Limited correction of lumbar lordosis in the treatment of degenerative scoliosis.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
May 2020
Historique:
entrez: 9 5 2020
pubmed: 10 5 2020
medline: 22 5 2020
Statut: ppublish

Résumé

Patients suffering from degenerative scoliosis (DS) were commonly associated with coronal and sagittal imbalance which made deformity correction surgery necessary. The study aimed to explore the efficacy and feasibility of the limited correction of lumbar lordosis (LL) in the treatment of patients with DS. This was a retrospective study including 58 DS patients who underwent spinal deformity correction surgery and were followed up at least 2 years between January 2013 and January 2017. According to the difference of postoperative LL, the patients were divided into 2 groups: the limited correction group: Pelvic incidence(PI)-18°≤ LL<PI-9° and the control group: PI-9°≤ LL<PI+9°. There were 31 patients in the limited group, and 27 patients in the control group. The clinical and radiographic outcomes were compared preoperatively and at the last follow-up evaluation. There was no significant difference between the 2 groups preoperatively (P > .05). In terms of surgery, the limited group had less intra-operative blood loss and operation time (P < .05). At the last follow-up, significant differences were found in terms of LL(-38.2 ± 4.7° and -46.9 ± 4.7°), PT (18.8 ± 5.2° and 11.1 ± 3.6°), sacrum slope (33.7 ± 7.0° and 41.4 ± 6.1°) (P < .05), while there were no significant differences in terms of lumbar Cobb angle (10.5 ± 9.3°and 8.3 ± 6.7°), Oswestry Disability Index scores (25.6 ± 10.2 and 26.4 ± 12.1), and JOA scores (23.6 ± 5.2 and 22.3 ± 5.7) (P > .05). Limited correction of LL in the treatment of DS patients can achieve favorable clinical outcomes including effective Cobb angle correction with less blood loss and operative time.

Sections du résumé

BACKGROUND BACKGROUND
Patients suffering from degenerative scoliosis (DS) were commonly associated with coronal and sagittal imbalance which made deformity correction surgery necessary. The study aimed to explore the efficacy and feasibility of the limited correction of lumbar lordosis (LL) in the treatment of patients with DS.
METHODS METHODS
This was a retrospective study including 58 DS patients who underwent spinal deformity correction surgery and were followed up at least 2 years between January 2013 and January 2017. According to the difference of postoperative LL, the patients were divided into 2 groups: the limited correction group: Pelvic incidence(PI)-18°≤ LL<PI-9° and the control group: PI-9°≤ LL<PI+9°. There were 31 patients in the limited group, and 27 patients in the control group. The clinical and radiographic outcomes were compared preoperatively and at the last follow-up evaluation.
RESULTS RESULTS
There was no significant difference between the 2 groups preoperatively (P > .05). In terms of surgery, the limited group had less intra-operative blood loss and operation time (P < .05). At the last follow-up, significant differences were found in terms of LL(-38.2 ± 4.7° and -46.9 ± 4.7°), PT (18.8 ± 5.2° and 11.1 ± 3.6°), sacrum slope (33.7 ± 7.0° and 41.4 ± 6.1°) (P < .05), while there were no significant differences in terms of lumbar Cobb angle (10.5 ± 9.3°and 8.3 ± 6.7°), Oswestry Disability Index scores (25.6 ± 10.2 and 26.4 ± 12.1), and JOA scores (23.6 ± 5.2 and 22.3 ± 5.7) (P > .05).
CONCLUSION CONCLUSIONS
Limited correction of LL in the treatment of DS patients can achieve favorable clinical outcomes including effective Cobb angle correction with less blood loss and operative time.

Identifiants

pubmed: 32384425
doi: 10.1097/MD.0000000000019624
pii: 00005792-202005080-00002
pmc: PMC7220324
doi:

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e19624

Références

Spine (Phila Pa 1976). 2009 Aug 1;34(17):1828-33
pubmed: 19644334
J Am Acad Orthop Surg. 2003 May-Jun;11(3):174-83
pubmed: 12828447
Neurosurg Focus. 2010 Mar;28(3):E1
pubmed: 20192655
Spine (Phila Pa 1976). 2002 Oct 15;27(20):2268-73
pubmed: 12394905
Spine (Phila Pa 1976). 2007 Sep 15;32(20):2238-44
pubmed: 17873817
Spine (Phila Pa 1976). 2012 Apr 15;37(8):693-700
pubmed: 22504517
Am J Orthop (Belle Mead NJ). 2003 Feb;32(2):77-82; discussion 82
pubmed: 12602636
J Orthop Traumatol. 2011 Dec;12(4):193-9
pubmed: 22065147
Spine (Phila Pa 1976). 2013 Mar 15;38(6):476-83
pubmed: 23492973
Spine (Phila Pa 1976). 1993 May;18(6):700-3
pubmed: 8516697
J Orthop Surg Res. 2014 Mar 07;9(1):15
pubmed: 24606963
Spine (Phila Pa 1976). 2014 Apr 15;39(8):E521-8
pubmed: 24480961
J Neurosurg Spine. 2007 Oct;7(4):387-92
pubmed: 17933311
Spine (Phila Pa 1976). 2012 Apr 20;37(9):E556-61
pubmed: 22281485
Spine (Phila Pa 1976). 2002 Feb 15;27(4):387-92
pubmed: 11840105

Auteurs

Yan Liang (Y)

Peking University People's Hospital.

Xiangyu Tang (X)

The General Hospital of Chinese People's Liberation Army (301 hospital) Beijing, China.

Yongfei Zhao (Y)

The General Hospital of Chinese People's Liberation Army (301 hospital) Beijing, China.

Kai Song (K)

The General Hospital of Chinese People's Liberation Army (301 hospital) Beijing, China.

Keya Mao (K)

The General Hospital of Chinese People's Liberation Army (301 hospital) Beijing, China.

Haiying Liu (H)

Peking University People's Hospital.

Zheng Wang (Z)

The General Hospital of Chinese People's Liberation Army (301 hospital) Beijing, China.

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Classifications MeSH