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Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy
BACKGROUND: Enhanced recovery after surgery (ERAS) reduces postoperative stress, increases patient satisfaction, and reduces postoperative stay and cost. In this study, we evaluated the feasibility and effectiveness of ERAS protocols compared with conventional perioperative care group and their effe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145634/ https://www.ncbi.nlm.nih.gov/pubmed/30271200 http://dx.doi.org/10.2147/CMAR.S168909 |
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author | Ji, Weiping Chandoo, Arvine Guo, Xiaoling You, Tao Shao, Zhuo Zheng, Kailian Wang, Juan Bi, Jianwei Smith, Fang Gao Tucker, Olga N Shen, Xian |
author_facet | Ji, Weiping Chandoo, Arvine Guo, Xiaoling You, Tao Shao, Zhuo Zheng, Kailian Wang, Juan Bi, Jianwei Smith, Fang Gao Tucker, Olga N Shen, Xian |
author_sort | Ji, Weiping |
collection | PubMed |
description | BACKGROUND: Enhanced recovery after surgery (ERAS) reduces postoperative stress, increases patient satisfaction, and reduces postoperative stay and cost. In this study, we evaluated the feasibility and effectiveness of ERAS protocols compared with conventional perioperative care group and their effect in gastric cancer patients undergoing gastrectomy. METHODS: A cohort of 366 patients were analyzed from a prospectively maintained database. The patients’ characteristics, tumor profile, surgical information data and postoperative complications were evaluated. RESULTS: Patients in the ERAS had a faster gastrointestinal function recovery and first flatus (3.26±0.64; P<0.001). Pain intensity of patients in the ERAS group was significantly lower than that of patients in the conventional care group on postoperative days 1 (2.33±0.98; P<0.001) and 3 (1.06±0.63; P<0.001). Postoperative hospital stays were significantly shorter in patients receiving ERAS program (6.66±3.36; P<0.001), than in those patients who received conventional perioperative care (9.02±2.61). CONCLUSION: ERAS can reduce postoperative stress, enhance the recovery of the gut, reduce the pain intensity, and increase satisfaction in gastric cancer patient undergoing curative gastrectomy. |
format | Online Article Text |
id | pubmed-6145634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61456342018-09-28 Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy Ji, Weiping Chandoo, Arvine Guo, Xiaoling You, Tao Shao, Zhuo Zheng, Kailian Wang, Juan Bi, Jianwei Smith, Fang Gao Tucker, Olga N Shen, Xian Cancer Manag Res Original Research BACKGROUND: Enhanced recovery after surgery (ERAS) reduces postoperative stress, increases patient satisfaction, and reduces postoperative stay and cost. In this study, we evaluated the feasibility and effectiveness of ERAS protocols compared with conventional perioperative care group and their effect in gastric cancer patients undergoing gastrectomy. METHODS: A cohort of 366 patients were analyzed from a prospectively maintained database. The patients’ characteristics, tumor profile, surgical information data and postoperative complications were evaluated. RESULTS: Patients in the ERAS had a faster gastrointestinal function recovery and first flatus (3.26±0.64; P<0.001). Pain intensity of patients in the ERAS group was significantly lower than that of patients in the conventional care group on postoperative days 1 (2.33±0.98; P<0.001) and 3 (1.06±0.63; P<0.001). Postoperative hospital stays were significantly shorter in patients receiving ERAS program (6.66±3.36; P<0.001), than in those patients who received conventional perioperative care (9.02±2.61). CONCLUSION: ERAS can reduce postoperative stress, enhance the recovery of the gut, reduce the pain intensity, and increase satisfaction in gastric cancer patient undergoing curative gastrectomy. Dove Medical Press 2018-09-13 /pmc/articles/PMC6145634/ /pubmed/30271200 http://dx.doi.org/10.2147/CMAR.S168909 Text en © 2018 Ji et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Ji, Weiping Chandoo, Arvine Guo, Xiaoling You, Tao Shao, Zhuo Zheng, Kailian Wang, Juan Bi, Jianwei Smith, Fang Gao Tucker, Olga N Shen, Xian Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy |
title | Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy |
title_full | Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy |
title_fullStr | Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy |
title_full_unstemmed | Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy |
title_short | Enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy |
title_sort | enhanced recovery after surgery decreases intestinal recovery time and pain intensity in patients undergoing curative gastrectomy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145634/ https://www.ncbi.nlm.nih.gov/pubmed/30271200 http://dx.doi.org/10.2147/CMAR.S168909 |
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