Predictors of failure for nonoperative management of spinal epidural abscess

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dc.contributor.author Hunter, Sarah
dc.contributor.author Cussen, Robert
dc.contributor.author Baker, Joseph F.
dc.date.accessioned 2019-12-09T11:37:11Z
dc.date.available 2019-12-09T11:37:11Z
dc.date.issued 2019-11-20
dc.identifier.citation Hunter, S., Cussen, R. and Baker, J. F. 'Predictors of Failure for Nonoperative Management of Spinal Epidural Abscess', Global Spine Journal, 0(0),[in press], 2192568219887915. (7pp.) doi: 10.1177/2192568219887915 en
dc.identifier.startpage 1 en
dc.identifier.endpage 7 en
dc.identifier.issn 0362-2436
dc.identifier.uri http://hdl.handle.net/10468/9361
dc.identifier.doi 10.1177/2192568219887915 en
dc.description.abstract Study Design: Retrospective cohort study. Objectives: The aim of this study is to identify predictive factors associated with failure of nonoperative management of spinal epidural abscess (SEA). Methods: Between January 2007 and January 2017, there were 97 patients 18 years or older treated for SEA at a tertiary referral center. Of these, 58 were initially managed nonoperatively. Details on presenting complaint, laboratory parameters, radiographic evaluation, demographics, comorbidities, and neurologic status (Frankel grades A-E) were collected. Success of treatment was defined as eradication of infection with no requirement for further antimicrobial therapy. Diagnosis of SEA was made via evaluation of imaging and intraoperative findings. Patients with repeat presentation of SEA, children, and those who were transferred for immediate surgical decompression were excluded. Results:Fifty-eight patients initially treated nonoperatively were included. Of these, 21 failed nonoperative management and required surgical intervention. The mean age was 60 years, 66% male, and 19% of Maori ethnicity. Abscess location was predominantly dorsal, and in the lumbar region (53%). Multivariate analysis identified Maori ethnicity, multifocal sepsis, and elevated white cell count as predictors of failure of nonoperative management. With 1 predictor the risk of failure was 44%. In the presence of 2 predictive variables, failure rate increased to 60%, and if all 3 variables were present, patients had a 75% risk of failure. Conclusion: Thirty-six percent of patients treated nonoperatively failed nonoperative management—the failure rate was significantly increased in patients with multifocal sepsis, in patients with elevated white cell count, and in patients of Maori ethnicity. en
dc.format.mimetype application/pdf en
dc.language.iso en en
dc.publisher Lippincott, Williams & Wilkins en
dc.rights © The Author(s) 2019. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (http://www.creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). en
dc.rights.uri http://www.creativecommons.org/licenses/by-nc-nd/4.0/ en
dc.subject Spinal epidural abscess en
dc.subject Pyogenic spinal column infection en
dc.subject Risk factors en
dc.title Predictors of failure for nonoperative management of spinal epidural abscess en
dc.type Article (peer-reviewed) en
dc.internal.authorcontactother Robert Cussen, University College Cork, Cork, Ireland. +353-21-490-3000 en
dc.internal.availability Full text available en
dc.description.version Published Version en
dc.description.status Peer reviewed en
dc.identifier.journaltitle Spine en
dc.identifier.articleid 2192568219887915 en
dc.internal.bibliocheck Check, vol, issue and article ID en
dc.identifier.eissn 1528-1159


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© The Author(s) 2019. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (http://www.creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). Except where otherwise noted, this item's license is described as © The Author(s) 2019. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (http://www.creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
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