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Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study
BACKGROUND: Postoperative pneumonia (PP) is one of the common complications following esophagectomy and associated with poor short- and long-term outcomes. Sevoflurane and propofol, which have inflammatory-modulating effects, are common used general anesthetics. This study aimed to compare the effec...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715630/ https://www.ncbi.nlm.nih.gov/pubmed/29202701 http://dx.doi.org/10.1186/s12871-017-0458-4 |
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author | Zhang, Guo-Hua Wang, Wen |
author_facet | Zhang, Guo-Hua Wang, Wen |
author_sort | Zhang, Guo-Hua |
collection | PubMed |
description | BACKGROUND: Postoperative pneumonia (PP) is one of the common complications following esophagectomy and associated with poor short- and long-term outcomes. Sevoflurane and propofol, which have inflammatory-modulating effects, are common used general anesthetics. This study aimed to compare the effects of anesthesia with sevoflurane and propofol on the development of PP after esophageal surgery for cancer. METHODS: The electronic medical records of patients who underwent elective esophagectomy between July 2013 and July 2016 were reviewed. We conducted univariate and multivariate logistics analysis and propensity score matching analysis to compare the effect of sevoflurane and propofol on the incidence of PP and to identify the risk factors for PP after esophagectomy. RESULTS: Overall, the incidence of postoperative pneumonia was 9.5%. There was no significant difference in the rates of PP between sevoflurane group and propofol group either before or after propensity score matching (9.6% vs 8.0%, P = 0.606; 7.7% vs 6.4%, P = 0.754, respectively). Univariate and multivariate analysis revealed that alcohol use (OR 1.513; 95% CI 1.062–2.156), surgical procedure (Sweet: referent; Ivor-Lewis: OR 1.993; 95% CI 1.190–3.337; Three-incision: OR 1.878; 95% CI 1.296–2.722) and surgeon experience (high-volume: referent; low-volume: OR 1.525; 95% CI 1.090–2.135) were significant risk factors of postoperative pneumonia. CONCLUSIONS: Sevoflurane did not differ from propofol in terms of affecting the risk of PP development after esophagectomy. |
format | Online Article Text |
id | pubmed-5715630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57156302017-12-08 Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study Zhang, Guo-Hua Wang, Wen BMC Anesthesiol Research Article BACKGROUND: Postoperative pneumonia (PP) is one of the common complications following esophagectomy and associated with poor short- and long-term outcomes. Sevoflurane and propofol, which have inflammatory-modulating effects, are common used general anesthetics. This study aimed to compare the effects of anesthesia with sevoflurane and propofol on the development of PP after esophageal surgery for cancer. METHODS: The electronic medical records of patients who underwent elective esophagectomy between July 2013 and July 2016 were reviewed. We conducted univariate and multivariate logistics analysis and propensity score matching analysis to compare the effect of sevoflurane and propofol on the incidence of PP and to identify the risk factors for PP after esophagectomy. RESULTS: Overall, the incidence of postoperative pneumonia was 9.5%. There was no significant difference in the rates of PP between sevoflurane group and propofol group either before or after propensity score matching (9.6% vs 8.0%, P = 0.606; 7.7% vs 6.4%, P = 0.754, respectively). Univariate and multivariate analysis revealed that alcohol use (OR 1.513; 95% CI 1.062–2.156), surgical procedure (Sweet: referent; Ivor-Lewis: OR 1.993; 95% CI 1.190–3.337; Three-incision: OR 1.878; 95% CI 1.296–2.722) and surgeon experience (high-volume: referent; low-volume: OR 1.525; 95% CI 1.090–2.135) were significant risk factors of postoperative pneumonia. CONCLUSIONS: Sevoflurane did not differ from propofol in terms of affecting the risk of PP development after esophagectomy. BioMed Central 2017-12-04 /pmc/articles/PMC5715630/ /pubmed/29202701 http://dx.doi.org/10.1186/s12871-017-0458-4 Text en © The Author(s). 2017 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 Zhang, Guo-Hua Wang, Wen Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study |
title | Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study |
title_full | Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study |
title_fullStr | Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study |
title_full_unstemmed | Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study |
title_short | Effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study |
title_sort | effects of sevoflurane and propofol on the development of pneumonia after esophagectomy: a retrospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715630/ https://www.ncbi.nlm.nih.gov/pubmed/29202701 http://dx.doi.org/10.1186/s12871-017-0458-4 |
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