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Predictors of persistent postoperative pain after surgery for idiopathic scoliosis

PURPOSE: To identify factors contributing to persistent postoperative pain in patients treated surgically for idiopathic scoliosis. METHODS: In total, 280 patients aged ten through 25 years at surgery, were identified in the Swedish Spine registry; all having preoperative and postoperative visual an...

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Autores principales: Charalampidis, Anastasios, Rundberg, Lina, Möller, Hans, Gerdhem, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Editorial Society of Bone & Joint Surgery 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582608/
https://www.ncbi.nlm.nih.gov/pubmed/34858532
http://dx.doi.org/10.1302/1863-2548.15.210090
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author Charalampidis, Anastasios
Rundberg, Lina
Möller, Hans
Gerdhem, Paul
author_facet Charalampidis, Anastasios
Rundberg, Lina
Möller, Hans
Gerdhem, Paul
author_sort Charalampidis, Anastasios
collection PubMed
description PURPOSE: To identify factors contributing to persistent postoperative pain in patients treated surgically for idiopathic scoliosis. METHODS: In total, 280 patients aged ten through 25 years at surgery, were identified in the Swedish Spine registry; all having preoperative and postoperative visual analogue scale (VAS) for back pain scores. The patients were divided into a high and low postoperative pain group based on the reported postoperative VAS for back pain scores (by using 45 mm on the 0 mm to 100 mm VAS scale as a cut-off). The patient-reported questionnaire included VAS for back pain, the 3-level version of EuroQol 5-dimensional (EQ-5D-3L) instrument, the EuroQol VAS (EQ-VAS) and the Scoliosis Research Society 22r instrument (SRS-22r). Predictors of postoperative back pain were searched in the preoperative data. RESULTS: The 67 (24%) patients that reported high postoperative VAS back pain (> 45 mm) also reported lower postoperative EQ-5D-3L, EQ-VAS and SRS-22r than patients with low postoperative VAS back pain (all p < 0.001). Two preoperative variables were independently associated with postoperative pain; each millimetre increase in preoperative VAS back pain (on the 0 mm to 100 mm scale) was associated with a higher risk of being in the high postoperative back pain group (odds ratio (OR) 1.03; 95% confidence interval (CI) 1.02 to 1.05) and each 1 point decrease on the preoperative SRS-22r mental health (scale from 1 to 5) was associated with a higher risk of being in the high postoperative back pain group (OR 1.68; 95% CI 1.03 to 2.73). CONCLUSION: High preoperative back pain and low preoperative mental health are independent predictors of back pain after surgery for idiopathic scoliosis. LEVEL OF EVIDENCE: III
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spelling pubmed-85826082021-12-01 Predictors of persistent postoperative pain after surgery for idiopathic scoliosis Charalampidis, Anastasios Rundberg, Lina Möller, Hans Gerdhem, Paul J Child Orthop Original Clinical Article PURPOSE: To identify factors contributing to persistent postoperative pain in patients treated surgically for idiopathic scoliosis. METHODS: In total, 280 patients aged ten through 25 years at surgery, were identified in the Swedish Spine registry; all having preoperative and postoperative visual analogue scale (VAS) for back pain scores. The patients were divided into a high and low postoperative pain group based on the reported postoperative VAS for back pain scores (by using 45 mm on the 0 mm to 100 mm VAS scale as a cut-off). The patient-reported questionnaire included VAS for back pain, the 3-level version of EuroQol 5-dimensional (EQ-5D-3L) instrument, the EuroQol VAS (EQ-VAS) and the Scoliosis Research Society 22r instrument (SRS-22r). Predictors of postoperative back pain were searched in the preoperative data. RESULTS: The 67 (24%) patients that reported high postoperative VAS back pain (> 45 mm) also reported lower postoperative EQ-5D-3L, EQ-VAS and SRS-22r than patients with low postoperative VAS back pain (all p < 0.001). Two preoperative variables were independently associated with postoperative pain; each millimetre increase in preoperative VAS back pain (on the 0 mm to 100 mm scale) was associated with a higher risk of being in the high postoperative back pain group (odds ratio (OR) 1.03; 95% confidence interval (CI) 1.02 to 1.05) and each 1 point decrease on the preoperative SRS-22r mental health (scale from 1 to 5) was associated with a higher risk of being in the high postoperative back pain group (OR 1.68; 95% CI 1.03 to 2.73). CONCLUSION: High preoperative back pain and low preoperative mental health are independent predictors of back pain after surgery for idiopathic scoliosis. LEVEL OF EVIDENCE: III The British Editorial Society of Bone & Joint Surgery 2021-10-01 /pmc/articles/PMC8582608/ /pubmed/34858532 http://dx.doi.org/10.1302/1863-2548.15.210090 Text en Copyright © 2021, The author(s) https://creativecommons.org/licenses/by-nc/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution-Non Commercial 4.0 International (CC BY-NC 4.0) licence (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed.
spellingShingle Original Clinical Article
Charalampidis, Anastasios
Rundberg, Lina
Möller, Hans
Gerdhem, Paul
Predictors of persistent postoperative pain after surgery for idiopathic scoliosis
title Predictors of persistent postoperative pain after surgery for idiopathic scoliosis
title_full Predictors of persistent postoperative pain after surgery for idiopathic scoliosis
title_fullStr Predictors of persistent postoperative pain after surgery for idiopathic scoliosis
title_full_unstemmed Predictors of persistent postoperative pain after surgery for idiopathic scoliosis
title_short Predictors of persistent postoperative pain after surgery for idiopathic scoliosis
title_sort predictors of persistent postoperative pain after surgery for idiopathic scoliosis
topic Original Clinical Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8582608/
https://www.ncbi.nlm.nih.gov/pubmed/34858532
http://dx.doi.org/10.1302/1863-2548.15.210090
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