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Relationship between postoperative lordosis distribution index and adjacent segment disease following L4-S1 posterior lumbar interbody fusion

Adjacent segment disease (ASD) is an acknowledged problem of posterior lumbar interbody fusion (PLIF). Many studies have been reported concerning the role of lordosis distribution index (LDI) in spinal biomechanics. However, few reports have been published about the impact of LDI on ASD following L4...

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Published in:Journal of orthopaedic surgery and research 2020-04, Vol.15 (1), p.129-129, Article 129
Main Authors: Zheng, Guoquan, Wang, Chunguo, Wang, Tianhao, Hu, Wenhao, Ji, Quanbo, Hu, Fanqi, Li, Jianrui, Chaudhary, Surendra K, Song, Kai, Song, Diyu, Zhang, Zhifa, Hao, Yongyu, Wang, Yao, Li, Jing, Zheng, Qingyuan, Zhang, Xuesong, Wang, Yan
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container_title Journal of orthopaedic surgery and research
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creator Zheng, Guoquan
Wang, Chunguo
Wang, Tianhao
Hu, Wenhao
Ji, Quanbo
Hu, Fanqi
Li, Jianrui
Chaudhary, Surendra K
Song, Kai
Song, Diyu
Zhang, Zhifa
Hao, Yongyu
Wang, Yao
Li, Jing
Zheng, Qingyuan
Zhang, Xuesong
Wang, Yan
description Adjacent segment disease (ASD) is an acknowledged problem of posterior lumbar interbody fusion (PLIF). Many studies have been reported concerning the role of lordosis distribution index (LDI) in spinal biomechanics. However, few reports have been published about the impact of LDI on ASD following L4-S1 PLIF. The study enrolled 200 subjects who underwent L4-S1 PLIF for degenerative spine disease from 2009 to 2014. The average follow-up term was 84 months. Several lower lumbar parameters were measured, including lower lumbar lordosis (LLL), lumbar lordosis (LL), pelvic incidence (PI), and LDI on the pre and postoperative radiograph. Perioperative information, comorbidities, and operative data were documented. Kaplan-Meier curves were plotted for the comparisons of ASD-free survival of 3 different types of postoperative LDI subgroups. The incidence of ASD was found to be 8.5%. LL and LLL increased by 3.96° (38.71° vs 42.67°; P < 0.001) and 3.60° (26.22° vs 28.82°; P < 0.001) after lower lumbar fusion surgery, respectively. Lordosis distribution index (LDI) increased by 0.03 (0.66 vs 0.69, P = 0.004) postoperatively. A significant difference (P = 0.001) was observed when comparing the incidence of ASD among postoperative LDI subgroups. The Kaplan-Meier curves showed a marked difference in ASD-free survival between low and moderate LDI subgroup (log-rank test, P = 0.0012) and high and moderate LDI subgroup (log-rank test, P = 0.0005). Patients with abnormal postoperative LDI were statistically more likely to develop ASD than those who had normal postoperative LDI. Moreover, patients with low postoperative LDI were at greater risk for developing ASD than those with high postoperative LDI over time.
doi_str_mv 10.1186/s13018-020-01630-9
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Many studies have been reported concerning the role of lordosis distribution index (LDI) in spinal biomechanics. However, few reports have been published about the impact of LDI on ASD following L4-S1 PLIF. The study enrolled 200 subjects who underwent L4-S1 PLIF for degenerative spine disease from 2009 to 2014. The average follow-up term was 84 months. Several lower lumbar parameters were measured, including lower lumbar lordosis (LLL), lumbar lordosis (LL), pelvic incidence (PI), and LDI on the pre and postoperative radiograph. Perioperative information, comorbidities, and operative data were documented. Kaplan-Meier curves were plotted for the comparisons of ASD-free survival of 3 different types of postoperative LDI subgroups. The incidence of ASD was found to be 8.5%. LL and LLL increased by 3.96° (38.71° vs 42.67°; P &lt; 0.001) and 3.60° (26.22° vs 28.82°; P &lt; 0.001) after lower lumbar fusion surgery, respectively. Lordosis distribution index (LDI) increased by 0.03 (0.66 vs 0.69, P = 0.004) postoperatively. A significant difference (P = 0.001) was observed when comparing the incidence of ASD among postoperative LDI subgroups. The Kaplan-Meier curves showed a marked difference in ASD-free survival between low and moderate LDI subgroup (log-rank test, P = 0.0012) and high and moderate LDI subgroup (log-rank test, P = 0.0005). Patients with abnormal postoperative LDI were statistically more likely to develop ASD than those who had normal postoperative LDI. 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Many studies have been reported concerning the role of lordosis distribution index (LDI) in spinal biomechanics. However, few reports have been published about the impact of LDI on ASD following L4-S1 PLIF. The study enrolled 200 subjects who underwent L4-S1 PLIF for degenerative spine disease from 2009 to 2014. The average follow-up term was 84 months. Several lower lumbar parameters were measured, including lower lumbar lordosis (LLL), lumbar lordosis (LL), pelvic incidence (PI), and LDI on the pre and postoperative radiograph. Perioperative information, comorbidities, and operative data were documented. Kaplan-Meier curves were plotted for the comparisons of ASD-free survival of 3 different types of postoperative LDI subgroups. The incidence of ASD was found to be 8.5%. LL and LLL increased by 3.96° (38.71° vs 42.67°; P &lt; 0.001) and 3.60° (26.22° vs 28.82°; P &lt; 0.001) after lower lumbar fusion surgery, respectively. 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Many studies have been reported concerning the role of lordosis distribution index (LDI) in spinal biomechanics. However, few reports have been published about the impact of LDI on ASD following L4-S1 PLIF. The study enrolled 200 subjects who underwent L4-S1 PLIF for degenerative spine disease from 2009 to 2014. The average follow-up term was 84 months. Several lower lumbar parameters were measured, including lower lumbar lordosis (LLL), lumbar lordosis (LL), pelvic incidence (PI), and LDI on the pre and postoperative radiograph. Perioperative information, comorbidities, and operative data were documented. Kaplan-Meier curves were plotted for the comparisons of ASD-free survival of 3 different types of postoperative LDI subgroups. The incidence of ASD was found to be 8.5%. LL and LLL increased by 3.96° (38.71° vs 42.67°; P &lt; 0.001) and 3.60° (26.22° vs 28.82°; P &lt; 0.001) after lower lumbar fusion surgery, respectively. Lordosis distribution index (LDI) increased by 0.03 (0.66 vs 0.69, P = 0.004) postoperatively. A significant difference (P = 0.001) was observed when comparing the incidence of ASD among postoperative LDI subgroups. The Kaplan-Meier curves showed a marked difference in ASD-free survival between low and moderate LDI subgroup (log-rank test, P = 0.0012) and high and moderate LDI subgroup (log-rank test, P = 0.0005). Patients with abnormal postoperative LDI were statistically more likely to develop ASD than those who had normal postoperative LDI. Moreover, patients with low postoperative LDI were at greater risk for developing ASD than those with high postoperative LDI over time.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>32245387</pmid><doi>10.1186/s13018-020-01630-9</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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1749-799X
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source Publicly Available Content Database; PubMed Central
subjects Adjacent segment disease
Age
Aged
Analysis
Arthritis
Back surgery
Biomechanics
Body mass index
Clinical outcomes
Comorbidity
Data collection
Degenerative disc disease
Disease susceptibility
Female
Follow-Up Studies
Fractures
Gender
Hospitals
Humans
Lordosis
Lordosis - diagnostic imaging
Lordosis - etiology
Lordosis distribution index
Lower lumbar lordosis
Lumbar lordosis
Lumbar Vertebrae - diagnostic imaging
Lumbar Vertebrae - surgery
Male
Middle Aged
Orthopedics
Patients
Posterior lumbar interbody fusion
Postoperative Complications - diagnostic imaging
Postoperative Complications - etiology
Postoperative period
Retrospective Studies
Sacrum - diagnostic imaging
Sacrum - surgery
Scoliosis
Spinal Diseases - diagnostic imaging
Spinal Diseases - surgery
Spinal Fusion - adverse effects
Spinal Fusion - trends
Spine (lumbar)
Statistical analysis
Surgeons
Surgery
Survival
title Relationship between postoperative lordosis distribution index and adjacent segment disease following L4-S1 posterior lumbar interbody fusion
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