TY - JOUR
T1 - Can distraction-based surgeries achieve minimum 18 cm thoracic height for patients with early onset scoliosis?
AU - Pediatric Spine Study Group
AU - ElBromboly, Yehia
AU - Hurry, Jennifer
AU - Johnston, Charles
AU - McClung, Anna
AU - Samdani, Amer
AU - Glotzbecker, Michael
AU - Hilaire, Tricia St
AU - Flynn, Tara
AU - El-Hawary, Ron
N1 - Funding Information:
Dr. Elbromboly, Ms Hurry, Ms McClung, Ms St. Hilaire, and Ms Flynn have nothing to disclose. Dr. Johnston reports other from Medtronic, other from Elsevier, outside the submitted work. Dr. Samdani reports personal fees from DePuy Synthes Spine, personal fees from Ethicon, personal fees from Globus Medical, personal fees from NuVasive, personal fees from Stryker, personal fees from Zimmer Biomet, outside the submitted work; and Executive Committee, Setting Scoliosis Straight Foundation Executive Committee, Children's Spine Study Group. Dr. Glotzbecker reports other from Orthobullets, other from Nuvasive, other from Depuy, other from Zimmer Biomet, other from Medtronic, other from GSSG, CSSG, HSG, outside the submitted work. Pediatric Spine Study Group reports grants from DePuy Synthes Spime, grants from Nuvasive, outside the submitted work. Dr. El-Hawary reports personal fees from Depuy Synthes Spine, personal fees from Medtronic Spine, grants from Depuy Synthes Spine, grants from Medtronic Spine, personal fees from Apifix Ltd., other from Children's Spine Foundation, other from Pediatric Orthopedic Society of North America, other from Scoliosis Research Society, personal fees from Wishbone Medical, outside the submitted work.
Funding Information:
No funding was received for the study. The research was supported by the Pediatric Spine Study Group. Acknowledgements
Publisher Copyright:
© 2020, Scoliosis Research Society.
PY - 2021/3
Y1 - 2021/3
N2 - Purpose: Karol et al. introduced the concept that 18 cm thoracic height is the critical point where a patient with early onset scoliosis (EOS) can maintain adequate pulmonary function. Our purpose was to determine if distraction-based surgeries will increase thoracic spine height to at least 18 cm in patients with EOS. Methods: Patients with EOS treated with distraction-based systems (minimum 5 years follow up, minimum five lengthenings). Radiographic analysis of thoracic spine height (T1–T12) at the last lengthening procedure. Results: One hundred and fifty-three patients (67 congenital, 21 neuromuscular, 38 syndromic, 27 idiopathic) with pre-operative mean age 4.6 years, scoliosis 75°, kyphosis 47° were evaluated. Their mean age at final lengthening procedure was 11 years (6–16), average number of lengthening procedures was 10.5 (4–21), mean final scoliosis was 53°, and mean final kyphosis was 58°. Final thoracic height was > 18 cm in 65% and was > 22 cm in 31% of patients. Based on etiology, only 48% of the congenital patients reached 18 cm compared to 81% neuromuscular, 84% syndromic and 67% idiopathic. This height gain was closely related to the percentage of scoliosis correction achieved for each etiology. Comparing congenital etiology to other etiologies, there was a lower percentage of patients in the congenital group that passed the 18 cm threshold (48% vs. 78%) (p < 0.05). Conclusion: At minimum 5 years follow up, distraction-based surgeries increased thoracic height for patients with EOS to greater than 18 cm in 65% of patients; however, only 48% of congenital patients reached this thoracic height threshold. Design: Retrospective review of prospectively collected registry data. LOI III.
AB - Purpose: Karol et al. introduced the concept that 18 cm thoracic height is the critical point where a patient with early onset scoliosis (EOS) can maintain adequate pulmonary function. Our purpose was to determine if distraction-based surgeries will increase thoracic spine height to at least 18 cm in patients with EOS. Methods: Patients with EOS treated with distraction-based systems (minimum 5 years follow up, minimum five lengthenings). Radiographic analysis of thoracic spine height (T1–T12) at the last lengthening procedure. Results: One hundred and fifty-three patients (67 congenital, 21 neuromuscular, 38 syndromic, 27 idiopathic) with pre-operative mean age 4.6 years, scoliosis 75°, kyphosis 47° were evaluated. Their mean age at final lengthening procedure was 11 years (6–16), average number of lengthening procedures was 10.5 (4–21), mean final scoliosis was 53°, and mean final kyphosis was 58°. Final thoracic height was > 18 cm in 65% and was > 22 cm in 31% of patients. Based on etiology, only 48% of the congenital patients reached 18 cm compared to 81% neuromuscular, 84% syndromic and 67% idiopathic. This height gain was closely related to the percentage of scoliosis correction achieved for each etiology. Comparing congenital etiology to other etiologies, there was a lower percentage of patients in the congenital group that passed the 18 cm threshold (48% vs. 78%) (p < 0.05). Conclusion: At minimum 5 years follow up, distraction-based surgeries increased thoracic height for patients with EOS to greater than 18 cm in 65% of patients; however, only 48% of congenital patients reached this thoracic height threshold. Design: Retrospective review of prospectively collected registry data. LOI III.
KW - Early onset scoliosis
KW - Growing rods
KW - Halifax method
KW - Sagittal spine length (SSL)
KW - Spine growth
KW - Thoracic height
KW - VEPTR
UR - http://www.scopus.com/inward/record.url?scp=85094630213&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85094630213&partnerID=8YFLogxK
U2 - 10.1007/s43390-020-00230-1
DO - 10.1007/s43390-020-00230-1
M3 - Article
C2 - 33123987
AN - SCOPUS:85094630213
SN - 2212-134X
VL - 9
SP - 603
EP - 608
JO - Spine Deformity
JF - Spine Deformity
IS - 2
ER -