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External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort

BACKGROUND: A prediction model for surgical site infection (SSI) after spine surgery was developed in 2014 by Lee et al. This model was developed to compute an individual estimate of the probability of SSI after spine surgery based on the patient’s comorbidity profile and invasiveness of surgery. Be...

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Autores principales: Janssen, Daniël M. C., van Kuijk, Sander M. J., d’Aumerie, Boudewijn B., Willems, Paul C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956755/
https://www.ncbi.nlm.nih.gov/pubmed/29769095
http://dx.doi.org/10.1186/s13018-018-0821-2
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author Janssen, Daniël M. C.
van Kuijk, Sander M. J.
d’Aumerie, Boudewijn B.
Willems, Paul C.
author_facet Janssen, Daniël M. C.
van Kuijk, Sander M. J.
d’Aumerie, Boudewijn B.
Willems, Paul C.
author_sort Janssen, Daniël M. C.
collection PubMed
description BACKGROUND: A prediction model for surgical site infection (SSI) after spine surgery was developed in 2014 by Lee et al. This model was developed to compute an individual estimate of the probability of SSI after spine surgery based on the patient’s comorbidity profile and invasiveness of surgery. Before any prediction model can be validly implemented in daily medical practice, it should be externally validated to assess how the prediction model performs in patients sampled independently from the derivation cohort. METHODS: We included 898 consecutive patients who underwent instrumented thoracolumbar spine surgery. To quantify overall performance using Nagelkerke’s R(2) statistic, the discriminative ability was quantified as the area under the receiver operating characteristic curve (AUC). We computed the calibration slope of the calibration plot, to judge prediction accuracy. RESULTS: Sixty patients developed an SSI. The overall performance of the prediction model in our population was poor: Nagelkerke’s R(2) was 0.01. The AUC was 0.61 (95% confidence interval (CI) 0.54–0.68). The estimated slope of the calibration plot was 0.52. CONCLUSIONS: The previously published prediction model showed poor performance in our academic external validation cohort. To predict SSI after instrumented thoracolumbar spine surgery for the present population, a better fitting prediction model should be developed.
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spelling pubmed-59567552018-05-24 External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort Janssen, Daniël M. C. van Kuijk, Sander M. J. d’Aumerie, Boudewijn B. Willems, Paul C. J Orthop Surg Res Research Article BACKGROUND: A prediction model for surgical site infection (SSI) after spine surgery was developed in 2014 by Lee et al. This model was developed to compute an individual estimate of the probability of SSI after spine surgery based on the patient’s comorbidity profile and invasiveness of surgery. Before any prediction model can be validly implemented in daily medical practice, it should be externally validated to assess how the prediction model performs in patients sampled independently from the derivation cohort. METHODS: We included 898 consecutive patients who underwent instrumented thoracolumbar spine surgery. To quantify overall performance using Nagelkerke’s R(2) statistic, the discriminative ability was quantified as the area under the receiver operating characteristic curve (AUC). We computed the calibration slope of the calibration plot, to judge prediction accuracy. RESULTS: Sixty patients developed an SSI. The overall performance of the prediction model in our population was poor: Nagelkerke’s R(2) was 0.01. The AUC was 0.61 (95% confidence interval (CI) 0.54–0.68). The estimated slope of the calibration plot was 0.52. CONCLUSIONS: The previously published prediction model showed poor performance in our academic external validation cohort. To predict SSI after instrumented thoracolumbar spine surgery for the present population, a better fitting prediction model should be developed. BioMed Central 2018-05-16 /pmc/articles/PMC5956755/ /pubmed/29769095 http://dx.doi.org/10.1186/s13018-018-0821-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Janssen, Daniël M. C.
van Kuijk, Sander M. J.
d’Aumerie, Boudewijn B.
Willems, Paul C.
External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort
title External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort
title_full External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort
title_fullStr External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort
title_full_unstemmed External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort
title_short External validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a Western European cohort
title_sort external validation of a prediction model for surgical site infection after thoracolumbar spine surgery in a western european cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956755/
https://www.ncbi.nlm.nih.gov/pubmed/29769095
http://dx.doi.org/10.1186/s13018-018-0821-2
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