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Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days
AIM: In recent years, with the concept of damage control resuscitation, hemostasis and preoperative fluid restriction have been carried out, but there is controversy regarding the effectiveness of fluid restriction. METHODS: From April 2007 to March 2013, 101 trauma patients presented with hemorrhag...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891115/ https://www.ncbi.nlm.nih.gov/pubmed/29657727 http://dx.doi.org/10.1002/ams2.328 |
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author | Matsuyama, Shigenari Miki, Ryusuke Kittaka, Hirotada Nakayama, Haruki Kikuta, Shota Ishihara, Satoshi Nakayama, Shinichi |
author_facet | Matsuyama, Shigenari Miki, Ryusuke Kittaka, Hirotada Nakayama, Haruki Kikuta, Shota Ishihara, Satoshi Nakayama, Shinichi |
author_sort | Matsuyama, Shigenari |
collection | PubMed |
description | AIM: In recent years, with the concept of damage control resuscitation, hemostasis and preoperative fluid restriction have been carried out, but there is controversy regarding the effectiveness of fluid restriction. METHODS: From April 2007 to March 2013, 101 trauma patients presented with hemorrhagic shock (systolic blood pressure ≤90 mmHg) at the prehospital or emergency department and were admitted to Hyogo Emergency Medical Center (Hyogo, Japan). They underwent emergency hemostasis by surgery and transcatheter arterial embolization. We compared two groups in a historical cohort study, the aggressive fluid resuscitation (AR) group, which included 59 cases treated in the period April 2007–March 2010, and the fluid restriction (FR) group, which included 42 cases treated in the period April 2010–March 2013. RESULTS: There was no difference between both groups in patient background (heart rate, 110 b.p.m.; systolic blood pressure, 70 mmHg). The Injury Severity Score was 34 (AR) versus 38 (FR) (not significant). Preoperative infusion volume of crystalloid significantly decreased, from 2310 mL (AR) to 1025 mL (FR) (P ≤ 0.01). There was no difference in mortality (36% [AR] versus 41% [FR]). Ventilator days significantly decreased, from 8.5 days (AR) to 5.5 days (FR) (P = 0.02). CONCLUSIONS: Preoperative fluid restriction for trauma patients with hemorrhagic shock did not improve mortality, but it decreased ventilator days by reducing the perioperative plus water balance and it might contribute to perioperative intensive care. |
format | Online Article Text |
id | pubmed-5891115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58911152018-04-13 Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days Matsuyama, Shigenari Miki, Ryusuke Kittaka, Hirotada Nakayama, Haruki Kikuta, Shota Ishihara, Satoshi Nakayama, Shinichi Acute Med Surg Original Articles AIM: In recent years, with the concept of damage control resuscitation, hemostasis and preoperative fluid restriction have been carried out, but there is controversy regarding the effectiveness of fluid restriction. METHODS: From April 2007 to March 2013, 101 trauma patients presented with hemorrhagic shock (systolic blood pressure ≤90 mmHg) at the prehospital or emergency department and were admitted to Hyogo Emergency Medical Center (Hyogo, Japan). They underwent emergency hemostasis by surgery and transcatheter arterial embolization. We compared two groups in a historical cohort study, the aggressive fluid resuscitation (AR) group, which included 59 cases treated in the period April 2007–March 2010, and the fluid restriction (FR) group, which included 42 cases treated in the period April 2010–March 2013. RESULTS: There was no difference between both groups in patient background (heart rate, 110 b.p.m.; systolic blood pressure, 70 mmHg). The Injury Severity Score was 34 (AR) versus 38 (FR) (not significant). Preoperative infusion volume of crystalloid significantly decreased, from 2310 mL (AR) to 1025 mL (FR) (P ≤ 0.01). There was no difference in mortality (36% [AR] versus 41% [FR]). Ventilator days significantly decreased, from 8.5 days (AR) to 5.5 days (FR) (P = 0.02). CONCLUSIONS: Preoperative fluid restriction for trauma patients with hemorrhagic shock did not improve mortality, but it decreased ventilator days by reducing the perioperative plus water balance and it might contribute to perioperative intensive care. John Wiley and Sons Inc. 2018-02-12 /pmc/articles/PMC5891115/ /pubmed/29657727 http://dx.doi.org/10.1002/ams2.328 Text en © 2018 The Authors. Acute Medicine & Surgery published by John Wiley & Sons Australia, Ltd on behalf of Japanese Association for Acute Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Matsuyama, Shigenari Miki, Ryusuke Kittaka, Hirotada Nakayama, Haruki Kikuta, Shota Ishihara, Satoshi Nakayama, Shinichi Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days |
title | Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days |
title_full | Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days |
title_fullStr | Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days |
title_full_unstemmed | Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days |
title_short | Preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days |
title_sort | preoperative fluid restriction for trauma patients with hemorrhagic shock decreases ventilator days |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891115/ https://www.ncbi.nlm.nih.gov/pubmed/29657727 http://dx.doi.org/10.1002/ams2.328 |
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