Please use this identifier to cite or link to this item: http://hdl.handle.net/11434/1041
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dc.contributor.authorMalham, Gregory-
dc.contributor.authorBlecher, Carl-
dc.contributor.otherEllis, Ngaire-
dc.contributor.otherParker, Rhiannon-
dc.contributor.otherWhite, Rohen-
dc.contributor.otherGoss, Ben-
dc.contributor.otherSeex, Kevin-
dc.date.accessioned2017-04-21T02:27:34Z-
dc.date.available2017-04-21T02:27:34Z-
dc.date.issued2017-03-
dc.identifier.citationClin Spine Surg. 2017 Mar;30(2):E90-E98.en_US
dc.identifier.issn2380-0186en_US
dc.identifier.issn2380-0194en_US
dc.identifier.urihttp://hdl.handle.net/11434/1041-
dc.description.abstractSTUDY DESIGN: A prospective single-surgeon nonrandomized clinical study. OBJECTIVE: To evaluate the radiographic and clinical outcomes, by fixation type, in extreme lateral interbody fusion (XLIF) patients and provide an algorithm for determining patients suitable for stand-alone XLIF. SUMMARY OF BACKGROUND DATA: XLIF may be supplemented with pedicle screw fixation, however, since stabilizing structures remain intact, it is suggested that stand-alone XLIF can be used for certain indications. This eliminates the associated morbidity, though subsidence rates may be elevated, potentially minimizing the clinical benefits. MATERIALS AND METHODS: A fixation algorithm was developed after evaluation of patient outcomes from the surgeon's first 30 cases. This algorithm was used prospectively for 40 subsequent patients to determine the requirement for supplemental fixation. Preoperative, postoperative, and 12-month follow-up computed tomography scans were measured for segmental and global lumbar lordosis and posterior disk height. Clinical outcome measures included back and leg pain (visual analogue scale), Oswestry Disability Index (ODI), and SF-36 physical and mental component scores (PCS and MCS). RESULTS: Preoperatively to 12-month follow-up there were increases in segmental lordosis (7.9-9.4 degrees, P=0.0497), lumbar lordosis (48.8-55.2 degrees, P=0.0328), and disk height (3.7-5.5 mm, P=0.0018); there were also improvements in back (58.6%) and leg pain (60.0%), ODI (44.4%), PCS (56.7%), and MCS (16.1%) for stand-alone XLIF. For instrumented XLIF, segmental lordosis (7.6-10.5 degrees, P=0.0120) and disk height (3.5-5.6 mm, P<0.001) increased, while lumbar lordosis decreased (51.1-45.8 degrees, P=0.2560). Back (49.8%) and leg pain (30.8%), ODI (32.3%), PCS (37.4%), and MCS (2.0%) were all improved. Subsidence occurred in 3 (7.5%) stand-alone patients. CONCLUSIONS: The XLIF treatment fixation algorithm provided a clinical pathway to select suitable patients for stand-alone XLIF. These patients achieved positive clinical outcomes, satisfactory fusion rates, with sustained correction of lordosis and restoration of disk height.en_US
dc.publisherWolters Kluwer Health, Inc.en_US
dc.subjectRadiographic Outcomesen_US
dc.subjectClinical Outcomesen_US
dc.subjectExtreme Lateral Interbody Fusionen_US
dc.subjectLumbar Lordosisen_US
dc.subjectXLIFen_US
dc.subjectFixation Algorithmen_US
dc.subjectVisual Analogue Scaleen_US
dc.subjectOswestry Disability Indexen_US
dc.subjectPhysical Component Scoresen_US
dc.subjectMental Component Scoresen_US
dc.subjectSegmental Lordosisen_US
dc.subjectTreatmentsen_US
dc.subjectFixation Typeen_US
dc.subjectStand-Alone XLIFen_US
dc.subjectPatient Outcomesen_US
dc.subjectSupplemental Fixationen_US
dc.subjectClinical Benefitsen_US
dc.subjectGlobal Lumbar Lordosisen_US
dc.subjectPosterior Disk Heighten_US
dc.subjectODIen_US
dc.subjectPhysical Component Scoresen_US
dc.subjectPCSen_US
dc.subjectMental Component Scoreen_US
dc.subjectMCSen_US
dc.subjectSF-36en_US
dc.subjectNeurosciences Clinical Institute, Epworth HealthCare, Victoria, Australiaen_US
dc.subjectEpworth Medical Imaging, Victoria, Australiaen_US
dc.titleMaintenance of segmental lordosis and disk height in stand-alone and instrumented extreme lateral interbody fusion (XLIF).en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1097/BSD.0b013e3182aa4c94en_US
dc.identifier.journaltitleClinical Spine Surgeryen_US
dc.description.pubmedurihttps://www.ncbi.nlm.nih.gov/pubmed/28207620en_US
dc.description.affiliatesNeurosurgery Department, Macquarie University, Sydney, NSW, Australia.en_US
dc.type.studyortrialProspective Studyen_US
dc.type.contenttypeTexten_US
Appears in Collections:Diagnostic Services
Musculoskeletal
Neurosciences

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