Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/35947
Title: Dynamic Posture-Related Preoperative Pain as a Single Clinical Criterion in Patient Selection for Extreme Lateral Interbody Fusion Without Direct Decompression.
Authors: Lim K.-Z.;Goldschlager T. ;Brown J. ;Daly C.
Institution: (Lim, Daly, Goldschlager) Department of Neurosurgery, Monash Health, Melbourne, VIC, Australia (Lim, Brown, Goldschlager) Department of Surgery, Monash University, Melbourne, VIC, Australia (Daly, Goldschlager) Hudson Institute of Medical Research, The Ritchie Centre, Melbourne, VIC, Australia
Issue Date: 4-Sep-2019
Copyright year: 2019
Publisher: SAGE Publications Ltd (E-mail: info@sagepub.co.uk)
Place of publication: United States
Publication information: Global Spine Journal. 9 (6) (pp 575-582), 2019. Date of Publication: 01 Sep 2019.
Journal: Global Spine Journal
Abstract: Study Design: Prospective cohort study. Objective(s): Evidence on predicting the success of indirect decompression via extreme lateral interbody fusion (XLIF) is scarce. The authors investigated if patients who could achieve a pain-free position preoperatively would derive clinical benefit from XLIF without direct decompression. Method(s): Data from 50 consecutive patients who underwent XLIF with and without direct decompression by a single surgeon from January 2014 to August 2017 was collected. Primary outcome is the rate of failure of patients who underwent XLIF without direct decompression, characterized by persistence of pain postoperatively that required reoperations within 6 months postoperatively. Secondary outcomes are clinical outcomes and patient-reported quality of life outcome data, including visual analogue scale for leg (VASL) and back (VASB) pain, Oswetry Disability Index (ODI), and Physical Component Score (PCS) and Mental Component Score (MCS) of SF-12, for up to 2 years postoperatively. Result(s): One patient with preoperative dynamic posture-related pain who underwent XLIF without direct decompression subsequently had a reoperation due to persisting pain. Statistically significant improvement was achieved across all patient reported outcomes (P <.05): improvement of 68% for VASL, 61% for VASB, 50% for ODI, 33% for PCS, and 11% for MCS of SF-12 at last follow-up. Six patients had thigh symptoms that resolved. Conclusion(s): The simple clinical criterion based on postural pain status preoperatively may help clinicians in patient selection for indirect decompression of XLIF without the need for direct decompression. Further studies with larger cohorts are warranted to establish the validity of the algorithm.Copyright © The Author(s) 2018.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1177/2192568218811317
ISSN: 2192-5682
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/35947
Type: Article
Subjects: hypotension/co [Complication]
incisional hernia/co [Complication]
leg pain
length of stay
male
neuromonitoring
osteosynthesis
Oswestry Disability Index
paresthesia/co [Complication]
*patient selection
*preoperative complication/co [Complication]
priority journal
prospective study
quality of life
radiculopathy
rehabilitation care
scoring system
spinal cord decompression
*spine fusion
spondylolisthesis
urine retention/co [Complication]
visual analog scale
weakness/co [Complication]
*extreme lateral interbody fusion
mental component score
physical component score
*preoperative pain/co [Complication]
patient-reported outcome
adult
aged
article
*body position
brain hemorrhage/co [Complication]
claudication
clinical article
clinical outcome
cohort analysis
decompression surgery
discectomy
dysesthesia/co [Complication]
female
follow up
fracture/co [Complication]
human
decompression surgery
discectomy
dysesthesia / complication
female
follow up
fracture / complication
human
hypotension / complication
incisional hernia / complication
leg pain
length of stay
neuromonitoring
osteosynthesis
Oswestry Disability Index
paresthesia / complication
*patient selection
patient-reported outcome
*preoperative complication / *complication
priority journal
prospective study
quality of life
radiculopathy
rehabilitation care
scoring system
adult
*spine fusion
spondylolisthesis
urine retention / complication
visual analog scale
weakness / complication
spinal cord decompression
aged
Article
*body position
brain hemorrhage / complication
claudication
clinical article
clinical outcome
cohort analysis
male
Type of Clinical Study or Trial: Observational study (cohort, case-control, cross sectional or survey)
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