EOS imaging, K2M, Medtronic, NuVasive and Zimmer Biomet. Harms Study Group Investigators: Aaron Buckland, MD: New York University; Amer Samdani, MD: Shriners Hospitals for Children—Philadelphia; Amit Jain, MD: Johns Hopkins Hospital; Baron Lonner, MD: Mount Sinai Hospital; Benjamin Roye, MD: Columbia University; Burt Yaszay, MD: Rady Children’s Hospital; Chris Reilly, MD: BC Children’s Hospital; Daniel Hedequist, MD: Boston Children’s Hospital; Daniel Sucato, MD: Texas Scottish Rite Hospital; David Clements, MD: Cooper Bone & Joint Institute New Jersey; Firoz Miyanji, MD: BC Children’s Hospital; Harry Shufflebarger, MD: Nicklaus Children's Hospital; Jack Flynn, MD: Children’s Hospital of Philadelphia; Jahangir Asghar, MD: Cantor Spine Institute; Jean Marc Mac Thiong, MD: CHU Sainte-Justine; Joshua Pahys, MD: Shriners Hospitals for Children—Philadelphia; Juergen Harms, MD: Klinikum Karlsbad-Langensteinbach, Karlsbad; Keith Bachmann, MD: University of Virginia; Larry Lenke, MD: Columbia University; Mark Abel, MD: University of Virginia; Michael Glotzbecker, MD: Boston Children’s Hospital; Michael Kelly, MD: Washington University; Michael Vitale, MD: Columbia University; Michelle Marks, PT, MA: Setting Scoliosis Straight Foundation; Munish Gupta, MD: Washington University; Nicholas Fletcher, MD: Emory University; Patrick Cahill, MD: Children’s Hospital of Philadelphia; Paul Sponseller, MD: Johns Hopkins Hospital; Peter Gabos, MD: Nemours/Alfred I. duPont Hospital for Children; Peter Newton, MD: Rady Children’s Hospital; Peter Sturm, MD: Cincinnati Children’s Hospital; Randal Betz, MD: Institute for Spine & Scoliosis; Ron Lehman, MD: Columbia University; Stefan Parent, MD: CHU Sainte-Justine; Stephen George, MD: Nicklaus Children's Hospital; Steven Hwang, MD: Shriners Hospitals for Children—Philadelphia; Suken Shah, MD: Nemours/Alfred I. duPont Hospital for Children; Tom Errico, MD: Nicklaus Children's Hospital; Vidyadhar Upasani, MD: Rady Children’s Hospital.
Funding Information:
Dale N. Segal, Keith J. Orland, Eric Yoon, Tracy Bastrom have no conflicts of interest to declare. Harms Study Group: Grants were received from DePuy Synthes Spine to the Setting Scoliosis Straight Foundation in support of Harms Study Group research. Nicholas D. Fletcher: reports grants from Harrison Foundation, personal fees from Orthopaediatrics, personal fees from Medtronic Spine, personal fees from Nuvasive, personal fees from Zimmer Biomet, outside the submitted work.
Publisher Copyright:
© 2020, Scoliosis Research Society.
PY - 2022/10
Y1 - 2022/10
N2 - Study design: Retrospective cohort study. Objective: To validate whether fusions that end proximal to the sagittal stable vertebrae are at risk for developing distal junctional kyphosis in adolescent idiopathic scoliosis. Background: Posterior spinal fusion is routinely used for the treatment of patients with adolescent idiopathic scoliosis. Fusions that end in either the lower thoracic or upper lumbar spine have the advantage of preserving motion segments. However, fusions ending proximal to the sagittal stable vertebrae has been shown to be at higher risk for developing distal junctional kyphosis. Methods: A multi-center database of prospectively enrolled subjects was queried for patients with adolescent idiopathic scoliosis that had Lenke type 1, 2 and 3 curves treated with posterior pedicle screw instrumentation. PA (posterior-anterior) and lateral full-length scoliosis films were obtained on each patient. PA radiographs were viewed to determine the coronal deformity and lateral radiographs to determine the sagittal deformity. Distal junctional kyphosis was defined as a greater than 10° increase in segmental kyphosis between the LIV and the LIV + 1 vertebra. Results: 346 patients were included with 85% being female and mean age of cohort 14.2 ± 2.08 years. At 5 years postoperatively, there was significant difference occurrence of distal junctional kyphosis dependent on whether the LIV relative to SSV with only 2.2% of fusions below the SSV developing DJK compared to 6.5% for fusions ending at the SSV and 15% for fusions with LIV above the SSV (p ' 0.001). There was no statistical difference in revision rates based on the relationship of LIV to SSV. Conclusion: There is an increased risk for development of DJK in patients with AIS treated with posterior fusion where the LIV was chosen proximal to the SSV. Level evidence: Level III.
AB - Study design: Retrospective cohort study. Objective: To validate whether fusions that end proximal to the sagittal stable vertebrae are at risk for developing distal junctional kyphosis in adolescent idiopathic scoliosis. Background: Posterior spinal fusion is routinely used for the treatment of patients with adolescent idiopathic scoliosis. Fusions that end in either the lower thoracic or upper lumbar spine have the advantage of preserving motion segments. However, fusions ending proximal to the sagittal stable vertebrae has been shown to be at higher risk for developing distal junctional kyphosis. Methods: A multi-center database of prospectively enrolled subjects was queried for patients with adolescent idiopathic scoliosis that had Lenke type 1, 2 and 3 curves treated with posterior pedicle screw instrumentation. PA (posterior-anterior) and lateral full-length scoliosis films were obtained on each patient. PA radiographs were viewed to determine the coronal deformity and lateral radiographs to determine the sagittal deformity. Distal junctional kyphosis was defined as a greater than 10° increase in segmental kyphosis between the LIV and the LIV + 1 vertebra. Results: 346 patients were included with 85% being female and mean age of cohort 14.2 ± 2.08 years. At 5 years postoperatively, there was significant difference occurrence of distal junctional kyphosis dependent on whether the LIV relative to SSV with only 2.2% of fusions below the SSV developing DJK compared to 6.5% for fusions ending at the SSV and 15% for fusions with LIV above the SSV (p ' 0.001). There was no statistical difference in revision rates based on the relationship of LIV to SSV. Conclusion: There is an increased risk for development of DJK in patients with AIS treated with posterior fusion where the LIV was chosen proximal to the SSV. Level evidence: Level III.
KW - Adolescent idiopathic scoliosis
KW - Distal junctional kyphosis
KW - Sagittal stable vertabrae
UR - http://www.scopus.com/inward/record.url?scp=85084793881&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85084793881&partnerID=8YFLogxK
U2 - 10.1007/s43390-020-00118-0
DO - 10.1007/s43390-020-00118-0
M3 - Article
C2 - 32405718
AN - SCOPUS:85084793881
SN - 2212-134X
VL - 8
SP - 983
EP - 989
JO - Spine deformity
JF - Spine deformity
IS - 5
ER -