The 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis

Background:. Thoracic spine height is cited as a crucial outcome measure in the treatment of early-onset scoliosis (EOS) because of its reported relationship to pulmonary function tests (PFTs). An 18-cm threshold has been proposed, although this single parameter might be overly simplistic for cases...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Charles E. Johnston, MD, Lori A. Karol, MD, David Thornberg, BS, Chanhee Jo, PhD, Pablo Eamara, MD
Formato: article
Lenguaje:EN
Publicado: Wolters Kluwer 2021
Materias:
Acceso en línea:https://doaj.org/article/f3e4dfb96c2d42c79ccec4fbdd8b11d7
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:f3e4dfb96c2d42c79ccec4fbdd8b11d7
record_format dspace
spelling oai:doaj.org-article:f3e4dfb96c2d42c79ccec4fbdd8b11d72021-11-25T07:59:02ZThe 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis2472-724510.2106/JBJS.OA.21.00093https://doaj.org/article/f3e4dfb96c2d42c79ccec4fbdd8b11d72021-12-01T00:00:00Zhttp://journals.lww.com/jbjsoa/fulltext/10.2106/JBJS.OA.21.00093https://doaj.org/toc/2472-7245Background:. Thoracic spine height is cited as a crucial outcome measure in the treatment of early-onset scoliosis (EOS) because of its reported relationship to pulmonary function tests (PFTs). An 18-cm threshold has been proposed, although this single parameter might be overly simplistic for cases of different etiologies and deformity magnitude. We aimed to reevaluate pulmonary function in patients undergoing corrective surgery, assessing the role of residual scoliosis as well as spine elongation Methods:. Patients undergoing EOS correction with a minimum of 5 years of follow-up since initial treatment were evaluated. Standard spirometry (forced vital capacity [FVC], forced expiratory volume in 1 second [FEV1]) was correlated to deformity magnitude and T1-T12 height. Patients were compared by age at first surgery (<5 or ≥5 years), final thoracic height (≤18 or >18 cm), and percentage of predicted pulmonary function (<60% or ≥60%). Results:. Twenty-nine patients (15 congenital, 11 syndromic, and 3 idiopathic cases) were tested at a mean of 8.5 years following initial surgery. Twenty-two patients (mean initial age, 4.8 years) had growth-sparing instrumentation, and 7 patients (age, 5.1 years) had definitive fusion performed. Age at initial surgery was not associated with a difference in PFT results at the time of follow-up, and both age groups had ominously low percentages of predicted pulmonary-function volumes (50% to 55%). Only 18 of the 29 patients achieved a T1-T12 height of >18 cm. Those with a thoracic height of ≤18 cm had similar percentage-of-predicted spirometry results at the time of follow-up as those with greater thoracic height, possibly because of increased deformity correction. Only 14 of 29 patients had spirometry of ≥60% of predicted volume at the time of follow-up. These 14 had slightly smaller curves and slightly greater T1-T12 heights but significantly better spirometry results than the 15 subjects with <60% of predicted volume. For those with a T1-T12 height of ≤18 cm, the residual Cobb angle negatively correlated with spirometry results. In those with a final T1-T12 height of >18 cm, spirometry did correlate with thoracic height, especially when residual deformity was ≥60°. Conclusions:. Regardless of thoracic height of ≤18 or >18 cm, with residual curves of >50o, pulmonary function was ominously low in fully half of the patients, raising doubt about the value of this threshold as an EOS outcome parameter. Level of Evidence:. Prognostic Level IV. See Instructions for Authors for a complete description of levels of evidence.Charles E. Johnston, MDLori A. Karol, MDDavid Thornberg, BSChanhee Jo, PhDPablo Eamara, MDWolters KluwerarticleOrthopedic surgeryRD701-811ENJBJS Open Access, Vol 6, Iss 4 (2021)
institution DOAJ
collection DOAJ
language EN
topic Orthopedic surgery
RD701-811
spellingShingle Orthopedic surgery
RD701-811
Charles E. Johnston, MD
Lori A. Karol, MD
David Thornberg, BS
Chanhee Jo, PhD
Pablo Eamara, MD
The 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis
description Background:. Thoracic spine height is cited as a crucial outcome measure in the treatment of early-onset scoliosis (EOS) because of its reported relationship to pulmonary function tests (PFTs). An 18-cm threshold has been proposed, although this single parameter might be overly simplistic for cases of different etiologies and deformity magnitude. We aimed to reevaluate pulmonary function in patients undergoing corrective surgery, assessing the role of residual scoliosis as well as spine elongation Methods:. Patients undergoing EOS correction with a minimum of 5 years of follow-up since initial treatment were evaluated. Standard spirometry (forced vital capacity [FVC], forced expiratory volume in 1 second [FEV1]) was correlated to deformity magnitude and T1-T12 height. Patients were compared by age at first surgery (<5 or ≥5 years), final thoracic height (≤18 or >18 cm), and percentage of predicted pulmonary function (<60% or ≥60%). Results:. Twenty-nine patients (15 congenital, 11 syndromic, and 3 idiopathic cases) were tested at a mean of 8.5 years following initial surgery. Twenty-two patients (mean initial age, 4.8 years) had growth-sparing instrumentation, and 7 patients (age, 5.1 years) had definitive fusion performed. Age at initial surgery was not associated with a difference in PFT results at the time of follow-up, and both age groups had ominously low percentages of predicted pulmonary-function volumes (50% to 55%). Only 18 of the 29 patients achieved a T1-T12 height of >18 cm. Those with a thoracic height of ≤18 cm had similar percentage-of-predicted spirometry results at the time of follow-up as those with greater thoracic height, possibly because of increased deformity correction. Only 14 of 29 patients had spirometry of ≥60% of predicted volume at the time of follow-up. These 14 had slightly smaller curves and slightly greater T1-T12 heights but significantly better spirometry results than the 15 subjects with <60% of predicted volume. For those with a T1-T12 height of ≤18 cm, the residual Cobb angle negatively correlated with spirometry results. In those with a final T1-T12 height of >18 cm, spirometry did correlate with thoracic height, especially when residual deformity was ≥60°. Conclusions:. Regardless of thoracic height of ≤18 or >18 cm, with residual curves of >50o, pulmonary function was ominously low in fully half of the patients, raising doubt about the value of this threshold as an EOS outcome parameter. Level of Evidence:. Prognostic Level IV. See Instructions for Authors for a complete description of levels of evidence.
format article
author Charles E. Johnston, MD
Lori A. Karol, MD
David Thornberg, BS
Chanhee Jo, PhD
Pablo Eamara, MD
author_facet Charles E. Johnston, MD
Lori A. Karol, MD
David Thornberg, BS
Chanhee Jo, PhD
Pablo Eamara, MD
author_sort Charles E. Johnston, MD
title The 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis
title_short The 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis
title_full The 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis
title_fullStr The 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis
title_full_unstemmed The 18-cm Thoracic-Height Threshold and Pulmonary Function in Non-Neuromuscular Early-Onset Scoliosis
title_sort 18-cm thoracic-height threshold and pulmonary function in non-neuromuscular early-onset scoliosis
publisher Wolters Kluwer
publishDate 2021
url https://doaj.org/article/f3e4dfb96c2d42c79ccec4fbdd8b11d7
work_keys_str_mv AT charlesejohnstonmd the18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT loriakarolmd the18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT davidthornbergbs the18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT chanheejophd the18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT pabloeamaramd the18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT charlesejohnstonmd 18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT loriakarolmd 18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT davidthornbergbs 18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT chanheejophd 18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
AT pabloeamaramd 18cmthoracicheightthresholdandpulmonaryfunctioninnonneuromuscularearlyonsetscoliosis
_version_ 1718413593673728000